Digital fluid teleportation, advanced biovirtualization, and large-scale integration of organ-on-chip and biomimetic models.

Abstract

This provides a method for predicting the biological behavior of target tissues. [Solution] The biomimetic platform includes a fluid synthesis device having a first fluid input unit selectively coupled to a source of a first input fluid solution, and a second fluid input unit selectively coupled to a source of a second input fluid solution. The fluid synthesis device further includes a fluid output unit. The biomimetic platform further includes a fluid addressing system having a fluid input unit fluidly coupled to the fluid output unit of the fluid synthesis device. The fluid addressing system further includes a first fluid output unit and a second fluid output unit. The biomimetic platform further includes a first biomimetic device having a fluid input unit fluidly coupled to the first fluid output unit of the fluid addressing system, and a second biomimetic device having a fluid input unit fluidly coupled to the second fluid output unit of the fluid addressing system.

Description

Background Art

[0001] Certain types of organ-on-chip devices can include microengineered biological cell culture compartments where tissue-level and organ-level elements of human physiology can be reproduced. Cells transplanted therein are expected to function and organize in a physiologically realistic and relevant manner, enabling accurate in vitro modeling of functional biological units of organ systems.

[0002] However, certain biofunctional chip systems cannot construct functional and realistic multi-organ networks, and thus cannot reproduce complex physiological reactions and multi-organ interactions at the whole-body level. Each biofunctional chip may require growth media of different compositions formulated with hormones, nutrients, and other molecules to mimic the natural microenvironment of the tissue of its specific organ. Since different cell types require different biochemical cues to maintain differentiated functions in different organs, it can be difficult to create a single universal media composition that can be carried between organ units and simultaneously support proper differentiation and long-term maintenance of all these multiple organ units.

[0003] Furthermore, in order to make these biofunctional chip devices into practical screening platforms, there may be a problem that the operation of these devices is complex. For example, the fluid within certain biofunctional chip devices needs to be driven either by a bulky syringe pump or manually by a researcher using a pipette. In processes such as screening of drug candidates, automated high-volume and high-throughput tests are required, and such throughput reduction may limit the adoption of biofunctional chip models in the pharmaceutical industry.

[0004] Therefore, there remains a need to improve the throughput and efficiency of the bio-chip devices. Furthermore, there is a need for improved bio-chip devices that can enable the specific transmission of cell-released signaling molecules, including hormones, between organs or tissues, while allowing specific growth medium formulations, which can define a particular tissue microenvironment, to be directed only to the organs in which they are intended. [Overview of the project]

[0005] Embodiments described herein relate to biomimetic platforms and methods for manufacturing the same. In some embodiments, the biomimetic platform may include a fluid synthesizer having a first fluid input section selectively coupled to a source of a first input fluid solution and a second fluid input section selectively coupled to a source of a second input fluid solution. The fluid synthesizer may further include a fluid output section. The fluid synthesizer may produce an output solution by mixing a first input fluid solution received from the first fluid input section with a second input fluid solution received from the second fluid input section, and discharge the output solution from the fluid output section. The biomimetic platform may further include a fluid addressing system having a fluid input section fluidically coupled to the fluid output section of the fluid synthesizer. The fluid addressing system may further include a first fluid output section and a second fluid output section. The fluid addressing system may transmit the output solution from the fluid input section of the fluid addressing system to one or both of the first and second fluid output sections. The biomimetic platform further includes a first biomimetic device having a fluid input unit fluidly coupled to the first fluid output unit of the fluid addressing system, and a second biomimetic device having a fluid input unit fluidly coupled to the second fluid output unit of the fluid addressing system. Each of the first and second biomimetic devices cultures biological tissue and perfuses the biological tissue with the output solution from the fluid synthesizer received at the fluid input unit of each biomimetic device via the fluid addressing system. In some embodiments, the fluid synthesizer has at least a third fluid input unit selectively coupled to at least a source of at least a third input fluid solution, and is further operable to produce the output solution by mixing one or both of the first input fluid solution received from the first fluid input unit and the second input fluid solution received from the second fluid input unit with at least a third input fluid solution received at at least a third fluid input unit.In some embodiments, the fluid synthesis apparatus may include a mixing chamber that is fluidly coupled to the fluid input and fluid output sections of the fluid synthesis apparatus and mixes the input fluid solution to produce the output solution. [Brief explanation of the drawing]

[0006] Throughout the figures, unless otherwise specified, the same reference numerals and letters are used to indicate similar features, elements, components, or parts of the illustrated embodiments. Furthermore, this disclosure will be described in detail hereafter with reference to the illustrated embodiments. [Figure 1] Figure 1 is a schematic diagram of a biomimetic platform according to one embodiment. [Figure 2] Figure 2A is a schematic diagram of the control system according to an embodiment, and Figure 2B is a schematic diagram of the biomimetic platform of Figure 1 engaged with the control system according to an embodiment. [Figure 3] Figure 3 is a schematic diagram showing the fluid synthesis apparatus of the biomimetic platform in Figure 1, according to an embodiment. [Figure 4] Figure 4 is a schematic diagram illustrating the fluid addressing system of the biomimetic platform shown in Figure 1, according to an embodiment. [Figure 5] Figures 5A to 5C are schematic diagrams showing one embodiment of a biomimetic device included in the biomimetic platform of Figure 1, respectively. Figure 5B is a schematic diagram of a horizontally configured biomimetic device, and Figure 5C is a schematic diagram of a vertically configured biomimetic device. [Figure 6] Figure 6A is a schematic top view of the arrangement of the biomimetic device and biosensor according to an embodiment; Figure 6B is an illustrative diagram of organ tissue culture included in the biomimetic device of Figures 6A and 6B; and Figure 6D is a detailed schematic top view of the biosensor of Figures 6A and 6B. [Figure 7]Figure 7A is a schematic diagram showing the increase in individual biomimetic devices using on-chip fluid synthesis equipment, and Figure 7B is a schematic diagram showing how individual biomimetic devices using on-chip fluid synthesis equipment are integrated into a single monolithic biomimetic platform. [Figure 8] Figure 8A is an explanatory diagram of a microphysiological platform according to one embodiment, which integrates a number of individual biomimetic devices and associated sensors into a single multilayer microfluidic device. Figures 8B, 8C, and 8D show a part of the biomimetic platform, illustrating the multilayer microfluidic device according to the embodiment. [Figure 9] Figure 9 is a schematic diagram of a fluid teleportation system according to one embodiment. [Figure 10] Figure 10 is a schematic diagram of a fluid teleportation system according to one embodiment. [Figure 11] Figures 11A to 11D are schematic diagrams illustrating different connection configurations of a fluid teleportation system according to various embodiments. [Figure 12] Figure 12 is a schematic diagram of a human function chip model, which includes multiple biomimetic devices, each replicating the physiology or function of a specific human tissue, organ, or system, and each connected to one or more other devices by digital fluid teleportation. [Figure 13] Figure 13 is a flowchart illustrating a fluid teleportation method according to one embodiment. [Figure 14] Figure 14 is an illustrative diagram illustrating an exemplary system hardware basic design concept of a biomimetic system including multiple biomimetic platforms, according to one embodiment. [Figure 15] Figures 15A and 15B are flowcharts illustrating a screen-forward mode method of fluid teleportation according to one embodiment. [Figure 16] Figures 16A to 16D are flow diagrams illustrating a screen-backward mode method for fluid transport according to one embodiment. [Figure 17]Figure 17A is an illustrative diagram of an exemplary user interface view of the system software, and Figure 17B is an illustrative diagram of an exemplary biomimetic device interconnection used in this exemplary embodiment to illustrate an active fluid teleportation connection according to one embodiment. [Figure 18] Figure 18 is an illustrative diagram illustrating an example of data collection using a virtual organization related to this disclosure. [Figure 19] Figure 19A is an illustrative diagram of exemplary coupling of a biomimetic device including a fluid synthesis device, a biological culture chamber, and a biosensor with another biomimetic device; Figure 19B is an illustrative diagram of exemplary coupling of a single biomimetic device with a dynamic system of multiple virtual tissues using exemplary embodiments of digital fluid teleportation as interconnection; Figure 19B is an illustrative diagram of exemplary coupling of a single biomimetic device to a dynamic system of multiple virtual tissues using exemplary embodiments of digital fluid teleportation as interconnection according to the present disclosure; and Figure 19C is an illustrative diagram of exemplary interfaces in which multiple virtual tissues are brought together by exemplary use of digital fluid teleportation to form a complete virtual according to various embodiments. [Figure 20] Figure 20 is a schematic diagram of a control device, such as the main control device of a control system, according to one embodiment. [Modes for carrying out the invention]

[0007] The disclosed subject matter provides systems and methods for one or more biomimetic devices, including integration, management, automation, analog interconnection, digital interconnection, maintenance, observation, analysis, or electronic control, or a combination thereof.

[0008] A technology for manufacturing a biomimetic platform comprising one or more biomimetic devices is disclosed herein. The disclosed subject matter allows for fully or partially automated biological culture to be performed using the biomimetic devices without requiring specialized personnel. In certain embodiments, feedforward and feedback effects between modeled biological systems or tissues can be modeled in multiple biomimetic devices, which can interconnect one or more subsets.

[0009] Basic design concepts for biomimetic platforms and control systems Figure 1 is a schematic diagram of a biomimetic platform 100 according to one embodiment. As shown in Figure 1, the biomimetic platform 100 may include a fluid synthesizer 110, a fluid addressing system, an array of biomimetic devices 130, an array of biosensors 140, a sensor data transmitter 150, and an outflow channel 160. Fluids can flow into the platform 100, such as the fluid input section 112 of the fluid synthesizer 110, through and between the components, and out of the platform 100, such as the fluid output section 164 of the outflow channel 160. Such fluids may include a cleaning fluid and one or more input solutions. As will be described in more detail below with reference to Figure 3, multiple input solutions received at the fluid input section 112 of the fluid synthesizer 110 can, in some embodiments, be mixed within the fluid synthesizer 110 under the control of a control input received by the fluid synthesizer 110, and the resulting customized solution can be output from the fluid output section 114. The fluid output section 114 is fluidically coupled to the fluid input section 122 of the fluid addressing system 120. As described below with reference to Figure 4, the fluid addressing system 120 can route individual boluses or continuous flows of the output solution from the fluid input unit 122 to one of the selected fluid output units 124. The routing of the fluid is controlled by a control input received by the fluid addressing system 120. Each fluid output unit 124 is fluidically connected to the input of a specific biomimetic device 130 in the array of biomimetic devices 130. As described in more detail below with reference to Figures 5A to 5C, each biomimetic device 130 may be implemented as an organ on a chip, and the solution delivered to the input of the biomimetic device 130 may interact with the contents of the device 130 and change its composition before reaching the output of the device 130. The output of the device 130 is fluidically connected to the input of one or more biosensors 140 in the array of biosensors 140 so that the boluses of the modified fluid can be received by one or more of the biosensors 140.As will be described in more detail below with partial reference to Figures 6A to 6D, each biosensor 140 can detect or measure one or more properties of the modified solution and generate a data signal indicating one or more properties. In some embodiments, the generated sensor data can be communicated to a sensor data transmitter 150, which can transmit the sensor data via a data output unit 154 to be received by a data receiver separate from the biomimetic platform 100. In some embodiments, the generated sensor data can be read directly from the biosensor 140 (i.e., without using the sensor data transmitter 150). In other words, the generated sensor data can be read without using a data transmission system. Each biosensor 140 has a liquid output that is fluidically connected to the input of the outflow channel 160 so that the modified fluid can be transported from the biosensor 140 to the outflow channel 160 and discharged from there to an outflow fluid separate from the biomimetic platform 100 via a fluid output unit 164 of the outflow channel 160. In some embodiments, the fluid output unit 164 can be routed for fluid reuse. In some embodiments, the fluid output unit 164 can route the fluid back to the fluid addressing system 120. In some embodiments, the fluid output unit 164 can route the fluid back to the fluid synthesizer 110. In some embodiments, the fluid output unit 164 can route the fluid back to the array of the biomimetic devices 130. In some embodiments, the fluid output unit 164 can undergo further processing before being reintegrated into the biomimetic platform 100.

[0010] In some embodiments, the fluid synthesis apparatus 110 can produce a microliter of a predetermined fluid mixture to perform conditional or combined cleaning on all or some of the biomimetic devices 130 within the biomimetic platform 100. In some embodiments, the fluid synthesis apparatus 110 can produce a specified fluid mixture in an amount ranging from less than a nanoliter to more than 1 milliliter. In some embodiments, the amount of one or more fluid mixtures produced depends on the requirements of a particular platform, intended experiment, biosystem, or combination thereof.

[0011] In some embodiments, the fluid addressing system 120 can be controlled manually, semi-automatically, or automatically to dynamically change which individual biomimetic devices or which subset of biomimetic devices are selected as input fluids or outputs for fluid delivery. In certain embodiments, the fluid addressing system 120 may include at least one valve configured to redirect the flow of the fluid mixture to a plurality of selected outputs or biomimetic devices 130.

[0012] In some embodiments, the fluid synthesis device 110 can repeatedly generate at least one target fluid mixture that can be delivered to a plurality of biomimetic devices 130 by the fluid addressing system 120. In non-limiting embodiments, such operation can be autonomously cyclical to create an automated biomimetic platform.

[0013] In some embodiments, the biomimetic platform 100 can include a first fluid synthesizer 110 for creating a first fluid mixture, a first fluid addressing system 120 for routing the first fluid mixture to all or a subset of at least one biomimetic device 130, and at least one biomimetic device 130 for culturing biological tissue or material with the first fluid mixture to produce a second fluid mixture. For example, the second fluid mixture can be produced by biochemical interactions between the first fluid mixture and the first biomimetic device.

[0014] In some embodiments, the biological tissue can include lung tissue, bone marrow tissue, bone tissue, pancreatic tissue, islet tissue, liver tissue, kidney tissue, placental tissue, eye tissue, intestinal tissue, bladder tissue, brain tissue, oral tissue, tongue tissue, dental tissue, nasal tissue, thymus tissue, lymph node tissue, lymphatic tissue, laryngeal tissue, or any combination thereof. In some embodiments, the biological tissue can include specific human tissue. In some embodiments, the specific human tissue can include one or more of a human organ, an organ subcomponent, a system of two or more organs, a system of general tissue elements (e.g., blood vessels or ligaments), or a specific cell type (e.g., fibroblasts that may be involved in a behavior of interest such as fibrosis). In some embodiments, the biological tissue can include specific human tissue that undergoes specific daily operations, lung tissue that breathes periodically, specific human tissue that undergoes an atypical condition, lung tissue that undergoes an asthma attack, specific human tissue that undergoes a specific interaction with an external drug, lung tissue that is infected with bacteria, lung tissue that is exposed to environmental factors, lung tissue that is exposed to contamination, lung tissue that is exposed to corrosive gases, specific human tissue that undergoes a specific interaction with an external drug intended to be used as a therapeutic agent, specific human tissue that undergoes a specific interaction with a drug, specific human tissue that undergoes a specific interaction with a biological antibody, specific human tissue that undergoes a specific interaction with a cell therapy, lung tissue that has undergone an asthma attack while monitoring the interaction with a bronchodilator as a treatment for asthma, or any combination thereof.

[0015] In some embodiments, the biosensor 140 can include at least one chemical sensor. In some embodiments, the at least one chemical sensor can be coupled to the at least one biomimetic device 130 to detect a target analyte in the second fluid mixture. In some embodiments, the at least one chemical sensor can include a thin conductive film for generating a resonant plasmon coupling with incident light and at least one biorecognition molecule for binding to at least one target analyte to form an SPR sensor. The thin film is configured to induce a perturbation or shift transmissible to the resonant coupling when the at least one biorecognition molecule binds to the target analyte. In a non-limiting embodiment, the at least one multiplexed plasmonic biosensor can include a transducer for transmitting measured target analyte data (e.g., the name and concentration of the target analyte) to an external receiver. In some embodiments, the biomimetic platform 100 can be configured to monitor and / or process the measured target analyte data and can include at least one external receiver. In some embodiments, the at least one sensor can utilize at least one sensing modality in addition to the SPR chemical sensing.

[0016] The biomimetic platform 100 is supported by a control system 170 schematically shown in Figure 2A, from which it receives fluid and control inputs and provides data and fluid output units. As shown in Figure 2A, the control system 170 may include a control unit, a data system 180, an engagement system 185, and a fluid system 190. The control unit may include a main control unit 172, one or more fluid synthesis device control units 174, one or more addressing system control units 176, and an external communicator 178. The data system 180 may include an imaging device 182 and one or more sensor data receivers 181. The engagement system 185 may include a mechanical support 186, one or more fluid couplings 187, and one or more control line couplings 188. The fluid system 190 may include one or more input solution containers 192, one or more wash solution containers 194, one or more fluid handlers 195, and one or more effluent containers 196.

[0017] For example, the control system 170 may include fluid containers such as a cleaning fluid container 194 and a container for the input solution of the fluid synthesizer 110, and / or provide fluid conduits to fluidically connect containers outside the control system 170 to supply fluid to each of the inputs on the biomimetic platform 100. It may also provide a container for a fluid output section 164 from the outflow passage 160 of the biomimetic platform 100, and / or provide fluid conduits to fluidically connect the(s) outflow containers outside the control system 170. The control system 170 may also include one or more controllers, such as the fluid synthesizer controller 174 which controls the operation of the fluid synthesizer 110 (e.g., controls the application of pneumatic pressure to valves within the fluid synthesizer 110), and the addressing system controller 176 which controls the operation of the fluid addressing system 120 (e.g., communicates with valves within the fluid addressing system 120 to guide the fluid flow). The control system 170 may include a data receiver 181 for receiving sensor data provided by the sensor data transmitter(s) 150 associated with the biosensor. It may also include an imaging device 182 (such as a charge-coupled device, active pixel sensor, optical microscope, magnetic resonance imaging device, computed tomography device, or MOS field-effect transistor sensor) capable of acquiring image data from the biomimetic device 130 and / or the biosensor 140. The control system 170 may also include a main control unit for receiving data from and / or providing instructions to other control devices and components, and may communicate with other devices or systems outside of the control system 170.

[0018] In some embodiments, the fluid handler 195 can selectively deliver fluid directly to a desired location on the biomimetic platform 100, including any one in the array of biomimetic devices 130. In other words, each of the biomimetic devices 130 can receive fluid not only from the fluid handler 195 but also from the fluid addressing system 120. In some embodiments, the fluid handler 195 may include one or more microinjectors and / or one or more pipettes. In some embodiments, the fluid handler 195 may be movable so that it can deliver fluid to a designated biomimetic device 130 in the array of biomimetic devices 130. This direct delivery can limit fluid loss. For example, if fluid A has been delivered to a designated biomimetic device 130 and a user needs to deliver fluid B to the biomimetic device 130, the user can do so without flushing fluid A out of the fluid addressing system 120 and the fluid synthesizer 110. This direct delivery capability can improve time efficiency because the user does not need to take time to flush out the fluid A line before delivering fluid B to the desired site. In some embodiments, the fluid handler 195 can be coupled to the same port on the biomimetic device 130 as the fluid addressing system 120. In some embodiments, the fluid addressing system 120 can be coupled to a first port on the biomimetic device 130, and the fluid handler 195 can be coupled to a second port on the biomimetic device 130.

[0019] In some embodiments, the fluid handler 195 can deliver fluid to an upstream location of the biomimetic device 130 (for example, upstream of the interface between the fluid addressing system 120 and the biomimetic device 130). In some embodiments, the fluid handler 195 can deliver fluid inline to the biomimetic device 130. In other words, ports can be integrated into one or more parts of the biomimetic device 130 for access by the fluid handler 195. In some embodiments, the fluid handler 136 can deliver fluid to a downstream location of the biomimetic device 130. In some embodiments, each of the biomimetic devices 130 may include a valve for injection from the fluid handler 195.

[0020] In some embodiments, the fluid handler 195 can draw fluid from one or more of the biomimetic devices 130. In some embodiments, the fluid handler 195 can draw fluid from a position upstream of the biomimetic devices 130. In some embodiments, the fluid handler 195 can draw fluid from an inline position relative to the biomimetic devices 130. In some embodiments, the fluid handler 195 can draw fluid from a position downstream of the biomimetic devices 130.

[0021] In some embodiments, the fluid handler 195 can deliver tissue, tissue precursor, stem cells, or any combination thereof to the biomimetic device 130. In some embodiments, the fluid handler 195 is used to express tissue in situ in the biomimetic device 130. In some embodiments, the tissue is expressed in the fluid handler 195.

[0022] In some embodiments, the fluid handler 195 can deliver or withdraw fluid from any part of the biomimetic platform 100. In some embodiments, the fluid handler 195 can deliver fluid to the fluid synthesizer 110. In some embodiments, the fluid handler 195 can withdraw fluid from the fluid synthesizer 110. In some embodiments, the fluid handler 195 can deliver fluid to the fluid addressing system 120. In some embodiments, the fluid handler 195 can withdraw fluid from the fluid addressing system 120. In some embodiments, the fluid handler 195 can deliver fluid to the biomimetic device 130. In some embodiments, the fluid handler 195 can withdraw fluid from the biomimetic device 130.

[0023] Figure 2B is a schematic diagram of one biomimetic platform 100 engaged with a control system 170. As shown, the mechanical support 186 positions the substrate 101 in contact with one or more components of the control system 170. In some embodiments, the mechanical support 186 may include clamps to engage with the substrate 101 and hold the substrate 101 in an operational relationship with one or more components of the control system 170. For example, the mechanical support 186 may support the substrate 101 in a read / write drive. In some embodiments, the mechanical support 186 may include structural components to hold the control line coupling 188 and the fluid coupling 187 in place. For example, the mechanical support 186 may include one or more platforms or clamps to hold the control line coupling 188 and the fluid coupling 187 in place. In some embodiments, the mechanical support 186 may function as, or include, a connecting tube for fluid coupling (for example, between the fluid synthesizer 110 and the fluid addressing system 120). In some embodiments, the mechanical support 186 may align the substrate 101 to a known position. In some embodiments, the position of the substrate 101 may be constrained so that one or more alignment pins (not shown) on the mechanical support 186, whose positions are known to the positioning system in the fluid handler 195 and the imaging device 182, can function as a reference for the position of different items. In some embodiments, these items may include tissue, objects of interest on the substrate 101, and / or the substrate 101 itself.

[0024] In some embodiments, the fluid coupling 187 can fluidly couple the wash container 194, the input solution container 192, and the effluent container 196 to the fluid synthesizer 110, the fluid addressing system 120, and the biomimetic device 130. In some embodiments, the fluid coupling 187 is established at an input to a component of the biomimetic rat form 100 (e.g., an input to the fluid synthesizer 110). In some embodiments, the fluid coupling 187 is established with an output from the biomimetic rat form 100 (e.g., the output from the outflow channel 160). In some embodiments, the control line coupling 188 is established with an input to a component of the biomimetic rat form 100 (e.g., an input to the fluid synthesizer 110). In some embodiments, the control line coupling 188 is established with an output from the biomimetic rat form 100 (e.g., the output from the outflow channel 160).

[0025] In some embodiments, the data receiver 181 can establish communication with the sensor data transmitter 150. In some embodiments, the data receiver 181 is configured to operate to perform passive readings from the biosensor 140.

[0026] In some embodiments, the imaging device 182 is configured to operate in order to image components of the biomimetic platform. In some embodiments, the imaging device 182 can use optical imaging techniques to detect fluids in the fluid synthesis device 110, the fluid addressing system 120, and / or various parts of the biomimetic device 130. In some embodiments, the imaging device 182 can be used to detect the type of cells or cell cultures within the biomimetic device 130 based on how light is absorbed, reflected, or scattered from the biomimetic device 130.

[0027] In some embodiments, the main control unit 172 can control the fluid blending device control unit 174, the addressing system control unit 176, the data receiver 181, and the imaging device 182. In some embodiments, the fluid blending device control unit 174 can control the valve opening and the fluid flow rate into and / or out of the fluid blending device 110 (i.e., the control line coupling 188). For example, a user can specify a particular mixing ratio and flow rate to be delivered to the fluid addressing system 120 via the fluid blending device control unit 174, and can open and close the appropriate valves within the fluid blending device 110 via the fluid blending device control unit 174.

[0028] In some embodiments, the addressing system control device 176 can control the valve opening and the flow rate of fluid to and / or out of the fluid addressing system 120. In some embodiments, the addressing system control device 176 can control the opening and closing of the valve between the fluid addressing system 120 and the biomimetic device 130. In some embodiments, the addressing system control device 176 can control the pressure in the fluid addressing system 120 and the biomimetic device 130 by controlling the valve in the fluid addressing system 120.

[0029] In some embodiments, the fluid synthesis device control unit 174, the addressing system control unit 176, the imaging device 182, and the data receiver 181 can be monitored and / or controlled via a single user interface (i.e., via the main control unit 172). In some embodiments, the fluid synthesis device control unit 174, the addressing system control unit 176, the imaging device 182, and the data receiver 181 can be monitored via separate user interfaces. In some embodiments, the main control unit 172 can communicate data to the user via an external communicator 178.

[0030] In some embodiments, the main control unit 172, the fluid synthesis unit control unit 174, and / or the addressing system control unit 176 may include a proportional control unit, an integral control unit, a differential control unit, a proportional-integral-derivative (PID) control unit, or any combination thereof. Any of the above-described control units can be implemented as a general-purpose computing unit. For example, the main control unit 172, schematically shown in Figure 20, may include a processor 172A, memory 172B, and one or more input / output devices 172C. The processor 172A may be configured to receive, process, analyze, compile, store, and access data, for example, via a network connection or via a physical connection to a device or storage medium (e.g., via a universal serial bus (USB) or any other type of port), as will be discussed in more detail herein. The processor 172A may be any suitable processing unit configured to execute and / or run a set of instructions or code, and may include one or more data processors, image processors, graphics processing units, physical processing units, digital signal processors, and / or central processing units. Each processor 172A may be, for example, a general-purpose processor, an FPGA (Field Programmable Gate Array), an ASIC (Application Specific Integrated Circuit), and / or similar. Each processor 172A may be configured to start and / or execute application processes and / or other modules, processes, and / or functions related to the system and / or its associated network. The underlying device technology can be provided in various component types (e.g., metal-oxide-semiconductor field-effect transistor (MOSFET) technology such as complementary metal-oxide-semiconductor (COMOS), bipolar technology such as emitter-coupled logic (ECL), polymer technology (e.g., silicon-conjugated polymers and metal-conjugated polymer-metal structures), mixed analog and digital, etc.).

[0031] Memory 172B may include a database (not shown) and may, for example, random access memory (RAM), memory buffers, hard drives, erasable programmable read-only memory (EPROM), electrically erasable read-only memory (EEPROM), read-only memory (ROM), flash memory, etc. Memory 172B may store instructions for causing the processor to execute modules, processes, and / or functions related to the communication device, such as patient data processing, sensor measurement, virus infection probability estimation, user device or patient monitoring and control, authentication, encryption, and / or communication. Some embodiments described herein relate to computer storage products having a persistent computer-readable medium (sometimes also called a persistent processor-readable medium) having instructions or computer code thereon for performing various computer implementation operations. The computer-readable medium (or processor-readable medium) is persistent in the sense that it does not itself contain transient propagating signals (e.g., propagating electromagnetic waves that carry information on a transmission medium such as space or a cable). The medium and computer code (sometimes also called code or algorithms) may be designed and constructed for a particular purpose or objective. Examples of persistent computer-readable media include, but are not limited to, magnetic storage media such as hard disks, floppy disks, and magnetic tapes; optical storage media such as compact discs / digital video discs (CDs / DVDs), compact disc read-only memory (CD-ROMs), and hologram devices; magneto-optical storage media such as optical discs; semiconductor storage devices such as solid-state drives (SSDs) and semiconductor hybrid drives (SSHDs); carrier signal processing modules; and hardware devices specifically configured to store and execute program code, such as application-specific integrated circuits (ASICs), programmable logic circuits (PLDs), read-only memory (ROM), and random access memory (RAM) devices.Other embodiments described herein relate to computer program products and may include, for example, instructions and / or computer code disclosed herein.

[0032] Each input / output device 172C can be coupled with processors 172A and 172B and configured to communicate with other devices (such as other control devices and components of the control system 170, other such control systems, and other devices such as via the external communicator 178). Each input / output device 172C may include a network interface configured to connect the computer device to other systems (e.g., the Internet, remote servers, databases) by wired or wireless connection. In some embodiments, the network interface may include radio frequency (RF) receivers, transmitters, and / or optical (e.g., infrared) receivers and transmitters configured to communicate with one or more devices and / or networks.

[0033] The biomimetic platform 100 and its components can be mounted on a chip or substrate 101. The substrate 101 can be manufactured through cleanroom nanofabrication and / or lithography processes similar to those used in the microprocessor manufacturing industry. For example, when incorporated into a single microfluidic substrate, the biomimetic platform can be fabricated by thermal embossing or stamping, and / or injection molding, which allows the intended microfluidic pattern to be imprinted on the thermoplastic material by integrally molding a thermosetting polymer into a mold defined by a negative photoresist. In certain embodiments, the platform can be fabricated from a plurality of bonded layers that can be optically aligned, for example, by utilizing complementary alignment markings. In certain embodiments, a platform fabricated from two or more layers can be bonded by applying heat, by an extruded adhesive, by applying an uncured thermosetting plastic containing uncured polydimethylsiloxane (PDMS) which then cures to provide adhesive strength, and / or by applying force in the layer-stratification direction to contain an encapsulating fluid or biocompound in a seal based on the resulting pressure. In some embodiments, the biosensor 140 can be integrated with the substrate 101. In some embodiments, the biosensor 140 may be positioned separately from the substrate 101 and / or outside the substrate 101. In some embodiments, the biosensor 140 can be integrated into a structure separate from the substrate 101.

[0034] In certain embodiments, the biomimetic platform 100 may include a variety of geometric features. These geometric features can be patterned on the biomimetic platform to influence the flow of the liquid. For example, the geometric features may include one or a combination of the following: selectively permeable membranes that restrict the passage of certain fluid compounds or phases but not others (e.g., selective permeability of gases or liquids); porous membranes; notches; pillars; edges that manipulate liquids by capillary action or surface tension trapping; micropillars; nanopillar arrays; surface metal deposition; thin-walled features that enable elastomer action; molded or mechanically punched holes for transporting liquids between adhesive layers; matching geometric features that enable mechanical alignment of at least two layers of a multilayer device by optical overlay or mechanical conformal fit; arrows or indicators for showing the user locations, ports, or zones of interest; and alignment marks that assist autofocus, stitching, motion, and position origin routines in imaging or automated analysis.

[0035] In some embodiments, the biomimetic platform 100 may include a microfluidic system capable of forming at least one inlet connection and at least one outlet connection. For example, as will be described in more detail below, the inlet connection may be a fluid input to a fluid synthesizer 110, an input control to a fluid addressing system 120, a fluid input to a component on the biomimetic platform such as a biomimetic device 130, or a combination thereof. The outlet connection may be a waste output, a sampling output, or a combination thereof. The disclosed system may include an external compressor for generating a controlled gas pressure. The gas pressure may drive the fluid flow and gate the fluid addressing system 120, as will be described in more detail below.

[0036] Figure 3 is a schematic diagram of a fluid synthesizer 110. The fluid synthesizer 110 can mix two or more input solutions together in individually specified ratios or proportions to create a custom fluid mixture or output solution. As shown in Figure 3, the fluid synthesizer 110 may include two or more fluid inputs 112, identified in Figure 3 as a fluid input 1 and a fluid output N (where N may be one or more). In some embodiments, the fluid entering the fluid synthesizer 110 through the fluid input 1 may be the same as the fluid entering the fluid synthesizer 110 through either the fluid input N or any other fluid input 112. In some embodiments, a first fluid may enter the fluid synthesizer 110 through a first fluid input 112, and a second fluid may enter the fluid synthesizer 110 through a second fluid input 112, wherein the second fluid is different from the first fluid. In some embodiments, many different fluids (e.g., at least about 3, at least about 4, at least about 5, at least about 6, at least about 7, at least about 8, at least about 9, at least about 10, at least about 20, at least about 30, at least about 40, at least about 50, at least about 60, at least about 70, at least about 80, at least about 90, or at least about 100) can enter the fluid synthesis apparatus 110 via the fluid input section 112. Each fluid input section 112 is fluidically connected to the mixing chamber 116 (e.g., by any suitable fluid tube or channel). Each fluid input section can be selectively fluidically coupled to a respective container of input solution (optionally part of the control system 170, not part of the biomimetic platform 100) to receive the input solution and transport it to the mixing chamber 116. For example, the container for input solution 1 can be connected to the fluid input unit 1 so that input solution 1 is delivered to the mixing chamber 116 via the fluid input unit 1, and the container for input solution N can be connected to the fluid input unit N so that input solution N is delivered to the mixing chamber 116 by the fluid input unit N.The desired amount (or flow rate) of input solution 1 and the desired amount (or flow rate) of input solution N are therefore received into the mixing chamber 116 and can be mixed together (e.g., passively or via an active mechanism such as a stirrer) to form the desired amount or bolus (or flow rate) of output solution. The mixing chamber 116 is fluidically coupled to the fluid output section 114 of the fluid synthesis apparatus 110, from which the output solution (a discrete bolus or a continuous flow at the desired flow rate) can be delivered to one or more of the biomimetic devices 130 via downstream components, such as a fluid addressing system 120.

[0037] The cleaning input 113 is fluidically coupled to the mixing chamber 116 and can be selectively fluidically coupled to a container of cleaning solution (not part of the biomimetic platform 100). After a desired amount of output solution is delivered from the fluid synthesizer 110 via the fluid output 114, a large amount of cleaning solution is transported to the mixing chamber 116 via the cleaning input 113, and the output solution can be discharged or cleared from the mixing chamber 116 via the fluid output 114 and downstream components. In some embodiments, the mixing chamber 116 may include an additional outlet flow (not shown) for discharging waste or for returning the fluid to the fluid synthesizer 110 for recirculation.

[0038] The amount (or flow rate) of each input solution delivered through each of the fluid input sections 112 can be controlled by the input solution container, for example, by the use of a pump that controls the flow of the fluid from the container, and / or a valve associated with the container. Alternatively, any one or more amounts (or flow rates) of the input solutions delivered to the mixing chamber 116 can be controlled by a separate mechanism, such as an active valve included in the fluid synthesis apparatus 110. As shown in Figure 3, the fluid coupling between each fluid input section 112 and the mixing chamber 116 may include a valve 115. The valve 115 can be in an open state, allowing the flow of the input solution to the mixing chamber 116, or in a closed state, blocking the flow of the input solution. Each valve 115 can be controlled by its respective control input (not part of the biomimetic platform 100), such as the fluid synthesis apparatus control device 174 included in the control system 170 as described above with reference to Figure 2. In some embodiments, the valve 115 may include a check valve, ball valve, globe valve, plug valve, needle valve, butterfly valve, pinch valve, gate valve, relief valve, or any combination thereof. In some embodiments, the fluid synthesizer 110 is controlled by a closed-loop control system, including, but not limited to, closed-loop fluid control of flow using a feedback control loop (including, but not limited to, a proportional-integral-differential control device or "PID" control device) between one or a combination of a flow sensor, a pressure regulator, and a flow control valve.

[0039] The fluid addressing system 120 is schematically illustrated in Figure 4. The fluid addressing system 120 can route the output solution from the fluid synthesizer 110 to a target location on the biomimetic platform 100. For example, the fluid addressing system 110 can convert the output solution to at least one biomimetic device 130. As shown in Figure 4, the fluid addressing system 120 functions as a demultiplexer component and can selectively route the fluid received at the fluid input unit 122 (e.g., the output of the fluid synthesizer 110) to one or more of the fluid output units 124 under the control of the control or selection line 125. The control line 125 includes control line 1 to control line S. The control line 125 controls the opening or closing of the valves 126A, 126B, 126C, 126D, 126E, and 126F (collectively referred to as valves 126). As shown, the valves 126 are arranged in pairs. For example, the control line 125 may include a "high" line and a "low" line, where the high line controls the first of each pair of valves 126, and the low line controls the second of each pair of valves 126. For example, control line 1 may include a high line and a low line. The high line of control line 1 may control valve 126A, while the low line of control line 1 may control valve 126B. Control line S may include a high line that controls valves 126C and 126E, and a low line that controls valves 126D and 126F. The advantage of such a system is that multiple valves can be controlled with a single line. However, the open / closed states of some of the valves 126 will interact with each other. In other words, it would not be possible to control each of the valves 126 independently. For example, valves 126C and 126E may have the same open / closed state, and valves 126D and 126F may have the same open / closed state. In some embodiments, one or more of the valves 126 may be dome-shaped membrane valves connected to the at least one biomimetic device 130 via a rectangular profile microchannel.In certain embodiments, one or more of the valves 126 can be operated by positive pressure. In certain embodiments, one or more of the valves 126 can be operated by the application of vacuum. In certain embodiments, one or more of the valves 126 can be operated by a combination of positive and negative pressure. In certain embodiments, one or more of the valves 126 can utilize rectangular profile microchannels.

[0040] In some embodiments, the fluid addressing system 120 can be implemented using a pneumatic gate or valve type demultiplexer component to select an output channel (fluid output section 124). The demultiplexer can operate using binary addressing logic with an integrated flow valve. For example, "0" can symbolize a closed valve, and "1" can symbolize an open valve. Each downstream biomimetic device 130 (or other device) in the biomimetic platform can have a numerical address, the binary representation of which can encode the valve state required to open the corresponding fluid addressing system output. The binary addressing logic can be controlled by a plurality of pneumatic or hydraulic control or selection lines 125. The mathematical relationship between the amount of the selection line (S) and the amount of the address (A) can be described by A = 2s. In some embodiments, each selection line can be controlled using two pneumatic or hydraulic connections, in which case the mathematical relationship between the amount of the selection line (S) and the amount of the address (A) can be described by A = 2S = 1. For example, in an implementation where the binary addressing logic has six selection lines, there could be 64 output addresses. Of course, the binary addressing logic may have fewer or more selection lines than six (for example, 10 selection lines to handle 1024 addresses). In one embodiment, each selection line can be operated by one external four-way valve, two external three-way valves, or two external two-way valves. In a non-limiting embodiment, the binary addressing system may include a total of seven two-way, four-port solenoid valves as pilot valves (e.g., 27 = 128 individually addressable fluid output units or outputs from the fluid addressing system), or a total of 14 two-way, four-port solenoid valves as pilot valves (e.g., 214 = 16,384 individually addressable fluid output units or outputs from the fluid addressing system).

[0041] In some embodiments, the fluid addressing system may include a “flush” output unit 127 for flushing any liquid or dead volume currently contained in the fluid addressing system or downstream channels. In some embodiments, the flush output unit 127 can be fluidically coupled to the outflow channel 160, as described above with reference to Figure 1. In some embodiments, the flush output unit 127 can be fluidically coupled to the fluid output unit 124. The fluid addressing system 120 provides great flexibility in operating the biomimetic platform 100 and in delivering customized fluids and / or flushing fluids to one or more, or all, downstream devices (such as biomimetic devices 130) of the fluid addressing system 120. For example, in some embodiments, the fluid addressing system 120 may include an “off” state in which all output units 124 are blocked. The fluid addressing system 120 may also open one of its fluid output units 124, one or more subsets of its fluid output units 124, or all of its fluid output units 124. In some embodiments, when the fluid addressing system 120 is dispensing fluid from its fluid input 122, the fluid addressing system 120 can simultaneously open all or a subset of the output channels connected to the biomimetic devices that require the fluid, thereby allowing all of the selected biomimetic devices to be perfused simultaneously.

[0042] Therefore, the customized fluid mixture produced by the fluid synthesis device 110 can be delivered to one or more biomimetic devices 130 by the fluid addressing system 120. The fluid addressing system 120 can open flow valves to the selected biomimetic device or device 130, allowing the customized fluid mixture produced by the fluid synthesis device 110 to flow into the target biomimetic device or device 130 while preventing it from entering any other biomimetic device or device 130.

[0043] In some embodiments, the fluid addressing system 120 may include a bypass selector 128 that can control the flushing of all fluids upstream of a selected biomimetic device 130. For example, downstream of the furthest downstream selection or control line 125 in the fluid addressing system 120, the fluid can either continue directly to the target biomimetic device 130 or be bypassed by the bypass selector 128 into a wastewater flow without interrupting the target biomimetic device 130. In other words, the bypass selector 128 can determine whether the fluid output from the fluid addressing system 120 reaches its target position in the array of biomimetic devices 130 or is switched to flow into a wastewater flow. This reduces the amount of wastewater if the user does not want the fluid currently in the fluid addressing system 120 to be sent to the biomimetic device 130. Using the bypass selector 128, only the fluid in the fluid addressing system 120 and the fluid upstream of it need to be flushed, and not the fluid in the biomimetic device 130, but rather into the effluent or wastewater flow. The binary addressing logic can be used to minimize the requirements for electromagnetic valves in order to create a biomimetic platform 100 for high-throughput screening or testing of a large number (e.g., hundreds to tens of thousands) of biomimetic devices 130. The biomimetic platform 100 may be a biomimetic chip system that includes at least one organ-on-a-chip.

[0044] In some embodiments, the fluid addressing system 120 can route the fluid flow to different layers of the biomimetic platform 100. In some embodiments, multiple layers of the biomimetic platform 100 can alternate between circular or dome-shaped microfluidic channels, which can be fabricated by photoresist reflow molding, and square or rectangular-shaped microfluidic channels, which can be fabricated by negative photoresist molding. Each of the circular, dome-shaped, square, and rectangular-shaped microfluidic channels can be located on the same layer or on different layers of the biomimetic platform 100. Such alternating arrangements of the microfluidic channels enable compatibility between membrane valves operating on circular-shaped microfluidic channels and biomimetic devices 130 operating on rectangular-shaped microfluidic channels. In some embodiments, the biomimetic platform 100 can include rectangular-shaped microfluidic channels used in combination with dome-shaped valves. In some embodiments, the rectangular fluid lines or microfluidic channels can be isolated from any expansion of pneumatically driven or hydraulically driven select lines. The aforementioned expansion can impart cross-sectional distortion to the pneumatic or hydraulic select line if higher pressure is used to enable more complete and / or rapid operation of the membrane valve. In some embodiments, the fluid flow can be transferred from a first flow layer to a second discrete valve layer ("out-of-plane" or "out-of-layer" valve) and then returned to the first flow layer in the fluid addressing system. The out-of-plane or out-of-layer valve can allow the pneumatic or hydraulic control valve to be positioned at any location on the footprint of the biomimetic platform 100. For example, the pneumatic or hydraulic control valve can be positioned at a location other than the one intended for valve mounting without unintended interference or pressure deflection of the fluid flow layer.

[0045] In some embodiments, fluid can flow between layers through holes (e.g., “vias”), which can be continuous between the microfluidic channels present in opposing layers of the apparatus. The arrangement of the vias can be utilized to traverse at least one of the second fluid channels without fluid contact by routing a first fluid channel on a first layer vertically to a second layer, and then returning the first fluid channel vertically across the second fluid channel to the first layer to create an overpass or underpass. In some embodiments, the vias are utilized to deliver fluid between microchannels having a rectangular cross-section and microchannels having a circular cross-section. A pneumatically or hydraulically controlled membrane valve can be placed in the layer having the circular cross-section, and the working membrane can form a more robust seal along the circular contour of the valved microchannel.

[0046] As described above with reference to Figure 1, the biomimetic platform 100 may include one or more sequences of biomimetic devices 130. Each of such biomimetic devices 130 may include a microengineered environment designed to stimulate the development of a physiologically relevant tissue or organ type. In some embodiments, all of the biomimetic devices 130 within the sequence and / or on the entire biomimetic platform may share the same general-purpose design. In other embodiments, the biomimetic devices 130 may have multiple designs and be distributed across different locations within the sequence or across multiple sequences on the biomimetic platform 100.

[0047] Each biomimetic device 130 of the biomimetic platform 100 can be configured to include one or more of tissues, cells, bacteria, viruses, other living organisms, biological scaffolds, or excised tissues, and is capable of replicating the structure and function of an organ or part thereof. In some embodiments, one or more of the biomimetic devices 130 can start as a naked structure. Thus, in the initial state of the biomimetic platform 100, it may lack any biological material, and the biomimetic devices 130 are configured to receive such material and then culture or grow it. Thus, in other states of the biomimetic platform 100, at any one or more stages of physiological development, one or more biomimetic devices 130 can contain biological material. Thus, in some embodiments, one or more of the biomimetic devices 130 can be seeded with tissue by introducing cells that can be supplied with a culture medium to grow into a tissue or organ. Such cells can be introduced into the biomimetic device by any one or more of several routes. In some embodiments, cells can be introduced directly into the biomimetic device, for example, by a fluid handler 195. Alternatively, or additionally, cells may be introduced into any one or more other parts of the biomimetic platform 100 that are fluidically coupled (or can be coupled) to the biomimetic device 130, such as in or upstream of the fluid synthesis device 110, or in or upstream of the fluid addressing system 120.

[0048] In some embodiments, the substrate 101 may include functionalized regions. In some embodiments, the functionalized regions on the substrate 101 may be functionalized to allow the cells to grow more easily. In some embodiments, the functionalized regions may be formed on the substrate 101 before the substrate 101 is enclosed to form the biomimetic device 130. In some embodiments, the functionalized regions may be formed within the biomimetic device 130 while the substrate 101 is in the enclosure or "nest". In some embodiments, the functionalized regions on the substrate 101 may be formed as a monolithic structure. In some embodiments, the functionalized regions on the substrate 101 may be decomposed across multiple components or structures.

[0049] In some embodiments, the cells may include cardiac cells, osteocytes, kidney cells, liver cells, intestinal cells, lung cells, or any combination thereof. In some embodiments, the biomimetic device 130 may be structured to model cardiac tissue, bone tissue, kidney tissue, liver tissue, intestinal tissue, lung tissue, or any combination thereof.

[0050] Figures 5A–5C are schematic diagrams of one embodiment of a biomimetic device 130 included in the biomimetic platform 100 of Figure 1. As shown, the biomimetic device 130 includes a tissue chamber 137 interposed by a channel 136. Each tissue chamber 137 may contain cells, organ tissue cultures, etc., in some states of the biomimetic device 130 and the biomimetic platform 100 (therefore, the tissue chamber 137 is also referred to as tissue 137 as appropriate in the context). In some embodiments, the tissue chamber 137 can be in fluid communication with the channel 136. In some embodiments, the tissue chamber 137 may include a fluid pathway through which tissue cultures can grow. In some embodiments, fluids and / or nutrients flow freely between the tissue chamber 137 and the channel 136. In some embodiments, the channel 136 can be used to deliver fluids to the tissue chamber 137 and / or the tissue contained therein. In some embodiments, the membrane can be positioned between the tissue chamber 137 and the channel 136, or between two or more different tissue types within the tissue chamber 137. In some embodiments, the membrane may include a semipermeable membrane. In some embodiments, the fluid within the tissue chamber 137 and the channel 136 may be held by surface tension rather than by a membrane. In other words, an open fluid communication may exist between the channel 136 and the tissue 137.

[0051] As shown, the tissue chamber or tissue 137 includes tissue chambers or tissue 1 up to tissue chamber or tissue N, while the channel 136 includes channels 1 through N, where N is an integer. In some embodiments, N can be 1, 2, 3, or more, up to any practical limit and to satisfy the requirements of any desired biofunctional chip or other structure. In some embodiments, the biomimetic device 130 can include N tissues 137 and N-1 channels. In other words, the tissues 137 can be located on the outer edge of the array of tissues 137 and channels 136 such that there is one fewer channel 136 than tissue 137. In some embodiments, the biomimetic device 130 can include N tissues 137 and N+1 channels 136. In other words, the channels 136 can be located on the outer edge of the array of tissues 137 such that there is one fewer tissue 137 than channel 136.

[0052] As shown, organization 1 includes an organization 1 fluid input A (132-1A) from the fluid addressing system 120 and an optional organization 1 fluid input B (132-1B) from the fluid handler 195, and channel 1 includes a channel 1 fluid input A (133-1A) from the fluid addressing system 120 and an optional channel 1 fluid input B (133-1B) from the fluid handler 195. Organization N includes an organization N fluid input A (132-NA) from the fluid addressing system 120 and an optional organization N fluid input B (132-NB) from the fluid handler 195, and channel N includes an optional channel N fluid input B (133-NB) from the channel N fluid input A (133-NA) and channel N fluid input B from the fluid addressing system 120. In some embodiments, the inputs (132-1A, 132-1B, 133-1A, 133-1B, 132-NA, 132-NB, 133-NA, 133-NB, hereinafter collectively referred to as inputs 132 and 133) may include injection ports. In some embodiments, the inputs 132 and 133 may include valves for regulating the flow of fluid.

[0053] As shown, tissue 1 includes tissue 1 fluid output section 138-1, channel 1 includes channel 1 fluid output section 139-1, tissue N includes tissue N fluid output section 138-N, and channel N includes channel N fluid output section 139-N. As shown, each of the outputs (138-1, 139-1, 138-N, and 139-N, collectively referred to herein as outputs 138, 139) is configured to discharge an output solution whose composition is based on the composition of the fluid solution received at the respective fluid input section to the channel from the fluid output section of the fluid synthesizer via the fluid addressing system, and is configured such that the fluid solution may interact with, modify, and / or supplement any tissue in the respective tissue chambers that are fluidly connected to the respective channels. In some embodiments, the outputs 138, 139 can reuse the fluid exiting tissue 137 and the channel 136. In some embodiments, the outputs 138, 139 can be supplied to a wastewater flow. In some embodiments, the outputs 138, 139 can further be supplied to a processing unit. As will be described in more detail below, each of the tissue chambers 137 or channels 136 may contain a separate sensor or set of sensors, or may be fluidically coupled. Figure 5B shows the tissue 137 and channels 136 oriented in a vertical configuration. In other words, the channels 136 are positioned above and below the tissue 137. Figure 5B includes axes, where the x-axis is horizontal and the z-axis is vertical. In Figure 5B, the fluid would flow horizontally through the tissue 137 and channels 136. Figure 5C shows the tissue 137 and channels 136 oriented in a horizontal configuration. Figure 5C includes axes, where the x-axis is horizontal and the z-axis is vertical. In Figure 5C, the fluid would flow vertically through the tissue 137 and channels 136.

[0054] Each or any of the biomimetic devices 130 can be implemented as any of a variety of non-limiting biofunctional chip models, including, for example, an eyeball model (e.g., the model disclosed in U.S. Patent No. 10,360,819), a placenta model (e.g., the model disclosed in U.S. Patent No. 10,360,819), a lung model (e.g., the model disclosed in U.S. Patent Publication No. 2018 / 0216058), an organ fibrosis model (e.g., the model disclosed in U.S. Patent Publication No. 2018 / 0230415), a cervix model (e.g., the model disclosed in U.S. Patent Publication No. 2018 / 0312810), a vascular system model (e.g., the model disclosed in International Publication No. 2019 / 191111), and / or a lung airway model (e.g., the model disclosed in International Publication No. 2020 / 073043). Furthermore, each or any of the biomimetic devices 130 may also include certain non-limiting functions for biofunctional chip models, including decellularized extracellular matrix (e.g., as disclosed in U.S. Patent Publication No. 2018 / 0126037), heterobifunctional crosslinking agents (e.g., as disclosed in U.S. Patent Publication No. 2018 / 0223251), and / or membrane inserts derived from natural extracellular matrix (e.g., as disclosed in U.S. Patent Publication No. 2020 / 0190456). The disclosures of each of the aforementioned patents and published patent applications are incorporated herein by reference.

[0055] As described above with reference to Figure 2, observation of the biomimetic device 130, for example, observation of the biomaterials, tissues, tissue structures contained therein, can be acquired by one or more associated and / or controlled imaging devices located within the control system. The imaging modalities or methods performed by such imaging devices may include optical microscopy, magnetic resonance imaging, or computed tomography (CT) scanning methods. Accordingly, the structure of the biomimetic device 130 on which the image data is acquired should be configured to enable effective acquisition of images by the desired imaging diagnostic technique. For example, in optical microscopy, the structure of the biomimetic device 130 and other structures of the biomimetic platform 100 between the imaging device and the biomimetic device 130 are required to sufficiently transmit the light frequencies employed by the optical microscope, and the refractive indices of different materials and the angle of incidence of light at their interfaces enable appropriate imaging. The data obtained from the use of one or a combination thereof of the imaging method on the contents of the biomimetic device 130 can be used for non-limited analytical purposes, including, but not limited to, creating a three-dimensional reconstruction of a biological entity within the biomimetic device; applying computer measurement techniques to the obtained data to obtain phenotypic data relating to a biological specimen or entity; measuring the deviation of the observed phenotype or physiology from the expected phenotype or physiology; or measuring the dynamic behavior of the observed biological entity over time, such as cell division rate, formation of biological networks, or development and function of biological tissues, organs, or functional subunits of organs, etc.

[0056] Other types of sensors include electronic sensors that monitor secondary or derived data (e.g., software reconstructions or models of biological or physical entities), or combinations thereof.

[0057] In addition to information collected from sensors such as the imaging device described above, which are not part of the biomimetic platform 100, information regarding the contents of each biomimetic device 130 may also be collected using one or more sensors coupled to or incorporated into the biomimetic platform 100. Such sensors can be incorporated into the biomimetic device 130 and / or can be incorporated, whole or partially, into one or more biosensors 140 that are operationally, for example, fluidically coupled (continuously or selectively) to the fluid output unit 134 of the biomimetic device 130. The sensors can be located locally, downstream, or upstream of each biomimetic device 130.

[0058] In some embodiments, the biomimetic device 130 may include at least one integrated sensor, which may include a chemical sensor, a mechanical sensor, an optical sensor, or a combination thereof. In some embodiments, the integrated sensor may be integrated inline into one or more of the biomimetic device 130. The at least one sensor may transmit one signal or a combination thereof. The signal may be generated from the biomimetic device, the biomimetic device's periphery, experimental factors or conditions related to the biomimetic device / platform, or a combination thereof.

[0059] In some embodiments where the sensor is a chemical sensor, the sensor or group of sensors can transmit chemical signals, whether integrated with or located downstream of the biomimetic device 130. Such chemical signals may include the presence and concentration of biological secretions (e.g., hormones, paracrine factors, extracellular matrix components, metabolic byproducts), biological consumption or uptake or modification of chemical substrates (e.g., consumption, uptake, or modification of nutrients, carbohydrates, amino acids, biotherapeutic drugs, drugs, pharmaceuticals, toxins, gases, dissolved solids, dissolved chemicals, or aerosolized compounds), pH of a liquid, osmotic pressure of a liquid, chemical composition of a liquid (names and concentrations of chemical components), multiplexed chemical sensing of multiple chemical targets (e.g., tens or hundreds of proteins by competitive binding to a dotted antibody microarray), environmental gas composition, or combinations thereof. In non-limiting embodiments, the biological consumption or uptake or modification of a chemical substrate can be determined by measuring the downstream concentration flowing out of the biomimetic device 130 relative to the concentration in the fluid upstream of the biomimetic device 130.

[0060] In some embodiments where the sensor is a mechanical sensor, whether integrated with or located downstream of the biomimetic device 130, the sensor or group of sensors can transmit mechanical signals including mechanical forces or force exertion by the biomimetic device 130 (e.g., pressure imposed by muscle tissue contraction or modeled tumor growth), mechanical forces or force application to the biomimetic device 130 (e.g., closed-loop pressure control or closed-loop electromechanical operation), ambient pressure, material properties (e.g., elastic modulus, shear modulus, periodic load characteristics), or a combination thereof.

[0061] In some embodiments where the sensor is a photosensor, whether integrated with or downstream of the biomimetic device 130, the sensor or sensor group can transmit optical signals including images acquired by light transmission microscopy, images acquired by fluorescence microscopy (e.g., confocal microscopy, light sheet microscopy, and super-resolution microscopy), quantitative optical measurements (e.g., transmittance, emission, electrochemiluminescence, fluorescence, and fluorescence resonance energy transfer (FRET) techniques), phenotypic observation, morphological and physiological observation in 3D computer reconstruction or reprojection, images of structural motifs (e.g., scaffold-tagged fluorescent markers, embedded quantum dots, second harmonic generation (SHG) imaging), or combinations thereof.

[0062] In some embodiments, the biomimetic device 130 may include a combination of chemical sensors, mechanical sensors, optical sensors, and modality-specific sensing methods. In non-limiting embodiments, additional sensor modalities may be integrated or applied. Such additional sensor modalities may include magnetic resonance, X-ray transmission, computed tomography, electronic monitoring of software reconstruction, software reconstruction of the biomimetic device, or a combination thereof. In some embodiments, the biomimetic device may include one or more surface plasmon resonance (SPR) biosensors for one or more corresponding target analytes, either alone or in combination with one or a combination of the sensors mentioned above.

[0063] When any fluid is delivered to the biomimetic device 130, an equal volume of the existing fluid can be displaced over the sensor itself, over the area the sensor is sensitive to, or within the volume the sensor is sensitive to, which can be located downstream of the biomimetic device 130, for example, as part of a biosensor 140.

[0064] As schematically shown in Figure 1, the biomimetic platform 100 may include an array of biosensors 140, the biosensors 140 of which can be fluidically coupled to the biomimetic device 130. The fluid-coupled array can be implemented in different ways. For example, the biomimetic device 130 may have a single biosensor 140 with a dedicated fluid coupling between them, i.e., the biosensor 140 can sense only the characteristics of the fluid output from the device 130. In some implementations, the relationship between the biomimetic device 130 and the biosensors 140 can be one-to-many (multiple biosensors fluidically coupled to or capable of being coupled to a single microfluidic device 130), many-to-one (a single biosensor fluidically coupled to or capable of being coupled to multiple microfluidic devices 130), or many-to-many, using appropriate microfluidic coupling, switching, multiplexing, and demultiplexing arrangements in the fluid pathway between the array of biomimetic devices 130 and the array of biosensors 140, as schematically shown in Figure 1. Any or all of these relationships between the biomimetic device 130 and the biosensor 140 can be used on a single biomimetic platform 100. Correspondingly, the biomimetic platform 100 can include multiple types of biosensors 140. For example, the biomimetic platform 100 may include electrochemical biosensors, optical biosensors, and / or fluorescent biosensors, and may include multiplexed biosensors. The types of biosensors 140 patterned adjacent to the biomimetic device 130 on the biomimetic platform 100 can be different. For example, a first biomimetic device 130 can be coupled with an optical fluorescence-based biosensor 140, a second biomimetic device 130 can be coupled with a pH sensor 140, and a third biomimetic device 130 can be coupled with a transepithelial electrical resistance (TEER) sensor 140. In some embodiments, the first biomimetic device 130 may have a first combination of sensor modalities different from the second combination of sensor modalities associated with the second biomimetic device 130.For example, variations in the combination of sensor modalities or variations in sensor targets can exist between biomimetic devices 130 contained within the same biomimetic platform 100.

[0065] In some embodiments, the biosensor 140 can be implemented, for example, as an unlabeled microfluidic biosensor and can be colocalized with or located downstream of the biomimetic device 130. In some embodiments, continuous acquisition from a plasmon biosensor multiplexed for multiple biological target analytes enables real-time characterization of the microenvironment and secretome of the biomimetic device 130 with high temporal resolution and avoids the costs of label-based biosensors, whose operating costs (primarily the consumption of label molecules) scale with the operating duration. An example of such an embodiment is the biomimetic device 230 and biosensor 240 shown in Figures 6A to 6D. In this embodiment, the surface plasmon resonance (SPR) based biosensor 240 is located close to the biomimetic device 230 to continuously monitor the biofunctional chip environment for target analytes in a fluid flow. In some embodiments, the biosensor 240 is located downstream of the biomimetic device 230. In some embodiments, the biosensor 240 can perform measurements inline with the biomimetic device 230. In some embodiments, the biosensor 240 can be integrated into the biomimetic device 230. In some embodiments, the biosensor 240 may include a colorimetric-based sensor. In some embodiments, the biosensor 240 may include a fluorescence-based sensor. In some embodiments, the biosensor 240 may be transmitted by a microscope. In some embodiments, the biosensor 240 may be electrical (e.g., cyclic voltammetry). In some embodiments, the biosensor 240 may be converted by a constant potential electrolysis device. In some embodiments, the biomimetic device 230 may include two inlets integrated into the biomimetic device 230. As described above with reference to Figures 5B and 5C, the inlets may be oriented towards the top and bottom of the biomimetic device 230. In some embodiments, the inlets may be oriented towards either side of the biomimetic device 230.

[0066] In some embodiments, the multiplexed biosensor 140 may include thin films and biorecognition molecules. The thin films can be deposited on the biosensor 140 by physical vapor deposition. For example, physical deposition of a gold thin film can be used to generate resonant plasmon bonding with laser emission at a specific, tightly controlled wavelength and critical incidence angle. Biorecognition molecules (e.g., antibodies, DNA, RNA, XNA, etc.) that can selectively act on the biomolecules of interest in the solution can be spotted on the surface. The binding of the biorecognition molecules adsorbed on the gold surface to the target molecules creates a surface load, the degree of which changes the critical angle at which the resonant bonding occurs. By tracking this angle for each of the spots, or by imaging all of them at once using a camera, the concentration of each target analyte in the solution can be measured without the need for additional labeling. The biosensor 140 is a label-free biosensor that can avoid adverse effects due to the potential toxicity of the labeling molecules to tissue culture. In some embodiments, the biosensor 140 may include multiple biorecognition elements that can simultaneously detect multiple target analytes.

[0067] In certain embodiments, the biosensor 140 can be integrated into at least one biomimetic device 130, enabling on-chip, real-time, and high-content data acquisition with reduced sample volume requirements. The biosensor 140 can automatically sample the fluid content within the biomimetic device 130 and quantify the target analyte in real time. Similar to a barcode reader, for example, the biosensor 140 and an optical transducer can sample and quantify the fluid content by utilizing the reflection of a laser beam as it scans the back of the SPR spot. Thus, the biosensor group 130 with the SPR can have improved data acquisition dimensions compared to ELISA or microscopic analysis.

[0068] In certain embodiments, biochemical, electrochemical / electrochemiluminescent, mechanical, and / or optical biosensing schemes can be incorporated into the biomimetic platform 100 through modifications of the components of the biosensor 140 or their on-chip placement. For example, given that multiplexed biosensor zones can utilize patterned gold deposition on glass, various biosensing schemes can be incorporated into similar gold pattern layers without additional manufacturing processes. For example, a series of interlocking microelectrode arrays for redox-based electrochemical biosensing can be realized by the disclosed technology.

[0069] In some embodiments, the measurements or readouts generated by the biosensor 140 are used for chemical or biological characterization of a biological entity being cultured or experimented with within the biomimetic device 130. This chemical or biological characterization may be based on the appearance, disappearance, or change in the concentration of one or more compounds. For example, the compounds may include chemical or biological compounds, chemical or biological sites, dissolved compounds, biologically secreted compounds, metabolized or altered compounds, target analytes, or combinations thereof. In some embodiments, this characterization is performed as a comparison between the composition of the solution at a first location upstream of the biomimetic device 130 and the composition of the solution at a second location downstream of the biomimetic device 130. In some embodiments, this measurement is used to infer, measure, or deduce one or a combination of characterization observations or factors relating to the biomimetic device 130. For example, the observations include: (1) the uptake of compounds, chemicals, drugs, or biopharmaceuticals from the solution into biological entities within the biomimetic device 130; (2) the uptake of complex biological entities, including extracellular vesicles, exosomes, viral particles, components of the extracellular matrix, polymers, enzymes, nucleic acids, peptides, or proteins, into the biological entities within the biomimetic device 130; (3) the secretion of compounds, chemicals, or biopharmaceuticals from the biological entities within the biomimetic device 130 into the surrounding liquid solution; and (4) the secretion of extracellular vesicles, exosomes, viral particles, and other substances. This may include: (5) secretion of the complex biological entity, comprising extracellular matrix components, polymers, enzymes, nucleic acids, peptides, or proteins, from the biological entity within the biomimetic device into the surrounding liquid solution; (6) modification of compounds, chemicals, drugs, or biological drugs in the solution by the biological entity within the biomimetic device 130; or (7) modification of complex biological entities such as extracellular vesicles, exosomes, viral particles, extracellular matrix components, polymers, enzymes, nucleic acids, peptides, or proteins by the biological entity within the biomimetic device 130.

[0070] As schematically shown in Figures 1 and 2A-2B, in some embodiments, one or more sensor data transmitters 150 can be associated with one or more of the biosensors 140 so that measurement data or data from the biosensors 140 can be transmitted to an external device of the biomimetic platform 100, such as a data receiver 181 which is part of a control system 170. This is also schematically shown in Figures 7AA and 7B. Figure 7A is an exemplary diagram of an augmentation of discrete biomimetic devices 330, each integrated with an on-chip fluid synthesizer 310. The biomimetic 330 further includes a chemical sensor or biosensor 340 located downstream of the biomimetic 330. Digitally converted data from one or more sensors can be transmitted by a sensor data transmitter 350 to an electronic device such as a computer C for continuous automatic monitoring and data processing. Figure 7B is an exemplary diagram of integrating multiple discrete biomimetic devices 430 into a single monolithic biomimetic platform 400, where the fluid output from a single fluid synthesizer 410 can be addressed to one or more selected individual biomimetic devices 430 using a fluid addressing system 420. Downstream of each individual biomimetic device 430 lies a biosensor 440 which can transmit the partial or whole chemical composition of a fluid and the composition measurement or measurement value, which can then be transmitted to an electronic device such as a computer C for data monitoring, data processing, or data monitoring and processing by a sensor data transmitter 450.

[0071] Returning to Figures 1 and 2A-2B, in some embodiments, a biosensor 140 having a sensor data transmitter 150 can characterize the concentration of a mixture of fluid components at a given location and electronically transmit this information to a fluid synthesizer, such as a fluid synthesizer 110, located at another location. This different location may refer to a different location within the same biomimetic platform 100, another biomimetic platform 100 engaging with the same control system, or another biomimetic platform or other device. The fluid synthesizer can then dynamically resynthesize and discharge this same fluid mixture. Since the connection can be made electronically, the link between the sensor and the fluid synthesizer may extend only a few millimeters on the same physical device (e.g., on the same biomimetic platform 100), or the link may extend to two or more disclosed biomimetic platforms located across different regions from each other. This enables the functions described in more detail below.

[0072] The biomimetic platform 100 described above provides the ability of the fluid synthesizer 110 to create a first fluid mixture which is delivered to a first biomimetic device 130 by the fluid addressing system 120. The fluid synthesizer 110 can then create a second fluid mixture which can subsequently be delivered to a second biomimetic device 130 by the fluid addressing system 120. This operation allows the biomimetic platform 100 to sequentially deliver at least one unique fluid mixture to at least one biomimetic device 130 integrated into the biomimetic platform 100. In some embodiments, this operation can circulate autonomously (e.g., under the control of the main control unit of the control system) to create an automated biomimetic platform 100. In some embodiments, the fluid synthesizer 110 can sequentially generate multiple fluid mixtures, and the fluid addressing system 120 can route the mixtures to designated biomimetic devices 130. In some embodiments, each biomimetic device 130 may have its own fluid synthesizer that delivers a unique fluid mixture. Alternatively, multiple fluid synthesis devices 110 incorporated into the biomimetic platform 100 can operate simultaneously at multiple locations. In some embodiments, the biomimetic platform 100 can perform diagnostic procedures that attempt to detect component failures, impending component failures, and component anomalies. Such diagnostic procedures can be performed at various points in time. For example, the diagnostic procedures can be performed prior to the start of an experiment, at one or more discrete intervals during the course of the experiment, continuously during the course of the experiment, at the end of the experiment, or a combination thereof. In some embodiments, such diagnostic procedures can include characterizing the fluid passing through components within the biomimetic platform 100 (e.g., biomimetic devices 130), activating valves or flow controls within the biomimetic platform 100, measuring one or more sensor readings, measuring fluid flow rates, measuring electrical properties, automatic or semi-automatic optical inspection, or a combination thereof.In some embodiments, the biomimetic platform 100 can passively monitor heuristics against expected or nominal values, performance measurements, performance metrics, or a combination thereof, to monitor the device itself for component failures or component anomalies without actively performing diagnostic procedures.

[0073] An exemplary embodiment of the biomimetic platform 100 is shown in Figures 8A to 8D. Figure 8A is a plan view of the biomimetic platform 500. As shown in Figure 8A, the biomimetic platform 500 is mounted on a flat, circular substrate 501 having a periphery 504. As shown in Figure 8A, in this exemplary embodiment, the components of the biomimetic platform 500 have a tiled or mirrored layout (similar to a specific tiled instruction execution core of a multicore microprocessor). That is, each half of the biomimetic platform includes a fluid synthesizer 510, a fluid addressing system 520, an array of biomimetic devices 530, and an array of biosensors 540. The two halves of the biomimetic platform share a common outflow channel 580.

[0074] In this embodiment, each biomimetic device 530 is paired with a dedicated biosensor 540 in a one-to-one relationship (similar to the embodiments shown in Figures 6A to 6D). Each array of biomimetic devices 530 includes 64 devices, and correspondingly, each array of biosensors 540 includes 64 biosensors. Figure 8B is a close-up view of the fluid synthesis device 510. As shown, the fluid synthesis device 510 includes a fluid inlet port 512, a valve control port 517, and a mixing chamber 516. As shown, there is a one-to-one relationship between the number of fluid inlet ports 512 and the number of fluid lines entering the mixing chamber 516. Figure 8C is a close-up view of part of the fluid addressing system 520, as well as part of the array of biomimetic devices 530 and part of the array of biosensors 540. As shown, the fluid addressing system 520 includes a fluid input section 522, a fluid output section 524, a control line 525, and a valve 526. The fluid inlet port 512 supplies fluid to the fluid input section 522, and the valve control port 517 and the control line 525 control the valve. In some embodiments, the biomimetic device 530 and the biosensor 540 are identical or substantially similar to the biomimetic device 230 and the biosensor 240 as described above with reference to Figures 6A to 6D. As shown, the biosensor 540 can be connected to the biomimetic device 530 via a meandering channel.

[0075] Figure 8D is a proximity view of the interface between the fluid addressing system 520 and the array of biomimetic devices 530. As shown, the biomimetic device 530 includes a tissue chamber or tissue 537, a channel 536, a tissue input 532A, a tissue input 532B, and a channel input 533BB. A fluid handler 595 is also shown. In some embodiments, the tissue input 532A is identical or substantially similar to input 132-1A or 132-NA, as described above with reference to Figure 5A. In other words, fluid can pass between the fluid addressing system 520 and the tissue chamber or tissue 537 via the tissue input 532A. In some embodiments, the tissue input 532B is identical or substantially similar to input 132-1B or 132-NB, as described above with reference to Figure 5A. In other words, fluid can pass between the fluid handler 595 and the tissue 537 via the tissue input 532B. In some embodiments, the channel input 533B is identical or substantially similar to input 133-1B or input 133-NB, as described above with reference to Figure 5A. In other words, fluid can pass between the fluid handler 595 and the channel 536 via the channel input 533B. In some embodiments, the biomimetic device 530 may include an inlet that creates a fluid path between the fluid addressing system 520 and the channel 536 (for example, identical or substantially similar to inputs 133-1A and 133-NA described above with reference to Figure 5A). Any combination of the fluid couplings described above may be included in the biomimetic platform 500.

[0076] In some embodiments, as shown in Figures 8A to 8D, the two processes of the component (e.g., the biomimetic device 530 and / or the sensor 540 associated with the biomimetic device 530) may be identical. This layout allows one process to function independently of one or more other processes to increase operational throughput, or to operate in an identical copy configuration for redundancy. For example, to improve statistical rigor or increase reproducibility, mirroring several components of the entire system across both sides to create two “core” processes can enable fault tolerance against operational anomalies (e.g., inlet blockage, fluid leak, valve perforation, component failure, or a combination thereof). In some embodiments, the mirrored or tiled components can be disabled without affecting other patterned processes. This redundancy allows a defective device to be “binned,” or operationally limited to a lower capacity or function set. Such binned or limited biomimetic platforms can be used for a variety of purposes. For example, the bin-type or restricted biomimetic platform can be sold or marketed to different levels of technical capability. Such a bin-type or restricted biomimetic platform can keep a portion of an ongoing experiment running or complete after a partial failure of one or more components. Such a bin-type or restricted biomimetic platform can also function as a substrate for testing, calibration, demonstration, or sampling procedures.

[0077] The biomimetic platform 500 shown in Figures 8A to 8D includes two processes of the same set of components, but in other embodiments, it may include two or more processes of components, for example, three, four, or more.

[0078] Fluid "teleportation" As described above, the biomimetic platform architecture described herein offers powerful capabilities. One of the key capabilities is “fluid teleportation,” “digital teleportation,” or virtual fluid coupling between components located on the same biomimetic platform or distributed across multiple platforms that are physically and geographically separated (e.g., multiple biomimetic platforms relating to the same control system, relating to different control systems within the same room or facility, relating to control systems distributed across regions, etc.). Fluid teleportation can also provide virtual duplication or multiple fluid couplings, for example, a single device can be virtually fluidically connected to many “downstream” devices. Fluid teleportation can also provide temporally distributed virtual fluid couplings (e.g., the time elapsed between the detection of the composition of a fluid leaving a first device and the synthesis of a fluid of the same composition for delivery to a second device (or a group of second devices) not fluidically coupled to the first device can be very short or very long). Details of fluid teleportation and exemplary implementations are described below.

[0079] As described above, fluid teleportation can enable the creation of fluid interconnections between at least two locations within a fluid or microfluidic network without altering the existing connection configuration or arrangement of the network (e.g., without bridging or connecting the locations by physical means). For example, the fluid interconnection can be established without connecting physical tubes or creating a physical interconnection between the locations that would allow for direct fluid flow. The interconnection is established between at least two discrete, isolated, or disconnected fluid networks (e.g., chambers or components). The interconnection can be established between at least two consecutive locations located opposite the direction of a unidirectional fluid flow (e.g., an interconnection between a first location and a second location upstream of the first location). The interconnection can be established between at least two locations separated by flow limiters, one-way valves, filters, components that selectively block the physical passage of chemical components of the fluid, or a combination thereof.

[0080] A simplified embodiment of the fluid teleportation system 600 is schematically shown in Figure 9. As shown, the fluid teleportation system 600 includes a first fluid synthesizer 610A, a first biomimetic device 630A, a first multianalyte fluid transducer / biosensor 640A, and a first sensor transmitter 650A integrated into the first device. As shown, the fluid teleportation system 600 further includes a second biomimetic device 630B, a second multianalyte fluid transducer / biosensor 640B, and a second fluid synthesizer 610B integrated into the second device. As shown in Figure 9, the outflow of the first biomimetic device 630A can be connected to the inlet of the second biomimetic device 630B without a direct fluid connection by using fluid-to-digital signal conversion, digital signal transmission, and then digital-to-fluid conversion, thereby forming a virtual fluid connection. As shown in Figure 9, the multi-analyte fluid transducer / biosensor 640A, located downstream of the first biomimetic device 630A, can convert the fluid composition of the first biomimetic device 630A into a digital signal that can be wirelessly transmitted by the sensor transmitter 650A to the second fluid synthesizer 610B, located upstream of the coupled second biomimetic device 630B, for reconstitution and subsequent perfusion.

[0081] Another embodiment of the fluid teleportation system 700 is schematically shown in Figure 10. In this embodiment, a plurality of biomimetic devices 730 are dynamically coupled by connections between the multi-analytical transducer / biosensor 740 and the sensor transmitter 750 of each device. Each of the biomimetic devices 730 can be connected via a fluid synthesizer 710 by fluid-to-digital and then digital-to-fluid conversion, so that the devices can be arbitrarily separated from each other, provided that digital communication is possible.

[0082] Figures 11A to 11D are schematic diagrams illustrating different connection configurations of a fluid teleportation system according to various embodiments. As shown in Figure 11A, signal transfer may be from a first device to a second device. More specifically, the control device of device 1 can control the fluid synthesizer, the biomimetic device, and / or the biosensor, and data from device 1 can be transmitted from the sensor data transmitter of device 1 to the control device of device 2. Based on the data transmitted from the sensor data transmitter of device 1 to the control device of device 2, the control device of device 2 can modify the control of the fluid synthesizer, the biomimetic device, and / or the biosensor of device 2. As shown in Figure 11B, the devices can be arranged in a serial virtual connection. In other words, data from device 1 can be applied to the deceased device of device 2 to control the operation of device 2, and data from device 2 can be applied to the control device of device 3 to control the operation of device 3. As shown in Figure 11C, data from the first device can be applied to control the operation of multiple additional devices in a multiplexed 1:2 (or 1:N) virtual connection. As shown in Figure 11C, data from device 1 is used to control the operation of devices 2 and 3. As shown in Figure 11D, the devices can be arranged in a feedback loop. In other words, the output from a downstream device (e.g., device 2) is transmitted to the input of an upstream device (e.g., device 1). In some embodiments, any desired teleportation device can be created by combining any of the connection configurations described above. An example of a complex arrangement of a teleportation device is shown in Figure 12.

[0083] Dynamic coupling between multiple biomimetic devices can be used, for example, to assemble a human body function chip model having a number of biomimetic devices, each replicating the physiology or function of a specific human tissue, organ, or system, and each connected to one or more other devices by digital fluid teleportation. This is schematically illustrated in an exemplary embodiment in Figure 12. As shown in Figure 12, the organ function chip biomimetic device system may include an intestinal device, a liver device, a kidney device, a bone device, a heart device, and a lung device. Oral drugs can be administered to the intestinal device (e.g., via a fluid synthesis device and a fluid addressing system, and / or directly to the device, e.g., by a fluid handler as described above), and aerosol drugs can similarly be administered to the lung device. As shown in Figure 12, oral drugs can be simulated at the inlet to the intestinal device, which can communicate with the liver device, kidney device, bone device, and heart device. Based on the data output from the intestinal device, the inputs to the liver device, kidney device, bone device, and heart device are controlled or operated. Based on the data output from the liver device, the kidney device, the bone device, and the heart device, the control unit of the lung device can operate the control unit of the intestine device. The operations and data forming the lung device are also influenced by the aerosol drug administered to the lung device. In some embodiments, the connections between the different organ devices can be virtual and / or physical. In some embodiments, the different bio-chip devices are contained on a single micro-biomimic platform or distributed across two or more bio-mimetic platforms. In some embodiments, a central control system can control each of the organ devices. In some embodiments, the central control system can be integrated into a single device containing each of the organ devices on a single bio-mimetic platform or on multiple bio-mimetic platforms. In some embodiments, one or more of the organ platforms can be implemented on removable disks.

[0084] In some embodiments, a digital fluid teleportation implementation (e.g., from one organ platform to another) may include measuring the concentration or presence of at least one target analyte in a first fluid at a first location and synthesizing a second fluid solution using a fluid synthesizer. The second fluid solution may contain at least one target analyte at the measured concentration or a concentration obtained by mathematical adjustment or transformation of the measured concentration. The second fluid may be the same as, a part of, or a derivative mixture of the first fluid. In certain embodiments, the method may further include flowing the second fluid solution from the fluid synthesizer to the second location without transporting the first fluid solution from the first location to the second location by a continuous fluid flow. For example, a whole or partial fluid composition characterized by at least one sensor at the first location can be "digitally teleported" to the second location by reconfiguring the first fluid whole or partially at the second location. These methods can be performed without requiring a physical connection between the first fluid at the first location and the second location. In certain embodiments, the digital fluid teleportation method makes it possible to copy an identical, partial, or derived mixture of the first fluid at the first location to one or more additional locations (by "digital fluid teleportation") across any distance, provided that means of data communication or data transport are present between at least two of those locations.

[0085] The method may include the steps of: preparing a first fluid mixture using a first fluid synthesis apparatus; incubating the first fluid mixture and a first biomimetic apparatus to produce a second fluid mixture; measuring the concentration of one or more target analytes in the second fluid mixture using a chemical sensor; and synthesizing a third fluid mixture by using the first fluid synthesis apparatus to reconstitute the same, partial, or derived mixture of the second fluid mixture. In a non-limiting embodiment, the method may further include incubating the third fluid mixture in the second biomimetic apparatus, the second biomimetic apparatus, at least two additional biomimetic apparatuses, or a combination thereof to produce a fourth fluid solution. In a non-limiting embodiment, the method may also include measuring the concentration of at least one target analyte in the fourth fluid solution for subsequent perfusion.

[0086] In certain embodiments, the method for digital fluid teleportation may further include transmitting the measured concentration to at least one external receiver. The external receiver may include at least one of a computer, an electronic control unit, an electronic control system, a network address, a network monitor, the first fluid synthesizer, one or more fluid synthesizers, and a control server. In non-limiting embodiments, the method for digital fluid teleportation may further include incubating the second tissue with the third fluid mixture to produce a fourth fluid mixture. In some embodiments, the method may further include measuring the concentration of the target analyte in the fourth fluid mixture for subsequent perfusion. In certain embodiments, digital fluid teleportation may enable fluid interconnection of at least two biomimetic devices without requiring the devices to be physically connected or to be positioned prior to each other along a sequential fluid path. In certain embodiments, the interconnection created by digital fluid teleportation may be enabled, disabled, rerouted, or a combination thereof, dynamically or discretely, continuously or at one or more intervals.

[0087] In certain embodiments, the disclosed subject matter provides a method for digital fluid teleportation between at least two bio-chip devices. In certain embodiments, a fluid chemical sensor or biosensor can perform real-time acquisition and readout of the composition of a first fluid or fluid mixture at its location in a first bio-chip device. This readout can be digitally transmitted so that it is dynamically resynthesized and discharged from a second location by a fluid synthesizer. The discharged resynthesized fluid can be directed to the second bio-chip device, which includes a fluid addressing system. In certain embodiments, an identical, partial, or derivative constituent mixture of the first fluid can be delivered to the second bio-chip without the requirement that the first bio-chip be connected to the second bio-chip. Thus, by combining one or more integrated fluid biosensors at different second locations on the chip with one or more fluid synthesizers capable of reproducing the same, partial, or derived component mixtures of the first sensor-characterizing fluid mixture, it is possible to "copy" the first fluid from one location and "paste" it to another location on the same platform, or to place it on another platform having a fluid synthesizer with a suitable inlet compound.

[0088] In certain embodiments, the sensor signals used for digital fluid teleportation can be transmitted wirelessly or digitally via any transmission network or protocol capable of transferring digital data. In certain embodiments, the digital signals can be transmitted back to the fluid synthesizer of the same biofunctional chip for the purpose of modeling a feedback loop.

[0089] In certain embodiments, digital fluid teleportation enables the digital transmission of a fluid composition to or from a location in a manner incompatible with physical fluid flow constraints. For illustrative purposes rather than limiting, such transmissions may include transmissions across air gaps or other obstacles blocking fluid flow (e.g., flow limiters or one-way valves), transmissions across distances at speeds faster than can be achieved through certain physical fluid conduits (since sensor signals are transmitted at the speed of light), or transmissions routing between destinations at speeds exceeding the capabilities of physical multi-directional valves, or a combination thereof.

[0090] In certain embodiments, the disclosed digital fluid teleportation method can connect two physically discrete organ models. As a non-limiting example, a model of a multi-organ system can be formed between at least two biomimetic devices within the integrated biomimetic platform without physical fluid connections directly linking the biomimetic devices or organ models. In certain embodiments, the disclosed system can operate without unintended leakage of the fluid biochemical microenvironment between the biomimetic devices or without fluid dilution of components between the organ models or biomimetic devices.

[0091] In certain embodiments, to connect a first biomimetic device to a second biomimetic device, the disclosed system can read the fluid composition for at least one fluid analyte or component at the outlet of the first biomimetic device using a biosensor, transmit the reading to a fluid synthesizer upstream of the second biomimetic device to synthesize a second fluid mixture having a mixture of identical, partial, or derivative components of the first fluid, and then flow this composition forward into the second biomimetic device. In non-limiting embodiments, a digital fluid teleportation method is applied to deliver one or more fluids between any one or combination of biomimetic devices integrated into the biomimetic platform shown in Figures 1 and 2. The fluid outflow of any microphysiological device can be sampled, reconstructed in the fluid synthesizer, and addressed to other biomimetic devices using the fluid addressing system. This process can be performed sequentially to link multiple biomimetic devices. For example, the output of a first biomimetic device can be reconstructed and supplied to a second biomimetic device. For example, the fluid outflow from the second biomimetic device is reconfigured and supplied to the third biomimetic device.

[0092] In certain embodiments, the connection established by digital fluid teleportation between two or more locations within the platform (e.g., between biomimetic devices) can be newly established, modified, or closed in real time or by other dynamic means. Unlike inflexible systems formed solely from physical fluid conduits, the disclosed subject allows coupling between biomimetic systems after a stable state, target state, or desired operating duration has been established. In non-limiting embodiments, the coupling can be disabled at a predetermined point in time. For example, the behavior of one biomimetic device can be evaluated with the other temporarily absent. In certain embodiments, the dynamic establishment of fluid connections by this digital fluid teleportation makes it possible to isolate and culture biofunctional chip models for a target period (e.g., one day, one week, or one month) and then fluidically couple them to model organ-to-organ or tissue-to-tissue interactions. In certain embodiments, the dynamic establishment of fluid connections by this digital fluid teleportation makes it possible to isolate and culture two different biomimetic devices for a target period (e.g., one day, one week, or one month). After the connection, it is possible to fluidly couple the biomimetic devices to construct a dynamic model (for example, the exposure of a first biological entity to secretions or chemical compounds produced by a second biological entity, a biological feedback phenomenon resulting from such unidirectional or bidirectional coupling, or a biological reaction of a chain reaction between two or more biological entities).

[0093] In certain embodiments, a fluid characterized by a single biosensor can be fluidically resynthesized by digital fluid teleportation to be delivered to multiple targets in order to generate dynamic fluid replicas. For example, the fluid, delivered to multiple biomimetic devices cultured as replicas (including, but not limited to, statistical rigor or hypothesis testing), can be simultaneously combined with a fluid composition measured in the effluent of a single drive biomimetic device. The effluent can be characterized by a sensor located at the outlet of the drive biomimetic device. Teleported to the fluid synthesizer, the fluid synthesizer can then reconstitute the mixture and deliver equal unit volumes of the same mixture to each of the replicated biomimetic devices via a fluid addressing system. In certain embodiments, the replicas to which the fluid mixture is delivered are biologically identical. In certain embodiments, the replicas to which the fluid mixture is delivered are nominally biologically identical for a predetermined purpose (e.g., classification or quantification of their resulting variations) (e.g., they can be cultured under identical initial conditions for the purpose of being identical replicas). In certain embodiments, the intentional variation may include the source of tissue cultured in different biomimetic devices, the pathophysiological state of the tissue cultured in the replicas, or the age of the tissue cultured in the replicas. In certain embodiments, the technique can be used to analyze different behaviors or responses exhibited by healthy organ models and diseased organ models in response to exposure to the same dynamic fluid environment.

[0094] In certain embodiments, the fluid can be replicated simultaneously to two locations by digital fluid teleportation, by which the sensor signal is transmitted to two fluid synthesizers. In certain embodiments, the fluid can be sequentially replicated to two locations by digital fluid teleportation, by teleporting to one fluid synthesizer whose output is addressed to a first location by a fluid addressing system. The fluid can then be teleported to the same fluid synthesizer to address the same fluid mixture as an output to a second location by the fluid addressing system. In certain embodiments, the desired fluid mixture can be replicated to three or more locations.

[0095] In certain embodiments, digital fluid teleportation can transport a fluid composition in a volume larger or smaller than the volume of fluid sampled by multiple sensors at a first location to one or more second locations. For illustrative and non-limiting purposes, a sensor at the first location may sample a chamber containing 0.1 milliliters of fluid, and this measured fluid composition can be transported by digital fluid teleportation to a second location where 1.0 ml of the same fluid composition can be synthesized by a fluid synthesizer.

[0096] In certain embodiments, sampled fluid compositions can be transported not only spatially but also temporally by digital fluid teleportation. In certain embodiments, temporal teleportation can be achieved by introducing a delay between one or more sensors at a first location and a fluid synthesis device that replicates the mixture at a second location. For illustrative purposes only and not limited thereto, this can be used to mimic natural phenomena. For example, natural phenomena include the transit time of hormones and biomimetic substances between tissues in the human body. When multiple biomimetic devices are interconnected by digital fluid teleportation, it is possible to sequentially transport metabolites or biological entities in a time series between multiple tissues or organs.

[0097] In certain embodiments, the one or more sensors can perform discrete or continuous recording of a fluid composition at a first location during a first time period. The sensors can also digitally store the sensor data constituting the recording. The recording can be reloaded to reproduce the recorded fluid composition through a fluid synthesis device. In certain embodiments, this method of loading a stored recording of a fluid composition can be used at a later date to reproduce the fluid composition from the recording. In certain embodiments, this method of storing and later loading a recording of a fluid composition can be used to store specific behaviors or dynamics observed in experiments on a biomimetic platform. The behaviors or dynamics can be reproduced at a later date in another biomimetic system. In certain embodiments, sensor readings over the duration of the entire experiment can be stored and made accessible later for various purposes. The purpose is the reproduction of all or part of the recording through real-time resynthesis of the recorded fluid composition in a fluid synthesis device. In certain embodiments, the technique of storing sensor data characterizing discrete or continuous fluid compositions can improve the experimental reproducibility of multi-organ-connected systems for investigating rare phenomena.

[0098] Figure 13 is a flowchart of a non-limiting embodiment of the digital fluid teleportation method 800. The method 800 includes receiving data indicating a measured concentration of a target analyte in a first fluid solution at a first location, as shown in 801. In some embodiments, the first location may be a biofunctional chip model. The method 800 further includes providing control commands to the fluid synthesizer to synthesize a second fluid solution containing the target analyte at the measured concentration or a concentration obtained from a mathematical adjustment or conversion of the measured concentration, thereby reconstructing the complete or partial composition of the first fluid solution, as shown in 802. In some embodiments, the second location may be on a biofunctional chip model. The method 800 further includes flowing the second fluid solution to a second location fluidically isolated from the first location, as shown in 803.

[0099] In some embodiments, the method 800 may include flowing the second solution to an additional location (i.e., a location different from the second location) where the additional location is fluidically isolated from the first location. In some embodiments, the first and second locations may be located on a single biomimetic platform. In some embodiments, the first location may be located on a first biomimetic platform, and the second location may be located on a second biomimetic platform. In some embodiments, the first and second biomimetic platforms may be engaged with a single control system. In some embodiments, the control system may receive data, provide control commands, and cause the second fluid solution to flow. In some embodiments, the first biomimetic platform may be engaged with a first control system, and the second biomimetic platform may be engaged with a second control system. In some embodiments, the method 800 may further include receiving second data, as shown in 804, indicating the measured concentration of the second target analyte in a third fluid solution resulting from the passage of the second fluid solution to the second biomimetic device. In some embodiments, the method 800 may further include providing a second control command to a second fluid synthesizer to cause the second fluid synthesizer to synthesize a fourth fluid solution containing the second target analyte at a measured concentration of the second target analyte or a concentration obtained from a mathematical adjustment or conversion of the measured concentration of the second target analyte, and reconstituting the complete or partial composition of the third fluid solution shown in 805. In some embodiments, the method 800 may further include flowing the fourth fluid solution into a third biomimetic device at a third position fluidically isolated from the first and second positions, as shown in 806.

[0100] In some embodiments, the fluid teleportation method may include measuring the constituent concentrations of dissolved chemical elements and solutes in the fluid by utilizing sensors specific to a first location. Optionally, mathematical transformations may be applied to the measured concentrations. These mathematical transformations, while illustrative and not limiting, may include doubling or halving the measured solute concentration during fluid production in a fluid synthesizer, adding two or more signals, component concentrations, or sets of components and their concentrations together, adding one or more constants to one or more component concentrations or signals, or combinations thereof. The concentrations may be transmitted to a control system or remote system. Fluid mixtures having equivalent chemical or solute concentrations are synthesized by mixing stock liquids together at a second location. In some embodiments, the mixture of stock liquids may include constituent mixtures of the same, partial, or derivative concentrations of the measured concentrations of the first fluid. The fluid mixture may be delivered to a third location. In some embodiments, the third location is discretely or physically separated from the first location. In some embodiments, the third position is discretely or physically separated from the second position. In some embodiments, the teleportation of the solution contents from the second position to the third position may be without a continuous fluid connection between the second and third positions.

[0101] In non-limiting embodiments, the biomimetic platform can record rare stimuli in the biomimetic device through multiple sensor modalities or targets, and the recording of such stimuli can be replicated in real time or at a later time by command. Multiple such recordings are replicated through multiple fluid synthesizers located remotely from each other. In non-limiting embodiments, the sampled fluid composition is modified and teleported to the fluid synthesizers in real time or at a later time. For example, the concentrations of multiple components belonging to the measured fluid composition transported by digital fluid teleportation can be modified from the concentrations or concentrations measured in the fluid recording. This technique allows characteristic outflow of the dynamic environment in the first biomimetic device to be reconstructed in the second biomimetic device without requiring the physical presence of the first biomimetic device in close proximity to and in fluid communication with the second biomimetic device. In certain embodiments, the fluid environment generated by the first biomimetic device can be resynthesized in the second biomimetic device at one or more later points in time without requiring the first biomimetic device to physically reproduce the measured environment locally in the first biomimetic device. Therefore, this technology can reduce costs, material requirements, and processing time.

[0102] In certain embodiments, the converted digital signals from a chemical or biosensor can be manipulated and adjusted before being resynthesized as part of digital fluid teleportation. In certain embodiments, a first fluid composition can be resynthesized as a second fluid by a fluid synthesizer such that the second fluid is a partial or derived mixture of the first fluid. In certain embodiments, the partial or derived mixture of the first fluid can contain at least one component of the concentration measured in the first fluid. The partial or derived mixture of the first fluid can be resynthesized into the second fluid at a different concentration than the measured concentration. The different concentration results from manipulation of the measured concentration by a process including algorithmic transformation, mathematical transformation, or transformation by signal processing techniques. For example, the disclosed technology enables characterizing a subset of components measured in the first fluid (e.g., determined by a linear combination of the storage fluid available to the fluid synthesizer or the storage fluid available to the fluid synthesizer), a subset of components measured in the first fluid (e.g., determined by experimental requirements such as incompatibility or toxicity between a particular compound at one location and a biological entity in a culture at a second location), a superset of components consisting of a mixture of some or all of the components in the first fluid mixture, additional components that are not present or measured in the first fluid mixture, or combinations thereof.

[0103] In certain embodiments, it is possible to prevent bulk transport of certain undesirable dissolved compounds in the first fluid by bulk fluid flow to the second location by digital fluid teleporting a partial or derived subset of the first sampled fluid at a first location to create a second fluid at a second location. In certain embodiments, such digital fluid teleportation of a partial or derived subset of the first sampled fluid can prevent bulk transport of certain undesirable dissolved compounds without requiring a physical mechanism to selectively filter the undesirable compounds from the bulk fluid mixture.

[0104] In certain embodiments, the biomimetic platform, which includes a plurality of individual biomimetic devices for culturing biofunctional chip models, can utilize digital fluid teleportation capabilities to selectively transport only a portion or derived subset of components in a first sampling fluid in a first biofunctional chip model to a second location corresponding to a second biofunctional chip model. In certain embodiments, this capability can be used to prevent the unintentional transport of dissolved compounds (e.g., growth factors, biological secretions, drugs, or chemical compounds) from the first biofunctional chip to the second biofunctional chip model. In some embodiments, the plurality of biofunctional chip models can be combined to form a “human body on a chip” configuration featuring a plurality of tissue types cultured in individual biofunctional chip models (each housed in a biomimetic device within the biomimetic platform) that are fluidically interconnected by digital fluid teleportation. In such embodiments for multi-organ or "human body on a chip" configurations, the ability to selectively transport only a partial or derived subset of components in the sampled fluid is utilized to transport a specific class of chemical compounds (e.g., biologically secreted compounds, hormones, paracrine factors, endocrine factors, signaling molecules, or combinations thereof) and not to transport undesirable compounds (e.g., growth factors for culturing only one type of tissue, metabolic waste, undesirable signaling molecules, organisms including viruses and bacteria, extracellular vesicles, or combinations thereof). In certain embodiments, the disclosed biomimetic platform is capable of preventing bulk leakage or transport of biochemical microenvironmental properties from a first biomimetic device or biofunctional chip model to a second biomimetic device or biofunctional chip model. The disclosed biomimetic platform prevents bulk leakage by fluidically synthesizing a mixture containing only the target set of concentrations of compounds in the fluid effluent of the first biomimetic device before introducing it into the second biomimetic device or a series of biomimetic devices.Such selectivity for components transported in a fluid is impossible in alternative systems configured to use direct fluid connections in which the entire fluid (or a volumetric subset thereof) moves physically in bulk by pump or directional flow in a sequential manner between multiple biological cultures connected in series.

[0105] In apparatuses having direct fluid connections between two or more sequential biological cultures, it is not possible to isolate or remove any dissolved components in a sequentially propagating fluid mixture without additional complex processes (e.g., chromatographic elution). Thus, the undesirable components can flow sequentially through all of the biological cultures. Such bulk, non-selective fluid flow prevents the mimicry or reconstruction of physiological processes (e.g., the natural isolation in the human body of specific local organ-specific biochemical microenvironments, biochemical signaling pathways, growth factors, morphogenetic agents, paracrine signaling compounds, or other biochemical components into a subset of just one tissue or space, in parallel with the large-scale or whole-body propagation of compounds such as endocrine or hormone signaling mechanisms).

[0106] In certain embodiments, fluid interconnections formed by digital fluid teleportation between multiple biomimetic devices can separate short-range biosignals or signaling cues within one tissue from biosignals inherent to, secreted, expected, or required in other tissues, and propagate selected signals by digital fluid teleportation, thereby overcoming the limitation of requiring a single "pluripotent stem cell culture medium" compatible with all biological tissues cultured in the biomimetic platform or system.

[0107] In certain embodiments, the biomimetic device can constitute a biological entity. The biomimetic device may include different growth media used for each tissue or biofunction chip model, superimposing the chemical signatures of compounds suspected to be involved in physiologically relevant inter-organ signaling. For example, for illustrative purposes rather than limiting purposes, the biomimetic platform may use the fluid addressing system to perfuse a first biomimetic device, a "pancreatic function chip," with a first specific culture medium formulation. The platform may sample the concentration of biologically secreted insulin in the effluent of the media formulation by the first pancreatic function chip biomimetic device, reconstitute the insulin concentration into a second media formulation using a fluid synthesis device, and subsequently deliver this second media formulation to a second biomimetic device, a "fat function chip." In certain embodiments, this process of selectively transporting a subset of chemical components allows for studying the binding effect of specific biocompounds without leakage between organs of the rest of the fluid environment. In certain embodiments, the concentration of a component or constituent in the fluid transported by digital fluid teleportation can be derived from one or more of the following: physical measurement, algorithmic manipulation of physical measurement, predicted value, or any other value.

[0108] In certain embodiments, the disclosed system is capable of amplifying the enrichment of multiple components in the measured signal to overcome proportional limits during the precise relative size determination of cultured biological tissue. For example, if the physical volume or cell mass of the biological tissue cultured in the first biomimetic device is insufficient to reproduce the physiological or desired concentration profile of a particular chemical substance resulting from other biological dynamic processes affecting the concentration of dissolved chemical compounds, such as biosecretion, biochemical modification, absorption, metabolism, or other soluble chemical compounds, the measured amount of the product secreted or absorbed by the biomimetic device can be mathematically transformed, scaled up, or scaled down linearly or nonlinearly or using a lookup table during the operation of the fluid synthesizer to conform to or mimic the physiological range or the desired target range. For example, individual pancreatic β-cells can secrete the same amount of insulin in a biomimetic device as in a human body. However, in a pancreatic function chip type biomimetic device, there are situations where a smaller number of islet β-cells cannot secrete the same physiologically relevant amount of insulin as produced in a human pancreas in response to an increase in glucose concentration in the medium. A fat-function chip biomimetic device, directly or by digital fluid teleportation, coupled to the pancreatic-function chip biomimetic device and exposed to the insulin, cannot induce sufficient glucose uptake to cause a significant change in the glucose content of the culture medium. In this example, the two biofunction chip biomimetic devices can be coupled in a physiologically appropriate manner, despite the size limitations in a particular embodiment of the biomimetic device, by amplifying both the detected concentration of the secreted insulin and the corresponding decrease in glucose in the medium when instructing the fluid synthesizer.

[0109] In certain embodiments, the disclosed system can reproduce a specific continuous fluid composition containing multiple chemical compounds and their target concentrations as a function of time at one or more designated locations, and can synthesize the fluid composition at those locations simultaneously or sequentially. In certain embodiments, by utilizing digital fluid teleportation to transmit fluid composition data over a communication network, including the Internet, the disclosed system can facilitate collaborative investigations of multi-tissue dynamics using resources and biomimetic platforms (and biomimetic devices within them) located in different facilities. In certain embodiments, collaboration between multiple laboratories, multiple institutions, and even multiple countries can be achieved by converting fluid composition from a biomimetic device into a digital signal, performing digital fluid teleportation, transmitting the signal to multiple biomimetic platforms, and converting the signal into a fluid mixture using a fluid synthesis device. Teams of experts in different organs and tissues can digitally connect their respective tissue models to form a human body model that spans the globe. For example, a cardiac function chip in France could be perfused to a lung function chip in Pennsylvania, a kidney function chip in California, and further connected to a liver function chip in Australia.

[0110] System Example As described above with reference to Figures 2A and 2B, the disclosed subject matter provides hardware-level components for operating and controlling its components, including, but not limited to, the biomimetic platform and biomimetic devices. These described components can be replaced, rearranged, modified, and redesigned to accommodate any possible variations of the system.

[0111] Figure 14 shows an exemplary system hardware architecture of one embodiment of a control system 970 operating with multiple biomimetic platforms 900 and various external devices and systems. As shown, the control system 970 includes a main control unit 972, a web client 973, a fluid synthesizer control unit 974, an addressing system control unit 976, a BioLine server 977, a network PC 979, a data receiver 981, and an imaging device 982. As shown, the biomimetic platform 900 includes a fluid synthesizer 910, a fluid addressing system 920, a biomimetic device 930, and a biosensor 940. In certain embodiments, the main control unit 972 is capable of running fault-tolerant control system software that can synchronize one or more of the following: digital fluid teleportation, fluid coupling, data acquisition, fluid control, pneumatic control, system monitoring, environmental monitoring, experimental feedback, user interaction, automatic response to nominal or fault conditions, environmental climate control, data transmission, web server operation, communication with additional biomimetic platforms, and synchronization with additional biomimetic platforms. In certain embodiments, the master control unit 972 can provide a web browser-based user interface to a local user's computer, laptop, and / or mobile device. In certain embodiments, the user interface to the control system of the biomimetic platform can run in a web browser, so as long as it has a web browser, it can be compatible with a variety of platforms, such as mobile or conventional desktops. In certain embodiments, a web-based user interface can eliminate the bottleneck that requires multiple users to share a single physical computer (e.g., the master control system itself). In some embodiments, the core software can run on the master control unit 972, and users can use or log in to a lightweight user interface or user client on their device (e.g., via a web client 973).In certain embodiments, but not limited to them, the user may use the user interface to do one or more of the following: design a new experiment, implement or sequence methods required for a new experiment, define a biomimetic apparatus experiment, modify an existing experiment, monitor acquired data, export data, plot data, perform graph elements or analyses, and manage digital fluid teleportation connections.

[0112] In some embodiments, the fluid synthesizer control unit 974 and / or the addressing system control unit 976 may include a shift register for port expansion that can be used for real-time control of the pneumatic valves on the biomimetic device 930. The fluid synthesizer control unit 974 and / or the addressing system control unit 976 may include an industrial microcontroller that can drive relays for valve operation and motion control (e.g., the imaging device 982) in response to higher-level control commands from the main control unit 972. In some embodiments, the imaging device 982 may include an SPR imaging camera. In some embodiments, the imaging device 982 may include a laser scanner. For example, each biomimetic platform 900 may have 14 valves (4 ports, 2 positions each) (7 on each side) for the fluid addressing system 920 and 48 valves (3 ports, 2 positions each) (1 to 24 on each side) for the fluid synthesizer 910. In non-limiting embodiments, each biomimetic platform 900 may have 12 four-way / two-position valves + 4 three-way / two-position valves, or 28 three-way / two-position valves. The latter configuration allows for depressurization of the entire fluid addressing system 920, thereby enabling simultaneous cleaning of all connected biomimetic devices 930. The connected compounds may be mixed in different ratios or in the same ratio. In some embodiments, two inlet solutions to the fluid synthesizer 910, which may be mixed in the same ratio, may be driven by a single valve. In some embodiments, the fluid synthesizer 910 may be expanded to accommodate 25 or more different mixture inputs on each side. As the number of valves required increases accordingly, latch-shift registers may be chained to create a parallel array of control pins for the pneumatic valves.

[0113] In certain embodiments, the biosensor 940 in each organ sensor unit is converted into a digital signal by the imaging device 982. The imaging device 982 can be connected to a networked PC 979 for the purpose of transmitting this converted data to the main control unit 972. In some embodiments, the networked PC 979 may include a small computer. In some embodiments, the networked PC 979 may include a laptop computer. The main control unit 972 can read the output directly from the imaging device 982 if the additional real-time data processing requirements do not cause any slowdown or interference. Connection from the local main control unit 972 to a software server (e.g., BioLine Server 977) connected to the Internet, cloud, or a SaaS (software-as-a-service) system makes it possible to establish software license management, access to a virtual tissue library, and real-time digital interoperability with offsite organ devices. Multiple biomimetic platforms 900 can be operated locally by a single main control unit 972. When interacting with off-site biomimetic platforms 900 and biomimetic devices 930 (platforms and devices operated by separate master control servers), data transmission can be mediated by the internet or cloud software servers. These technologies can enable improved quality and easily established connectivity that can be maintained and monitored for events including, but not limited to, connection dropouts, prediction of bandwidth requirements, consideration of load balancing, and optimization of data traffic routing.

[0114] The disclosed subject matter provides software applications and techniques for operating the biomimetic platform 900. Disclosed biological virtualization techniques for statistical data processing and modeling virtual tissues and virtual organs are integrated into the main control unit 972 and can be configurable in the user client. In a non-limiting example, the disclosed system may have a main control unit 972 capable of providing fault-tolerant software for synchronizing and managing all operations of the biomimetic platform 900 in real time. The software of the main control unit 972 can determine a pulse-width modulation (PWM) bias in the fluid synthesizer 910 based on user settings and transmitted signals from the biosensor 940. In a non-limiting example, the opening and closing cycle of a flow metering valve controlled by pulse-width modulation can enable proportional control of flow rates via microfluidic valves (e.g., in the fluid addressing system 920 or the fluid synthesizer 910). In certain embodiments, the PWM can be applied at a certain frequency to enable a complete opening and closing cycle in the valve. For example, if a pulse width of 0% corresponds to a normally closed valve and a pulse width of 100% corresponds to a normally open valve, a valve with a pulse width of 60% can remain open twice as long in each pulse cycle as a valve with a pulse width of 30%. The fluid velocity can be controlled by adjusting the opening period. In certain embodiments, the PWM is applied at a certain frequency to prevent complete operation (closing or opening) of the valve between the signal-high and signal-low portions of the pulse. For example, a sufficiently high PWM frequency allows such an elastomer valve to oscillate or undulate closely around a steady position, thereby enabling a valve with a 60% pulse width to maintain a steady position that allows twice the flow of a valve with a 30% pulse width. In certain embodiments, a fluid-filled fluid control line can be integrated into the microfluidic valve of the biomimetic platform 900 and driven using a syringe pump or a peristaltic pump.

[0115] The software of the main control unit 972 can control the biomimetic platform 900 by sending commands to a microcontroller (e.g., the fluid synthesizer control unit 974 and / or the addressing system control unit 976) to activate specific biomimetic device 930 addresses within the fluid addressing system 920 for monitoring flow rate, fluid level, and pneumatic line pressure. In certain embodiments, the software of the main control unit 972 can control the biomimetic platform 900 to perform data processing, host a local web server for web client logins, package data for transmission to local web clients (e.g., a data receiver 981, a local data storage location, and a local data server), and maintain connections to one or more of the data servers and control servers. In certain embodiments, National Instruments LabView may be used to implement the control software. In certain embodiments, other programming languages ​​may be used to implement the control software, including, but not limited to, one or a combination of C++, C#, Python, and Java.

[0116] In certain embodiments, the control system 970 can detect leaks, blockages, or a combination of leaks and blockages in the biomimetic platform 900 by polling data from the outlet flow meter and alert the user by email, text message, or other direct or indirect means of communication. In certain embodiments, upon detection of a leak or blockage event, the control system 970 can be configured to take immediate action (e.g., interrupting flow to the blocked biomimetic device 930, interrupting flow throughout the device 930, pausing the experiment, or continuing as normal).

[0117] In certain embodiments, the control system 970 may provide user client software. For example, a user of the control system 970 may design, monitor, and process experiments on a software client provided by the main control unit 972 or by an internet server, which can be run on their web browser. In certain embodiments, the user client software may run as a local application on a computer (e.g., the network PC 979) or as a distributed application across multiple computers. In certain embodiments, the software may present aspects of an ongoing experiment (including, but not limited to, portions of measurement data) alongside a head-up display of the current state of the fluid addressing system 920 on the biomimetic device 930, shown alongside two columns of the biomimetic device 930. In certain embodiments, a user may click on an individual biomimetic device 930 to expand a settings box. In certain embodiments, each biomimetic device 930 may be customizable (e.g., by giving it a name, a distinctive icon, visual features, or a combination thereof). In certain embodiments, each biomimetic device 930 may have all of its sensors 940 and flow characteristics specified in the user interface. In certain embodiments, real-time data can be visualized in graph form on a subpanel of the interface, allowing for an at-a-glance summary of the biomimetic device's status. In certain embodiments, the user interface can enable the import of supplementary data and its association with multiple aspects of existing data, including timestamps or sensor recordings.

[0118] In certain embodiments, and exemplary but not limiting, in response to seeing unexpected sensor readings, the user can image the biomimetic device 930 in question and associate the image as an accompanying data file with the corresponding point in time of recorded sensor or platform operation for later analysis. In non-limiting embodiments, the real-time data subpanel can be minimized. In certain embodiments, a digital fluid teleportation outline can provide a visualization of the connections between biomimetic devices 930 on multiple biomimetic platforms 900. In certain embodiments, the interface design can improve functionality and clarity of obtained data by providing visual aesthetics in the form of bold colors. In certain embodiments, the visual style of the user interface can complement the clarity of the presented data. The software generated by the disclosed subject can support alternative colors and improved contrast schemes to enable access for users with color blindness or visual impairment. In some embodiments, the biomimetic devices 930 can be presented in the user interface as movable blocks, and the synthesized fluid connections can be established by dragging and dropping visual links or relationships between the movable blocks. In certain embodiments, experiments can be designed in a user interface using graphic elements including blocks, lines, or curves. In certain embodiments, experiments can be designed through interaction with the biomimetic platform and platform software via a command-line interface (CLI).

[0119] In certain embodiments, the disclosed subject provides internet-accessible software that can run on a centralized software server. In certain embodiments, the internet-accessible software can manage the installation of multiple biomimetic platforms, client licensing and communication between accounts, and provides access to templates, optimization protocols, and standard libraries for virtual organizations as part of a subscription service. In certain embodiments, the disclosed system can operate across distributed cloud platforms (e.g., Amazon AWS and / or Microsoft Azure).

[0120] Screen forward implementation In some embodiments, the biomimetic platform and control system architecture described above can function collectively as a high-throughput screening system. The screening system can define one or more target conditions (e.g., chemical compounds, therapeutic agents, treatments, and / or fluid compositions) and identify the responses of cultured tissue in the biomimetic device (e.g., time-dependent responses and / or endpoint responses) that may arise from the defined conditions. The screening process can begin with known conditions or externally applied condition profiles (e.g., drug concentration profiles mimicking dietary administration) and identify endpoints arising from each such condition (e.g., a "screenforward" approach). An example of such a screenforward approach is shown in the flowcharts of Figures 15A and 15B illustrating method 1000. For example, as shown in Figures 15A and 15B, compounds, chemical concentration profiles, conditions, and / or physiological modifiers can be defined for the biological screening shown in 1001. If the exemplary system includes a software-guided experimental design determined in 1002, then software-guided statistical analyses (e.g., power analysis, combinatorial or factorial analysis, orthogonal experimental design, D-optimal experimental design, and / or experimental cost management) as shown in 1003 can be performed. A specific experimental design (e.g., the quantity or arrangement of biological replicas in a biomimetic apparatus) can be determined without a software-guided experimental design, as shown in 1004. Then, based on the experimental design, biological replicas (e.g., tissues, organ models, organ model systems, or combinations thereof) can be distributed into the biomimetic apparatus of the exemplary microfluidic system, as shown in 1005. The biological replicas can be exposed immediately or after a maturation period to predefined experimental conditions (e.g., specific concentrations of nutrients, drugs, bacteria, viruses, gene editing agents, or combinations thereof) as shown in 1006.If present and valid, as determined in 1007 of the exemplary system, the integrated biosensor can perform sequential or discrete sensing of a target (e.g., DNA, RNA, protein, growth factor, hormone) as shown in 1008. The detected results and data can be stored and displayed in a graphical user interface as shown in 1009. The biological replicas can be cultured for a predetermined period as shown in 1010. If the integrated biosensor is not determined to be present and valid in 1007, 1008 and 1009 are skipped, and method 100 proceeds to 1010. Upon reaching the experimental endpoint period, endpoint measurements can be performed according to the experimental design shown in 1011. For illustrative and non-limiting purposes, the endpoint measurements may include one or a combination of immunohistochemistry (IHC) staining, immunocytochemistry (ICC), tissue extraction, microscopy, RNA or DNA isolation, transcriptomics, proteomics, and cell isolation. The measured endpoint data can be stored and reported to the user as shown in 1012.

[0121] In non-limiting embodiments, the disclosed system can screen multiple conditions. Various dynamic and continuous conditions (e.g., drug concentration profiles and / or predetermined drug concentrations based on drug splitting models) can be compounded in real time by the disclosed fluid synthesizer. In certain embodiments, the disclosed system can test one or a combination of dynamic and continuous conditions for screening. As a non-limiting example, the disclosed system can determine the effect of different concentrations of vascular endothelial growth factor (VEGF) receptor inhibitors on tumor angiogenesis, the effect of administering VEGF inhibitors at different frequencies or concentrations on tumor angiogenesis, or the effect of administering the VEGF inhibitors in dynamic concentration profiles that mimic metabolism and / or transport in the human body.

[0122] In a particular embodiment of the Screen-Backward Implementation, the disclosed system can perform a screening study or screening experiment by identifying known endpoints and finding the conditions that cause or generate such endpoints. The disclosed system can define a target endpoint state and search for a set of initial conditions or conditional profiles that can generate the target endpoint state through one or a series of iterative refinements (i.e., a “screen-backward” approach). For example, Figures 16A–16D depict method 1100, in which a biological endpoint target state, profile, performance, and / or morphology is defined, as shown in 1101. If the exemplary system can include a software-inducible experimental design, such as that determined in 1102, then software-inducible statistical analysis (e.g., power analysis, combinatorial analysis, orthogonal experimental design, D-optimal experimental design, experimental cost control, experimental modifiers, drugs, therapeutic compounds, chemical profiles, and tissue composition determining the dimensions of the experimental space) as shown in 1103 is possible. A specific experimental design (e.g., experimental modifiers, drugs, therapeutic compounds, chemical profiles, and / or tissue compositions) can be determined without the software-guided experimental design shown in 1104. Based on the experimental design, biological replicas (e.g., tissues, organ models, organ model systems, or combinations thereof) can then be distributed into the exemplary microfluidic biomimetic apparatus shown in 1105. The distributed biological replicas can be immediately or, after a maturation period, exposed to predefined experimental conditions (e.g., nutrients, drugs, bacteria, viruses, and / or gene editing agents in concentrations of 1 or a range) as shown in 1106. If an integrated biosensor exists and is active, as determined in 1107, the method 1100 may, in 1108, include performing sequential or individual sensing of a target (e.g., DNA, RNA, proteins, growth factors, hormones). The detected results and data can be stored and displayed in the graphical user interface shown in 1109.As shown in 1110, 1111, and 1112, the screen-backward mode method includes determining whether an integrated biosensor is present and enabled, whether the experimental duration, if defined, has been reached, and whether sensor-based feedback is enabled, respectively. If both sensor-based feedback and the integrated biosensor are enabled and the experimental duration has not been reached, method 1100 includes using sensor measurements to perform feedback control of biological behavior by modifying culture conditions, as shown in 1113. This loop continues until the experimental duration is reached. In a non-limiting embodiment, the biosensor may provide real-time feedback based on detected data regarding the experimental duration and / or biological behavior. The detected data can be used to modify the culture conditions, as shown in 1112. The biological replica in the biomimetic device is cultured for the predetermined period, as shown in 1114. Method 1114 occurs when the experimental duration is reached or when the integrated biosensor is not present and not enabled. When the experimental endpoint duration or phase is reached, endpoint measurements can be performed according to the experimental design, as shown in 1115. The measured endpoint data is stored and can be reported to the user as shown in 1116. If any replica can achieve the target endpoint state shown in 1116, the experimental conditions required to achieve the target endpoint state can be presented to the user as shown in 1118. Otherwise, the disclosed system can loop back to 1105 by repeating the screen-backward procedure sequentially or iteratively via 1119 until the target endpoint state can be achieved. As a non-limiting example, various experimental conditions can be iteratively defined for the following series of experiments. The experimental conditions can be defined automatically or semi-automatically by software induction, or by one or more manual inputs, requirements, and / or constraints.

[0123] In non-limiting embodiments, the disclosed system can define a state in which tumor angiogenesis is restricted and systemic toxicity-induced cell death is restricted, and then screen for time-dependent administration conditions of a VEGF inhibitor that result in this intended endpoint. In non-limiting embodiments, the disclosed system can be used for biological screening procedures. For example, the system can be employed on tissue cultured from a reporter cell line of human pancreatic beta cells that express a fluorescent protein during insulin secretion. The target endpoint state can be defined as a specific time-dependent fluorescence intensity profile (correlated to a time-dependent insulin release profile) in response to exposure to an increased glucose concentration in a fluid mixture. The disclosed system can iteratively screen for combinations of culture conditions (e.g., from a series of growth factor, glucose, and drug compound precursor solutions) and time-dependent profiles that can produce this target endpoint response.

[0124] In certain embodiments, the disclosed screen-forward and / or screen-backward modes are selected for multiple devices or multiple tissue models defined in a biomimetic device on one biomimetic platform or multiple connected biomimetic platforms. The screen-forward or screen-backward modes can define the target state or target condition for multiple systems. For example, the screen-forward or screen-backward conditions or constraints can be applied to one tissue or to multiple tissues. The conditions or constraints can be defined as an ideal target range for a certain biological behavior or biochemical reaction. In non-limiting embodiments, the conditions or constraints can be optimized as a ranking of priorities or as a cost function related to the health of one tissue as seen from the other. For example, a target final state can be defined for the screen-forward and / or screen-backward modes that prevents a behavior in one tissue while minimizing the effects of drug toxicity in another tissue.

[0125] In certain embodiments, the user interface is designed as shown in Figures 17A and 17B, for illustrative purposes only and not limiting. In certain embodiments, the operating mode of the biomimetic platform may affect the elements, layout, and functionality of the user interface.

[0126] Virtual Tissues The disclosed subject matter provides, in certain embodiments, systems and methods for developing and integrating “Virtual Tissues.” Where the response of a biomimetic device (e.g., the biomimetic device 130 described above with reference to Figure 1, a specific biological entity, or a biological tissue) to a given input space of possible combinations of stimuli is characterized, the physical embodiment of that particular biomimetic device can be replaced by a virtualized simulated representation based on predicted or pre-established behavior or response. For example, any of the devices described above with reference to Figures 11A–11D and Figure 12 may include a virtual or simulated device (e.g., a virtual tissue representation). In certain embodiments, this virtual device (e.g., a virtual tissue) is computationally simulated by creating a predictive or statistical model of expected behavior based on data gathered from observations of the physical embodiment of the device being simulated (within the biomimetic device, in animals, in humans, gathered from scientific literature, or a combination thereof). In certain embodiments, this virtual device is computationally simulated based on heuristics, rules, or datasets. In certain embodiments, this virtual device is simulated based on inference-based predictions. The digital output of the virtual device can be similar to or identical to the output measured by a sensor from the corresponding physical version in which the virtual device is replaced. Thus, such a virtual device can be coupled with one or more additional physical biomimetic devices or additional virtual devices, and the response, absorption / secretion, and behavior of the first virtual device can be modeled computationally.

[0127] In certain embodiments, the biological behavior of a target tissue can be predicted by using a virtual tissue, and this includes creating a statistical predictive model of the target tissue based on physical observations of the target tissue, and applying the statistical predictive model to predict mutations in a first fluid solution. The mutations may include chemical or biological changes induced when the first fluid solution is cultured with the target tissue to produce the second fluid solution. In non-limiting embodiments, the first fluid solution may be the input to the virtual tissue, and the second fluid solution may be the output of the virtual tissue. In some embodiments, a first continuous mathematical function or continuous measurement may be used as the input to the virtual tissue, and a second continuous mathematical function may be produced as the corresponding output. For example, the continuous mathematical function may be a continuous relationship with time. For illustrative purposes only, and not as an limitation, the continuous input function to a virtual tissue for compound "A" whose concentration increases linearly as a function of time can be written as A(t) = A0t, where "A0" is a constant defining the accumulation rate. If the virtual tissue secretes compound "B" and the concentration of compound "B" is always kept at twice that of "A", then the continuous output function of the virtual tissue for compound "B" is B(t) = 2A(t), which can also be written as B(t) = 2A0t. In certain embodiments, by symbolically linking the input and output of the virtual tissue in this way, these equations can be rapidly calculated by numerical or analytical methods, and simulation results can be generated. In certain embodiments, output data can be generated by utilizing any mathematical transformation of the numerical values ​​generated by the virtual tissue output.

[0128] In certain embodiments, predicting the biological behavior of a target tissue using virtual tissues may further include combining at least two virtual tissues by connecting the output of a first virtual tissue to the input of a subsequent virtual tissue. In non-limiting embodiments, a network of at least three virtual tissues is established. Each virtual tissue can receive at least one input and produce at least one output. Each of the at least one output can be connected to zero or at least one input of a virtual tissue. In non-limiting embodiments, each of the at least one input and output is mathematically transformed before or after being connected to a virtual tissue. At least one input and output data from each virtual tissue can be recorded discretely or continuously over a duration within the scope of the experiment.

[0129] In a particular embodiment, predicting the biological behavior of a target tissue using a virtual tissue may further include the steps of identifying the components of the second fluid solution calculated from the output of the virtual tissue, and synthesizing a fluid solution based on the identified components using a fluid synthesis apparatus.

[0130] In certain embodiments, the reactions, absorption / secretion, and behavior of multiple virtual tissues can also be computationally modeled in this manner. In certain embodiments, the observations can be derived from existing data in scientific or medical literature. In certain embodiments, the observations can be derived from measurements performed on a biomimetic platform. The observations are used to predict the behavior of biological entities (cultured in certain embodiments within a biomimetic device), allowing the biological entities to be simulated as virtual tissues rather than physically deployed within the biomimetic device. These models can range from computationally simple (for example, a virtual tissue can be embodied by a lookup table mapping the concentration of a single input factor or chemical to a corresponding amount of a second secreting compound) to computationally complex models based on statistical algorithms used in machine learning (see Figure 18). In certain embodiments, for illustrative and non-limiting purposes, the virtual tissues are simulated by neural networks, decision trees, ensembles of multiple machine learning methods, or statistical inference. Digital signals converted from biosensors associated with actual biological entities cultured within a biomimetic device can be inputs to the virtual tissue or a subset of the virtual tissue inputs, and the outputs of the virtual tissue can then be used as digital inputs to a fluidity synthesizer that supplies the medium mixture (including secretions from the virtual tissue) to the tissue in physical culture. In certain embodiments, multiple virtual tissues can be coupled or linked to each other.

[0131] For example, as shown in Figure 18, a biomimetic chip model cultured in a biomimetic device can be characterized by acquiring a substantial amount of data through the use of the biomimetic platform under a wide variety of culture conditions. The dynamic response of the cultured tissue under predetermined conditions can then be computationally predicted based on the collected data, which maps the input conditions to phenotype, behavior, and secreted factors and compounds. In certain embodiments, the prediction method may use interpolation of existing data to generate predictions. In certain embodiments, machine learning or statistical learning techniques may be employed to generate predictions. Tissue virtualization can be achieved by replacing real tissue with virtual tissue and digitally interfaced to a fluid synthesizer for real tissue or other digital inputs for virtual tissue. Thus, the disclosed virtual tissue technology can enable the expansion or enhancement of the biomimetic device with additional virtual tissues to allow whole-body functional chip analysis for all real tissues in culture (for example, by simulating all other tissues or organs in a whole-body model).

[0132] In certain embodiments, the disclosed virtual tissue system can statistically model real biomimetic devices based on sensor or image data measured in real time while they are running. In certain embodiments, the virtual tissue system can use the measured sensor or image data to display a predictive extrapolation of its behavior to the user. In certain embodiments, if a local biomimetic device is engaged in digital fluid teleportation connectivity to an off-site biomimetic device in a multi-center collaborative study, continuous statistical modeling and machine learning algorithms can be used to provide a transient virtual tissue as a substitute during temporary dropouts of data connectivity.

[0133] In certain embodiments, a method for predicting the biological behavior of a target tissue or target multi-tissue interaction using the virtual tissue may further include coupling the virtual tissue to the biomimetic device by delivering the composition of the output solution of the virtual tissue to the biomimetic device as a synthesized fluid solution. In certain embodiments, the measured partial or complete composition of the fluid flowing out of the biomimetic device may be used as the data input to the virtual tissue. In non-limiting embodiments, at least one virtual tissue may be coupled with at least one biomimetic device by delivering the synthesized fluid solution to the at least one biomimetic device via the fluid addressing system. In some embodiments, the method may further include creating a mixed network of biomimetic devices and virtual tissues by coupling at least one virtual tissue with at least one biomimetic device. For example, multiple virtual tissues and / or multiple real tissues in biomimetic devices within a biomimetic system may be coupled by digital fluid teleportation, and the “fluid” teleported to or from the virtual tissue is processed only as a digital signal (resulting in the absence of a physical tissue to which the fluid analog is delivered for interaction). If multiple types of tissue cultures in a biomimetic platform are characterized to the same degree, multiple virtual tissues and / or multiple real tissue units can be combined in a manner similar to that previously described for systems having only physical ("real") biomimetic device cultures.

[0134] Figure 19A shows an exemplary coupling of a physical biomimetic device via digital transmission. Figure 19B shows an exemplary coupling of a single physical biomimetic device with a dynamic system of multiple virtual tissues. The virtual tissue receives digitally transmitted fluid effluent from the physical biomimetic device and can process the data according to the characterized behavior of the virtualized biological entity. The virtual tissue then transmits the digital output of the corresponding fluid to the fluid synthesizer of the physical tissue, where it can be reconstituted into a physical mixture. The virtual tissue then transmits the digital fluid output of the corresponding effluent to the fluid synthesizer of the physical tissue, where it can be reconstituted into a physical mixture. In a non-limiting embodiment, a complete virtual system can be established by linking two or more virtual tissues, as shown in Figure 19C. In certain embodiments, the screen-forward and screen-backward operating modes can be used with virtual tissue models to substitute for a particular physical model in the disclosed system. In certain embodiments, a screen-forward or screen-backward approach consisting solely of virtual tissues can be used to identify the most promising conditions or predicted results of a series of experiments. In certain embodiments, the identified prediction can be used to select physical experiments to be performed on a biomimetic device.

[0135] In certain embodiments, the method for predicting the biological behavior of a target tissue using a virtual tissue may further include generating behavioral or observational data from the at least one biomimetic device. The behavioral or observational data may be used to improve a statistical predictive model. In non-limiting embodiments, the target tissue may be cultured with the at least one biomimetic device under predetermined conditions to provide the behavioral or observational data for improving the statistical predictive model. In some embodiments, at least one component of the behavioral or observational data may be provided to train the statistical predictive model. In certain embodiments, at least one virtual tissue may be used to predict the biological behavior of the target tissue.

[0136] In certain embodiments, feedback data can be obtained using a disclosed biosensor (e.g., the biosensor 140 as described above with reference to Figure 1). In some embodiments, the biosensor can be integrated on-chip (i.e., on a substrate such as the substrate 101 as described above with reference to Figure 1). In some embodiments, the biosensor can be detachable. For example, the disclosed system can function perfectly well without a biosensor. An exemplary system without a biosensor can still use the fluid synthesizer to prepare fluids or fluid mixtures in real time from fluid reagents connected to the system or more. For example, there may be multiple precursor fluid inlet connections from which a composite solution can be prepared. The number of such connections can be expanded based on the need. An exemplary system without a biosensor can use the fluid addressing system to deliver the fluid preparation to a target culture chamber by selecting the target chamber as the intended destination for the fluid. The fluid synthesizer can change the composition of this fluid in real time to create dynamic fluid formulations. In some embodiments, output data from the device can be delivered to an external sensor (e.g., an "off-chip" sensor) on the substrate. In some embodiments, the output data can be sent to a vial outflow line and / or a fluid processing system to sample the fluid downstream of the device and supply the fluid to the biosensor.

[0137] In certain embodiments, exemplary systems without integrated biosensors can generate microliters of a specified fluid mixture to perform conditional or combined cleaning on selected culture chambers. Instead of using integrated biosensors, the effluent can be sampled from the system's outlet port, and the endpoints used to quantify the results of the screening conditions can be measured from the sampled fluid. For example, the endpoint measurements may include biochemical secretion, metabolism, measurement of biochemical processes, bright-field imaging of the contents of the culture chamber, fluorescence imaging of the contents of the culture chamber, electrophysiological measurements (e.g., transepithelial electrical resistance (TEER) measurement), genomic / transcriptome / proteomics quantification of cells or subsets of cells in the culture chamber, cell retrieval for subsequent processing (e.g., paraffin sectioning or processing for electron microscopy), or a combination thereof.

[0138] In certain embodiments, an exemplary system without a biosensor can record a fluid composition on an external biosensor platform and digitally teleport the recorded fluid composition to a fluid synthesizer. For illustrative and non-limiting purposes, the tissue secretion can be sampled into a plurality of discrete collectibles over a time series, and the concentration of the secretion can be measured using conventional evaluation techniques (e.g., by ELISA). Following the measurement of these samples, the obtained concentration profiles can be used as a fluid synthesizer, and thus such records can be replicated through at least one fluid synthesizer that may be located remotely from each other. In non-limiting embodiments, the sampled fluid composition can be modified and teleported to a fluid synthesizer. As a non-limiting example, the concentration of the teleported fluid composition can be modified from the concentration measured in the fluid record.

[0139] In certain embodiments, exemplary systems without biosensors can perform the screen-forward and / or screen-backward screenings. Initial conditions (whether fixed in the screen-forward approach or generated heuristically / iteratively in the screen-backward approach) can be formulated by the fluid synthesizer, and sensor feedback is not required. Similarly, endpoints in either mode can be selected so that quantification can be generated off-chip. In non-limiting embodiments, the biosensors can be integrated into the disclosed system to collect more data related to biological characterization and / or enhancement of associated virtual tissue models.

[0140] In certain embodiments, the virtual tissue can reduce the physical complexity of the biomimetic platform (compared to the use of equivalent real / physical models) at the expense of increased computational complexity. By incorporating virtual tissue as a substitute for biomimetic devices, scientific experiments or investigations conducted using the subject can become less expensive and less time-consuming. For example, the virtual tissue is free from the risk of biological contamination and may not require biological supplementation with culture media or growth factors. Furthermore, the statistical model of the virtual tissue may be deterministically reproducible. In some embodiments, the virtual tissue can operate in training mode. In such training mode, the biomimetic platform can challenge one or more tissues in real time, as determined by the statistical uncertainty of the virtual tissue, using physical biomimetic devices, with the aim of improving the predictive effectiveness of the virtual tissue in areas or situations where its existing predictive ability is weakest or most error-prone. In certain embodiments, these regimes or situations may include, without limitation, a series of fluid compositions not previously encountered in order to measure the response of the real tissue and thereby populate any missing areas in its statistical observation space. The disclosed training mode can provide edge cases in real organizations and contemplate useful situations in order to enhance the virtual model through a machine learning approach. The disclosed training mode can ensure that the virtual organization does not over-interpolate from physically obtained data during actual experiments in order to maximize its predictive power and minimize errors.

[0141] In certain embodiments, the experiments performed by the disclosed subject matter may consist solely of virtual tissues for predictive modeling. In non-limiting examples, the disclosed applications of biovirtualization can be used in both screen-forward and screen-backward computational solutions. In certain embodiments, the disclosed virtual tissue system can answer exemplary predictive questions, including, but are not limited to, "given these initial conditions, what tissue dynamics will be predicted to be observed over four weeks?" or "given these desired mechanical properties of a tissue, what formulation of initial conditions will be predicted to produce the said properties?" In certain embodiments, the disclosed computational techniques can be used in drug development in both drug candidate screening (forward calculation of drug effects, in non-limiting examples, "how the behavior of tissue will change under the influence of this drug") and drug candidate identification (forward calculation of desired drug targets, in non-limiting examples, "given that progression to a healthy state over four weeks depends on these initially calculated changes in cellular behavior, what types of drugs would cause these changes?").

[0142] In certain embodiments, the disclosed subject provides a browseable virtual tissue library that can be accessed from a user software client during configuration. The virtual tissue library can provide access to various virtual tissue modules. Furthermore, the virtual tissue library can provide an interface to real tissue that can be cultured in a biomimetic device, which can be seeded and cultured at a central location and interact with the client's local tissue culture by fluid teleportation away from the site, with a client-configurable seeding date. Thus, the virtual library can be a cheaper alternative for the user than continuously culturing their own large-scale libraries of cells and tissues in tissue culture and managing costs such as ordering flasks, growth media, and cell lines.

[0143] In certain embodiments, the disclosed subject matter provides a method for connecting a biomimetic device to a virtual tissue. An exemplary method may include, in the biomimetic device, characterizing a fluid solution by measuring the concentration of at least one target analyte with a sensor, generating an input to the virtual tissue based on the measurement, and providing the input to the virtual tissue.

[0144] Examples of tissue culture use In certain embodiments, the disclosed subject matter can provide a system for creating large quantities of functional tissue. The biomimetic platform described herein (e.g., the biomimetic platform 100 as described above with reference to Figure 1) can be used for therapeutic tissue engineering by creating a target quantity of tissue for transplantation. The biomimetic platform can create tissue on a scale that generates sufficient tissue volume to culture functional tissue. For example, a fluid synthesizer (e.g., the fluid synthesizer 110 as described above with reference to Figure 1) can control the biochemical environment of multiple devices (e.g., tissue culture chambers) that produce tissue with low morphological variation. A fluid addressing system (e.g., the fluid addressing system 120 as described above with reference to Figure 1) can utilize fluid input to support a large number of biomimetic devices (e.g., hundreds, thousands, or more) with a consistent flow rate, a consistent flow rate duration, and a consistent fluid composition. The biomimetic platform described herein can enable the cultivation of functional tissue on an improved scale compared to conventional tissue culture methods, which include the deployment of tissue cultures in the limited footprint of manual dispensing or well plate systems.

[0145] In certain embodiments, the disclosed subject can provide a system for differentiating and maturing tissues. For example, a biomimetic platform can be formulated such that the entire differentiation process of organoid tissue is automated by a fluid synthesis device and a fluid addressing system. The fluid synthesis device and fluid addressing system can generate and supply the solutions required for differentiation to a target device. The required solutions can be a biological growth medium that can contain various compounds for tissue differentiation (e.g., growth factors, transcription inhibitors, and / or nutrients). In non-limiting embodiments, the disclosed screen-forward and screen-backward operating modes are used to optimize organoid growth, differentiation, and biological function. In some embodiments, the integrated biosensor (e.g., the biosensor 140 described above with reference to Figure 1) can provide continuous feedback on the state of the organoid. The integrated biosensor can enable a feedback-based differentiation protocol in which the culture conditions can be dynamically changed. In some embodiments, the disclosed system can also provide fixed conditions for developing organoid tissue.

[0146] Other usage examples In certain embodiments, the disclosed system can be used to evaluate the effects of genetic modification on tissue. In non-limiting examples, the fluid synthesis apparatus and the fluid addressing system can be used to produce a culture medium having a drug capable of modifying, introducing, or knocking out specific genes in cells. The gene editing agent may include various components used in various gene editing technologies (e.g., CRISPR-Cas9, TALEN, meganucleases, zinc fingers, and / or gene therapy). In non-limiting embodiments, the disclosed system can be used to evaluate the effects of the genetic modification on the tissue scale. In certain embodiments, the disclosed system can deliver a drug capable of performing genetic modification on a targeted subset or subpopulation of cells. The integrated biosensor can monitor the state of the tissue and provide real-time feedback.

[0147] In certain embodiments, the disclosed system can be used to deliver cells or bacteria to tissue within a culture chamber. The fluid synthesis device can add living organisms to the fluid mixture, which can then be delivered by the fluid addressing system. The disclosed system having living organisms in the fluid mixture can be used to screen living tissues. For example, the effect of bacterial infection on lung tissue can be screened by delivering one or more types of bacteria to one or more target tissues cultured within the device. In non-limiting embodiments, the disclosed system can be used to screen immunotherapies. In a non-limiting example, certain modified human cells, including T cells enhanced with chimeric antigen receptors (i.e., CAR-T cells), can be flowed into one or more tissues in a culture chamber on the device. The binding efficacy of different CAR-T cells to specific tissues, cancers, cells, drugs, and / or living organisms can be evaluated. In some embodiments, specific cancer tissue can be cultured within the biomimetic device, and immunotherapies, including CAR-T cell therapy, can be screened for their efficacy targeting the cancer tissue using either the screen-forward or screen-backward operating mode.

[0148] In certain embodiments, the disclosed system can deliver a virus to tissue cultured therein in a biomimetic apparatus. The fluid synthesis apparatus can add a specific virus to the fluid mixture, which can be delivered by the fluid addressing system. The disclosed system having a specific virus can be used to evaluate the susceptibility of the cultured tissue to the virus. In non-limiting embodiments, the system may include a vaccine and can be used to evaluate the effectiveness of the vaccine or other prophylactic agents against viral infection.

[0149] In certain embodiments, the disclosed system can deliver a specific gas to cultured tissue within a biomimetic device via the fluid addressing system. The disclosed system having the gas delivered to the tissue can be used to model embolism and / or human airway tissue. In non-limiting embodiments, the specific gas may be contained in a fluid mixture and delivered to one or more biomimetic devices. In some embodiments, the gas composition may be designed to mimic hypoxic or hyperxic conditions. In certain embodiments, a lung model may be exposed to hypoxic or hyperxic conditions, and the resulting behavior can be investigated by the disclosed system. In non-limiting embodiments, a specific toxic gas may be delivered to cultured tissue within the culture chamber to evaluate its effect on or damage to the tissue.

[0150] The disclosed subject matter provides systems and methods for forming biomimetic platforms by physically modeling, computationally modeling, or combining the two. The multiple biomimetic devices can be interconnected. In certain embodiments, the interconnected biological tissues, organisms, or systems can span numerous scales of biological and population-level entities. For example, the multiple interconnected biological tissues or systems can model interactions of different cell types, different biological organs, different organisms (e.g., to model disease transmission between two humans), different species (e.g., to model infection of human tissue by a bacterial culture), different biological scales (e.g., to model the effect of metabolite secretion from a culture of one cell type to a culture of tissue in a human donor population), or combinations thereof.

[0151] In certain embodiments, the disclosed biomimetic devices can be spatially patterned and connected to at least one microfluidic channel or fluid connection to form a biomimetic platform or a subset of biomimetic platforms. In certain embodiments, the at least one microfluidic channel can be used to deliver fluid to at least one biomimetic device spatially patterned within the microfluidic channel or microfluidic channel network. For example, the fluid may include cell culture media, nutrients, glucose, amino acids, biopharmaceuticals, drugs, pharmaceutical products, toxins, gases, dissolved solids, dissolved chemicals, aerosolized compounds, biologically active chemical fixatives, or combinations thereof. In non-limiting embodiments, the fluid may be delivered over a plurality of discrete periods. In certain embodiments, a predetermined range of doses of the fluid may be delivered to the biomimetic device in doses. In certain alternative embodiments, the fluid may be delivered to the biomimetic device continuously.

[0152] In certain embodiments, the chemical composition of the fluid delivered to the biomimetic platform may require modification. Such modification may be based on biological experiments (e.g., to maintain homeostasis or in response to sensor readings). In certain embodiments, such modification to the chemical composition of the fluid may be dynamic and continuous. In non-limiting embodiments, such modification may be discrete or performed stepwise.

[0153] In certain embodiments, the disclosed fluid synthesis apparatus may be incorporated into a biomimetic platform to synthesize a fluid of a desired chemical composition. The desired chemical composition can be synthesized by mixing or combining discrete components, divided fluids, inlet solutions, reagents, or combinations thereof at predetermined concentrations corresponding to the desired composition. In non-limiting embodiments, the synthesized fluid mixture may be delivered to multiple biomimetic devices / platforms using a delivery mechanism (e.g., microfluidic channels or fluid conduits).

[0154] The disclosed subject matter provides a system and method for manufacturing a “human function chip” system or a system consisting of multiple interconnected “biofunction chip” models using multiple biomimetic devices that are not in physical fluid communication or are not physically fluidically accessible. In certain embodiments, digital fluid teleportation can fluidly interconnect biomimetic devices or biomimetic platforms between scientists in different laboratories, different institutions, or with different experimental capabilities.

[0155] The foregoing is merely illustrative of the principles of this disclosure, and it will be understood that various modifications are possible by those skilled in the art without departing from the scope and spirit of this disclosure.

Claims

1. A method for predicting the biological behavior of a target tissue, The process includes a step of applying one or more first inputs to a statistical prediction model to predict the biological behavior of the target tissue, The statistical prediction model is created based on one or more second inputs provided to the cultured tissue in at least one biomimetic device, and observational data of the cultured tissue acquired by one or more sensors. A method wherein the cultured tissue is of the same tissue type as the target tissue.

2. The method according to claim 1, wherein the observational data includes one or more of phenotypic data, morphological data, metabolic data, genotypic data, and proteomics data.

3. A method according to claim 1, wherein the observation data includes the composition of the fluid output from the cultured tissue and the biological composition of the cultured tissue after exposure to the fluid input.

4. A method according to claim 1, wherein the cultured tissue is incubated in at least one biomimetic device under predetermined conditions based on one or more second inputs.

5. A method according to claim 1, wherein the one or more second inputs and the observation data are provided for training a virtual tissue model.

6. A method according to claim 1, wherein the observational data is used to evaluate the biological efficacy or safety of at least one compound or condition to humans or animals.

7. A method according to claim 1, wherein the observational data is used for drug discovery or screening.

8. The method according to claim 1, wherein the statistical prediction model includes a virtual organization model.

9. The method according to claim 1, wherein the statistical prediction model includes one or more of a neural network, a decision tree, and statistical inference.

10. A method according to claim 1, wherein the step of applying the one or more first inputs to the statistical prediction model in order to predict the biological behavior of the target tissue further comprises applying a mathematical transformation to the numerical values ​​generated by the statistical prediction model.

11. A method according to claim 1, wherein the one or more sensors include at least one of an imaging device and a biosensor.

12. A method according to claim 11, wherein the biosensor includes an analyte sensor.

13. The method according to claim 11, wherein the imaging device is configured to collect image information from the at least one biomimetic device.

14. The method according to claim 11, wherein the imaging apparatus is configured to perform at least one of bright-field imaging, optical microscopy, fluorescence microscopy, magnetic resonance imaging, and computed tomography (CT) scanning.

15. A method according to claim 11, wherein the biosensor includes a chemical reaction or bioreaction recognition element configured to interact with a target analyte to produce a measurement of the amount or concentration of the target analyte, and a recording system configured to record the measurement and the operation of the biomimetic device.

16. A method according to claim 1, wherein the target tissue includes one or more of the following: lung tissue, bone marrow tissue, bone tissue, pancreatic tissue, endocrine islet tissue, liver tissue, kidney tissue, placental tissue, eye tissue, intestinal tissue, bladder tissue, brain tissue, mouth tissue, tongue tissue, tooth tissue, nasal tissue, thymic tissue, lymph node tissue, lymphatic tissue, throat tissue, specific human tissue, specific human tissue undergoing specific daily activities, lung tissue undergoing periodic respiration, specific human tissue undergoing an atypical state, lung tissue undergoing an asthma attack, specific human tissue undergoing specific interactions with external drugs, lung tissue infected with bacteria, lung tissue exposed to environmental factors, lung tissue exposed to contamination, lung tissue exposed to corrosive gases, specific human tissue undergoing specific interactions with external drugs intended for use as therapeutic agents, specific human tissue undergoing specific interactions with drugs, specific human tissue undergoing specific interactions with biological antibodies, specific human tissue undergoing specific interactions with cell therapy, or lung tissue undergoing an asthma attack while being monitored for interaction with bronchodilators as a treatment for asthma.

17. A method according to claim 1, wherein the one or more second inputs include one or more of the composition of a fluid input to the cultured tissue, the biological composition of the cultured tissue before exposure to the fluid input, and predetermined incubation conditions.

18. The method according to claim 17, wherein the composition of the fluid input to the cultured tissue comprises one or more of a predetermined culture medium, a chemical stimulus, and a biological stimulus.

19. The method according to claim 17, wherein the predetermined incubation conditions include one or more of temperature, incubation period, and gas composition.

20. The method according to claim 17, wherein the one or more second inputs are defined by a continuous function.

21. In the method described in claim 1, further, The steps include: binding the statistical prediction model to the cultured tissue in the at least one biomimetic device; A step of applying one or more third inputs to the statistical prediction model to predict the biological behavior of the cultured tissue, The method comprises the step of supplying a synthesized fluid solution as the fluid input to the cultured tissue in at least one biomimetic device, based on the predicted biological behavior of the cultured tissue. A method wherein the one or more third inputs are based on the cultured tissue in the at least one biomimetic device.

22. In the method described in claim 21, further, A method comprising the step of supplying the synthesized fluid solution to the cultured tissue in the at least one biomimetic device through a fluid addressing system.

23. A method according to claim 1, wherein the biological behavior of the target tissue includes phenotypic behavior, genotypic behavior, and proteomics behavior.

24. A method according to claim 1, wherein the statistical predictive model of the target tissue is based on off-chip observational data including one or more measurements of biochemical secretion, metabolism, biochemical processes, electrophysiological measurements, and quantification of the genome, transcriptome, and / or proteomics of cells or subsets of cells in the cultured tissue.

25. It is a system, A control system comprising a control device configured to predict the biological behavior of a target tissue by applying one or more first inputs to a statistical prediction model, The statistical prediction model is created based on one or more second inputs provided to the cultured tissue in at least one biomimetic device, and observational data of the cultured tissue acquired by one or more sensors. The system wherein the cultured tissue is of the same tissue type as the target tissue.

26. The system according to claim 25, wherein the at least one biomimetic device includes a material configured for optical imaging.

27. The system according to claim 25, wherein the cultured tissue in the at least one biomimetic device is an organ-inept chip model.

28. A method for predicting the biological behavior of a target tissue using a statistical predictive model, The process of obtaining the statistical prediction model from a browsable statistical prediction model library, A step of applying one or more first inputs to the statistical prediction model to predict the biological behavior of the target tissue. It has, The statistical prediction model is based on one or more second inputs provided to cultured tissue in at least one biomimetic device, and observational data acquired by one or more sensors. A method wherein the cultured tissue is of the same tissue type as the target tissue.

29. A method for creating a statistical predictive model, A step of providing one or more first inputs to cultured tissue in at least one biomimetic device, A step of obtaining observational data from the cultured tissue, A method comprising the step of creating the statistical prediction model by correlating the first input with the observation data.

Images