2723 results about "Microfluidic chip" patented technology

The invention provides an agricultural environment monitoring method and system based on the Internet of Things. According to the method, multi-source data weights are dynamically distributed through a soil sensor array connected with Internet of Things nodes, and a global soil parameter set is generated; deploying a micro-electro-mechanical micro-fluidic chip in the coverage area to carry out soil solution selective permeation, converting the target ion concentration into an electric signal, and synchronously transmitting the electric signal and soil parameters; historical time series data are extracted, coherence is established through time correlation analysis, and undeployed area data are filled in combination with a spatial interpolation algorithm to construct a dynamic prediction model; according to the nutrient space change trend output by the model, crop growth requirements are matched to generate a fertilization amount adjustment instruction, and the fertilization amount adjustment instruction is issued to field fertilization equipment through the Internet of Things to execute dynamic regulation. Space-time precise sensing of soil nutrients and self-adaptive fertilization regulation and control are realized, and the utilization efficiency of agricultural resources and crop growth sustainability are improved.

The invention relates to the technical field of fertilizer preparation, and discloses an ecological balance fertilizer for yield increase and disease resistance of peanuts and a preparation method of the ecological balance fertilizer. The preparation process comprises the following steps: constructing a PLGA core containing trichoderma harzianum spores and magnesium carbonate through a micro-fluidic chip low-temperature water-in-oil emulsion method; coating bacillus amyloliquefaciens and potassium silicate with ultraviolet-induced cross-linked temperature-sensitive hydrogel to form a middle layer; loading rhizobium by using aminated mesoporous S < iO2 >, and spraying and assembling an enzyme response shell through a fluidized bed; finally, the hydroxyapatite nanorod and a binder are combined and granulated and formed through a fluidized bed. Precise controlled release of functional bacteria and nutrients is realized by constructing a temperature-sensitive-enzyme response type release system, and the activity of a fungicide is guaranteed to be preserved by virtue of trichoderma harzianum-rhizobium synergistic interaction and silicon bond linkage soil remediation in combination with a low-temperature fluidized bed process, so that a'fertilizer-bacterium-soil 'ecological cycle system is finally constructed.

The invention discloses a dynamic optimization system and method for a compound essential oil ratio, and aims to solve the problems that the traditional technology depends on artificial experience, the optimization efficiency is low and the quality tracing is insufficient. According to the method, raw material molecular fingerprint data are collected in real time through a high-precision spectrum sensor array and a micro-fluidic chip, a production environment field domain is constructed in combination with a computational fluid mechanics model, a formula optimization problem is encoded into an Ising model by using a quantum annealing algorithm, and global search is realized through a quantum tunneling effect. The system integrates digital twin bodies, covers molecular dynamics simulation, phase equilibrium prediction and olfactory receptor activation probability simulation, and accurately maps a physical system state; a multi-modal data fusion network and a reinforcement learning framework are adopted to dynamically adjust formula parameters, and an NSGA-III algorithm is combined to optimize efficacy collaboration degree, cost and stability indexes. And the execution control module realizes nanoscale flow regulation through the piezoelectric micro-injection valve array, and realizes non-tampering evidence storage of formula parameters and quality data based on a block chain technology. Dynamic closed-loop optimization of the compound essential oil ratio is achieved, the production efficiency, the product consistency and the supply chain transparency are remarkably improved, and the method is suitable for the field of intelligent manufacturing of high-end essential oil.

The invention relates to the technical field of model analysis, in particular to an imaging flow cytometry cell detection method based on an improved model. The method comprises the following steps: introducing a cell sample to be detected into an imaging flow cytometry system integrated with a micro-fluidic chip for continuous image acquisition to generate an initial cell image sequence; an automatic digital focusing algorithm is applied to the initial cell image sequence, and a cell image frame set with the optimal focal plane is screened out; inputting the cell image frame set into a preset PA-YOLO improved model for multi-dimensional extraction and fusion, and generating a multi-scale cell characteristic spectrum; carrying out refined feature learning and cell target positioning and classification on the multi-scale cell feature spectrum, and outputting a cell detection result; and carrying out validity verification on the cell detection result, and carrying out comparative analysis in combination with an imaging flow cytometry system to generate a cell detection report. According to the method, the imaging quality and the detection accuracy of cell images with different depths can be remarkably improved.

The present invention belongs to the field of microbead preparation technology, and specifically relates to a microbead production process with adjustable internal phase based on microfluidic technology and its application. The microbead production process includes the following steps: (1) raw material transportation: the required materials are transported to the microfluidic chip separately through a pump under heat preservation conditions; (2) logistics shearing: the required materials are sheared in the microfluidic chip to obtain composite droplets; (3) cooling and molding: after the sheared droplets are cooled, they are cooled and solidified using a cooling medium to form microbead particles; (4) product collection: the microbead particles and the cooling medium are subjected to solid-liquid separation, filtered, and collected to obtain microbeads. The microbead production process of the present invention can quickly realize the continuous production of double-layer microbeads, realize the precise regulation of the inner layer of the double-layer microbeads, and quickly and accurately control the particle size of the microbeads; at the same time, it can quickly realize the production conversion between single-layer microbeads and double-layer microbeads.

The invention provides a micro-fluidic chip for combined detection of C-reactive protein and ferritin and application thereof.The micro-fluidic chip comprises a substrate and a cover plate pressed on the substrate, a micro-channel is defined by the substrate and the cover plate, the left end of the micro-channel is communicated with a buffer solution sample adding hole formed in the cover plate, the right end of the micro-channel is communicated with a waste liquid area, and the left end of the micro-channel is communicated with a buffer solution sample adding hole formed in the cover plate. The waste liquid area is provided with a movable water-absorbing paper sheet, the microchannel is sequentially provided with a marking area, a detection area and a sample adding area from left to right, the marking area is provided with a marked anti-human CRP antibody, a marked anti-human SF antibody, a marked second antibody and a marked antigen, the first detection site is provided with an anti-human CRP antibody, and the second detection site is provided with an anti-human SF antibody. The first reference point is provided with a first antibody which reacts with the labeled second antibody, the second detection site is provided with an anti-human SF antibody, and the second reference point is provided with an antibody which reacts with the labeled antigen. The detection process of C-reactive protein and ferritin can be simplified, and the detection time is shortened.

The utility model discloses a micro-fluidic chip imaging positioning device, and belongs to the technical field of micro-fluidic chip positioning. According to the technical scheme, the system comprises a microcosmic illumination module, a microcosmic imaging module, a chip moving and macroscopic illumination module, a macroscopic imaging module and an optical path multiplexing module; the microscopic illumination module comprises a fly's-eye lens assembly, the fly's-eye lens assembly comprises two fly's-eye lenses, the optical axes of the two fly's-eye lenses are parallel to each other, and the focus of each lens array element in one fly's-eye lens coincides with the center of the lens array element at the corresponding position of the other fly's-eye lens. The micro-fluidic chip clamp is applied to the aspect of micro-fluidic chip imaging positioning, overcomes the defects caused by an existing micro-fluidic chip clamp, solves the technical problems of universality, automation and high precision of micro-fluidic chip positioning, and has the characteristics of rapidness, automation, high precision and universality.

The invention discloses a generative odor real-time synthesis method and system based on cross-modal potential space mapping, and belongs to the technical field of artificial intelligence and olfaction calculation. The method comprises the following steps: acquiring a multi-modal input stream of a current scene, and extracting an emotion semantic feature vector by using a deep neural network; mapping the semantic features into target odor chemical feature vectors by using nonlinear projection through a pre-constructed vision-smell joint embedding space; constructing a convex optimization model based on olfactory perception, and calculating a basic liquid optimal mixing proportionality coefficient matrix capable of fitting the target vector; the matrix is converted into a micro-fluidic driving signal, and the target smell is synthesized in situ in the micro-fluidic chip. The invention further discloses a self-adaptive cleaning logic and olfactory fatigue compensation mechanism based on scene mutation detection. The method solves the problems that in the prior art, label matching is dependent, new smell cannot be synthesized, and dynamic transition is lacked, and olfactory replicating and real-time generation of abstract semantic scenes are achieved.

The invention belongs to the technical field of microbead preparation, and particularly relates to a microbead production process with an adjustable internal phase based on a microfluidic technology and application of the microbead production process. The micro-bead production process comprises the following steps: (1) conveying raw materials: respectively conveying required materials to a micro-fluidic chip through a pump under a heat preservation condition; (2) material flow shearing: shearing the required material in the micro-fluidic chip to obtain composite liquid drops; (3) cooling and forming: cooling and curing the sheared liquid drops by using a cooling medium after the sheared liquid drops are cooled, so as to form microbead particles; and (4) product collection: carrying out solid-liquid separation on the microbead particles and a cooling medium, filtering, and collecting to obtain the microbeads. According to the microbead production process disclosed by the invention, continuous production of double-layer microbeads can be quickly realized, accurate regulation and control of inner layers of the double-layer microbeads are realized, and the particle sizes of the microbeads are quickly and accurately controlled; and meanwhile, the production conversion of single-layer microbeads and double-layer microbeads can be quickly realized.

The utility model discloses a device for preparing a double-droplet microsphere. The device comprises a fluid injection unit, a liquid injection unit and a control unit, the micro-fluidic chip comprises a cover glass, one side of the cover glass is provided with a dispensing needle a, the dispensing needle a is connected with an internal phase glass capillary tube, the internal phase glass capillary tube is partially nested in an intermediate phase glass capillary tube, the intermediate phase glass capillary tube is partially nested in an external phase glass capillary tube, and the external phase glass capillary tube is connected with the external phase glass capillary tube. A dispensing needle b is vertically arranged above one end, which is overlapped with the inner phase glass capillary, of the intermediate phase glass capillary, and a dispensing needle c is vertically arranged above one end, which is overlapped with the intermediate phase glass capillary, of the outer phase glass capillary; and a micro-droplet collection unit. According to the utility model, through the coaxially arranged glass capillary tube and the dispensing needle head communicated with the glass capillary tube, the double-droplet microsphere is prepared, meanwhile, the groove is formed in the dispensing needle head, so that the construction of a coaxial glass capillary tube micro-fluidic chip is facilitated, the preparation equipment is simple, and the operation is simple.

The invention relates to an organ-like core-shell microsphere as well as a preparation method and application thereof. The preparation method comprises the steps that 1, raw materials are prepared, specifically, shell raw materials and inner core raw materials are prepared, the shell raw materials comprise a photoinitiator and methacrylated hyaluronic acid (HAMA), and the inner core raw materials comprise organoid precursor cell suspension and matrigel; 2) molding: extruding the dispersion phase of the shell raw material wrapping the core raw material to a continuous phase by using a micro-fluidic chip and a high-precision injection pump, cutting the dispersion phase into liquid drops by the continuous phase, and performing illumination curing on the liquid drops to form core-shell microspheres; and (3) incubating, namely culturing the core-shell microspheres in a culture medium, so that the organoid precursor cells in the inner core are developed into organoids. According to the preparation method, rapid forming and curing of the organ-like precursor cells carried by the matrigel are achieved, so that the time of the organ-like precursor cells staying in the oil phase is shortened, the cells can obtain oxygen and nutrient substances, and the cell activity is improved.

The invention relates to the technical field of medical instruments, in particular to an intelligent wound nursing system which comprises a dressing body, and the dressing body comprises a skin-friendly layer, a functional layer and a protective layer. A monitoring module, a control module, a medicine leading-in module, a flexible circuit layer and an alarm module are integrated in the functional layer. According to the method, the infection misdiagnosis rate is reduced through multi-sensor fusion monitoring and a preset infection risk threshold algorithm; according to the design, the micro-fluidic chip and the biological probe are integrated in the percolate component sensor, so that the infection detection rate is increased; a temperature-sensitive hydrogel micro-valve array and nanofiber membrane slow release technology is adopted, so that medicine waste or poor treatment effect is reduced; through a multi-sensor data fusion algorithm, the detection accuracy is improved; the layout of the micro-valve array and the annularly distributed independent medicine storage cavities is adopted, so that the release error is reduced; through the ultrathin flexible framework, the snakelike wiring circuit and flip chip packaging, circuit breakage is avoided, and the clinical failure rate is reduced.

The invention discloses an ultrasonic phased array driven graphene oxide flow stripping and closed-loop regulation and control system and method, and the system comprises an ultrasonic phased array module, and a piezoelectric transducer array element in the ultrasonic phased array module controls sound beam focusing and energy distribution through a phase delay controller, and carries out the stripping of graphite oxide flowing in a flow channel; a micro-Raman spectrometer in the micro-fluidic-Raman detection module collects characteristic peak data of a graphene oxide sheet layer in a micro-fluidic chip in real time and sends the characteristic peak data to a signal analysis unit; and the feedback control module is used for receiving the layer number distribution data output by the signal analysis unit, dynamically adjusting ultrasonic parameters of the phase delay controller, and controlling the diverter valve to guide substandard products into a secondary treatment channel and finally return the substandard products to the flow channel for stripping again. The system and the method for stripping the graphene oxide based on coupling of the ultrasonic phased array and the micro-fluidic chip have the advantages of efficient stripping, accurate detection, closed-loop optimization and the like.

The invention relates to a centrifugal micro-fluidic chip for automatic detection of a nano-enzyme test strip and application of the centrifugal micro-fluidic chip. The centrifugal micro-fluidic chip integrates the steps of sample adding, chromatography, color development and the like of the nano-enzyme test strip, and full automation of nano-enzyme experiments on the micro-fluidic chip is realized. Comprising a reaction structure main body, a bottom runner layer, a vertical through hole layer, a pressing layer, a top runner layer and a sealing body. The closed structure of the chip effectively reduces the interference of external environmental factors on the experiment, reduces the risk of sample pollution, and ensures the high reliability of the detection result.

The invention belongs to the technical field of microfluidics, and particularly relates to a liquid separation-convergence integrated liquid drop micro-fluidic chip and a liquid drop preparation method.The liquid separation-convergence integrated liquid drop micro-fluidic chip is characterized in that a liquid drop generation unit is arranged at the communication position of a branch splitting channel and a convergence channel which is correspondingly communicated with the branch splitting channel; and under the action of continuous phase shearing force, the dispersed phase solution is sheared off by the continuous phase solution, so that liquid drops are formed. The droplet generation units are symmetrically arranged along the circumference of the channel, the distance from each unit to the center is equal, and a continuous phase solution and a dispersed phase solution encountered at each droplet generation unit are almost equivalent, so that the sizes of the generated droplets are consistent, the droplets with basically consistent sizes are obtained at a collection port, and high-flux preparation of microspheres with uniform sizes is realized.

The invention discloses an inertial micro-fluidic chip integrating cell focusing and sorting and a preparation method thereof. The inertial micro-fluidic chip comprises a cover plate layer, a runner layer and a substrate layer, a chip inlet, a first chip outlet and a second chip outlet are formed in the cover plate layer; the flow channel layer is provided with a sample liquid flow channel inlet, a first flow channel outlet and a second flow channel outlet, the chip inlet is communicated with the sample liquid flow channel inlet, the first chip outlet is communicated with the first flow channel outlet, and the second chip outlet is communicated with the second flow channel outlet. The flow channel layer is provided with a spiral cell sorting flow channel and a cell focusing flow channel, the front end of the spiral cell sorting flow channel is communicated with a sample liquid flow channel inlet, the tail end of the spiral cell sorting flow channel is communicated with the cell focusing flow channel and a first flow channel outlet, and the tail end of the cell focusing flow channel is communicated with a second flow channel outlet. Through a microfluid vortex focusing technology and a spiral flow channel inertia sorting technology, accurate sorting and focusing of cells are realized, and the problems that the focusing state of the sorted cells is influenced and the cell counting detection precision is low are effectively solved.

The invention discloses a portable nucleic acid detection micro-fluidic chip, a nucleic acid detection device and a nucleic acid detection method, and belongs to the field of micro-fluidic chips, a detection module comprises a quantitative chamber, a micro-channel, a reaction chamber, a first connecting channel and a color developing module; the reaction chamber comprises an RPA reaction chamber in which an RPA amplification reagent is pre-embedded, a porous filter membrane and a CRISPR reaction chamber in which a CRISPR detection component is pre-embedded, and the RPA reaction chamber, the porous filter membrane and the CRISPR reaction chamber are sequentially positioned at the same position of the three adjacent chip layers; the aperture of the porous filter membrane is larger than the particle size of an RPA amplification product and smaller than the particle size of a core enzyme in a CRISPR detection component; two ends of the micro-channel are respectively communicated with the quantitative chamber and the RPA reaction chamber; two ends of the first connecting channel are respectively communicated with the CRISPR reaction chamber and the color developing module; the flow resistance of the first connecting channel is smaller than that of the micro-channel. According to the invention, the sequential reaction of RPA amplification and CRISPR cleavage can be completed without depending on artificial transfer of amplification products.

The utility model relates to the technical field of cell cultivators, in particular to a pump-free perfusion micro-fluidic chip for multi-cell three-dimensional co-culture, which comprises a liquid storage layer, a liquid inlet and outlet layer, an upper channel layer, a lower channel layer and a packaging layer, realizes a one-way circulation perfusion dynamic co-culture system without a pumping system, reduces the occupied space of equipment, and is convenient to operate. Operation is simple, culture medium consumption is reduced, and cost is reduced; the separation of free NK cells and tumor infiltration NK cells is realized, and conditions are provided for researching molecular biological characteristics of different types of NK cells. The migration and interaction of the tumor spheres and the NK cells are observed in real time at the same time, so that the problem that a microfluid pump integrated by an external system is needed for separating free immune cells and tumor infiltration immune cells by existing equipment is solved.

The invention discloses a closed-loop control digital microfluidic system and a method thereof, and relates to the technical field of microfluidics, and the method comprises the following steps: initializing a digital microfluidic chip electrode array, setting an electrode spacing, an electrode size and a voltage upper limit, collecting a no-load state signal, and generating initial reference data; liquid drops are formed at the preset position of the digital micro-fluidic chip, and according to the initial reference data, the initial position, the volume and the form information of the liquid drops are collected, and a liquid drop initial state data set is generated; inputting the initial state data set of the liquid drop into a pre-trained closed-loop prediction model, performing kinetic analysis and trajectory prediction calculation, generating an expected motion trajectory of the liquid drop, and comparing the expected motion trajectory with the real-time state data flow of the liquid drop to generate deviation feedback data of the liquid drop; and dynamically adjusting the initial driving voltage parameter according to the droplet deviation feedback data to generate a closed-loop driving voltage sequence. The liquid drop trajectory control precision is improved, and motion errors caused by environmental disturbance and electrode response differences are reduced.

The invention discloses a tear total IGE detection method and system based on multi-modal data fusion. The method comprises the following steps: acquiring ocular surface images, physiological parameters and environmental allergen data, and acquiring historical medical data from a hospital information system; preprocessing and feature extraction are performed, patient symptom description is analyzed in combination with a natural language processing technology, and related image block features are recognized; adjusting a space-time attention weight based on frequency domain analysis and transfer learning, inputting a lightweight Transform model, and predicting a tear total IgE concentration and an allergy risk score; whether a trace tear sampling program is started or not is judged, and the actually measured concentration of total tear IgE is detected through a disposable micro-fluidic chip; and integrating all information by using a Bayesian adaptive filtering algorithm to determine the total tear IgE level. By implementing the method provided by the invention, the sampling amount is extremely small, the detection time is short, the environmental interference can be dynamically corrected, and the absolute concentration value is output, so that the dual requirements of clinical precise diagnosis and treatment and home monitoring are met.

The invention discloses a micro-fluidic chip, extraction equipment and an exosome extraction method, which can be used for an enzymatic detection device. Wherein the micro-fluidic chip comprises a chip base body with a rotation center, the chip base body is provided with a sample introduction unit, a reagent unit, a filtering unit, a capturing unit, a waste liquid bin, a collecting unit and a switching structure, and the filtering unit is arranged on the downstream of the sample introduction unit in the centrifugal direction, communicates with the sample introduction unit and is used for filtering impurities in a sample; the capturing unit is arranged on the downstream of the filtering unit in the centrifugal direction and communicated with the filtering unit, the capturing unit is communicated with the reagent unit and located on the downstream of the reagent unit, and the capturing unit is used for capturing or releasing the extracted target object; the waste liquid bin and the collecting unit are arranged on the downstream of the capturing unit in the centrifugal direction, and the waste liquid bin communicates with the capturing unit through a communicating structure; the switching structure is arranged in the communication structure, the switching structure can selectively block the communication structure, and the switching structure can enable the capturing unit to be communicated with the collecting unit.

The invention discloses a batch processing technology of micro-fluidic chips, and relates to the technical field of chip processing. The method comprises the following steps: firstly, providing at least two layers of polymer coiled materials, namely a first coiled material for forming a micro-channel structure and a second coiled material for closing a micro-channel, the coiled materials are continuous coiled materials selected from polyethylene glycol terephthalate (PET), cycloolefin polymer (COP), polycarbonate (PC) or polymethyl methacrylate (PMMA), and the coiled materials are continuous coiled materials selected from polyethylene glycol terephthalate (PET), cycloolefin polymer (COP), polycarbonate (PC) or polymethyl methacrylate (PMMA); the thickness of the coiled material is 50-500 microns; secondly, carrying out continuous compression molding processing on the surface of the first coiled material through a roll-to-roll processing platform; through a roll-to-roll continuous process, micro-channel mold pressing, functional deposition, precise alignment bonding and online cutting are integrated, high-efficiency, high-consistency and high-integration-level batch manufacturing of the micro-fluidic chip is realized, and manual intervention and production cost are remarkably reduced.

The utility model relates to the technical field of micro-fluidic chips, in particular to a micro-fluidic chip which comprises a chip main body, a sample injection hole, a flow channel, a reaction hole and an air injection hole, the sample injection hole, the flow channel and the reaction hole are positioned on the chip main body, the sample injection hole, the flow channel and the reaction hole are sequentially connected, and the air injection hole is communicated with the flow channel. The flow channel comprises a sample injection flow channel and a driving flow channel, the sample injection hole, the sample injection flow channel, the flow blocking part, the driving flow channel and the reaction hole are sequentially connected, an inner cavity of the flow blocking part is provided with a flow blocking plug capable of preventing the sample injection flow channel from being communicated with the driving flow channel, the flow blocking plug is in sliding connection with the flow blocking part, and the gas injection hole is located in the driving flow channel. A sealing plug is slidably connected into the gas injection hole. According to the micro-fluidic chip disclosed by the utility model, when the sample liquid in the flow channel is driven to advance by extruding the gas, the gas can be prevented from flowing back in the flow channel, and the volume of the sample liquid entering the reaction area can be obtained through the volume of the gas injected into the flow channel, so that the quantitative control of the sample liquid is realized.

The invention discloses a micro-fluidic chip for basalt CO2 mineralization reaction and a preparation method, the micro-fluidic chip comprises a bottom glass plate, a middle epoxy resin layer and a top glass plate, the preparation process comprises the following steps: installing a metal injection / outpouring pipeline on the bottom glass plate drilled with corresponding bolt holes, and forming an accommodating cavity by using a sealing ring; preparing and screening basalt particles according to the particle size distribution of a target reservoir, and filling the accommodating cavity with the basalt particles; quantitatively analyzing a particle arrangement structure based on a digital image processing technology, ensuring that the geometric similarity between the particle arrangement structure and a target reservoir is greater than or equal to 90%, and if the particle arrangement structure does not reach the standard, refilling; after the verification is passed, covering a top glass plate and pressing by using a bolt; and finally, pouring epoxy resin and sealing to form the micro-fluidic chip. The chip can bear high temperature and high pressure, supports visual observation and quantitative analysis of CO2 mineralization reaction in a deep geological environment, has high-precision pore reproduction, long-period sealing performance and high preparation efficiency, and is suitable for interdisciplinary research in the fields of energy environment and geophysics.

The invention relates to a microfluidic nucleic acid detection device, and relates to the field of detection. Comprising a bottom plate, a chip inlet and outlet module erected on one side above the bottom plate, a chip table erected on the chip inlet and outlet module and used for bearing a micro-fluidic chip with a liquid bag, a displacement module erected above the chip table, and a crushing module erected on the displacement module and used for squeezing liquid in the liquid bag into the micro-fluidic chip, the liquid transferring module is erected on one side of the crushing module and is used for transferring liquid in the micro-fluidic chip to flow; the pneumatic module is erected above the front end of the bottom plate and is used for controlling a flow channel of the micro-fluidic chip to be opened and closed; the heating module is erected on the other side above the bottom plate and is used for locally heating the micro-fluidic chip and automatically detecting the temperature; and the fluorescent module is used for acquiring a fluorescent signal of the micro-fluidic chip. The micro-fluidic chip detection device has the advantages that different types of micro-fluidic chips can be rapidly detected, and an accurate result can be obtained.

The invention discloses a gene sequencing sample data matching method based on a micro-fluidic chip, relates to the technical field of gene sequencing sample matching, and aims to solve the problem that the matching rate is reduced due to inaccurate analysis of gene sequencing samples. According to the method, multi-strategy comparison and candidate set screening are adopted, multi-dimensional comparison of sequences, variation and functions is combined, the accuracy is improved, the adaptability to complex samples is enhanced through quantitative index and biological verification evaluation and dynamic optimization of comparison strategies, the matching reliability and practical value are remarkably improved, the clinical and scientific research diversified requirements are met, and the method is worthy of popularization and application. Sample types such as blood and cells are adapted through a differential lysis strategy, impurities such as proteins and salts are removed through stepped purification, and the nucleic acid concentration and the fragment state are unified in combination with standardized treatment, so that interference is reduced from the source.

The invention discloses a temperature control system and method of a micro-fluidic chip, and relates to the technical field of micro-fluidic temperature control, and the method comprises the following steps: in the manufacturing process of the micro-fluidic chip, embedding topological insulator nanowires into a substrate in a directional arrangement mode to form a pre-locking array, and meanwhile, generating an anisotropic heat conduction network under the continuous action of a sound-magnetic field, a topological vortex invariant is calculated, and a heat conduction weight coefficient is generated; arranging a fluorescent layer on the surface of a micro-reaction cavity of the anisotropic heat conduction network, collecting a fluorescence lifetime attenuation curve in real time, and calculating a transient temperature value and a temperature change rate according to a heat conduction constraint variation model and a heat conduction weight system; nonlinear feed-forward compensation power is calculated according to the transient temperature value and the temperature change rate, feedback compensation power is calculated in combination with a deviation field of the target temperature and the real-time temperature, and a compensation power instruction is generated; according to the method, the thermal pilot frequency domain filtering function is constructed through the compensation power instruction, so that the uniformity and response speed of thermal response are improved.

The invention provides a micro-fluidic chip capable of culturing oral squamous cell carcinoma organoid and a preparation method thereof, and relates to the technical field of micro-fluidic chips, the chip comprises a four-layer structure: the first layer is a closed layer, the second layer is a culture solution / drug pool layer (containing a concentration gradient injection channel and a slow flow channel), the third layer is a matrix culture pool layer, and the fourth layer is a matrix culture pool layer. The fourth layer is a matrigel inflow layer (containing an S-shaped flow channel); the second layer and the third layer are integrally formed, and all the layers are connected through oxygen plasma welding; the problems that in the prior art, matrigel is prone to shifting, drug gradient regulation and control is poor, operation is tedious, and adaptability is insufficient are solved, the matrigel and organoids can be stably fixed, the drug concentration gradient can be precisely regulated and controlled, the nutrition supply efficiency is enhanced, the structural integration level and operation convenience are improved, and the application prospect is wide. The method is suitable for oral squamous cell carcinoma organoid culture, drug screening and tumor mechanism research.

A microfluidic chip liquid inlet device disclosed by the present invention comprises a bottom plate and supporting legs, a liquid inlet structure is arranged above the bottom plate, the liquid inlet structure comprises a liquid inlet mechanism, a liquid injection mechanism and a feeding mechanism, and the liquid inlet mechanism comprises a first motor, a rotating rod, a mounting plate, a rotating rod and a first bearing plate. The output end of the first motor is connected with the bottom of the rotating rod, the top of the rotating rod is connected with the bottom of the mounting plate, and the bottom of the mounting plate is connected with the top of the rotating rod. According to the invention, micro-fluidic chips with different sizes can be rapidly and conveniently clamped and fixed, and a plurality of micro-fluidic chips can be subjected to liquid feeding work at the same time, so that the problem that the plurality of micro-fluidic chips cannot be rapidly and conveniently used at the same time is solved; and moreover, the problem that the micro-fluidic chips with different sizes cannot be quickly and conveniently clamped and fixed is solved, and the working efficiency of the liquid inlet device is improved.

The invention discloses a detection kit and method for detecting allergic inflammatory factors based on a centrifugal micro-fluidic chip, and relates to the field of kits, the detection kit comprises the centrifugal micro-fluidic chip and a preset reagent; the centrifugal micro-fluidic chip comprises a chip base body, a sample adding cavity, a liquid level sensor, a liquid level sensor, a liquid level sensor, a liquid level sensor and a liquid level sensor, the nucleic acid extraction and purification cavity comprises a plurality of amplification cavities; a reagent storage chamber; a waste liquid chamber; and a capillary valve. The functions of nucleic acid extraction, variable temperature amplification and multi-target synchronous detection are integrated through the centrifugal micro-fluidic chip, full-closed operation is achieved by means of centrifugal force or other driving force such as air pressure and electroosmotic flow, and the pollution risk caused by manual step-by-step operation is thoroughly eliminated; a multi-wavelength distinguishable fluorescent probe and a grouping preset primer combination are adopted to synchronously complete parallel detection of the allergic inflammatory factor mRNA and the drug accompanying diagnosis target, cross interference is avoided, and large instruments and equipment do not need to be relied on.