157 results about "Biological cell" patented technology

The invention discloses a biological cell image classification method and system and a storage medium, and relates to the field of biomedical analysis, and the method comprises the steps: obtaining a to-be-classified biological cell image, employing a pre-trained AlexNet network as a basic feature extractor, and obtaining a one-dimensional feature vector; key feature information is obtained through feature selection and dimension reduction, one-dimensional feature vectors after dimension reduction are mapped to different feature spaces, and different feature representations are generated through reconstruction; constructing a multi-modal feature, converting the multi-modal feature into a feature map by adopting an attention mechanism, and generating a biological cell portrait; a classification model is constructed based on a graph convolutional network, pre-training is carried out by using transfer learning, a biological cell portrait to be recognized is used as input, and the category probability of each biological cell image is acquired. According to the method, deep learning and multi-modal fusion technologies are combined, the biological cell image classification precision is improved through feature reconstruction and transfer learning, and reliable technical support is provided for biomedicine and clinical diagnosis.

A system includes a flow cell and a fluidics system under pressure causing sheath and sample biological fluids to flow. The fluidics system includes a gas bubble remover to remove and eliminate gas bubbles in the sheath fluid. The flow cell receives sheath fluid from the fluidics system, wherein the sample biological fluid flows with cells or particles through the flow cell to be surrounded by the sheath fluid. A deflection chamber under the flow cell receives drops of the sample biological fluid and sheath fluid out of the flow cell to selectively deflect one or more of the drops along one or more deflection paths. A droplet deposition unit system in communication with the deflection chamber receives the selectively deflected drops in the stream of the sample biological fluid with the one or more biological cells or particles into one or more containers.

The invention discloses a method for generating an enhanced image of a bright-field microscope, and the method comprises the steps: simulating an optical imaging model of optical Zernike phase contrast microscope imaging through a computer system based on the optical imaging principle of a conventional optical Zernike phase contrast microscope; extra hardware such as an annular diaphragm and an annular phase plate does not need to be added in an illumination light path and an imaging light path of the bright-field microscope, enhancement of the phase contrast of a bright-field digital microscopic image is achieved, energy loss of an illumination optical system is avoided, and the design and manufacturing cost of the microscopic optical system is greatly reduced; the optical Zernike phase contrast microscope can be universally used for different bright field microscopes, halo artifacts caused by interference effects in a traditional optical Zernike phase contrast microscope do not exist, finer structural features in biological cells can be distinguished, the resolution of the optical Zernike phase contrast microscope can be close to the resolution limit of objective lens design, and the technical requirements for users are greatly reduced.

The utility model provides a biological cell dyeing device and relates to the field of biological cells. Comprising a base, a fixing device is arranged on the upper surface of the base and comprises a sliding plate, the upper surface of the sliding plate is fixedly connected with the fixed end of a first electric telescopic rod, the telescopic end of the first electric telescopic rod is fixedly connected with the middle of the lower surface of a concave frame, and the interior of the upper surface of the concave frame is fixedly connected with one end of a spring; the other end of the spring is fixedly connected with the lower surface of the fixing frame. According to the biological cell dyeing device, through the synergistic effect of a sliding plate, a first electric telescopic rod, a concave frame, a spring and a fixing frame, biological cells can be conveniently dyed, when the biological cells need to be dyed, a cell slide is placed on the fixing frame, the cell slide is fixed through the fixing frame, and the spring plays a buffering role; a first electric telescopic rod is convenient for a worker to quickly take the slide, so that the cell slide is fixed.

Photocatalytic sterilization technology is a technology that uses active substances generated by specific materials under light conditions to kill bacteria, viruses and other microorganisms. This technology mainly relies on the performance of photocatalytic materials, especially semiconductor materials such as titanium dioxide (TiO2). When the photocatalyst is irradiated by light of a specific wavelength, the electrons in the material transition from the valence band to the conduction band, forming electron-hole pairs. These electrons and holes have high chemical activity and can react with water or oxygen to generate free radicals with strong oxidizing ability, which can destroy the cell wall or cell membrane of microorganisms, causing the leakage of intracellular substances, thereby achieving the effect of sterilization. The present application aims to solve the problems of low light utilization rate and insufficient active sites of TiO2 photocatalytic materials, and proposes a TiO2@Ag / Ti-MOF functional material. The TiO2@Ag / Ti-MOF functional material is based on the Ti-MOF skeleton to construct Ag-MOF, realizing the controlled slow release of Ag ions and having a long-term effective sterilization effect.

Systems and methods for encapsulating cells in hydrogel tubes for cell growth within hydrogel tubes are described. In aspects, a system includes a plurality of peristaltic pumps and a plurality of pulse dampeners to provide oscillatory-controlled flow rates of each of a cell solution, a hydrogel solution, and a cross-linking solution to an extruder configured to form hollow hydrogel tubes having suspended biological cells in an interior

The invention discloses a multilayer imaging method for terahertz near-field system tomography, and belongs to the technical field of terahertz near-field imaging. Aiming at the problem that internal depth quantitative calibration is difficult to realize in existing terahertz near-field three-dimensional imaging, the method proposes that a signal with deepest internal imaging is determined through primary scanning, then multiple data processing is carried out through secondary or multiple scanning, bias voltages of different acquired signals are respectively adjusted under the same magnification times, and the internal depth quantitative calibration is realized in the terahertz near-field three-dimensional imaging. The offset values are arranged in an arithmetic progression, thereby obtaining imaging data representing different linear depths. According to the method, multilayer imaging of internal depth calibration can be realized, a three-dimensional tomographic image with quantitative depth information is formed, and the method is suitable for observation of internal structures of biological cells and nondestructive testing of internal defects of materials.

The present invention relates to a method of preparing a microbial cell product, the method comprising: providing an aqueous suspension comprising microbial cells; subjecting said suspension to mechanical cell dissociation at a temperature in the range of 15 DEG C to 35 DEG C, preferably at a pH in the range of 9 to 11, to obtain an aqueous suspension comprising dissociated microbial cells; separating the suspension to provide an extract rich in small cell debris and an extract rich in large cell debris; and combining at least a portion of the extracts to provide the microbial cell product. The invention further relates to a microbial cell product obtained or obtainable by said method. The invention further relates to the use of said products in food products, for example as a replacement for egg white; in animal food; and / or use in cosmetic formulations.

The present invention discloses a multifunctional oscillating culture integrated shaker and method based on cell culture, which relates to the technical field of enzyme biological cells. A split oscillating platform for placing containers is configured inside the body. The oscillating platform is composed of multiple oscillating plates, and clamping members are configured on the upper part of the oscillating plates to clamp the containers. A driving module connected to the oscillating platform is configured inside the body. The driving module includes an oscillating unit and a connecting unit. The connecting unit connects the oscillating unit and the oscillating plates. The connecting unit is configured with two transmission states for adjacent oscillating plates through a differential, and the differential is configured to drive multiple oscillating plates to oscillate at the same speed or at different speeds by the driving module. In this application, the oscillating platform is split into multiple oscillating plates. When oscillating enzyme biological cells, the enzyme biological cells that require different oscillating parameters are placed on different oscillating plates, and multiple enzyme biological cells can be oscillated in the same shaker through oscillating plates with different oscillating frequencies.

The present invention belongs to the technical field of photothermal materials, and specifically relates to a thorn-shaped photothermal anode material and its application in sterilization in an electro-Fenton system. The thorn-shaped photothermal anode material provided by the present invention has a nano-thorn-like structure, which has a capture and puncture effect on cells, and can assist the free radicals generated by the electro-Fenton sterilization system to enter the microbial cells and react with cellular substances, thereby improving the utilization efficiency of hydroxyl radicals and enhancing the sterilization and disinfection effect; further, the thorn-shaped photothermal anode material has oxygen vacancies, which can serve as active centers to activate hydrogen peroxide to produce hydroxyl radicals, reduce the amount of reagent added, reduce iron sludge formation, and improve the operating efficiency of the system. The application of the thorn-shaped photothermal anode material to the construction of an electro-Fenton sterilization system can significantly improve the sterilization efficiency.

The invention discloses a mouse primary cardiac endothelial cell extraction method, and belongs to the technical field of biological cell extraction. The method comprises the following steps: step 1, obtaining pure myocardial tissues; 2, the treated heart tissue is transferred into an intelligent tissue grinding system to be ground; step 3, transferring the ground heart tissue into a temperature-controlled enzymolysis reactor, automatically monitoring the digestion process, and terminating the reaction when a preset digestion degree is reached; step 4, carrying out primary cell separation, carrying out magnetic separation by using anti-CD31 magnetic beads, and specifically enriching heart endothelial cells; 5, transferring the purified endothelial cells to an intelligent microenvironment culture system, and automatically optimizing a culture medium replacement period to adapt to a cell metabolism state; and step 6, performing multi-dimensional quality evaluation on the endothelial cells, wherein the multi-dimensional quality evaluation comprises marker expression analysis, in-vitro lumen formation experiment, AI-assisted morphological analysis and digital quality scoring.

The application relates to the field of sewage treatment, and discloses a sulfur autotrophic denitrification biofilter composite filler and a preparation method thereof. The method comprises the following steps: carrying out a silane hydrolysis reaction on a silane coupling agent containing a mercaptan group to prepare a hydrolysis solution, and then adding hydroxylated polystyrene microspheres into the hydrolysis solution to carry out a grafting reaction and prepare the sulfur autotrophic denitrification biofilter composite filler. The method grafts mercaptan groups to the surface of the polystyrene microspheres by using the silane coupling agent containing the mercaptan group. The mercaptan groups can specifically combine with sulfur transport proteins on the cell membrane of sulfur autotrophic denitrification microorganisms, so that the sulfur autotrophic denitrification microorganisms can selectively colonize on the surface of the polystyrene microspheres, competition between other microorganisms and the sulfur autotrophic microorganisms can be avoided, the colonization stability of the sulfur autotrophic microorganisms is improved, and the biofilm formation efficiency is improved.

A self-organizing swarm robot system and control method based on cellular soft and hard mechanisms are disclosed. The system includes several individual robots. Each robot includes an upper shell, a middle support, a lower support chassis, electrically driven legs, a magnetically connected actuator, a PCB control board, and light-emitting elements. The PCB control board is equipped with an ESP-NOW wireless communication module, a light sensor, and a multi-pose sensor. The magnetically connected actuator includes static and dynamic actuators alternately distributed along the circumference. This invention can simulate the adhesion force regulation and morphological expansion and contraction mechanism between biological cells, achieving dynamic control between swarm robots under mechanical action. It exhibits high flexibility and fast response speed, enabling multi-degree-of-freedom movement and posture adjustment in complex environments. By using ESP-NOW wireless communication technology in conjunction with light sensors and multi-pose sensors to construct a high-precision distributed sensing and control system, it supports the self-organization, collaboration, and task execution capabilities of swarm robots in weak information environments.

The invention discloses a tyrosinase near-infrared fluorescent probe as well as a preparation method and application thereof, and belongs to the technical field of analytical chemistry. According to the technical scheme, the tyrosinase near-infrared fluorescent probe is characterized in that the structural formula of the tyrosinase near-infrared fluorescent probe is shown in the specification. The invention further specifically discloses a preparation method of the tyrosinase near-infrared fluorescent probe and application of the tyrosinase near-infrared fluorescent probe to selective detection of tyrosinase in a water environment, a biological cell system and living organisms. The near-infrared fluorescent probe disclosed by the invention has the advantages of fluorescence emission in a near-infrared region, good selectivity, high sensitivity and the like.

The application discloses a system and method for controlling liposome drug directional delivery based on a spectrum space phase gradient light field, and belongs to the technical field of light field regulation of biological cells; in the application, quasi-plane waves are irradiated onto a spatial light modulator, the amplitude of a target light field is embedded into a phase by using Fourier expansion, and then a holographic template of the reconstructed light field is generated; the holographic template is loaded onto the spatial light modulator, and after filtering through a 4f system, the light beam is projected to an objective lens; on the focal plane of the objective lens, with the help of the existence of the phase gradient, the drug-loaded liposome is transported along a preset track in a directional manner, and is captured by an intensity gradient optical trap at the end of the track; the application can design any drug delivery track according to requirements, and without moving the equipment platform, the two manipulations of any track delivery and target capture can be realized through a single light beam, and the convenience and efficiency of drug directional delivery are improved.

The invention discloses a novel molecular chaperone-mediated autophagy (CMA) activating agent, relates to the technical field of biological cells, and is characterized in that the novel molecular chaperone-mediated autophagy activating agent is a novel anti-tumor drug chidamide, and the novel molecular chaperone-mediated autophagy activating agent is a novel anti-tumor drug chidamide. The chidamide can obviously up-regulate the mRNA and protein level of the key protein LAMP2A in the CMA process. According to the present invention, by constructing a human THP1-LAMP2luciferase reporter gene system, the compound capable of activating the LAMP2 promoter is screened from the bulk drug; through cell level primary screening, secondary screening and animal level verification, an effective CMA activator chidamide is finally determined. A good tool is provided for basic research of CMA, and novel drugs are further researched and developed by taking CMA as a target spot.

The utility model discloses a biological cell storage cabinet, which comprises a cabinet body, a baffle plate, a storage frame, a lifting spoon and a cell culture plate, a support block is arranged at the upper end in the cabinet body, the baffle plate is placed in the cabinet body, and the bottom of the baffle plate is attached to the top of the support block. The lifting spoon and the connecting rod are additionally arranged, liquid nitrogen can be conveniently added and transferred by a worker, direct contact between the liquid nitrogen and the storage plate is avoided, the opening used for adding the liquid nitrogen is additionally formed in the baffle, liquid nitrogen can be conveniently added into the lifting spoon, liquid nitrogen splashing is avoided, and the liquid nitrogen at the opening is isolated through the cover plate when the liquid nitrogen storage device is not used. The observation hole for placing the wooden stick is additionally formed in the cover plate, the liquid level height is measured by observing the frosting length of the wooden stick, liquid nitrogen in the observation hole is isolated through the end cover when the cell culture plate is not used, leakage of the liquid nitrogen is further reduced, a plurality of transversely-arranged insertion rods are additionally arranged, when a single cell culture plate is taken and placed, the other cell culture plates cannot be inclined and fall off, and the cell culture plate is convenient to use. The cells are convenient to take and place.

The present invention relates to a method and platform for generating CAR-T cells and processing biological cells within a single functionally closed container. The method involves introducing host cells into a sealed container with multiple sterile channels, performing genetic modifications, and maintaining the cells under controlled conditions monitored by real-time feedback until a desired fraction of genetically modified cells is obtained. The container also supports target cell separation using antibody or aptamer functionalized buoyant microbubbles, facilitating the separation of target cells from non-target cells during centrifugation. Waste separation and cell harvesting are performed using pneumatic pressure, enabling high purity cell recovery. The platform includes modules for cell enrichment, sequestration, and isolation, enabling high recovery and high purity of therapeutic cell populations. This integrated closed system approach ensures sterile conditions, efficient processing, and high quality cell products for advanced therapeutic applications.

Synthetic human cell mimic hydrogel particles and their use in cytometric or coulter device applications are described. The synthetic human cell mimic hydrogel particles described herein are selectively tunable to have at least one optical, volumetric, or capacitance property that is substantially similar to a corresponding optical, volumetric, or capacitance property of the human cell mimic hydrogel particle's natural biological cell counterpart.

The invention discloses a reactive copper ion near-infrared fluorescent probe as well as a preparation method and application thereof, and belongs to the technical field of copper ion near-infrared fluorescent probes. According to the technical scheme, the reactive copper ion near-infrared fluorescent probe is characterized in that the structural formula of the reactive copper ion near-infrared fluorescent probe is shown in the specification. The invention further specifically discloses a preparation method of the reactive copper ion near-infrared fluorescent probe and application of the reactive copper ion near-infrared fluorescent probe to selective detection of copper ions in an aqueous solution, a biological cell system and animal tissue. The near-infrared fluorescent probe disclosed by the invention has the advantages of fluorescence emission in a near-infrared region, good selectivity, low detection limit and the like.

The invention relates to the technical field of grain detection, in particular to a gas detector for grain mildew real-time monitoring, which comprises an acquisition module for acquiring data information of the environment where grains are located, including temperature, humidity, illumination intensity, oxygen content, PH value, radiation intensity and the like. Trace microbial particles can be detected by utilizing intrinsic fluorescence characteristics of microbial cells; the whole detection process can be completed in a short time, and the rapid detection requirement is met; destructive treatment on the grain sample is not needed, and the integrity of the sample is kept; the detection process can realize high automation, and manual operation errors are reduced; the microorganism counting method based on microorganism intrinsic fluorescence does not need any reagent and complex manual operation process, can be used for carrying out real-time, automatic and continuous detection on the concentration of microorganisms in grains, and has very important significance on detection and early warning of change states of food crops.

A method of manipulating and / or investigating cellular bodies (9) is provided. The method comprises the steps of: providing a sample holder (3) comprising a holding space (5) for holding a fluid medium (11); providing a sample (7) comprising one or more cellular bodies (9) in a fluid medium (11) in the holding space (5); generating an acoustic wave in the holding space exerting a force (F) on the sample (7) in the holding space (5). The method further comprises providing the holding space (5) with a functionalised wall surface portion (17) to be contacted by the sample (7) and the sample (7) is in contact with the functionalised wall surface portion (17) during at least part of the step of application of the acoustic wave. A system and a sample holder (3) are also provided.

The invention relates to an antibacterial and deodorant insole material and a preparation method thereof, and belongs to the technical field of insole materials. The antibacterial and deodorant insole material comprises the following components: EVA, TPU, an antibacterial material, a dispersing agent and a compatilizer, the preparation method comprises the following steps: adding the EVA, the TPU, the antibacterial material, the dispersing agent and the compatilizer into a double-screw extruder, and extruding and granulating to obtain the antibacterial and deodorant insole material. According to the invention, the o-aminobenzoic acid-syringaldehyde composite carrier destroys microbial cell membranes to enhance the sterilization permeation efficiency of nano-silver, and syringaldehyde neutralizes odor molecules to achieve synergistic interaction, so that the integration of dual functions of bacteriostasis and deodorization is realized.

The utility model relates to the technical field of reagent bottles, and discloses a reagent bottle for biological cell separation, which comprises a reagent bottle, a cover body is inserted into a bottle opening of the reagent bottle, a rubber ring is fixedly connected to the bottom of the cover body, and a fixing mechanism is arranged on the surface of the bottle opening of the reagent bottle. Through a fixing mechanism, after a reagent bottle is filled with a reagent, the reagent bottle is covered with a cover body, the bottom of a rubber ring is located at the top of the reagent bottle, then a pulling plate is pulled to enable a disc to move, then a connecting frame is rotated to enable the disc to rotate to the position above the cover body, then the pulling plate is loosened, and at the moment, the disc can move downwards through the elastic force of a spring; the cover body is tightly pressed by the bottom of the disc, so that the reagent bottle is tightly pressed by the rubber ring, the smell of a reagent in the reagent bottle does not fly out of the reagent bottle, a pungent smell is generated in a laboratory, and the personal safety of workers in the laboratory is further protected.

The present invention relates to a system for collecting, separating, concentrating, and reinfusing blood components from whole blood. The system further includes cell modification. The system includes a blood processing device and a fluid flow circuit.

The invention relates to the technical field of biological cells, in particular to a method for forming a derived mammary gland organoid based on induced differentiation of pluripotent stem cells, the adopted culture technical means is no longer rough, more specific and refined, different culture media are customized and used in different stages of cell reproduction, and the culture efficiency is greatly improved. And the old culture medium is taken out in time to replace a proper amount of new and appropriate culture medium, so that normal proliferation of cells is promoted, cell death is reduced, and the pluripotent stem cells can be quickly differentiated to form the derived mammary gland organs. The method is supported by national key research and development plan projects, the project name is microenvironment adaptive type organoid assembly technology research and development based on full liquid phase printing, and the project number is 2024YFC3407600.

The invention discloses a multi-scene inflatable portable cell culture device, and relates to the technical field of biological cell culture.The device comprises a culture cabin, a system cabin and an air cabin, the culture cabin is of a three-layer structure comprising a wear-resistant layer, an inflatable layer and an antibacterial layer and is connected with the system cabin and the air cabin through a double-layer zipper, and the culture cabin is provided with a transparent window and an openable double-layer bottom plate; and a zipper assembly with an automatic sealing structure is connected between the bottom plate and the culture cabin. A heating plate and a temperature sensor are arranged in the antibacterial layer, the system cabin is provided with a temperature controller, a gas controller and a control panel, and the gas cabin is provided with a gas pump and a gas cylinder, supplies gas to the inflation layer and the culture cabin respectively and is electrically connected with the gas controller. The culture cabin of the device can be folded and stored, is good in portability, can be arranged outside a scientific research instrument in a sleeving manner to construct a culture environment in situ, is adaptive to multiple experiment scenes, can accurately regulate and control temperature and gas parameters of the culture cabin, is good in sealing antibacterial activity and convenient to operate, and solves the problems that a traditional culture box is poor in portability and cannot be matched with the scientific research instrument for use.

The invention provides an oscillation mixing device for biological cell culture, and belongs to the technical field of cell culture.The oscillation mixing device comprises a shell, an openable shell door is arranged on the front side of the shell, an inner cavity is reserved in the shell, an oscillation unit is arranged at the bottom of the inner cavity, and an assembly table is arranged on the oscillation unit; a containing unit is arranged on the upper portion of the assembling table, substrates are arranged on the two sides of the upper portion of the assembling table, first linkage units are arranged on the sides, close to each other, of the substrates, the first linkage units are provided with high-low displacement units, and the high-low displacement units are provided with reset units. According to the invention, the problem that the whole culture container is not convenient to load and unload because the culture container close to the outside is convenient to load and unload and the culture container close to the inside needs to be probed and controlled by an operator when the culture container is close to the inside during the constraint of the culture container is solved.

Rotationally symmetric dielectric structure (2) for optical beam shaping and for capturing and manipulating individual particles and living biological cells in an aqueous medium, which is mounted concentrically on the facet of a single-mode optical fiber (1), wherein the structure (2) comprises at least three total reflection surfaces (S1, S1', S2) configured to divide a light field emerging from the single-mode optical fiber (1) into at least two separate light paths, and wherein the at least three total reflection surfaces (S1, S1', S2) are further configured to combine the separate light paths as a ring beam at a common focal point.