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71results about How to "Meet the needs of clinical applications" patented technology

Latex enhanced turbidimetric immunoassay kit of quantitatively detecting procalcitonin PCT

The invention relates to a latex enhanced turbidimetric immunoassay kit of quantitatively detecting procalcitonin PCT. The kit comprises an R1 reagent, an R2 reagent and a calibrator, wherein the R1 reagent comprises a protecting agent, a reaction enhancing agent, a preservative and buffer solution; the R2 reagent comprises a protecting agent, a preservative, buffer solution and anti-human PCT antibody coated sensitization polystyrene latex particles; the calibrator comprises a protecting agent, a preservative, buffer solution and PCT recombinant protein; the human PCT antibody in the R2 reagent is linked with polystyrene latex particles through streptavidin-biotin; and the particle diameter of the latex particles in the R2 reagent is 40-500 nm. The kit can be used on a biochemical analyzer and a scatter turbidimetry analyzer for quantitatively detecting the PCT content in human blood. The invention provides the PCT detection kit which has the advantages of convenience, quickness, high sensitivity, strong specificity and accurate quantification; and the kit has high instrument compatibility, is low in detection cost and meets the requirements on PCT turbidimetric products in clinical use.
Owner:NANJING NORMAN BIOLOGICAL TECH

Preparation method of ultrasound and magnetic resonance two-mode contrast medium having lymph targeting

The invention discloses a preparation method of an ultrasound and magnetic resonance two-mode contrast medium having lymph targeting. The preparation method comprises the following steps: adding a surfactant to an alkaline solution, stirring, adding a silicon source to the solution after the surfactant is dissolved completely, continuously stirring, adding a magnetic compound to generate a sol mixture, stirring, washing and carrying out centrifugal drying to obtain a powdery product; carrying out high-temperature calcination on the product to obtain powdery nanometer mesoporous silica particles without the surfactant; dispersing the particles in an organic solvent, adding a silane coupling agent, stirring, washing with ethyl alcohol and water, and carrying out centrifugal drying to obtain a powdery product; dispersing the powder in deionized water, adding a cross-linking agent and sodium hyaluronate, stirring, washing with water and carrying out centrifugal drying to obtain nano-particles; and dispersing the particles in deionized water, dropwise adding fluorocarbon, stirring, washing with water and drying to obtain the contrast medium. By utilizing the preparation method, integration of double imaging modes can be realized, and two imaging manners can be developed.
Owner:SHANGHAI JIAO TONG UNIV +1

Immunofluorescence kit for quantitatively detecting content of troponin I and preparation method

The invention discloses an immunofluorescence kit for quantitatively detecting the content of troponin I and a preparation method. The preparation method comprises the following steps: preparing a troponin antibody-large-particle fluorescent particle conjugate; preparing a nitrocellulose membrane labeled antibody; assembling a reagent card; preparing a TNI calibration product; establishing a standard curve; calculating the content of the troponin in a sample to be detected. The immunofluorescence kit for quantitatively detecting the content of the troponin I comprises a nitrocellulose membrane, a reagent and the calibration product. The lowest detection limit of the kit can reach 0.1ng/ml and the requirement of clinical application is met; the fastest time of a process from sample acquisition to detection result presentation only needs 10 to 15 minutes so that more expensive time for patients is provided, and illness states of the patients can be dynamically detected. The immunofluorescence kit for quantitatively detecting the content of the troponin I has good result relevance, no remarkable difference and an accurate and reliable detection result, and can be used for clinically replacing imported products; the detection cost is greatly reduced.
Owner:苏州联辰生物技术有限公司

Preparation, product and application of sandwich type degradable stent for alveolar bone repair

The invention relates to a preparation method of a sandwich type degradable stent for alveolar bone repair as well as a product and application thereof. The preparation method comprises the following steps: preparing a self-curing hydroxyapatite and PLGA double-layer stent through double-nozzle 3D printing; and afterwards, performing amination of the surface of the polyester, and chemically fixing the silk fibroin coating loaded with the endothelial growth promoting medicine through an EDC/NHS coupling reaction. The hydroxyapatite stent matched with bone trauma is prepared, the bioactive coating modified PLGA provides a matched base for external fixation of bone wounds, the hydroxyapatite stent is used in cooperation with bone glue, bone nails and suture lines to achieve the fixing effect, and accurate bone grafting is achieved. All the materials are biodegradable, the degradation rate of the materials is suitable for growth of new bones, the silk fibroin coating loaded with VEGF improves the compatibility of PLGA and mucous membranes, the defects that a traditional titanium mesh stent is exposed outside the mucous membranes in advance and cannot be degraded in vivo are overcome, and the requirements of clinical application are met.
Owner:SHANGHAI NAT ENG RES CENT FORNANOTECH

Method for obtaining maternal mesenchymal stem cells from placenta

The invention discloses a method for obtaining maternal mesenchymal stem cells from placenta. The method for obtaining the maternal mesenchymal stem cells from the placenta comprises the following steps: obtaining placenta tissues from a position, which are within 5cm away from the radius of an umbilical cord and are 0.5 cm away from a fetal surface, of the placenta; and carrying out enzyme digestion treatment on placenta tissues by adopting an enzyme digestion solution, and then carrying out cell culture on a product of the enzyme digestion treatment to obtain the maternal mesenchymal stem cells. According to the method disclosed by the invention, the technical problem of separating the maternal mesenchymal stem cells from the placenta is solved, the prepared maternal mesenchymal stem cells are large in quantity and high in purity, neonatal cells are not easy to mix, and the clinical application requirements can be met; the method provided by the invention solves the problems that thequantity of the maternal mesenchymal stem cells obtained from the decidua basalis is small and the decidua basalis is easy to lose, and provides a new scheme and way for obtaining the maternal mesenchymal stem cells from the placenta.
Owner:深圳华大基因细胞科技有限责任公司

Preparation of polyester/periodic mesoporous bone-filling composite material with fluorescently-labeled degradation rate, product and application

ActiveCN109568675AImprove luminous efficiency and stabilityImprove dispersion uniformityTissue regenerationProsthesisPoly l lactic acidNanoparticle
The invention relates to preparation of polyester/periodic mesoporous bone-filling composite material with a fluorescently-labeled degradation rate, a product and application. The preparation comprises the steps of firstly, synthesizing rare-earth periodic mesoporous nanoparticles with fluorescence performance, then, subjecting the rare-earth periodic mesoporous nanoparticles to chemical modification by taking poly-L-lactic acid with low molecular weight as a modifier, and finally, adding the modified nanoparticles into a polyester matrix by a solution blending method. The invention further provides the product obtained by the method and application of the product in bone restoration as a composite bone filling material. The fluorescent mesoporous material obtained by the method provided by the invention is uniformly dispersed in an organic matrix, mechanical properties of a polyester are improved greatly, and the degradation behavior of the composite bone filling material can be monitored in real time. The preparation process is simple, and the composite bone filling material can serve as a bone filling material of load bearing bone parts with relatively high performance index requirements. The obtained composite material can meet the requirements of clinical application.
Owner:SHANGHAI NAT ENG RES CENT FORNANOTECH

No-mark surgery registration method used for optical surgery navigation system

The invention discloses a no-mark surgery registration method used for an optical surgery navigation system. The no-mark surgery registration method used for the optical surgery navigation system comprises the following steps of: S1: importing the CT sequence of a focus position, processing a CT image, and extracting an upper surface skin outline; S2: reconstructing a two-dimensional skin outline into a three-dimensional point set, and carrying out preliminary coordinate transformation on the CT coordinate system of the point set; S3: calibrating a structured light camera to the coordinate system of a surgical space; S4: utilizing the structured light camera to collect the point cloud of the surgical space, and finishing segmentation and transformation of the point cloud; S5: removing outliers in the surgical space, and adopting resolution ratio consistency to carry out downsampling to obtain a simplified image and the simplified point cloud of the surgical space; and S6: carrying out registration on the point cloud of a CT image space to the surgical space to finish surgery registration. A surgery registration process disclosed by the invention does not need human intervention, and enough surgery navigation accuracy can be guaranteed while surgery registration operation complexity is lowered and operation time is shortened.
Owner:SHANGHAI UNIV
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