30results about How to "Help adhesion" patented technology

The invention relates to a preparation method of a mechanically-enhanced cell-loaded microchannel hydrogel, which comprises the following steps: preparing a mixed solution of hydrogel sol and cell culture fluid, and pouring the sol-cell mixed liquid into a polymethyl methacrylate die into which capillary tubes or fibers are inserted, thereby enabling primary crosslinking; drawing out the capillary tubes or fibers, introducing the hydrogel sol into microchannels of the cell-loaded hydrogel, and reinserting the capillary tubes or fibers, or sucking excess hydrogel sol out of the microchannels and carrying out ultraviolet irradiation, thereby enabling secondary crosslinking, so that the cell-loaded hydrogel with thick hydrogel layer is formed in the wall regions of the microchannels; and drawing out the capillary tubes or fibers, introducing endothelial cell culture fluid into the microchannels of the cell-loaded hydrogel, and culturing so that the endothelial cells grow and spread to form endothelial microchannels. The introduction of the thick hydrogel layer can maintain the stability of the microchannels in the hydrogel, and prevent shedding and intrusion of the endothelial cells;and the culture fluid in the microchannels can be filtered and screened.

The present invention relates to one kind of micro carrier for large scale cell culture. The micro carrier is prepared with chitosan and gelatin and through the following steps: mixing chitosan and acetic acid aqua and gelatin aqua in certain ratio to form composite chitosan-gelatin aqua; adding mineral oil with Span to form stable chitosan-gelatin water-in-oil preparation; adding glutaraldehyde to cure; filtering with 100 / 280 micron mesh and collecting solid micro carrier, or filtering with 450 / 600 micron mesh, freeze drying and collecting porous micro carrier; processing with glycine to close un-reacted aldehyde group; and finally processing with NaOH to eliminate residual acetic acid and to obtain the micro carrier. The micro carrier is favorable to cell adhesion and can maintain cell function for long time. In addition, the method of the present invention can control various parameters of the micro carrier in relatively wide range, has low cost and is suitable for industrial production.

The invention relates to a protein adhered to the surface layers of bacteria and an application thereof. The invention discloses an application of an integration membrane protein STY in preparing a reagent for promoting the adhesion of cells. The invention also discloses a method for changing the adhesion property of the cells by utilizing the integration membrane protein STY. The invention also discloses a specific antibody of the integration membrane protein STY.

The invention discloses a power battery. The power battery comprises a battery shell, an electrode group and an electrolyte, wherein the electrode group is coated in the battery shell; the electrode group is formed by superposing a plurality of positive plates, negative plates and diaphragms; the positive plate is coated with a high-nickel positive electrode material composition, the negative plate is coated with a silicon-based negative electrode material composition, and the high-nickel positive electrode material is adopted to be matched with the silicon-based negative electrode material, so that the energy density of the single battery reaches 281Wh / kg, and the capacity is kept at 80% after the single battery is charged and discharged at the rate of 1C for 350 times at the room temperature; a lithium-rich positive electrode material is adopted to be matched with the silicon-based negative electrode material, so that the energy density of a single battery reaches 302Wh / kg, and the capacity is kept at 80% after the single battery is charged and discharged at the rate of 0.5C for 195 times at the room temperature circulation. Meanwhile, the invention further provides a battery cloud platform management method, model parameter changes of a polarization link are considered, battery safety design is guided through model research, battery manufacturing process parameters are controlled through a digital intelligent manufacturing technology, and the battery manufacturing consistency is guaranteed.

The invention provides a drug coating solution for a drug-coated balloon and a drug-coated balloon, which belong to the technical field of pharmacy. The drug coating liquid of the present invention uses pectin as the excipient of the drug coating balloon, and after being mixed with the active drug (paclitaxel or docetaxel), it helps the adhesion of the drug coating liquid to the blank balloon. When the drug-coated balloon reaches the lesion, pectin helps the active drug to be released from the surface of the balloon coating quickly and deposited on the surface of the blood vessel wall to reach an effective drug concentration. Arginine-glycine-aspartic acid (RGD) peptides are structural recognition motifs for cell surface integrins, including ανβ3 and α5β1, associated with the process of anchoring to the extracellular matrix. The present invention adds RGDS-OCH to the drug coating liquid 2 (CH 2 ) 6 CH 3 , can act as an integrin targeting vascular endothelial cells, enhance the absorption of active drugs, and reduce the loss of active drugs during delivery.

The invention provides a preparation method of an electronic circuit board cleaning agent. The preparation method comprises the following steps: firstly, mixing ethylene glycol monomethyl ether, 1-hydroxy-ethanesulfonic acid and a polyol solvent to obtain a premixed solution; dissolving polyethylene glycol oleate, sodium diethylhexyl sulfosuccinate, secondary alkyl sodium sulfonate, alkyl polyglucoside and potassium pyrophosphate into deionized water, adding the premixed solution, N-methyl-2-pyrrolidone, modified silica gel and 2, 2 '-azodiisobutylamidine dihydrochloride, and carrying out reflux reaction in a nitrogen atmosphere so as to obtain the product. The cleaning agent is suitable for cleaning electronic circuit boards and has a good cleaning effect and does not cause corrosion andrusting of the electronic circuit boards.

The invention relates to a preparation method of a mechanically-enhanced cell-loaded microchannel hydrogel, which comprises the following steps: preparing a mixed solution of hydrogel sol and cell culture fluid, and pouring the sol-cell mixed liquid into a polymethyl methacrylate die into which capillary tubes or fibers are inserted, thereby enabling primary crosslinking; drawing out the capillary tubes or fibers, introducing the hydrogel sol into microchannels of the cell-loaded hydrogel, and reinserting the capillary tubes or fibers, or sucking excess hydrogel sol out of the microchannels and carrying out ultraviolet irradiation, thereby enabling secondary crosslinking, so that the cell-loaded hydrogel with thick hydrogel layer is formed in the wall regions of the microchannels; and drawing out the capillary tubes or fibers, introducing endothelial cell culture fluid into the microchannels of the cell-loaded hydrogel, and culturing so that the endothelial cells grow and spread to form endothelial microchannels. The introduction of the thick hydrogel layer can maintain the stability of the microchannels in the hydrogel, and prevent shedding and intrusion of the endothelial cells;and the culture fluid in the microchannels can be filtered and screened.

The invention discloses a rapid preparation method for dry silver-stained samples of freshwater ciliates, belonging to the field of biotechnology. The method of the present invention comprises: (1) picking and collecting ciliates, and cleaning the surface of the ciliates; (2) adhering the clean worm liquid obtained from cleaning to the surface of a clean glass slide treated with polylysine, and removing the ciliate liquid Divide into several small drops and blow dry; (3) Add silver nitrate solution dropwise to the surface of the worm body, and clean the residue after standing; (4) Use a halogen cold light source to irradiate and develop; (5) Rinse the scum and dry it; (6) Add neutral gum dropwise to the surface of the worm body, add a cover slip and seal the slide. The method of the invention can efficiently and high-quality prepare dry silver-stained samples of freshwater ciliates, and at the same time greatly simplifies the film-making steps, and the invention does not need to use a developing solution, thereby saving raw material costs. In addition, the sample of the present invention is irradiated and developed under a cold halogen light source after being stained with silver nitrate, which is not affected by weather factors and is easier to control.

The invention discloses a mesoporous molecular sieve composite laser direct forming material, which comprises the following components in terms of weight percentage: 70-95% polycarbonate; 1-10% laser direct forming additive; 1-5wt% Phosphate ester / mesoporous molecular sieve hybrid material; 1-15wt% toughening agent; 0.5-5% other additives. The phosphate ester / mesoporous molecular sieve hybrid material is prepared from phosphate ester and mesoporous molecular sieve. The invention also discloses a phosphate / mesoporous molecular sieve hybrid material and a preparation method thereof. The beneficial effects of the present invention are: the phosphate / mesoporous molecular sieve hybrid material can promote the char formation in the laser activation process and help to shorten the plating time; at the same time, the special structure of the mesoporous molecular sieve is helpful for the metal to be deposited on the surface of the substrate. Adhesion, and can significantly improve the bonding strength between the coating and the substrate.

The invention relates to a protein adhered to the surface layers of bacteria and an application thereof. The invention discloses an application of an integration membrane protein STY in preparing a reagent for promoting the adhesion of cells. The invention also discloses a method for changing the adhesion property of the cells by utilizing the integration membrane protein STY. The invention also discloses a specific antibody of the integration membrane protein STY.

The invention provides a drug coating solution used for a drug-coated balloon and the drug-coated balloon, and belongs to the technical field of pharmacy. The drug coating solution provided by the invention takes pectin as an excipient of the drug-coated balloon, and is conducive to adhesion of the drug coating solution and an empty balloon after being mixed with an active drug (paclitaxel or docetaxel). When the drug-coated balloon reaches a damaged site, the pectin is conducive to quick release of the active drug from the coating surface of the balloon, and the active drug deposits on the surface of a blood vessel wall to reach effective drug concentration. An arginine-glycine-aspartic acid (RGD) peptide is a structural recognition motif of cell surface integrin, including alpha-nu-beta3 and alpha-5-beta-1, and is associated with the process of anchoring an extracellular matrix. RGDS-OCH2(CH2)6CH3 is added into the drug coating solution provided by the invention, can be used as integrin on targeting vascular endothelial cells, enhances absorption of the active drug, and meanwhile, reduces the loss of the active drug during delivery.

The invention discloses application of sodium hypochlorite in preparing a single-layer double-sided polypropylene / polydopamine patch. According to the application disclosed by the invention, by usingthe principles that sodium hypochlorite can quickly peel a polydopamine film from polypropylene and the polypropylene patch density is smaller than that of a saturated saline solution, a single-layerpatch is divided into two sides on nanoscale, one side is a polypropylene / polydopamine film face which can effectively prevent the patch from being attached to organs in the enterocoelia, and the other side is a polypropylene face which is exposed after the polydopamine nanofilm is peeled; the polypropylene face is internally in contact with peritoneum to improve abdominal wall tension, so that displacement risk is reduced, the structure of the patch is more reasonable, and requirements in the peritoneum and the enterocoelia are met simultaneously. Meanwhile, the preparation method is not related to stacked composition of varieties of composite materials, the thickness of the obtained patch is macroscopically kept as the thickness of a pure PP patch, and the patch is lighter and thinner and has a great clinical application value.

The invention belongs to the technical field of biological medicines, and particularly relates to a biomimetic composite patch. The biomimetic composite patch mainly comprises an isolating membrane, wherein holes are evenly distributed in two sides of the isolating membrane respectively; a cell induction layer is formed at one side of the isolating membrane; an outer layer space is formed at the other side of the isolating membrane; an induction space is formed in the middle of the isolating membrane; an impermeable layer covers the outer layer space, so as to provide a space for two-way growth of cells. The patch can absorb an electrospinning patch formed by a degradable material and a function factor complex. The invention provides a preparation method of the patch and use of the patch in the aspects of pasting, sealing, blocking, stopping bleeding, isolating, repairing and preventing adhesion of defective tissues in a surgical operation. The patch also can be used as a controlled release carrier of a medicament and a tissue engineering scaffold material.

The invention relates to a bionic in-situ regeneration repair nano sticking patch, which is formed by overlapping an layer A with a cationic group material and a layer B with an anionic group material sequentially, wherein the sticking patch comprises 20 to 80 percent by mass of the A layer with the cationic group material and the balance of the layer B with the anionic group material; layer A with the cationic group material comprises at least one of polysaccharide with a cationic group, protein with the cationic group or opypeptide (polypeptide) with the cationic group; layer B with the anionic group material comprises at least one of polysaccharide with an anionic group, protein with the anionic group or opypeptide (polypeptide) with the anionic group; and the sticking patch comprises not more than 10 percent by mass of added functional factors and / or functional polypeptide. The raw materials used by the invention are materials which can be degraded in vitro and have biocompatibility. The sticking patch is flexible, has good tissue adhesivity, is suitable for concave-convex surfaces of visceral organs, has strong stretching resistance and air pressure resistance, is suitable for application of sticking, sealing, leak stoppage, hemostasia, isolation, repair, adhesion prevention and artificial meninges of defect tissues and can also be used as a slowly-releasing carrier of a medicament and a nano-grade tissue engineering support material.

The invention provides an artificial dental planting body, which consists of a head part and a body part, wherein the body part comprises an inner side part, an outer side part and an anchoring part;the inner side part is a mandrel; the outer side part is a porous metal material sleeve and sleeves the mandrel; the anchoring part is fixed at one end of the mandrel; holes of the porous metal material of the sleeve are uniform; the length of projected ribs of the outer side surface of the sleeve is 30 to 50 percent of the pore diameter; the increase of friction between the surface of the porousmetal material and the peripheral bone tissue can be facilitated; the friction is uniform; the bone tissues are stimulated, and are promoted to uniformly grow into the porous metal material; the mandrel and the anchoring part prepared by the nanometer porous metal are favorable for the cell adhesion, differentiation and migration; and the storage of many growth factors and medicine is facilitated.The artificial dental planting body has the advantages that the uniform combination of the sleeve and the bone tissues can be realized; the fixation is firm; and the bone combination time is reduced.

The invention discloses a method for preparing a regenerated rubber asphalt mixture, which belongs to the field of asphalt technology. The main points of the technical solution include the following steps: S1: weighing 10-30 parts of rubber oil and 60-80 parts of rubber powder in parts by weight, Add rubber powder into rubber oil and swell for more than 6 hours at a temperature of 20°C-40°C to obtain a mixture; S2: add 60-80 parts by weight of new aggregates in the container for mixing, and then mix the Add the mixture, then add 20-40 parts of pavement reclaimed material in parts by weight, 4-10 parts of matrix rock asphalt, 1.7-2.8 parts of 70# asphalt, and 6-12 parts of filler to obtain the recycled rubber asphalt mixture, so as to improve the regeneration of the recycled asphalt mixture. The effect of low temperature resistance performance.

The invention discloses a functional structured ion implantation modified layer on the surface of biomedical pure magnesium, which comprises a manganese modified layer ion-implanted and evenly distributed on the surface of the pure magnesium, and the manganese modified layer includes manganese in the inner layer Elemental substance and manganese oxide located on the surface with increasing content from inside to outside. The invention also discloses a preparation method of the biomedical pure magnesium surface functional structured ion implantation modification layer. The invention also discloses the application of a biomedical pure magnesium surface functional structured ion implantation modified layer in a degradable bone implant material. The invention enables pure magnesium to form uniform galvanic corrosion at the initial stage of immersion in simulated body fluid, and promotes the deposition of calcium-phosphorus compounds similar to human bone components. As time goes on, the corrosion type changes to uniform corrosion, achieving controllable degradation. On the basis of effectively improving the corrosion resistance of biomedical magnesium, the biocompatibility is further improved and the application range is expanded.