422 results about "Cell survival rate" patented technology

The invention relates to the technical field of carbon ion radiotherapy relative biological effects, and discloses a cell survival rate prediction method and system based on Monte Carlo simulation carbon ion spectrum distribution. The method comprises the following steps: collecting experimental data of isolated cells to construct a cell database; based on the energy range of carbon ion radiotherapy particles and the type of secondary particles, a monte carlo method is used to construct a monoenergetic particle DNA damage database. And then constructing a cell survival rate prediction model based on DNA damage repair, and fitting cell radiation specificity parameters of the model based on a cell database to accurately reflect the radiation sensitivity of the cells. Then on the basis of the monoenergetic particle DNA damage database, the mixed beam DNA damage characteristics are determined in a dose weighting mode, the mixed beam DNA damage characteristics are input into the model subjected to parameter fitting to predict the cell survival rate, the secondary particle biological effect is considered, and the prediction accuracy of the clinical carbon ion beam relative biological effect can be improved.

The invention provides a liposuction needle cannula system and method, and the system comprises a cannula assembly which is used for forming a liposuction space at a liposuction part; the liposuction needle assembly is arranged in the sleeve assembly in a sliding and penetrating mode and used for conducting liposuction operation in the liposuction space. According to the technical scheme, tissue damage is reduced, and the fat cell survival rate and the liposuction efficiency are improved.

The invention relates to the field of biological medicine, and discloses a rhizoma polygonati-fructus lycii heterozygous exosome, a preparation method and application thereof and an antioxidant composition. The hybrid exosome comprises miRNA-156a (micro Ribonucleic Acid) and miRNA-396b (micro Ribonucleic Acid), and the expression quantity ratio of the miRNA-156a to the miRNA-396b is (1.2 to 1.8): 1; the heterozygous exosome is loaded with a polygonatum kingianum characteristic active component and a Chinese wolfberry fruit characteristic active component. The rhizoma polygonati-fructus lycii heterozygous exosome is good in biocompatibility and capable of remarkably improving the cell survival rate, and brand-new and efficient raw materials and technical supports are provided for development of anti-aging and anti-oxidation functional products.

The invention provides an anti-aging repair composition containing PDRN, and lipid nanoparticles and application thereof. The composition provided by the invention is prepared from polydeoxyribonucleotide, micro-current tetrapeptide-1 and palmitoyl tripeptide-5. According to the application, the polydeoxyribonucleotide, the micro-current tetrapeptide-1 and the palmitoyl tripeptide-5 are compounded for use, so that the composition has a synergistic effect in the aspects of promoting cell proliferation, inhibiting an intracellular ROS (reactive oxygen species) level and the like, and has remarkable antioxidant, anti-inflammatory, anti-aging, soothing and repairing effects. The PDRN-containing composition is prepared into the lipid nanoparticles, so that the stability of the PDRN-containing composition is improved, the permeability of the PDRN-containing composition on the skin surface is improved, the bioavailability of the PDRN-containing composition is improved, the cell survival rate and cell uptake are promoted, the expression of adenosine A2A receptors, the synthesis of collagen, angiogenesis and the inhibition of anti-inflammatory factors are promoted, and a remarkable anti-aging effect is achieved.

The invention discloses an antibacterial peptide based on D-type amino acid and application of the antibacterial peptide, and the antibacterial peptide is characterized in that the amino acid sequence is w-r-r-w-r-r-w-w-r-k-r (dTrp-dArg-dArg-dTrp-dArg-dArg-dTrp-dTrp-dArg-dLys-dArg). The antibacterial peptide can be synthesized through an Fmoc solid-phase chemical method, the synthesis difficulty is low, and the in-vivo antibacterial activity is good. The antibacterial peptide especially has broad-spectrum killing activity on carbapenem-resistant pseudomonas aeruginosa, pseudomonas aeruginosa, klebsiella pneumoniae, escherichia coli, methicillin-resistant staphylococcus aureus and staphylococcus aureus, is low in hemolytic toxicity, can reach half or more of cell survival rate under medium and low concentration, almost has no toxic effect on cells, and can be used for preparing the antibacterial peptide with a broad-spectrum killing activity on carbapenem-resistant pseudomonas aeruginosa, klebsiella pneumoniae, escherichia coli, methicillin-resistant staphylococcus aureus and staphylococcus aureus. The stability is good, the operability is high, and the cost is low.

The invention discloses a construction method of a microplastic toxicity prediction model based on transcriptomics and a QSAR (Quantitative Synthetic Aperture Radar) model, which comprises the following steps: measuring actual observation values of cell survival rates of different microplastic samples after contamination and changes of genes in the cells, and screening out the genes as specific genes; selecting a physicochemical descriptor and then determining a gene expression descriptor of the specific gene; establishing a training set and a test set; a plurality of machine learning algorithms are utilized to construct QSAR models respectively, and an optimal QSAR model is selected according to a performance evaluation result; and carrying out performance verification on the optimal QSAR model, and screening out a microplastic toxicity prediction range suitable for the optimal QSAR model. The construction method of the microplastic toxicity prediction model can realize reliable prediction of toxicity, and can effectively support safety evaluation and biotoxicity mechanism research of microplastics.

The invention discloses a therapeutic nano-vesicle preparation rich in mitochondrial functional protein, a preparation method of the therapeutic nano-vesicle preparation and application of the therapeutic nano-vesicle preparation in treatment of radioactive skin injury. The preparation method comprises the following steps: culturing, amplifying and cleaning umbilical cord mesenchymal stem cells, dispersing the umbilical cord mesenchymal stem cells in a suspension, mechanically extruding the umbilical cord mesenchymal stem cells into a crude solution through a multistage aperture polycarbonate membrane, and centrifuging, concentrating and purifying the crude solution to obtain the preparation. The preparation has the remarkable advantages that local administration can be realized, inflammation can be quickly inhibited, oxidative stress is reduced, and a repair pathway is activated, so that the preparation is suitable for treating acute radioactive skin injury; the preparation method is easy to standardize and scale, high in stability and convenient for emergency storage and delivery, and avoids the defects of cell therapy; a plurality of targets such as immune inflammation, oxidative stress and the like can be synergistically regulated, the biological effect of hUMSCs is simulated and partially replaced, and the limitation caused by the cell survival rate and the microenvironment dependency is avoided; the key function of hUMSCs is covered in function, and the clinical feasibility, safety and emergency suitability of the application level are higher.

The invention relates to the technical field of microfluidics, in particular to a high-throughput and high-efficiency cell extrusion microfluidic system and a particle introduction method. And a closed-loop control system integrating real-time cell deformation sensing, dynamic parameter decision and physical extrusion and alternating electric field cooperative application is constructed. The chip is provided with an inlet shunting device, a micro-channel and a channel structure of a microelectrode. The method comprises the steps of real-time deformation image acquisition and analysis and dynamic extrusion parameter decision and cooperative application. The invention provides a high-flux and high-efficiency cell extrusion microfluidic system and a particle introduction method, and aims to solve the problems that the drug loading efficiency and the survival rate are difficult to consider due to heterogeneity in the existing cell extrusion technology and a physical extrusion and electroporation coordinated regulation strategy is lacked, so that personalized precise treatment of cells is realized, and the cell quality is improved. The drug loading efficiency, the cell survival rate and the high throughput are obviously improved.

The invention discloses an application of an antibacterial peptide and an application of the antibacterial peptide in preparation of antibacterial drugs for treating carbapenem-resistant pseudomonas aeruginosa, klebsiella pneumoniae (ATCC700603), escherichia coli (ATCC25922), staphylococcus aureus and methicillin-resistant staphylococcus aureus, the antibacterial peptide is characterized in that the sequence is w-r-r-w-k-r-w-w-r-r, and the sequence is shown in the description. All amino acids are D-type amino acids; the antibacterial peptide can be used as an antibacterial substance in wash supplies, food preservative additives, medical consumable antibacterial agents and cosmetics, can be synthesized through an Fmoc solid-phase chemical method, and is low in synthesis difficulty and good in in-vivo antibacterial activity. Particularly, the antibacterial peptide has broad-spectrum killing activity against carbapenem pseudomonas aeruginosa, klebsiella pneumoniae (ATCC700603), escherichia coli (ATCC25922), staphylococcus aureus and methicillin-resistant staphylococcus aureus, the cell survival rate of the antibacterial peptide within the range of medium and low concentration (2 mu g / mL-32 mu g / mL) reaches half or more, the toxicity is small, the toxicity is almost avoided, the operability is high, and the antibacterial peptide can be widely applied to the field of medical application. The cost is low.

The invention belongs to the technical field of biological medicines, and particularly relates to a wheat peptide with antioxidant stress activity and a preparation method and application thereof. The invention provides a wheat peptide with antioxidant stress activity. The amino acid sequence of the wheat peptide is as shown in SEQ ID NO: 1. The invention discloses a wheat peptide FGWPGPK for protecting oxidative stress nerve cells as well as a screening method and application of the wheat peptide FGWPGPK. A target peptide fragment is identified from wheat germs through enzymolysis and multi-dimensional screening strategies, and it is proved that the target peptide fragment can significantly improve the survival rate of PC-12 cells damaged by H2O2 (72.88%) and reduce the ROS level (125.54%). The peptide fragment has strong antioxidant activity and nerve targeting property, and is suitable for preventing and treating neurodegenerative diseases such as Alzheimer's disease.

The invention provides an intelligent decision-making method and system for free flap riser anastomosis based on hemodynamics. According to the method, firstly, the blood flow direction, the flow speed and the blood vessel wall tension parameter of a target blood vessel are collected, and a dynamic correlation model of intravascular fluid mechanics and external tissue deformation is established; a three-dimensional blood flow pressure gradient map is generated based on the model, then, a system automatically screens an anastomosis path meeting a blood flow resistance threshold value and the endothelial cell survival rate requirement, and the optimal anastomosis pose is determined by analyzing the blood vessel wall elasticity matching degree and the turbulence generation probability. Then, guiding the accurate adjustment of the clamping direction of the blood vessel and the suture needle pitch in the operation, ensuring that the pressure of the lumen of the anastomosed blood vessel is kept balanced when the anastomosed blood vessel is axially stretched, meanwhile, effectively inhibiting local vortex, and remarkably improving the long-term smoothness of the anastomosis of the blood vessel. According to the method, mechanical precise matching and blood flow stable control of free flap vascular anastomosis are achieved, and the postoperative risk is remarkably reduced.

The invention relates to a culture medium for high-density serum-free suspension culture of BHK-21 cells and application of the culture medium. The culture medium contains inorganic salt, amino acid, vitamins, energy substances, a buffer substance, an antioxidant, sterol, polyamine, an additive and an indicator, and the antioxidant comprises dihydrolipoic acid and S-acetyl-L-glutathione. According to the invention, the culture medium for serum-free suspension culture of the BHK-21 cells, which is clear in components and remarkable in culture effect, can be provided. The added dihydrolipoic acid and S-acetyl-L-glutathione are combined as antioxidants of the culture medium, so that the survival rate of BHK-21 cells cultured in the culture medium is improved while the oxidation resistance of the serum-free suspension culture medium is improved.

The invention discloses a molecular chaperone synergistic blue-copper peptide and application thereof, belongs to the technical field of skin care, and particularly relates to a blue-copper peptide composition formed by compounding blue-copper peptide and N-acetylneuraminic acid, and the structure of the blue-copper peptide is that copper is connected to glycyl-L-histidyl-L-lysine; the blue copper peptide and the N-acetylneuraminic acid are mixed according to the mass ratio of 1: (0.1-1) for use, and further, phenylalanine derivatives can be added into the mixture for compounding. When the blue copper peptide composition obtained by the invention is applied to cells, the cell survival rate is high, the non-enzymatic glycosylation inhibition rate is good, and the expression of Elastin, Col-I and Col-IV mRNA in the cells is high. Therefore, the blue copper peptide composition disclosed by the invention is high in cell survival rate, good in non-enzymatic glycosylation inhibition rate and capable of improving the mRNA expression of Elastin, Col-I and Col-IV in cells, and the application of the blue copper peptide composition.

The invention belongs to the technical field of cell cryopreservation, and particularly relates to a cell cryopreservation solution and a cell cryopreservation method. The cell freezing medium comprises the following components in percentage by volume: 95% of fetal calf serum and 5% of dimethyl sulfoxide. The temperature conditions for cryopreserving the cells by adopting the cell cryopreservation liquid are as follows: standing for 90 minutes at 4 DEG C, then standing for more than 12 hours or overnight at-70 DEG C, and then immersing into liquid nitrogen for long-term storage. According to the cell cryopreservation liquid and the cell cryopreservation method provided by the invention, the problems that a traditional cell cryopreservation technology and an improved cell cryopreservation box are tedious in operation and low in cell resuscitation success rate, and the improved cell cryopreservation liquid is relatively high in cost are solved, and the cell cryopreservation liquid is simple in ingredient, simple in operation, low in cost and high in cell survival rate.

The invention discloses a gelatin microcarrier lysate as well as a preparation method and application thereof. The gelatin microcarrier lysis buffer comprises lyase, a cell protective agent, a cell energy metabolism protective agent, an antioxidant, a buffer solution and a chelating agent. The gelatin microcarrier lysate has extremely strong protectiveness to cells, abandons damaging trypsin and EDTA, and innovatively adds a cell protection combination of a cell protective agent L-arginine, a cell energy metabolism protective agent sodium pyruvate and an antioxidant vitamin C, so that the cell survival rate (gt; 98%) and the retention rate (gt; the method is high in cell yield, good in safety and wide in range.

The invention discloses application of a 3D hypoxia mesenchymal stem cell derived exosome preparation in preparation of an immune cell proliferation inhibitor or a medicine for treating acute myocardial infarction, belongs to the technical field of biology, and solves the problems of low cell survival rate and immunological rejection in application of a cell treatment method in the prior art. The 3D hypoxia mesenchymal stem cell derived exosome is used as a medium for treating acute myocardial infarction, and the problem of immunological rejection can be solved.

The invention discloses a pyranopyridone alkaloid compound as well as a preparation method and application thereof, and belongs to the technical field of medicines. The pyranopyridone alkaloid compound with the activity of resisting the acetaminophen-induced acute liver injury is extracted from a fermentation product of a marine fungus Aspergillus aculeatusWHUF0198, and the pyranopyridone alkaloid compound improves the cell survival rate of mouse hepatocytes treated by acetaminophen and reduces the glutamic-pyruvic transaminase level in a cell supernatant. The pyranopyridone alkaloid compound has the advantages that the pyranopyridone alkaloid compound has the activity of resisting the acetaminophen-induced acute liver injury, and the pyranopyridone alkaloid compound has the activity of resisting the acetaminophen-induced acute liver injury; the pyran pyridone alkaloid compound disclosed by the invention can be used for preparing a medicine for treating acute liver injury. Aiming at the current situation that the types of medicines for treating acute liver injury caused by acetaminophen are deficient at present, the traditional Chinese medicine composition is rich in potential economic benefit.

The invention discloses a preparation method and application of cubilose peptide. The amino acid sequence of the cubilose peptide is KPAPPKPEPK. The cubilose peptide prepared by the invention has strong ultraviolet damage resistance, and can improve the cell survival rate, improve the antioxidant enzyme level in serum, scavenge free radicals and reduce the inflammatory factor level in skin tissues. When the cubilose peptide is used for developing anti-ultraviolet damage products, the efficacy of cubilose can be deeply excavated, and the quality and economic value of cubilose products are improved.

The invention belongs to the technical field of gene transfection, and discloses a transfection enhancement method for improving transient transfection efficiency of plasmids, which comprises the following steps: step 1, plasmid extraction: extracting plasmids by using an endotoxin-removing plasmid extraction kit; 2, preparing cells before transfection; and the cells are recovered and cultured, so that the density of the cells reaches 70-90% during transfection. Step 3, transfection: 1) adding a proper amount of the serum-free culture medium into one centrifugal tube under a sterile condition, then adding a transfection reagent, and fully and uniformly mixing; 2) adding the serum-free culture medium and a reinforcing agent into the other centrifugal tube, fully and uniformly mixing, and then adding plasmids. According to the scheme, the transient transfection efficiency and effect of plasmids are comprehensively improved from plasmid extraction, cell preparation, transfection compound formation to subsequent treatment through a series of optimization steps. Meanwhile, cytotoxicity and stress reaction are reduced, and the cell survival rate and the target protein expression quantity are improved, so that the transfection method becomes an efficient and reliable transfection method.

The invention discloses composite hydrogel and application of the composite hydrogel in preparation of a diabetes wound repair dressing. The gel comprises Metformin (Met) loaded Mg-MOF / Met nano-particles, a hydrogel carrier and a hydrogel carrier, wherein the Mg-MOF / Met nano-particles are prepared from the following components of Mg-MOF / Met nano-particles; the hydrogel network is formed by cross-linking chitosan (CA) modified by arginine and oxidized dextran through a Schiff base reaction; wherein the Mg-MOF / Met nano particles are uniformly dispersed in the hydrogel network, and the Mg-MOF / Met nano particles are uniformly dispersed in the hydrogel network. An animal model verifies that after 14 days, the healing rate reaches 92.1%, the antibacterial rate is larger than 95%, the ROS clearance rate is 85.2%, the cell survival rate is larger than 95%, and remarkable application prospects are shown in the field of diabetes wound repair.

The invention discloses algin with anti-photoaging activity as well as a preparation method and application of the algin, and belongs to the technical field of deep processing of seaweed. The molecular weight of the algin is 10-350kDa, the total sugar content is 40wt%-80wt%, the reducing sugar content is 3wt%-16wt%, and the uronic acid content is 40wt%-80wt%. The preparation method of the algin specifically comprises the following steps: (1) degrading dielectric barrier discharge plasma; and (2) dialyzing and freeze-drying. The algin can significantly improve the inhibition rate of elastase and the cell survival rate of HaCaT cells after ultraviolet irradiation, has significant anti-photoaging activity, and can be used for developing anti-photoaging functional foods and skin care products. Meanwhile, the preparation method adopting the dielectric barrier discharge plasma is simple and convenient to operate, rapid, efficient, green, environment-friendly and free of addition of exogenous chemical substances, and the molecular weight of the algin can be remarkably reduced, so that the additional value of the algin is improved, the application range of the algin is widened, and the algin has a good application prospect.

According to the cell electroporation method and device, an electroporation loading part formed by buckling a first electrode plate and a second electrode plate is arranged, and the number of electrode plates welded to each electrode plate is the same as the number of cell culture pore cavities of a standard cell porous plate; the adjacent first electrode plates and second electrode plates are combined to form a complete positive and negative electrode group, and the positions of the positive and negative electrode groups are in one-to-one correspondence with the cell culture pore cavities, so that a standard cell culture porous plate for bearing a cell suspension can be embedded into the electroporation loading part for direct electroporation without transferring the cell suspension; the non-contact butt joint between the standard cell culture porous plate and the electroporation loading part is realized, the damage of electroporation to cells is smaller, the cell survival rate is improved, a cell porous plate of a special specification does not need to be customized, plug-and-play is realized, the problem that an existing electroporation instrument is not matched with the standard cell culture porous plate is solved, the cost is reduced, the operation process is simplified, and the operation efficiency is improved. And the high-flux electrotransfection is realized.

Provided are a novel high-concentration cell preservation liquid and a high-concentration cell preservation method.　The cell preservation liquid is for preserving cells in a non-frozen state. The cell preservation liquid contains a basal medium and an additive added to the basal medium. The basal medium is a culture medium used for cell culture. The additive contains at least genetically modified albumin and ascorbic acid (ascorbic acid derivative). The cell preservation liquid stores the cells at a cell concentration of at least 1 × 107 cells / mL. For example, when cells are preserved in a cell preservation liquid at 4°C at a cell concentration of 1 × 108 cells / mL, the cell survival rate when 72 hours has elapsed is 80% or more.

The application discloses a kind of live cell dynamic monitoring method, comprising the following steps: obtaining the cell scanning picture group that live cell grown in culture vessel is photographed under specified condition, and the picture is preprocessed;Cell scanning picture group after pre-processing is input into trained cell identification model, and output cell growth state chart group;Cell growth state chart group is input into trained survival rate calculation model, and the survival rate of cell in each cell growth state chart is output;The cell survival rate numerical value obtained is drawn into cell survival rate-time curve chart;The cell survival rate-time curve chart generated is combined with nonlinear regression statistical method, and the half inhibitory concentration value of the efficacy of specified parameter calculation is selected.The growth state of cell under specified condition is monitored, and the survival rate of cell and the half inhibitory concentration value of the efficacy are calculated based on these data;It can significantly improve the efficiency and accuracy in the field of drug research and development, drug screening, treatment scheme effect, etc.

To provide a method for exposing a poorly water-soluble test substance to cultured cells.SOLUTION: Provided is a method for exposing a poorly water-soluble test substance to cultured cells is provided, wherein an emulsified product comprising (A) the poorly water-soluble test substance, (B) polyoxyethylene sorbitan fatty acid ester, and (C) a medium is obtained, and then the emulsified product is exposed to the cultured cells for a predetermined period of time, the method using a cell survival rate of the cultured cells as an indicator to evaluate the presence or absence of cytotoxicity or single-dose toxicity of the poorly water-soluble test substance.SELECTED DRAWING: None

The invention provides 3D printing bio-ink as well as a preparation method and application thereof. The 3D printing bio-ink is prepared from the following components: methacrylic anhydride gelatin, oxidized hyaluronic acid, carboxymethyl chitosan and 2-methacryloyloxyethyl phosphorylcholine. By designing the specific composition of the 3D printing bio-ink, the 3D printing bio-ink which is good in printing performance, mechanical strength and electrical conductivity and high in cell survival rate after printing is prepared, and then a 3D printing stent with high cell-stent interaction is prepared and can be used for preparing a skin injury repair material.

The invention relates to a non-gadolinium magnetic resonance contrast agent and a preparation method thereof, and belongs to the field of contrast agents. The invention aims to provide a non-gadolinium contrast agent with high biological safety aiming at the risks of renal fibrosis and cerebral deposition existing in a gadolinium-based magnetic resonance contrast agent. The invention provides a phosphate group modified non-gadolinium magnetic resonance contrast agent. The phosphate group modified non-gadolinium magnetic resonance contrast agent consists of a ligand of a phosphate group substituted trans-cyclohexanediamine tetraacetic acid derivative (tmPCDTA or tqPCDTA) and metal ions Fe < 3 + > or Mn < 2 + >, the contrast agent disclosed by the invention is high in biological safety: endogenous Fe < 3 + > / Mn < 2 + > is used for replacing gadolinium, and cell experiments prove that the survival rate of 4T1 cells is not influenced at the concentration of 500 mu M; clinical applicability is high, kidney excretion is rapid, bladder signals are enhanced 3-5 minutes after mouse intravenous injection, and liver retention is avoided.

The invention belongs to the technical field of biology, and particularly relates to application of carboplatin in preparation of a medicine for preventing and / or treating negative chain RNA virus infection. Experimental results show that the carboplatin has no obvious influence on the cell survival rate, and the virus titer in the Vero cells treated by the carboplatin is obviously reduced; the replication of PPRV in Vero cells can be significantly inhibited, and the inhibition effect is most significant when the concentration of carboplatin is 100 [mu] M; and the N protein level in Vero cells treated by carboplatin (100 [mu] M) is remarkably reduced, so that the method has a wide application prospect.

The invention provides a method for improving the success rate of single cell culture under external stimulation, belongs to the field of cell culture, and can solve the problem that the contradiction between a Raman spectrum signal and the survival rate can be formed by improving laser energy in the existing single cell culture. The method comprises the following steps: preparing a working solution containing an allogenic material; pretreating an experimental strain by using a culture medium containing the allogenic material to obtain a cell suspension; introducing the cell suspension into chambers of a micro-fluidic chip, and adjusting the cell suspension until each chamber contains at most one cell; in the presence of the allogenic material, culturing the single cell; wherein the allogenic substance is selected from one or more of an antioxidant substance, an anti-radiation substance, an anti-apoptosis substance and a repair promoting substance. According to the method, the exogenous material is added into the culture medium, and the micro-fluidic chip with a plurality of chambers is adopted for single cell culture, so that the survival rate and the clone formation rate of the single cells after Raman sorting can be remarkably improved, meanwhile, the advantage of low background interference is kept, and the survival rate of the single cells is improved.

The invention discloses a degradable outer clip for an absorbable ligature clip, the degradable outer clip comprises an outer clip main body made of Mg-Zn-Ca-Y alloy, the outer side of the outer clip main body is coated with a PLGA (poly (lactic-co-glycolic acid)) coating, and the Mg-Zn-Ca-Y alloy forming the outer clip main body comprises the following components: 0.8-5.0 wt% of Zn, 0.2-1.2 wt% of Ca, 0.6-4.0 wt% of Y and the balance of Mg. The PLGA coating is composed of the following components in parts by weight: 80-90 parts of PLGA, 5-10 parts of calcium carbonate nanoparticles and 5-15 parts of PEG, a solvent is a composite solvent of dichloromethane and acetone, and the concentration of solid components in a coating solution in the solvent is 8-12% w / v. By optimizing the synergistic effect of the Mg-Zn-Ca-Y alloy matrix and the functional PLGA coating, the complete degradation time can be accurately controlled to be about 6 months and is synchronous with blood vessel healing, and premature failure or long-term foreign matter residue is avoided; the bonding strength of the coating is high, the clamping force retention rate exceeds 75% within two weeks, and blood vessel pressure fluctuation is effectively resisted; the biocompatibility is excellent, the cell survival rate is high, and the inflammatory response is obviously reduced.