Medicament coating material and preparation method
A drug coating and drug technology, applied in coating, medical science, prosthesis, etc., can solve the problem of inhibition of vascular re-endothelialization process, and achieve the effect of protecting vascular endothelial cells, increasing drug concentration, and inhibiting cholesterol synthesis.
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Embodiment 1
[0030] The drug is ferulic acid, and the drug carrier is a copolymer of hydroxybutyrate and hydroxycaproate (molecular weight: 200000; the molar percentage of hydroxycaproate is 12%), and the weight ratio is 1:20.
[0031] In this embodiment, the specific steps of the preparation method of the drug coating material are as follows:
[0032] (1) dissolving the drug and the drug carrier in ethyl acetate, and after being ultrasonically and uniformly dissolved, a drug coating material solution is obtained, and the concentration of the drug coating material solution is 5wt%;
[0033] (2) The drug coating material is prepared by solution casting method. The uniformly dissolved drug coating material solution is poured into a glass vessel, and the solvent is evaporated under vacuum at 25°C for 24 hours to form a film, and then heated to 35°C. Thoroughly evaporate the solvent for 48 hours, and then use it after sterilization.
Embodiment 2
[0035] The drug is ferulic acid, and the drug carrier is a copolymer of hydroxybutyrate and hydroxycaproate (molecular weight: 200000; the molar percentage of hydroxycaproate is 12%), and the weight ratio is 1:10.
[0036] In this embodiment, the specific steps of the preparation method of the drug coating material are as follows:
[0037] (1) dissolving the drug and the drug carrier in ethyl acetate, and after being ultrasonically and uniformly dissolved, a drug coating material solution is obtained, and the concentration of the drug coating material solution is 10wt%;
[0038] (2) The drug coating material is prepared by solution casting method. The uniformly dissolved drug coating material solution is poured into a glass vessel, and the solvent is evaporated under vacuum at 25°C for 24 hours to form a film, and then heated to 35°C. Thoroughly evaporate the solvent for 48 hours, and then use it after sterilization.
Embodiment 3
[0040] According to Example 1, the drug-loaded coating was prepared for in vitro platelet adhesion test. like figure 1 As shown, the test results prove that the number of adhered platelets on the surface of the drug-loaded coating and the non-medicated coating is relatively small after 0.5 hours of contact with plasma. After 3 hours of contact with plasma, the number of surface-attached platelets increased. However, compared with the non-drug-loaded coating, the number of platelets adhered to the surface of the drug-loaded coating and the degree of platelet aggregation and deformation are smaller, indicating that the drug-loaded coating can effectively inhibit the adhesion of platelets on the coating. and activate.
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