Iron-base alloy implanted medical device and manufacturing method thereof
A technology for implanting medical devices and iron-based alloys, which is applied in medical formulas, medical preparations containing active ingredients, medical science, etc., and can solve problems such as limited therapeutic effects and side effects of drugs
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Embodiment 1
[0030] Using ethyl acetate as the solvent, the polylactic acid-glycolic acid with a weight average molecular weight of 100,000 and paclitaxel were mixed and dissolved in ethyl acetate at a mass ratio of 3:1, and the solution was coated on the surface of the pure iron stent to form a drug carrier Coating, the thickness of the drug-loaded coating is 15μm, the pore size is 0.2μm, and the amount of paclitaxel on the stent substrate area is 200μg / cm 2 . The prepared drug-loaded stents were implanted into the abdominal aorta of rabbits, and samples were taken at 1 day, 7 days, 14 days, and 28 days. The test showed that the drug release percentages on the stent were 20%, 40%, 50%, and 65%, respectively. The experimental results show that the stent drug-loaded coating prepared in this example has a controllable drug release performance.
Embodiment 2
[0032] Dissolve polysuccinate and rapamycin with a weight average molecular weight of 200,000 in a chloroform solution in a ratio of 4:1, and spray on the surface of the stent to form a polysuccinate-rapamycin drug carrier Coating, the thickness of the coating is about 5μm, the pore diameter is less than 0.1μm, and the amount of rapamycin on the stent substrate area is 50μg / cm 2 ; Then the chloroform solution with a molecular weight of 60,000 polysuccinate is coated on the surface of the drug-carrying coating of the iron-zinc alloy stent substrate, as the top layer, with a thickness of 10 μm and a pore diameter of less than 0.1 μm. The prepared drug-loaded stent was implanted into the abdominal aorta of rabbits, and samples were taken at 1, 7, 14, and 28 days. The test results showed that the drug release percentages were 15%, 35%, 50%, and 65%, respectively. The experimental results showed The stent drug-loaded coating prepared in this embodiment has a controllable drug release...
Embodiment 3
[0034] Using acetone as the solvent, dissolve polyracemic lactic acid with a weight average molecular weight of 300,000, polyglycolic acid and dexamethasone in a mass ratio of 1:1:1, and coat the solution on the nitriding iron with a cavity A drug-loaded coating is formed in the cavity of the base alloy stent. The thickness of the drug-loaded coating is 25μm, the pore diameter is 2μm, and the amount of active drug on the stent substrate area is 300μg / cm 2 . The prepared drug-loaded stent was implanted into the rabbit's abdominal aorta, and samples were taken at 1, 7, 14, and 28 days. The test results showed that the drug release percentages were 40%, 50%, 60%, and 80%. The experimental results showed The stent drug-loaded coating prepared in this embodiment has a controllable drug release performance.
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