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Drug sustained release magnesium alloy stent and preparation method thereof

A magnesium alloy stent and drug technology, applied in the field of medical devices, can solve the problems of unfavorable large-scale production, affecting the treatment effect, and negative effects on the human body, and achieve the effects of high market promotion value, increased service time, and easy preparation

Inactive Publication Date: 2015-07-08
日照天一生物医疗科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, in the existing protective measures, substances harmful to the human body are usually introduced into the magnesium alloy stent, which will have a negative effect on the human body and affect the therapeutic effect; or there are many process steps, which is not conducive to large-scale production

Method used

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  • Drug sustained release magnesium alloy stent and preparation method thereof

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preparation example Construction

[0040] In addition, the present invention also provides a method for preparing a drug sustained-release magnesium alloy stent, which can be used to prepare the above-mentioned drug sustained-release magnesium alloy stent, comprising the following steps:

[0041] S100: The base of the laser-engraved magnesium alloy stent is dried 100°, polished, washed with water, then dipped in the first coating for 0.25-5 minutes, taken out and then dried and cured to obtain a magnesium alloy stent covered with the first coating. The first coating comprises silane coupling agent KH550, dehydrated alcohol and the first solvent, wherein, the first solvent is water, and the volume ratio of silane coupling agent KH550, dehydrated alcohol and water is 2~5:90~95: 3~6.

[0042] In the present invention, there are many ways to polish the magnesium alloy stent backbone 100, and electrochemical polishing is preferred.

[0043] In this step, the first coating 210 (ie, the coating of silane coupling age...

Embodiment 1

[0057] (1) Polish the base of the laser-engraved ZK60 magnesium alloy stent, wash it with water after polishing, then place it in the first coating and dip it for 0.25min, dry it at room temperature, put it in a drying oven, and sinter it at 120°C for 15min to obtain a surface coated with The magnesium alloy stent of the first coating; wherein, the volume ratio of each component in the first coating is: silane coupling agent KH550: absolute ethanol: water = 2:94:4, and the thickness of the first coating is 200nm;

[0058] (2) The surface of the magnesium alloy stent obtained in step (1) is ultrasonically sprayed with the second coating, then placed in a vacuum drying oven, dried in vacuum at 30°C for 12 hours, then heated to 80°C, and kept for 60 minutes to obtain a surface covered with the second coating. A coated magnesium alloy stent; wherein the second coating is composed of rapamycin, DL-PLCL and chloroform, and the sum of the mass of rapamycin and DL-PLCL is 0.5% of the t...

Embodiment 2

[0061] (1) Polish the base of the AE21 magnesium alloy stent that has been laser-engraved, wash it with water, then place it in the first coating for 2 minutes, dry it at room temperature, put it in a drying oven, and sinter it at 80°C for 60 minutes to obtain the surface coated with the first coating. A coated magnesium alloy stent; wherein, the volume ratio of each component in the first coating is: silane coupling agent KH550: absolute ethanol: water = 5:90:5, and the thickness of the first coating is 1 μm;

[0062](2) The surface of the magnesium alloy stent obtained in step (1) is ultrasonically sprayed with the second coating, then placed in a vacuum drying oven, dried in vacuum at 10°C for 24 hours, then heated to 50°C, and kept for 120min to obtain a surface covered with the second coating. A coated magnesium alloy stent; wherein the second coating is composed of paclitaxel, DL-PLCL and dichloromethane, and the sum of the mass of paclitaxel and DL-PLCL is 2% of the tota...

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Abstract

The invention discloses a drug sustained release magnesium alloy stent and a preparation method thereof. The drug sustained release magnesium alloy stent comprises a magnesium alloy stent backbone and composite coatings, and the composite coatings comprise a first coating covering the surface of the magnesium alloy stent backbone, a second coating covering the surface of the first coating and a third coating covering the surface of the second coating; the first coating is a silane coupling agent KH550 coating, the second coating is a DL-PLCL medicine carrying layer, and the third coating is a medicine carrying layer formed by at least one of PLGA and PLLA. According to the drug sustained release magnesium alloy stent and the preparation method thereof, the composite coatings can effectively separate the magnesium alloy stent backbone from an outside corrosive medium and can effectively increase the supporting time of the magnesium alloy stent in the body, the composite coatings are degradable coatings, and degradation products are harmless to a human body.

Description

technical field [0001] The invention relates to the technical field of medical devices, in particular to a drug slow-release magnesium alloy stent and a preparation method thereof. Background technique [0002] With the development of modern medical technology and the improvement of medical equipment, interventional stent therapy has become a major means of interventional cardiovascular therapy. However, the current clinical cardiovascular stents are still mainly made of non-degradable metal materials, such as stainless steel, cobalt-chromium alloy, etc. These metal stents are biologically inert, and they exist in the body for a long time after implantation, which may cause thrombosis For this reason, patients need to take anticoagulant drugs for a long time. [0003] Magnesium alloy stent, as a degradable stent, has gradually become a development trend and research hotspot of vascular stent. However, the corrosion and degradation rate of magnesium alloy stents in the bloo...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61F2/07A61L31/10A61L31/16A61L31/14
Inventor 郭高东吕树铮杨柯葛长江张炳春罗兆坤
Owner 日照天一生物医疗科技有限公司