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采用温度诱导法在支架上对雷帕霉素进行表面结晶。

Surface crystallization of rapamycin on stents using a temperature induced process.

机构信息

School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Israel, 91120.

出版信息

Langmuir. 2012 Apr 17;28(15):6207-10. doi: 10.1021/la300364y. Epub 2012 Apr 2.

Abstract

Metallic drug eluting stents (DES) are usually prepared by coating with a drug-polymer matrix as a rate controlling diffusion barrier. However, coating materials may display numerous problems, thus carrier-free DES are desired, yet releasing drug over long period of time. For this, we are reporting a novel temperature induced (TI) crystallization process for coating rapamycin on stents. Rapamycin crystals with a defined morphology and target drug load were applied from supersaturated solution. This method enables fabrication of controllable and homogeneous crystalline coatings on stent scaffolds and allowing the drug to release for several weeks.

摘要

金属药物洗脱支架(DES)通常通过涂覆药物-聚合物基质作为控释扩散屏障来制备。然而,涂层材料可能会显示出许多问题,因此需要无载体的 DES,并且需要长时间释放药物。为此,我们报告了一种新的温度诱导(TI)结晶工艺,用于在支架上涂覆雷帕霉素。从过饱和溶液中应用了具有明确定型形态和目标药物负载的雷帕霉素晶体。该方法能够在支架支架上制造可控且均匀的结晶涂层,并允许药物释放数周。

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