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Polyurethane membrane with porous surface for controlled drug release in drug eluting stent

机译:具有多孔表面的聚氨酯膜,用于在药物洗脱支架中控制药物释放

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BackgroundMembrane covered drug eluting stents (DES) were prepared to prevent tumor ingrowth and to control drug release. Polyurethane (PU) is commonly used for DES coating material because of high tensile strength. The release of paclitaxel (PTX) may increase from porous PU membrane. ResultsPolyethylene glycol (PEG) was incorporated into PU membranes to form porous structure and control the release of hydrophobic anti-cancer drug such as PTX. The bare metal stents were coated with PEG incorporated PU and then, PEG was washed out to form porous structure. The crystallization of PTX was inhibited in porous PU membranes and the release of PTX from porous PU membranes was approximately 8.6% more extended over 19?days. ConclusionsThe enhanced release of PTX from porous PU membranes may increase the patency for the DES covering materials.
机译:背景制备了覆盖膜的药物洗脱支架(DES),以防止肿瘤向内生长并控制药物释放。聚氨酯(PU)由于抗张强度高,通常用于DES涂层材料。紫杉醇(PTX)从多孔PU膜的释放可能会增加。结果将聚乙二醇(PEG)掺入PU膜中以形成多孔结构并控制疏水性抗癌药物如PTX的释放。用掺有PEG的PU涂覆裸金属支架,然后将PEG洗出以形成多孔结构。 PTX的结晶在多孔PU膜中受到抑制,PTX从多孔PU膜中的释放持续了19天多了约8.6%。结论PTX从多孔PU膜释放的增强可能会增加DES覆盖材料的通畅性。

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