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Treatments of paclitaxel with poly(vinyl pyrrolidone) to improve drug release from poly(ε-caprolactone) matrix for film-based stent

机译:聚乙烯吡咯烷酮对紫杉醇的处理,以改善薄膜支架的药物从聚ε-己内酯基质中的释放

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摘要

Drug-loaded biodegradable films as a principal part of film-based stent were investigated for controlled drug delivery systems. In this study, solid dispersion technique, a pretreatment method of paclitaxel (PTX), was applied to prepare the PTX-loaded poly(ε-caprolactone) (PCL) films. Drug dissolution rates and characteristics of the poly(vinyl pyrrolidone) (PVP)/PTX solid dispersions (SDs) and physical mixtures (PMs) were investigated to show that the PVP/PTX SDs were successfully prepared before being incorporated in biodegradable films. Afterwards, the effect of the application of SDs on improving drug release behavior, weightlessness, crystalline states, and surface and internal morphologies of the films were studied. It was found that, the films with SDs showed a higher drug release rate than the films with PMs or pure PTX. In addition, the content of PVP in the SDs also had impact on drug release behavior: the more PVP in SDs, the faster the drug was released. According to the drug release test and weightlessness study, the possible drug release mechanism was put forward for the films with SDs. The application of solid dispersion technique showed a remarkable effect on improving drug release behavior for film-based biodegradable stent drug delivery systems.
机译:研究了载药生物可降解膜作为基于膜的支架的主要部分,用于可控药物输送系统。在这项研究中,固体分散技术是紫杉醇(PTX)的预处理方法,用于制备负载PTX的聚(ε-己内酯)(PCL)薄膜。研究了聚乙烯吡咯烷酮(PVP)/ PTX固体分散体(SDs)和物理混合物(PMs)的药物溶出速率和特性,表明在将PVP / PTX SD掺入可生物降解薄膜之前已成功制备了该产品。随后,研究了SDs的应用对改善药物释放行为,失重,结晶态以及薄膜表面和内部形态的影响。发现具有SDs的膜比具有PMs或纯PTX的膜显示更高的药物释放速率。此外,SD中PVP的含量也对药物释放行为产生影响:SD中PVP越多,药物释放速度越快。根据药物释放试验和失重研究,提出了具有SDs的薄膜可能的药物释放机理。固体分散技术的应用在改善基于膜的生物可降解支架药物递送系统的药物释放行为方面显示出显着效果。

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