首页> 外文期刊>Journal of Applied Polymer Science >Comparison of the degradation and release behaviors of poly(lactide-co-glycolide)-methoxypoly(ethylene glycol) microspheres prepared with single- and double-emulsion evaporation methods
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Comparison of the degradation and release behaviors of poly(lactide-co-glycolide)-methoxypoly(ethylene glycol) microspheres prepared with single- and double-emulsion evaporation methods

机译:单乳液和双乳液蒸发法制备的聚(丙交酯-共-乙交酯)-甲氧基聚(乙二醇)微球的降解和释放行为比较

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The purpose of this study was to compare the degradation and release behaviors of poly(lactide-co-glycolide) (PLGA)-methoxypoly(ethylene glycol) microspheres fabricated by the single-emulsion evaporation method (DEEM) and double-emulsion evaporation methods (DEEM). Vancomycin and mizolastine were used as the hydrophilic and hydrophobic model drugs, and they were encapsulated into microspheres through DEEM and SEEM, respectively. The two types of microspheres were similar in size distribution, but the mizolastine-loaded microspheres showed a much higher encapsulation efficiency than those loaded with vancomycin. Scanning electron microscopy, size, and molecular weight (Mw) analyses during the degradation revealed that the microspheres fabricated by DEEM underwent a bulk degradation process and showed a faster MW reduction rate during the early degradation period than the microspheres fabricated by SEEM, which exhibited a surface-to-bulk degradation process according to the Mw and morphological changes. The mass loss rates of the two types of microspheres were similar, but the mean size decrease rates showed a little difference. The mizolastine-loaded microspheres exhibited an approximately linear release profile after the initial burst release, whereas the vancomycin-loaded microspheres showed a more severe burst release, a faster release rate, and thus, a shorter time to full release. (c) 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41943.
机译:这项研究的目的是比较通过单乳液蒸发法(DEEM)和双乳液蒸发法制备的聚(丙交酯-共-乙交酯)(PLGA)-甲氧基聚(乙二醇)微球的降解和释放行为(认为)。万古霉素和咪唑斯汀分别用作亲水性和疏水性模型药物,分别通过DEEM和SEEM封装到微球中。两种类型的微球的尺寸分布相似,但与装有万古霉素的微球相比,负载有咪唑斯汀的微球的包封效率高得多。降解过程中的扫描电子显微镜,尺寸和分子量(Mw)分析表明,DEEM制备的微球经历了整体降解过程,并且在降解早期,其MW还原速率比SEEM制备的微球更快。从表面到整体的降解过程根据Mw和形态变化而定。两种类型的微球的质量损失率相似,但平均尺寸减小率差异不大。最初的突释释放后,负载咪唑斯汀的微球表现出近似线性的释放曲线,而负载万古霉素的微球表现出更严重的突释释放,更快的释放速率,从而缩短了完全释放的时间。 (c)2015 Wiley Periodicals,Inc. J. Appl。 Polym。科学2015,132,41943。

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