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作 者:赵仲[1] 孟乐乐[2] 陈霓祥[2] 胡振华[2] 陈思源[2] 王薪懿[1] 林清[2] 苏靖[1]
机构地区:[1]上海交通大学,上海200240 [2]上海交通大学医学院附属新华医院,上海200092
出 处:《现代生物医学进展》2011年第24期4801-4803,共3页Progress in Modern Biomedicine
基 金:上海交通大学医工结合基金(YG2010MS11);国家自然科学基金(81001416)
摘 要:目的:研究装载于不同分子量的PLGA中的5-氟尿嘧啶微球的制备方法及其在体外条件下的缓释行为。方法:以水包油包固复乳法将5-氟尿嘧啶包裹在高分子聚乳酸-聚羟基乙酸共聚物(PLGA)中,形成缓释微球,考察其大小,外观,包封率等理化性质,以紫外分光光度法为检测方法研究其体外释放行为。结果:经扫描电子显微镜观察,所制备的微球形态完整,大小较均匀。具有一定得包封率和载药量,体外释放研究表明其处方1和处方2的缓释时间为8天和23天。结论:以水包油包固复乳法制备的PLGA 5-氟尿嘧啶微球能够达到缓释的目的。Objective: To investigate the preparation method and in vitro release behavior of 5-Fluorouracil loaded in sustained-re-lease microspheres prepared by PLGA of different molecular weight.Methods: 5-Fluorouracil was microencapsulated into PLGA micro-spheres by solid-in-oil-in-water(S/O/W) multiple emulsion technique,then the sustained-release microspheres were obtained.The physical and chemical properties of the microspheres such as the particle size,appearance and encapsulation efficiency were detected.The micro-spheres' in vitro release behaviors were detected by the way of UV spectrophotometry.Results: The microspheres had complete shape,uniform particle size.They had certain encapsulation efficiency and loading capacity.The research of in vitro release showed that the formulation1 and formulation 2 can release 5-Fu 8 days and 23 days respectively.Conclusion: The microspheres prepared by the way of solid-in-oil-in-water(S/O/W) multiple emulsion technique can reach the target of sustained-release of 5-Fu.
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