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作 者:任甜甜[1] 郑瑞媛[1] 胡振华[1] 蔡云鹏[1] 陈晓静[1] 朱涵蕾[1] 袁伟恩[1]
机构地区:[1]上海交通大学,上海200240
出 处:《现代生物医学进展》2011年第11期2034-2036,共3页Progress in Modern Biomedicine
基 金:国家重大专项-"重大新药创制"科技重大专项-创新药物研究开发技术平台(2009ZX09310-007);上海科委项目(No.0952nm03700和No.1052nm03900);上海交通大学大学生创新项目(IPP2090)
摘 要:目的:由于长期服用左旋多巴治疗帕金森病,其药物浓度波动刺激易引起异动症,本实验旨在制备突释小,药物释放浓度稳定的左旋多巴甲酯微球制剂。方法:将左旋多巴甲酯用复乳法包裹于PLGA微球内,采用C18反相色谱研究药物包封率和体外释放行为。结果:通过调节药物浓度和不同高分子组合筛选出突释小,包封率高且缓慢释放的处方。结论:左旋多巴甲酯包裹于PLGA能实现理想的缓释效果,降低药物浓度波动,为后期药效学实验提供基础。Objective: Chronic administration of levodopa in the treatment of PD leads to debilitated involuntary movements, we aimed to prepare levodopa methyl ester-loaded sustained release microspheres without initial burst. Methods: Levodopa methyl ester (LDME) were microencapsulated into PLGA microspheres by multiple emulsion technique. The encapsulation efficiency and vitro release of microspheres were detected using HPLC system equipped with a C18 reverse column. Results: By adjusting LDME concentration and different polymer combinations, we achieved microspheres with high encapsulation efficiency, low initial burst and sustained release. Conclusions: LDME would achieve sustained release while encapsulated into PLGA microspheres, which provided a basis for later pharmacodynamic study.
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