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马钱子碱聚乳酸载药纳米粒的制备和体外评价
引用本文:赵继会,刘召林,许洁,于燕燕,冯年平. 马钱子碱聚乳酸载药纳米粒的制备和体外评价[J]. 中国中药杂志, 2009, 34(17): 46-48
作者姓名:赵继会  刘召林  许洁  于燕燕  冯年平
作者单位:上海中医药大学 药剂教研室, 上海 201203
基金项目:上海市博士点基金(2006B02);上海市教委项目(07ZZ53);上海市教委重点学科项目(J50302)
摘    要:目的:制备和评价马钱子碱聚乳酸载药纳米粒(Bru-PLA-NPs)。方法:采用溶剂扩散法制备Bru-PLA-NPs,并对其进行表征和体外释药评价。结果:制得的Bru-PLA-NPs的平均粒径为95 nm,多分散指数为0.362,Zeta电位为-15.68 mV。Bru的平均载药量和包封率分别为7%,37%。体外释药试验表明,与Bru溶液相比Bru-PLA-NPs具有明显的缓释作用。结论:采用溶剂扩散法制备的Bru-PLA-NPs粒径小,载药量高,具有明显的缓释作用。

关 键 词:马钱子碱;聚乳酸纳米粒;体外释放
收稿时间:2009-01-16

Preparation and in vitro evaluation of brucine-loaded Polylacticacid Nanoparticles
ZHAO JiHui,LIU ZhaoLin,XU Jie,YU YanYan and FENG NianPing. Preparation and in vitro evaluation of brucine-loaded Polylacticacid Nanoparticles[J]. China Journal of Chinese Materia Medica, 2009, 34(17): 46-48
Authors:ZHAO JiHui  LIU ZhaoLin  XU Jie  YU YanYan  FENG NianPing
Abstract:Objective: To prepare and evaluate Brucine-loaded polylacticacid nanoparticles (Bru-PLA-NPs). Method: The Bru-PLA-NPs were prepared by solvent diffusion method. The physical, chemical properties and in vitro release behavior of the prepared Bru-PLA-NPs were evaluated, respectively. Result: The mean particle size of the prepared Bru-PLA-NPs is 95 nm with polydispersity index of 0.362. The zeta potential is -15.68 mV. The mean loading and entrapment efficiency of Bru were 7% and 37%, separately. Compared with Bru solution, an obvious sustained release behavior of Bru from Bru-PLA-NPs was observed in the in vitro release experiment. Conclusion: The Bru-PLA-NPs prepared by solvent diffusion method exhibited small particle size, high Bru-loading efficiency, and obvious sustained release in vitro
Keywords:brucine   PLA nanoparticles   in vitro release
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