›› 2011, Vol. 38 ›› Issue (10): 228-231.

• 经验交流 • 上一篇    下一篇

黄体酮聚乳酸微球制备及其体外释药特性研究

高豪1, 方炳虎1, 刘雅红1, 陈朝喜2, 唐咏泳1, 陈建新1   

  1. 1. 华南农业大学兽医学院 广东省兽药研制与安全评价重点实验室,广东广州 510642;2. 西南民族大学生命科学与技术学院,四川成都 610041
  • 收稿日期:1900-01-01 修回日期:2011-04-08 出版日期:2011-10-20 发布日期:2011-10-20
  • 通讯作者: 陈建新

Preparation and in vitro Release Property of Polylactic Acid Microspheres Containing Progesterone

GAO Hao1, FANG Bing-hu1, LIU Ya-hong1, CHEN Chao-xi2, TANG Yong-yong1, CHEN Jian-xin1   

  1. 1. College of Veterinary Medicine, Guangdong Provincial Key Laboratory of Veterinary Pharmaceutics Development and Safety Evaluation, South China Agricultural University, Guangzhou 510642, China;2. Department of Life Science and Technology, Southwest University for Nationalities, Chengdu 610041, China
  • Received:1900-01-01 Revised:2011-04-08 Online:2011-10-20 Published:2011-10-20

摘要: 本试验旨在制备黄体酮聚乳酸微球,并考察其体外释药性能。以包封率、载药量为主要评价指标,考察制备黄体酮微球的主要影响因素,筛选出最佳工艺条件。扫描电子显微镜观察微球形态,紫外—可见分光光度法测定微球的包封率、载药量和体外释药特性。最佳工艺所制备的微球光滑、圆整、均匀、分散性好,包封率为(80.60±1.00)%,载药量为(10.63±0.05)%,在7 d内累积释药率达53.41%。制备微球包封率和载药量高,具有明显的缓释效果,能有效地延长药物作用时间。

关键词: 黄体酮; 聚乳酸微球; 体外释放

Abstract: To prepare progesterone PLA microspheres by emulsification solvent evaporation process and investigate the characteristics of progesterone PLA microspheres in vitro release.Progesterone PLA microspheres formulation and preparation parameters were investigated and established basing on the entrapment efficiency and content of the drug. Seven factors were selected to establish the optimal conditions. The morphology of microspheres was characterized by SEM. UV spectrometry was used to determine the entrapment efficiency, the drug loading and release property in vitro. The progesterone PLA microspheres were smooth, round, well dispersed and consistent diameters. The entrapment efficiency of the progesterone PLA microspheres was (80.60±1.00)%, drug loading was (10.63±0.05)%,cumulative release in 7 days was 53.41% in vitro.The progesterone PLA microspheres had distinct slow-release effect and could prolong the medicine action time.

Key words: progesterone; polylactic acid microspheres; in vitro release

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