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环丙沙星聚乳酸微球体外释药性能的研究

Study on the release of ciprofloxacin polylactic acid microspheres in vitro

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【作者】 杨帆韩芸冯穗生金描真张志宏

【Author】 YANG Fan ,HAI Yun ,FENG Shui-sheng ,JIN Miao-zhen ,ZHANG Zhi-hong(1. Dept. of Pharmaceuticals, Guangdong College of Pharmacy, Guangzhou, Guangdong 510224 ;2. Nanhai Pingzhou Hospital)

【机构】 广东药学院药剂学教研室南海平洲医院 广东广州510224广东广州510224广东南海510000

【摘要】 目的:考察环丙沙星聚乳酸微球的体外释药性能。方法:采用体外释放度试验中的浆法测定环丙沙星微球的体外释药情况,并对聚乳酸浓度对微球体外释放度的影响进行了考察。结果:在聚乳酸浓度为10%的情况下,环丙沙星微球的体外释药情况为:53.2 h的累积释药量为84.0%,T1/2为31.9 h,Higuchi方程为Q=-0.0043+0.0039t1/2,r=0.994。结论:环丙沙星聚乳酸微球具有明显的缓释效果。

【Abstract】 Objective :To study the release of ciprofloxacin polylactic acid microspheres in vitro . Metheds: The release of the ciprofloxacin microspheres were examined by paddle method. The relation between the concentration of polylactic acid and the release of ciprofloxacin microspheres was also examined. Results; The accumulated release percentage of the ciprofloxacin microspheres with 10% polylactic acid was 84. 0% after 53. 2 h. The release half - life T1/2 was 31. 9 h and the Higuchi equation was Q = - 0. 0043 + 0. 0039t1/2 , r = 0. 994. Conclusion: The ciprofloxacin polylactic acid microspheres showed significant sustained release effect.

【关键词】 环丙沙星聚乳酸微球体外释药
【Key words】 ciprofloxacinpolylactic acidmicrospheresrelease in vitro
  • 【文献出处】 广东药学院学报 ,Academic Journal of Guangdong College of Pharmacy , 编辑部邮箱 ,2002年04期
  • 【分类号】R94
  • 【被引频次】5
  • 【下载频次】117
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