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马蔺子素脂质体的体外药剂学性质研究

Pharmaceutical characteristics of irisquinone liposomes in vitro

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【作者】 孙锋戴俊东吕万良张?李德华张强

【Author】 SUN Feng, DAI Jun-dong, L(?) Wan-liang, ZHANG Xuan, LI De-hua, ZHANG Qiang(Department of Pharmaceutics, School of Phamaceutical Sciences, Peking University, Beijing 100083, China)

【机构】 北京大学药学院药剂学系北京大学药学院药剂学系 北京 100083北京 100083北京 100083

【摘要】 目的:研究马蔺子素脂质体的体外药剂学性质。方法:采用反相蒸发(REV)法制备马蔺子素脂质体,建立马蔺子素的HPLC含量测定法。检验其各项物理化学性质,考察其稳定性与体外释放。结果:马蔺子素脂质体包封率达到98%以上,粒径在100nm左右,3个月内稳定性良好,体外释放48h不超过30%。结论:所制得的马蔺子素脂质体的物理化学性质优良,稳定性良好,体外释放较缓慢。

【Abstract】 Objective: To characterize the irisquinone liposomes in vitro. Methods: Irisquinone liposomes prepared by the REV technique were quantified by HPLC. The physicochemical characteristics including the stability and drug release in vitro were determined. Results: The encapsulation rate of irisquinone achieved more than 98 percent with the particle size around 100nm. Irisquinone Iiposomes remained stable for 3 months and showed a drug release rate of less than 30% within 48 hours in vitro. Conclusion :The stable irisquinone liposomes have advantages of sustained release.

  • 【文献出处】 中国新药杂志 ,Chinese New Drugs Journal , 编辑部邮箱 ,2005年01期
  • 【分类号】R283;
  • 【被引频次】14
  • 【下载频次】336
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