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柔红霉素聚氰基丙烯酸正丁酯毫微粒体外释药规律研究 被引量:4

The in vitro Release Kinetics of Daunorubicin Polybutylcyanoacrylate Nanoparticles
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摘要 作者用动态膜透析法考察了柔红霉素聚氰基丙烯酸正丁酯毫微粒冻干针剂体外释药规律,并用6种数学模型对释药过程进行拟合,以残差平方和、拟合度、AIC等参数为指标,评价了各数学模型的拟合优度。结果表明双指数函数模型能较好地描述毫微粒中柔红霉素的释药规律。 The in vitro release kinetics of Daunorubicin Polybutylcyanoacrylate Nanoparticles(DNRPBCANP) was studied by dynamic dialysis system. The concentration of Daunorubicin was determined by spectrophotometry. The result showed the in vitro release kinetics of DNRPBCANP could be well characterized by a biexponential equation. There were two phases in the process of drug release. The initial phase was a fast release phase (the burst effect).The second phase was a slow release phase.
出处 《华西医科大学学报》 CAS CSCD 1999年第2期168-170,184,共4页 Journal of West China University of Medical Sciences
关键词 柔红霉素 正丁酯 毫微粒 体外释药 DNR-PBCA-NP DaunorubicinPolybutylcyanoacrylate nanoparticlesDrug release in vitroBiexponential equation
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参考文献1

  • 1奚念朱,药物动力学,1990年,109页

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