王齐放, 李三鸣, 张天弘, 于 净, 胡忠盛, 李 岳. 异维A酸与直链淀粉包合物的制备及酶控释放动力学研究J. 药学学报, 2012,47(9): 1227-1230.
引用本文: 王齐放, 李三鸣, 张天弘, 于 净, 胡忠盛, 李 岳. 异维A酸与直链淀粉包合物的制备及酶控释放动力学研究J. 药学学报, 2012,47(9): 1227-1230.
WANG Qi-fang, LI San-ming, ZHANG Tian-hong, YU Jing, HU Zhong-sheng, LI Yue. The preparation and kinetic study on enzymatically-controlled drug release of isotretinoin/amylose inclusion complexJ. 药学学报, 2012,47(9): 1227-1230.
Citation: WANG Qi-fang, LI San-ming, ZHANG Tian-hong, YU Jing, HU Zhong-sheng, LI Yue. The preparation and kinetic study on enzymatically-controlled drug release of isotretinoin/amylose inclusion complexJ. 药学学报, 2012,47(9): 1227-1230.

异维A酸与直链淀粉包合物的制备及酶控释放动力学研究

The preparation and kinetic study on enzymatically-controlled drug release of isotretinoin/amylose inclusion complex

  • 摘要:

    以直链淀粉为包合载体, 采用密封控温包合技术制备异维A酸包合物, 通过粉末X-射线衍射及DSC测试验证包合物的形成。运用动力学原理建立异维A/直链淀粉包合物的酶控释放动力学方程, 通过方程推断在α-淀粉酶作用下药物释放的动力学规律。结果表明, 在无α-淀粉酶存在时, 药物释放符合一级动力学模型; α-淀粉酶存在时, 药物释放是由脱包和酶解共同作用的加速过程。预示异维A/直链淀粉包合物可通过加入α-淀粉酶调控药物的释放。

     

    Abstract:

    The inclusion complex of isotretinoin was prepared by sealed-control temperature method and amylose was used as carrier.  The formation of inclusion complex was confirmed by powder X-ray diffraction and DSC.  The equation of enzymatically-controlled drug release was established by kinetic theory, and the release characteristic of drug was confirmed by using the kinetic equation.  The results show that the drug release was attributed to first order reaction without α-amylase.  However, with α-amylase, the drug release was an acceleration process by the effect of both dissociation and enzymatic hydrolysis simultaneously.  The research indicates that drug release from the inclusion complex was modulated by the addition of a-amylase.

     

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