蒋新国, 王孝俊, 朱芳海, 李正伟, 奚念朱. 海藻酸钠的分子量与缓释作用J. 药学学报, 1994, 29(4): 306-310.
引用本文: 蒋新国, 王孝俊, 朱芳海, 李正伟, 奚念朱. 海藻酸钠的分子量与缓释作用J. 药学学报, 1994, 29(4): 306-310.
XG Jlang.XJ Wang.FH Zhu.ZW Li, NZ Xi, . SODIUM ALGINATE:ITS MOLECULAR WEIGHT AND SUSTAINED RELEASE EFFECTJ. Acta Pharmaceutica Sinica, 1994, 29(4): 306-310.
Citation: XG Jlang.XJ Wang.FH Zhu.ZW Li, NZ Xi, . SODIUM ALGINATE:ITS MOLECULAR WEIGHT AND SUSTAINED RELEASE EFFECTJ. Acta Pharmaceutica Sinica, 1994, 29(4): 306-310.

海藻酸钠的分子量与缓释作用

SODIUM ALGINATE:ITS MOLECULAR WEIGHT AND SUSTAINED RELEASE EFFECT

  • 摘要: 以盐酸普罗帕酮、盐酸地尔硫和硝酸异山梨酯为模型药物,研究它们在不同分子量的海藻酸钠骨架片中的释药规律。结果表明:海藻酸钠的分子量与释药速度间有良好的线性关系。根据这一关系可以预测已知分子量海藻酸钠的释药情况,为海藻酸钠缓释片剂的处方设计及其实际应用提供理论依据。

     

    Abstract: This paper deals With the pattern of release of propafenone hydrochloride(PF),diltiazem hydrochloride(DH)and isosorbide dinitrate(ID)from matrices of sodium alginate(NaAlg)with different molecular weights.The results revealed that the molecular weight of NaAlg wasinversely proportional to the release rate of these drugs.According to the above relationship,therelease rate of drugs from NaAlg with any molecular weight can be predicted,This result mightprovide a theoretical consideration for formulation design of sustained release preparations andespecially for the applieation of NaAlg。

     

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