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黄芩苷固体分散体的研制
引用本文:岳红坤,周冉,王景翔,马珊珊.黄芩苷固体分散体的研制[J].井冈山大学学报(自然科学版),2013(2):89-93.
作者姓名:岳红坤  周冉  王景翔  马珊珊
作者单位:石家庄学院化工学院,河北石家庄050035
摘    要:目的研制黄芩苷固体分散体,并对其进行考察。方法以PEG6000为载体,用溶剂法、熔融法、溶剂.熔融法、研磨法制备黄芩苷固体分散体,并通过紫外、红外、溶解度、溶出度的考察比较不同药物与载体的比例对固体分散体的影响。结果溶剂法即共沉淀法,药物与PEG6000的比例为1:8时的固体分散体最优。结论制备方法和药物与载体的比例都会影响黄芩苷-PEG6000固体分散体的质量。

关 键 词:黄芩苷  固体分散体  溶出度  溶剂法

RESEARCH ON BAICALIN SOLID DISPERSION
YUE Hong-kun,ZHOU Ran,WANG Jing-xiang,MA Shan-shan.RESEARCH ON BAICALIN SOLID DISPERSION[J].Journal of Jinggangshan University(Natural Sciences Edition),2013(2):89-93.
Authors:YUE Hong-kun  ZHOU Ran  WANG Jing-xiang  MA Shan-shan
Institution:(College of Cheminal Technology, Shijiazhuang University, Shijiazhuang, Hebei 050035, China)
Abstract:Objective : To prepare and investigate baicalin solid dispersion. Methods: Using PEG6000 as cartier, baicalin solid dispersion was prepared by solvent, melting, solvent-melting, grinding methods. The influence on solid dispersion of different proportion was studied by UV, IR, solubility and dissolution rate. Results: The solid dispersions of solvent method and the ratio of the drug and PEG6000 1:8 is the best. Conclusion: The quality of solid dispersion was affected by the preparation method and the ratio.
Keywords:baicalin  solid dispersion  dissolution rate  solvent method
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