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生物分配胶束色谱法预测中药制剂消炎利胆片膜通透性的研究
引用本文:侯晓蓉,陈英颖,李成平,宋必卫. 生物分配胶束色谱法预测中药制剂消炎利胆片膜通透性的研究[J]. 药物分析杂志, 2012, 0(6): 1069-1075
作者姓名:侯晓蓉  陈英颖  李成平  宋必卫
作者单位:浙江工业大学药学院;浙江树人大学生物与环境学院
基金项目:浙江省自然科学基金(Y2080137);浙江省科技厅公益计划研究社会发展项目(2011C23006)
摘    要:目的:基于生物分配胶束色谱法进行复杂中药制剂消炎利胆片的分离和膜通透性预测。方法:考察了生物分配胶束色谱的保留因子与药物膜通透性的相关性,以非离子型表面活性剂Brij 35作为流动相,模拟生物体内环境,得到各受试药物的保留因子Log k,与膜通透性参数(口服吸收率、Log Papp、Log BB)数据进行相关分析得出定量保留-膜通透性(QRPR)模型。结果:预测了消炎利胆片10个主要保留成分的透膜吸收情况。结论:生物分配胶束色谱可以用于中药复杂成分的分离,以及预测药物主成分的透膜吸收活性。

关 键 词:生物分配胶束色谱  定量保留-膜通透性模型  消炎利胆片  穿心莲内酯  脱水穿心莲内酯  药物活性分析  透膜吸收

Predicting permeability of Xiaoyanlidan tablets by biopartitioning micellar chromatography
HOU Xiao-rong,CHEN Ying-ying,LI Cheng-ping,SONG Bi-wei. Predicting permeability of Xiaoyanlidan tablets by biopartitioning micellar chromatography[J]. Chinese Journal of Pharmaceutical Analysis, 2012, 0(6): 1069-1075
Authors:HOU Xiao-rong  CHEN Ying-ying  LI Cheng-ping  SONG Bi-wei
Affiliation:1 (1.College of Pharmacy,Zhejiang University of Technology,Hangzhou 310014,China; 2.College of Biology and Environment Engineering,Zhejiang Shuren University,Hangzhou 310015,China)
Abstract:Objective:To separate the complex ingredients in traditional Chinese medicine(TCM) Xiaoyanlidan tablets and estimate the permeability by biopartitioning micellar chromatography(BMC).Methods:The correlation between retention factors in BMC and drug permeability was investigated.Non-ionic Brij35 was used as mobile phase to mimic the in vivo environment,and different concentrations of Brij-35 were studied.The logarithm of capacity factor(Log k) and permeability parameter data(date of oral absorption,Log Papp,Log BB) of test drugs were fitted to model the quantitative retention-permeability relationship(QRPR) models.Results:The permeability of the ten retained components in Xiaoyanlidan tablets were calculated and discussed.Conclusion:The results indicate that BMC can separate the complex components in TCM,as well as predict the membrane absorption activity.
Keywords:biopartitioning micellar chromatography  quantitative retention-permeability relationships models  Xiaoyanlidan tablets  andrographolide  dehydroandrographolide  pharmacological activity analysis  semipermeable membrane absorption
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