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多成分药物序贯代谢方法用于川芎水煎液多成分不同阶段吸收代谢研究
引用本文:刘洋,罗志强,吕贝然,赵海誉,董玲. 多成分药物序贯代谢方法用于川芎水煎液多成分不同阶段吸收代谢研究[J]. 中国中药杂志, 2016, 41(7): 1178-1182
作者姓名:刘洋  罗志强  吕贝然  赵海誉  董玲
作者单位:北京中医药大学, 北京 100102,北京中医药大学, 北京 100102,北京中医药大学, 北京 100102,中国中医科学院 中药研究所, 北京 100700,北京中医药大学, 北京 100102
基金项目:国家自然科学基金项目(81473362);北京中医药大学在读研究生项目(2015-JYB-XS061)
摘    要:中药作为多成分药物,其代谢与吸收相关性问题,可以通过序贯代谢方法开展,并为生物药剂学分类系统中决定吸收的肠渗透性成分选择提供遴选依据。该研究以川芎为研究载体,采用在体封闭肠环的实验方法,并且结合液质联用技术对川芎水煎液中的多成分口服给药吸收和序贯代谢过程进行了研究。结果在川芎水煎液中鉴别了14个主要成分,其中阿魏酸,洋川芎内酯F,G,I,J,3-羟基丁基苯肽6个成分以原型吸收入血,可作为中药生物药剂学分类系统中首选肠渗透性评价成分。正丁基苯酞,E-藁本内酯,Z-藁本内酯,新蛇床内酯,洋川芎内酯A,Q,在所有样品中均不存在,说明这6个成分不吸收或者在进入肝门静脉血前已经被代谢;洋川芎内酯H会被肝代谢;洋川芎内酯M会被肠道菌和肝代谢。通过这一研究,川芎水煎液多成分口服给药吸收代谢变化得以清晰展示出来,从而将静态的吸收入血成分转变为动态地、连续地、整体地多成分吸收代谢过程。

关 键 词:多成分药物  药物代谢  序贯代谢  整体吸收  液质联用
收稿时间:2015-12-18

Absorption and metabolism of Chuanxiong Rhizoma decoction with multi-component sequential metabolism method
LIU Yang,LUO Zhi-qiang,LV Bei-ran,ZHAO Hai-yu and DONG Ling. Absorption and metabolism of Chuanxiong Rhizoma decoction with multi-component sequential metabolism method[J]. China Journal of Chinese Materia Medica, 2016, 41(7): 1178-1182
Authors:LIU Yang  LUO Zhi-qiang  LV Bei-ran  ZHAO Hai-yu  DONG Ling
Affiliation:Beijing University of Chinese Medicine, Beijing 100102, China,Beijing University of Chinese Medicine, Beijing 100102, China,Beijing University of Chinese Medicine, Beijing 100102, China,Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China and Beijing University of Chinese Medicine, Beijing 100102, China
Abstract:The multiple components in Chinese herbal medicines (CHMS) will experience complex absorption and metabolism before entering the blood system. Previous studies often lay emphasis on the components in blood. However, the dynamic and sequential absorption and metabolism process following multi-component oral administration has not been studied. In this study, the in situ closed-loop method combined with LC-MS techniques were employed to study the sequential process of Chuanxiong Rhizoma decoction (RCD). A total of 14 major components were identified in RCD. Among them, ferulic acid, senkyunolide J, senkyunolide I, senkyunolide F, senkyunolide G, and butylidenephthalide were detected in all of the samples, indicating that the six components could be absorbed into blood in prototype. Butylphthalide, E-ligustilide, Z-ligustilide, cnidilide, senkyunolide A and senkyunolide Q were not detected in all the samples, suggesting that the six components may not be absorbed or metabolized before entering the hepatic portal vein. Senkyunolide H could be metabolized by the liver, while senkyunolide M could be metabolized by both liver and intestinal flora. This study clearly demonstrated the changes in the absorption and metabolism process following multi-component oral administration of RCD, so as to convert the static multi-component absorption process into a comprehensive dynamic and continuous absorption and metabolism process.
Keywords:multi-component drug  drug metabolism  sequential metablism  integral absorption  LC-MS
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