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[黄芩苷吸收性药物芩百清肺浓缩丸药物配伍的药代动力学比较]

[Pharmacokinetic comparison of baicalin absorption medicine Qinbai Qingfei concentrated pellets drug compatibility].

作者信息

Li Hai-Long, Feng Wen-Cheng, Yao Lin, Sun Yan, Song Ya-Juan, Hu Hao, Wang Wei-Ming

出版信息

Zhongguo Zhong Yao Za Zhi. 2014 May;39(10):1933-6.

PMID:25282909
Abstract

The Qinbai Qingfei concentrated pellets by traditional Chinese medicine theoryand party and group, the rats were given the drugs group, comparison of pharmacokinetics parameters changes of baicalin , discusses the rationality of Qinbai prescription. The rats were gavaged monarch drug group (Huang Qincu extract, mainly forbaicalin), and official medicine group, adjuvant group, medicine group and Qinbai group (Quan Fangzu) the content of baicalin equal as the monarch drug group, in the 28 h collection in rat plasma at different time point, application of HPLC determination of baicalin glycosides in rat plasmaconcentration time curve, with 3P97 practical pharmacokinetics program to process the data Based on the data analysis, baicalin in rat plasma of Qinbai group Cmax is 4 times as big as monarch druggroup, AUC is 6 times as big as monarch drug group; the content of baicalin in plasma of rats the highest is Qinbai group, the minister drug group, adjuvant group, medicine group of baicalin in rat plasma content of less than the Qinbai group, but was significantly higher than that of monarch drug group; the medicine group is slightly higher than that adjuvant the content of baicalin in plasma of rats. The pharmacokinetic results show that the measured plasma concentration in rats that Qinbai can significantly increase Cmax and AUC of baicalin, other components of qinbai can promoted the baicalin absorption in vivo. It showed that the reasonable of Qinbai compound compatibility. The minister drug can promote the absorption of baicalin in vivo.

摘要

按照中医理论和方剂配伍制备芩百清肺浓缩丸,将大鼠分为给药组,比较黄芩苷药代动力学参数变化,探讨芩百方剂的合理性。对大鼠灌胃君药组(黄芩粗提物,主要成分为黄芩苷)、臣药组、佐药组、使药组及芩百组(全方组),使各给药组黄芩苷含量与君药组相等,于28 h内不同时间点采集大鼠血浆,应用高效液相色谱法测定大鼠血浆中黄芩苷的浓度-时间曲线,用3P97实用药代动力学程序处理数据。数据分析结果显示,芩百组大鼠血浆中黄芩苷的Cmax为君药组的4倍,AUC为君药组的6倍;大鼠血浆中黄芩苷含量最高的是芩百组,臣药组、佐药组、使药组大鼠血浆中黄芩苷含量低于芩百组,但显著高于君药组;使药组大鼠血浆中黄芩苷含量略高于佐药组。药代动力学结果表明,测定大鼠血浆浓度显示芩百能显著提高黄芩苷的Cmax和AUC,芩百其他成分可促进黄芩苷在体内的吸收。这表明芩百复方配伍合理,臣药可促进黄芩苷在体内的吸收。

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