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氢化阿托酸在大鼠体内时间药代动力学参数的立体选择性
引用本文:何跃生,路红莉,王殿英,何绍雄.氢化阿托酸在大鼠体内时间药代动力学参数的立体选择性[J].药学学报,1993,28(11):817-822.
作者姓名:何跃生  路红莉  王殿英  何绍雄
作者单位:天津医药科学研究所,天津医药科学研究所,天津医药科学研究所,天津医药科学研究所 天津 300070,天津 300070,天津 300070,天津 300070
基金项目:国家自然科学基金,No.3880273
摘    要:研究了氢化阿托酸在大鼠体内的立体选择药代动力学参数,结果表明,在标准明暗周期下,T1/2α和CL具有立体择性,而反相明暗周期下,有立体选择性的药代动力学参数为T1/2β,AUC,CL,Vc和MRT。比较两种明暗周期各相应参数,除极少数几个参数外,都无显著差异。

关 键 词:氢化阿托酸  非甾体抗炎药  立体选择药代动力学参数
收稿时间:1993-02-16

THE STEREOSELECTIVITY OF CHRONO-PHARMACOKINETIC PARAMETERS OF HYDRATROPIC ACID IN RATS
YS He,HL Lu,DY Wang and SX He.THE STEREOSELECTIVITY OF CHRONO-PHARMACOKINETIC PARAMETERS OF HYDRATROPIC ACID IN RATS[J].Acta Pharmaceutica Sinica,1993,28(11):817-822.
Authors:YS He  HL Lu  DY Wang and SX He
Abstract:The stereoselective chrono-pharmacokinetic parameters of hydratropic acid in rats were studied. The results showed that under standard light—dark cycle pharmacokinetic parameters of T1/2α and CL are stereoselective and under reverse light—dark cycle, parameters T1/2β, AUC, CL, Vc and MRT were shown to be stereoselective. To compare the corresponding parameters of the two different light—dark cycles using t—test, no differences were found in most of them.
Keywords:Hydratropic acid  Nonsteroidal antiinflammatory drug  Stereoselective chronopharmacokinetic parameters
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