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.
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.
YS He, HL Lu, DY Wang , SX He, . THE STEREOSELECTIVITY OF CHRONO-PHARMACOKINETIC PARAMETERS OF HYDRATROPIC ACID IN RATSJ. Acta Pharmaceutica Sinica, 1993, 28(11): 817-822.
Citation: YS He, HL Lu, DY Wang , SX He, . THE STEREOSELECTIVITY OF CHRONO-PHARMACOKINETIC PARAMETERS OF HYDRATROPIC ACID IN RATSJ. Acta Pharmaceutica Sinica, 1993, 28(11): 817-822.

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

THE STEREOSELECTIVITY OF CHRONO-PHARMACOKINETIC PARAMETERS OF HYDRATROPIC ACID IN RATS

  • 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。

     

    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.

     

/

返回文章
返回