淫羊藿次苷Ⅰ在大鼠体内的药动学和组织分布研究

刘子琛;徐英;陈世忠

中国药学杂志 ›› 2008, Vol. 43 ›› Issue (11) : 848-851.

中国药学杂志 ›› 2008, Vol. 43 ›› Issue (11) : 848-851.
论著

淫羊藿次苷Ⅰ在大鼠体内的药动学和组织分布研究

  • 刘子琛;徐英;陈世忠
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Study on Pharmacokinetics and Tissue Distribution of IcarisideⅠ in Rats by HPLC-UV Assay

  • LIU Zi-chen,XU Ying,CHEN Shi-zhong
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摘要

目的研究淫羊藿次苷Ⅰ在血液和各组织中的HPLC检测方法及在大鼠体内的药动学和组织分布。方法采用Dikma-C18色谱柱(4.6mm×250mm,5μm),流动相甲醇-0.2%磷酸(73:27),流速1.0mL·min-1,检测波长270nm,柱温20℃。大鼠按淫羊藿次苷Ⅰ单剂量10mg·kg-1尾静脉注射后,采用高效液相色谱法测定给药后不同时间的淫羊藿次苷Ⅰ血药浓度和各组织浓度,用3P97程序计算药动学参数。结果淫羊藿次苷Ⅰ的血药浓度-时间曲线符合二室模型,并在心脏和肌肉组织有一定程度的蓄积。结论此方法简便、准确、稳定,可用于淫羊藿次苷Ⅰ的药动学和组织分布研究。

Abstract

OBJECTIVE To establish a HPLC-UV assay for the determination of icarisideⅠ in blood and tissue samples,and to study its pharmacokinetics and tissue distribution in rats.METHODS IcarisideⅠ was analyzed on a Dikma C18 column with the mobile phase consisting of methnol-0.2% phosphate acid(73∶27) at 1.0 mL·min-1 flow rate and with column temperature at 20 ℃.The wavelength of UV detector was set at 270 nm.A single dose of 10 mg·kg-1 icarisideⅠ was administrated intravascularly in rats.The icariside Ⅰ concentrations in blood and tissues were assayed by HPLC-UV method.The pharmacokinetic parameters of icarisideⅠ were calculated by 3P97 program.RESULTS The concentration-time curve of icarisideⅠ was fitted to a two-compartment model.IcarisideⅠ was remained in heart and muscle in some degree.CONCLUSION The method was convenient,accurate and specific.It was suitable for the study on pharmacokinetis and tissue distribution of icariside Ⅰ.

关键词

淫羊藿次苷 / 淫羊藿 / 高效液相色谱 / 药动学

Key words

icariside / epimedium / HPLC-UV / pharmacokinetics

引用本文

导出引用
刘子琛;徐英;陈世忠. 淫羊藿次苷Ⅰ在大鼠体内的药动学和组织分布研究[J]. 中国药学杂志, 2008, 43(11): 848-851
LIU Zi-chen;XU Ying;CHEN Shi-zhong. Study on Pharmacokinetics and Tissue Distribution of IcarisideⅠ in Rats by HPLC-UV Assay [J]. Chinese Pharmaceutical Journal, 2008, 43(11): 848-851

参考文献

[1] LIU T H,WANG Y,WANG B X,et al. Studies on the metabolism of icariin by intestinal bacteria partⅠ: The transformation of icariin by intestinal flora[J] .Chin Tradit Herb Drugs(中草药),2000,31(11):834-837. [2] QIU F,CHEN Y J,KANO Y,et al. Metabolism of orally administered icariin in rats[J] .Acta Pharm Sin(药学学报),1999,34(3):222-226. [3] LENOBLE R,RICHHEIMER S,BAILEY D T,et al. Compositions comprising icarisideⅠ and anhydroicaritin and methods for making the same:PCT,WO 02/13842 A1[P] .2002-02-21. [4] XIN Z C,YUAN Y M,FU J,et al. Effects of icariin on intracavernosal pressure and systematic arterial blood pressure of rat[J] . Natl Med J Chin(中华医学杂志),2004,84(2):142-145. [5] TIAN L,XIN Z C,LIU W J,et al. Effects of icariin on the erectile function and expression of nitrogen oxide synthase isoforms in corpus cavernosum of arteriogenic erectile dysfunction rat model[J] . Natl Med J Chin(中华医学杂志),2004,84(11):954-957. [6] YE L K,CHEN J M,LIU S H,et al. Pharmacokinetics of icariin in rats[J] .Chin Pharm J(中国药学杂志),1999,34(1):33-36.

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