A liquid chromatography/tandem mass spectrometry method for the simultaneous quantification of valsartan and hydrochlorothiazide in human plasma

被引:74
作者
Li, Hao
Wang, Yingwu
Jiang, Yao
Tang, Yunbiao
Wang, Jiang
Zhao, Limei
Gu, Jingkai [1 ]
机构
[1] Jilin Univ, Coll Life Sci, Res Ctr Drug Metab, Changchun 130021, Peoples R China
[2] Chinese Med Univ, Clin Hosp 2, Shenyang 110004, Peoples R China
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 852卷 / 1-2期
关键词
valsartan; hydrochlorothiazide; LC/MS/MS; pharmacokinetics;
D O I
10.1016/j.jchromb.2007.02.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC/MS/MS) method was developed and validated for simultaneous quantification of valsartan and hydrochlorothiazide in human plasma. After a simple protein precipitation using acetonitrile, the analytes were separated on a Zorbax SB-Aq C18 column using acetonitrile -10 mM ammonium acetate (60:40, v/v, pH 4.5) as mobile phase at a flow rate of 1.2 mL/min. Valsartan and hydrochlorothiazide were eluted at 2.08 min and 1.50 min, respectively, ionized using ESI source, and then detected by multiple reaction monitoring (MRM) mode. The precursor to product ion transitions of m/z 434.2-350.2 and m/z 295.9-268.9 were used to quantify valsartan and hydrochlorothiazide, respectively. The method was linear in the concentration range of 4-3600 ng/mL for valsartan and 1-900 ng/mL for hydrochlorothiazide. The method was successfully employed in a pharmacokinetic study after an oral administration of a dispersible tablet containing 80 mg valsartan and 12.5 mg hydrochlorothiazide to each of the 20 healthy volunteers. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:436 / 442
页数:7
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