Hydrophilic interaction liquid chromatography-tandem mass spectrometry for the determination of levosulpiride in human plasma

被引:52
作者
Paek, IB
Moon, Y
Ji, HY
Kim, HH
Lee, HW
Lee, YB
Lee, HS [1 ]
机构
[1] Wonkwang Univ, Drug Metab & Bioanal Lab, Coll Pharm, Iksan 570749, South Korea
[2] Wonkwang Univ, Phytofermentat Res Ctr, Iksan 570749, South Korea
[3] Chonnam Natl Univ, Coll Pharm, Kwangju 500757, South Korea
[4] Chonnam Natl Univ, Inst Bioequivalence & Bridging Study, Kwangju 500757, South Korea
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 809卷 / 02期
关键词
levosulpiride;
D O I
10.1016/j.jchromb.2004.07.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid, sensitive and selective hydrophilic interaction liquid chromatography-tandem mass spectrometric (HILIC-MS/MS) method for the determination of levosulpiride in human plasma was developed. Levosulpiride and internal standard, tiapride were extracted from human plasma with ethyl acetate at pH 11 and analyzed on an Atlantis HILIC silica column with the mobile phase of acetonitrile-ammonium formate (190 mM, pH 3.0) (94:6, v/v). The analytes were detected using an electrospray ionization tandem mass spectrometry in the multiple-reactionmonitoring mode. The standard curve was linear (r = 0.999) over the concentration range of 1.00-200 ng/ml. The lower limit of quantification for levosulpiride was 1.00 ng/ml using 100 mul plasma sample. The coefficient of variation and relative error for intra- and inter-assay at three quality control (QC) levels were 3.8-9.1 and -2.9 to -0.1%, respectively. The recoveries of levosulpiride ranged from 80.5 to 87.4%, with that of tiapride (internal standard) being 84.6%. This method was successfully applied to the pharmacokinetic study of levosulpiride in humans. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:345 / 350
页数:6
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