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采用固相萃取-高效液相色谱法测定雷贝拉唑对映体及其代谢产物。

Determination of rabeprazole enantiomers and their metabolites by high-performance liquid chromatography with solid-phase extraction.

作者信息

Miura Masatomo, Tada Hitoshi, Satoh Shigeru, Habuchi Tomonori, Suzuki Toshio

机构信息

Department of Pharmacy, Akita University Hospital, 1-1-1 Hondo, Akita 010-8543, Japan.

出版信息

J Pharm Biomed Anal. 2006 May 3;41(2):565-70. doi: 10.1016/j.jpba.2005.12.016. Epub 2006 Jan 18.

DOI:10.1016/j.jpba.2005.12.016
PMID:16442771
Abstract

Here, we describe the development of a rapid, simple and sensitive high-performance liquid chromatography (HPLC) method for the simultaneous quantitative determination of rabeprazole enantiomers (1a,b) and their metabolites, rabeprazole-thioether (2) and rabeprazole sulfone (3), in human plasma. Analytes and the internal standard (omeprazole-thioether) were separated using a mobile phase of 0.5 M NaClO4-acetonitrile (6:4, v/v) over a Chiral CD-Ph column. Analysis required only 100 microl of plasma and involved solid-phase extraction with an Oasis HLB cartridge, which gave high recovery (>91.8%) with good selectivity for all analytes. The lower limit of quantification was 5 ng/ml for analytes 1a, 1b and 3 and 10 ng/ml for 2. Linearity of this assay was determined to lie between 5 and 1000 ng/ml for 1a, 1b and 3 and 10 and 1000 ng/ml for 2 (r2>0.982 of the regression line). Inter- and intra-day coefficients of variation were less than 7.8% and accuracies were within 8.4% over the linear range for all analytes. Our results indicate that this method is applicable to the simultaneous monitoring of plasma levels of rabeprazole enantiomers and associated metabolites in human plasma.

摘要

在此,我们描述了一种快速、简便且灵敏的高效液相色谱(HPLC)方法的开发,用于同时定量测定人血浆中雷贝拉唑对映体(1a,b)及其代谢产物雷贝拉唑硫醚(2)和雷贝拉唑砜(3)。使用0.5 M高氯酸钠 - 乙腈(6:4,v/v)的流动相在Chiral CD-Ph柱上分离分析物和内标(奥美拉唑硫醚)。分析仅需100微升血浆,并采用Oasis HLB柱进行固相萃取,所有分析物的回收率均高于91.8%,且具有良好的选择性。分析物1a、1b和3的定量下限为5 ng/ml,2的定量下限为10 ng/ml。该测定法的线性范围为1a、1b和3在5至1000 ng/ml之间,2在10至1000 ng/ml之间(回归线的r2>0.982)。在所有分析物的线性范围内,日内和日间变异系数均小于7.8%,准确度在8.4%以内。我们的结果表明,该方法适用于同时监测人血浆中雷贝拉唑对映体及其相关代谢产物的血浆水平。

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