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手性液相色谱-串联质谱法同时测定人血浆中奥美拉唑、雷贝拉唑、兰索拉唑和泮托拉唑对映体。

Simultaneous enantioselective determination of omeprazole, rabeprazole, lansoprazole, and pantoprazole enantiomers in human plasma by chiral liquid chromatography-tandem mass spectrometry.

机构信息

Research Division of Clinical Pharmacology, First Affiliated Hospital of Nanjing Medical University, Nanjing, P. R. China.

Department of Pharmacy, Nanjing Jinling Hospital, Nanjing, P. R. China.

出版信息

J Sep Sci. 2020 Aug;43(16):3183-3196. doi: 10.1002/jssc.202000226. Epub 2020 Jun 23.

Abstract

Proton pump inhibitors, including omeprazole, rabeprazole, lansoprazole, and pantoprazole, achieved simultaneous enantioselective determination in the human plasma by chiral liquid chromatography-tandem mass spectrometry. The four corresponding stable isotope-labeled proton pump inhibitors were adopted as the internal standards. Each enantiomer and the internal standards were extracted with acetonitrile containing 0.1% ammonia, then separated with a Chiralpak IC column (5 µm, 4.6 mm × 150 mm) within 10 min. The mobile phase was composed of acetonitrile-ammonium acetate (10 mM) containing 0.2% acetic acid (50:50, v/v). To quantify all enantiomers, an API 4000 tandem mass spectrometer was used, and multiple reaction monitoring transitions were performed on m/z 360.1→242.1, 384.1→200.1, 370.1→252.1, and 346.1→198.1, respectively. No significant matrix effect was observed for all analytes. The calibration curve for all enantiomers were linear from 1.25 to 2500 ng/mL. The precisions for intra- and inter-run were < 14.2%, and the accuracy fell in the interval of -5.3 to 8.1%. Stability of samples was confirmed under the storage and processing conditions. The developed method was also suitable for separation and determination of ilaprazole enantiomers. The validated method combining the equilibrium dialysis method was applied to the protein binding ratio studies of four pairs proton pump inhibitor enantiomers in human plasma.

摘要

质子泵抑制剂,包括奥美拉唑、雷贝拉唑、兰索拉唑和泮托拉唑,通过手性液相色谱-串联质谱法在人血浆中实现了同时对映选择性测定。采用四种相应的稳定同位素标记的质子泵抑制剂作为内标。每个对映体和内标均用含 0.1%氨的乙腈提取,然后在 10 分钟内用 Chiralpak IC 柱(5 µm,4.6 mm×150 mm)分离。流动相由含 0.2%乙酸的乙腈-乙酸铵(10 mM)(50:50,v/v)组成。为了定量所有对映体,采用 API 4000 串联质谱仪,在 m/z 360.1→242.1、384.1→200.1、370.1→252.1 和 346.1→198.1 处进行多重反应监测转换。所有分析物均未观察到显著的基质效应。所有对映体的校准曲线在 1.25 至 2500 ng/mL 范围内呈线性。日内和日间精密度均<14.2%,准确度在-5.3 至 8.1%的区间内。在储存和处理条件下确认了样品的稳定性。所开发的方法也适用于艾普拉唑对映异构体的分离和测定。结合平衡透析法的验证方法用于研究人血浆中四对对映体质子泵抑制剂的蛋白结合率。

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