High-Throughput Chiral LC-MS/MS Method Using Overlapping Injection Mode for the Determination of Pantoprazole Enantiomers in Human Plasma with Application to Pharmacokinetic Study

被引:7
作者
Li, Shengni [1 ,2 ]
Jiang, Huafang [2 ]
Wang, Yiya [2 ]
Liu, Yinli [1 ]
Shen, Xiaohang [2 ]
Liang, Wenzhong [2 ]
Hong, Zhanying [1 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmaceut Anal, 325 Guohe Rd, Shanghai 200433, Peoples R China
[2] WuXi AppTec Co Ltd, Bioanalyt Serv, 288 Fute Zhong Rd, Shanghai 200131, Peoples R China
基金
中国国家自然科学基金;
关键词
chiral separation; human plasma; LC-MS/MS; overlapping injection; pantoprazole enantiomers; PERFORMANCE LIQUID-CHROMATOGRAPHY; PROTON PUMP INHIBITORS; HEALTHY-VOLUNTEERS; STATIONARY-PHASE; DOG PLASMA; VALIDATION; QUANTIFICATION;
D O I
10.1002/chir.22616
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A sensitive and high-throughput chiral liquid chromatography-tandem mass spectrometry method was developed and validated for the quantification of R-pantoprazole and S-pantoprazole in human plasma. Sample extraction was carried out by using ethyl acetate liquid-liquid extraction in 96-well plate format. The separation of pantoprazole enantiomers was performed on a CHIRALCEL OJ-RH column and an overlapping injection mode was used to achieve a run time of 5.0 min/sample. The mobile phase consisted of 1) 10 mM ammonium acetate in methanol: acetonitrile (1: 1, v/v) and 2) 20 mM ammonium acetate in water. Isocratic elution was used with flow rate at 500 mu L/min. The enantiomers were quantified on a triple-quadrupole mass spectrometer under multiple reaction monitoring (MRM) mode with m/z 382.1/230.0 for pantoprazole and m/z 388.4/230.1 for pantoprazole-d7. Linearity from 20.0 to 5000 ng/mL was established for each enantiomer (r(2) > 0.99). Extraction recovery ranged from 91.7% to 96.4% for R-pantoprazole and from 92.5% to 96.5% for S-pantoprazole and the IS-normalized matrix factor was 0.98 to 1.07 for R-pantoprazole and S-pantoprazole, respectively. The method was demonstrated with acceptable accuracy, precision, selectivity, and stability and the method was applied to support a pharmacokinetic study of a phase I clinical trial of racemic pantoprazole in healthy Chinese subjects. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:569 / 575
页数:7
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