CHENG Dong-xia, DAI Xiao-jian, ZHANG Yi-fan, WU Yong-qian, SHI Chong-tie, MA Xi-feng, LI Jin, CHEN Xiao-yan, ZHONG Da-fang. Determination of anaprazole in human plasma by LC-MS/MS in pharmacokinetic studyJ. Acta Pharmaceutica Sinica, 2016,51(12): 1885-1890. doi: 10.16438/j.0513-4870.2016-0508
Citation: CHENG Dong-xia, DAI Xiao-jian, ZHANG Yi-fan, WU Yong-qian, SHI Chong-tie, MA Xi-feng, LI Jin, CHEN Xiao-yan, ZHONG Da-fang. Determination of anaprazole in human plasma by LC-MS/MS in pharmacokinetic studyJ. Acta Pharmaceutica Sinica, 2016,51(12): 1885-1890. doi: 10.16438/j.0513-4870.2016-0508

Determination of anaprazole in human plasma by LC-MS/MS in pharmacokinetic study

  • Anaprazole is a proton pump inhibitor clinically used for curing peptic ulcer. A rapid, sensitive and convenient LC-MS/MS method was first established for the determination of anaprazole in human plasma. d3, 13C-anaprazole was used as internal standard (IS). After extraction from human plasma by protein precipitation with acetonitrile, all components were separated on an Extend C18 column (100 mm×4.6 mm, 3.5 μm). The assay was linear over the concentration range of 5.00-3 000 ng·mL-1 (r2 > 0.995). The method was successfully applied to a pharmacokinetic study of 40 mg anaprazole enteric-coated tablets in 14 Chinese healthy volunteers under fasting or high fat diet conditions. Cmax was (1 020±435) ng·mL-1 and AUC0-t was (2 370±754) h·ng·mL-1 under fasting condition. And Cmax was (538±395) ng·mL-1 and AUC0-t was (1 610±650) h·ng·mL-1 under high fat diet condition. The plasma results suggest that the exposure of anaprazole is reduced by the high fat diet.
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