A simple, rapid and sensitive method based on an ultra-performance liquid chromatography tandem mass spectrometry （UPLC-MS/MS） has been developed and validated for the determination of pimavanserin in rat plasma. Th...A simple, rapid and sensitive method based on an ultra-performance liquid chromatography tandem mass spectrometry （UPLC-MS/MS） has been developed and validated for the determination of pimavanserin in rat plasma. The analyte was extracted by protein precipitation with methanol and separated on an ACQUITY BEH C18 column （100 mm × 2.1 mm, 1.7μm; Waters, USA）, with an isocratic elution of acetonitrile-water containing 10 mM ammonium acetate （70：30, v/v）, at a flow rate of 0.2 mL/min for 2.5 rain. The analyte and clarithromyein （the internal standard） were detected and quantified in positive ion mode using multiple reaction monitoring transitions at m/z 428.2 - 223.0 for pimavanserin and m/z 748.5 - 589.5 for clarithromycin. Relative coefficient （r） for the calibration curve was more than 0.9980. The intra-day and inter-day precisions （relative standard deviation, RSD%） were less than 13.3% and 10.5%, respectively, and the accuracy （relative error, RE%） was within ± 11.5%. The analytical method was successfully applied to a routine pharmacokinetic study of pimavanserin in rats after oral administration at the dose of 10 mg/kg.展开更多
基金supported in part by a grant of the Scientific Research Program of Hainan Province (ZDYF2016143), China
文摘A simple, rapid and sensitive method based on an ultra-performance liquid chromatography tandem mass spectrometry （UPLC-MS/MS） has been developed and validated for the determination of pimavanserin in rat plasma. The analyte was extracted by protein precipitation with methanol and separated on an ACQUITY BEH C18 column （100 mm × 2.1 mm, 1.7μm; Waters, USA）, with an isocratic elution of acetonitrile-water containing 10 mM ammonium acetate （70：30, v/v）, at a flow rate of 0.2 mL/min for 2.5 rain. The analyte and clarithromyein （the internal standard） were detected and quantified in positive ion mode using multiple reaction monitoring transitions at m/z 428.2 - 223.0 for pimavanserin and m/z 748.5 - 589.5 for clarithromycin. Relative coefficient （r） for the calibration curve was more than 0.9980. The intra-day and inter-day precisions （relative standard deviation, RSD%） were less than 13.3% and 10.5%, respectively, and the accuracy （relative error, RE%） was within ± 11.5%. The analytical method was successfully applied to a routine pharmacokinetic study of pimavanserin in rats after oral administration at the dose of 10 mg/kg.
