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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study
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Liquid chromatography-tandem mass spectrometry method for simultaneous quantification of urapidil and aripiprazole in human plasma and its application to human pharmacokinetic study

机译:液相色谱-串联质谱法同时测定人血浆中乌拉地尔和阿立哌唑的含量及其在人体药代动力学研究中的应用

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摘要

A sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous determination of urapidil and aripiprazole in human plasma. A simple liquid-liquid extraction with ethyl acetate was used for the sample preparation. Chromatographic separation was achieved on a Phenomenex C18 (4.6×50 mm, 5 μm) column with 0.1% formic acid-acetonitrile (10:90, v/v) as the mobile phase with flow rate of 0.6 mL/min. The quantitation of the target compounds was determined in a positive ion multiple reaction monitoring mode. Calibration plots were linear over the range of 2.0-2503.95 ng/mL for urapidil and 1.0-500.19 ng/mL for aripiprazole. The lower limit of quantitation for urapidil and aripiprazole was 2.0 and 1.0 ng/mL, respectively. Mean recovery was in the range of 69.94-75.62% for both analytes and internal standards. Intra-day and inter-day precisions of the assay at three concentrations were 2.56-5.89% with accuracy of 92.31-97.83% for urapidil, and 3.14-6.84% with accuracy of 91.38-94.42% for aripiprazole. The method was successfully applied to human pharmacokinetic study of urapidil and aripiprazole in healthy human male volunteers.
机译:建立了灵敏且选择性的液相色谱-串联质谱(LC-MS / MS)方法,并验证了该方法可同时测定人血浆中的乌拉地尔和阿立哌唑。使用乙酸乙酯的简单液-液萃取用于样品制备。在Phenomenex C18(4.6×50 mm,5μm)色谱柱上以0.1%甲酸-乙腈(10:90,v / v)作为流动相以0.6 mL / min的流速进行色谱分离。目标化合物的定量以阳离子多重反应监测模式确定。乌拉地尔在2.0-2503.95 ng / mL范围内和阿立哌唑在1.0-500.19 ng / mL范围内的校准图呈线性。乌拉地尔和阿立哌唑的定量下限分别为2.0和1.0 ng / mL。分析物和内标物的平均回收率均在69.94-75.62%的范围内。在三种浓度下,日间和日间分析的精确度分别为2.56-5.89%,对于乌拉地尔为92.31-97.83%,对阿立哌唑为3.14-6.84%,对精度为91.38-94.42%。该方法已成功地应用于乌吡地尔和阿立哌唑在健康人类男性志愿者中的人体药代动力学研究。

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