Development and validation of an LC-MS/MS method for the quantitative determination of aripiprazole and its main metabolite, OPC-14857, in human plasma

被引:85
作者
Kubo, M
Mizooku, Y
Hirao, Y
Osumi, T
机构
[1] Otsuka Pharmaceut Co Ltd, Dept Clin Res & Dev, Chuo Ku, Osaka 5400021, Japan
[2] Sumika Chem Anal Serv, Pharmaceut Anal Lab, Pharmaceut Business Div, Konohana Ku, Osaka 5540022, Japan
[3] Otsuka Pharmaceut Co Ltd, Tokushima Res Inst, Drug Safety Res Ctr, Dept Drug Metabol, Tokushima 7710192, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2005年 / 822卷 / 1-2期
关键词
aripiprazole; OPC-14857; LC-MS/MS;
D O I
10.1016/j.jchromb.2005.06.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An accurate, sensitive, reproducible, and selective liquid chromatography/tandem mass spectrometry (LC-MS/MS) method for determination of aripiprazole and its main metabolite, OPC-14857, in human plasma was developed and validated. Chromatographic separation was achieved isocratically on a Cl 8 reversed-phase column within 7.5 min. The calibration curve, ranging from 0.1 to 100 ng/ml, was fitted to a 1/y(2)-weighted linear regression model. The assay showed no significant interference. Lower limit of quantitation (LLOQ) for both analytes was 0.1 ng/ml using 0.4 ml of plasma. Intra- and inter-assay precision and accuracy values for aripiprazole and OPC-14857 were within regulatory limits. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:294 / 299
页数:6
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