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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Development and validation of an LC-MS/MS method for the quantitative determination of aripiprazole and its main metabolite, OPC-14857, in human plasma
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Development and validation of an LC-MS/MS method for the quantitative determination of aripiprazole and its main metabolite, OPC-14857, in human plasma

机译:建立和验证LC-MS / MS方法用于定量测定人血浆中阿立哌唑及其主要代谢物OPC-14857

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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.
机译:开发并验证了测定人血浆中阿立哌唑及其主要代谢物OPC-14857的准确,灵敏,可重现和选择性液相色谱/串联质谱(LC-MS / MS)方法。色谱分离在7.5分钟内在Cl 8反相色谱柱上等度完成。校准曲线的范围从0.1到100 ng / ml,拟合到1 / y(2)加权线性回归模型。该测定显示无明显干扰。使用0.4 ml血浆,两种分析物的定量下限(LLOQ)为0.1 ng / ml。阿立哌唑和OPC-14857的测定内和测定间精密度和准确度值均在规定的范围内。 (c)2005 Elsevier B.V.保留所有权利。

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