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采用气相色谱-质谱联用仪测定血浆中的奈韦拉平。

Determination of nevirapine in plasma by GC-MS.

作者信息

Vogel M, Bertram N, Wasmuth J C, Emmelkamp J, Rockstroh J K, Reichel C

机构信息

Department of Internal Medicine I, Bonn University, Bonn, Germany.

出版信息

J Chromatogr Sci. 2010 Feb;48(2):91-4. doi: 10.1093/chromsci/48.2.91.

Abstract

Here we describe a simple, stable, and specific gas chromatography-mass spectrometry (GC-MS) method for the determination of nevirapine in plasma. After precipitation of proteins, the non-nucleoside reverse transcriptase inhibitor nevirapine was extracted with dichloromethane. For the determination and quantification of nevirapine, 1 microL of the organic layer was injected onto the GC-MS system. Linear calibration curves were obtained with BIRH 0414BS as internal standard in a range from 0.01 to 15 microg/mL. Intra- and inter-day accuracy and precision of this method were good with an accuracy between 96-109% and a precision between 2-8% across the therapeutic range of nevirapine. GC-MS proved to be a valid alternative to high-performance liquid chromatography and liquid chromatography-MS.

摘要

在此,我们描述了一种用于测定血浆中奈韦拉平的简单、稳定且特异的气相色谱-质谱联用(GC-MS)方法。蛋白质沉淀后,用二氯甲烷提取非核苷类逆转录酶抑制剂奈韦拉平。为了测定和定量奈韦拉平,将1微升有机层注入GC-MS系统。以BIRH 0414BS作为内标,在0.01至15微克/毫升的范围内获得线性校准曲线。该方法的日内和日间准确度及精密度良好,在奈韦拉平的治疗范围内,准确度在96%至109%之间,精密度在2%至8%之间。事实证明,GC-MS是高效液相色谱和液相色谱-质谱联用的有效替代方法。

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