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Sensitive Liquid Chromatography-Tandem Mass Spectrometry Method for the Determination of Olanzapine in Human Urine

机译:灵敏液相色谱-串联质谱法测定人尿中的奥氮平

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摘要

A sensitive and selective liquid chromatographic-tandem mass spectrometric (LC-MS-MS) method was developed to determine olanzapine (OLZ) in human urine. After solid-phase extraction with SPE cartridge, the urine sample was analysed on a C_(18) column (Symmetry 3.5 μm, 50 x 4.6 mm i.d) interfaced with a triple quadrupole tandem mass spectrometer. Positive electrospray ionization was employed as the ionization source. The mobile phase consisted of ammonium acetate (pH 7.8)-acetonitrile (10:90, v/v). The method was linear over a concentration range of 1-100 ngml~(-1). The lower limit of quantitation was 1 ngml~(-1). The intra-day and inter-day relative standard deviation across three validation runs over the entire concentration range was <11.5 %. The accuracy determined at three concentrations (8.0, 50.0 and 85.0 ngml~(-1) OLZ) was within ±1.21 % in terms of relative errors.
机译:建立了灵敏且选择性的液相色谱-串联质谱(LC-MS-MS)方法来测定人尿中的奥氮平(OLZ)。用SPE柱固相萃取后,在与三重四极串联质谱仪连接的C_(18)色谱柱(对称3.5μm,50 x 4.6 mm i.d)上分析尿液样品。正电喷雾电离用作电离源。流动相由乙酸铵(pH 7.8)-乙腈(10:90,v / v)组成。该方法在1-100 ngml〜(-1)的浓度范围内是线性的。定量下限为1 ngml〜(-1)。在整个浓度范围内进行的三次验证运行的日内和日间相对标准偏差<11.5%。就相对误差而言,在三种浓度(8.0、50.0和85.0 ngml〜(-1)OLZ)下测定的准确度在±1.21%以内。

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