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A validated high-resolution accurate mass LC-MS assay for quantitative determination of metoprolol and α-hydroxymetoprolol in human serum for application in pharmacokinetics

机译:一种经过验证的高分辨率精确质量液相色谱-质谱法,用于定量测定人血清中的美托洛尔和α-羟基美托洛尔,用于药代动力学

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To determine metoprolol and its metabolite α-hydroxymetoprolol in human serum we validated a method on an LC system with an Exactive? Orbitrap mass spectrometer (Thermo Scientific) as detector and isotope-labelled metoprolol-d7 as internal standard. A simple sample preparation was used with water-acetonitrile (15:85, v/v) as precipitation reagent. This method has a chromatographic run time of 15 min and linear calibration curves in the range of 5.0-250 μg/L for both metoprolol and α-hydroxymetoprolol. Validation showed the method to be accurate, with a good precision, selective and with a lower limit of quantitation of 2.0 μg/L for metoprolol and 1.0 μg/L for α-hydroxymetoprolol, respectively. This validated LC-Orbitrap MS analysis for metoprolol and α-hydroxymetoprolol can be used for application in human pharmacokinetics.
机译:为了确定人血清中的美托洛尔及其代谢物α-羟基美托洛尔,我们验证了一种具有Exactive?的LC系统方法。 Orbitrap质谱仪(Thermo Scientific)作为检测器,同位素标记的美托洛尔-d7作为内标。使用简单的样品前处理,以水-乙腈(15:85,v / v)作为沉淀试剂。该方法的美托洛尔和α-羟基美托洛尔的色谱运行时间为15分钟,线性校准曲线在5.0-250μg/ L范围内。验证显示该方法准确,准确度高,选择性好,并且对美托洛尔的定量下限分别为2.0μg/ L和对α-羟基美托洛尔的定量下限分别为1.0μg/ L。经验证的美托洛尔和α-羟基美托洛尔的LC-Orbitrap MS分析可用于人体药代动力学。

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