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

Sjoukje Postma-Kunnen, J. Yska, Gerard Hommema, Sikke Koopmans, B. Wilffert, E. Roon
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引用次数: 4

Abstract

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.
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高效液相色谱-质谱联用法定量测定人血清中美托洛尔和α-羟美托洛尔的药代动力学。
为了测定人血清中美托洛尔及其代谢物α-羟美托洛尔,我们建立了以Exactive®Orbitrap质谱仪(Thermo Scientific)为检测器,以同位素标记美托洛尔-d7为内标的液相色谱系统。用水-乙腈(15:85,v/v)作为沉淀剂进行简单的样品制备。美托洛尔和α-羟美托洛尔的色谱运行时间为15 min,线性校准曲线在5.0 ~ 250µg/L范围内。验证结果表明,该方法准确、精密度好、选择性好,美托洛尔的定量下限为2.0µg/L, α-羟美托洛尔的定量下限为1.0µg/L。美托洛尔和α-羟基美托洛尔的LC-Orbitrap质谱分析方法可用于人体药代动力学研究。
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