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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of levophencynonate and its metabolite demethyl levophencynonate in human plasma by liquid chromatography tandem mass spectrometry
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Simultaneous determination of levophencynonate and its metabolite demethyl levophencynonate in human plasma by liquid chromatography tandem mass spectrometry

机译:液相色谱-串联质谱法同时测定人血浆中的左旋壬酸及其代谢产物脱甲基左旋壬酸

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A sensitive and convenient high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) method was developed to determine levophencynonate and demethyl levophencynonate levels in human plasma simultaneously. Chromatographic separation was achieved on a SHIMADZU Shim-Pack XR C8 column and mass spectrometric analysis was performed by an API5000 mass spectrometer coupled with an electro-spray ionization (ESI) source in the positive ion mode. The MRM transitions of m/z 358.4 -> 156.4 and 344.5 -> 144.2 were used to quantify levophencynonate and demethyl levophencynonate, respectively. This analytical method was fully validated with specificity, linearity, lower limit of quantitation (LLOQ), accuracy, precision, stability, matrix effect and recovery. The linearity of this method were developed to be within the concentration ranges of 10-4000 pg/mL for levophencynonate and 25-8000 pg/mL for demethyl levophencynonate in human plasma. This method was used in a clinical study which was administrated with single oral dose for Chinese healthy subjects to investigate the pharmacokinetics of levophencynonate and demethyl levophencynonate. (C) 2016 Elsevier B.V. All rights reserved.
机译:建立了灵敏,方便的高效液相色谱串联质谱法(HPLC-MS / MS),用于同时测定人血浆中左旋壬酸和去甲基左旋壬酸的水平。在SHIMADZU Shim-Pack XR C8色谱柱上进行色谱分离,并通过API5000质谱仪结合电喷雾电离(ESI)源以正离子模式进行质谱分析。 m / z 358.4-> 156.4和344.5-> 144.2的MRM跃迁分别用于量化左旋壬酸和去甲基左旋壬酸。该分析方法经过特异性,线性,定量下限(LLOQ),准确性,精密度,稳定性,基质效应和回收率的充分验证。在人血浆中,该方法的线性被开发为在左旋壬酸的浓度范围为10-4000 pg / mL和对去甲基左旋壬酸的浓度范围为25-8000 pg / mL。该方法被用于对中国健康受试者进行单次口服给药的临床研究中,以研究左旋壬酸和去甲基左旋壬酸的药代动力学。 (C)2016 Elsevier B.V.保留所有权利。

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