首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >UPLC-MS/MS assay for simultaneous determination of four compounds in rat plasma: application to pharmacokinetic study after oral administration of Caulis Spatholobi extract
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UPLC-MS/MS assay for simultaneous determination of four compounds in rat plasma: application to pharmacokinetic study after oral administration of Caulis Spatholobi extract

机译:UPLC-MS / MS测定法同时测定大鼠血浆中的四种化合物:口服鸡血藤提取物后在药代动力学研究中的应用

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An ultra-performance liquid chromatography tandem mass spectrometry method was developed for the simultaneous determination of protocatechuic acid, catechin, gallocatechin and formononetin in rat plasma, with genkwanin as the internal standard in this study. Plasma samples were prepared by liquid-liquid extraction with ethyl acetate. The four components were separated on an Agilent Zorbax Eclipse Plus C-18 column (2.1x50mm, 1.8m) with the mobile phase consisting of water containing 0.05% formic acid and methanol (35:65, v/v), and detected by negative ion electrospray ionization in the selected reaction monitoring mode. The method was linear for all analytes over the investigated ranges, with all correlation coefficients >0.99. The validated lower limit of quantification was 0.5ng/mL for protocatechuic acid, catechin, and gallocatechin and 0.8ng/mL for formononetin. The intra- and inter-day precisions (RSD, %) were <13.1%, and accuracy (RE, %) ranged from -13.8 to 9.9%. The mean absolute extraction recoveries of the analytes and internal standard from rat plasma were all >80.7%. The validated method was successfully applied for the first time to investigate the pharmacokinetics of four chemical ingredients after oral administration of Caulis Spatholobi Extract in rats. Copyright (c) 2016 John Wiley & Sons, Ltd.
机译:建立了一种超高效液相色谱串联质谱法同时测定大鼠血浆中原儿茶酸,儿茶素,没食子儿茶素和formononetin的方法,其中以那香苷为内标。通过用乙酸乙酯进行液-液萃取来制备血浆样品。在Agilent Zorbax Eclipse Plus C-18色谱柱(2.1x50mm,1.8m)上分离四种成分,流动相由含有0.05%甲酸和甲醇(35:65,v / v)的水组成,并通过负离子检测在选定的反应监控模式下进行离子电喷雾电离。该方法对于研究范围内的所有分析物都是线性的,所有相关系数均> 0.99。经验证,原儿茶酸,儿茶素和没食子儿茶素的定量下限为0.5ng / mL,甲萘醌的定量下限为0.8ng / mL。日内和日间精度(RSD,%)均<13.1%,精度(RE,%)的范围为-13.8至9.9%。从大鼠血浆中分析物和内标物的平均绝对提取回收率均> 80.7%。经验证的方法首次成功地用于研究口服鸡血藤提取物后四种化学成分的药代动力学。版权所有(c)2016 John Wiley&Sons,Ltd.

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