首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Application of a sensitive and specific LC-MS/MS method for determination of eriodictyol-8-C-beta-D-glucopyranoside in rat plasma for a bioavailability study
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Application of a sensitive and specific LC-MS/MS method for determination of eriodictyol-8-C-beta-D-glucopyranoside in rat plasma for a bioavailability study

机译:灵敏而特异的LC-MS / MS方法在大鼠血浆中测定芥酸8-C-β-D-吡喃葡萄糖苷的生物利用度研究中的应用

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摘要

This study is the first to detail the development and validation of a rapid, sensitive and specific LC-ESI-MS/MS method for the determination of eriodictyol-8-C--d-glucopyranoside (EG) in rat plasma. A simple protein precipitation method was used for plasma sample preparation. Chromatographic separation was successfully achieved on an Agilent Zorbax XDB C-18 column (2.1x50mm, 3.5 mu m) using a step gradient program with the mobile phase of 0.1% formic acid aqueous solution and acetonitrile with 0.1% formic acid. EG and the internal standard (IS) were detected using an electrospray negative ionization mass spectrometry in the multiple reaction monitoring mode. This method demonstrated good linearity and did not show any endogenous interference with the active compound and IS peaks. The lower limit of quantification of EG was 0.20ng/mL in 50L rat plasma. The average recoveries of EG and IS from rat plasma were both above 80%. The inter-day precisions (relative standard deviation) of EG determined over 5days were all within 15%. The present method was successfully applied to a quantification and bioavailability study of EG in rats after intravenous and oral administration. The oral absolute bioavailability of EG in rats was estimated to be 7.71 +/- 1.52%. Copyright (c) 2014 John Wiley & Sons, Ltd.
机译:这项研究是第一个详细开发和验证快速,灵敏和特异的LC-ESI-MS / MS方法,用于测定大鼠血浆中的香茅醇8-C-d-吡喃葡萄糖苷(EG)的方法。一种简单的蛋白质沉淀方法用于血浆样品制备。在Agilent Zorbax XDB C-18色谱柱(2.1x50mm,3.5μm)上,使用0.1%甲酸水溶液和0.1%甲酸的乙腈流动相,成功地完成了色谱分离。 EG和内标(IS)使用电喷雾负离子质谱仪在多反应监测模式下进行检测。此方法显示出良好的线性,并且对活性化合物和IS峰均未显示任何内源性干扰。在50L大鼠血浆中EG的定量下限为0.20ng / mL。从大鼠血浆中EG和IS的平均回收率均高于80%。在5天内确定的EG的日间精度(相对标准偏差)均在15%以内。本方法成功地用于大鼠静脉内和口服给药后EG的定量和生物利用度研究。 EG在大鼠中的口服绝对生物利用度估计为7.71 +/- 1.52%。版权所有(c)2014 John Wiley&Sons,Ltd.

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