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首页> 外文期刊>Bulletin of the Korean Chemical Society >Pentafluorophenylprophyl Ligand-based Liquid Chromatography-Tandem Mass Spectrometric Method for Rapid and Reproducible Determination of Metformin in Human Plasma
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Pentafluorophenylprophyl Ligand-based Liquid Chromatography-Tandem Mass Spectrometric Method for Rapid and Reproducible Determination of Metformin in Human Plasma

机译:基于五氟苯基异丙醇配体的液相色谱-串联质谱法快速,可重复测定人血浆中的二甲双胍

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摘要

This paper describes first development and validation of pentafluorophenylprophyl ligand-based liquid chromatography coupled to tandem mass spectrometry (PFPLC-MS/MS) method to determine metformin, a highly polar compound, in human plasma. Metformin and Phenformin (internal standard) were extracted from human plasma 50 μL with a single-step protein precipitation. The chromatographic separation was performed using a linear gradient elution of mobile phase involving 5.0 mM ammonium formate solution with 0.1% formic acid (A) and acetonitrile (B) over 3.0 min of run time on a Phenomenex Luna PFP column. The detection was performed using a triple-quadrupole tandem mass spectrometer (Waters Quattro micro) with electrospray ionization in the mode of positive ionization and multiple-reaction monitoring (MRM). The developed method was validated with 5.0 ng/mL of lower limit of quantification (LLOQ). The calibration curve was linear over 5-3000 ng/mL of the concentration range (R~2>0.99). The specificity, selectivity, carry-over effect, precision, accuracy and stability of the method met the acceptance criteria. The method developed in this study had had rapidness, simplicity and ruggedness. The reliable method was successfully applied to high throughput analysis of real samples for a practical purpose of a pharmacokinetic study.
机译:本文介绍了基于五氟苯基脯氨酸配体的液相色谱与串联质谱法(PFPLC-MS / MS)联用测定人血浆中高极性二甲双胍的方法的首次开发和验证。通过单步蛋白质沉淀从50μL人血浆中提取二甲双胍和苯乙双胍(内标)。在Phenomenex Luna PFP色谱柱上,在3.0分钟的运行时间内,使用包含5.0 mM甲酸铵溶液和0.1%甲酸(A)和乙腈(B)的流动相进行线性梯度洗脱,进行色谱分离。使用具有正电离和多反应监测(MRM)模式的电喷雾电离的三重四极串联质谱仪(Waters Quattro micro)进行检测。用5.0 ng / mL的定量下限(LLOQ)对开发的方法进行了验证。校准曲线在5-3000 ng / mL的浓度范围内呈线性(R〜2> 0.99)。该方法的特异性,选择性,残留效应,精密度,准确性和稳定性均达到了可接受的标准。本研究开发的方法具有快速,简便和耐用的特点。可靠的方法已成功地用于实际样品的高通量分析,用于药代动力学研究的实际目的。

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