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Sensitive liquid chromatography-tandem mass spectrometry method for the determination of scutellarin in human plasma: Application to a pharmacokinetic study

机译:灵敏液相色谱-串联质谱法测定人血浆中的黄rin素:在药代动力学研究中的应用

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摘要

A sensitive and selective liquid chromatographic-tandem mass spectrometric (LC-MS/MS) method for the determination of scutellarin in human plasma has been developed. Samples were prepared using solid phase extraction and analyzed on a C-18 column interfaced with a triple quadrupole tandem mass spectrometer. Positive electrospray ionization was employed as the ionization source. The mobile phase consisted of methanol-water (0.1% formic acid), using gradient procedure. The analyte and internal standard baicalin were both detected by use of selected reaction monitoring mode. The method was linear in the concentration range of 0.2-20.0 ng/mL. The lower limit of quantification (LLOQ) was 0.2 ng/mL. The intra- and inter-day relative standard deviation across three validation runs over the entire concentration range was less than 12.4%. The accuracy determined at three concentrations (1.0, 5.0 and 10.0 ng/mL for scutellarin) was within +/- 5.0% in terms of relative error. The method herein described was successfully applied for the evaluation of pharmacokinetic profiles of scutellarin guttate pills in 20 healthy volunteers. (c) 2005 Elsevier B.V. All rights reserved.
机译:已经开发了一种灵敏的选择性液相色谱-串联质谱法(LC-MS / MS),用于测定人血浆中的黄cut素。使用固相萃取制备样品,并在与三重四极杆串联质谱仪连接的C-18色谱柱上进行分析。正电喷雾电离用作电离源。流动相由甲醇-水(0.1%甲酸)组成,采用梯度方法。分析物和内标黄mode苷均通过选择的反应监测模式进行检测。该方法在0.2-20.0 ng / mL的浓度范围内是线性的。定量下限(LLOQ)为0.2 ng / mL。在整个浓度范围内进行的三次验证运行的日内和日间相对标准偏差均小于12.4%。就相对误差而言,在三种浓度(黄素的浓度为1.0、5.0和10.0 ng / mL)下测定的准确度在+/- 5.0%之内。本文描述的方法已成功地用于评估20例健康志愿者中黄cut胶点滴药的药代动力学概况。 (c)2005 Elsevier B.V.保留所有权利。

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