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采用液相色谱-电喷雾串联质谱法定量紫杉醇及其两种主要代谢物。

Quantitation of paclitaxel and its two major metabolites using a liquid chromatography-electrospray ionization tandem mass spectrometry.

机构信息

Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jul 15;879(22):2018-22. doi: 10.1016/j.jchromb.2011.05.024. Epub 2011 May 25.

Abstract

A sensitive and selective liquid chromatographic-tandem mass spectrometric (LC-MS/MS) method for the determination of paclitaxel (Taxol) and its two major metabolites in human plasma has been developed. Samples were prepared after liquid-liquid extraction and analyzed on a C(18) column interfaced with a Q-Trap tandem mass spectrometer. Positive electrospray ionization was employed as the ionization source. The mobile phase consisted of acetonitrile-water (0.05% formic acid) (65:35) at the flow rate of 0.25 mL/min. The analytes and internal standard docetaxel were both detected by use of multiple reaction monitoring mode. The method was linear in the concentration range of 0.5-500.0 ng/mL for paclitaxel, 6α-hydroxypaclitaxel and p-3'-hydroxypaclitaxel, respectively. The lower limit of quantification (LLOQ) was 0.5 ng/mL for paclitaxel, 6α-hydroxypaclitaxel and p-3'-hydroxypaclitaxel, respectively. The intra- and inter-day relative standard deviation across three validation runs over the entire concentration range was less than 8.18%. The accuracy determined at three concentrations was within ±10.8% in terms of relative error. The total run time was 7.0 min. This assay offers advantages in terms of expediency, and suitability for the analysis of paclitaxel and its metabolites in various biological fluids.

摘要

已经开发出一种灵敏且选择性的液质联用(LC-MS/MS)方法,用于测定人血浆中的紫杉醇(Taxol)及其两种主要代谢物。样品经液液萃取后进行制备,并在 C(18)柱上进行分析,该柱与 Q-Trap 串联质谱仪相连接。采用正电喷雾电离作为离子源。流动相由乙腈-水(0.05%甲酸)(65:35)组成,流速为 0.25 mL/min。分析物和内标多西他赛均采用多重反应监测模式进行检测。紫杉醇、6α-羟基紫杉醇和 p-3'-羟基紫杉醇的浓度范围分别为 0.5-500.0 ng/mL 时,方法呈线性。紫杉醇、6α-羟基紫杉醇和 p-3'-羟基紫杉醇的定量下限(LLOQ)分别为 0.5 ng/mL。三个验证运行的整个浓度范围内,日内和日间相对标准偏差(RSD)均小于 8.18%。以相对误差计,三个浓度点的准确度均在±10.8%范围内。总运行时间为 7.0 分钟。该方法具有快速、适用于分析各种生物体液中紫杉醇及其代谢物的优点。

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