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LC-MS/MS 法测定人血浆中几种联合心血管治疗药物

LC-MS/MS method for the determination of several drugs used in combined cardiovascular therapy in human plasma.

机构信息

Analytical Chemistry Department, Science and Technology Faculty, Basque Country University/EHU, P.O. Box 644, 48080 Bilbao, Basque Country, Spain.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Oct 15;878(28):2685-92. doi: 10.1016/j.jchromb.2010.07.026. Epub 2010 Aug 6.

Abstract

A simple, fast and validated method is reported for the simultaneous analysis, in human plasma, of several drugs usually combined in cardiovascular therapy (atenolol, bisoprolol, hydrochlorothiazide, chlorthalidone, salicylic acid, enalapril and its active metabolite enalaprilat, valsartan and fluvastatin) using high performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) with electrospray ionization (ESI), working in multiple reaction monitoring mode (MRM). Separation of analytes and internal standard (pravastatin) was performed on a Luna C18(2) (150mm×4.6mm, 3μm) column using a gradient elution mode with a run time of 15min. The mobile phase consisted of a mixture of acetonitrile and water containing 0.01% formic acid and 10mM ammonium formate at pH 4.1. Sample treatment consisted of a simple protein precipitation with acetonitrile, enabling a fast analysis. The method showed good linearity, precision (RSD% values between 0.7% and 12.7%) and accuracy (relative error values between 0.9% and 14.0%). Recoveries were within 68-106% range and the ion-suppression was not higher than 22% for any analyte. The method was successfully applied to plasma samples obtained from patients under combined cardiovascular treatment.

摘要

本文报道了一种简单、快速且经过验证的方法,可用于同时分析人血浆中的几种药物(通常联合用于心血管治疗的药物),包括阿替洛尔、比索洛尔、氢氯噻嗪、氯噻酮、水杨酸、依那普利及其活性代谢物依那普利拉、缬沙坦和氟伐他汀,采用高效液相色谱-串联质谱法(LC-MS/MS),以电喷雾电离(ESI)为离子源,工作模式为多反应监测(MRM)。分析物和内标(普伐他汀)的分离在 Luna C18(2)(150mm×4.6mm,3μm)柱上进行,采用梯度洗脱模式,运行时间为 15min。流动相由含 0.01%甲酸和 10mM 甲酸铵的乙腈和水的混合物组成,pH 值为 4.1。样品处理采用乙腈简单的蛋白沉淀法,可实现快速分析。该方法具有良好的线性、精密度(RSD%值在 0.7%至 12.7%之间)和准确度(相对误差值在 0.9%至 14.0%之间)。回收率在 68-106%范围内,任何分析物的离子抑制均不超过 22%。该方法成功应用于接受联合心血管治疗的患者的血浆样本。

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