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采用液相色谱-串联质谱法同时测定血浆中醋氯芬酸及其三种代谢物。

Simultaneous determination of aceclofenac and its three metabolites in plasma using liquid chromatography-tandem mass spectrometry.

作者信息

Kang Wonku, Kim Eun-Young

机构信息

College of Pharmacy, Catholic University of Daegu, Kyoungbuk 712-702, South Korea.

出版信息

J Pharm Biomed Anal. 2008 Feb 13;46(3):587-91. doi: 10.1016/j.jpba.2007.11.009. Epub 2007 Nov 17.

DOI:10.1016/j.jpba.2007.11.009
PMID:18096348
Abstract

A new LC/MS/MS-based method allows simultaneous determination of aceclofenac and its three metabolites (4'-OH-aceclofenac, diclofenac, and 4'-OH-diclofenac) in plasma. After acetonitrile-induced precipitation of proteins from the plasma samples, aceclofenac, 4'-OH-aceclofenac, diclofenac, 4'-OH-diclofenac, and flufenamic acid (an internal standard) were chromatographed on a reverse-phase C(18) analytical column. The isocratic mobile phase of acetonitrile/0.1% formic acid((aq)) [80:20 (v/v)] was eluted at 0.2 mL/min. Quantification was performed on a triple-quadrupole mass spectrometer employing electrospray ionization, and the ion transitions were monitored in multiple reaction-monitoring mode. The monitored transitions for aceclofenac, diclofenac, 4'-OH-diclofenac, 4'-OH-aceclofenac and flufenamic acid were m/z 352.9-->74.9, 296.1-->251.7, 311.8-->267.7, 368.9-->74.9, and 279.9-->235.9, respectively. The coefficient of variation of the assay precision was less than 6.5%, and the accuracy ranged from 93% to 103%. The limits of detection were 2 ng/mL for aceclofenac and 0.2 ng/mL for both diclofenac and 4'-OH-diclofenac. This method was used successfully to measure the concentrations of aceclofenac and its three metabolites in plasma from healthy subjects after administration of a single 100-mg oral dose of aceclofenac. This analytic method is a very simple, sensitive, and accurate way to determine the pharmacokinetics of aceclofenac and its metabolites.

摘要

一种基于液相色谱-串联质谱的新方法可同时测定血浆中的醋氯芬酸及其三种代谢物(4'-羟基醋氯芬酸、双氯芬酸和4'-羟基双氯芬酸)。血浆样品经乙腈诱导蛋白质沉淀后,将醋氯芬酸、4'-羟基醋氯芬酸、双氯芬酸、4'-羟基双氯芬酸和氟芬那酸(内标)在反相C(18)分析柱上进行色谱分离。以乙腈/0.1%甲酸(水溶液)[80:20(v/v)]作为等度流动相,以0.2 mL/min的流速洗脱。采用电喷雾电离在三重四极杆质谱仪上进行定量分析,并在多反应监测模式下监测离子跃迁。醋氯芬酸、双氯芬酸、4'-羟基双氯芬酸、4'-羟基醋氯芬酸和氟芬那酸的监测跃迁分别为m/z 352.9→74.9、296.1→251.7、311.8→267.7、368.9→74.9和279.9→235.9。该分析方法的精密度变异系数小于6.5%,准确度范围为93%至103%。醋氯芬酸的检测限为2 ng/mL,双氯芬酸和4'-羟基双氯芬酸的检测限均为0.2 ng/mL。该方法成功用于测定健康受试者单次口服100 mg醋氯芬酸后血浆中醋氯芬酸及其三种代谢物的浓度。这种分析方法是测定醋氯芬酸及其代谢物药代动力学的一种非常简单、灵敏且准确的方法。

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