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小鼠血浆中双氯芬酸及其三种主要代谢物的液相色谱-串联质谱测定法

Liquid chromatography-tandem mass spectrometric assay for diclofenac and three primary metabolites in mouse plasma.

作者信息

Sparidans Rolf W, Lagas Jurjen S, Schinkel Afred H, Schellens Jan H M, Beijnen Jos H

机构信息

Universiteit Utrecht, Faculty of Science, Department of Pharmaceutical Sciences, Section of Biomedical Analysis, Division of Drug Toxicology, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Sep 1;872(1-2):77-82. doi: 10.1016/j.jchromb.2008.07.012. Epub 2008 Jul 18.

Abstract

The first liquid chromatography-tandem mass spectrometric assay for the simultaneous determination of diclofenac, 4'-hydroxy-diclofenac, 5-hydroxy-diclofenac and diclofenac-acyl-glucuronide in mouse plasma, using a simple sample pre-treatment procedure, was developed and validated. Analytes in plasma were stabilized using acetic acid and ascorbic acid. After addition of the internal standard D(4)-diclofenac to a 10 microl sample volume and protein precipitation with acetonitrile, the supernatant was supplemented with an equal volume of water and injected into the chromatographic system. A polar embedded reversed-phase column with gradient elution using formic acid and ammonium acetate in water-methanol were used. The eluate was totally transferred into an electrospray interface with positive ionization and the analytes were quantified using triple quadrupole mass spectrometry. The assay was validated in the ranges 10-5000 ng/ml for 4'-hydroxy-diclofenac and 20-10,000 ng/ml for the other analytes, the lowest levels of these ranges (10 or 20 ng/ml) being the lower limits of quantification. Within day precisions were < or = 10%, between day precisions < or = 13% and accuracies were between 90 and 108%. The analytes were chemically stable under all relevant conditions. The assay was successfully applied in a pharmacokinetic study with diclofenac in mice.

摘要

建立并验证了首个采用简单样品预处理程序同时测定小鼠血浆中双氯芬酸、4'-羟基双氯芬酸、5-羟基双氯芬酸和双氯芬酸酰基葡萄糖醛酸苷的液相色谱-串联质谱分析法。血浆中的分析物用乙酸和抗坏血酸进行稳定化处理。向10微升样品体积中加入内标D(4)-双氯芬酸并用乙腈进行蛋白沉淀后,向上清液中加入等体积的水并注入色谱系统。使用在水-甲醇中采用甲酸和乙酸铵进行梯度洗脱的极性内嵌反相柱。洗脱液完全转移至带正离子化的电喷雾接口,分析物采用三重四极杆质谱法进行定量。该分析法在4'-羟基双氯芬酸10 - 5000纳克/毫升以及其他分析物20 - 10,000纳克/毫升的范围内进行了验证,这些范围的最低水平(10或20纳克/毫升)为定量下限。日内精密度≤10%,日间精密度≤13%,准确度在90%至108%之间。分析物在所有相关条件下化学性质稳定。该分析法成功应用于双氯芬酸在小鼠体内的药代动力学研究。

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