Liquid chromatography-electrospray mass spectrometry determination of free and total concentrations of ropivacaine in human plasma

被引:20
作者
Mathieu, O
Hillaire-Buys, D
Dadure, C
Barnay, F
Mathieu-Daudé, JC
Bressolle, F
机构
[1] Univ Montpellier I, Fac Pharm, Clin Pharmacokinet Lab, F-34093 Montpellier 5, France
[2] Lapeyronie Hosp, Intens Care Unit, Montpellier, France
[3] Arnaud de Villeneuve Hosp, INSERM, U454, Montpellier, France
[4] Lapeyronie Hosp, Dept Med Pharmacol & Toxicol, Montpellier, France
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2006年 / 831卷 / 1-2期
关键词
ropivacaine; local anaesthetics; equilibrium-dialysis; plasma; quantitation LC-ESI-MS;
D O I
10.1016/j.jchromb.2005.11.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A specific and sensitive liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) method was developed for the determination of free and total ropivacaine in human plasma. The work-up procedure involved a simple precipitation of plasma proteins with methanol. Etidocaine served as the internal standard. After microscale equilibrium-dialysis, measurement of free ropivacaine levels was performed after direct injection of the dialysate into the chromatograph. The system used a Zorbax eclipse XD8 C8 analytical column packed with 5 mu m diameter particles as the stationary phase. The mobile phase consisted of a 15-min gradient (mobile phase A: 0.05% (v/v) trimethylamine in acetonitrile, mobile phase 13: 2 mM ammonium formate buffer (pH 3)). Mass spectrometric data were acquired in single ion monitoring mode at m/z 275 for ropivacaine and m/z 277 for etidocaine. The drug/internal standard peak area ratios (plasma) or peak areas (dialysate) were linked via a quadratic relationship to concentrations. Precision ranged from I to 7.6% and accuracy was between 92.6 and 109%. The lower limits of quantitation were 1 mu g/1 in plasma and 2 mu g/l in the dialysate. This method was found suitable for the analysis of plasma samples collected during a clinical trial performed in 30 infants undergoing epidural anaesthesia or continuous psoas compartment block. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 98
页数:8
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