Determination of buprenorphine and norbuprenorphine in whole blood by liquid chromatography mass spectrometry

被引:49
作者
Hoja, H
Marquet, P
Verneuil, B
Lotfi, H
Dupuy, JL
Lachatre, G
机构
[1] UNIV HOSP LIMOGES,DEPT PHARMACOL & TOXICOL,F-87042 LIMOGES,FRANCE
[2] FAC PHARM,TOXICOL LAB,F-87025 LIMOGES,FRANCE
关键词
D O I
10.1093/jat/21.2.160
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and highly specific method for the determination of buprenorphine and norbuprenorphine in postmortem and hemolyzed whole blood using combined liquid chromatography and mass spectrometry (LC-MS) with electrospray ionization was developed. After enzymatic hydrolysis and deproteinization with acetonitrile, Extrelut-3 cartridges were used for a preliminary basic sample cleanup. Elution by toluene-ether (50:50, v/v) was followed by an acid wash with 0.05M H3PO4 and a basic re-extraction into ether. A Nucleosil C18 (150 x 1-mm i.d.) reversed-phase column was used for the chromatographic separation together with a mixture of 2mM ammonium formate buffer (pH 3) and acetonitrile (55:45, v/v) as the mobile phase. Recoveries were between 56 and 60%, and detection limits were 0.05 ng/mL for both analyses. The coefficient of variation for repeatability was lower than 4%. Limits of quantitation were 0.1 ng/mL for buprenorphine and norbuprenorphine. Reproducibility was good, and linearity was excellent in the range of 0.1 to 100 ng/mL (r > 0.9999, n = 7).
引用
收藏
页码:160 / 165
页数:6
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