Evaluation of various derivatization approaches for gas chromatography-mass spectrometry analysis of buprenorphine and norbuprenorphine

被引:8
作者
Wu, Chih-Hung [1 ]
Yang, Shu-Ching [1 ]
Wang, Yu-Shan [1 ]
Chen, Bud-Gen [1 ]
Lin, Ching-Chiang [1 ]
Liu, Ray H. [1 ]
机构
[1] Fooyin Univ, Dept Med Technol, Kaohsiung 83102, Taiwan
关键词
buprenorphine; alkylation; acylation; silylation; derivatization; GC-MS;
D O I
10.1016/j.chroma.2007.11.063
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Various chemical derivatization approaches have been adapted for the analysis of buprenorphine and its major metabolite (norbuprenorphine) by GC-MS based methodologies. These approaches included alkylation, acylation, and silylation resulting in the formation of methyl, acetyl, trifluoroacetyl, pentafluoropropionyl, heptafluorobutyryl, and trimethylsilyl derivatives. This study conducted a comprehensive evaluation on the merits of these approaches based on the following criteria: reaction yields and ionization efficiency of the derivatization products; chromatographic characteristics; and cross-contributions to the intensities of ions designating the analytes and the internal standards. Under acidic derivatization conditions, the analytes could form three artifact products. Overall, derivatization by acetyl anhydride resulted in best performance characteristics. (c) 2008 Published by Elsevier B.V.
引用
收藏
页码:93 / 112
页数:20
相关论文
共 22 条
[1]   Evaluation of buprenorphine CEDIA assay versus GC-MS and ELISA using urine samples from patients in substitution treatment [J].
Böttcher, M ;
Beck, O .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2005, 29 (08) :769-776
[2]  
CHEN BG, IN PRESS J AM SOC MA
[3]  
CONE EJ, 1984, DRUG METAB DISPOS, V12, P577
[4]   STABILITY OF THE "6,14-ENDO-ETHANOTETRAHYDROORIPAVINE ANALGESICS - ACID-CATALYZED REARRANGEMENT OF BUPRENORPHINE [J].
CONE, EJ ;
GORODETZKY, CW ;
DARWIN, WD ;
BUCHWALD, WF .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (02) :243-246
[5]   The hair analysis proficiency testing program of the French Society of Analytical Toxicology [J].
Deveaux, M ;
Kintz, P ;
Goullé, JP ;
Bessard, J ;
Pépin, G ;
Gosset, D .
FORENSIC SCIENCE INTERNATIONAL, 2000, 107 (1-3) :389-394
[6]  
DICANDIA D, 2003, CONTRIBUTI ORIGNALI, V24, P19
[7]  
Everhart ET, 1997, CLIN CHEM, V43, P2292
[8]   Opioid receptor imaging and displacement studies with [6-O-[C-11]methyl]buprenorphine in baboon brain [J].
Galynker, I ;
Schlyer, DJ ;
Dewey, SL ;
Fowler, JS ;
Logan, J ;
Gatley, J ;
MacGregor, RR ;
Ferrieri, RA ;
Holland, MJ ;
Brodie, J ;
Simon, E ;
Wolf, AP .
NUCLEAR MEDICINE AND BIOLOGY, 1996, 23 (03) :325-331
[9]   The development and application of a rapid gas chromatography-mass spectrometry method to monitor buprenorphine withdrawal protocols [J].
George, S ;
George, C ;
Chauhan, A .
FORENSIC SCIENCE INTERNATIONAL, 2004, 143 (2-3) :121-125
[10]   Characterization of the pharmacokinetics of buprenorphine and norbuprenorphine in rats after intravenous bolus administration of buprenorphine [J].
Gopal, S ;
Tzeng, TB ;
Cowan, A .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 15 (03) :287-293