Liquid chromatography/atmospheric pressure ionization-mass spectrometry in drug metabolism studies

被引:273
作者
Kostiainen, R
Kotiaho, T
Kuuranne, T
Auriola, S
机构
[1] Univ Helsinki, Dept Pharm, Viikki Drug Discovery Technol Ctr, DDTC, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Pharm, Div Pharmaceut Chem, FIN-00014 Helsinki, Finland
[3] Univ Kuopio, Dept Pharmaceut Chem, FIN-70211 Kuopio, Finland
来源
JOURNAL OF MASS SPECTROMETRY | 2003年 / 38卷 / 04期
关键词
drug metabolism; liquid chromatography/atmospheric pressure ionization-mass spectrometry;
D O I
10.1002/jms.481
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The study of the metabolic fate of drugs is an essential and important part of the drug development process. The analysis of metabolites is a challenging task and several different analytical methods have been used in these studies. However, after the introduction of the atmospheric pressure ionization (API) technique, electrospray and atmospheric pressure chemical ionization, liquid chromatography/mass spectrometry (LC/MS) has become an important and widely used method in the analysis of metabolites owing to its superior specificity, sensitivity and efficiency. In this paper the feasibility of LC/API-MS techniques in the identification, structure characterization and quantitation of drug metabolites is reviewed. Sample preparation, LC techniques, isotope labeling, suitability of different MS techniques, such as tandem mass spectrometry, and high-resolution MS in drug metabolite analysis, are summarized and discussed. Automation of data acquisition and interpretation, special techniques and possible future trends are also the topics of the review. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:357 / 372
页数:16
相关论文
共 152 条
  • [51] Fernández-Metzler CL, 1999, DRUG METAB DISPOS, V27, P32
  • [52] FOUDA HG, 1993, 41 ANN ASMS C MASS S, pA49
  • [53] Structural elucidation of metabolites of ritonavir and indinavir by liquid chromatography-mass spectrometry
    Gangl, E
    Utkin, I
    Gerber, N
    Vouros, P
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2002, 974 (1-2) : 91 - 101
  • [54] Evaluation of accelerator mass spectrometry in a human mass balance and pharmacokinetic study-experience with 14C-labeled (R)-6-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone (R115777), a farnesyl transferase inhibitor
    Garner, RC
    Goris, I
    Laenen, AAE
    Vanhoutte, E
    Meuldermans, W
    Gregory, S
    Garner, JV
    Leong, D
    Whattam, M
    Calam, A
    Snel, CAW
    [J]. DRUG METABOLISM AND DISPOSITION, 2002, 30 (07) : 823 - 830
  • [55] A review of membrane sampling from biological tissues with applications in pharmacokinetics, metabolism and pharmacodynamics
    Garrison, KE
    Pasas, SA
    Cooper, JD
    Davies, MI
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 17 (1-2) : 1 - 12
  • [56] Gibson G.G., 1994, Introduction to Drug Metabolism, V2nd, P1
  • [57] GILBERT JD, 1995, ACS S SERIES, V619
  • [58] Analysis of O-glucuronide conjugates in urine by electrospray ion trap mass spectrometry
    Gu, JK
    Zhong, DF
    Chen, XY
    [J]. FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1999, 365 (06): : 553 - 558
  • [59] HENDEE WR, 1973, RADIOACTIVE ISOTOPES
  • [60] Increasing bioanalytical throughput using pcSFC-MS/MS: 10 minutes per 96-well plate
    Hoke, SH
    Tomlinson, JA
    Bolden, RD
    Morand, KL
    Pinkston, JD
    Wehmeyer, KR
    [J]. ANALYTICAL CHEMISTRY, 2001, 73 (13) : 3083 - 3088