Matrix effects: The Achilles heel of quantitative high-performance liquid chromatography-electrospray-tandem mass spectrometry

被引:1024
作者
Taylor, PJ
机构
[1] Princess Alexandra Hosp, Dept Clin Pharmacol, Brisbane, Qld 4102, Australia
[2] Princess Alexandra Hosp, Australian Bioanalyt Serv Pty Ltd, Brisbane, Qld 4102, Australia
关键词
electrospray; tandem mass spectrometry; matrix effects; quantitation;
D O I
10.1016/j.clinbiochem.2004.11.007
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
High-performance liquid chromatography coupled by an electrospray ion source to a tandem mass spectrometer (HPLC-EST-MS/ MS) is the current analytical method of choice for quantitation of analytes in biological matrices. With HPLC-ESI-MS/MS having the characteristics of high selectivity, sensitivity, and throughput, this technology is being increasingly used in the clinical laboratory. An important issue to be addressed in method development, validation, and routine use of HPLC-ESI-MS/MS is matrix effects. Matrix effects are the alteration of ionization efficiency by the presence of coeluting substances. These effects are unseen in the chromatograrn but have deleterious impact on methods accuracy and sensitivity. The two common ways to assess matrix effects are either by the postextraction addition method or the postcolumn infusion method. To remove or minimize matrix effects, modification to the sample extraction methodology and improved chromatographic separation must be performed. These two parameters are linked together and form the basis of developing a successful and robust quantitative HPLC-EST-MS/MS method. Due to the heterogenous nature of the population being studied, the variability of a method must be assessed in samples taken from a variety of subjects. In this paper, the major aspects of matrix effects are discussed with an approach to address matrix effects during method validation proposed. (c) 2004 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:328 / 334
页数:7
相关论文
共 44 条
[1]   Ion suppression in mass spectrometry [J].
Annesley, TM .
CLINICAL CHEMISTRY, 2003, 49 (07) :1041-1044
[2]   Quantitative characterization of differential ion suppression on liquid chromatography/atmospheric pressure ionization mass spectrometric bioanalytical methods [J].
Avery, MJ .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (03) :197-201
[3]  
Bayliss MK, 2000, RAPID COMMUN MASS SP, V14, P2039, DOI 10.1002/1097-0231(20001115)14:21<2039::AID-RCM130>3.0.CO
[4]  
2-2
[5]  
Bonfiglio R, 1999, RAPID COMMUN MASS SP, V13, P1175, DOI 10.1002/(SICI)1097-0231(19990630)13:12<1175::AID-RCM639>3.3.CO
[6]  
2-S
[7]   Atmospheric pressure ionization LC/MS/MS techniques for drug disposition studies [J].
Brewer, E ;
Henion, J .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (04) :395-402
[8]   LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY WITH IONSPRAY AND ELECTROSPRAY INTERFACES IN PHARMACEUTICAL AND BIOMEDICAL-RESEARCH [J].
BRUINS, AP .
JOURNAL OF CHROMATOGRAPHY, 1991, 554 (1-2) :39-46
[9]   Quantitation of SR 27417 in human plasma using electrospray liquid chromatography tandem mass spectrometry: A study of ion suppression [J].
Buhrman, DL ;
Price, PI ;
Rudewicz, PJ .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1996, 7 (11) :1099-1105
[10]   Development of a method for rapid quantitation of amino acids by liquid chromatography-tandem mass spectrometry (LC-MSMS) in plasma [J].
Casetta, B ;
Tagliacozzi, D ;
Shushan, B ;
Federici, G .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2000, 38 (05) :391-401