Systematic and comprehensive strategy for reducing matrix effects in LC/MS/MS analyses

被引:615
作者
Chambers, Erin [1 ]
Wagrowski-Diehl, Diane M. [1 ]
Lu, Ziling [1 ]
Mazzeo, Jeffrey R. [1 ]
机构
[1] Waters Corp, Chem Appl Technol, Milford, MA 01757 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2007年 / 852卷 / 1-2期
关键词
matrix effects; quantitative bioanalysis; mass spectrometry; phospholipids; UPLC; HPLC; sample preparation;
D O I
10.1016/j.jchromb.2006.12.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A systematic, comprehensive strategy that optimizes sample preparation and chromatography to minimize matrix effects in bioannalytical LC/MS/MS assays was developed. Comparisons were made among several sample preparation methods, including protein precipitation (PPT), liquid-liquid extraction (LLE), pure cation exchange solid-phase extraction (SPE), reversed-phase SPE and mixed-mode SPE. The influence of mobile phase pH and gradient duration on the selectivity and sensitivity for both matrix components and basic analytes was investigated. Matrix effects and overall sensitivity and resolution between UPLC (R) technology and HPLC were compared. The amount of specific matrix components, or class of matrix components, was measured in the sample preparation extracts by LC/MS/MS with electrospray ionization (ESI) using both precursor ion scanning mode and multiple reaction monitoring (MRM). PPT is the least effective sample preparation technique, often resulting in significant matrix effects due to the presence of many residual matrix components. Reversed-phase and pure cation exchange SPE methods resulted in cleaner extracts and reduced matrix effects compared to PPT. The cleanest extracts, however, were produced with polymeric mixed-mode SPE (both reversed-phase and ion exchange retention mechanisms). These mixed-mode sorbents dramatically reduced the levels of residual matrix components from biological samples, leading to significant reduction in matrix effects. LLE also provided clean final extracts. However, analyte recovery, particularly for polar analytes, was very low. Mobile phase pH was manipulated to alter the retention of basic compounds relative to phospholipids, whose retention tends to be relatively independent of pH. In addition to the expected resolution, speed and sensitivity benefits of UPLC (R) technology, a paired t-test demonstrated a statistically significant improvement with respect to matrix effects when this technology was chosen over traditional HPLC. The combination of polymeric mixed-mode SPE, the appropriate mobile phase pH and UPLC (R) technology provides significant advantages for reducing matrix effects resulting from plasma matrix components and in improving the ruggedness and sensitivity of bioanalytical methods. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 34
页数:13
相关论文
共 42 条
[1]  
AHNOFF M, 2004, POSTER MPN211
[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]  
BENNETT P, 2003, POSTER 6006
[4]  
BENNETT P, TANDEM CAPABILITIES
[5]   Liquid chromatography/tandem mass spectrometry method for simultaneous determination of risperidone and its active metabolite 9-hydroxyrisperidone in human plasma [J].
Bhatt, Jignesh ;
Subbaiah, Gunta ;
Singh, Sadhana .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2006, 20 (14) :2109-2114
[6]   AN ALTERNATIVE EXPEDITIOUS ANALYSIS OF PHOSPHOLIPID-COMPOSITION IN HUMAN BLOOD-PLASMA BY P-31 NMR-SPECTROSCOPY [J].
BRADAMANTE, S ;
BARCHIESI, E ;
BARENGHI, L ;
ZOPPI, F .
ANALYTICAL BIOCHEMISTRY, 1990, 185 (02) :299-303
[7]   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
[8]   Matrix effects on accurate mass measurements of low-molecular weight compounds using liquid chromatography-electrospray-quadrupole time-of-flight mass spectrometry [J].
Calbiani, F ;
Careri, M ;
Elviri, L ;
Mangia, A ;
Zagnoni, I .
JOURNAL OF MASS SPECTROMETRY, 2006, 41 (03) :289-294
[9]  
CAPKA V, TANDEM CAPABILITIES
[10]   Chiral liquid chromatography-tandem mass spectrometric methods for stereoisomeric pharmaceutical determinations [J].
Chen, JW ;
Korfmacher, WA ;
Hsieh, Y .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 820 (01) :1-8