Method for internal standard introduction for quantitative analysis using on-line solid-phase extraction LC-MS/MS

被引:11
作者
Alnouti, Y [1 ]
Li, M [1 ]
Kavetskaia, O [1 ]
Bi, HG [1 ]
Hop, CECA [1 ]
Gusev, AI [1 ]
机构
[1] Pfizer Global Res & Dev, Groton, CT 06340 USA
关键词
D O I
10.1021/ac051806q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel approach for on-line introduction of internal standard (IS) for quantitative analysis using LC-MS/MS has been developed. In this approach, analyte and IS are introduced into the sample injection loop in different steps. Analyte is introduced into the injection loop using a conventional autosampler (injector) needle pickup from a sample vial. IS is introduced into the sample injection loop on-line from a microreservoir containing the IS solution using the autosampler. As a result, both analyte and IS are contained in the sample loop prior to the injection into the column. Methodology allowed to reliably introduce IS and demonstrated injection accuracy and precision comparable to those obtained using off-line IS introduction (i.e., IS and analyte are premixed before injection) while maintaining chromatographic parameters (i.e., analyte and IS elution time and peak width). This new,, technique was applied for direct analysis of model compounds in rat plasma using on-line solid-phase extraction (SPE) LC-MS/MS quantification. In combination with on-line SPE, IS serves as a surrogate IS and compensates for signal variations attributed to sample preparation and instrumentation factors including signal suppression. The assays yielded accuracy (85-119%), precision (2-16%), and analyte recovery comparable to those obtained using off-line IS introduction. Furthermore, on-line IS introduction allows for nonvolumetric sample (plasma) collection and direct analysis without the need of measuring and aliquoting a fixed sample volume prior to the on-line SPE LC-MS/MS analysis. Therefore, this methodology enables direct sample (plasma) analysis without any sample manipulation and preparation.
引用
收藏
页码:1331 / 1336
页数:6
相关论文
共 16 条
[1]   Development and application of a new on-line SPE system combined with LC-MS/MS detection for high throughput direct analysis of pharmaceutical compounds in plasma [J].
Alnouti, Y ;
Srinivasan, K ;
Waddell, D ;
Bi, HG ;
Kavetskaia, O ;
Gusev, AI .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1080 (02) :99-106
[2]   QUANTITATIVE TRACE ANALYSIS BY COMBINED CHROMATOGRAPHY AND MASS-SPECTROMETRY USING EXTERNAL AND INTERNAL STANDARDS [J].
BOYD, RK .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1993, 7 (04) :257-271
[3]   Postcolumn introduction of an internal standard for quantitative LC-MS analysis [J].
Choi, BK ;
Gusev, AI ;
Hercules, DM .
ANALYTICAL CHEMISTRY, 1999, 71 (18) :4107-4110
[4]   LC-MS/MS signal suppression effects in the analysis of pesticides in complex environmental matrices [J].
Choi, BK ;
Hercules, DM ;
Gusev, AI .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2001, 369 (3-4) :370-377
[5]   Deferred standards, an on-line qualification, validation and system stability probe for chromatographic assay [J].
Clarot, I ;
Dreyfuss, MF ;
Domelier, R ;
Battu, S ;
Cardot, PJP .
JOURNAL OF CHROMATOGRAPHY A, 2002, 958 (1-2) :79-88
[6]   A dual electrospray ionization source combined with hexapole accumulation to achieve high mass accuracy of biopolymers in fourier transform ion cyclotron resonance mass spectrometry [J].
Hannis, JC ;
Muddiman, DC .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2000, 11 (10) :876-883
[7]   Ionization enhancement in atmospheric pressure chemical ionization and suppression in electrospray ionization between target drugs and stable-isotope-labeled internal standards in quantitative liquid chromatography/tandem mass spectrometry [J].
Liang, HR ;
Foltz, RL ;
Meng, M ;
Bennett, P .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (24) :2815-2821
[8]  
Niessen WMA, 2000, REV ANAL CHEM, V19, P289
[9]   Determination of N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC) in urine by high-performance liquid chromatography combined with mass spectrometry [J].
Perico, A ;
Baglioni, S ;
Bavazzano, P .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2004, 18 (16) :1865-1868
[10]  
PINTO MS, 2002, ANAL CHIM ACTA, V466, P345