Flow injection with chemical reaction interface-isotope ratio mass spectrometry:: An alternative to off-line combustion for detecting low levels of enriched 13C in mass balance studies

被引:9
作者
Chen, P [1 ]
Teffera, Y [1 ]
Black, GE [1 ]
Abramson, FP [1 ]
机构
[1] George Washington Univ, Sch Med & Hlth Sci, Dept Pharmacol RE6640, Washington, DC 20037 USA
关键词
D O I
10.1016/S1044-0305(98)00133-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have evaluated the potential of flow injection chemical reaction interface isotope-ratio mass spectrometry to replace radioactive labeling techniques in material balance studies. A sample is flow injected and transmitted through a desolvation system followed by combustion to form (CO2)-C-13 with a microwave-powered chemical reaction interface. We can detect trace amounts of a C-13-labeled drug (3'-azido-3'-deoxythymidine, AZT) in urine or feces. Our ability to quantify less than 100 ng/mL of excess C-13 (similar to 1 mu g/mL of C-13-labeled AZT) from a sample equivalent to 10 mu L of urine is superior to previous detection limits for C-13 in urine that use off-line combustion methods. Parallel studies using C-14-labeled AZT showed that our stable isotope method provides comparable percent excretion data for urine and feces. These results support previous findings that mass balance studies could be carried out with isotope-ratio mass spectrometer, here using doses as low as 1-2 mg/kg. (J Am Soc Mass Spectrom 1999, 10, 153-158) (C) 1999 American Society for Mass Spectrometry.
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收藏
页码:153 / 158
页数:6
相关论文
共 13 条
[1]  
Abramson FP, 1996, DRUG METAB DISPOS, V24, P697
[2]   CRIMS - CHEMICAL-REACTION INTERFACE MASS-SPECTROMETRY [J].
ABRAMSON, FP .
MASS SPECTROMETRY REVIEWS, 1994, 13 (04) :341-356
[3]  
AHMED AE, 1991, J PHARMACOL EXP THER, V257, P479
[4]   PERFORMANCE OF HUMAN MASS BALANCE METABOLITE IDENTIFICATION STUDIES USING STABLE ISOTOPE (C-13, N-15) LABELING AND CONTINUOUS-FLOW ISOTOPE-RATIO MASS-SPECTROMETRY AS AN ALTERNATIVE TO RADIOACTIVE LABELING METHODS [J].
BROWNE, TR ;
SZABO, GK ;
AJAMI, A ;
WAGNER, D .
JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 33 (03) :246-252
[5]  
CHEN P, 1997, P 45 ASMS C MASS SPE, P707
[6]  
DEMIRANDA P, 1990, DRUG METAB DISPOS, V18, P315
[7]   Liquid chromatography chemical reaction interface mass spectrometry as an alternative to radioisotopes for quantitative drug metabolism studies [J].
Goldthwaite, CA ;
Hsieh, FY ;
Womble, SW ;
Nobes, FJ ;
Blair, A ;
Klunk, LJ ;
Mayol, RF .
ANALYTICAL CHEMISTRY, 1996, 68 (17) :2996-3001
[8]   RAPID PROCEDURE FOR ISOLATION OF DRUGS AND DRUG METABOLITES FROM PLASMA [J].
HORNING, MG ;
HORNING, EC ;
BOUCHER, EA ;
STAFFORD, M .
CLINICA CHIMICA ACTA, 1972, 37 (NMAR) :381-&
[9]   Element- and isotope-specific detection for high-performance liquid chromatography using chemical reaction interface mass spectrometry [J].
McLean, M ;
Vestal, ML ;
Teffera, Y ;
Abramson, FP .
JOURNAL OF CHROMATOGRAPHY A, 1996, 732 (02) :189-199
[10]  
Miller J. C., 1993, STAT ANAL CHEM, P117