DEVELOPMENT OF A FE-19-NMR METHOD FOR STUDIES ON THE INVIVO AND INVITRO METABOLISM OF 2-FLUOROANILINE

被引:47
作者
VERVOORT, J [1 ]
DEJAGER, PA [1 ]
STEENBERGEN, J [1 ]
RIETJENS, IMCM [1 ]
机构
[1] AGR UNIV WAGENINGEN,DEPT MOLEC PHYS,6703 HA WAGENINGEN,NETHERLANDS
关键词
D O I
10.3109/00498259009046882
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. A 19F-n.m.r. method has been developed for study of the metabolism of 2-fluoroaniline both after in vivo exposure of rats and in in vitro model systems. 2. From the 19F-n.m.r. spectrum of the 24 h urine it was calculated that over 90% of the dose was excreted within 24 h. The metabolic pattern showed that 85% of the metabolites were para-hydroxylated, 72% sulphated, 13% glucuronidated and 29% N-acetylated, 4-amino-3-fluorophenyl sulphate being the main urinary metabolite (53%). 3. In vitro studies of phase I metabolism of 2-fluoroaniline with rat liver microsomes was representative for the in vivo metabolism as hydroxylation in both systems was observed only at the para-position. 4. Phase I + II metabolism was studied in vitro in either isolated rat hepatocytes in suspension or in a 1 h recirculating liver perfusion system. In both these in vitro systems para-hydroxylation, N-acetylation, sulphation and glucuronidation of 2-fluoroaniline were observed. The ratio between glucuronidation and sulphation was dependent on sulphate availability 5. Of the in vitro systems tested, hepatocytes in Krebs Ringer (sulphate limited) medium was the best model for in vivo metabolism. 6. The detection limit for fluoro-containing metabolites in this 19F-n.m.r. method was 1 μM for an overnight run using a Bruker CXP 300 spectrometer. From this it can be concluded that 19F-n.m.r. urine analysis is a useful tool in biomonitoring studies. For 2-fluoroaniline the method appears to be more sensitive than currently available h.p.l.c./t.l.c. methods. In addition, concentration of urine samples can result in either lower detection limits, or in shorter times needed for n.m.r. data acquisition. 7. N-acetylation is known to show genetic polymorphism. Therefore, the 19F-n.m.r. method, detecting all 2-fluoroaniline metabolites, has the additional advantage of eliminating the risk of obtaining false negatives for fast acetylators. © 1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
引用
收藏
页码:657 / 670
页数:14
相关论文
共 16 条
[1]  
AYMES JD, 1980, B SOC CHIM FR, V3, P175
[2]   THE METABOLISM OF 3-CHLORO-4-FLUORO-ANILINE IN DOG AND RAT [J].
BALDWIN, MK ;
HUTSON, DH .
XENOBIOTICA, 1980, 10 (02) :135-144
[3]   THE PREPARATION OF ORTHO-AMINOPHENYL SULPHATES [J].
BOYLAND, E ;
MANSON, D ;
SIMS, P .
JOURNAL OF THE CHEMICAL SOCIETY, 1953, (NOV) :3623-3628
[4]  
BRODIE BB, 1948, J PHARMACOL EXP THER, V94, P22
[5]   2,4-DIFLUOROANILINE AND 4-FLUOROANILINE EXPOSURE - MONITORING BY METHEMOGLOBIN AND URINE ANALYSES [J].
EADSFORTH, CV ;
LOGAN, CJ ;
MORRISON, BJ ;
WARBURTON, PA .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 1984, 54 (03) :223-232
[6]   THE METABOLISM OF ORTHO-FLUOROANILINE BY RATS, RABBITS AND MARMOSETS [J].
EADSFORTH, CV ;
COVENEY, PC ;
HUTSON, DH ;
LOGAN, CJ ;
SAMUEL, AJ .
XENOBIOTICA, 1986, 16 (06) :555-566
[7]   KINETICS OF THE FORMATION AND SECRETION OF THE ANILINE METABOLITE 4-AMINOPHENOL AND ITS CONJUGATES BY ISOLATED RAT HEPATOCYTES [J].
EVELO, CTA ;
VERSTEEGH, JFM ;
BLAAUBOER, BJ .
XENOBIOTICA, 1984, 14 (05) :409-416
[8]   BIOTRANSFORMATION OF NITROSOBENZENE, PHENYLHYDROXYLAMINE, AND ANILINE IN THE ISOLATED PERFUSED-RAT-LIVER [J].
EYER, P ;
KAMPFFMEYER, H ;
MAISTER, H ;
ROSCHOEHME, E .
XENOBIOTICA, 1980, 10 (7-8) :499-516
[9]  
GROSSMAN SJ, 1986, DRUG METAB DISPOS, V14, P689
[10]  
PAINE AJ, 1979, LIVER QUANTITATIVE A, P215