Identification and quantification of metabolites of 2,3,5,6-tetrafluoro-4-trifluoromethylaniline in rat urine using 19F nuclear magnetic resonance spectroscopy, high-performance liquid chromatography-nuclear magnetic resonance spectroscopy and high-performance liquid chromatography-mass spectrometry
被引:8
作者:
Scarfe, GB
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机构:Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
Scarfe, GB
Clayton, E
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机构:Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
Clayton, E
Wilson, ID
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机构:Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
Wilson, ID
Nicholson, JK
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机构:Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
Nicholson, JK
机构:
[1] Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, London SW7 2AZ, England
[2] AstraZeneca Pharmaceut, Dept Drug Metab & Pharmacokinet, Macclesfield SK10 4TG, Cheshire, England
来源:
JOURNAL OF CHROMATOGRAPHY B
|
2000年
/
748卷
/
01期
关键词:
2,3,5,6-tetrafluoro-4-trifluoromethylaniline;
D O I:
10.1016/S0378-4347(00)00321-2
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The urinary excretion profile and identity of the metabolites of 2,3,5,6-tetrafluoro-4-triflouromethylaniline, following i.p. administration to the rat at 50 mg kg(-1), were determined using a combination of F-19-NMR, HPLC-NMR and HPLC-MS. A total of 388 of the dose was eliminated in the urine as five metabolites. The major routes of metabolism were N-glucuronidation, sulfation and oxidation with a significant amount of metabolic defluorination to give a number of ortho-ring hydroxylated metabolites. The oxidised metabolites were excreted as glucuronide and/or sulfate conjugates. (C) 2000 Elsevier Science B.V. All rights reserved.