Identification of new urinary metabolites of famprofazone in humans

被引:11
|
作者
Shin, HS [1 ]
Park, BB
Choi, SN
Oh, JJ
Hong, CP
Ryu, H
机构
[1] Kongju Natl Univ, Dept Environm Educ, Kong Ju 314701, Chungcheungnam, South Korea
[2] Kongju Natl Univ, Dept Chem, Kong Ju 314701, Chungcheungnam, South Korea
[3] Kongju Natl Univ, Dept Chem Educ, Kong Ju 314701, Chungcheungnam, South Korea
关键词
D O I
10.1093/jat/22.1.55
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Urinary metabolites of famprofazone following oral administration in humans were identified by gas chromatography-mass spectrometry with electron impact-ionization and comparison with the spectra and retention times of authentic standards. The metabolites were determined following selective derivatization with N-methyl-bis-trifluoroacetamide (MBTFA) and N-methyl-N- trimethyl silyl trifluoroacetamide (MSTFA). Famprofazone was rapidly and extensively metabolized by N-dealkylation, β-hydroxylation, and p- hydroxylation. The major metabolite, representing approximately 15% of the dose, was methamphetamine. The other metabolites, which were present in minor amounts, were amphetamine, norephedrine, norpseudoephedrine, ephedrine, pseudoephedrine, p hydroxyamphetamine, p-hydroxymethamphetamine, and p- hydroxydemethyl famprofazone.
引用
收藏
页码:55 / 60
页数:6
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