IDENTIFICATION OF URINARY AND BILIARY METABOLITES OF ALPRENOLOL IN THE RAT

被引:15
作者
HOFFMANN, KJ
ARFWIDSSON, A
BORG, KO
SKANBERG, I
机构
[1] Research Laboratories, AB Hässle, Fack, S-431 20, Mölndal
关键词
D O I
10.3109/00498257909038710
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. After oral administration of alprenolol to rat, 12 metabolites were isolated and characterized as trifiuoroacetyl, trimethylsilyl and n-butylboronate derivatives, using a g.l.c.-mass spectrometry-computer system. Fragmentation pathways of derivatives in the mass-spectrometric. analysis are discussed. 2. Metabolic reactions involved are oxidative degradation of the propanoliso-propylamine side-chain, aromatic hydroxylation, oxidation of the allyl group, and conjugation. A method for direct analysis of epoxide functions in the allyl group is described. 3. In comparison with metabolism of alprenolol in vitro, more polar metabolites are formed in vivo but the same principal metabolic pathways are valid. Structural features for biliary excretion are discussed. © 1979 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
引用
收藏
页码:93 / 106
页数:14
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