ORAL PHARMACOKINETICS OF FLUAZIFOP-BUTYL IN HUMAN VOLUNTEERS

被引:11
作者
WOOLLEN, BH
HART, TB
BATTEN, PL
LAIRD, WJD
DAVIES, DS
DOLLERY, CT
机构
[1] ICI PLC,AGROCHEM,FERNHURST,ENGLAND
[2] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT CLIN PHARMACOL,LONDON W12 0HS,ENGLAND
来源
HUMAN & EXPERIMENTAL TOXICOLOGY | 1991年 / 10卷 / 01期
关键词
D O I
10.1177/096032719101000107
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1 Fluazifop-butyl, the active ingredient of FUSILADE, a selective herbicide, was administered orally to three male volunteers at a dose level of 0.07 mg kg-1 body weight. Over a period of 6 d between 80 and 93% of the dose was excreted in urine as the metabolite fluazifop, the majority within the first 24 h. Peak plasma concentrations of fluazifop occurred 1-2.5 h after administration. 2 The elimination of fluazifop from plasma and urine can be described by a one-compartment pharmacokinetic model and the elimination half-life was estimated from blood and urine data to be within the range 9-37 h. Fluazifop was found to bind to serum proteins. 3 The study indicates that the amount of fluazifop-butyl absorbed in exposed persons can be assessed by measuring fluazifop concentrations in urine.
引用
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页码:39 / 43
页数:5
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