INFLUENCE OF METABOLITES ON PROTEIN-BINDING OF VERAPAMIL ENANTIOMERS

被引:6
|
作者
JOHNSON, JA
AKERS, WS
机构
[1] Department of Clinical Pharmacy, College of Pharmacy, University of Tennessee, Memphis
关键词
VERAPAMIL; ENANTIOMERS; PROTEIN BINDING; METABOLITES;
D O I
10.1111/j.1365-2125.1995.tb04492.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study investigated the effect of verapamil metabolites on R-and S-verapamil protein binding in plasma samples collected from subjects prior to rac-verapamil dosing and following single dose and steady state rac-verapamil dosing. Iri vitro studies of the effects of norverapamil, D617 and D620 on R- and S-verapamil protein binding were also performed. Protein binding of R- and S-verapamil was unchanged following single and multiple doses of rac-verapamil as compared with protein binding in pre-dose samples. In vitro, norverapamil had no effect on R- and S-verapamil protein binding up to 1000 ng ml(-1). Norverapamil 5000 ng ml(-1) caused a 30% increase in free fraction of both R- and S-verapamil. D617 and D620 concentrations up to 5000 ng ml(-1) had no effect on R- and S-verapamil protein binding. We conclude the metabolites of verapamil have no clinically significant effect on R- and S-verapamil protein binding.
引用
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页码:536 / 538
页数:3
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