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Stereoselective interaction between the R enantiomer of warfarin and cimetidine.

机译:华法林的R对映异构体和西咪替丁之间的立体选择性相互作用。

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摘要

The stereoselectivity of the pharmacokinetic interaction between warfarin and cimetidine was investigated in eight healthy volunteers. The warfarin enantiomers were given separately as single doses (15 mg) alone and during chronic administration of cimetidine (1 g day-1). Cimetidine did not interact with S warfarin but there was an interaction with the R enantiomer of warfarin. Cimetidine caused a significant increase in the mean plasma half-life of R warfarin (from 47.8 h to 57.8 h) and a significant decrease in its mean plasma clearance (from 2.3 to 1.7 ml h-1 kg-1) (P less than 0.02). Administration of a pharmacological dose of vitamin K1 together with the enantiomers of warfarin was necessary clinically and resulted in elevation of vitamin K1 2,3-epoxide concentrations, which were similar in each case.
机译:在八名健康志愿者中研究了华法林与西咪替丁之间药代动力学相互作用的立体选择性。华法林对映体分别以单剂量(15 mg)和在长期服用西咪替丁期间(1 g day-1)服用。西咪替丁不与华法林S相互作用,但与华法林R对映异构体存在相互作用。西咪替丁引起华法林R的平均血浆半衰期显着增加(从47.8 h到57.8 h),并且平均血浆清除率显着降低(从2.3 ml -1 h-1 kg-1减少)(P小于0.02) )。临床上必须给予药理剂量的维生素K1和华法林对映异构体,导致维生素K1的2,3-环氧化物浓度升高,每种情况下相似。

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