Literature DB >> 6121675

Comparative pharmacokinetics of frusemide in female rhesus monkeys, cynomolgus monkeys and baboons.

E Doyle, L F Chasseaud, J N Miller.   

Abstract

1. The pharmacokinetics of frusemide have been compared in 3 non-human primate species after single intravenous dose of 3 mg/kg of the drug. 2. Peak mean plasma concentrations of frusemide were 31.6, 33.6, 43.6 micrograms/ml in the rhesus monkey, cynomolgus monkey and baboon respectively, and concentrations declined with a half-life of about 20 min. 3. There were no notable differences in the pharmacokinetic parameters estimated from either a one-compartment or two-compartment open model. 4. There were statistically significant species-related differences in clearance, half-lives and volumes of distribution adjusted for bodyweight. 5. The pharmacokinetics of frusemide in the cynomolgus monkey are closer to those in man than are those in the rhesus monkey, the baboon or other commonly used laboratory animal species.

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Year:  1982        PMID: 6121675     DOI: 10.1016/0306-4492(82)90015-6

Source DB:  PubMed          Journal:  Comp Biochem Physiol C        ISSN: 0306-4492


  2 in total

1.  SB-239063, a potent and selective inhibitor of p38 map kinase: preclinical pharmacokinetics and species-specific reversible isomerization.

Authors:  K W Ward; J W Proksch; L M Azzarano; K L Salyers; J E McSurdy-Freed; T M Molnar; M A Levy; B R Smith
Journal:  Pharm Res       Date:  2001-09       Impact factor: 4.200

2.  Interspecies scaling and prediction of human clearance: comparison of small- and macro-molecule drugs.

Authors:  Yeamin Huh; David E Smith; Meihau Rose Feng
Journal:  Xenobiotica       Date:  2011-09-05       Impact factor: 1.908

  2 in total

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