作者: E. Doyle , L.F. Chasseaud , J.N. Miller
DOI: 10.1016/0306-4492(82)90015-6
关键词: Primate 、 Distribution (pharmacology) 、 Baboon 、 Intravenous dose 、 Open model 、 Physiology 、 Pharmacology 、 Animal species 、 Plasma concentration 、 Pharmacokinetics 、 Medicine
摘要: Abstract 1. The pharmacokinetics of frusemide have been compared in 3 non-human primate species after a single intravenous dose mg/kg the drug. 2. Peak mean plasma concentrations were 31.6, 33.6, 43.6 μg/ml rhesus monkey, cynomolgus monkey and baboon respectively, declined with half-life about 20 min. 3. There no notable differences pharmacokinetic parameters estimated from either one-compartment or two-compartment open model. 4. statistically significant species-related clearance, half-lives volumes distribution adjusted for bodyweight. 5. are closer to those man than other commonly used laboratory animal species.