Evaluation of rat intestinal absorption data and correlation with human intestinal absorption

被引:95
作者
Zhao, YH
Abraham, MH
Le, J
Hersey, A
Luscombe, CN
Beck, G
Sherborne, B
Cooper, I
机构
[1] UCL, Dept Chem, London WC1H 0AJ, England
[2] GlaxoSmithKline, DMPK, Mechanism & Extrapolat Technol, Ware SG12 0DP, Herts, England
[3] Biofocus Plc, Saffron Walden CB10 1XL, Essex, England
[4] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
[5] Millennium Pharmaceut Ltd, Cambridge CB1 6ET, England
关键词
human intestinal absorption; rat intestinal absorption; correlation; evaluation;
D O I
10.1016/S0223-5234(03)00015-1
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The absorption of 111 drug and drug-like compounds was evaluated from 111 references based on the ratio of urinary excretion of drugs following oral and intravenous administration to intact rats and biliary excretion of bile duct-cannulated rats. Ninety-eight drug compounds for which both human and rat absorption data were available were selected for correlation analysis between the human and rat absorption. The result shows that the extent of absorption in these two species is similar. For 94% of the drugs the absorption difference between humans and rats is less than 20% and for 98% of drugs the difference is less than 30%. There is only one drug for which human absorption is significantly different from rat absorption. The standard deviation is 11% between human and rat absorption. The linear relationship between human and rat absorption forced through the origin, as determined by least squares regression, is %Absorption (human) = 0.997%Absorption (rat) (n = 98, SD = 11). It is suggested that the absorption in rats could be used as an alternative method to human absorption in pre-clinical oral absorption studies. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:233 / 243
页数:11
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