作者: Iftekhar Mahmood , Chandra Sahajwalla
DOI: 10.1002/JPS.10174
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摘要: Abstract The objective of this study is to predict clearance drugs in humans from animals which are excreted the bile. Clearance ( CL ) eight known be bile were randomly selected literature. Scaling was performed using at least three animal species. Using simple allometry, × mean life‐span potential (MLP) or × brain weight, s studied predicted humans. choice one methods depended on ‘rule exponents' as described by Mahmood and Balian. A ‘correction factor' calculated adjusting flow rate based species body weight (bile flow = mL/day/kg weight) liver weight). combining it with factor', biliary Predicted allometry several times higher for all (% error [range] = 46–1703). a report provided substantial improvement [range] = 5–91) prediction drugs. results indicate that drug may overpredicted applying employed here, predictability data significantly improved. © 2002 Wiley‐Liss, Inc. American Pharmaceutical Association J Pharm Sci 91:1908–1914,