J Clin Pharmacol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     

Sign In to gain access to subscriptions and/or personal tools.
First published on June 16, 2008
The Journal of Clinical Pharmacology 2008, doi:10.1177/0091270008320369
© 2008 the American College of Clinical Pharmacology
This Article
Right arrow Full Text (JCP OnlineFirst[PDF])
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Google Scholar
Right arrow Articles by Goteti, K.
Right arrow Articles by Garner, C. E.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Goteti, K.
Right arrow Articles by Garner, C. E.
©© 2008 American College of Clinical Pharmacology, Inc.
The Journal of Clinical Pharmacology, 10.1177/0091270008320369


Article

Estimation of Human Drug Clearance Using Multiexponential Techniques

Kosalaram Goteti 1*, Patrick J. Brassil 1, Steven S. Good 1, and C. Edwin Garner 1

1 Infection and Cancer Discovery, AstraZeneca R&D Boston

* To whom correspondence should be addressed. E-mail: kosalaram.goteti{at}astrazeneca.com.


   Abstract
A multiexponential allometry (MA) method was developed to predict human drug clearance from preclinical data. Separate data sets containing clearances from human and preclinical species were chosen for the study. Human clearance was estimated using the MA technique according to the equation: CL = aBWb + cBWd, where CL is clearance in milliliters/minute, and a, b, c, and d are constants derived from preclinical pharmacokinetic data. Simple allometry (SA) gave the poorest prediction using any data set, and the percentage outliers remained larger than MA or monkey liver blood flow within 1.5-, 2-, and 3-fold error. Analysis of compounds common to both data sets suggested that MA could accurately predict human clearances within approximately 10% of 3-fold error. The analysis also showed that monkey is an important species for scaling, and MA is a better predictor of human clearance when the slope of SA is >0.7.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2008 by the American College of Clinical Pharmacology