期刊
PHARMACOLOGY & THERAPEUTICS
卷 229, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2021.107938
关键词
Albumin-mediated hepatic uptake; in vitro-to-in vivo extrapolation (IVIVE); Organic anions; Organic anion transporting polypeptide (OATP)
资金
- Japanese Ministry of Education, Culture, Sports, Sciences, and Technology [19H03392, 18K06608]
- Grants-in-Aid for Scientific Research [19H03392, 18K06608] Funding Source: KAKEN
Considering albumin-mediated hepatic uptake can improve the prediction accuracy for hepatic clearance of highly protein-bound anionic drugs. This has important clinical and physiological relevance for in vitro-to-in vivo extrapolation of drug metabolism and uptake/efflux processes.
The accuracy in predicting in vivo hepatic clearance of drugs from in vitro data (often termed as in vitro-to-in vivo extrapolation, IVIVE) has improved in part by applying the extended-clearance concept that considers the interplay between hepatic metabolism and uptake/efflux processes. However, the IVIVE-based prediction performs poorly in predicting the hepatic uptake clearance of highly albumin-bound anionic drugs. Their hepatic uptake clearances tend to be much higher than expected based on the free-drug theory. Such observation can be attributable to a phenomenon called albumin-mediated hepatic uptake, for which various models have been thus far proposed. Our group has been applying a facilitated-dissociation model, which assumes the enhanced dissociation of the drug-albumin complex upon interaction with the cell surface. By considering the albumin-mediated hepatic uptake (using the facilitated-dissociation model or alternative kinetic models), a number of investigations demonstrated the improvement in the prediction accuracy for the hepatic clearance of highly protein bound anionic drugs that are substrates for hepatic uptake transporters. This review summarizes the reported kinetic analyses of the albumin-mediated hepatic uptake of highly albumin-bound drugs concerning the IVIVE and the clinical and physiological relevance. (C) 2021 Published by Elsevier Inc.
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