Kinetic characterization of rat hepatic uptake of 16 actively transported drugs

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Abstract

To explore the determinants of hepatic uptake, 16 compounds were investigated with different physicochemical and disposition characteristics, including five statins, three sartans, saquinavir, ritonavir, erythromycin, clarithromycin, nateglinide, repaglinide, fexofenadine, and bosentan. Freshly isolated rat hepatocytes in suspension were used with the oil-spin method to generate kinetic parameters. Clearances, via passive diffusion (P diff) and active uptake (CL active, characterized by maximal uptake rate and K m), were estimated from the initial uptake rate data over a 0.01 to 100 μM concentration range. The K m values had a range of 15-fold, with 10 of the 16 drugs with K m <10 μM (median 6 μM). Both CL active and P diff ranged over 100-fold (median 188 and 14 μl/min/10 6 cells). Assessment of the relative contribution of P diff and CL active indicated that, at low concentrations (approximately 0.1 μM), the active process contributes >80% to the overall uptake for 13 drugs. Although high P diff values were obtained for ritonavir and repaglinide, active process contributed predominantly to uptake; in contrast, high passive permeability dominates over transporter-mediated uptake for saquinavir over the full concentration range. For bosentan and erythromycin, active and passive processes were equally important. Hepatocyte-to-medium unbound concentration ratio was >10 for 9 of the 16 drugs, ranging from 2 to 494 for bosentan and atorvastatin, respectively. Some drugs showed extensive intracellular binding (fraction unbound range 0.01-0.6), which was not correlated with active uptake. LogD 7.4 correlated significantly with P diff and the extent of intracellular binding but not with active uptake. This study provides systematic assessment of the role of active uptake relative to the passive process; implications of the findings are discussed. Copyright © 2011 by The American Society for Pharmacology and Experimental Therapeutics.

Bibliographical metadata

Original languageEnglish
Pages (from-to)1808-1814
Number of pages6
JournalDrug Metabolism and Disposition
Volume39
Issue number10
DOIs
Publication statusPublished - Oct 2011