The Role of P-Glycoprotein in the Pharmacokinetics and Tissue Distribution of a Hepatitis C Virus Protease Inhibitor

Author(s): Kevin X. Chen, Bancha Vibulbhan, Tongtong Liu, Lisa Broske, Genfeng Wang, Cheng Li, F. George Njoroge, Annette S. Uss, K.-C. Cheng.

Journal Name: Drug Metabolism Letters

Volume 3 , Issue 4 , 2009

Become EABM
Become Reviewer


S5, a hepatitis C virus protease inhibitor, displays partially saturable efflux in the Caco-2 system. In addition, the efflux can be reversed by cyclosporine, indicating that S5 may be a human Pglycoprotein (P-gp) substrate. S5 can also activate the ATPase activity in vesicle membranes containing mouse P-gp 1a and 1b, suggesting that S5 may be a substrate for mouse P-gp. The pharmacokinetics and tissue distribution of S5 were evaluated after intravenous and oral administration to wild-type and 1a/1b knockout mice. Plasma and kidney levels of this compound in knockout mice were transiently higher than those in wild-type mice only after oral dosing, indicating effective P-gp efflux occurs in wild-type mice. The levels of S5 in brain samples from knockout mice were higher than those from wild-type mice after both intravenous and oral administration, but much more significantly after intravenous administration. The levels in liver were four time higher in knockout mice than in wild-type mice after oral administration, but were not different between knockout and wild-type mice after intravenous administration. These results suggest that P-gp efflux limits exposure to S5 in the brain and liver, and that the effect is dependent on the route of administration.

Keywords: P-glycoprotein, P-gp knockout mice, HCV protease inhibitor, tissue distribution, pharmacokinetics

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2009
Page: [290 - 295]
Pages: 6
DOI: 10.2174/187231209790218091
Price: $58

Article Metrics

PDF: 3