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Comparative pharmacokinetics of vinblastine after a 96-hour continuous infusion in wild-type mice and mice lacking
J van Asperen1, O van Tellingen, A H Schinkel
1Department of Clinical Chemistry, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
The Journal of Pharmacology and Experimental Therapeutics
|March 23, 1999
Abstract:
To determine the tissue-specific impact of P-glycoprotein on the accumulation of a substrate drug, we have studied the tissue distribution of vinblastine in mdr1a(-/-) and wild-type mice at approximately similar, relatively low plasma levels. Vinblastine was administered as a 96-h continuous infusion at dose rates of 1 to 10 microgram/h, which were delivered by a s.c.-implanted osmotic pump. Drug concentrations were determined in plasma and tissues by HPLC. In comparison to wild-type mice, 4.4- to 9.6-fold higher drug concentrations were observed in the brains of mdr1a(-/-) mice (p