Despite the small sample size of the animal collectives used in the present study, the good tolerability and at least partially significant evidence pointing to a higher bioavailability might justify consideration of the microemulsion as a promising formulation for further rodent studies involving oral and intraperitoneal administration of tariquidar.
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Pharmacokinetics of the P-gp Inhibitor Tariquidar in Rats After Intravenous, Oral, and Intraperitoneal Administration.
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