A pharmacokinetic evaluation of HIV protease inhibitors, cyclic ureas, in rats and dogs

• Published in: Biopharmaceutics & drug disposition Vol. 15; no. 7; p. 535
• Main Authors: Wong, Y N, Burcham, D L, Saxton, P L, Erickson-Viitanen, S, Grubb, M F, Quon, C Y, Huang, S M
• Format: Journal Article
• Language: English
• Published: England 01.10.1994
• Subjects: Administration, Oral; Animals; Biological Availability; Chromatography, High Pressure Liquid; Computer Simulation; Cross-Over Studies; Dogs; Half-Life; HIV - drug effects; HIV Protease Inhibitors - administration & dosage; HIV Protease Inhibitors - blood; HIV Protease Inhibitors - pharmacokinetics; HIV Protease Inhibitors - pharmacology; Injections, Intravenous; Male; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship; Urea - analogs & derivatives; Virus Replication - drug effects
• ISSN: 0142-2782
• DOI: 10.1002/bdd.2510150702

The pharmacokinetics of a series of novel cyclic, non-peptide inhibitors of HIV protease were studied in rats or dogs after intravenous and oral administration. Six symmetrically substituted cyclic urea compounds (XK234, XM311, XM320, XM321, XM323, and XM412), which effectively inhibited HIV virus replication, with IC90 values of 0.03-1.0 microM (0.017-0.76 microgram mL-1), were evaluated. Plasma concentrations were measured in rats and dogs using specific and sensitive HPLC methods. In rats, the maximum plasma concentrations of 0.21-1.88 micrograms mL-1 were detected within 1 h of oral administration of 10 mg kg-1 of the compounds. The elimination half-lives ranged from 1.25 to 3.3 h in rats and the absolute oral bioavailability ranged from 18 to 100%. In dogs, the maximum plasma concentration and absolute oral bioavailability were 4.37 micrograms mL-1 and 48%, 1.07 micrograms mL-1 and 16%, and 1.48 mg ML-1 and 38% for XK234, XM311, and XM323, respectively. The data demonstrated that the maximum plasma concentrations of these cyclic ureas were several times higher than the IC90 for inhibition of viral replication after single doses of 10 mg kg-1 in rats and dogs. With this combination of high potency against virus replication and good oral bioavailability, these cyclic ureas represent a new class of compounds that are suitable for development as therapeutic agents for the treatment of HIV-associated diseases.