TY - JOUR T1 - Disposition of the Dipeptidyl Peptidase 4 Inhibitor Sitagliptin in Rats and Dogs JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 525 LP - 532 DO - 10.1124/dmd.106.013110 VL - 35 IS - 4 AU - Maria G. Beconi AU - James R. Reed AU - Yohannes Teffera AU - Yuan-Qing Xia AU - Christopher J. Kochansky AU - David Q. Liu AU - Shiyao Xu AU - Charles S. Elmore AU - Suzanne Ciccotto AU - Donald F. Hora AU - Ralph A. Stearns AU - Stella H. Vincent Y1 - 2007/04/01 UR - http://dmd.aspetjournals.org/content/35/4/525.abstract N2 - The pharmacokinetics, metabolism, and excretion of sitagliptin [MK-0431; (2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine], a potent dipeptidyl peptidase 4 inhibitor, were evaluated in male Sprague-Dawley rats and beagle dogs. The plasma clearance and volume of distribution of sitagliptin were higher in rats (40–48 ml/min/kg, 7–9 l/kg) than in dogs (∼9 ml/min/kg, ∼3 l/kg), and its half-life was shorter in rats, ∼2 h compared with ∼4 h in dogs. Sitagliptin was absorbed rapidly after oral administration of a solution of the phosphate salt. The absolute oral bioavailability was high, and the pharmacokinetics were fairly dose-proportional. After administration of [14C]sitagliptin, parent drug was the major radioactive component in rat and dog plasma, urine, bile, and feces. Sitagliptin was eliminated primarily by renal excretion of parent drug; biliary excretion was an important pathway in rats, whereas metabolism was minimal in both species in vitro and in vivo. Approximately 10 to 16% of the radiolabeled dose was recovered in the rat and dog excreta as phase I and II metabolites, which were formed by N-sulfation, N-carbamoyl glucuronidation, hydroxylation of the triazolopiperazine ring, and oxidative desaturation of the piperazine ring followed by cyclization via the primary amine. The renal clearance of unbound drug in rats, 32 to 39 ml/min/kg, far exceeded the glomerular filtration rate, indicative of active renal elimination of parent drug. The American Society for Pharmacology and Experimental Therapeutics ER -