RT Journal Article SR Electronic T1 PHARMACOKINETICS AND METABOLISM OF [14C]EPLERENONE AFTER ORAL ADMINISTRATION TO HUMANS JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP 1448 OP 1455 DO 10.1124/dmd.31.11.1448 VO 31 IS 11 A1 Chyung S. Cook A1 Loren M. Berry A1 Roy H. Bible A1 Jeremy D. Hribar A1 Elisabeth Hajdu A1 Norman W. Liu YR 2003 UL http://dmd.aspetjournals.org/content/31/11/1448.abstract AB A pharmacokinetics and metabolism study was conducted in eight healthy human volunteers. After oral administration of [14C]eplerenone (EP) at a dose of 100 mg per person as an aqueous solution, blood, saliva, breath, urine, and fecal samples were collected at various time points. All matrices were analyzed for total radioactivity and/or for EP and its open-lactone-ring form (EPA). EP was well absorbed, and a mean EP Cmax of 1.72 μg/ml was achieved 1.2 h postdose. After the Cmax, plasma concentrations of EP declined with a half-life of 3.0 h. Plasma concentrations of EPA were much lower than EP concentrations, and the area under the plasma-concentration time curve (AUC) for EPA was only 4% of the EP AUC. Plasma protein binding was moderate (33-60%) but concentration-dependent over the therapeutic concentration range. EP and its metabolites did not preferentially partition into the red blood cells and blood concentrations of total radioactivity were lower than plasma concentrations. Approximately 66.6% and 32.0% of the radioactive dose were excreted in urine and feces, respectively. The majority of urinary and fecal radioactivity was due to metabolites, indicating extensive metabolism of EP. The major metabolic pathways were 6β- and/or 21-hydroxylation and 3-keto reduction. There was no evidence for any alteration of the 9,11-epoxide ring or the methyl ester. As a percentage of dose, the primary metabolic products excreted in urine and feces included 6β-hydroxy-EP (6β-OHEP) (32.0%), 6β,21-OHEP (20.5%), 21-OHEP (7.89%), and 2α,3β,21-OHEP (5.96%). The amounts of the other metabolites excreted were less than 5% each. The American Society for Pharmacology and Experimental Therapeutics