RT Journal Article SR Electronic T1 Distribution and excretion of furobufen in rats and dogs. JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP 125 OP 128 VO 9 IS 2 A1 M N Cayen A1 E S Ferdinandi A1 E Greselin YR 1981 UL http://dmd.aspetjournals.org/content/9/2/125.abstract AB Groups of male rats and dogs were given single doses of 50 mg of 14C-furobufen per kg orally or intravenously. In rats, tissue radioactivity levels were generally lower than that of serum. Radioactivity accumulated in and was retained by white adipose tissue. The radioactivity in fat was due to a conjugate of dibenzofuranacetic acid, the major metabolite of furobufen. Approximately one-half of the dose was excreted each in the urine and feces of rats after oral and intravenous administration of 14C-furobufen. A similar excretion pattern was observed in dogs after an oral dose.