The pharmacokinetics and metabolism of 14C-carprofen in man

✍ Scribed by John E. Ray; Denis N. Wade

• Publisher: John Wiley and Sons
• Year: 1982
• Tongue: English
• Weight: 510 KB
• Volume: 3
• Category: Article
• ISSN: 0142-2782
• DOI: 10.1002/bdd.2510030105

✦ Synopsis

Abstract

Three healthy male subjects received single 100mg oral doses of carprofen containing 20 μCi of ^14^C‐carprofen. Venous blood samples were drawn during the first 48 h after the dose and urine and feces were collected for 120h. Concentrations of carprofen and its metabolites in body fluids were determined by TLC and mass spectral analysis. After a lag time of 0.3±0.41h (mean ±S.D.), carprofen was absorbed rapidly and peak concentrations in the plasma were reached in 2.7 ± 1.3 h. The ^14^C plasma concentrations declined in a biphasic fashion. The mean half‐lives of the initial (α) and terminal (β) phases were 1.1 h and 20.6 ± 6.1 h, respectively. Biotransformation to a glucuronide metabolite appeared to be the major mechanism of carprofen clearance. In 48 h 74.0 per cent of administered radioactivity was recovered in urine and 14.1 per cent was recovered in feces. A glucuronide of carprofen comprised 85.0 per cent of the radiolabelled compounds in urine. The remaining radioactivity was comprised of parent drug (12.0 per cent) and un unidentified acid‐labile conjugate of the parent drug (3.0 per cent). This pattern of metabolism and excretion is different from that in the dog and rat and may explain species differences in drug activity and toxicity.