Species Differences in Absorption, Metabolism and Excretion of Pranoprofen, a 2-Arylpropionic Acid Derivative, in Experimental Animals

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Absorption, metabolism and excretion of 2-(5H-[1] benzopyrano-[2,3-b] pyridin-7-yl) propionic acid (pranoprofen), an anti-inflammatory drug, were investigated in mice, rats, guinea pigs and rabbits using ^<14>C-labeled compound ([^<14>C] pranoprofen) at a dose of 5 mg/kg. After the oral administration of [^<14>C] pranoprofen the radioactivity was rapidly and almost completely absorbed from the digestive organs of the animals tested. The radioactivity in the blood reached the maximum at 30-60 min after the oral administration of [^<14>C] pranoprofen in all species tested, and the biological half-lives of the radioactivity were 4.1 h in rats, 2.6 h in guinea pigs, 1.3 h in mice and 0.9 h in rabbits, respectively. When [^<14>C] pranoprofen was orally administered, urinary and fecal excretions of the radioactivity within 3 d were 81.1% and 18.7% of the dose in mice, 51.5% and 39.4% in rats, 81.8% and 9.0% in guinea pigs, and 93.2% and 3.6% in rabbits, respectively. A major metabolite of pranoprofen was its acyl glucuronide in rats, guinea pigs and rabbits. However, it was shown that acyl glucosidation is also a predominant metabolic pathway of pranoprofen in mice.
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