Title of article :
Disposition of Suprofen Enantiomers in the Cat
Author/Authors :
CASTRO، نويسنده , , E.F. and SORACI، نويسنده , , A.L. and FRANCI، نويسنده , , R. and FOGEL، نويسنده , , F.A. and TAPIA، نويسنده , , M.O.، نويسنده ,
Issue Information :
فصلنامه با شماره پیاپی سال 2001
Abstract :
Suprofen (SPF) is a non-steroidal anti-inflammatory drug (NSAID), which belongs to the 2-arylpropionic acids subclass. As a result of their chiral characteristics, these compounds have shown a marked enantioselective behaviour with a high degree of interspecies variation. They are mainly eliminated by glucuronidation. Plasma, biliary and urine disposition of SPF was investigated in the cat after intravenous administration of the racemate (dose 2 mg/kg). Both enantiomers exhibited similar disposition profiles in plasma with no evidence of chiral inversion. During bile sampling time, recovered acylglucuronides of R (–) and S (+) SPF were less than 1% of the total dose administered. Only free SPF was recovered in the urine, representing 0.12% of the administered racemic SPF dose. The results indicate that neither chiral inversion nor glucuronidation predominate in SPF disposition in cats.
Keywords :
Cats , Suprofen , chiral inversion , glucuronidation. , enantioselective
Journal title :
The Veterinary Journal
Journal title :
The Veterinary Journal