INVESTIGADORES
SORACI Alejandro Luis
artículos
Título:
Disposition of suprofen enantiomers in the cat
Autor/es:
CASTRO, E.; SORACI, A. L.; FRANCI, R.; FOGEL, F. A.; TAPIA, M. O.
Revista:
The Veterinary Journal
Editorial:
ELSEVIER SCI LTD
Referencias:
Año: 2001 vol. 162 p. 38 - 43
ISSN:
1090-0233
Resumen:
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.