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Pharmacokinetics and metabolism of 14C isobytylnaphtyl acetic acid in rat.
Jacquot, C; Payan-Lepain, E; Christen, M O; Achtert, G; Hausleiter, H J; Borchers, F.
Afiliación
  • Jacquot C; Lab. Pharmacocinetique experimentale, Faculte de Pharmacie, Paris XI, Chatenay Malabry, France.
Eur J Drug Metab Pharmacokinet ; 14(4): 249-56, 1989.
Article en En | MEDLINE | ID: mdl-2633918
After oral administration to rats, absorption of INAA was slow but complete. Plasma level curves reached a plateau for INAA as well as for the two metabolites, which were rapidly formed (MI and MII). The plateau concentration led to an increase of the apparent elimination half-life, which was short after i.v. administration due to the small volume of distribution and to the high rate of metabolism. In any case the half-life was independent of the dose and the pharmacokinetics of INAA remained linear from 1.5 to 15 mg/kg. The two rapidly formed plasma metabolites were eliminated more slowly than INAA. INAA and its metabolites were distributed only sparsely in all tissues under investigation, probably due to the high protein binding. Both routes of administration resulted in elimination of the radioactivity mainly by the urine. Besides the two main metabolites with known structures (MI and MII) small amounts of INAA and two additional metabolites were detected.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Naftalenoacéticos Límite: Animals Idioma: En Revista: Eur J Drug Metab Pharmacokinet Año: 1989 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácidos Naftalenoacéticos Límite: Animals Idioma: En Revista: Eur J Drug Metab Pharmacokinet Año: 1989 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Francia