| Autor: |
Walker, D. K., Ackland, M. J., James, G. C., Muirhead, G. J., Rance, D. J., Wastall, P., Wright, P. A. |
| Předmět: |
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| Zdroj: |
Xenobiotica; Mar1999, Vol. 29 Issue 3, p297-310, 14p |
| Abstrakt: |
1. Pharmacokinetics were studied in mouse, rat, rabbit, dog and man after single intravenous and or oral doses of sildenafil or [14C]-sildenafil (ViagraTM). 2. In man, absorption from the gastrointestinal tract was essentially complete. With the exception of male rat, Tmax occurred at 1h or less. Bioavailability was attenuated by presystemic hepatic metabomlism in all species. 3. The volume of distribution was similar in rodents and humans (1-2 l/kg) but was greater in dog (5.2 l/kg), due to lower plasma protein binding (84 versus 94-96% respectively). 4. High clearance was the principal determinant of short elimination half-lives in rodents (0.4-1.3 h), whereas moderate clearance in dog and man resulted in longer halflives (6.1 and 3.7 h respectively). Clearances were in agreement with in vitro metabolism rates by liver microsomes from the various species. 5. After single oral or intravenous doses of [14C]-sildenafil, the majority of radioactivity was excreted in the faeces of all species. No unchanged drug was detected in the excreta of man. 6. Five principal pathways of metabolism in all species were piperazine N -demethylation, pyrazole N-demethylation, loss of a two-carbon fragment from the piperazine ring (N, N-deethylation), oxidation of the piperazine ring and aliphatic hydroxylation. Additional metabolites arose through combinations of these pathways. 7. Sildenafil was the major component detected in human plasma. Following oral doses, AUC for the piperazine N-desmethyl and piperazine N, N-desethyl metabolites were 55 and 27% that of parent compound respectively. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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