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1.
Am J Vet Res ; 48(12): 1725-32, 1987 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-3434919

RESUMO

The pharmacokinetic disposition of florfenicol was studied in male veal calves given 11 mg of florfenicol/kg of body weight, IV and 11 mg of florfenicol/kg PO every 12 hours for 7 doses. After florfenicol administration IV, the median elimination half-life was 222.8 minutes, whereas the median half-life of the distribution phase was 7.94 minutes. Median body clearance and apparent volume of distribution were 2.87 ml/kg/min and 0.907 L/kg, respectively. After florfenicol administration, PO, there was a wide variation in the calculated half-life, which was attributed to variation in the rate of florfenicol absorption. The half-life was 167.4 to 534.9 minutes after the first oral dose and 190 to 808.8 minutes after the seventh dose. The median bioavailability after the first oral dose was 0.8888. Peak and trough concentrations of florfenicol were increased after subsequent doses were administered, compared with those after the first oral dose. The percentage of protein binding in serum from one adult cow was 22% to 26%. Florfenicol concentrations in tissues and body fluids of male veal calves were studied after the seventh dose of 11 mg of florfenicol/kg. High concentrations of florfenicol were measured in the urine, kidney, and bile. Low concentrations were measured in the brain, CSF, and aqueous humor. Concentrations in all other tissues and fluids studied were similar to the concurrent serum concentration.


Assuntos
Antibacterianos/farmacocinética , Bovinos/metabolismo , Tianfenicol/análogos & derivados , Administração Oral , Animais , Antibacterianos/administração & dosagem , Esquema de Medicação , Injeções Intravenosas , Masculino , Tianfenicol/administração & dosagem , Tianfenicol/farmacocinética , Distribuição Tecidual
2.
J Vet Pharmacol Ther ; 9(4): 412-25, 1986 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-3806782

RESUMO

The pharmacokinetic disposition of florfenicol was described in veal calves after administration of a single 22-mg/kg dose intravenously, orally after a 12-h fast and orally 5 min post feeding. Both serum concentrations and urinary excretion were studied. After intravenous administration the median elimination half-life was 171.9 min while the half-life of the distribution phase was 5.9 min. The median body clearance (Cl) and apparent volume of distribution (Vz) were 2.85 ml/kg/min and 0.78 l/kg, respectively. Following oral administration the median bio-availability (f) was 0.88 for calves dosed after a 12-h fast and 0.65 for calves dosed 5 min post feeding. Calves given the oral doses had a complex absorption pattern with delayed absorption. Slightly more than 50% of the administered dose both orally and intravenously was recovered as unchanged florfenicol in the urine by 30 h.


Assuntos
Tianfenicol/análogos & derivados , Administração Oral , Animais , Disponibilidade Biológica , Bovinos , Feminino , Injeções Intravenosas , Absorção Intestinal , Cinética , Taxa de Depuração Metabólica , Tianfenicol/administração & dosagem , Tianfenicol/sangue , Tianfenicol/metabolismo
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