Journal
JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS
Volume 35, Issue 5, Pages 503-507Publisher
WILEY-BLACKWELL
DOI: 10.1111/j.1365-2885.2011.01340.x
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- Intervet Inc. d/b/a Merck Animal Health, Summit, NJ, USA
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Gaunt, P. S., Langston, C., Wrzesinski, C., Gao, D., Adams, P., Crouch, L., Sweeney, D., Endris, R. Single intravenous and oral dose pharmacokinetics of florfenicol in the channel catfish (Ictalurus punctatus). J. vet. Pharmacol. Therap. 35, 503-507. Plasma distribution and elimination of florfenicol in channel catfish were investigated after a single dose (10 mg/kg) of intravenous (i.v.) or oral administration in freshwater at a mean water temperature of 25.4 degrees C. Florfenicol concentrations in plasma were analyzed by means of liquid chromatography with MS/MS detection. After i.v. florfenicol injection, the terminal half-life (t1/2), volume of distribution at steady state (Vss), and central volume of distribution (Vc) were 8.25 h, 0.9 and 0.381 L/kg, respectively. After oral administration of florfenicol, the terminal t1/2, Cmax, Tmax, and oral bioavailability (F) were 9.11 h, 7.6 mu g/mL, 9.2 h, and 1.09, respectively. There was a lag absorption time of 1.67 h in oral dosing. Results from these studies support that 10 mg florfenicol/kg body weight in channel catfish is an efficacious dosage following oral administration.
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