Abstract

The purpose of this study was to investigate the comparative pharmacokinetics of difloxacin in male goat kids and lambs. Difloxacin was administered in a crossover as a single dose of 5 mg kg −1 b.wt. by the intravenous (i.v.) and intramuscular (i.m.) routes in kids and lamb. The concentrations of the drug in the plasma were measured using high-performance liquid chromatography (HPLC) with fluorescence detection. Following i.v. injection, the elimination half-life ( t 1/2 β ) in goat kids (3.57 ± 0.39 h) was higher than in lambs (2.63 ± 0.29 h). The apparent volume of distribution ( V dss) and the total body clearance (Cl tot) in goat kids were 0.48 ± 0.03 l kg −1 and 0.12 ± 0.01 l kg −1 h −1, respectively. The corresponding values in lambs were 0.49 ± 0.04 l kg −1 and 0.11 ± 0.01 l kg −1 h −1, respectively. After i.m. administration, difloxacin reached a peak plasma concentration ( C max) of 4.95 ± 0.53 and 4.25 ± 0.47 μg ml −1 at a post-injection time ( T max) of 1.85 ± 0.23 and 1.31 ± 0.2 h in goat kids and lambs, respectively. The mean bioavailability ( F) in both goat kids and lambs were 97.5 ± 20.61% and 97.1 ± 21.5%, respectively. The in vitro plasma protein binding % of difloxacin were 10.31 and 12.98 for goat kids and lambs, respectively. Using the surrogate marker C max/MIC and AUC 24/MIC 90, difloxacin could be effective by the i.m. route at 5 mg kg −1 against isolates with MIC ≤ 0.5 and 0.4 μg ml −1 for goat kids and lambs, respectively, after i.m. dosing.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call