Abstract

Pasteurella multocida (P.multocida) infection causes substantial economic loss in the duck industry. Danofloxacin, a fluoroquinolone solely used in animals, shows good antibacterial activity against P.multocida. In this study, the in vitro pharmacodynamics of danofloxacin against P.multocida was studied. The serum and lung tissue pharmacokinetics of danofloxacin were studied in healthy and P.multocida infected ducks following oral administration of a single dose of 5mg/kg body weight (b.w.). The MIC, MBC and MPC of danofloxacin against P.multocida (C48-1 ) were 0.25, 1 and 3.2μg/ml, respectively. The Cmax was 0.34μg/ml, attained at 2.03hr in healthy ducks, and was 0.35μg/ml, attained at 2.87hr in diseased ducks. Compared to the serum pharmacokinetics of danofloxacin in healthy ducks, the absorption rate and extent were similar in healthy and diseased animals. In contrast, the elimination rate was slower, with an elimination half-life (T1/2β ) of 13.17 and 16.18hr for healthy and infected animals, respectively; the AUCs in the two groups were 5.70 and 7.68μghr/ml, respectively, which means the total amount of drug in the circulation was increased in the infected ducks. The maximum concentration in lung tissues between healthy and infected animals was not significantly different (8.96 vs. 8.93μg/g). However, the Tmax in healthy ducks was longer than that in infected ducks (4hr vs. 1.75hr), which means that the distribution rate of danofloxacin was slower in healthy ducks. The concentration of danofloxacin in lung tissues was approximately 24-fold higher than that in the serum. In the serum pharmacokinetic profiles, the ƒAUC0-24hr /MIC was 18.19 in healthy ducks and was 25.04 in P.multocida infected ducks at the clinical recommended dose, which is far from the PK/PD target (125hr) of fluoroquinolones. Danofloxacin, at a dose of 5mg/kg b.w., seems to be insufficient for ducks infected with P.multocida, with an MIC equal to 0.25μg/ml.

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