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The pharmacokinetic properties of levofloxacin alone and with amprolium or toltrazuril were determined in broiler chickens after a single IV and oral administrations. After IV injection, levofloxacin serum concentration was best to be described by a two-compartment open model. Amprolium resulted in a significance increase in Vdss and Cltot (3.05 ± 0.17 and 0.65 ± 0.023 L/kg, respectively). In contrast, toltrazuril induced a significance decrease in Vdss and Cltot (1.71 ± 0.17 and 0.32 ± 0.015 L/kg, respectively) compared with levofloxacin alone (2.36 ± 0.34 and 0.44±0.009 L /kg, respectively). The elimination half-life and the mean residence time of levofloxacin were 4.07 ± 0.24 and 5.40 ± 0.26, 3.89 ± 0.24 and 4.77 ± 0.28, 4.10 ± 0.45 and 5.38 ± 0.36 h. in control, amprolium and toltrazuril respectively. Following oral dosing the maximum serum concentration was 3.27 ± 0.13, 2.17 ± 0.097 and 2.95 ± 0.11 µg/ml reached at 1.32 ± 0.096, 0.92 ± 0.057 and 1.30 ± 0.037h in control, amprolium and toltrazuril respectively. Amprolium and toltrazuril resulted in a significance decrease in interval between doses (19.10 ± 0.58 and 19.29 ± 0.51h respectively), compared with levofloxacin alone (27.39 ± 1.80 h.). Oral bioavailability was found to be 107.47 ± 9.23, 75.74 ± 4.50 and 53.51 ± 2.45% in control, amprolium and toltrazuril respectively. It was concluded that the pretreatment of (amprolium and toltrazuril) with levofloxacin altered the pharmacokinetic profile of levofloxacin.

Influence of amprolium and toltrazuril on the disposition kinetics of levofloxacin in broiler chickens