Comparative pharmacokinetics of diaveridine in pigs and chickens following single intravenous and oral administration

Journal of Veterinary Pharmacology and Therapeutics
Y-F LiZ-L Zeng


Comparative pharmacokinetic profiles of diaveridine following single intravenous and oral dose of 10 mg/kg body weight in healthy pigs and chickens were investigated, respectively. Concentrations of diaveridine in plasma samples were determined using a validated high-performance liquid chromatography-ultraviolet (HPLC-UV) method. The concentration-time data were subjected to noncompartmental kinetic analysis by WinNonlin program. The corresponding pharmacokinetic parameters in pigs or chickens after single intravenous administration were as follows, respectively: t1/2β(elimination half-life) 0.74 ± 0.28 and 3.44 ± 1.07 h; Vd(apparent volume of distribution) 2.70 ± 0.99 and 3.86 ± 0.92 L/kg; ClB(body clearance) 2.59 ± 0.62 and 0.80 ± 0.14 L/h/kg; and AUC0-∞(area under the blood concentration vs. time curve) 4.11 ± 1.13 and 12.87 ± 2.60 μg∙h/mL. The corresponding pharmacokinetic parameters in pigs or chickens after oral administration were as follows, respectively: t1/2β1.78 ± 0.41 and 2.91 ± 0.57 h; Cmax(maximum concentration) 0.43 ± 0.24 and 1.45 ± 0.57 μg/mL; Tmax(time to reach Cmax) 1.04 ± 0.67 and 3.25 ± 0.71 h; and AUC0-∞1.33 ± 0.55 and 9.28 ± 2.69 μg∙h/mL. The oral bioavailability (F) of diaveridine in pigs or chickens was...Continue Reading


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Jul 8, 2014·Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences·Hui WangXianhui Huang
Sep 24, 2015·Environmental Toxicology and Pharmacology·Jianzhong WangXingyuan Cao

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