Pharmacokinetics of levamisole in sheep after intravenous administration

Authors: Garcia JJ, Teran MT, Diez MJ, Fernandez M, Sierra M
Publication: New Zealand Veterinary Journal, Volume 45, Issue 2, pp 63-66, Apr 1997
Publisher: Taylor and Francis

Animal type: Livestock, Production animal, Ruminant, Sheep
Subject Terms: Alimentary system/gastroenterology, Animal remedies/veterinary medicines, Anthelmintics, Parasite control, Parasites - internal, Metabolic disease, Nematode, Pharmacology, Treatment/therapy
Article class: Scientific Article
Abstract: The pharmacokinetics of levamisole at doses of 5, 7.5 and 10 mg/kg were determined after its intravenous administration to eighteen healthy Merino sheep. Using compartmental analysis, the disposition of the drug best fitted a two-compartmental open model. The mean values for the compartmental volume of distribution at steady state (Vss) were 2.034 ± 0.23 I, 2.347 ± 0.720 and 2.001 ± 0.367 I/kg for each dose, respectively, and values obtained using the statistical moment theory were 2.141 ± 0.269,2.390 ± 0.536 and 2.140 ± 0.345 l/kg for each dose, respectively. There were no dose-related differences (one-way ANOVA) in the constants describing distribution and elimination phases (α and β) or Vss, but significant differences were detected in the total body clearance (Cl) and the area under the plasma concentration-time curve (AUC). After non-compartmental analysis, no significant differences were found when the parameters λ (the linear terminal slope) and Vss were compared, but significant differences were detected in Cl and AUC. There were no significant differences between the values obtained using the compartmental and non-compartmental analysis when λ -β, Cl, Vss, and AUC were compared.
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