Literature DB >> 3841151

Pharmacokinetics of ivermectin administered intravenously to cattle.

P K Wilkinson, D G Pope, F P Baylis.   

Abstract

Ivermectin, a macrocyclic lactone disaccharide antiparasitic agent, was administered intravenously to six young calves (one bull, five steers) as a bolus dose of 200 micrograms/kg. The disposition kinetics of ivermectin in cattle can be described by a three-compartment open model with elimination from the central compartment. Compartmental analysis yielded mean parameters as follows: terminal elimination rate constant (beta) = 0.258 d-1, biological half-life (t 1/2 beta) = 2.7 d; apparent volume of distribution of the central compartment (Vd1) = 0.45 L/kg; apparent volume of distribution at steady state (Vdss) = 2.4 L/kg. The area under the plasma concentration-time curve (AUC) was 254 ng X d/mL. Noncompartmental parameters, obtained by utilizing statistical moment theory, mean residence time (MRT), clearance (CL), and Vdss were calculated to be 2.8 d, 0.79 L/kg X d, and 2.2 L/kg, respectively.

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Year:  1985        PMID: 3841151     DOI: 10.1002/jps.2600741020

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  2 in total

1.  The relative systemic availability of ivermectin after administration as capsule, tablet, and oral solution.

Authors:  G Edwards; A Dingsdale; N Helsby; M L Orme; A M Breckenridge
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

2.  The distribution and some pharmacokinetic parameters of ivermectin in pigs.

Authors:  E W Scott; Q A McKellar
Journal:  Vet Res Commun       Date:  1992       Impact factor: 2.459

  2 in total

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