Pharmacokinetics and bioequivalence of parenterally administered doramectin in cattle
- 1 August 1995
- journal article
- Published by Wiley in Journal of Veterinary Pharmacology and Therapeutics
- Vol. 18 (4), 290-298
- https://doi.org/10.1111/j.1365-2885.1995.tb00593.x
Abstract
Plasma concentrations of doramectin in 40 cattle dosed by subcutaneous (sc) or intramuscular (i.m.) injection (200 μg/kg) were compared to assess the bioequivalence of the two routes of administration. Peak concentration (Cmax), and areas under the concentration curve (AUC0–) were determined from plasma concentrations. Animals treated by the sc route showed a mean AUC0– of 457 ± 66 ng±day/mL (± SD) and a mean Cmax of 27.8 ± 7.9 ng/mL. Results from the i.m. treatment group showed a mean AUC0– of 475 ± 82 ng-day/mL and a mean Cmax of 33.1 ± 9.0 ng/mL Absorption constants (ka) determined by modelling were 0.542 ± 0.336 day-1after sc administration and 0.710 ± 0.357 day-1after i.m. administration. The 90% confidence limits on the difference between mean AUC0– values for the sc and i.m. groups fell within 20% of the mean value for the subcutaneous group. Cmax was somewhat greater for the i.m. route. The 90% confidence limits on the difference in mean In (Tmax+1) also fell within 20% of the mean sc value. Based on this analysis, bioequivalence of the sc and i.m. formulation has been established.Keywords
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