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Assessment of the long‐acting ivermectin formulation in sheep: Further insight into potential pharmacokinetic interactions
Author(s) -
Ballent Mariana,
Maté Maria Laura,
Dominguez Paula,
Virkel Guillermo,
Albérich Melanie,
Lespine Anne,
Lanusse Carlos,
Lifschitz Adrian Luis
Publication year - 2019
Publication title -
journal of veterinary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.527
H-Index - 60
eISSN - 1365-2885
pISSN - 0140-7783
DOI - 10.1111/jvp.12739
Subject(s) - ivermectin , pharmacokinetics , abamectin , pharmacology , bioavailability , in vivo , chemistry , plasma concentration , drug , medicine , biology , microbiology and biotechnology , veterinary medicine , pesticide , agronomy
The aim of the current study was to evaluate the in vivo pharmacokinetic of ivermectin ( IVM ) after the administration of a long‐acting ( LA ) formulation to sheep and its impact on potential drug‐drug interactions. The work included the evaluation of the comparative plasma profiles of IVM administered at a single therapeutic dose (200 μg/kg) and as LA formulation at 630 μg/kg. Additionally, IVM was measured in different gastrointestinal tissues at 15 days posttreatment with both IVM formulations. The impact of the long‐lasting and enhanced IVM exposure on the disposition kinetics of abamectin ( ABM ) was also assessed. Plasma ( IVM and ABM ) and gastrointestinal ( IVM ) concentrations were analyzed by HPLC with fluorescent detection. In plasma, the calculated C max and AUC 0‐t values of the IVM ‐ LA formulation were 1.47‐ and 3.35‐fold higher compared with IVM 1% formulation, respectively. The T 1/2ab and T max collected after administration of the LA formulation were 2‐ and 3.5‐fold longer than those observed after administration of IVM 1% formulation, respectively. Significantly higher IVM concentrations were measured in the intestine mucosal tissues and luminal contents with the LA formulation, and in the liver, the increase was 7‐fold higher than conventional formulation. There was no drug interaction between IVM and ABM after the single administration of ABM at 15 days post‐administration of the IVM LA formulation. The characterization of the kinetic behavior of the LA formulation to sheep and its potential influence on drug‐drug interactions is a further contribution to the field.