Comparative plasma disposition kinetics of albendazole, fenbendazole, oxfendazole and their metabolites in adult sheep
- 28 June 1995
- journal article
- Published by Wiley in Journal of Veterinary Pharmacology and Therapeutics
- Vol. 18 (3) , 196-203
- https://doi.org/10.1111/j.1365-2885.1995.tb00578.x
Abstract
The comparative plasma disposition kinetics of albendazole (ABZ), fenbendazole (FBZ) and oxfendazole (OFZ) following their oral administration (5 mg/kg) to adult sheep was characterized. Jugular blood samples were taken serially over a 144 h period and plasma was analysed by high performance liquid chromatography (HPLC) for ABZ, ABZ sulphoxide (ABZSO) and ABZ sulphone (ABZSO2) (ABZ treatment), and for FBZ, OFZ and FBZ sulphone (FBZSO2) (FBZ and OFZ treatments). While the ABZ parent drug was not detected at any time post-treatment, ABZSO and ABZSO2 were the analytes recovered in plasma, after oral administration of ABZ to sheep. The active ABZSO metabolite was the main analyte recovered in plasma (between 0.25 and 60h post-treatment), accounting for 71 % of the total AUC. FBZ, OFZ and FBZSO2 were the analytes detected in plasma following the oral administration of both FBZ and OFZ to sheep. Low concentrations of FBZ were found in plasma between 4 (FBZ treatment) or 8 h (OFZ treatment) and 72 h post-treatment. The plasma profile of each analyte followed a similar pattern after both treatments; OFZ being the main component detected in plasma. The plasma disposition of ABZ metabolites was markedly different to that of FBZ derivatives. ABZSO exhibited faster absorption and a higher Cmax than OFZ (both treatments). Furthermore, while ABZSO declined relatively rapidly in plasma reaching non-detectable concentrations at 60 h post-ABZ administration, OFZ was found in plasma for up to 120 (FBZ treatment) and 144 h (OFZ treatment). The extended detection of OFZ in plasma in both treatments correlated with the prolonged t1/2β (18 h) and mean residence time (MRT) (30–33 h) obtained for this metabolite compared to those of ABZSO (t1/2β= (7.0 h); MRT= 12.5 h). These differences between the disposition of ABZ and FBZ metabolites may account for differences in their patterns of efficacy and tissue residues.Keywords
This publication has 28 references indexed in Scilit:
- Mode of action of benzimidazolesPublished by Elsevier ,2003
- Biliary secretion and enterohepatic recycling of fenbendazole metabolites in sheepJournal of Veterinary Pharmacology and Therapeutics, 1993
- Comparative efficacies of various anthelmintics against benzimidazole-resistant strains of sheep nematodesPublished by Wiley ,1993
- Comparative sulphoxidation of albendazole by sheep and cattle liver microsomes and the inhibitory effect of methimazoleXenobiotica, 1993
- Benzimidazoles: Veterinary usesParasitology Today, 1990
- The oxidative metabolism of fenbendazole: a comparative studyJournal of Veterinary Pharmacology and Therapeutics, 1988
- Sulphoxidation of albendazole by the FAD-containing and cytochrome P-450 dependent mono-oxygenases from pig liver microsomesXenobiotica, 1987
- Interaction of Fasciola hepatica with albendazole and its metabolitesJournal of Veterinary Pharmacology and Therapeutics, 1984
- Noncompartmental Determination of the Steady-State Volume of Distribution for Any Mode of AdministrationJournal of Pharmaceutical Sciences, 1982
- ESTRIP, a BASIC Computer Program for Obtaining Initial Polyexponential Parameter EstimatesJournal of Pharmaceutical Sciences, 1978