Comparative disposition of ricobendazole enantiomers after intravenous and subcutaneous administration of a racemic formulation to calves
✍ Scribed by Carles Cristòfol; Guillermo Virkel; Luis Álvarez; Margarida Arboix; Carlos E. Lanusse
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 210 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0142-2782
- DOI
- 10.1002/bdd.246
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The enantioselective disposition kinetics of the benzimidazole anthelmintic, ricobendazole (RBZ), have been characterized after its intravenous (iv) and subcutaneous (sc) administration as a racemic formulation to cattle. The (+) and (−) RBZ enantiomeric forms were recovered in plasma after iv and sc administration of the racemic RBZ formulation, using a chiral phase based HPLC method. A biexponential plasma concentration versus time curve was observed for both RBZ enantiomers following the iv treatment. Total body clearance was higher for (−) RBZ (150.4 mL/h · kg) compared with that obtained for the (+) RBZ antipode (78.1 mL/h · kg). The elimination half‐life of the (−) RBZ enantiomer was shorter (T1/2β: 2.67 h) compared with the (+) enantiomer (T1/2β: 5.41 h). The plasma availability (expressed as AUC) was significantly higher for (+) RBZ compared with that obtained for the (−) antipode following both treatments. The enantiomeric ratio in plasma at T~0~ was close to unity (50% of each enantiomer); the analysis of the concentration ratios (+) RBZ/(−) RBZ, demonstrated an increase in the proportion of (+) RBZ during the time course of the kinetics after both iv and sc treatments. The results presented herein show the enantioselective disposition kinetics of RBZ in cattle and are a further contribution to the understanding of the kinetic behaviour of these sulphoxide‐containing benzimidazole anthelmintics in ruminants. Copyright © 2000 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
Verapamil is a chiral calcium channel blocking drug which is useful clinically as the racemate in treating hypertension and arrhythmia. The published pharmacokinetic data for verapamil enantiomers in the rat model are limited. Utilizing a stereospeci®c highperformance liquid chromatographic (HPLC) a