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Xenobiotica
the fate of foreign compounds in biological systems
Volume 44, 2014 - Issue 4
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Animal Pharmacokinetics and Metabolism

Pharmacokinetic study in pigs and in vitro metabolic characterization in pig- and human-liver microsomes reveal marked differences in disposition and metabolism of tiletamine and zolazepam (Telazol)

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Pages 379-390 | Received 18 Jun 2013, Accepted 06 Aug 2013, Published online: 11 Sep 2013
 

Abstract

1. An equal-dose combination of tiletamine and zolazepam (Telazol®) is used as a veterinary anesthetic. There also have been reports of human abuse of Telazol®. The pharmacokinetics and metabolic fate of tiletamine and zolazepam and the rationale for their administration as an equal-dose combination are unclear.

2. The single-dose pharmacokinetics of intramuscular tiletamine and zolazepam (3 mg/kg each) in 16 Yorkshire-crossbred pigs were determined. The metabolites of tiletamine and zolazepam in pig plasma and urine were identified by mass spectrometry. The metabolic stability of tiletamine and zolazepam and the kinetics of formation of their metabolites by pig- and human-liver microsomes were determined.

3. Higher concentrations of zolazepam were observed in pig plasma and it was cleared more slowly compared to tiletamine (apparent clearance: 11 versus 134 l/h; half-life: 2.76 versus 1.97 h). Three metabolites of zolazepam and one metabolite of tiletamine were identified in pig urine, plasma and in microsomal incubations. In vitro formation of each of these metabolites in microsomes was biphasic involving a high-affinity/low-capacity and a low-affinity/high-capacity enzyme. The in vitro metabolic stability of tiletamine was considerably lower compared to zolazepam.

4. These results collectively point to major pharmacokinetic and metabolic differences between the two components of this fixed-dose anesthetic combination.

Acknowledgements

We thank the staff at the Experimental Surgery Services of University of Minnesota and Kristine Mulier for assistance with conduct of pharmacokinetic experiments in pigs. Analytical work was conducted in the Epilepsy and Research Education Program laboratory at the University of Minnesota (RPR, supervisor). Dr Charles Locuson of Pfizer Animal Health kindly provided the metabolites of tiletamine and zolazepam.

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