L- and D-threo ethylphenidate concentrations, pharmacokinetics, and pharmacodynamics in horses

Author:

Knych Heather K.12ORCID,McKemie Dan S.1,Seminoff Kelsey1,Hartmann Petra3,Hovda Lynn4,Benson Dionne5

Affiliation:

1. K.L. Maddy Equine Analytical Chemistry Laboratory, School of Veterinary Medicine; University of California; Davis California

2. Department of Veterinary Molecular Biosciences, School of Veterinary Medicine; University of California; Davis California

3. Industrial Laboratories; Wheat Ridge Colorado

4. Minnesota Racing Commission; Shakopee Minnesota

5. Racing Medication and Testing Consortium; Lexington Kentucky

Funder

Racing Medication and Testing Consortium

California Horse Racing Board

Publisher

Wiley

Subject

Spectroscopy,Pharmaceutical Science,Environmental Chemistry,Analytical Chemistry

Reference21 articles.

1. “Chasing the high”-experiences of ethylphenidate as described on international internet forums;Soussan;Subst Abus,2015

2. Carboxylesterase transesterification of meperidine (Demerol) and methylphenidate (Ritalin) in the presence of [(2)H(6)] ethanol: preliminary in vitro findings using a rat liver preparation;Bourland;J Pharm Sci,1997

3. Detection of the novel metabolite ethylphenidate after methylphenidate overdose with alcohol coingestion;Markowitz;J Clin Psychopharmacol,1999

4. Ethylphenidate formation in human subjects after the administration of a single dose of methylphenidate and ethanol;Markowitz;Drug Metab Dispos,2000

5. A review of ethylphenidate in deaths in east and west Scotland;Parks;Forensic Sci Int,2015

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