1. Academic Validation
  2. Hydroxy levamisole and its phase II conjugates as potential indicators of levamisole doping in thoroughbred horses

Hydroxy levamisole and its phase II conjugates as potential indicators of levamisole doping in thoroughbred horses

  • Rapid Commun Mass Spectrom. 2022 Nov 16;e9430. doi: 10.1002/rcm.9430.
Moses Philip 1 Abdul Khader Karakka Kal 1 Michael Benedict Subhahar 1 Tajudheen K Karatt 1 Binoy Mathew 1 Zubair Perwad 1 Fatma Mohammed Graiban 1 Marina Rodriguez Caveney 1 Ramy Sayed 1 Ahmed Mahmoud Kadry 1
Affiliations

Affiliation

  • 1 Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
Abstract

Rationale: According to previous research articles, aminorex is the major metabolite of levamisole; however, in the screening of levamisole positive racehorse urine and plasma samples, aminorex could only be detected in trace amounts or not at all. In forensic laboratories, hydroxy levamisole and its phase II conjugates make it easier to confirm levamisole misuse and to differentiate between the abuse of levamisole and aminorex. This study aimed to identify the major levamisole metabolites that can be detected along with the parent drug.

Methods: The study describes levamisole and its metabolites in thoroughbred horses following oral administration and in vitro with equine liver microsomes. The plausible structures of the detected metabolites were postulated using liquid chromatography-high-resolution mass spectrometry.

Results: Under the experimental conditions twenty-six metabolites (seventeen phase I, two phase II, and seven conjugates of phase I metabolites) were detected (M1-M26). The major phase I metabolites identified were formed by hydroxylation. In phase II, the glucuronic acid conjugates of levamisole and hydroxy levamisole were detected as the major metabolites. In plasma, the parent drug and major metabolites are detectable for up to eight days, while in urine, they are detectable for up to twenty days. Levamisole levels rapidly increased at 45 minutes following administration, then declined gradually until detectable levels were reached approximately 8 days after administration, according to the pharmacokinetics study.

Conclusions: A prolonged elimination profile and relatively high concentration of hydroxyl metabolites suggest that the detection of hydroxyl metabolites is imperative for investigating levamisole doping in horses.

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