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Characterizing Lomerizine metabolites in camel urine: High-resolution mass spectrometry method development and validation for enhanced doping control.
Nalakath, Jahfar; Rasik, Rasik Puzhithinipra; Kadry, Ahmed; Babu, Ansar; Waseem, Ibrahim; Ok, Praseen; Hebel, Christiana; Selvapalam, Narayanan; Nagarajan, Erumaipatty Rajagounder.
Afiliación
  • Nalakath J; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Rasik RP; Department of Chemistry, Kalasalingam Academy of Research and Education, Krishnan Kovil, Tamil Nadu, India.
  • Kadry A; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Babu A; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Waseem I; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Ok P; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Hebel C; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Selvapalam N; Camel Forensic Laboratory, Central Veterinary Research Laboratory, Dubai, UAE.
  • Nagarajan ER; Department of Chemistry, Kalasalingam Academy of Research and Education, Krishnan Kovil, Tamil Nadu, India.
Rapid Commun Mass Spectrom ; 38(17): e9846, 2024 Sep 15.
Article en En | MEDLINE | ID: mdl-38923663
ABSTRACT
RATIONALE Lomerizine (LMZ) is an antimigraine drug that works as a calcium channel blocker and has selective effects on the central nervous system. It is metabolized into trimetazidine (TMZ), which is a prohibited substance owing to its performance-enhancing effects in both human and animal sports. Effective doping control measures are imperative to distinguish the source of TMZ in samples to ensure integrity and fairness of the sport, therefore a comprehensive analysis of LMZ metabolites is essential to identify potential biomarkers in camel urine for effective doping control.

METHODS:

Camel urine samples were collected from four healthy animals following a single oral administration of LMZ at a dosage of 1 mg/kg body weight. In vitro studies were conducted using homogenized camel liver samples. Lomerizine and its metabolites were extracted using solid-phase extraction and analyzed with a Thermo Fisher Orbitrap Exploris liquid chromatography mass spectrometry system. The acquired data was processed with the Compound Discoverer software.

RESULTS:

The study conducted a comprehensive analysis of LMZ metabolites in camels and identified 10 phase I and one phase II metabolites. The primary pathway for the formation of phase I metabolites was de-alkylation, while phase II metabolite was formed through alkylation of the parent drug. The study provided valuable insights into the unique metabolic pathways of LMZ in camels under specific experimental conditions.

CONCLUSION:

The developed method enables the detection and characterization of LMZ and its metabolites in camels. The identified metabolites has the potential to act as marker metabolites for the distinctive detection of LMZ in camel urine to ensure efficient analytical strategies for routine doping control applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Camelus / Doping en los Deportes Límite: Animals Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Camelus / Doping en los Deportes Límite: Animals Idioma: En Revista: Rapid Commun Mass Spectrom Año: 2024 Tipo del documento: Article