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Journal of chromatography1987; 423; 123-130; doi: 10.1016/0378-4347(87)80334-1

Identification of a flunixin metabolite in the horse by gas chromatography-mass spectrometry.

Abstract: The main metabolite of flunixin, a hydroxylated product, has been identified by gas chromatography-mass spectrometry and 1H NMR spectroscopy in equine urine and plasma. The method also permits the qualitative monitoring of the urinary elimination of the drug and its metabolite. The two products are detected up to 175 and 54 h, respectively, after a single intravenous administration at the dose of 1 mg/kg. Simultaneous detection of the two compounds increases the reliability of anti-doping control analysis.
Publication Date: 1987-12-25 PubMed ID: 3502127DOI: 10.1016/0378-4347(87)80334-1Google Scholar: Lookup
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  • Journal Article

Summary

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This research article discusses a study on identifying a key metabolite of flunixin, a veterinary medication primarily used in horses, through methods such as gas chromatography-mass spectrometry and 1H NMR spectroscopy. The research further explores how these methods contribute to enhancing the effectiveness of anti-doping control analysis in horses by tracking the urinary elimination of the drug and its metabolite.

Identification of Flunixin Metabolite

  • The research focuses on isolating and identifying the primary metabolite of flunixin – a hydroxylated substance. Metabolites are derivatives or by-products of the body metabolizing or processing a certain drug. In this case, flunixin, known for its anti-inflammatory, analgesic (pain-relieving), and antipyretic (fever-reducing) properties in horses, was the drug under consideration.
  • The identification was conducted using both gas chromatography-mass spectrometry (GC-MS) and 1H NMR spectroscopy. GC-MS is a method that combines features of gas-liquid chromatography and mass spectrometry to identify different substances within a test sample. 1H NMR spectroscopy is a form of nuclear magnetic resonance spectroscopy, which uses the magnetic properties of specific atoms to determine the structure of compounds and their function in the body.

Monitoring Urinary Elimination of the Drug and Metabolite

  • Another crucial aspect of the study involved observing how flunixin and its metabolite are eliminated from the body. Tracking the urinary elimination of the drug and its metabolite could give important insights into the body’s efficiency in processing the drug and how long it stays in the system.
  • After a single intravenous administration of flunixin at a dose of 1 mg/kg, the drug and its primary metabolite were detected up to 175 hours and 54 hours respectively. This reveals how long the substances remain detectable following administration, which is crucial information for anti-doping purposes.

Enhancement of Anti-Doping Control Analysis

  • The ability to simultaneously detect flunixin and its metabolite significantly enhances the reliability of anti-doping control analysis. Detecting both the administered drug and its primary by-product ensures a more comprehensive tracking of drug use. This can be particularly beneficial in ensuring the fairness and integrity of competitive horse sports where such drugs might be used to gain an unfair advantage.
  • This also serves as a useful scientific reference for authorities dealing with doping in other equine athletic events, contributing to the development of more effective testing and control measures.

Cite This Article

APA
Jaussaud P, Courtot D, Guyot JL, Paris J. (1987). Identification of a flunixin metabolite in the horse by gas chromatography-mass spectrometry. J Chromatogr, 423, 123-130. https://doi.org/10.1016/0378-4347(87)80334-1

Publication

NlmUniqueID: 0427043
Country: Netherlands
Language: English
Volume: 423
Pages: 123-130

Researcher Affiliations

Jaussaud, P
  • INRA-ENVL Research Laboratory for Sport Equine, National School of Veterinary Medicine, Charbonnières, France.
Courtot, D
    Guyot, J L
      Paris, J

        MeSH Terms

        • Animals
        • Anti-Inflammatory Agents, Non-Steroidal / analysis
        • Anti-Inflammatory Agents, Non-Steroidal / blood
        • Anti-Inflammatory Agents, Non-Steroidal / urine
        • Biotransformation
        • Clonixin / analogs & derivatives
        • Clonixin / analysis
        • Clonixin / blood
        • Clonixin / urine
        • Gas Chromatography-Mass Spectrometry
        • Horses
        • Magnetic Resonance Spectroscopy
        • Male
        • Nicotinic Acids / analysis
        • Spectrophotometry, Infrared

        Citations

        This article has been cited 2 times.
        1. Knych HK, Finno CJ, Baden R, Arthur RM, McKemie DS. Identification and characterization of the enzymes responsible for the metabolism of the non-steroidal anti-inflammatory drugs, flunixin meglumine and phenylbutazone, in horses. J Vet Pharmacol Ther 2021 Jan;44(1):36-46.
          doi: 10.1111/jvp.12891pubmed: 32757313google scholar: lookup
        2. Radi AE, Abd El-Ghany N, Wahdan T. Voltammetric Determination of Flunixin on Molecularly Imprinted Polypyrrole Modified Glassy Carbon Electrode. J Anal Methods Chem 2016;2016:5296582.
          doi: 10.1155/2016/5296582pubmed: 27242945google scholar: lookup