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Determination of zearalenone and its metabolites in urine, plasma and faeces of horses by HPLC-APCI-MS.

Abstract: The paper describes a method for the sensitive and selective determination of zearalenone and its metabolites in urine, plasma and faeces of horses by high performance liquid chromatography and atmospheric pressure chemical ionisation (APCI) mass spectrometry (MS). While only one step sample clean-up by an immunoaffinity column (IAC) was sufficient for plasma samples, urine and faeces samples had to be prepared by a combination of a solid-phase extraction (SPE) and an immunoaffinity column. The method allows the simultaneous determination of zearalenone and all of its metabolites; alpha-zearalenol, beta-zearalenol, alpha-zearalanol, beta-zearalanol and zearalanone. Dideuterated zearalanone was used as internal standard for quantification and the study of the matrix effect. Recovery rates between 56 and slightly above 100% were achieved in urine samples, and more than 80% in plasma and faeces samples. The limits of detection ranged from 0.1-0.5 microg/l or microg/kg, the limits of quantification from 0.5-1.0 microg/l or microg/kg. The practical use of the method is demonstrated by the analysis of spiked and naturally contaminated urine, plasma and faeces of horses.
Publication Date: 2006-07-07 PubMed ID: 16828347DOI: 10.1016/j.jchromb.2006.06.012Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper discusses the development and testing of a new method for detecting zearalenone and its metabolic byproducts in the urine, blood plasma, and feces of horses.

Research Methodology

  • The researchers developed a method using high performance liquid chromatography and atmospheric pressure chemical ionisation (APCI) mass spectrometry (MS) to selectively and sensitively determine the presence of zearalenone and its metabolites.
  • The paper studied zearalenone and its metabolites; alpha-zearalenol, beta-zearalenol, alpha-zearalanol, beta-zearalanol and zearalanone.
  • The testing process involved the use of a sample clean-up step conducted through an immunoaffinity column (IAC). This step was found sufficient for plasma samples but needed to be combined with solid-phase extraction (SPE) for urine and feces samples.
  • In the quantification and study of the matrix effect, Dideuterated zearalanone was used as an internal standard.

Findings

  • The new method showed promising results with recovery rates showing great variation in urine samples, ranging from 56% to slightly over 100%. For plasma and feces samples, the hit rate was more than 80%.
  • The limit of detection for this method was found to be between 0.1-0.5 microg/l or microg/kg, and the limits of quantification being between 0.5-1.0 microg/l or microg/kg.
  • The practical applicability of the method was demonstrated by conducting analysis of spiked and naturally contaminated urine, plasma and faeces of horses.

Significance and Implications

  • This research offers a potential new approach for detecting and identifying the presence of zearalenone and its metabolites in horse samples.
  • It further contributes to existing knowledge on analytical methodologies for toxicological research on animal species, focusing on horses in this case.
  • Given the accuracy and efficiency of this method, it can serve as an essential tool for regulating horse doping, ensuring animal health, and determining the presence of harmful substances in animal farming and racing sectors.

Cite This Article

APA
Songsermsakul P, Sontag G, Cichna-Markl M, Zentek J, Razzazi-Fazeli E. (2006). Determination of zearalenone and its metabolites in urine, plasma and faeces of horses by HPLC-APCI-MS. J Chromatogr B Analyt Technol Biomed Life Sci, 843(2), 252-261. https://doi.org/10.1016/j.jchromb.2006.06.012

Publication

ISSN: 1570-0232
NlmUniqueID: 101139554
Country: Netherlands
Language: English
Volume: 843
Issue: 2
Pages: 252-261

Researcher Affiliations

Songsermsakul, P
  • Department of Veterinary Public Health, Institute of Nutrition, University of Veterinary Medicine, Veterinärplatz 1, A-1210 Vienna, Austria.
Sontag, G
    Cichna-Markl, M
      Zentek, J
        Razzazi-Fazeli, E

          MeSH Terms

          • Analytic Sample Preparation Methods
          • Animals
          • Chromatography, High Pressure Liquid / methods
          • Feces / chemistry
          • Horses
          • Mass Spectrometry / methods
          • Tandem Mass Spectrometry
          • Zearalenone / analysis
          • Zearalenone / metabolism

          Citations

          This article has been cited 14 times.
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