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Biological mass spectrometry1991; 20(3); 109-114; doi: 10.1002/bms.1200200303

The development of a gas chromatographic/mass spectrometric screening procedure to detect the administration of anabolic steroids to the horse.

Abstract: A screening procedure for anabolic steroid residues in horse urine has been developed based upon solid-phase extraction and gas chromatographic/mass spectrometric analysis in the selected ion mode. For moderate sample throughput the method provides a viable alternative to radioimmunoassay screening and has advantages over the latter technique due to its flexibility, specificity and ability to detect a number of steroids in a single analysis. Full automation of the gas chromatographic/mass spectrometric analysis is an additional feature of the methodology.
Publication Date: 1991-03-01 PubMed ID: 2069982DOI: 10.1002/bms.1200200303Google Scholar: Lookup
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  • Journal Article

Summary

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The research article is about the development of a new screening method for detecting anabolic steroids in horse urine using gas chromatography and mass spectrometry, which presents an alternative to radioimmunoassay screening.

Overview of the Study

  • In this study, the researchers established a new procedure for screening anabolic steroid residues in horse urine. Their method is mainly comprised of solid-phase extraction and gas chromatographic/mass spectrometric analysis in a selected ion mode. This means that the screening was focused on detecting particular anabolic steroids.
  • The goal of this research is to provide an alternative method to the current predominantly used technique, the radioimmunoassay screening. They aimed to create a method that offers more flexibility, specificity, and the capability to detect a multitude of steroids in a single analysis. This is particularly important in order to more accurately detect the administration of anabolic steroids to horses, a problem concerning ethics in sports and health of the animals.

Advantages of the Method

  • The method presented by the researchers has several important advantages, compared to the currently most widely used technique, radioimmunoassay.
  • Firstly, the new procedure is more flexible, meaning it could be adjusted or manipulated according to the needs of a specific analysis.
  • Secondly, it is more specific, in other words, it can precisely identify the specific type or types of steroids present in the urine sample. This specificity allows the analysis to differentiate between different anabolic steroids, something which is not assessable using radioimmunoassay.
  • Lastly, their method has the capability to detect multiple anabolic steroids in a single analysis. This fundamentally makes the approach more efficient, as it reduces the time, effort and resources needed to test for different steroids separately.

Automation

  • Another highlighted feature of the methodology proposed in the research article is its amenability to full automation.
  • An automated gas chromatographic/mass spectrometric analysis implies that this screening procedure can be conducted with minimal human intervention, which could considerably improve the accuracy of the results (by reducing potential human error) and increase time-efficiency.

Cite This Article

APA
Teale P, Houghton E. (1991). The development of a gas chromatographic/mass spectrometric screening procedure to detect the administration of anabolic steroids to the horse. Biol Mass Spectrom, 20(3), 109-114. https://doi.org/10.1002/bms.1200200303

Publication

ISSN: 1052-9306
NlmUniqueID: 9102982
Country: England
Language: English
Volume: 20
Issue: 3
Pages: 109-114

Researcher Affiliations

Teale, P
  • Horseacing Forensic Laboratory Limited, Newmarket, Suffolk, UK.
Houghton, E

    MeSH Terms

    • Anabolic Agents / urine
    • Animals
    • Gas Chromatography-Mass Spectrometry / methods
    • Horses

    Citations

    This article has been cited 1 times.
    1. Oda SS, El-Ashmawy IM. Adverse effects of the anabolic steroid, boldenone undecylenate, on reproductive functions of male rabbits.. Int J Exp Pathol 2012 Jun;93(3):172-8.