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Journal of analytical toxicology1995; 19(3); 182-186; doi: 10.1093/jat/19.3.182

Determination of triamcinolone acetonide in equine serum and urine by liquid chromatography-atmospheric pressure ionization mass spectrometry.

Abstract: Urine and serum samples collected from four standard-bred mares after 30-mg intraarticular administrations of triamcinolone acetonide were analyzed using combined high-performance liquid chromatography-atmospheric pressure ionization mass spectrometry. Maximum triamcinolone acetonide concentrations of 32.3, 14.8, 24.3, and 29.4 ng/mL in the urine and 2.7, 1.9, 2.3, and 2.5 ng/mL in the serum samples were observed. The peak concentrations of the drug were detected approximately 22 h (urine) and 12 h (serum) after administration. The drug elimination profiles for both urine and serum are presented and discussed.
Publication Date: 1995-05-01 PubMed ID: 7564297DOI: 10.1093/jat/19.3.182Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper is about a scientific study that sought to determine the presence of the drug triamcinolone acetonide in the serum and urine of horses, using high-performance liquid chromatography-atmospheric pressure ionization mass spectrometry.

Methodology

  • The research involved the collection of urine and serum samples from four standard-bred mares who were administered with 30-mg intraarticular doses of triamcinolone acetonide.
  • The researchers then used a rigorous analytical technique known as combined high-performance liquid chromatography-atmospheric pressure ionization mass spectrometry (LC-API-MS) to analyze these samples. This method involves the separation of compounds (in this case, traces of the drug) in a liquid suspension by their varying properties. The separated compounds are then ionized using atmospheric pressure and their mass-to-charge ratios are measured, which aids in their identification and quantification.

Findings

  • The maximum concentrations of triamcinolone acetonide found in the urine were 32.3, 14.8, 24.3, and 29.4 ng/mL, and in the serum samples were 2.7, 1.9, 2.3, and 2.5 ng/mL.
  • In addition, the peak concentrations of the drug were detected approximately 22 hours after administration in the urine samples and 12 hours after administration in the serum samples.

Implications

  • The findings of this study contribute valuable data on the pharmacokinetics of triamcinolone acetonide in horses, particularly the timeline of its maximum concentration and elimination from the body. This information is crucial for establishing drug detection times and managing its therapeutic use among horses.
  • The demonstration of the use of LC-API-MS for the detection and quantification of the drug in equine urine and serum could be employed by veterinarians and those in horse racing and equestrian sports for drug testing.

Cite This Article

APA
Koupai-Abyazani MR, Yu N, Esaw B, Laviolette B. (1995). Determination of triamcinolone acetonide in equine serum and urine by liquid chromatography-atmospheric pressure ionization mass spectrometry. J Anal Toxicol, 19(3), 182-186. https://doi.org/10.1093/jat/19.3.182

Publication

ISSN: 0146-4760
NlmUniqueID: 7705085
Country: England
Language: English
Volume: 19
Issue: 3
Pages: 182-186

Researcher Affiliations

Koupai-Abyazani, M R
  • Can Test Laboratories Ltd., Vancouver, BC, Canada.
Yu, N
    Esaw, B
      Laviolette, B

        MeSH Terms

        • Animals
        • Chromatography, High Pressure Liquid
        • Horses
        • Mass Spectrometry
        • Triamcinolone Acetonide / blood
        • Triamcinolone Acetonide / urine

        Citations

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