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Equine veterinary journal2013; 45(6); 715-720; doi: 10.1111/evj.12059

Pharmacokinetics of triamcinolone acetonide following intramuscular and intra-articular administration to exercised Thoroughbred horses.

Abstract: The use of triamcinolone acetonide (TA) in performance horses necessitates establishing appropriate withdrawal times prior to performance. Objective: To describe the plasma pharmacokinetics of TA and time-related urine and synovial fluid concentrations following i.m. and intra-articular administration to exercised Thoroughbred horses. Methods: Block design. Methods: Twelve racing fit adult Thoroughbred horses received a single i.m. administration of TA (0.1 mg/kg bwt). After an appropriate washout period, the same horses then received a single intra-articular TA administration (9 mg) into the right antebrachiocarpal joint. Blood, urine and synovial fluid samples were collected prior to, and at various times, up to 60 days post drug administration and analysed using liquid chromatography-mass spectrometry. Plasma data were analysed using noncompartmental analysis. Results: Maximum measured plasma TA concentrations were 0.996 ± 0.391 at 13.2 h and 1.27 ± 0.278 ng/ml at 6.5 h for i.m. and intra-articular administration, respectively. The plasma terminal elimination half-life was 11.4 ± 6.53 and 0.78 ± 1.00 days for i.m. and intra-articular administration, respectively. Following i.m. administration, TA was below the limit of detection (LOD) by Days 52 and 60 in plasma and urine, respectively. Following intra-articular administration TA was undetectable by Day 7 in plasma and Day 8 in urine. Triamcinolone acetonide was also undetectable in any of the joints sampled following i.m. administration and remained above the limit of quantitation (LOQ) for 21 days following intra-articular administration. Conclusions: This study extends previous studies describing the pharmacokinetics of TA following i.m. and intra-articular administration to the horse and suggests that plasma and urine concentrations are not a good indicator of synovial fluid concentrations. Furthermore, results of this study supports an extended withdrawal time for TA given i.m.
Publication Date: 2013-04-09 PubMed ID: 23574452DOI: 10.1111/evj.12059Google Scholar: Lookup
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  • Clinical Trial
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research investigates the plasma concentration and elimination rate of the drug triamcinolone acetonide (TA) in Thoroughbred racehorses after intramuscular and intra-articular administration. The findings emphasize the need for adequate withdrawal times before racing and highlight a discrepancy between drug concentrations in plasma, urine, and synovial fluid samples.

Research Methodology

  • Twelve adult fit racing Thoroughbreds were given a single intramuscular (i.m.) dose of TA. Post the appropriate washout period, the same horses received a single intra-articular dose of TA.
  • The researchers collected blood, urine, and synovial fluid samples before and at various points up to 60 days after administering the drug.
  • The samples were analyzed using liquid chromatography-mass spectrometry and the plasma data was evaluated using noncompartmental analysis.

Results

  • Results showed the peak plasma TA concentrations post 13.2 hours and 6.5 hours for intramuscular and intra-articular administration respectively.
  • The plasma elimination half-life demonstrates the time body takes to reduce the drug’s concentration in plasma by half. The study found it to be approximately 11.4 days for i.m. administration and 0.78 days for intra-articular administration.
  • Apart from plasma, the presence of the drug was also examined in urine and synovial fluid.
  • Post i.m. administration, the drug was undetectable in plasma by Day 52 and in urine by Day 60. Post intra-articular administration, it was untraceable on Day 7 in plasma and Day 8 in urine.
  • Interestingly, TA was undetectable in any sampled joints following i.m. administration but remained quantifiable till 21 days after intra-articular administration.

Conclusions

  • This study adds to existing knowledge on how TA behaves in a horse’s body post administration via different routes.
  • It pointed out the discrepencies between plasma, urine, and synovial fluid concentrations of TA, suggesting they may not be reliable indicators of each other.
  • The study highlights the need for an extended withdrawal period for TA administered intramuscularly, as the drug remains detectable in the body for an extended period after administration.

Cite This Article

APA
Knych HK, Vidal MA, Casbeer HC, McKemie DS. (2013). Pharmacokinetics of triamcinolone acetonide following intramuscular and intra-articular administration to exercised Thoroughbred horses. Equine Vet J, 45(6), 715-720. https://doi.org/10.1111/evj.12059

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 45
Issue: 6
Pages: 715-720

Researcher Affiliations

Knych, H K
  • K.L. Maddy Equine Analytical Chemistry Laboratory, School of Veterinary Medicine, University of California, USA; Department of Veterinary Molecular Biosciences, School of Veterinary Medicine, University of California, USA.
Vidal, M A
    Casbeer, H C
      McKemie, D S

        MeSH Terms

        • Animals
        • Anti-Inflammatory Agents / administration & dosage
        • Anti-Inflammatory Agents / blood
        • Anti-Inflammatory Agents / pharmacokinetics
        • Area Under Curve
        • Female
        • Half-Life
        • Horses / metabolism
        • Injections, Intra-Articular
        • Injections, Intramuscular
        • Male
        • Physical Conditioning, Animal / physiology
        • Triamcinolone Acetonide / administration & dosage
        • Triamcinolone Acetonide / blood
        • Triamcinolone Acetonide / pharmacokinetics

        Citations

        This article has been cited 6 times.
        1. Shahinfar S, Maibach H. Enigma of Intramuscular Triamcinolone Acetonide (Kenalog(®)) Efficacy.. Clin Pharmacokinet 2023 Sep;62(9):1189-1199.
          doi: 10.1007/s40262-023-01297-5pubmed: 37598107google scholar: lookup
        2. Knych HK, Weiner D, Harrison L, McKemie DS. Pharmacokinetics and pharmacodynamics of intra-articular isoflupredone following administration to horses with lipopolysaccharide-induced synovitis.. BMC Vet Res 2022 Dec 13;18(1):436.
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        3. Tou K, Cawley A, Bowen C, Sornalingam K, Fu S. Measurements of hydrocortisone and cortisone for longitudinal profiling of equine plasma by liquid chromatography-tandem mass spectrometry.. Drug Test Anal 2022 May;14(5):943-952.
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        4. Johnson JP, Vinardell T, David F. Ultrasound-guided injections of the equine head and neck: review and expert opinion.. J Equine Sci 2021 Dec;32(4):103-115.
          doi: 10.1294/jes.32.103pubmed: 35023988google scholar: lookup
        5. El-Rahman GIA, Behairy A, Elseddawy NM, Batiha GE, Hozzein WN, Khodeer DM, Abd-Elhakim YM. Saussurea lappa Ethanolic Extract Attenuates Triamcinolone Acetonide-Induced Pulmonary and Splenic Tissue Damage in Rats via Modulation of Oxidative Stress, Inflammation, and Apoptosis.. Antioxidants (Basel) 2020 May 8;9(5).
          doi: 10.3390/antiox9050396pubmed: 32397156google scholar: lookup
        6. Ekstrand C, Bondesson U, Giving E, Hedeland M, Ingvast-Larsson C, Jacobsen S, Löfgren M, Moen L, Rhodin M, Saetra T, Ranheim B. Disposition and effect of intra-articularly administered dexamethasone on lipopolysaccharide induced equine synovitis.. Acta Vet Scand 2019 Jun 20;61(1):28.
          doi: 10.1186/s13028-019-0464-2pubmed: 31221173google scholar: lookup