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American journal of veterinary research2004; 65(11); 1479-1482; doi: 10.2460/ajvr.2004.65.1479

Pharmacokinetics of R(-) and S(+) carprofen after administration of racemic carprofen in donkeys and horses.

Abstract: To compare plasma disposition of the R(-) and S(+) enantiomers of carprofen after IV administration of a bolus dose to donkeys and horses. Methods: 5 clinically normal donkeys and 3 clinically normal horses. Methods: Blood samples were collected from all animals at time 0 (before) and at 10, 15, 20, 30, and 45 minutes and 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10, 24, 28, 32, and 48 hours after IV administration of a bolus of carprofen (0.7 mg/kg). Plasma was analyzed in triplicate via high-performance liquid chromatography to determine the concentrations of the carprofen enantiomers. A plasma concentrationtime curve for each donkey and horse was analyzed separately to estimate noncompartmental pharmacokinetic variables. Results: In donkeys and horses, the area under the plasma concentration versus time curve (AUC) was greater for the R(-) carprofen enantiomer than it was for the S(+) carprofen enantiomer. For the R(-) carprofen enantiomer, the AUC and mean residence time (MRT) were significantly less and total body clearance (CIT) was significantly greater in horses, compared with donkeys. For the S(+) carprofen enantiomer, AUC and MRT were significantly less and CIT and apparent volume of distribution at steady state were significantly greater in horses, compared with donkeys. Conclusions: Results have suggested that the dosing intervals for carprofen that are used in horses may not be appropriate for use in donkeys.
Publication Date: 2004-11-30 PubMed ID: 15566084DOI: 10.2460/ajvr.2004.65.1479Google Scholar: Lookup
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  • Comparative Study
  • Journal Article

Summary

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This research is an investigation of the pharmacokinetics of two forms of carprofen, R(-) and S(+), when given intravenously to both horses and donkeys. The results suggest that the dosage intervals typically used for horses may not be suitable for donkeys.

Study Methodology

  • The study was conducted using five clinically normal donkeys and three clinically normal horses.
  • A bolus dose of carprofen was intravenously administered to these animals and blood samples were collected at distinct intervals for 48 hours.
  • The samples were studied through high-performance liquid chromatography to determine the concentrations of the carprofen enantiomers.
  • A plasma concentration-time curve was plotted for each animal to estimate pharmacokinetic variables.

Findings and Conclusion

  • Both in donkeys and horses, the area under the plasma concentration versus time curve (AUC) was found greater for the R(-) carprofen enantiomer than S(+) carprofen enantiomer.
  • In case of the R(-) carprofen enantiomer, the AUC and mean residence time (MRT) were found to be significantly less and total body clearance (CIT) was significantly greater in horses compared to donkeys.
  • For the S(+) carprofen enantiomer, AUC, MRT were significantly less and CIT and apparent volume of distribution at steady state were significantly greater in horses than in donkeys.
  • These differences in pharmacokinetic properties of carprofen between horses and donkeys suggest that the dosing intervals used for horses may not be appropriate for donkeys.

Cite This Article

APA
Mealey KL, Matthews NS, Peck KE, Burchfield ML, Bennett BS, Taylor TS. (2004). Pharmacokinetics of R(-) and S(+) carprofen after administration of racemic carprofen in donkeys and horses. Am J Vet Res, 65(11), 1479-1482. https://doi.org/10.2460/ajvr.2004.65.1479

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 65
Issue: 11
Pages: 1479-1482

Researcher Affiliations

Mealey, Katrina L
  • Department of Veterinary Clinical Sciences, Washington State University, Pullman, WA 99164, USA.
Matthews, Nora S
    Peck, Kenneth E
      Burchfield, Melissa L
        Bennett, Brad S
          Taylor, Tex S

            MeSH Terms

            • Animals
            • Anti-Inflammatory Agents, Non-Steroidal / blood
            • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
            • Area Under Curve
            • Carbazoles / blood
            • Carbazoles / pharmacokinetics
            • Chromatography, High Pressure Liquid
            • Equidae / blood
            • Horses / blood
            • Isomerism
            • Time Factors

            Citations

            This article has been cited 7 times.
            1. Ebner L, O O, Simon B, Lizarraga I, Smith J, Cox S. Pharmacokinetics of butorphanol following intravenous and intramuscular administration in donkeys: A preliminary study. Front Vet Sci 2022;9:979794.
              doi: 10.3389/fvets.2022.979794pubmed: 36213418google scholar: lookup
            2. Gómez-Segura L, Boix-Montañes A, Mallandrich M, Parra-Coca A, Soriano-Ruiz JL, Calpena AC, Gimeno Á, Bellido D, Colom H. Swine as the Animal Model for Testing New Formulations of Anti-Inflammatory Drugs: Carprofen Pharmacokinetics and Bioavailability of the Intramuscular Route. Pharmaceutics 2022 May 12;14(5).
              doi: 10.3390/pharmaceutics14051045pubmed: 35631631google scholar: lookup
            3. Gómez-Segura L, Parra A, Calpena AC, Gimeno Á, Boix-Montañes A. Carprofen Permeation Test through Porcine Ex Vivo Mucous Membranes and Ophthalmic Tissues for Tolerability Assessments: Validation and Histological Study. Vet Sci 2020 Oct 10;7(4).
              doi: 10.3390/vetsci7040152pubmed: 33050372google scholar: lookup
            4. Ingrao JC, Johnson R, Tor E, Gu Y, Litman M, Turner PV. Aqueous stability and oral pharmacokinetics of meloxicam and carprofen in male C57BL/6 mice. J Am Assoc Lab Anim Sci 2013 Sep;52(5):553-9.
              pubmed: 24041210
            5. Boocock H, Flyps J, Escobar A, Redondo JI, Taylor PM, Gozalo-Marcilla M, Johnston GM, Bettschart-Wolfensberger R, Sullivan R. Donkey and Hybrid Anaesthetic Mortality in an Observational, Prospective, Multicentre Cohort Study. Animals (Basel) 2025 Jun 25;15(13).
              doi: 10.3390/ani15131880pubmed: 40646777google scholar: lookup
            6. Alipour-Khairkhah H, Azizi S, Asri-Rezaei S. Stress, lipid profile and inflammatory responses to flunixin meglumine administration in surgical and non-surgical castration in donkeys. Vet Anim Sci 2025 Mar;27:100423.
              doi: 10.1016/j.vas.2024.100423pubmed: 39835330google scholar: lookup
            7. Akyol BA, Gokbulut C. The effect of intravenous lipid emulsion (ILE) on the pharmacokinetic/toxicokinetic dispositions of ivermectin and carprofen in rabbits. Naunyn Schmiedebergs Arch Pharmacol 2024 Mar;397(3):1841-1852.
              doi: 10.1007/s00210-023-02738-5pubmed: 37768375google scholar: lookup