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Research in veterinary science2010; 89(2); 236-241; doi: 10.1016/j.rvsc.2010.02.011

Determination of oral tramadol pharmacokinetics in horses.

Abstract: The determination of the pharmacokinetic parameters of tramadol in plasma and a better characterization of its metabolites after oral administration to horses is necessary to design dosage regimens to achieve target plasma concentrations that are associated with analgesia. The purpose of this study was to determine the pharmacokinetics and elimination pattern in urine of tramadol and its metabolites after oral administration to horses. Tramadol was administered orally to six horses and its half-life, T(max) and C(max) in plasma were 10.1, 0.59 h, and 132.7 ng/mL, respectively. The half-life, T(max) and C(max) for M1 in plasma were 4.0, 0.59 h, and 28.0 ng/mL, respectively. Tramadol and its metabolites were detectable in urine between 1 and 24 h after the administration. In conclusion, the PK data reported in this study provides information for the design of future studies of tramadol in horses.
Publication Date: 2010-03-12 PubMed ID: 20223494DOI: 10.1016/j.rvsc.2010.02.011Google Scholar: Lookup
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  • Journal Article

Summary

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This research looks into the metabolism rate of oral tramadol in horses, by determining its half-life and peak levels after administration. Through understanding these pharmacokinetic properties, more effective dosage regimens for pain relief can be designed for horses.

Introduction to Research

This work examines the pharmacokinetics of tramadol, an opioid analgesic commonly used to manage pain, when administered orally to horses. The research revolves around understanding how tramadol is metabolized within the organism, and the implications this has for designing effective dosage regimens.

Research Methodology

  • The study involved administering tramadol orally to six horses.
  • The team monitored concentration levels in the horses’ plasma over a set time after administration.
  • They determined key pharmacokinetic parameters, such as half-life (time taken for concentration to reduce by half), T(max) (time taken to reach peak concentration), and C(max) (maximum concentration).
  • This process was repeated for M1, a metabolite of tramadol.
  • The elimination pattern of tramadol and its metabolites was observed and measured by examining horses’ urine samples collected 1 and 24 hours post-administration.

Results

  • For tramadol in plasma, the determined half-life was 10.1 hours, T(max) was 0.59 hours, and C(max) was 132.7 ng/mL.
  • For M1 in plasma, the half-life was slightly shorter at 4.0 hours, with a T(max) of 0.59 hours, and a C(max) of 28.0 ng/mL.
  • Traces of tramadol and its metabolites were found in horses’ urine within 1 hour of consumption and remained detectable up to 24 hours.

Conclusions and Implications

The data obtained offers insight into how tramadol is metabolized in horses, providing key information for future studies on tramadol usage in equines. This knowledge could aid in formulating dosage regimens that take into account tramadol’s half-life and concentration, in turn optimizing its analgesic effect. The research also contributes to the broader understanding of drug metabolism in large mammals, which could have applications beyond equine pain management.

Cite This Article

APA
Cox S, Villarino N, Doherty T. (2010). Determination of oral tramadol pharmacokinetics in horses. Res Vet Sci, 89(2), 236-241. https://doi.org/10.1016/j.rvsc.2010.02.011

Publication

ISSN: 1532-2661
NlmUniqueID: 0401300
Country: England
Language: English
Volume: 89
Issue: 2
Pages: 236-241

Researcher Affiliations

Cox, S
  • Department of Comparative Medicine, University of Tennessee, College of Veterinary Medicine, 2407 River Drive, Knoxville, TN 37996, United States. scox6@utk.edu
Villarino, N
    Doherty, T

      MeSH Terms

      • Administration, Oral
      • Analgesics, Opioid / administration & dosage
      • Analgesics, Opioid / blood
      • Analgesics, Opioid / pharmacokinetics
      • Animals
      • Area Under Curve
      • Female
      • Half-Life
      • Horses / blood
      • Horses / metabolism
      • Tramadol / administration & dosage
      • Tramadol / blood
      • Tramadol / pharmacokinetics

      Citations

      This article has been cited 1 times.
      1. Kelly KR, Pypendop BH, Christe KL. Pharmacokinetics of tramadol following intravenous and oral administration in male rhesus macaques (Macaca mulatta).. J Vet Pharmacol Ther 2015 Aug;38(4):375-82.
        doi: 10.1111/jvp.12194pubmed: 25488714google scholar: lookup