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Research in veterinary science1988; 44(2); 233-236;

Pharmacokinetics of sodium amoxicillin in horses.

Abstract: The pharmacokinetics of sodium amoxicillin were investigated after intravenous and intramuscular administration of a single dose of 15 mg kg-1 body-weight to five horses. A rapid distribution phase was noted after intravenous administration (t1/2 alpha about 20 minutes). The t1/2 beta values obtained after the intravenous and the intramuscular administration were significantly different (P less than 0.05). The bioavailability obtained was about 67 per cent. Plasma protein binding, evaluated in vitro, showed that the percentage of bound fraction was 37 to 38 per cent. It was concluded that sodium amoxicillin administration at 15 mg kg-1 four times a day should be effective in the treatment of several systemic infections in the horse.
Publication Date: 1988-03-01 PubMed ID: 3387678
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study investigates the pharmacokinetics of sodium amoxicillin in horses by administering a single dose of the drug, intravenously and intramuscularly, to five horses. The results suggest that a dosage of 15 mg kg-1 four times a day should effectively treat systemic infections.

Introduction to Pharmacokinetics Study

  • This study investigated the pharmacokinetics of sodium amoxicillin, a common antibiotic used to treat bacterial infections, in horses.
  • The aim was to better understand how the drug is absorbed, distributed, metabolized, and excreted in horses, an area that had not been thoroughly explored before.

Experimental Design and Execution

  • The researchers administered a single dose of sodium amoxicillin (15 mg kg-1 body weight) to five horses either via intravenous injection or intramuscular injection.
  • After administration, they closely monitored the horses and carried out various measurements including the half-life (t1/2) of the drug and the degree to which it bound to plasma proteins.

Results and Findings

  • The researchers found that after intravenous administration, there was a rapid distribution phase of the drug within the horses. This was characterized by a half-life (t1/2 alpha) of approximately 20 minutes.
  • The half-life values (t1/2 beta) obtained after both the intravenous and intramuscular administration were significantly different, suggesting that the route of administration could impact the pharmacokinetics of the drug.
  • The bioavailability of the drug, or the proportion of the drug that entered the circulation and could have an active effect, was found to be about 67 percent.
  • They also noted that around 37-38 percent of the drug was bound to plasma proteins. This is an important aspect as it can affect the distribution and excretion of the drug within the body.

Conclusions and Recommendations

  • Based on their results, the researchers concluded that when dosed at 15 mg kg-1 four times a day, sodium amoxicillin should be able to effectively treat various systemic infections in horses.
  • This study aids in guiding the proper use of sodium amoxicillin in treating infections in horses. The findings could potentially help in reducing the chances of antibiotic resistance or other adverse effects associated with improper antibiotic usage.

Cite This Article

APA
Montesissa C, Carli S, Sonzogni O, Garlappi R. (1988). Pharmacokinetics of sodium amoxicillin in horses. Res Vet Sci, 44(2), 233-236.

Publication

ISSN: 0034-5288
NlmUniqueID: 0401300
Country: England
Language: English
Volume: 44
Issue: 2
Pages: 233-236

Researcher Affiliations

Montesissa, C
  • Institute of Veterinary Pharmacology, Toxicology and Experimental Therapy, University of Milan, Italy.
Carli, S
    Sonzogni, O
      Garlappi, R

        MeSH Terms

        • Amoxicillin / administration & dosage
        • Amoxicillin / pharmacokinetics
        • Animals
        • Biological Availability
        • Horses / metabolism
        • Injections, Intramuscular
        • Injections, Intravenous / veterinary
        • Male

        Citations

        This article has been cited 3 times.
        1. Yáñez JA, Remsberg CM, Sayre CL, Forrest ML, Davies NM. Flip-flop pharmacokinetics--delivering a reversal of disposition: challenges and opportunities during drug development. Ther Deliv 2011 May;2(5):643-72.
          doi: 10.4155/tde.11.19pubmed: 21837267google scholar: lookup
        2. Elsheikh HA, Taha AA, Khalafalla AE, Osman IA, Wasfi IA. Pharmacokinetics of amoxicillin trihydrate in Desert sheep and Nubian goats. Vet Res Commun 1999 Dec;23(8):507-14.
          doi: 10.1023/a:1006318623854pubmed: 10672967google scholar: lookup
        3. Dubbelboer IR, Olsén L, Pelander L, Lacroix MZ, Claustre L, Roques B, Ekstrand C. Pharmacokinetics of Amoxicillin in the Cat. J Vet Pharmacol Ther 2025 Sep;48(5):380-388.
          doi: 10.1111/jvp.70003pubmed: 40454567google scholar: lookup