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Journal of veterinary pharmacology and therapeutics2004; 27(5); 293-298; doi: 10.1111/j.1365-2885.2004.00596.x

Cefotaxime kinetics in plasma and synovial fluid following intravenous administration in horses.

Abstract: Cefotaxime powder was diluted with sterile water to a concentration of 100 mg/mL. The volume of solution was adjusted for each experimental horse to provide a total dose of 15, 20, and 25 mg/kg and was administered by infusion through a jugular vein catheter over a 10-min period. All three doses were administered to each of the six experimental horses at three different times. Cefotaxime concentrations in plasma and synovial fluid samples were measured by high-performance liquid chromatography (HPLC). Standard compartmental analysis techniques and the WinSAAM modeling program were used to determine standard pharmacokinetic parameters for cefotaxime. The plasma and synovial fluid data from the five horses administered the 25 mg/kg dose was analyzed. Plasma cefotaxime concentrations appeared to be linearly related to dose infused and declined in parallel, suggesting linear drug kinetics. Moreover, cefotaxime concentrations declined monotonically suggesting that its disposition kinetics could essentially be described by a one-compartment model rather than the fact that sampling occurred after the infusion was discontinued. Maximum concentration of cefotaxime in plasma occurred immediately after cessation of the infusion. Minimum inhibitory concentrations were determined for Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae, common isolates from septic arthritis in horses. Based on our pharmacokinetic data, a regimen of 25 mg/kg administered i.v. every 6 h appears appropriate for susceptible joint infections in adult horses.
Publication Date: 2004-10-27 PubMed ID: 15500566DOI: 10.1111/j.1365-2885.2004.00596.xGoogle Scholar: Lookup
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  • Clinical Trial
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the effects of three different doses of Cefotaxime, an antibiotic, on horses. The study finds that the highest dosage tested (25 mg/kg) is most effective for treating joint infections in horses.

Experimental Procedure

  • Cefotaxime powder was prepared at a concentration of 100 mg/mL using sterile water. The solution was then tailored to each horse to provide doses of 15 mg/kg, 20 mg/kg, and 25 mg/kg.
  • The solution was administered to each horse intravenously via a jugular vein catheter over a 10-minute period. The varying doses were given to all six experimental horses at different times.
  • Both plasma and synovial fluid samples were collected from the horses to measure Cefotaxime concentrations using high-performance liquid chromatography (HPLC).

Data Analysis

  • The collected data was analyzed using standard compartmental analysis techniques and the WinSAAM modeling program to determine pharmacokinetic parameters for Cefotaxime.
  • The researchers found that the plasma Cefotaxime concentrations seemed to directly relate to the infused dose and decreased in parallel, suggesting the drug follows a linear kinetic process.
  • The study also revealed steady declines in Cefotaxime concentrations, which suggests that the drug’s kinetics can be described using a one-compartment model, rather than being dependent on the timing of sampling post-infusion.

Antimicrobial Effectiveness

  • The maximum concentration of Cefotaxime in plasma was recorded immediately after the halt of the infusion.
  • The research also evaluated Minimum Inhibitory Concentrations (MIC), the lowest concentration of an antimicrobial that inhibits visible bacterial growth, for Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. These bacteria are commonly known to cause septic arthritis in horses.
  • Based on the pharmacokinetic data and bacterial MIC values, the researchers proposed a dosage regimen of 25 mg/kg of Cefotaxime administered intravenously every 6 hours as an effective treatment protocol for susceptible joint infections in adult horses.

Cite This Article

APA
Orsini JA, Moate PJ, Engiles J, Norman T, Poppenga R, Benson CE, Boston RC. (2004). Cefotaxime kinetics in plasma and synovial fluid following intravenous administration in horses. J Vet Pharmacol Ther, 27(5), 293-298. https://doi.org/10.1111/j.1365-2885.2004.00596.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 27
Issue: 5
Pages: 293-298

Researcher Affiliations

Orsini, J A
  • Department of Clinical Studies, New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, 382 West Street Road, Kennett Square, PA 19348, USA. orsini@vet.upenn.edu
Moate, P J
    Engiles, J
      Norman, T
        Poppenga, R
          Benson, C E
            Boston, R C

              MeSH Terms

              • Animals
              • Anti-Bacterial Agents / administration & dosage
              • Anti-Bacterial Agents / blood
              • Anti-Bacterial Agents / pharmacokinetics
              • Anti-Bacterial Agents / pharmacology
              • Arthritis, Infectious / drug therapy
              • Arthritis, Infectious / microbiology
              • Arthritis, Infectious / veterinary
              • Cefotaxime / administration & dosage
              • Cefotaxime / blood
              • Cefotaxime / pharmacokinetics
              • Cefotaxime / pharmacology
              • Chromatography, High Pressure Liquid / veterinary
              • Drug Administration Schedule
              • Escherichia coli / drug effects
              • Horse Diseases / drug therapy
              • Horses / metabolism
              • Infusions, Intravenous / veterinary
              • Joint Diseases / drug therapy
              • Joint Diseases / microbiology
              • Joint Diseases / veterinary
              • Klebsiella pneumoniae / drug effects
              • Microbial Sensitivity Tests
              • Pseudomonas aeruginosa / drug effects
              • Staphylococcus aureus / drug effects
              • Synovial Fluid / metabolism

              Citations

              This article has been cited 2 times.
              1. Altayban A, Kandeel M, Tahoun A, Al-Nazawi M. Cefotaxime pharmacokinetics in Arabian camel (Camelus dromedarius) calves after single intravenous injection. Trop Anim Health Prod 2020 Mar;52(2):887-891.
                doi: 10.1007/s11250-019-02080-0pubmed: 31696417google scholar: lookup
              2. Yilmaz M, Arslan F, Mert A. Community Acquired Chronic Arthritis due to Pseudomonas aeruginosa in a Previously Healthy Pregnant Woman. Case Rep Infect Dis 2014;2014:272306.
                doi: 10.1155/2014/272306pubmed: 25371836google scholar: lookup