Pharmacokinetic/pharmacodynamic analysis of cephalothin after intramuscular administration in Thoroughbred horses.
Abstract: A pharmacokinetic/pharmacodynamic (PK/PD) approach was used to determine a dosage regimen of cephalothin (CET) after intramuscular (IM) administration in horses. CET plasma concentrations were measured in eight horses after a single IM administration of 11 mg/kg bwt of CET. The data were modeled using a nonlinear mixed-effect model, and the probability of target attainment (PTA) of the PK/PD target was calculated for 5,000 horses generated by Monte Carlo simulations. IM administrations of CET at 11 mg/kg bwt q 8 hr and q 6 hr achieved a PTA of 90% against the MIC90 of S. zooepidemicus and S. aureus, respectively, and were considered to be effective dosage regimens. The total dose for the IM administration recommended in this study was lower than that for intravenous (IV) administration in previous studies.
©2023 The Japanese Society of Equine Science.
Publication Date: 2024-01-18 PubMed ID: 38274556PubMed Central: PMC10806359DOI: 10.1294/jes.34.111Google Scholar: Lookup
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Summary
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This research article investigates the most effective dosage schedule of cephalothin, a type of antibiotic, when administered intramuscularly to Thoroughbred horses. Using a mathematical modelling approach, the study found that a dosage of 11 mg/kg every 8 or 6 hours provided 90% probability of successfully treating S. zooepidemicus and S. aureus infections.
Study Design
- The study employs a pharmacokinetic/pharmacodynamic (PK/PD) approach. This involves studying the rate at which a drug is processed in the body (pharmacokinetics) and the effects it has on the body (pharmacodynamics).
- The PK/PD model was applied to cephalothin (CET), an antibiotic, to find an effective dosage regimen when given by intramuscular (IM) injection.
- The research involved a sample size of eight Thoroughbred horses, each given a single IM dose of CET at 11 mg/kg body weight.
Methodology and Results
- The researchers measured CET plasma concentrations in the horses after the drug was administered.
- The measurements were processed using a nonlinear mixed-effect model, a statistical tool used in drug testing to account for variability between different subjects.
- The probability of target attainment (PTA) was calculated. This is basically the likelihood that the drug treatment will reach the intended effect.
- Using a Monte Carlo simulation, a computational technique that generates random sampling outcomes, the PTA was calculated for 5,000 horses.
- The study found that administering CET via IM injection at 11 mg/kg body weight every 8 hours and every 6 hours achieved a PTA of 90% in treating S. zooepidemicus and S. aureus infections, respectively.
Implications of the Findings
- This suggests these are effective dosage regimens for treating these types of infections in horses.
- The research also indicated that the total dose suggested for IM administration in this study was lower than that recommended for intravenous (IV) administration in previous studies.
- This research could potentially have an impact on horse health management, optimization of drug treatments, and could contribute to more cost-effective use of antibiotics.
Cite This Article
APA
Kuroda T, Minamijima Y, Niwa H, Mita H, Tamura N, Fukuda K, Ohta M.
(2024).
Pharmacokinetic/pharmacodynamic analysis of cephalothin after intramuscular administration in Thoroughbred horses.
J Equine Sci, 34(4), 111-114.
https://doi.org/10.1294/jes.34.111 Publication
Researcher Affiliations
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
- Laboratory of Racing Chemistry, Tochigi 320-0851, Japan.
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
- Equine Research Institute, Japan Racing Association, Tochigi 329-0412, Japan.
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