Pharmacokinetics and body fluid and endometrial concentrations of cefoxitin in mares.
Abstract: Four healthy adult mares were each given a single injection of sodium cefoxitin (20 mg/kg of body weight, IV), and serum cefoxitin concentrations were measured serially during a 6-hour period. The mean elimination rate constant was 1.08/hour and the elimination half-life was 0.82 hour. The apparent volume of distribution (at steady state) and the clearance of the drug were estimated at 0.12 L/kg and 259 ml/hr/kg, respectively. Each mare and 2 additional mares were then given 4 consecutive IM injections of sodium cefoxitin (400 mg/ml) at a dosage of 20 mg/kg. Cefoxitin concentrations in serum, synovial fluid, peritoneal fluid, CSF, urine, and endometrium were measured serially. After IM administration, the highest mean serum concentration was 23.1 micrograms/ml 30 minutes after the 2nd injection. The highest mean synovial concentration was 11.4 micrograms/ml 1 hour after the 4th injection. The highest mean peritoneal concentration was 10.4 micrograms/ml 2 hours after the 4th injection. The highest mean endometrial concentration was 4.5 micrograms/g 4 hours after the 4th injection. Mean urine concentrations reached 11,645 micrograms/ml. Cefoxitin did not readily penetrate the CSF. Bioavailability of cefoxitin given IM was 65% to 89% (mean +/- SEM = 77% +/- 5.9%). One of the 6 mares developed acute laminitis during the IM experiment.
Publication Date: 1986-08-01 PubMed ID: 3752682
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- Journal Article
- Research Support
- U.S. Gov't
- Non-P.H.S.
Summary
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The research article is about a study conducted on four mares to ascertain the body fluid distribution and pharmacokinetics of Cefoxitin, an antibiotic commonly used for bacterial infections, after both intravenous and intramuscular administration.
Methodology
- Four healthy adult mares were administered a single dose of sodium Cefoxitin (20 mg/kg of body weight, IV) and then serum Cefoxitin concentrations were measured at intervals over a period of 6 hours.
- Values including, the mean elimination rate, elimination half-life, apparent volume of distribution (Vd) and clearance of the drug were calculated.
- This same set of mares along with an additional two were then given four intramuscular injections of sodium Cefoxitin (400 mg/ml) at a dosage of 20 mg/kg.
- Cefoxitin concentrations in serum, synovial fluid, peritoneal fluid, cerebrospinal fluid (CSF), urine, and endometrium were measured intermittently.
Results
- The mean elimination rate constant was found to be 1.08/hour and the elimination half-life was 0.82 hour.
- Apparent volume of distribution (Vd) was 0.12 L/kg and clearance was 259 ml/hr/kg.
- Peak serum concentration of 23.1 micrograms/ml was observed 30 minutes after the 2nd intramuscular injection.
- Peak concentration values were also calculated for synovial, peritoneal, and endometrial fluids.
- Cefoxitin concentration in urine was seen to be significantly high.
Implications and Conclusions
- Cefoxitin did not easily penetrate the CSF, implying its limited use in treating CNS infections.
- The bioavailability of Cefoxitin, when given intramuscularly, was calculated to be between 65% to 89%, with a mean of 77%, which indicates high absorption and systemic use.
- However, the study also reported an instance of one horse developing acute laminitis during the course of the study which hints at potential side effects.
- This research provides critical insights into the distribution, clearance, and bioavailability of Cefoxitin, particularly valuable for equine veterinary medicine.
Cite This Article
APA
Brown MP, Gronwall RR, Houston AE.
(1986).
Pharmacokinetics and body fluid and endometrial concentrations of cefoxitin in mares.
Am J Vet Res, 47(8), 1734-1738.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cefoxitin / blood
- Cefoxitin / metabolism
- Endometrium / metabolism
- Female
- Horses / metabolism
- Kinetics
- Peritoneal Cavity / metabolism
- Synovial Fluid / metabolism
- Time Factors
Citations
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