Cefadroxil in the horse: pharmacokinetics and in vitro antibacterial activity.
Abstract: Sodium cefadroxil was administered as a single intravenous dose (25 mg/kg) to six healthy adult mares. Plasma samples were collected over a 24-h period and cefadroxil concentrations were measured by microbiological assay. The pharmacokinetic behavior of the drug was appropriately described in terms of a one-compartment open model. Values for the major pharmacokinetic terms were: extrapolated initial plasma concentration = 59.2 +/- 15.0 micrograms/ml; half-life = 46 +/- 20 min; apparent volume of distribution = 462 +/- 191 ml/kg; and body clearance = 7.0 +/- 0.6 ml/min.kg. In a subsequent study, a suspension of cefadroxil monohydrate was administered intragastrically (25 mg/kg) to the same six horses. Plasma concentrations of the drug peaked at 1-2 h but, in general, absorption was both poor and inconsistent. The data were unsuitable for determination of cefadroxil bioavailability from this oral dosage form. Ninety-nine isolates of eleven bacterial species obtained from clinically ill horses were tested for susceptibility to cefadroxil. All strains of Streptococcus equi, Streptococcus zooepidemicus, coagulase-positive staphylococci, Corynebacterium pseudotuberculosis and five out of six strains of Actinobacillus suis were highly susceptible to the drug (MIC less than 4 micrograms/ml). Escherichia coli, Klebsiella pneumoniae and Salmonella sp. showed intermediate susceptibility (MIC 4-16 micrograms/ml), while all isolates of Corynebacterium (Rhodococcus) equi, Enterobacter cloacae and Pseudomonas aeruginosa proved to be highly resistant to cefadroxil (MIC greater than 128 micrograms/ml).
Publication Date: 1985-09-01 PubMed ID: 4057345DOI: 10.1111/j.1365-2885.1985.tb00953.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research investigated the behavior and effects of the antibiotic cefadroxil in horses and tested its effectiveness against various bacterial strains. Main findings showed the cefadroxil had varying effectiveness depending on the bacterial strain and mode of administration in horses.
Research Method
- An antibiotic drug, Sodium cefadroxil, was administered as a single dose through the vein to six adult mares.
- The concentration of the drug in their plasma was measured over 24 hours using a microbiological assay.
- The distribution and removal of the drug from the body was modeled and key parameters calculated.
- In a separate experiment, a suspension of the drug was administered into the stomach of the same six horses.
- Samples were taken to measure peak plasma levels and absorption of the drug.
Pharmacokinetics of Cefadroxil
- Cefadroxil’s activity in the horse’s body was best described using a one-compartment open model. This is a standard model used in pharmacokinetics to describe the absorption, distribution, metabolism, and excretion of drugs.
- The main pharmacokinetic terms, which provide information about the drug action in the body, were identified. This includes the initial plasma concentration, half-life, volume of distribution, and body clearance rate.
- The drug’s half-life—a measure of how long it takes for half the drug to be removed from the body—was found to be 46 minutes on average.
- The other identified parameters were the initial plasma concentration (59.2 micrograms/ml), the volume of distribution (462 ml/kg), and the body clearance rate (7.0 ml/min.kg).
Antibacterial Activity of Cefadroxil
- The researchers tested the susceptibility of 99 bacterial strains from 11 species to cefadroxil. These bacteria were collected from horses suffering from clinical illnesses.
- The strains of bacteria demonstrated varying degrees of susceptibility to the antibiotic. Streptococcus equi, Streptococcus zooepidemicus, coagulase-positive staphylococci, Corynebacterium pseudotuberculosis, and most strains of Actinobacillus suis were highly susceptible to cefadroxil.
- However, some strains such as Escherichia coli, Klebsiella pneumoniae, and Salmonella sp. showed intermediate susceptibility and others including Corynebacterium (Rhodococcus) equi, Enterobacter cloacae and Pseudomonas aeruginosa proved to be highly resistant to cefadroxil.
- This finding allows for selection of this antibiotic in case of infections with these susceptible bacteria, while alternative treatments would need to be considered against the cefadroxil-resistant strains.
Cite This Article
APA
Wilson WD, Baggot JD, Adamson PJ, Hirsh DC, Hietala SK.
(1985).
Cefadroxil in the horse: pharmacokinetics and in vitro antibacterial activity.
J Vet Pharmacol Ther, 8(3), 246-253.
https://doi.org/10.1111/j.1365-2885.1985.tb00953.x Publication
Researcher Affiliations
MeSH Terms
- Animals
- Bacteria / drug effects
- Biological Availability
- Cefadroxil / metabolism
- Cefadroxil / pharmacology
- Female
- Horse Diseases / microbiology
- Horses / metabolism
- Kinetics
- Microbial Sensitivity Tests
Citations
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