Pharmacokinetics of intravenously and orally administered pyrimethamine in horses.
Abstract: Single-dose pharmacokinetic variables of pyrimethamine were studied in horses. Pyrimethamine (1 mg/kg of body weight) was administered IV and orally to 6 adult horses, and plasma samples were obtained at frequent intervals thereafter. Plasma pyrimethamine concentration was assayed by gas chromatography, and concentration-time data were analyzed, using a pharmacokinetic computer program. The IV and oral administration data were best described by 3-compartment and 1-compartment models, respectively. The median volume of distribution at steady state after IV administration was 1,521 ml/kg and the median elimination half-time was 12.06 hours. Mean plasma concentration after oral administration fluctuated between a maximal concentration of 0.18 microgram/ml and 0.09 microgram/ml (24 hours after dosing). Bioavailability after oral administration was 56%.
Publication Date: 1992-12-01 PubMed ID: 1476310
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- Journal Article
Summary
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The research article studies the behavior of Pyrimethamine, an antimalarial drug, in horses when given through both intravenous (IV) and oral administrations. The results provide important information on how the administered drug is metabolized and cleared from the horse’s body.
Research Methodology
- The research begins with the administration of Pyrimethamine to six fully-grown horses. This was done in two methods namely intravenously (IV) and orally. In each case, the horses were given 1 mg/kg of their body weight.
- The researchers took plasma samples from the horses at frequent intervals after administering the plasma. These samples were then used to measure the concentration of the drug through a method known as gas chromatography.
- Pharmacokinetic computer programming was used to analyze the data collected from the concentration-time of the plasma samples. This allowed the researchers to determine how the drug moves in and out of the body and its overall metabolism.
Research Results
- Findings from the intravenously administered drugs indicated that the data was best explained by a 3-compartment model, a term generally used in pharmacokinetics to describe how a drug is distributed and eliminated from the body.
- The volume of distribution at steady state after being given IV was a median of 1,521 ml/kg. The elimination half-time, which describes the time it takes for half of the administered drug to be removed from the body, was 12.06 hours.
- Data from the orally administered drugs, on the other hand, worked best with a 1-compartment model.
- The average plasma concentration fluctuated from a maximum concentration of 0.18 micrograms/ml to a minimum of 0.09 micrograms/ml 24 hours after dosage. The bioavailability, which is a measure of the amount of drug that reaches systemic circulation, was 56% after oral administration. This implies that the drug was more readily available in the body when orally administered than when given intravenously.
The research findings are key to understanding the pharmacokinetic parameters of Pyrimethamine in horses and could lead to more effective treatment strategies using the drug.
Cite This Article
APA
Clarke CR, Burrows GE, MacAllister CG, Spillers DK, Ewing P, Lauer AK.
(1992).
Pharmacokinetics of intravenously and orally administered pyrimethamine in horses.
Am J Vet Res, 53(12), 2292-2295.
Publication
Researcher Affiliations
- Department of Physiological Sciences, College of Veterinary Medicine, Oklahoma State University, Stillwater 74078.
MeSH Terms
- Administration, Oral
- Animals
- Chromatography, Gas / veterinary
- Female
- Horses / metabolism
- Injections, Intravenous / veterinary
- Male
- Models, Biological
- Pyrimethamine / blood
- Pyrimethamine / pharmacokinetics
Citations
This article has been cited 1 times.- Almond DS, Szwandt IS, Edwards G, Lee MG, Winstanley PA. Disposition of intravenous pyrimethamine in healthy volunteers. Antimicrob Agents Chemother 2000 Jun;44(6):1691-3.
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