Pharmacokinetic studies of theophylline in horses.
Abstract: The pharmacokinetics of theophylline were determined in Standardbred trotters after single intravenous and oral administration. A bi-exponential equation was fitted to the intravenous data and a tri-exponential equation to the oral data. The biological half-life of theophylline was found to be 14.8 h, the volume of distribution 1.02 l/kg and the total plasma clearance 0.86 ml/kg/min. The oral absorption of the drug was complete (bioavailability 108%) and rapid (absorption half-life 0.4 h).
Publication Date: 1985-03-01 PubMed ID: 3989903DOI: 10.1111/j.1365-2885.1985.tb00927.xGoogle Scholar: Lookup
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- Journal Article
Summary
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The research is about studying the behavior of the drug theophylline in horses, particularly in Standardbred trotters. The study tracked how the drug moves in the horse’s body after it was administered both intravenously and orally.
Overview of the Research and Methodology
- The research focused on studying the pharmacokinetics of theophylline, which essentially means how the drug gets absorbed, distributed, metabolized, and excreted by the body of the Standardbred trotters.
- The theophylline was administered in two common methods, intravenous (directly into the bloodstream) and oral (by mouth).
- The scientists used a bi-exponential equation to fit the data gathered from the intravenous method and a tri-exponential equation for the data from the oral method. These models enabled them to accurately describe how the levels of the drug changed over time in the body.
Findings
- The biological half-life, which refers to the time needed for half of the drug to be naturally eliminated from the body, was determined to be 14.8 hours. This suggests that theophylline has a relatively long duration of action in the horse’s body.
- The volume of distribution of the drug, which gives an idea of how extensively the drug has spread throughout the tissues in the horse’s body, was found to be 1.02 liters per kilogram. This suggests the theophylline spreads widely in the horse body’s tissues.
- The total plasma clearance rate, the rate at which the drug is removed from the plasma, was calculated to be 0.86 milliliters per kilogram per minute. This refers to the effectiveness of the body (primarily the liver and kidneys) in removing the drug.
- The overall oral absorption of the drug, also known as its bioavailability, was complete at 108%. This means that slightly more of the drug becomes available in the bloodstream after oral administration than would be expected.
- Furthermore, the absorption half-life was rapid, at only 0.4 hours. This indicates that the drug is quickly absorbed into the bloodstream after oral administration.
Conclusion
- This research provides useful information about the pharmacokinetics of theophylline in Standardbred trotters, which is important for optimizing the therapeutic use of this drug in these animals.
- Understanding the pharmacokinetics of the drug in various administration routes offers clinicians valuable insights for designing optimal dosage regimens.
Cite This Article
APA
Ingvast-Larsson C, Paalzow G, Paalzow L, Ottosson T, Lindholm A, Appelgren LE.
(1985).
Pharmacokinetic studies of theophylline in horses.
J Vet Pharmacol Ther, 8(1), 76-81.
https://doi.org/10.1111/j.1365-2885.1985.tb00927.x Publication
Researcher Affiliations
MeSH Terms
- Administration, Oral
- Animals
- Biological Availability
- Female
- Half-Life
- Horses / metabolism
- Injections, Intravenous
- Kinetics
- Male
- Theophylline / administration & dosage
- Theophylline / metabolism
Citations
This article has been cited 1 times.- Errecalde JO, Landoni MF. The pharmacokinetics of a slow-release theophylline preparation in horses after intravenous and oral administration. Vet Res Commun 1992;16(2):131-8.
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