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Journal of veterinary pharmacology and therapeutics2015; 38(5); 500-503; doi: 10.1111/jvp.12210

The effect of feeding on the pharmacokinetic variables of two commercially available formulations of omeprazole.

Abstract: The objectives of this study were to investigate the impact of formulation (enteric coated and buffered) and feeding on pharmacokinetic variables associated with the oral administration of omeprazole in the horse. Six thoroughbred racehorses were studied in a crossover design. Each received 2 g of an enteric coated or buffered formulation in both the fed and fasted state. Plasma omeprazole concentrations were determined by UHPLC-MS. The effects of feeding or formulation on AUC0-inf_obs, half-life, Tmax or Cmax were not statistically significant. However, a wider-than-expected degree of variation was present and examination of the raw data suggests that an effect of feeding, wherein the bioavailability of omeprazole may be reduced in the fed animal, may be present. Further investigation in a larger population of animals to assess the factors that contribute to the wide degree of absorption observed is warranted.
Publication Date: 2015-02-10 PubMed ID: 25676888DOI: 10.1111/jvp.12210Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study investigates the impact of different formulations of orally administrated omeprazole and feeding conditions on pharmacokinetic factors in racehorses. Though not statistically significant, hints of reduced drug bioavailability in fed animals were noted, suggesting the need for further study.

Objective of the Study

  • The main aim of this research was to delve into the effects of formulation (specifically enteric coated and buffered versions) and feeding conditions on different pharmacokinetic variables. This was done in the context of oral administration of omeprazole in horses.

Study Design and Methodology

  • The experiment included six thoroughbred racehorses and was carried out using a crossover design. This type of design is a type of longitudinal study in which subjects receive a sequence of different treatments. It’s often used to reduce confounding variables and improve the reliability of findings.
  • Each horse received 2 grams of either an enteric-coated or buffered formulation. These two treatment regimes were introduced in both the fed and fasted state.
  • The concentration of omeprazole in the horse’s plasma was determined utilising UHPLC-MS (ultra-high performance liquid chromatography-mass spectrometry), a method often used for drug detection and analysis.

Findings and Interpretations

  • Upon analyzing the results, the researchers observed that the effects of feeding or the specific formulation of the drug on various pharmacokinetic parameters such as AUC0-inf_obs (the total drug exposure over time from zero to infinity), half-life, Tmax (the time it takes for a drug to reach its maximum concentration in the blood), or Cmax (the maximum or peak concentration of a drug after administration) were not statistically significant.
  • Despite this, the study highlighted a wider-than-expected range of variation. This refers to the variability noticed in the drug absorption levels among the horses.
  • Scrutinizing the raw data suggested that horse feeding could potentially affect the formulation, where the bioavailability (the degree to which a drug is absorbed into the bloodstream) of omeprazole may be reduced in the fed animal.
  • While this possible effect of feeding was not statistically significant in their sample size, the researchers recognized that it may warrant investigation in a broader population of animals to identify the factors that contribute to the broad absorption range observed.

Future Research

  • The researchers recommend further investigation in a larger animal population to understand the elements that contribute to the wide-ranging degree of absorption noticed. Additional research would further verify if the feeding does in fact have a noticeable impact on the absorption of the omeprazole.

Cite This Article

APA
Sykes BW, Underwood C, McGowan CM, Mills PC. (2015). The effect of feeding on the pharmacokinetic variables of two commercially available formulations of omeprazole. J Vet Pharmacol Ther, 38(5), 500-503. https://doi.org/10.1111/jvp.12210

Publication

ISSN: 1365-2885
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 38
Issue: 5
Pages: 500-503

Researcher Affiliations

Sykes, B W
  • School of Veterinary Sciences, The University of Queensland, Gatton, Qld, Australia.
Underwood, C
  • School of Veterinary Sciences, The University of Queensland, Gatton, Qld, Australia.
McGowan, C M
  • Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, UK.
Mills, P C
  • School of Veterinary Sciences, The University of Queensland, Gatton, Qld, Australia.

MeSH Terms

  • Administration, Oral
  • Animals
  • Anti-Ulcer Agents / administration & dosage
  • Anti-Ulcer Agents / blood
  • Anti-Ulcer Agents / pharmacokinetics
  • Eating / physiology
  • Fasting / metabolism
  • Female
  • Horses / blood
  • Horses / metabolism
  • Male
  • Omeprazole / administration & dosage
  • Omeprazole / blood
  • Omeprazole / pharmacokinetics

Citations

This article has been cited 3 times.
  1. Gough S, Hallowell G, Rendle D. Evaluation of the treatment of equine glandular gastric disease with either long-acting-injectable or oral omeprazole. Vet Med Sci 2022 Mar;8(2):561-567.
    doi: 10.1002/vms3.728pubmed: 35167731google scholar: lookup
  2. Wise JC, Hughes KJ, Edwards S, Jacobson GA, Narkowicz CK, Raidal SL. Pharmacokinetic and pharmacodynamic effects of 2 registered omeprazole preparations and varying dose rates in horses. J Vet Intern Med 2021 Jan;35(1):620-631.
    doi: 10.1111/jvim.15971pubmed: 33340169google scholar: lookup
  3. Sykes BW, Hewetson M, Hepburn RJ, Luthersson N, Tamzali Y. European College of Equine Internal Medicine Consensus Statement--Equine Gastric Ulcer Syndrome in Adult Horses. J Vet Intern Med 2015 Sep-Oct;29(5):1288-99.
    doi: 10.1111/jvim.13578pubmed: 26340142google scholar: lookup