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Biomedical chromatography : BMC1994; 8(1); 29-31; doi: 10.1002/bmc.1130080108

A liquid chromatographic method for the determination of fenoprofen in equine plasma and urine.

Abstract: A high performance liquid chromatographic method to measure plasma and urine fenoprofen levels in equine biofluids is described. Liquid-liquid extraction with diethylether was used to isolate the drug from plasma and urine. The accuracy and reproducibility of the method were within acceptable limits over the concentration range 0-10 micrograms/mL and 0-20 micrograms/mL respectively from plasma and urine. Detection limits were 0.05 microgram/mL (2 mL plasma) and 0.2 microgram/mL (0.5 mL urine). This procedure was applied to ascertain the pharmacokinetics of a 3 g dose of fenoprofen calcium in a horse.
Publication Date: 1994-01-01 PubMed ID: 8130630DOI: 10.1002/bmc.1130080108Google Scholar: Lookup
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  • Journal Article

Summary

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The research presents a reliable method using high performance liquid chromatography (HPLC) to measure fenoprofen, a type of non-steroidal anti-inflammatory drug, in horse plasma and urine.

Understanding the Research Methodology

This research primarily focuses on implementing a high performance liquid chromatographic method to analyze Fenoprofen in biofluids of a horse, namely plasma and urine. Liquid-liquid extraction with diethylether was the chosen technique for drug isolation from these fluids. The key features of the methodology can be defined as follows:

  • Liquid-liquid extraction is a simple process where a solution is separated into two liquid phases by the addition of a solvent in which the item of interest is soluble.
  • Diethylether was used as the solvent for drug extraction, this choice might be influenced by its various characteristics like a greater degree of polarity and lower density than water.
  • The chosen method of separation and analysis is High Performance Liquid Chromatography (HPLC), which is a highly accurate and reproducible method for separation and identification of compounds. It works on the principle that different compounds will elute, or come off the column, at different times.

Evaluating the Performance of the Method

The reliability and accuracy of the established method depend on several parameters. In this research those measures where:

  • Accuracy and reproducibility of the method: The research team found accurate results within acceptable limits over the concentration range 0-10 micrograms/mL from plasma and 0-20 micrograms/mL from urine.
  • Detection limits: The detection limits were considerably low, at 0.05 micrograms/mL for plasma samples (2mL) and 0.2 micrograms/mL for urine samples (0.5mL). These low detection limits indicate high sensitivity of the method.

Applying the Method to Study Pharmacokinetics

Upon establishing the reliability of the method, it was applied to investigate the pharmacokinetics of a 3-gram dose of Fenoprofen calcium in a horse. Here, the study would likely look at the absorption, distribution, metabolism, and excretion of the drug. The findings from such a study could provide vitally important data for understanding the drug’s effects, its optimal dosage in equine medicine, and potential side effects.

Cite This Article

APA
Delbeke FT, Debackere M. (1994). A liquid chromatographic method for the determination of fenoprofen in equine plasma and urine. Biomed Chromatogr, 8(1), 29-31. https://doi.org/10.1002/bmc.1130080108

Publication

ISSN: 0269-3879
NlmUniqueID: 8610241
Country: England
Language: English
Volume: 8
Issue: 1
Pages: 29-31

Researcher Affiliations

Delbeke, F T
  • Faculteit Diergeneeskunde, Universiteit Gent, Belgium.
Debackere, M

    MeSH Terms

    • Animals
    • Chromatography, High Pressure Liquid / methods
    • Chromatography, High Pressure Liquid / standards
    • Female
    • Fenoprofen / blood
    • Fenoprofen / urine
    • Horses / blood
    • Horses / urine
    • Reproducibility of Results

    Citations

    This article has been cited 1 times.
    1. Shiri S, Alizadeh K, Abbasi N. A novel technique for simultaneous determination of drugs using magnetic nanoparticles based dispersive micro-solid-phase extraction in biological fluids and wastewaters. MethodsX 2020;7:100952.
      doi: 10.1016/j.mex.2020.100952pubmed: 32596135google scholar: lookup