Analyze Diet
Journal of analytical toxicology1999; 23(3); 200-209; doi: 10.1093/jat/23.3.200

Etodolac in equine urine and serum: determination by high-performance liquid chromatography with ultraviolet detection, confirmation, and metabolite identification by atmospheric pressure ionization mass spectrometry.

Abstract: A high-performance liquid chromatographic method was used for the detection of etodolac in equine serum and urine. The method consisted of a one-step liquid-liquid extraction, separation on a reversed-phase (RP-18) column and detection using an ultraviolet detector. Additional confirmation methods included a HPLC coupled with an atmospheric pressure chemical ionization mass spectrometer (APCI-MS). Free (unbound) etodolac and its conjugates were present in the samples. Concentrations of the drug in the serum and urine samples collected from four standardbred mares after a single oral administration of Ultradol were determined. Maximum etodolac concentrations of 712, 716, 568, and 767 microg/mL in urine and 4.1, 3.6, 3.1, and 2.2 microg/mL in serum were observed. The peak concentrations of the drug were detected 2-10 h (urine) and 40 min-6 h (serum) after administration to four horses. The maximum detection time was 79 h in urine and 48 h in serum after the drug administration. The drug-elimination profiles for both urine and serum are presented and discussed. Method ruggedness and precision and stability studies of etodolac in serum and urine are presented. Three major metabolites were detected in the urine by liquid chromatography-APCI-MS. All three metabolites were identified as monohydroxylated etodolac.
Publication Date: 1999-06-16 PubMed ID: 10369330DOI: 10.1093/jat/23.3.200Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article presents a method for detecting a drug known as etodolac in horses’ urine and serum, using high-performance liquid chromatography and atmospheric pressure ionization mass spectrometry. It also discusses the times and concentrations at which peak drug effects occur, the duration of its detectability, and shows that etodolac is converted into monohydroxylated etodolac in the body.

Method for Detection of Etodolac

  • The researchers used a high-performance liquid chromatographic method for detecting etodolac in equine serum and urine.
  • This method involves a one-step liquid-liquid extraction, separation on a reversed-phase column and detection using an ultraviolet detector.
  • For additional confirmation, the high-performance liquid chromatography method was paired with an atmospheric pressure chemical ionization mass spectrometer.

Concentration and Detection Time of Etodolac

  • The scientists administered Ultradol, a drug containing etodolac, orally to four standardbred mares.
  • The concentration of etodolac in the urine and serum samples was measured and tracked over time.
  • Maximum etodolac concentrations were between 568 and 767 micrograms per milliliter (μg/mL) in urine and between 2.2 and 4.1 μg/mL in serum.
  • Peak concentrations were detected within 2 to 10 hours in urine and within 40 minutes to 6 hours in serum, post-administration.
  • Etodolac was detectable up to 79 hours in urine and up to 48 hours in serum post-administration.

Method Ruggedness and Stability Studies

  • The study also included a ruggedness and precision study of the methods used to detect etodolac in serum and urine.
  • These findings discuss the method’s reliability and dependability for its intended use, an essential component in its validity and potential for wider adoption.

Identification of Metabolites

  • Finally, the researchers identified three main metabolites of etodolac from the horse urine via liquid chromatography-APCI-MS.
  • All three metabolites were identified as monohydroxylated etodolac, offering insights into how the drug is processed within the equine body.

Cite This Article

APA
Koupai-Abyazani MR, Esaw B, Laviolette B. (1999). Etodolac in equine urine and serum: determination by high-performance liquid chromatography with ultraviolet detection, confirmation, and metabolite identification by atmospheric pressure ionization mass spectrometry. J Anal Toxicol, 23(3), 200-209. https://doi.org/10.1093/jat/23.3.200

Publication

ISSN: 0146-4760
NlmUniqueID: 7705085
Country: England
Language: English
Volume: 23
Issue: 3
Pages: 200-209

Researcher Affiliations

Koupai-Abyazani, M R
  • CANTEST Laboratories Ltd., Vancouver, British Columbia, Canada.
Esaw, B
    Laviolette, B

      MeSH Terms

      • Animals
      • Anti-Inflammatory Agents, Non-Steroidal / blood
      • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
      • Anti-Inflammatory Agents, Non-Steroidal / urine
      • Chromatography, High Pressure Liquid / methods
      • Drug Stability
      • Etodolac / blood
      • Etodolac / pharmacokinetics
      • Etodolac / urine
      • Female
      • Horses
      • Mass Spectrometry / methods
      • Reproducibility of Results
      • Sensitivity and Specificity
      • Spectrophotometry, Ultraviolet / methods

      Citations

      This article has been cited 0 times.