Determination of methocarbamol in equine serum and urine by high-performance liquid chromatography with ultraviolet detection and atmospheric pressure ionization-mass spectrometric confirmation.
Abstract: Urine and serum samples collected from four standard-bred mares after and oral regimen administration of methocarbamol were extracted and analyzed. The method consisted of enzyme hydrolysis followed by a one-step liquid-liquid extraction, separation on a reversed-phase (RP-18) column, and detection using an ultraviolet (UV) detector. The confirmation was carried out using a liquid chromatography-atmospheric pressure ionization-mass spectrometry (LC-API-MS) system. Maximum methocarbamol concentrations of 1498, 1734, 1547, 2322 micrograms/mL in urine and 4.9, 1.7, and 3.6 micrograms/mL in serum were observed. The peak concentrations of the drug were detected 1-4 h (urine) and 10-60 min (serum) after administration to four horses. The method validation results and drug elimination profiles for both urine and serum are presented and discussed.
Publication Date: 1997-07-01 PubMed ID: 9248949DOI: 10.1093/jat/21.4.301Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research paper discusses a method for measuring the concentration of methocarbamol, a muscle relaxant, in horse urine and serum using high-performance liquid chromatography and mass spectrometry.
Methods
- The research paper describes a method to detect the presence and concentration of methocarbamol, a muscle relaxant drug commonly used in veterinary medicine, in both the urine and serum of horses.
- For the research, urine and serum samples were collected from four standard-bred mares after an oral regimen administration of methocarbamol was given.
- The method involved first hydrolyzing the samples with enzymes, followed by a one-step liquid-liquid extraction.
- The samples were then separated using a reversed-phase column (RP-18) and detected with an ultraviolet (UV) detector.
Confirmation Process
- The researchers confirmed their findings with a liquid chromatography-atmospheric pressure ionization-mass spectrometry (LC-API-MS) system.
- This system is instrumental in providing very specific results as it can isolate and detect individual molecules in a sample, making it a precise tool for drug detection.
Results
- Upon analysis, maximum concentrations of 1498, 1734, 1547, 2322 micrograms/mL of methocarbamol in urine and 4.9, 1.7, and 3.6 micrograms/mL in serum samples were observed.
- The peak concentrations of the drug were detected 1-4 hours after administration in urine and 10-60 minutes after administration in serum. The variance in detection times between the two mediums is likely due to the body’s metabolic and excretory processes.
Discussion
- The research team discussed the results of their method validation and the observed drug elimination profiles for both urine and serum.
- The findings of the research would be significant for doping control in equestrian sports, understanding the pharmacokinetics of methocarbamol in horses, and ensuring the safe and effective use of the drug in veterinary practice.
Cite This Article
APA
Koupai-Abyazani MR, Esaw B, Laviolette B.
(1997).
Determination of methocarbamol in equine serum and urine by high-performance liquid chromatography with ultraviolet detection and atmospheric pressure ionization-mass spectrometric confirmation.
J Anal Toxicol, 21(4), 301-305.
https://doi.org/10.1093/jat/21.4.301 Publication
Researcher Affiliations
- Can Test Laboratories Ltd., Vancouver, British Columbia, Canada.
MeSH Terms
- Animals
- Atmospheric Pressure
- Chromatography, High Pressure Liquid / methods
- Horses / blood
- Horses / urine
- Mass Spectrometry / methods
- Methocarbamol / blood
- Methocarbamol / urine
- Muscle Relaxants, Central / blood
- Muscle Relaxants, Central / urine
- Reproducibility of Results
- Spectrophotometry, Ultraviolet
Citations
This article has been cited 1 times.- Walash M, Belal F, Eid M, EL Abass SA. Spectrofluorometric determination of methocarbamol in pharmaceutical preparations and human plasma. J Fluoresc 2011 Mar;21(2):555-61.
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