Analyze Diet
Journal of chromatography1987; 404(1); 223-232; doi: 10.1016/s0021-9673(01)86852-7

Analysis of detomidine in horse blood, plasma and urine samples utilizing a sensitive gas chromatography-mass spectrometry method.

Abstract: Chemical ionization- and electron impact ionization-selective ion monitoring provided a simple and sensitive method for measuring detomidine (Domosedan), a potent sedative-analgesic drug for horses and cattle. Chemical ionization was at least 10 times more sensitive than electron impact ionization. By using propranolol as an internal standard, we found that the recovery of detomidine from the extraction procedure used in this study was greater than 75% for plasma, whole blood, or urine samples. Approximately 68% of detomidine was bound to plasma protein and 53% was bound to red blood cells.
Publication Date: 1987-08-28 PubMed ID: 3680434DOI: 10.1016/s0021-9673(01)86852-7Google 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

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 new method for measuring detomidine, a sedative-analgesic drug for horses and cattle, in their blood, plasma, and urine. The method used is more sensitive and the recovery rate of the drug from samples is significantly high.

Methodology

  • The study employed two methods to monitor the presence of detomidine – chemical ionization and electron impact ionization-selective ion monitoring.
  • Propranolol was used as an internal standard to determine the level of detomidine.
  • The researchers subjected the blood, plasma, and urine samples to an extraction procedure to retrieve detomidine from them.

Findings

  • The researchers discovered that chemical ionization was at least 10 times more sensitive in detecting the presence of detomidine compared to electron impact ionization. This means the chemical ionization method has a higher chance of identifying detomidine presence even in small amounts.
  • The extraction method produced high recovery rates of detomidine in all types of samples used. More than 75% of detomidine was recovered from plasma, whole blood, or urine samples. This suggests that the extraction process was efficient in retrieving the drug from the samples.
  • It was found that 68% of detomidine binds to plasma protein and 53% of it binds to red blood cells. These findings show how detomidine interacts with bodily fluids once administered to horses or cattle, which is vital for understanding its effects and behavior within the body.

Significance

  • This study gives insight into a particularly potent and sensitive method for measuring levels of detomidine. This could help improve the precision and accuracy in checking drug dosage in livestock.
  • The high recovery rate indicates that the extraction method used is quite efficient and may be utilized in similar research involving measurement of drug concentrations in bodily fluids.
  • By understanding how detomidine binds to plasma proteins and red blood cells, veterinarians and scientists can gain insights into the drug’s bodily interactions and influence their usage and dosage decisions.

Cite This Article

APA
Singh AK, Mishra U, Ashraf M, Abdennebi EH, Granley K, Dombrovskis D, Hewetson D, Stowe CM. (1987). Analysis of detomidine in horse blood, plasma and urine samples utilizing a sensitive gas chromatography-mass spectrometry method. J Chromatogr, 404(1), 223-232. https://doi.org/10.1016/s0021-9673(01)86852-7

Publication

NlmUniqueID: 0427043
Country: Netherlands
Language: English
Volume: 404
Issue: 1
Pages: 223-232

Researcher Affiliations

Singh, A K
  • Department of Veterinary Diagnostic Investigation, College of Veterinary Medicine, University of Minnesota, St. Paul 55108.
Mishra, U
    Ashraf, M
      Abdennebi, E H
        Granley, K
          Dombrovskis, D
            Hewetson, D
              Stowe, C M

                MeSH Terms

                • Analgesics / analysis
                • Analgesics / blood
                • Analgesics / urine
                • Animals
                • Blood Proteins / metabolism
                • Chromatography, Thin Layer
                • Erythrocytes / metabolism
                • Gas Chromatography-Mass Spectrometry
                • Horses
                • Imidazoles / analysis
                • Imidazoles / blood
                • Imidazoles / urine
                • Protein Binding

                Citations

                This article has been cited 0 times.