Detection of fenspiride and identification of in vivo metabolites in horse body fluids by capillary gas chromatography-mass spectrometry: administration, biotransformation and urinary excretion after a single oral dose.
Abstract: Studies related to the in vivo biotransforrmation and urinary excretion of fenspiride hydrochloride in the horse are described. After oral administration, the drug is metabolised by both phase I functionalisation and phase II conjugation pathways. Following enzymatic deconjugation, fenspiride and its phase I metabolites were isolated from post-administration biofluids using bonded co-polymeric mixed mode solid-phase extraction cartridges to isolate the basic compounds. Following trimethylsilylation (TMS), the parent drug and metabolites were identified by capillary gas chromatography-mass spectrometry (GC-MS). Fenspiride (A) and seven metabolites (B-->G) arising from oxidation on both the aromatic and heterocyclic substructures were detected in urine. The positive ion electron ionisation mass spectra of the TMS derivatives of fenspiride and its metabolites provided useful information on its metabolism. Positive ion methane chemical ionisation-GC-MS of the derivatives provided both derivatised molecular mass and structural information. Unchanged fenspiride can be detected in post-administration plasma and urine samples for up to 24 h. Maximum urinary levels of 100-200 ng ml(-1) were observed between 3 and 5 h after administration. After enzymatic deconjugation, the major phenolic metabolite (G) can be detected in urine for up to 72 h. This metabolite is the analyte of choice in the GC-MS screening of post-race equine urine samples for detection of fenspiride use. However, a distinct difference was observed in the urinary excretion of this metabolite between the thoroughbred horses used in UK study and the quarterbred and standardbred horses used for the USA administrations.
Publication Date: 2002-02-28 PubMed ID: 11863284DOI: 10.1016/s0378-4347(01)00556-4Google Scholar: Lookup
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- Journal Article
Summary
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This research article examines the biotransformation and urinary excretion of the drug fenspiride hydrochloride in horses. It highlights how the drug and its metabolites can be isolated and identified in horse body fluids through testing methods, and discusses the timeframes in which the unchanged drug and its major metabolite can be detected in post-administration samples. It also notes a significant difference in the urinary excretion of the major metabolite among different horse breeds.
Drug Administration and Metabolism
- The drug in focus is fenspiride hydrochloride, a bronchodilatory drug known to suppress cough reflexes, often used in treating respiratory diseases.
- After being administered orally to a horse, the drug is metabolized through a two-step process: Firstly, phase I functionalisation, followed by phase II conjugation pathways, which is a common metabolic pathway for drugs.
Metabolite Detection and Identification
- In post-administration biofluids, both fenspiride and its phase I metabolites were isolated using a technique called bonded co-polymeric mixed-mode solid-phase extraction, specifically meant for isolating basic compounds.
- After undergoing a process called trimethylsilylation (TMS), these elements were identified using a testing method known as capillary gas chromatography-mass spectrometry (GC-MS)
- In the urine, the researchers detected fenspiride along with seven metabolites resulting from the drug’s oxidation. They acquired important data about fenspiride’s metabolism through the positive ion electron ionisation mass spectra of the TMS derivatives of the drug and its metabolites.
Excretion Timeframe and Detection in Horse Species
- The unchanged drug can be identified in both plasma and urine samples up to 24 hours after administration.
- The major phenolic metabolite (designated as ‘G’) is the primary element surveyed in post-racing tests looking for the presence of fenspiride in equine urine samples. This metabolite can be detected up to 72 hours post administration.
- A key observation was the noticeable difference in the excretion of metabolite G between different breeds of horses. Specifically, the thoroughbred horses used in the UK study displayed a different metabolic response compared to the quarterbred and standardbred horses used in the USA.
Cite This Article
APA
Dumasia MC, Houghton E, Hyde W, Greulich D, Nelson T, Peterson J.
(2002).
Detection of fenspiride and identification of in vivo metabolites in horse body fluids by capillary gas chromatography-mass spectrometry: administration, biotransformation and urinary excretion after a single oral dose.
J Chromatogr B Analyt Technol Biomed Life Sci, 767(1), 131-144.
https://doi.org/10.1016/s0378-4347(01)00556-4 Publication
Researcher Affiliations
- Department of Drug Metabolism, Research Division, Horseracing Forensic Laboratory Ltd, Ely, Cambridgeshire, UK. mdumasia@hfl.co.uk
MeSH Terms
- Animals
- Biotransformation
- Body Fluids / metabolism
- Calibration
- Gas Chromatography-Mass Spectrometry / methods
- Horses
- Male
- Spiro Compounds / pharmacokinetics
- Spiro Compounds / urine
Citations
This article has been cited 1 times.- Yuan M, Breitkopf SB, Asara JM. Serial-omics characterization of equine urine. PLoS One 2017;12(10):e0186258.
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