Detection of 17alpha-hydroxyprogesterone caproate in equine plasma by gas chromatography/tandem mass spectrometry.
Abstract: A method was developed for the analysis of the synthetic progestin 17alpha-hydroxyprogesterone caproate in equine plasma following its administration by intramuscular injection. The method employed a reversed-phase solid-phase extraction followed by enol-trimethylsilylation and analysis by gas chromatography/tandem mass spectrometry. The intact ester was detectable in the plasma for up to 2 weeks after a single therapeutic dose, and was found to be stable in equine whole blood for at least 2 months.
Copyright (c) 2006 John Wiley & Sons, Ltd.
Publication Date: 2006-05-18 PubMed ID: 16705648DOI: 10.1002/rcm.2526Google Scholar: Lookup
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- Journal Article
Summary
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This research focuses on developing a method to detect the presence of a synthetic hormone, 17alpha-hydroxyprogesterone caproate, in horse’s blood plasma using a technique called gas chromatography/tandem mass spectrometry.
Methodology
- The researchers established an approach to analyze 17alpha-hydroxyprogesterone caproate, a synthetic progesterone, in equine plasma. This hormone was administered through intramuscular injection.
- The method used is called reverse-phase solid-phase extraction – a procedure that isolates compounds from a mixture based on their physical and chemical properties.
- This extraction method was followed by enol-trimethylsilylation – a chemical process used to make substances more volatile – thus, easier to be detected in the mass spectrometry step.
- The team then utilized gas chromatography (a technique used to separate and analyze compounds that can be vaporized without decomposition) combined with tandem mass spectrometry (a method that identifies the quantity and type of chemicals in a sample) for the analysis.
Results
- The intact ester of the hormone was detectable in the plasma for up to two weeks after a single therapeutic dose was administered. This suggests that the synthetic hormone’s effects could be traced for fourteen days following injection.
- Further, the hormone was found to be stable in equine whole blood for at least two months. This indicates its long-term stability and possibly prolonged effects.
Significance
- The findings of this study are crucial for veterinary medicine and animal sports. In equine sports, for instance, horse doping is an ongoing concern.
- This research provides a sophisticated method to detect the presence of this particular synthetic hormone in a horse’s blood, which enables better monitoring and regulation.
Cite This Article
APA
McKinney AR, Suann CJ, Stenhouse AM.
(2006).
Detection of 17alpha-hydroxyprogesterone caproate in equine plasma by gas chromatography/tandem mass spectrometry.
Rapid Commun Mass Spectrom, 20(12), 1855-1858.
https://doi.org/10.1002/rcm.2526 Publication
Researcher Affiliations
- Australian Racing Forensic Laboratory, P.O. Box 528, Kensington, NSW 1465, Australia. amckinney@racingnsw.com.au
MeSH Terms
- 17 alpha-Hydroxyprogesterone Caproate
- Animals
- Gas Chromatography-Mass Spectrometry / methods
- Horses
- Hydroxyprogesterones / blood
- Hydroxyprogesterones / pharmacokinetics
- Hydroxyprogesterones / urine
- Injections, Intramuscular
- Male
- Progestins / blood
- Progestins / pharmacokinetics
- Progestins / urine
- Substance Abuse Detection / methods
- Tandem Mass Spectrometry / methods
Citations
This article has been cited 2 times.- Zhang S, Mada SR, Sharma S, Torch M, Mattison D, Caritis S, Venkataramanan R. Simultaneous quantitation of 17alpha-hydroxyprogesterone caproate, 17alpha-hydroxyprogesterone and progesterone in human plasma using high-performance liquid chromatography-mass spectrometry (HPLC-MS/MS).. J Pharm Biomed Anal 2008 Dec 1;48(4):1174-80.
- Zhang S, Mada SR, Mattison D, Caritis S, Venkataramanan R. Development and validation of a high-performance liquid chromatography-mass spectrometric assay for the determination of 17alpha-hydroxyprogesterone caproate (17-OHPC) in human plasma.. J Chromatogr B Analyt Technol Biomed Life Sci 2007 Sep 1;856(1-2):141-7.
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