Liquid chromatography clean-up method to improve identification of anabolic agents in human urine by gas chromatography-mass spectrometry [An article from: Analytica Chimica Acta] Buy on Amazon

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Liquid chromatography clean-up method to improve identification of anabolic agents in human urine by gas chromatography-mass spectrometry [An article from: Analytica Chimica Acta]

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PublisherElsevier
ISBN / ASINB000RR04CU
ISBN-13978B000RR04C8
AvailabilityAvailable for download now
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
A confirmatory procedure to allow the unequivocal identification of the presence of urinary anabolic steroids and metabolites banned for use in sport by athletes is presented. A single liquid chromatography (LC) procedure was developed to selectively isolate the metabolites of the most abused anabolic agents. Five millilitre urine samples, with trenbolone added as a retention time marker, were concentrated by solid-phase extraction, enzymatically hydrolysed and directly injected onto the LC system. Chromatographic separation was carried out on a 150mmx4.6mm I.D. column, packed with 3@mm Hypersil BDS-C"1"8 with gradient elution and UV absorbance detection (340nm). Fractions containing compounds of interest were collected and evaporated. After solvent evaporation and derivatisation to form trimethylsilyl (TMS) derivatives, fractions were analysed by GC/MS in full scan mode with an external ionisation ion trap mass spectrometer. A validation procedure for qualitative analysis was performed for the anabolic agents with special sensitivity requirements according to the International Olympic Committee (IOC) and the World Anti-Doping Agency (WADA). Appropriate precision, accuracy and recoveries were found. The selectivity of the method showed that no interfering peaks were observed at the retention time of the analytes, allowing obtaining full scan spectra even at the low concentrations required (2ng/ml).
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