Development of an analytical method for the determination of the misuse in sports of boldenone through the analysis of urine by on-line coupling liquid chromatography-gas chromatography-combustion-isotope ratio mass spectrometry

被引:4
|
作者
Toledano, R. M. [1 ]
Diaz-Plaza, E. M. [3 ]
Cortes, J. M. [2 ]
Aragon, A. [2 ]
Vazquez, A. M. [2 ]
Villen, J. [1 ]
Munoz-Guerra, J. [3 ]
机构
[1] Univ Castilla La Mancha, Escuela Tecn Super Ingenieros Agronomos, Albacete 02071, Spain
[2] Univ Castilla La Mancha, Fac Educ, Albacete 02071, Spain
[3] Agencia Espanola Protecc Salud El Deporte, Lab Control Dopaje, Madrid 28040, Spain
关键词
On-line LC-GC-C-IRMS; TOTAD interface; Boldenone; Doping; Steroid analysis; C-13/C-12; RATIOS; STEROIDS; CARBON; OILS;
D O I
10.1016/j.chroma.2014.10.049
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Boldenone (Bo), androsta-1,4-dien-17 beta-ol-3-one, is an anabolic androgenic steroid not clinically approved for human application. Despite this, many cases are reported every year of athletes testing positive for Bo or its main metabolite 5 beta-androst-1-en-17 beta-0l-3-one (BoM). Recently the capability of different human intestinal bacteria to produce enzymes able to modify endogenous steroids in Bo has been demonstrated. When a urinary concentration of Bo and/or BoM between 5 and 30 ng/mL is measured a complementary analysis by gas chromatography combustion isotope ratio mass spectrometry (GC-C-IRMS) must be carried out to discriminate the endogenous or exogenous origin. In the present work, a novel analytical method that couples LC-GC by means of the TOTAD interface with C-IRMS is described. The method is based on a first RPLC separation of unacetyled steroids, followed by acetylation and automated on-line LC-GC-C-IRMS, which includes a second RPLC clean-up of acetyl Bo and BoM, isolation of the two fractions in a fraction collector and their consecutive analysis by GC-C-IRMS. The method has been applied to the analysis of urine samples fortified at 5 and 10 ng/mL, where it has shown a good performance. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 178
页数:8
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