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Applications of Isotope Ratio Mass Spectrometry in Sports Drug Testing Accounting for Isotope Fractionation in Analysis of Biological Samples.
Piper, Thomas; Thevis, Mario.
Afiliação
  • Piper T; Center for Preventive Doping Research-Institute of Biochemistry, German Sport University Cologne, Cologne, Germany. Electronic address: t.piper@biochem.dshs-koeln.de.
  • Thevis M; Center for Preventive Doping Research-Institute of Biochemistry, German Sport University Cologne, Cologne, Germany.
Methods Enzymol ; 596: 403-432, 2017.
Article em En | MEDLINE | ID: mdl-28911778
ABSTRACT
The misuse of anabolic-androgenic steroids (AAS) in sports aiming at enhancing athletic performance has been a challenging matter for doping control laboratories for decades. While the presence of a xenobiotic AAS or its metabolite(s) in human urine immediately represents an antidoping rule violation, the detection of the misuse of endogenous steroids such as testosterone necessitates comparably complex procedures. Concentration thresholds and diagnostic analyte ratios computed from urinary steroid concentrations of, e.g., testosterone and epitestosterone have aided identifying suspicious doping control samples in the past. These ratios can however also be affected by confounding factors and are therefore not sufficient to prove illicit steroid administrations. Here, carbon and, in rare cases, hydrogen isotope ratio mass spectrometry (IRMS) has become an indispensable tool. Importantly, the isotopic signatures of pharmaceutical steroid preparations commonly differ slightly but significantly from those found with endogenously produced steroids. By comparing the isotope ratios of endogenous reference compounds like pregnanediol to that of testosterone and its metabolites, the unambiguous identification of the urinary steroids' origin is accomplished. Due to the complex urinary matrix, several steps in sample preparation are inevitable as pure analyte peaks are a prerequisite for valid IRMS determinations. The sample cleanup encompasses steps such as solid phase or liquid-liquid extraction that are presumably not accompanied by isotopic fractionation processes, as well as more critical steps like enzymatic hydrolysis, high-performance liquid chromatography fractionation, and derivatization of analytes. In order to exclude any bias of the analytical results, each step of the analytical procedure is optimized and validated to exclude, or at least result in constant, isotopic fractionation. These efforts are explained in detail.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Isótopos de Carbono / Congêneres da Testosterona / Anabolizantes / Cromatografia Gasosa-Espectrometria de Massas Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Isótopos de Carbono / Congêneres da Testosterona / Anabolizantes / Cromatografia Gasosa-Espectrometria de Massas Idioma: En Ano de publicação: 2017 Tipo de documento: Article