1. Academic Validation
  2. Analytical approaches for the detection of emerging therapeutics and non-approved drugs in human doping controls

Analytical approaches for the detection of emerging therapeutics and non-approved drugs in human doping controls

  • J Pharm Biomed Anal. 2014 Dec;101:66-83. doi: 10.1016/j.jpba.2014.05.020.
Mario Thevis 1 Wilhelm Schänzer 2
Affiliations

Affiliations

  • 1 Center for Preventive Doping Research - Institute of Biochemistry, German Sport University Cologne, Am Sportpark Müngersdorf 6, 50933 Cologne, Germany. Electronic address: thevis@dshs-koeln.de.
  • 2 European Monitoring Center for Emerging Doping Agents, Cologne/Bonn, Germany.
Abstract

The number and diversity of potentially performance-enhancing substances is continuously growing, fueled by new pharmaceutical developments but also by the inventiveness and, at the same time, unscrupulousness of black-market (designer) drug producers and providers. In terms of sports drug testing, this situation necessitates reactive as well as proactive research and expansion of the analytical armamentarium to ensure timely, adequate, and comprehensive doping controls. This review summarizes literature published over the past 5 years on new drug entities, discontinued therapeutics, and 'tailored' compounds classified as doping agents according to the regulations of the World Anti-Doping Agency, with particular attention to analytical strategies enabling their detection in human blood or urine. Among these compounds, low- and high-molecular mass substances of peptidic (e.g. modified insulin-like growth factor-1, TB-500, hematide/peginesatide, growth hormone releasing Peptides, AOD-9604, etc.) and non-peptidic (selective Androgen Receptor modulators, hypoxia-inducible factor stabilizers, siRNA, S-107 and ARM036/aladorian, etc.) as well as inorganic (cobalt) nature are considered and discussed in terms of specific requirements originating from physicochemical properties, concentration levels, metabolism, and their amenability for chromatographic-mass spectrometric or alternative detection methods.

Keywords

Anti-myostatin antibody; Doping; Emerging drugs; Mass spectrometry; Sport; Stamulumab.

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