Comprehensive plasma-screening for known and unknown substances in doping controls
Article first published online: 18 MAR 2010
Copyright © 2010 John Wiley & Sons, Ltd.
Rapid Communications in Mass Spectrometry
Volume 24, Issue 8, pages 1124–1132, 30 April 2010
How to Cite
Thomas, A., Guddat, S., Kohler, M., Krug, O., Schänzer, W., Petrou, M. and Thevis, M. (2010), Comprehensive plasma-screening for known and unknown substances in doping controls. Rapid Commun. Mass Spectrom., 24: 1124–1132. doi: 10.1002/rcm.4492
- Issue published online: 19 MAR 2010
- Article first published online: 18 MAR 2010
- Manuscript Accepted: 29 JAN 2010
- Manuscript Revised: 28 JAN 2010
- Manuscript Received: 23 DEC 2009
Occasionally, doping analysis has been recognized as a competitive challenge between cheating sportsmen and the analytical capabilities of testing laboratories. Both have made immense progress during the last decades, but obviously the athletes have the questionable benefit of frequently being able to switch to new, unknown and untested compounds to enhance their performance. Thus, as analytical counteraction and for effective drug testing, a complementary approach to classical targeted methods is required in order to implement a comprehensive screening procedure for known and unknown xenobiotics. The present study provides a new analytical strategy to circumvent the targeted character of classical doping controls without losing the required sensitivity and specificity. Using 50 µL of plasma only, the method potentially identifies illicit drugs in low ng/mL concentrations. Plasma provides the biological fluid with the circulating, unmodified xenobiotics; thus the identification of unknown compounds is facilitated. After a simple protein precipitation, liquid chromatographic separation and subsequent detection by means of high resolution/high accuracy orbitrap mass spectrometry, the procedure enables the determination of numerous compounds from different classes prohibited by the World Anti-Doping Agency (WADA). A new hyphenated mass spectrometry technology was employed without precursor ion selection for higher collision energy dissociation (HCD) fragmentation experiments. Thus the mass spectra contained all the desired information to identify unknown substances retrospectively. The method was validated for 32 selected model compounds for qualitative purposes considering the parameters specificity, selectivity, limit of detection (<0.1–10 ng/mL), precision (9–28%), robustness, linearity, ion suppression and recovery (80–112%). In addition to the identification of unknown compounds, the plasma samples were simultaneously screened for known prohibited targets. Copyright © 2010 John Wiley & Sons, Ltd.