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Anti-Doping Control Using Comprehensive Multidimensional Gas Chromatography Time-of-Flight Mass Spectrometry (GCxGC-TOFMS) for Enhanced Detection of Anabolic Steroids in Urine

Posters | 2010 | LECOInstrumentation
GCxGC, GC/MSD, GC/TOF
Industries
Forensics
Manufacturer
Agilent Technologies, GERSTEL, LECO

Summary

Importance of the Topic


Urine-based steroid screening is pivotal in anti-doping control to ensure fair competition. The complexity of urinary matrices and low analyte concentrations require analytical methods with high resolution and sensitivity. Comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (GCxGC-TOFMS) offers enhanced peak capacity and rapid data acquisition, enabling reliable detection of trace anabolic steroids.

Objectives and Study Overview


This study aimed to demonstrate the capabilities of GCxGC-TOFMS for anti-doping analysis by:
  • Resolving steroid analytes that coelute in one-dimensional chromatography
  • Achieving detection limits at or below World Anti-Doping Agency cut offs (2 ng/mL)
  • Evaluating quantitative performance across a calibration range of 2 to 100 ng/mL

Methodology and Instrumentation


Urine samples were spiked with five trimethylsilyl-derivatized steroid standards at concentrations ranging from 2 to 100 ng/mL. Sample preparation involved:
  • Acid hydrolysis with beta glucuronidase at 50°C for one hour
  • pH adjustment and liquid–liquid extraction with methyl tert butyl ether
  • Drying under nitrogen followed by derivatization with MSTFA NH4I ethanethiol

Instrumentation used:
  • Gas chromatograph with dual stage thermal modulator and automated sampler
  • Primary column Rxi-5ms (30 m × 0.25 mm × 0.25 μm) and secondary column BPX-50 (1.20 m × 0.10 mm × 0.10 μm)
  • Time-of-flight mass spectrometer Pegasus 4D operating at 100 spectra per second over 45 to 750 m/z

Key Results and Discussion


  • Enhanced peak capacity of GCxGC fully resolved coeluting TMS derivatives of stanozolol and hydroxystanozolols
  • True signal deconvolution separated trace anabolic steroids from endogenous interferences, enabling clear spectral identification
  • Calibration curves of di- and tri-TMS derivatives exhibited linearity greater than 99.9% over 2–100 ng/mL
  • Limits of detection at or below 2 ng/mL were achieved for all five target steroids, meeting or exceeding WADA minimum required performance levels

Benefits and Practical Applications


GCxGC-TOFMS offers:
  • Significantly improved resolution in complex biological samples
  • Reliable detection and quantification of anabolic steroids at ultra-trace levels
  • Automated deconvolution for simultaneous qualitative and quantitative analysis in a single run

Future Trends and Opportunities


Potential developments include:
  • Integration of high-resolution accurate mass spectrometry to further enhance selectivity
  • Advancements in modulation technology to increase throughput and peak capacity
  • Application of machine learning algorithms for automated data interpretation and deconvolution

Conclusion


This study demonstrates that GCxGC-TOFMS significantly improves the detection, separation, and quantitation of anabolic steroids in urine compared to one-dimensional GCMS. The method reliably meets stringent WADA guidelines, offering robust performance for routine anti-doping laboratories.

References


  • John Heim, Doug Staples, Joe Binkley. Anti-Doping Control Using GCxGC-TOFMS for Enhanced Detection of Anabolic Steroids in Urine. LECO Corporation.

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