AI Article Synopsis

  • Dried blood spot (DBS) testing offers a quick and minimally invasive way to collect small blood samples, which is useful in anti-doping by providing information on banned substances like ephedrine during competition.
  • This study compared DBS samples from different sites (upper-arm and finger-prick) with venous plasma to evaluate how well they correlate in measuring ephedrine concentrations after administering low and high doses.
  • Findings indicated that alternative sampling sites are effective for ephedrine detection in doping control, but differences in concentration between DBS and venous plasma could require separate analysis standards.

Article Abstract

Dried blood spot (DBS) testing allows fast, easy and minimally invasive collection of microvolumes of blood. In an anti-doping context, DBS testing has particular relevance for substances prohibited in-competition only such as ephedrine, which is currently detected by urine analysis, because DBS can add information about the blood drug concentrations during the in-competition period. Several collection methods and devices exist for DBS collection from different anatomical sites. Thus, agreements between concentrations of target analytes in DBS samples from different sampling sites, along with between DBS and those in conventional venous plasma samples, need to be evaluated. Herein, we collected matched upper-arm DBS, fingerprick DBS and venous plasma samples from eight healthy male subjects in an 8-h period following oral administrations of 20 mg ('low dose') and 60 mg ('high dose') of ephedrine. We show that the use of alternative sampling sites and matrices is a feasible possibility for ephedrine analysis in doping control. We observed very good agreement between collection sites and that specificity and sensitivity can be upheld despite use of an alternative collection site. However, potential concentration differences between DBS and venous plasma should be considered, and distinct threshold might be necessary if implementing both blood matrices in ephedrine analysis.

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Source
http://dx.doi.org/10.1002/dta.3338DOI Listing

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