Dried blood spots for doping controls—Development of a comprehensive initial testing procedure with fully automated sample preparation

Author:

Garzinsky Ann‐Marie1,Thomas Andreas1,Guddat Sven1,Görgens Christian1,Dib Josef1,Thevis Mario12ORCID

Affiliation:

1. Center for Preventive Doping Research/Institute of Biochemistry German Sport University Cologne Cologne Germany

2. European Monitoring Center for Emerging Doping Agents Cologne/Bonn Germany

Abstract

AbstractCurrently, primarily urine, whole blood and serum samples are analyzed for doping‐relevant substances in professional sports, but recently dried blood spots (DBS) have been introduced as complementary matrix, offering advantageous features, e.g. a minimally invasive sampling procedure. In order to cope with the increased application of DBS, a comprehensive initial testing procedure (ITP) was developed, optimized and validated, comprising a total of 233 substances representing all groups on the World Anti‐Doping Agency's (WADA's) Prohibited List. The sample preparation was conducted by employing a fully automated system using an efficient flow‐through extraction of a 4 mm diameter spot followed by LC–HRMS/MS analysis. The procedure was successfully validated in terms of selectivity, limit of detection, reproducibility, carryover and robustness with respect to an alternative manual sample preparation, an alternative dried blood collection device and the sample extract stability, and was thus found to meet the required criteria of the relevant guidelines published by WADA for routine application. As a proof‐of‐concept, DBS samples were analyzed after the administration of the glucocorticoids prednisone and dexamethasone, as well as the stimulant pseudoephedrine and the beta‐blocker propranolol. All substances were detected in post‐administration samples for at least 4 h and up to 24 h after intake, depending on the collection time period, using the developed testing procedure. In particular, for substances that are only banned in‐competition, data obtained from DBS samples can be useful for the interpretation of adverse analytical findings. In conclusion, the developed ITP accounts for the anticipated increasing relevance of DBS in anti‐doping analysis in the future and provides a foundation for optimized approaches for specific substance classes.

Funder

Bundesministerium des Innern, für Bau und Heimat

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

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