| Literature DB >> 33450134 |
Christian Reichel1,2, Damir Erceg3,4,5,6,7, Barbara Lorenc1, Veronika Scheiblhofer1, Letizia Farmer1, Katharina Zanitzer1, Thomas Geisendorfer1, Günter Gmeiner1, Mario Thevis8,2.
Abstract
Erythropoietin (EPO) is a hormone, which stimulates the production of red blood cells. Due to its performance-enhancing effect, it is prohibited by the World Anti-Doping Agency (WADA). In order to reduce the detection window of EPO doping, athletes have been applying low doses of recombinant EPO (e.g., <10 IU/kg body weight, daily or every second day) instead of larger doses twice or more per week (e.g., 30 IU/kg). Microdoses of Retacrit (epoetin zeta), an EPO biosimilar, were administered intravenously and subcutaneously to human males and females. Urine and serum samples were collected and analysed applying the new biotinylated clone AE7A5 EPO antibody and a further optimized sarcosyl polyacrylamide gel electrophoresis (SAR-PAGE) protocol. With the improved protocol, microdosed Retacrit (7.5 IU/kg body weight [BW]) was detectable for at least 52 h after intravenous administration. Detection windows were approximately the same for serum and urine and doubled after subcutaneous administration (~104 h). Previous studies applying different electrophoretic techniques and the not further optimized SAR-PAGE protocol revealed considerably shorter detection windows for recombinant human erythropoietin (rhEPO) microdoses. Because the new biotinylated antibody performed significantly more sensitive than the nonbiotinylated version, the new protocol will improve the sensitivity and hence detectability of recombinant EPO in doping control.Entities:
Keywords: SAR-PAGE; doping control; epoetin zeta; erythropoietin; microdosis
Year: 2021 PMID: 33450134 DOI: 10.1002/dta.2989
Source DB: PubMed Journal: Drug Test Anal ISSN: 1942-7603 Impact factor: 3.345