- Mar 4, 2010
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From an interview with norwegian anti-doping researcher Yvette Dehnes:
I assume she is referring to this study.
Detection of recombinant EPO in blood and urine samples with EPO WGA MAIIA, IEF and SAR-PAGE after microdose injections
http://onlinelibrary.wiley.com/doi/10.1002/dta.1579/abstract
7.5 IU/kg would be about 500 IU for a GC-rider. That is the smallest micro-dose I've seen mentioned by various whistleblowers. Since the idea behind micro-dosing is to take your EPO in the evening and not glow in the morning, an 18-24 hour window of detection is unacceptable.
Through her research, Dehnes has shown that micro doses can be detected up to a day later.
- I felt it was pretty encouraging, and partly due to the improvement of the analytical methods we have for EPO. If we tested subjects within 18-24 hours, we could actually see that they had doped.
- It is no longer the case that they can inject in the evening and be safe in the morning.
I assume she is referring to this study.
Detection of recombinant EPO in blood and urine samples with EPO WGA MAIIA, IEF and SAR-PAGE after microdose injections
http://onlinelibrary.wiley.com/doi/10.1002/dta.1579/abstract
The misuse of microdoses of performance enhancing drugs like erythropoietin (EPO) constitutes a major challenge in doping analysis. When injected intravenously, the half-life of recombinant human EPO (rhEPO) like epoetin alfa, beta, and zeta is only a few hours and hence, the window for direct detection of rhEPO in urine is small. In order to investigate the detection window for rhEPO directly in blood and urine with a combined affinity chromatography and lateral flow immunoassay (EPO WGA MAIIA), we recruited nine healthy people who each received six intravenously injected microdoses (7.5 IU/kg) of NeoRecormon (epoetin beta) over a period of three weeks. Blood and urine samples were collected in the days following the injections and analyzed with EPO WGA MAIIA as well as the current validated methods for rhEPO; isoelectric focusing (IEF) and sarcosyl polyacrylamide gel electrophoresis (SAR-PAGE). For samples collected 18 h after a microdose, the sensitivity of the EPO WGA MAIIA assay was 100% in plasma and 87.5% in urine samples at the respective 98% specificity threshold levels. In comparison, the sensitivity in plasma and urine was 75% and 100%, respectively, with IEF, and 87.5% in plasma and 100% in urine when analyzed with SAR-PAGE. We conclude that EPO WGA MAIIA is a sensitive assay for the detection of rhEPO, with the potential of being a fast, supplemental screening assay for use in doping analysis.
7.5 IU/kg would be about 500 IU for a GC-rider. That is the smallest micro-dose I've seen mentioned by various whistleblowers. Since the idea behind micro-dosing is to take your EPO in the evening and not glow in the morning, an 18-24 hour window of detection is unacceptable.