Affiliation:
1. Australian Racing Forensic Laboratory, Racing NSW Sydney NSW Australia
2. New Zealand Racing Laboratory Services Ltd, Avondale Auckland New Zealand
3. Harness Racing NSW Bankstown NSW Australia
Abstract
AbstractAn improved screening workflow and a robust capillary flow LC–MS confirmatory method for the detection of recombinant human erythropoietin (rHuEPO) has been implemented to increase the sensitivity of rHuEPO detection and to reduce the number of suspect samples committed to confirmatory testing. The influence of repeated dosing of epoetin‐β on the detection window of rHuEPO in equine plasma was assessed using the optimised method.Samples were initially assessed using an economical R&D Human EPO Duo‐Set ELISA Development System. Samples indicating a result greater than the batch baseline were analysed using the complementary R&D Human EPO Quantikine IVD ELISA kit. All samples recording an abnormal screening result were subjected to confirmatory analysis. Confirmation of rHuEPO in plasma (≥2.5 ml) in the range of 4–13 mIU/ml (n = 6) was achieved using immunoaffinity enrichment, tryptic digestion, and capillary flow LC–MS/MS.Four horses were administered a single dose of epoetin‐β (10,000 IU) via the subcutaneous and intravenous routes, on two occasions, seven days apart. The excretion profile was rapid with epoetin‐β detection times of 48 to 72 h following each administration, with no appreciable difference observed between the two routes of administration. This workflow has been shown as an effective anti‐doping strategy related to rHuEPO misuse and supports the use of out‐of‐competition testing of horses in the 2 to 3‐day period prior to race‐day.