Screening and confirmation of recombinant human follistatin in equine plasma for doping control purposes

Abstract

Recombinant human follistatin (rhFST) is a potential performance‐enhancing agent owing to its stimulating effect on muscle growth. Administration of rhFST to athletes is prohibited in human sports by the World Anti‐Doping Agency (WADA) and in horseracing according to Article 6 of the International Agreement on Breeding, Racing and Wagering published by the International Federation of Horseracing Authorities (IFHA). For effective control of the potential misuse of rhFST in flat racing, methods for screening and confirmatory analysis are required. This paper describes the development and validation of a complete solution for detecting rhFST and confirming its presence in plasma samples collected from racehorses. A high‐throughput analysis of rhFST with a commercially available enzyme‐linked immunosorbent assay (ELISA) was evaluated for the screening of equine plasma samples. Any suspicious finding would then be subjected to a confirmatory analysis using immunocapture, followed by nano‐liquid chromatography/high‐resolution tandem mass spectrometry (nanoLC‐MS/HRMS). The confirmation of rhFST by nanoLC‐MS/HRMS was achieved by comparing the retention times and relative abundances of three characteristic product‐ions with those from the reference standard in accordance with the industry criteria published by the Association of Official Racing Chemists. The two methods achieved comparable limit of detection (~2.5–5 ng/mL) and limit of confirmation (2.5 ng/mL or below), as well as adequate specificity, precision and reproducibility. To our knowledge, this is the first report of the screening and confirmation methods for rhFST in equine samples.