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Detection of extracellular hemoglobin from Arenicola marina in doping control serum samples by means of liquid chromatography and high‐resolution tandem mass spectrometry

作   者:
Soizic GochardKatja WalpurgisAileen G?deAndreas ThomasPhilippe DelahautMario Thevis
作者机构:
Laboratoire de Toxicologie Centre Hospitalier Universitaire Tizi‐OuzouUniversité Paris‐SaclayCER GroupePig For Life SACER GroupeGerman Sport University Cologne Institute of Biochemistry/Center for Preventive Doping
关键词:
blood substitutedopingLC‐HRMS/MSlugwormultrafiltrationhemoglobinhemoglobin‐based oxygen carrier (HBOC)
期刊名称:
Drug testing and analysis
i s s n:
1942-7603
年卷期:
2023 年 15 卷 11/12 期
页   码:
1430-1438
页   码:
摘   要:
Abstract The manipulation of blood and blood components in sports is prohibited at all times, and besides blood transfusions, also hemoglobin‐based oxygen carriers (HBOCs) can be employed to artificially improve the oxygen transport capacity of the blood. But while most drug candidates based on stabilized hemoglobin (Hb) were found to be characterized by serious side effects, the natural giant extracellular Hb from the marine invertebrate Arenicola marina (lugworm) could be another candidate for transfusion medicine and cheating athletes, as it was found to be well tolerated in preclinical animal studies. Within this research project, lugworm Hb was implemented into the existing doping control detection method for bovine HBOCs based on ultrafiltration, tryptic digestion, and liquid chromatography coupled with high‐resolution tandem mass spectrometry (LC‐HRMS/MS). For the mass spectrometric identification of lugworm Hb, two precursor–product ion pairs for a total of four tryptic peptides originating from subunits hbA2 (T6), hbB1 (T3 and T6), and the linker chain (T16) were employed. The modified approach was comprehensively characterized and found to allow for the specific and sensitive detection of lugworm Hb down to concentrations of 10?μg/mL from 50?μL of serum/plasma. Therefore, it can serve as confirmation procedure for lugworm Hb following visual or electrophoretic screening. Moreover, a proof‐of‐concept rat administration study was conducted, and the observed detection windows of at least 4 (dose: 200?mg/kg) and 8?h (dose: 600?mg/kg) suggest that the approach can be readily employed to efficiently test in‐competition doping control samples for the presence of the drug candidate.
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