在运动药物检测中检测 GH 类似物 somatrogon:免疫学方法和 LC-HRMS/MS。

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Drug Testing and Analysis Pub Date : 2024-07-11 DOI:10.1002/dta.3766
Katja Walpurgis, Andreas Thomas, Mitsuhiko Sato, Masato Okano, Hans Geyer, Mario Thevis
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引用次数: 0

摘要

由于人类生长激素(hGH)被认为具有溶脂和合成代谢的特性,因此在体育运动中,无论是赛内还是赛外,都禁止滥用人类生长激素(hGH)及其合成类似物。在本研究项目中,研究人员利用目前世界反兴奋剂机构批准的 hGH 和 hCG 兴奋剂控制检测方法,对 somatrogon(一种 22 kDa hGH 和人绒毛膜促性腺激素(hCG)β 亚基 C 端肽(CTP)的重组融合糖蛋白)的可检测性进行了调查。为此,进行了交叉反应试验和给药研究,结果证明只有 "试剂盒 2 "的 GH 异构体差异免疫测定法适用于检测血清中的给药情况。在尿液中,对总 hCG 的特异性免疫测定在几个给药后样本中得出了推定阳性结果,这可能是由于存在 hCG β 亚基的免疫活性片段。由于这些方法对索马曲贡的检测能力有限,因此通过与 GH 受体(GHR)结合的磁珠亲和纯化、蛋白水解消化和液相色谱高分辨串联质谱法(LC-HRMS/MS),开发出了血清样本中该药物的高特异性检测方法(LOD:10 ng/mL)。因此,该方法可用于确认血清样本中是否存在索马特罗贡,而目前使用的免疫测定试剂盒中只有 "试剂盒 2 "会产生异常高的 Rec/Pit 比值。
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Detection of the GH analog somatrogon in sports drug testing: Immunological approaches and LC-HRMS/MS.

Due to the presumed lipolytic and anabolic properties, the misuse of human growth hormone (hGH) and its synthetic analogs in sports is prohibited both in- and out-of-competition. Within this research project, the detectability of somatrogon, a recombinant fusion glycoprotein of 22 kDa hGH and the C-terminal peptide (CTP) of the human chorionic gonadotropin (hCG) β-subunit, with current WADA-approved doping control assays for hGH and hCG was investigated. For that purpose, cross-reactivity tests and a somatrogon administration study were conducted, and only "Kit 2" of the GH isoform differential immunoassays proved applicable to the detection of somatrogon administration in serum. In urine, the immunoassay specific for total hCG yielded presumptively positive findings for several post-administration samples, which can probably be attributed to the presence of an immunoreactive fragment of the hCG β-subunit. As the detectability of somatrogon with these approaches was found to be limited, a highly specific detection assay (LOD: 10 ng/mL) for the drug in serum samples was developed by using affinity purification with GH receptor (GHR)-conjugated magnetic beads, proteolytic digestion, and liquid chromatography high-resolution tandem mass spectrometry (LC-HRMS/MS). Following optimization, the approach was comprehensively characterized, and authentic post-administration serum samples were successfully analyzed as proof-of-concept, indicating a detection window of at least 96 h. Consequently, the presented method can be employed to confirm the presence of somatrogon in serum samples, where only "Kit 2" of the currently used immunoassay kits yielded an abnormally high Rec/Pit ratio.

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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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