Probing for peptidic drugs (2-10 kDa) in doping control blood samples.

IF 3 Q2 CHEMISTRY, ANALYTICAL Analytical science advances Pub Date : 2022-08-22 eCollection Date: 2022-08-01 DOI:10.1002/ansa.202200027
Andreas Thomas, Sam Thilmany, Amelie Hofmann, Mario Thevis
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Abstract

Bioactive peptides with a molecular mass between 2 and 10 kDa represent an important class of substances banned in elite sports, which has been recognized with an increasing number and variety of substances by anti-doping organizations. Also, the annually renewed list of prohibited substances of the World Anti-Doping Agency (WADA) explicitly mentions more and more of these peptides, and efficient testing procedures are required. Even under simplified sample preparation conditions, liquid chromatography coupled to high-resolution mass spectrometry (with resolution properties > 100,000 full width at half maximum) offers suitable conditions for this task and can therefore be used as an initial testing procedure. In contrast to urine, blood analysis essentially relies on the detection of intact peptide hormones, and the expected concentrations are commonly higher in blood samples than in urine. This facilitates the analysis, and a generic sample preparation by means of mixed-mode solid-phase extraction could be realized in this study. Co-extraction and analysis of several different peptides such as insulins (human, lispro, aspart, glulisine, tresiba, detemir, glargine, bovine insulin and porcine insulin), growth hormone releasing hormones (sermorelin, CJC-1295 and tesamorelin), insulin-like growth factors (long-R3-IGF-I, R3-IGF-I and Des1-3-IGF-I) and mechano growth factors (human MGF and MGF-Goldspink) with criteria that fulfil the requirements of the WADA documents (TD2022 MRPL) for doping controls. The proof of principle was shown by the analysis of post administration samples after treatment with synthetic insulin analogues.

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检测兴奋剂控制血液样本中的肽类药物(2-10 kDa)
分子质量在 2 至 10 kDa 之间的生物活性肽是精英体育运动中禁用的一类重要物 质,反兴奋剂组织已经认识到这类物质的数量和种类都在不断增加。此外,世界反兴奋剂机构(WADA)每年更新的禁用物质清单中也明确提到了越来越多的此类多肽,因此需要高效的检测程序。即使在简化的样品制备条件下,液相色谱法与高分辨率质谱法(分辨率大于 100,000 全宽半最大值)也能为这一任务提供合适的条件,因此可用作初始检测程序。与尿液相比,血液分析主要依靠检测完整的肽类激素,血液样本中的预期浓度通常高于尿液。这就为分析提供了便利,在本研究中可以通过混合模式固相萃取实现通用的样品制备。对几种不同的肽进行共萃取和分析,如胰岛素(人胰岛素、利舒胰岛素、天冬胰岛素、格列胰岛素、特瑞沙胰岛素、地特米胰岛素、格列胰岛素、牛胰岛素和猪胰岛素)、生长激素释放激素(sermorelin、CJC-1295 和 tesamorelin)、胰岛素样生长因子(长-R3-IGF-I、R3-IGF-I 和 Des1-3-IGF-I)和机械生长因子(人 MGF 和 MGF-Goldspink),其标准符合世界反兴奋剂机构兴奋剂控制文件(TD2022 MRPL)的要求。通过对合成胰岛素类似物治疗后的用药后样本进行分析,证明了这一原则。
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