通过固相提取和LC-HRMS在干血斑点中敏感检测低分子质量的类药物
Wei Chang1, Siyu Yan2,3, Xiya Yan2,3
1Beijing Anti-Doping Laboratory, Beijing Sport University, Beijing, People's Republic of China. nadl.changwei@bsu.edu.cn.
Analytical and bioanalytical chemistry
|August 24, 2024
概括
一种新方法增强了抗兴奋剂中低分子质量 (LMMP) 药物的干血斑 (DBS) 分析. 这种敏感的技术提高了没有二甲基硫氧化物 (DMSO) 的检测极限,有助于常规药物查.
科学领域:
- 分析化学 分析化学
- 生物化学 生物化学
- 运动科学 运动科学 运动科学
背景情况:
- 干血斑点 (DBS) 分析在反兴奋剂中越来越受欢迎,因为样品的稳定性和易用性.
- 在DBS中的小样本体积限制了对禁止物质的敏感检测方法的应用.
- 开发高度敏感的检测方法对于使用DBS的有效反兴奋剂策略至关重要.
研究的目的:
- 在干血斑点 (DBS) 中建立低分子量 (LMMP) 药物的敏感检测方法.
- 在不使用二甲基硫氧化物 (DMSO) 的情况下,优化DBS中LMMPs的检测策略.
- 根据世界反兴奋剂机构 (WADA) 的指导方针,验证开发的常规反兴奋剂分析方法.
主要方法:
- 应用了系统优化策略来检测DBS中的LMMP.
- 该方法是在不使用DMSO的情况下开发的,以提高质谱仪的电离效率.
- 该方法根据WADA的指导方针进行了验证,包括一个后给药研究.
主要成果:
- 开发的方法实现了LMMPs的检测极限 (LOD),从0.05到3.74 ng/mL.
- 这些LOD明显低于之前报告的方法 (0.5-20 ng/mL).
- 该方法证明了在DBS中对LMMP药物的常规分析的适用性,以及同时检测LMMP和小分子药物的潜力.
结论:
- 在DBS中成功建立并验证了一种新的,敏感的LMMP检测方法.
- 与现有技术相比,该方法提供了更好的检测极限,并且避免了使用DMSO.
- 这种方法支持常规的反兴奋剂分析,并有可能在DBS中获得更广泛的药物查应用.
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