School of Pharmacy, De Montfort University, Leicester LE2 9BH, UK.
Department of Biosciences and Chemistry, Sheffield Hallam University, Sheffield S1 1WB, UK.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Jul 15;1178:122584. doi: 10.1016/j.jchromb.2021.122584. Epub 2021 Feb 21.
Anti-doping analysis requires an exceptional level of accuracy and precision given the stakes that are at play. Current methods rely on the application of chromatographic techniques linked with mass spectrometry to provide this. However, despite the effectiveness of these techniques in achieving good selectivity and specificity, some issues still exist. In order to reach the minimum required performance level as set by WADA, labs commonly use selective monitoring by quadrupole mass spectrometry. This can be potentially fooled through the use of masking agents or by moving the peaks, as often only a small portion of the spectrum is used for analysis. Further issues exist in the inability to detect new or modified compounds, or to reanalyse samples/spectra. One technique that could overcome these problems is that of comprehensive 2D chromatography. Here a second separation column is employed to generate greater separative power. Compared to conventional separation, GCxGC allows for a greater peak capacity (i.e., number of peaks that can be resolved within a given time) and greater separation of coeluting compounds, which makes the technique promising for the complex task required in anti-doping. When combined with Time of Flight Mass Spectrometry this technique demonstrates vast potential allowing for full mass range datasets to be obtained for retroactive analysis. Similarly, LCxLC provides improvements in resolving power compared to its 1D counterpart and can be used both online as part of the analysis or offline solely as a purification step. In this review we summarise the work in this field so far, how comprehensive chromatography has been applied to anti-doping studies, and discuss the future application for this technique.
抗兴奋剂分析需要极高的准确性和精密度,因为这涉及到重大的利益。目前的方法依赖于与质谱联用的色谱技术来提供这种分析。然而,尽管这些技术在实现良好的选择性和特异性方面非常有效,但仍存在一些问题。为了达到世界反兴奋剂机构规定的最低性能要求,实验室通常采用四极杆质谱进行选择性监测。通过使用掩蔽剂或移动峰,这种方法可能会被愚弄,因为通常只有一小部分光谱用于分析。另外,还存在无法检测新的或修饰的化合物,或重新分析样品/光谱的问题。一种可以克服这些问题的技术是二维全面色谱。在这里,使用第二根分离柱来产生更大的分离能力。与传统的分离相比,GCxGC 允许更大的峰容量(即在给定时间内可以分辨的峰数)和共洗脱化合物的更好分离,这使得该技术在反兴奋剂复杂任务中具有很大的潜力。当与飞行时间质谱联用时,该技术显示出巨大的潜力,允许获得用于追溯分析的全质量范围数据集。同样,LCxLC 与 1D 相比在分辨率方面有所提高,并且可以在线作为分析的一部分或离线仅作为纯化步骤使用。在这篇综述中,我们总结了迄今为止该领域的工作,全面色谱技术如何应用于反兴奋剂研究,并讨论了该技术的未来应用。