Department of Chemistry, Center for Innovative Technology, Institute of Chemical Biology, Institute for Integrative Biosystems Research and Education, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37235, United States.
Brazilian Doping Control Laboratory (LBCD), Chemistry Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, RJ 21941-598, Brazil.
Anal Chem. 2021 Aug 10;93(31):10990-10998. doi: 10.1021/acs.analchem.1c02163. Epub 2021 Jul 28.
The detection and unambiguous identification of anabolic-androgenic steroid metabolites are essential in clinical, forensic, and antidoping analyses. Recently, sulfate phase II steroid metabolites have received increased attention in steroid metabolism and drug testing. In large part, this is because phase II steroid metabolites are excreted for an extended time, making them a potential long-term chemical marker of choice for tracking steroid misuse in sports. Comprehensive analytical methods, such as liquid chromatography-tandem mass spectrometry (LC-MS/MS), have been used to detect and identify glucuronide and sulfate steroids in human urine with high sensitivity and reliability. However, LC-MS/MS identification strategies can be hindered by the fact that phase II steroid metabolites generate nonselective ion fragments across the different metabolite markers, limiting the confidence in metabolite identifications that rely on exact mass measurement and MS/MS information. Additionally, liquid chromatography-high-resolution mass spectrometry (LC-HRMS) is sometimes insufficient at fully resolving the analyte peaks from the sample matrix (commonly urine) chemical noise, further complicating accurate identification efforts. Therefore, we developed a liquid chromatography-ion mobility-high resolution mass spectrometry (LC-IM-HRMS) method to increase the peak capacity and utilize the IM-derived collision cross section (CCS) values as an additional molecular descriptor for increased selectivity and to improve identifications of intact steroid analyses at low concentrations.
检测和明确鉴定合成代谢雄性类固醇代谢物在临床、法医和反兴奋剂分析中至关重要。最近,类固醇代谢和药物检测中越来越关注硫酸酯相 II 代谢物。在很大程度上,这是因为相 II 类固醇代谢物的排泄时间延长,使它们成为追踪运动中类固醇滥用的潜在长期化学标志物选择。综合分析方法,如液相色谱-串联质谱法 (LC-MS/MS),已被用于检测和鉴定人尿中葡萄糖醛酸和硫酸盐类固醇,具有高灵敏度和可靠性。然而,LC-MS/MS 鉴定策略可能会受到以下事实的阻碍,即相 II 类固醇代谢物会在不同的代谢物标记物之间产生非选择性离子碎片,从而限制了对依赖于精确质量测量和 MS/MS 信息的代谢物鉴定的信心。此外,液相色谱-高分辨率质谱法 (LC-HRMS) 有时不足以完全从样品基质(通常为尿液)化学噪声中分辨出分析物峰,这进一步增加了准确鉴定的难度。因此,我们开发了一种液相色谱-离子淌度-高分辨率质谱法 (LC-IM-HRMS) 方法,以增加峰容量,并利用 IM 衍生的碰撞截面 (CCS) 值作为增加选择性的附加分子描述符,并提高低浓度完整类固醇分析的鉴定。