Görgens Christian, Guddat Sven, Orlovius Anne-Katrin, Sigmund Gerd, Thomas Andreas, Thevis Mario, Schänzer Wilhelm
Institute of Biochemistry, Center for Preventive Doping Research, German Sport University Cologne, Am Sportpark Müngersdorf 6, 50933, Cologne, Germany.
Anal Bioanal Chem. 2015 Jul;407(18):5365-79. doi: 10.1007/s00216-015-8699-x. Epub 2015 Apr 30.
In the field of LC-MS, reversed phase liquid chromatography is the predominant method of choice for the separation of prohibited substances from various classes in sports drug testing. However, highly polar and charged compounds still represent a challenging task in liquid chromatography due to their difficult chromatographic behavior using reversed phase materials. A very promising approach for the separation of hydrophilic compounds is hydrophilic interaction liquid chromatography (HILIC). Despite its great potential and versatile advantages for the separation of highly polar compounds, HILIC is up to now not very common in doping analysis, although most manufacturers offer a variety of HILIC columns in their portfolio. In this study, a novel multi-target approach based on HILIC high resolution/high accuracy mass spectrometry is presented to screen for various polar stimulants, stimulant sulfo-conjugates, glycerol, AICAR, ethyl glucuronide, morphine-3-glucuronide, and myo-inositol trispyrophosphate after direct injection of diluted urine specimens. The usage of an effective online sample cleanup and a zwitterionic HILIC analytical column in combination with a new generation Hybrid Quadrupol-Orbitrap® mass spectrometer enabled the detection of highly polar analytes without any time-consuming hydrolysis or further purification steps, far below the required detection limits. The methodology was fully validated for qualitative and quantitative (AICAR, glycerol) purposes considering the parameters specificity; robustness (rRT < 2.0%); linearity (R > 0.99); intra- and inter-day precision at low, medium, and high concentration levels (CV < 20%); limit of detection (stimulants and stimulant sulfo-conjugates < 10 ng/mL; norfenefrine; octopamine < 30 ng/mL; AICAR < 10 ng/mL; glycerol 100 μg/mL; ETG < 100 ng/mL); accuracy (AICAR 103.8-105.5%, glycerol 85.1-98.3% at three concentration levels) and ion suppression/enhancement effects.
在液相色谱 - 质谱联用(LC - MS)领域,反相液相色谱是体育药物检测中分离各类违禁物质的主要选择方法。然而,高极性和带电荷的化合物由于在反相材料上的色谱行为困难,在液相色谱中仍是一项具有挑战性的任务。一种非常有前景的分离亲水性化合物的方法是亲水作用液相色谱(HILIC)。尽管HILIC在分离高极性化合物方面具有巨大潜力和多种优势,但到目前为止,它在兴奋剂分析中并不常见,尽管大多数制造商在其产品组合中提供了各种HILIC柱。在本研究中,提出了一种基于HILIC高分辨率/高精度质谱的新型多目标方法,用于在直接注射稀释尿液样本后筛选各种极性兴奋剂、兴奋剂磺基共轭物、甘油、AICAR、葡萄糖醛酸乙酯、吗啡 - 3 - 葡萄糖醛酸和肌醇三磷酸酯。使用有效的在线样品净化和两性离子HILIC分析柱,结合新一代混合四极杆 - 轨道阱®质谱仪,能够检测高极性分析物,无需任何耗时的水解或进一步纯化步骤,远远低于所需的检测限。考虑到参数特异性、稳健性(相对保留时间rRT < 2.0%)、线性(R > 0.99)、低、中、高浓度水平的日内和日间精密度(变异系数CV < 20%)、检测限(兴奋剂和兴奋剂磺基共轭物 < 10 ng/mL;去甲伪麻黄碱;章鱼胺 < 30 ng/mL;AICAR < 10 ng/mL;甘油 100 μg/mL;葡萄糖醛酸乙酯 < 100 ng/mL)、准确度(三个浓度水平下AICAR为103.8 - 105.5%,甘油为85.1 - 98.3%)以及离子抑制/增强效应,该方法已针对定性和定量(AICAR、甘油)目的进行了全面验证。