Doping Control Laboratory of Athens, Olympic Athletic Center of Athens 'Spiros Louis', 37 Kifissias Ave., 151 23 Maroussi, Greece.
Rapid Commun Mass Spectrom. 2010 Jun 15;24(11):1595-609. doi: 10.1002/rcm.4554.
Unification of the screening protocols for a wide range of doping agents has become an important issue for doping control laboratories. This study presents the development and validation of a generic liquid chromatography/time-of-flight mass spectrometry (LC/TOFMS) screening method of 241 small molecule analytes from various categories of prohibited substances (stimulants, narcotics, diuretics, beta(2)-agonists, beta-blockers, hormone antagonists and modulators, glucocorticosteroids and anabolic agents). It is based on a single-step liquid-liquid extraction of hydrolyzed urine and the use of a rapid-resolution liquid chromatography/high-resolution time-of-flight mass spectrometric system acquiring continuous full scan data. Electrospray ionization in the positive mode was used. Validation parameters consisted of identification capability, limit of detection, specificity, ion suppression, extraction recovery, repeatability and mass accuracy. Detection criteria were established on the basis of retention time reproducibility and mass accuracy. The suitability of the methodology for doping control was demonstrated with positive urine samples. The preventive role of the method was proved by the case where full scan acquisition with accurate mass measurement allowed the retrospective reprocessing of acquired data from past doping control samples for the detection of a designer drug, the stimulant 4-methyl-2-hexanamine, which resulted in re-reporting a number of stored samples as positives for this particular substance, when, initially, they had been reported as negatives.
将各种兴奋剂的筛查方案统一起来已成为兴奋剂检测实验室的一个重要问题。本研究建立并验证了一种通用的液相色谱/飞行时间质谱(LC/TOFMS)筛查方法,用于检测 241 种来自各种禁用物质类别的小分子分析物(兴奋剂、麻醉剂、利尿剂、β2-激动剂、β-阻滞剂、激素拮抗剂和调节剂、糖皮质激素和合成代谢制剂)。该方法基于水解尿液的一步液-液萃取,以及使用快速分辨液相色谱/高分辨飞行时间质谱系统采集连续全扫描数据。采用正离子电喷雾电离模式。验证参数包括鉴定能力、检测限、特异性、离子抑制、提取回收率、重复性和质量准确性。检测标准基于保留时间重现性和质量准确性来建立。该方法通过阳性尿液样本证明了其在兴奋剂检测中的适用性。通过全扫描采集精确质量测量的方式,可以对过去的兴奋剂检测样本进行回溯性数据再处理,以检测一种设计药物——兴奋剂 4-甲基-2-己胺,这一案例证明了该方法的预防作用,从而导致一些先前报告为阴性的存储样本重新被报告为阳性,这是因为该物质的检测结果得到了重新确认。