Grucza Krzysztof, Kwiatkowska Dorota, Kowalczyk Katarzyna, Wicka Mariola, Szutowski Mirosław, Chołbiński Piotr
Department of Toxicology, Medical University of Warsaw, Poland.
Department of Anti-Doping Research, Institute of Sport - National Research Institute, Warsaw, Poland.
Drug Test Anal. 2018 Jun;10(6):1017-1024. doi: 10.1002/dta.2331. Epub 2017 Dec 1.
Higenamine (Norcoclaurine) is a very popular substance in Chinese medicine and is present in many plants. The substance may be also found in supplements or nutrients, consumption of which may result in violation of anti-doping rules. Higenamine is prohibited in sport at all times and included in Class S3 (β-2-agonists) of the World Anti-Doping Agency (WADA) 2017 Prohibited List. The presence of higenamine in urine samples at concentrations greater than or equal to 10 ng/mL constitutes an adverse analytical finding (AAF). This work presents a new metabolite of higenamine in urine sample which was identified by means of ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Samples were prepared according to 2 protocols - a Dilute and Shoot (DaS) approach and a method involving acid hydrolysis and double liquid-liquid extraction (LLE). To meet the requirements typical for a confirmatory analysis, the screening procedure was further developed. In samples prepared by the DaS method, 2 peaks were observed; the earlier one was specific for higenamine and the later one unknown. MS scan analysis showed mass about 80 Da higher than that of higenamine. In turn, in samples prepared in accordance with the protocol involving hydrolysis, an increase in the area under peak for higenamine was observed, while the second peak was absent. It seems that the described strategy of detection of higenamine in urine avoids false negative results.
去甲乌药碱(去甲粉防己碱)是一种在中药中非常常见的物质,存在于许多植物中。该物质也可能存在于补充剂或营养物中,食用这些可能导致违反反兴奋剂规则。去甲乌药碱在体育赛事中始终被禁止使用,并被列入世界反兴奋剂机构(WADA)2017年禁用清单的S3类(β-2-激动剂)。尿样中去甲乌药碱浓度大于或等于10 ng/mL即构成阳性分析结果(AAF)。这项工作展示了尿样中去甲乌药碱的一种新代谢物,它是通过超高效液相色谱-串联质谱法(UPLC-MS/MS)鉴定出来的。样品按照两种方案制备——稀释进样(DaS)方法和一种涉及酸水解及双液-液萃取(LLE)的方法。为满足确证分析的典型要求,进一步改进了筛查程序。在采用DaS方法制备的样品中,观察到两个峰;较早出现的峰对去甲乌药碱具有特异性,较晚出现的峰未知。质谱扫描分析显示其质量比去甲乌药碱高约80 Da。相应地,在按照涉及水解的方案制备的样品中,观察到去甲乌药碱的峰面积增加,而第二个峰不存在。看来所描述的尿样中去甲乌药碱检测策略可避免假阴性结果。