Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.
Center of Sports Nutrition Science (CSN), University of Physical Education, Budapest, Hungary.
Drug Test Anal. 2021 Jan;13(1):128-139. doi: 10.1002/dta.2929. Epub 2020 Oct 9.
The aim of the present research was the identification and quantification of specific anabolic androgenic steroids (AASs) and other sterane structured compounds in dietary supplements (DSs). The adulteration of DSs by these compounds is of a particular concern in athletes, because it might lead to a positive doping result. The research was focused on the optimization of a highly sensitive and selective GC-based analytical strategy using triple quadrupole MS as detector. Chromatographic method and multiple reaction monitoring (MRM) transitions of 28 target compounds were optimized. Sample clean-up was carried out by using a solid phase extraction (SPE) procedure, while the derivatization of AASs was performed by using N-methyl-N-(trimethylsilyl)-trifluoroacetamide (MSTFA). The method was validated, and the following parameters were investigated: linearity range, limit of detection, accuracy, and precision expressed in terms of intra-day precision. The calibration curves were evaluated by using regression model and resulting in a good determination coefficients (R ≥ 0.9912). The residuals were scattered randomly around zero. The limits of detection (LODs) were lower than 7.0 ng g or ng ml . The accuracy assessment was evaluated in different forms of DSs characterized by high sample-to-sample variability (liquid, powder, tablet, capsule, protein, and herbal-based). Intra-day assay precision was in all cases lower than 20%. The developed analytical method was successfully applied to the analysis of 67 commercially available dietary supplements. In five cases, one or more steroid-type compounds were found in the concentration of 5 ng g -100 μg g , which might result adverse analytical findings in athletes.
本研究的目的是鉴定和定量检测膳食补充剂(DSs)中的特定合成代谢雄激素类固醇(AASs)和其他甾烷结构化合物。这些化合物在运动员中受到特别关注,因为它们可能导致阳性兴奋剂检测结果。研究重点是优化一种基于气相色谱的高灵敏度和选择性分析策略,使用三重四极杆质谱作为检测器。优化了 28 种目标化合物的色谱方法和多反应监测(MRM)转换。采用固相萃取(SPE)程序进行样品净化,采用 N-甲基-N-(三甲基硅基)-三氟乙酰胺(MSTFA)对 AASs 进行衍生化。对方法进行了验证,考察了以下参数:线性范围、检测限、准确度和精密度(日内精密度)。通过回归模型评估校准曲线,得到了良好的决定系数(R≥0.9912)。残差随机散布在零附近。检测限(LOD)低于 7.0 ng g 或 ng ml 。准确度评估以高样品间变异性为特征的不同形式的 DSs 进行评价(液体、粉末、片剂、胶囊、蛋白质和草药基)。在所有情况下,日内测定精密度均低于 20%。所开发的分析方法成功应用于 67 种市售膳食补充剂的分析。在五种情况下,发现一种或多种甾体化合物的浓度在 5 ng g -100 μg g 之间,这可能导致运动员出现不良分析结果。