Strano-Rossi Sabina, Odoardi Sara, Castrignanò Erika, Serpelloni Giovanni, Chiarotti Marcello
Institute of Public Health, Forensic Toxicology Laboratory, Università Cattolica del S. Cuore, Rome, Italy.
Institute of Public Health, Forensic Toxicology Laboratory, Università Cattolica del S. Cuore, Rome, Italy.
J Pharm Biomed Anal. 2015 Mar 15;106:144-52. doi: 10.1016/j.jpba.2014.06.011. Epub 2014 Jun 14.
The paper describes a liquid chromatography/high resolution mass spectrometry LC/HRMS method for the simultaneous identification and quantification of stimulants (ephedrines, caffeine, anorectic drugs such as phentermine, phendimetrazine, phenmetrazine, fenfluramine, benfluorex, mephentermine, fencanfamine, sibutramine) and PDE5I (sildenafil, vardenafil and tadalafil) in food supplements using a benchtop Orbitrap mass spectrometer. The mass detector, with a nominal resolving power of 100,000 (FWHM at m/z 200), operated in full scan mode in ESI positive ionization mode. Analytes were identified by retention times, accurate masses and correspondence of experimental and calculated isotopic patterns. The limits of detection (LOD) obtained varied from 1 to 25 ng g(-1) and limits of quantification (LOQ) were 50 ng g(-1) for all compounds. The method was linear for all the analytes in the ranges from 50 to 2000 ng g(-1), giving correlation coefficients>0.99. Accuracy (intended as %E) and repeatability (% CV) were always lower than 15%. The method was applied to the analysis of 36 dietary supplements, revealing the presence of ephedrine and/or pseudoephedrine in four of them, caffeine in eight of them and sildenafil in four of them. In one case, ephedrine was not reported on the label of the dietary supplement, as well as for caffeine in other two cases. A further confirmation of the analytes identity in positive samples was obtained through in-source fragmentation and comparison of the obtained fragments and their relative abundances with those from certified standards. As the acquisition mode is full scan, it would be also possible to re-process a previously acquired datafile for the investigation of untargeted analytes.
本文描述了一种液相色谱/高分辨率质谱(LC/HRMS)方法,该方法使用台式轨道阱质谱仪同时鉴定和定量食品补充剂中的兴奋剂(麻黄碱、咖啡因、食欲抑制剂如苯丁胺、苯双甲吗啉、苯甲吗啉、芬氟拉明、苄氟雷司、美芬丁胺、芬坎法明、西布曲明)和磷酸二酯酶5抑制剂(西地那非、伐地那非和他达拉非)。质量检测器的标称分辨率为100,000(m/z 200处的半高宽),在电喷雾电离正离子模式下以全扫描模式运行。通过保留时间、精确质量以及实验和计算的同位素模式的对应关系来鉴定分析物。所获得的检测限(LOD)在1至25 ng g⁻¹之间,所有化合物的定量限(LOQ)均为50 ng g⁻¹。该方法对于所有分析物在50至2000 ng g⁻¹范围内呈线性,相关系数>0.99。准确度(以%E表示)和重复性(%CV)始终低于15%。该方法应用于36种膳食补充剂的分析,发现其中4种含有麻黄碱和/或伪麻黄碱,8种含有咖啡因,4种含有西地那非。在一个案例中,膳食补充剂标签上未标明麻黄碱,在另外两个案例中未标明咖啡因。通过源内裂解以及将获得的碎片及其相对丰度与认证标准品的碎片及其相对丰度进行比较,对阳性样品中的分析物身份进行了进一步确认。由于采集模式为全扫描,也可以重新处理先前采集的数据文件以研究非靶向分析物。