Division of Advanced Analysis, Toxicological Evaluation and Research Department, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Cheongju-si, Chungcheongbuk-do, Republic of Korea.
J Sep Sci. 2017 Dec;40(24):4677-4688. doi: 10.1002/jssc.201700879. Epub 2017 Nov 13.
Adulterated products are continuously detected in society and cause problems. In this study, we developed and validated a method for determining synthetic sedative-hypnotics and sleep inducers, including barbital, benzodiazepam, zolpidem, and first-generation antihistamines, in adulterated products using Quadrupole-Orbitrap mass spectrometry and ultrahigh performance liquid chromatography with tandem mass spectrometry. In Quadrupole-Orbitrap mass spectrometry analysis, target compounds were confirmed using a combination of retention time, mass tolerance, mass accuracy, and fragment ions. For quantification, several validation parameters were employed using ultrahigh performance liquid chromatography with tandem mass spectrometry. The limit of detection and limit of quantitation was 0.05-53 and 0.17-177 ng/mL, respectively. The correlation coefficient for linearity was more than 0.995. The intra- and interassay accuracies were 86-110 and 84-111%, respectively. Their precision values were evaluated as within 4.0 (intraday) and 10.7% (interday). Mean recoveries of target compounds in adulterated products ranged from 85 to 116%. The relative standard deviation of stability was less than 10.7% at 4°C for 48 h. The 144 adulterated products obtained over 3 years (2014-2016) from online and in-person vendors were tested using established methods. After rapidly screening with Quadrupole-Orbitrap mass spectrometry, the detected samples were quantified using ultrahigh performance liquid chromatography with tandem mass spectrometry. Two of them were adulterated with phenobarbital.
伪劣产品不断在社会中被检测到,并引发问题。在本研究中,我们开发并验证了一种使用四极杆轨道阱质谱和超高效液相色谱串联质谱法测定掺杂物中的合成镇静催眠药和睡眠诱导剂(包括苯巴比妥、苯二氮䓬类、唑吡坦和第一代抗组胺药)的方法。在四极杆轨道阱质谱分析中,通过保留时间、质量容限、质量精度和碎片离子的组合来确认目标化合物。对于定量分析,使用超高效液相色谱串联质谱法采用了多个验证参数。检测限和定量限分别为 0.05-53 和 0.17-177ng/mL。线性的相关系数大于 0.995。日内和日间准确度分别为 86-110%和 84-111%。精密度值评估为 4.0%(日内)和 10.7%(日间)以内。目标化合物在掺杂物中的平均回收率为 85-116%。在 4°C 下放置 48 小时,稳定性的相对标准偏差小于 10.7%。使用建立的方法对 3 年来(2014-2016 年)从在线和现场销售人员处获得的 144 种掺杂物进行了测试。使用四极杆轨道阱质谱快速筛选后,使用超高效液相色谱串联质谱法对检测到的样品进行定量分析。其中两个掺杂物中掺有苯巴比妥。