Qualitative and Quantitative Analysis of Five Indoles or Indazole Amide Synthetic Cannabinoids in Suspected E-Cigarette Oil by GC-MS.

Cui-Mei Liu, Wei Jia, Chun-Hui Song, Zhen-Hua Qian, Zhen-Dong Hua, Yue-Meng Chen
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Abstract

Objectives: To establish the GC-MS qualitative and quantitative analysis methods for the synthetic cannabinoids, its main matrix and additives in suspicious electronic cigarette (e-cigarette) oil samples.

Methods: The e-cigarette oil samples were analyzed by GC-MS after diluted with methanol. Synthetic cannabinoids, its main matrix and additives in e-cigarette oil samples were qualitatively analyzed by the characteristic fragment ions and retention time. The synthetic cannabinoids were quantitatively analyzed by using the selective ion monitoring mode.

Results: The linear range of each compound in GC-MS quantitative method was 0.025-1 mg/mL, the matrix recovery rate was 94%-103%, the intra-day precision relative standard deviations (RSD) was less than 2.5%, and inter-day precision RSD was less than 4.0%. Five indoles or indazole amide synthetic cannabinoids were detected in 25 e-cigarette samples. The main matrixes of e-cigarette samples were propylene glycol and glycerol. Additives such as N,2,3-trimethyl-2-isopropyl butanamide (WS-23), glycerol triacetate and nicotine were detected in some samples. The content range of synthetic cannabinoids in 25 e-cigarette samples was 0.05%-2.74%.

Conclusions: The GC-MS method for synthesizing cannabinoid, matrix and additive in e-cigarette oil samples has good selectivity, high resolution, low detection limit, and can be used for simultaneous qualitative and quantitative analysis of multiple components; The explored fragment ion fragmentation mechanism of the electron bombardment ion source of indole or indoxamide compounds helps to identify such substances or other compounds with similar structures in cases.

气相色谱-质谱联用分析疑似电子烟油中5种吲哚或吲哚酰胺类合成大麻素。
目的:建立可疑电子烟(电子烟)油样品中合成大麻素及其主要基质和添加剂的气相色谱-质谱联用定性和定量分析方法。方法:采用甲醇稀释后的气相色谱-质谱法对电子烟油样品进行分析。通过特征碎片离子和保留时间对电子烟油样品中的合成大麻素及其主要基质和添加剂进行定性分析。采用选择性离子监测模式对合成大麻素进行定量分析。结果:各化合物在GC-MS定量方法中线性范围为0.025 ~ 1 mg/mL,基质回收率为94% ~ 103%,日内精密度相对标准偏差(RSD) < 2.5%,日内精密度RSD < 4.0%。在25份电子烟样品中检出5种吲哚类或吲哚胺类合成大麻素。电子烟样品的主要基质为丙二醇和甘油。在部分样品中检测到N,2,3-三甲基-2-异丙基丁酰胺(WS-23)、三乙酸甘油和尼古丁等添加剂。25份电子烟样品中合成大麻素的含量范围为0.05% ~ 2.74%。结论:采用气相色谱-质谱法合成电子烟油样品中的大麻素、基质和添加剂,选择性好,分辨率高,检出限低,可同时对多组分进行定性和定量分析;所探索的吲哚或吲哚酰胺类化合物的电子轰击离子源的碎片离子碎裂机制,有助于在某些情况下识别这类物质或具有类似结构的其他化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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