气相色谱法同时测定电子烟油中的20种合成大麻素类物质

Simultaneous Determination of 20 Synthetic Cannabinoids in Electronic Cigarette Oil by Gas Chromatography

  • 摘要: 建立了气相色谱同时对电子烟油中20种合成大麻素类物质进行定量分析的方法. 样品经甲醇提取后,在色谱柱初始温度250 ℃保持1 min,然后以10 ℃/min的速率升温至310 ℃并保持21 min的条件下,采用基质外标法,实现电子烟油中20种合成大麻素类物质的定量分析. 结果表明,在1.0~100.0 μg/mL范围内,20种合成大麻素类物质线性关系良好,相关系数(r)均大于0.999,检出限为0.01~0.11 μg/mL,定量限为0.03~0.36 μg/mL. 在2、10、50 μg/mL 3个基质加标水平下,各目标物的加标回收率为83.74%~114.82%,相对标准偏差(RSDs, n=6)为0.44%~4.11%. 对公安机关缴获的10份可疑样品进行分析,检出4F-ABUTINACA、MDMB-4en-PINACA、ADB-BUTINACA、4F-MDMB-BUTICA、5F-MDMB-PICA和MDMB-BUTINACA 6种合成大麻素,含量在0.0050%~0.2009%之间. 方法具有准确、简便、快速等优点,能够满足相关鉴定工作的需求.

     

    Abstract: A method for simultaneous quantitative determination of 20 synthetic cannabinoids (SCs) in electronic cigarette oil by gas chromatography (GC) has been established. The samples were extracted using methanol. The initial temperature of the column was 250 ℃ and stayed for 1 min, and then the temperature was rised to 310 ℃ by the rate of 10 ℃/min and stayed for 21 min. Combined with the external standard method, the 20 SCs in electronic cigarette oil were successfully identified. The 20 SCs had a good linear relationship between 1.0~100.0 μg/mL, and the correlation coefficients (r) were higher than 0.999. The limits of detection (LODs) were 0.01~0.11 μg/mL, and the limits of quantitation (LOQs) were 0.03~0.36 μg/mL. At the three spiked levels (2, 10, 50 μg/mL), the spiked recoveries ranged from 83.74% to 114.82%, the relative standard deviations (RSDs, n=6) were between 0.44% and 4.11%. The 10 suspicious samples seized by the public security authorities were analyzed, and 4F-ABUTINACA, MDMB-4en-PINACA, ADB-BUTINACA, 4F-MDMB-BUTICA, 5F-MDMB-PICA and MDMB-BUTINACA were detected, the content were between 0.0050% and 0.2009%. The method is accurate, simple and rapid, which could satisfy the requirements of relevant identification work.

     

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