任雁明, 解润芳, 王蕊, 熊积斌, 赵臣飞, 杨盛晔, 杨永祎, 李树华, 张瑞林. 超高效液相色谱−串联质谱法快速测定大麻植物中8种大麻素[J]. 云南大学学报(自然科学版), 2021, 43(6): 1212-1219. doi: 10.7540/j.ynu.20210093
引用本文: 任雁明, 解润芳, 王蕊, 熊积斌, 赵臣飞, 杨盛晔, 杨永祎, 李树华, 张瑞林. 超高效液相色谱−串联质谱法快速测定大麻植物中8种大麻素[J]. 云南大学学报(自然科学版), 2021, 43(6): 1212-1219. doi: 10.7540/j.ynu.20210093
REN Yan-ming, XIE Run-fang, WANG Rui, XIONG Ji-bin, ZHAO Chen-fei, YANG Sheng-ye, YANG Yong-yi, LI Shu-hua, ZHANG Rui-lin. Rapid determination of eight cannabinoids in cannabis plants by ultra performance liquid chromatography-tandem mass spectrometry[J]. Journal of Yunnan University: Natural Sciences Edition, 2021, 43(6): 1212-1219. DOI: 10.7540/j.ynu.20210093
Citation: REN Yan-ming, XIE Run-fang, WANG Rui, XIONG Ji-bin, ZHAO Chen-fei, YANG Sheng-ye, YANG Yong-yi, LI Shu-hua, ZHANG Rui-lin. Rapid determination of eight cannabinoids in cannabis plants by ultra performance liquid chromatography-tandem mass spectrometry[J]. Journal of Yunnan University: Natural Sciences Edition, 2021, 43(6): 1212-1219. DOI: 10.7540/j.ynu.20210093

超高效液相色谱−串联质谱法快速测定大麻植物中8种大麻素

Rapid determination of eight cannabinoids in cannabis plants by ultra performance liquid chromatography-tandem mass spectrometry

  • 摘要: 建立一种基于超高效液相色谱−串联质谱(UPLC-MS/MS)同时测定大麻植物中8种大麻素的方法. 样品经甲醇提取后,采用CHIMADZU Shim-pack Velox PFPP色谱柱,以20 mmol/L乙酸铵和0.1%甲酸缓冲液及乙腈为流动相进行梯度洗脱,电喷雾离子源正负离子多反应监测模式进行质谱分析,外标法定量分析大麻植物中的8种大麻素. 8种大麻素在5~500 μg/L线性范围内线性良好,检测限(limit of detection,LOD)和定量限(limit of quantification,LOQ)分别为0.13~1.26 μg/L和0.39~3.83 μg/L,保留时间和定量离子峰面积的相对标准偏差分别为0.10%~0.43%和3.46%~13.41%. 建立的UPLC-MS/MS技术的大麻素定量分析方法灵敏度高、重现性好、分析效率高,可用于检测大麻植物样品中的大麻素含量.

     

    Abstract: A method based on ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established for the simultaneous determination of eight cannabinoids in cannabis plants. The sample was extracted with methanol. Using CHIMADZU Shim-pack Velox PFPP chromatographic column, gradient elution with 20 mmol/L ammonium acetate, 0.1% formic acid buffer and acetonitrile as mobile phases, electrospray ion source positive and negative ion multi-reaction monitoring were used for mass spectrometry analysis, and the external standard method was used to quantitatively analyze the eight cannabinoids in cannabis plants. The eight cannabinoids have good linearity in the linear range of 5~500  μg/L, and the limit of detection (LOD) and limit of quantification (LOQ) are 0.13~1.26  μg/L and 0.39~3.83  μg/L, respectively. The relative standard deviations of retention time and quantitative ion peak area are 0.10%~0.43% and 3.46%~13.41%, respectively. The UPLC-MS/MS technology of cannabinoid quantitative analysis method show high sensitivity, good reproducibility and high analysis efficiency, and can be used to detect cannabinoid content in cannabis plant.

     

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