食品科学 ›› 2021, Vol. 42 ›› Issue (24): 305-310.doi: 10.7506/spkx1002-6630-20201206-068

• 安全检测 • 上一篇    

基于QuEChERS-高效液相色谱-质谱联用技术检测食用菌中8 种烟碱类化合物

陈荣锋,陈凤明,潘裕添,张国广,张峰   

  1. (1.中国检验检疫科学研究院,北京 100176;2.闽南师范大学菌物产业工程技术中心,福建 漳州 363000;3.国家卫生健康委职业安全卫生研究中心,北京 102308)
  • 发布日期:2021-12-30
  • 基金资助:
    “十三五”国家重点研发计划重点专项(2017YFC1601600);国家“万人计划”科技创新领军人才项目

Determination of Eight Nicotine Compounds in Edible Fungi by QuEChERS-High Performance Liquid Chromatography-Mass Spectrometry

CHEN Rongfeng, CHEN Fengming, PAN Yutian, ZHANG Guoguang, ZHANG Feng   

  1. (1. Chinese Academy of Inspection and Quarantine, Beijing 100176, China;2. Engineering Research Center of Fungal Industry, Minnan Normal University, Zhangzhou 363000, China;3. National Center for Occupational Safety and Health, National Health Commission, Beijing 102308, China)
  • Published:2021-12-30

摘要: 建立QuEChERS-高效液相色谱-质谱联用法测定食用菌中8?种烟碱类化合物的检测方法。食用菌经粉碎、提取和净化后,进入液相色谱-质谱检测系统,经HILIC色谱柱分离,利用0.1%甲酸-10?mmol/L乙酸铵溶液和乙腈(20∶80,V/V)作为流动相,等度洗脱,电喷雾离子源正离子模式,多反应监测扫描。在优化条件下8?种烟碱类化合物在一定质量浓度范围内线性关系良好,相关系数大于0.99,方法定量限和检出限分别在0.012~0.12?μg/kg和0.004~0.04?μg/kg之间,方法的回收率在78.7%~107.8%之间,日内精密度和日间精密度分别在1.8%~10.3%和2.8%~11.1%之间,基质效应为81.5%~106.6%。本方法简便、快速、准确,灵敏,完全满足对食用菌中尼古丁等物质的检测。

关键词: 高效液相色谱-质谱联用法;食用菌;烟碱类化合物

Abstract: A method for the determination of eight nicotine compounds in edible fungi by QuEChERS (quick, easy, cheap, effective, rugged and safe) extraction followed by high performance liquid chromatography-mass spectrometry (HPLC-MS) was developed. The compounds in crushed edible fungi were extracted and purified before being injected into the HPLC-MS system. The chromatographic separation was accomplished on an HILIC column by isometric elution using a mobile phase comprising 10 mmol/L ammonium acetate aqueous solution containing 0.1% formic acid and acetonitrile (20:80, V/V). The chromatographic peaks were detected by electrospray ionization (ESI) in the positive ion mode using multiple reaction monitoring (MRM). Under the optimal conditions, the calibration curve for each analyte was linear over a certain concentration range with a correlation coefficient of greater than 0.99. The limit of quantification (LOQ) and limit of detection (LOD) of the developed method were 0.012–0.12 and 0.004–0.04 μg/kg, respectively. The recoveries of the method were in the range of 78.7%–107.8%. The relative standard deviations for intra-day and inter-day precision were 1.8%–10.3% and 2.8%–11.1%, respectively. The matrix effect rates of the method were 81.5%–106.6%.?In conclusion, this method is simple, rapid, accurate and sensitive, and is suitable for the detection of nicotine compounds in edible fungi.

Key words: high performance liquid chromatography-mass spectrometry; edible fungi; nicotine compounds

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