食品科学 ›› 2025, Vol. 46 ›› Issue (10): 290-298.doi: 10.7506/spkx1002-6630-20240808-067

• 安全检测 • 上一篇    下一篇

超高效液相色谱-高分辨质谱法快速测定食品中107种那非类非法添加物

冯峰,常启智,孙晓,杜容竹,张峰   

  1. (1.中国检验检疫科学研究院食品安全研究所,北京 100176;2.国家市场监督管理总局重点实验室(食品质量与安全),北京 100176;3.中国医科大学药学院,辽宁 沈阳 110122;4.西安市食品药品检验所,陕西 西安 710119)
  • 出版日期:2025-05-25 发布日期:2025-05-07
  • 基金资助:
    中国检验检疫科学研究院基本科研业务费项目(2023JK009;2024JK017)

Rapid Determination of 107 Illegally Added Nafils in Foods by Ultra-high Performance Liquid Chromatography-High Resolution Mass Spectrometry

FENG Feng, CHANG Qizhi, SUN Xiao, DU Rongzhu, ZHANG Feng   

  1. (1. Institute of Food Safety, Chinese Academy of Inspection and Quarantine, Beijing 100176, China; 2. Key Laboratory of Food Quality and Safety, State Administration for Market Regulation, Beijing 100176, China; 3. School of Pharmacy, China Medical University, Shenyang 110122, China; 4. Xi’an Institute for Food and Drug Control, Xi’an 710119, China)
  • Online:2025-05-25 Published:2025-05-07

摘要: 基于超高效液相色谱-四极杆/静电场轨道阱高分辨质谱法建立快速测定压片糖果、蜂蜜和液体饮料3 种类型食品中107 种那非类非法添加物的分析方法。样品经甲醇提取、Waters Acquity UPLC BEH C18色谱柱(2.1 mm×100 mm,1.7 μm)分离,以乙腈和0.1%甲酸溶液作为流动相进行梯度洗脱,正、负离子同时扫描模式检测,采用一级母离子全扫描和数据依赖的二级碎片离子扫描模式采集数据。结果表明:107 种那非类物质在4~300 µg/L质量浓度范围内线性关系良好,相关系数(R2)均大于0.99;方法检出限为0.1~1 mg/kg,定量限为0.2~2 mg/kg;在2、5、10 mg/kg 3 个水平下的平均加标回收率为82.5%~117.0%,相对标准偏差为0.9%~10.0%(n=6)。该方法检测速率快、准确度高、灵敏度高,可用于食品中那非类非法添加物的快速识别和定量。

关键词: 超高效液相色谱;高分辨质谱;非法添加物;那非类物质

Abstract: A rapid method for the determination 107 illegally added nafils in compressed candies, honey and beverage was developed by ultra-high performance liquid chromatography coupled with quadrupole orbitrap high-resolution mass spectrometry. The samples were extracted with methanol and separated on a Waters Acquity UPLC BEH C18 column (2.1 mm × 100 mm, 1.7 μm) with gradient elution using a mobile phase consisting of acetonitrile and 0.1% formic acid in water. The detection was conducted in both positive and negative ion modes, and a full MS scan/data dependent MS2 mode was used to collect data. The 107 nafils showed good linearity in the concentration range of 4–300 μg/L, with correlation coefficients (R2) greater than 0.99. The limits of detection (LODs) were 0.1–1 mg/kg, and the limits of quantification (LOQs) were 0.2–2 mg/kg. The average recoveries ranged from 82.5% to 117.0% at three spiked levels of 2, 5, 10 mg/kg, with relative standard deviations of 0.9%–10.0% (n = 6). This method was fast, accurate, sensitive, and suitable for the rapid identification and quantification of illegal additives in foods.

Key words: ultra-high performance liquid chromatography; high-resolution mass spectrometry; illegal additives; nafils

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