食品科学 ›› 2026, Vol. 47 ›› Issue (5): 335-341.doi: 10.7506/spkx1002-6630-20250823-166

• 安全检测 • 上一篇    

超声辅助提取-衍生化反应结合超高效液相色谱-高分辨质谱同时测定食品中23 种醛酮类化合物

朱洲海,徐艳群,朱丽,刘美燕,杨玺,尹志豇,彭琪媛,高茜,任达兵,朱瑞芝   

  1. (1.云南省烟草化学重点实验室,云南中烟工业有限责任公司技术中心,云南 昆明 650231;2.昆明理工大学食品科学与工程学院,云南 昆明 650500)
  • 发布日期:2026-04-13
  • 基金资助:
    云南中烟工业有限公司科技项目(2024ZK01)

Ultrasound-Assisted Extraction Combined with Derivatization for the Simultaneous Determination of 23 Aldehydes and Ketones in Foods by UPLC-HRMS

ZHU Zhouhai, XU Yanqun, ZHU Li, LIU Meiyan, YANG Xi, YIN Zhijiang, PENG Qiyuan, GAO Qian, REN Dabing, ZHU Ruizhi   

  1. (1. Yunnan Provincial Key Laboratory of Tobacco Chemistry, Technology Center of China Tobacco Yunnan Industry Co. Ltd., Kunming 650231, China; 2. Faculty of Food Science and Engineering,Kunming University of Science and Technology, Kunming 650500, China)
  • Published:2026-04-13

摘要: 提出一种创新性方法,通过衍生化处理结合超高效液相色谱-高分辨质谱联用技术,实现食品样本中23 种醛酮类化合物(aldehydes and ketones,AKs)的同步定量分析。通过系统考察提取方法、酸溶液类型与组成、衍生化试剂质量浓度等关键因素,对提取与衍生化效率进行优化。最优条件下,选用超声辅助提取法(功率50 W、时间10 min、温度30 ℃)作为固体样品中AKs的最佳提取方式;以磷酸(1%,V/V)为优选酸溶液;2,4-二硝基苯肼衍生化试剂质量浓度为50 μg/mL。该方法展现出宽动态线性范围(R2≥0.995)、高灵敏度(定量限:0.002 0~0.132 4 µg/mL)及良好准确度。应用本方法成功测定了茶叶与咖啡样本中的23 种AKs。相较于现有方法,本研究实现了更高通量,同时显著缩短了分析时长。

关键词: 醛酮成分;高分辨质谱;衍生化反应;同时定量分析

Abstract: In this study, we introduced a novel method that utilizes derivatization treatments in conjunction with ultra-high performance liquid chromatography coupled with high-resolution mass spectrometry (UPLC-HRMS) for the simultaneous quantification of 23 aldehydes and ketones (AKs) in food samples. Several key factors including the extraction procedure, the type and composition of acid solutions, and derivatizing agent concentration were optimized which influenced the extraction and derivatization efficiencies. Under optimal conditions, ultrasound-assisted extraction (50 W, 10 min, and 30 ℃) was selected as the most suitable method for extracting AKs from solid samples, with phosphoric acid (1%, V/V) as the preferred acid and 2,4-dinitrophenylhydrazine (DNPH) at a concentration of 50 μg/mL as the derivatizing agent. The proposed method exhibited good linearity over a wide concentration range (R2 ≥ 0.995), high sensitivity with limits of quantification (LOQs) of 0.002 0–0.132 4 µg/mL, and high accuracy. Using the developed method, 23 AKs were successfully determined in tea and coffee samples. Compared with existing methods, this method achieves higher throughput while significantly reducing analysis time.

Key words: aldehydes and ketones; high-resolution mass spectrometry; derivatization; simultaneous quantification

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