食品科学 ›› 2025, Vol. 46 ›› Issue (2): 240-247.doi: 10.7506/spkx1002-6630-20240602-001

• 安全检测 • 上一篇    下一篇

QuEChERS结合HPLC检测辣椒及其制品中天然辣椒素、二氢辣椒素和合成辣椒素

成璐瑶,温雅君,石文婷,周子莹,马丽艳   

  1. (1.中国农业大学食品科学与营养工程学院,北京 100083;2.北京市农产品质量安全中心,北京 100029;3.农业农村部农产品质量检验测试中心(北京),北京 100083)
  • 出版日期:2025-01-25 发布日期:2024-12-30
  • 基金资助:
    科技创新2030——重大项目(2023ZD0406309-01)

Determination of Natural Capsaicin, Dihydrocapsaicin and Synthetic Capsaicin in Hot Pepper and Its Products by QuEChERS Combined with HPLC

CHENG Luyao, WEN Yajun, SHI Wenting, ZHOU Ziying, MA Liyan   

  1. (1. College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China; 2. Beijing Agricultural Products Quality and Safety Center, Beijing 100029, China; 3. Quality Inspection and Testing Center for Agri-products (Beijing), Ministry of Agriculture and Rural Affairs, Beijing 100083, China)
  • Online:2025-01-25 Published:2024-12-30

摘要: 建立一种QuEChERS结合高效液相色谱快速检测辣椒及其制品中的天然辣椒素、二氢辣椒素和合成辣椒素的方法。样品用乙腈提取,无水硫酸镁、十八烷基硅烷(C18)、乙二胺-N-丙基硅烷化硅胶、石墨化炭黑复合吸附剂净化。采用Agilent Eclipse Plus C18(150 mm×4.6 mm,5 μm)分离,以0.4%磷酸水溶液和90%乙腈溶液为流动相进行梯度洗脱,荧光检测器进行检测。结果表明:天然辣椒素、二氢辣椒素和合成辣椒素在0.20~100 mg/L范围内线性关系良好,决定系数(R2)均大于0.999。天然辣椒素的方法检出限为0.014~0.069 mg/kg,定量限为0.046~0.23 mg/kg;二氢辣椒素的方法检出限为0.023~0.12 mg/kg,定量限为0.077~0.39 mg/kg;合成辣椒素的方法检出限为0.018~0.088 mg/kg,定量限为0.059~0.30 mg/kg。在干辣椒、鲜辣椒、香菇酱、辣椒油4 种基质中,3 个不同添加水平下的加标回收率为91.6%~117.2%,相对标准偏差为0.2%~6.1%。该方法简便、准确,不仅适用于干、鲜辣椒,而且适用于高油、高蛋白等辣椒制品中天然辣椒素、二氢辣椒素和合成辣椒素含量的检测。

关键词: QuEChERS;高效液相色谱;辣椒;辣椒素;合成辣椒素

Abstract: A QuEChERS combined with high performance liquid chromatography (HPLC) method was developed for the rapid determination of natural capsaicin, dihydrocapsaicin and synthetic capsaicin in hot pepper and its products. The samples were extracted with acetonitrile and purified by sequential use of anhydrous magnesium sulfate, octadecylsilane (C18), ethylenediamine-N-propylsilane silica gel (PSA) and graphitized carbon black (GCB). An Agilent Eclipse Plus C18 column (150 mm × 4.6 mm, 5 μm) was used for separation, gradient elution was performed with a mobile phase comprising 0.4% phosphoric acid aqueous solution and 90% acetonitrile in water, and a fluorescence detector was used for detection. The results showed that natural capsaicin, dihydrocapsaicin and synthetic capsaicin had a good linear relationship in the range of 0.20–100 mg/L, with determination coefficients (R2) greater than 0.999. The limits of detection (LOD) and quantification (LOQ) of natural capsaicin were 0.014–0.069 mg/kg and 0.046–0.23 mg/kg, respectively. The LOD and LOQ of dihydrocapsaicin were 0.023–0.12 mg/kg and 0.077–0.39 mg/kg, respectively. The LOD and LOQ of synthetic capsaicin were 0.018–0.088 mg/kg and 0.059–0.30 mg/kg, respectively. The recovery rates were 91.6%–117.2% and the relative standard deviation (RSD) were 0.2%–6.1% for dry hot pepper, fresh hot pepper, shiitake mushroom paste with hot pepper and chili oil at three different spiked levels. The developed method is simple, accurate and suitable for the determination of not only dried and fresh hot peppers, but also natural capsaicin, dihydrocapsaicin and synthetic capsaicin in high oil and high protein hot pepper products.

Key words: QuEChERS; high performance liquid chromatography; hot pepper; capsaicin; synthetic capsaicin

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