食品科学 ›› 2026, Vol. 47 ›› Issue (1): 1-7.doi: 10.7506/spkx1002-6630-20250721-166

• 食品安全快速检测专栏 •    

量子点荧光微球侧流免疫层析法灵敏快速检测食用油中辣椒素类物质

白宇琛,杨洋,姜嘉群,沈建忠,王战辉   

  1. (1.山西医科大学公共卫生学院,营养与食品卫生学教研室,煤炭环境致病与防治教育部重点实验室,山西 太原 030001;2.中国农业大学动物医学院,兽医公共卫生安全全国重点实验室,北京 100193)
  • 发布日期:2026-02-04
  • 基金资助:
    国家自然科学基金青年科学基金项目(82404321); 山西省基础研究计划(自由探索类)青年项目(202203021222260);山西省高等教育“百亿工程”科技引导专项

Sensitive and Rapid Detection of Capsaicinoids in Edible Oils by Lateral Flow Immunoassay with Quantum Dot Beads

BAI Yuchen, YANG Yang, JIANG Jiaqun, SHEN Jianzhong, WANG Zhanhui   

  1. (1. Department of Nutrition and Food Hygiene, MOE Key Laboratory of Coal Environmental Pathogenicity and Prevention, School of Public Health, Shanxi Medical University, Taiyuan 030001, China; 2. State Key Laboratory of Veterinary Public Health and Safety, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China)
  • Published:2026-02-04

摘要: 目的:建立基于量子点荧光微球(quantum dot beads,QBs)对食用油中的辣椒素类物质(capsaicinoids,CPCs)快速定量检测的侧流免疫层析方法(lateral flow immunoassay,LFIA)。方法:以QBs作为信号探针标记抗体,通过系统优化缓冲液pH值、抗体标记量、荧光探针使用量以及包被抗原质量浓度关键实验参数,建立一种用于定量检测CPCs的QBs-LFIA。结果:经实验确定,QBs-LFIA体系的最佳反应条件包括:磷酸盐缓冲液pH 7.5,抗体标记量30 μg,荧光探针用量2 μL,包被抗原质量浓度0.5 mg/mL。在最优条件下QBs-LFIA对缓冲液中CPC的半数抑制浓度为0.022 ng/mL,线性范围为0.009~0.054 ng/mL;对食用油样本中CPCs的检测限为0.14~0.47 µg/kg,加标回收率为77.6%~115.2%,变异系数低于8.0%;与CPCs类似物香兰素类化合物的交叉反应率低于0.1%;对20 份含不同含量CPCs的食用油样本的检测结果表明该方法与液相色谱-串联质谱法相关性良好(R2>0.90)。结论:本研究建立的QBs-LFIA灵敏度高、特异性强、可靠性高,适用于食用油中CPCs的现场快速检测。

关键词: 侧流免疫层析方法;量子点荧光微球;辣椒素类物质;定量检测;食用油

Abstract: Objective: To establish a lateral flow immunoassay (LFIA) based on quantum dot beads (QBs) for the rapid and quantitative detection of capsaicinoids (CPCs) in edible oils. Methods: QBs were used as fluorescent probes to label antibodies, and experimental conditions such as buffer pH, the amount of labeled antibody, fluorescent probe dosage, and coating antigen concentration were optimized to establish a novel method for the quantitative detection of CPCs. Results: The optimal reaction conditions were as follows: buffer pH 7.5, 30 μg of antibodies labeled, 2 μL of fluorescent probe, and coating antigen concentration 0.5 mg/mL. Under the optimal conditions, the half maximal inhibitory concentration (IC50) for CPC in the buffer solution was 0.022 ng/mL. The method was linear over the concentration range of 0.009–0.054 ng/mL. The limit of detection (LOD) for CPCs in edible oil samples was 0.14–0.47 µg/kg. The recoveries in spiked samples ranged from 77.6% to 115.2%, with a coefficient of variation (CV) of less than 8.0%. The cross-reaction rates with CPC analogues were less than 0.1%. When the method was applied for the analysis of 20 edible oil samples containing different amounts of CPCs, the results were well correlated with those of liquid chromatography-tandem mass spectrometry (LC-MS/MS) (R2 > 0.90). Conclusion: The QBs-LFIA method is highly sensitive, specific and reliable, and is suitable for the rapid on-site detection of CPCs in edible oil samples.

Key words: lateral flow immunoassay; quantum dot beads; capsaicinoids; quantitative detection; edible oil

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