食品科学 ›› 2026, Vol. 47 ›› Issue (15): 297-306.doi: 10.7506/spkx1002-6630-20251226-221

• 安全检测 • 上一篇    下一篇

微流控电化学芯片的构建及其对食物过敏标志物的检测

李可,宋吉雨,张文静,周瑾茹,傅玲琳,管玉雯,何建敏   

  1. (1.浙江省检验检疫科学技术研究院,浙江?杭州 310008;2.浙江工商大学食品与生物工程学院,浙江?杭州 310018)
  • 出版日期:2026-08-15 发布日期:2026-08-24
  • 基金资助:
    国家自然科学基金青年科学基金项目(32402165);海关总署科研项目(2024HK108)

Development of a Microfluidic Electrochemical Chip for the Detection of Food Allergy Biomarkers

LI Ke, SONG Jiyu, ZHANG Wenjing, ZHOU Jinru, FU Linglin, GUAN Yuwen, HE Jianmin   

  1. (1. Zhejiang Academy of Science & Technology for Inspection & Quarantine, Hangzhou 310008, China; 2. School of Food Science and Biotechnology, Zhejiang Gongshang University, Hangzhou 310018, China)
  • Online:2026-08-15 Published:2026-08-24

摘要: 本研究基于微流控技术与电化学免疫传感原理,构建一种用于检测食品过敏标志物的新型微流控电化学免疫传感器。该传感器以丝网印刷碳电极为基底,通过电化学沉积金纳米颗粒构建金纳米电极,并集成微流控芯片实现自动化样品处理与检测。构建基于链霉亲和素-生物素的抗体固定体系,结合氧化还原介质K3[Fe(CN)6]的阻抗响应变化,经电化学工作站将微通道内的化学变化转化为电极阻抗信号,最终依据阻抗值实现对过敏标志物OX40L的定量检测。结果表明,该传感器检测线性范围为10~7 500 pg/mL,检测限低至10 pg/mL,变异系数小于10%,且可实现电极再生。进一步将传感器与肠道芯片集成,成功实现对卵白蛋白、麦醇溶蛋白等4 种致敏原刺激下细胞因子的实时动态监测,其中,通过外接电化学工作站等设备,能够实现对卵白蛋白连续80 h监测。综上,该集成系统兼具微型化、高灵敏度和自动化优势,可为过敏机制研究和食品安全检测提供新型技术平台。

关键词: 微流控芯片;电化学免疫传感器;金纳米电极;食物过敏标志物

Abstract: This study developed a novel microfluidic electrochemical immunosensor based on microfluidic technology and electrochemical immunosensing for the detection of food allergy biomarkers. The sensor utilized screen-printed carbon electrodes (SPCEs) modified with electrodeposited gold nanoparticles (AuNPs) to construct gold nanoelectrodes and was integrated with microfluidic chips to achieve automated sample processing and detection. An 11-mercaptoundecanoic acid (11-MUA) self-assembled monolayer (SAM) was used as the immobilization substrate to construct a streptavidin-biotinylated antibody system. Using the impedance response variation of the redox mediator K3[Fe(CN)6], the chemical changes within the microchannels were converted into electrode impedance signals by an electrochemical workstation, ultimately enabling quantitative detection of the allergen biomarker OX40L based on the impedance values. The sensor exhibited a linear range from 10 to 7 500 pg/mL, a low detection limit (LOD) of 10 pg/mL, and coefficient of variation < 10%, and allowed successful electrode regeneration. Furthermore, the integration of the sensor with a gut-on-a-chip platform achieved real-time dynamic monitoring of cytokines stimulated by four allergens (e.g., ovalbumin, gliadin), and interfacing it with external devices such as electrochemical workstations allowed continuous monitoring of ovalbumin for up to 80 hours. In summary, this integrated system offers the advantages of miniaturization, high sensitivity, and automation, providing a novel technical platform for allergy mechanism research and food safety detection.

Key words: microfluidic chip; electrochemical immunosensor; gold nanoelectrode; food allergy biomarkers

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