食品科学 ›› 2026, Vol. 47 ›› Issue (9): 333-340.doi: 10.7506/spkx1002-6630-20251021-139

• 安全检测 • 上一篇    下一篇

基于5-羟色胺释放原理构建结缔微组织传感器检测肌酸激酶

蒋栋磊,张思迪,徐阳,王柯,王立峰   

  1. (南京财经大学食品科学与工程学院,江苏省现代粮食流通与安全协同创新中心,江苏 南京 210023)
  • 出版日期:2026-05-15 发布日期:2026-06-03
  • 基金资助:
    江苏省现代农业重点项目(BE2022317);“十四五”国家重点研发计划青年科学家项目(2022YFF1102700); 国家自然科学基金面上项目(32172297;32472430);江苏高校优势学科建设工程资助项目(PAPD)

A 5-Hydroxytryptamine Release-Based Biomimetic Microtissue Sensor for Detecting Creatine Kinase

JIANG Donglei, ZHANG Sidi, XU Yang, WANG Ke, WANG Lifeng   

  1. (Collaborative Innovation Center for Modern Grain Circulation and Safety, College of Food Science and Engineering, Nanjing University of Finance & Economics, Nanjing 210023, China)
  • Online:2026-05-15 Published:2026-06-03

摘要: 根据肌酸激酶刺激肥大细胞释放5-羟色胺(5-hydroxytryptamine,5-HT)的原理,利用5-HT在电极表面的氧化电流变化实现对肌酸激酶的定量分析。采用金纳米粒子、Fe3O4纳米颗粒和多壁碳纳米管共同修饰丝网印刷碳电极,同时将肥大细胞与甲基丙烯酰化明胶的复合物作为生物墨水,通过3D生物打印技术制备具有网状结构的结缔组织模型,联动电化学工作站,构建基于5-HT释放原理的电化学仿生结缔微组织传感器。传感器的检测范围为0.3~5.0 μg/mL,线性回归方程为IDPV=0.236 39lg C+1.944 38,决定系数为0.993(n=3),检测限为0.042 μg/mL。以上结果证实了通过检测过敏反应中细胞分泌物的水平,从而间接确定过敏原浓度的可行性,同时也为过敏原的快速检测提供了新思路。

关键词: 过敏原;肌酸激酶;炎症介质;电化学传感器;5-羟色胺

Abstract: Based on the principle of creatine kinase (CK)-induced release of 5-hydroxytryptamine (5-HT) from mast cells, the quantitative analysis of CK was achieved by detecting changes in the oxidation current of 5-HT on the electrode surface. Gold nanoparticles (AuNPs), Fe3O4 nanoparticles and multi-walled carbon nanotube (MWCNT) were used jointly to modify the screen-printed carbon electrode (SPCE). Meanwhile, the composite of mast cells and gelatin methacryloyl (GelMA) was used as bio-ink to prepare a connective tissue model with a network structure through 3D bioprinting, which was then combined with an electrochemical workstation to develop a bionic sensor to detect CK. The sensor demonstrated a linear response to CK concentrations ranging from 0.3 to 5.0 μg/mL, which was fitted to the equation: IDPV = 0.236 39lgC + 1.944 38 (R2 = 0.993, n = 3). The limit of detection (LOD) was determined to be 0.042 μg/mL. The above results confirmed the feasibility of indirectly quantifying food allergen concentrations by detecting cellular secretion during allergic reactions. This study provides a new strategy for rapid allergen detection.

Key words: allergens; creatine kinase; inflammatory mediator; electrochemical sensor; 5-hydroxytryptamine

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