食品科学 ›› 2023, Vol. 44 ›› Issue (4): 337-343.doi: 10.7506/spkx1002-6630-20220224-202

• 安全检测 • 上一篇    

铂壳金核纳米酶介导的磁弛豫免疫传感器快速检测食源性沙门氏菌

董永贞,陈瑞,吴紫荆,陈翊平,潘晖,刘明军   

  1. (1.华中农业大学食品科学技术学院,湖北 武汉 430070;2.岭南现代农业科学与技术广东省实验室,广东 广州 510000 3.荆州市食品药品检验所,湖北 荆州 434000)
  • 发布日期:2023-03-01
  • 基金资助:
    岭南现代农业实验室自主科研项目(NZ2021036)

Gold Core@Platinum Shell-Nanozyme-Mediated Magnetic Relaxation Immunosensor for the Rapid Detection of Foodborne Salmonella

DONG Yongzhen, CHEN Rui, WU Zijing, CHEN Yiping, PAN Hui, LIU Mingjun   

  1. (1. College of Food Science and Technology, Huazhong Agricultural University, Wuhan 430070, China; 2. Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510000, China; 3. Jingzhou Institute for Food and Drug Control, Jingzhou 434000, China)
  • Published:2023-03-01

摘要: 构建了一种基于铂壳金核(Au@Pt)纳米酶介导顺磁离子价态转变的磁弛豫免疫传感器,并用于鸡蛋中沙门氏菌的快速、高灵敏检测。首先通过微波水热法合成了稳定性高、催化性能强的Au@Pt纳米酶,并利用其过氧化氢类酶活性催化过氧化氢(H2O2),而剩余的H2O2可将MnO4-还原为Mn2+。由于MnO4-/Mn2+两者之间磁信号差异显著,可实现H2O2的定量分析。结合免疫反应,沙门氏菌浓度与“检测抗体-Au@Pt纳米酶”含量呈正比,而Au@Pt纳米酶可调控H2O2介导的MnO4-/Mn2+转化体系,进而控制磁信号的变化,最终实现沙门氏菌的定量分析。本方法的检出限为50 CFU/mL,线性范围为1×102~5×107 CFU/mL,对鸡蛋样品的检测结果与荧光定量聚合酶链式反应方法具有良好的一致性。该方法灵敏度高、稳定性好、操作简单、成本低,在食源性致病菌快速检测方面具有良好的应用前景。

关键词: 沙门氏菌;铂壳金核纳米酶;顺磁离子;磁弛豫免疫传感器;过氧化氢

Abstract: In this study, a magnetic relaxation immunosensor based on gold core@platinum shell (Au@Pt) nanozyme-mediated paramagnetic ion valence transition was constructed and used for the rapid detection of Salmonella in foods. Pt@Au nanozyme with high stability and good catalytic performance was synthesized by a microwave-assisted hydrothermal (MAH) method, and its catalase-like activity was used to catalyze hydrogen peroxide (H2O2). The remaining H2O2 could convert MnO4- into Mn2+ through a redox reaction. The significant difference in magnetic signals between MnO4? and Mn2+ allowed the quantitative analysis of hydrogen peroxide. In the immunoreaction, the concentration of Salmonella was directly proportional to the content of “detection antibody-Pt@Au”. Au@Pt could regulate the H2O2-mediated MnO4?/Mn2+ conversion system and consequently control the change of magnetic signal, ultimately allowing the quantitative analysis of Salmonella. The detection limit of this method for Salmonella was 50 CFU/mL, and the linear range was 1 × 102–5 × 107 CFU/mL. The results of this method for Salmonella in eggs were in good agreement with those of fluorescence quantitative polymerase chain reaction (PCR). This method has the advantages of high sensitivity, good stability, simple operation and low cost, thus having a good application prospect in the rapid detection of foodborne pathogens.

Key words: Salmonella; platinum shell@gold core nanozyme; paramagnetic ions; magnetic relaxation switching immunosensor; hydrogen peroxide

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