刘雪平,梁 峰,张 岩,刘继红,王红旗.基于电化学适体传感器的一步法快速检测 赭曲霉毒素A[J].食品安全质量检测学报,2016,7(5):1915-1919
基于电化学适体传感器的一步法快速检测 赭曲霉毒素A
One-step rapid detection of ochratoxin A by the electrochemical aptasensor
投稿时间:2016-04-19  修订日期:2016-05-17
DOI:
中文关键词:  赭曲霉毒素A  核酸适配体  电化学传感器  二茂铁
英文关键词:ochratoxin A  aptamer  electrochemical sensor  ferrocene
基金项目:河南省高等学校重点科研项目(16A610005)、国家公益性行业(农业)项目(201203094)、国家自然科学基金项目(21305031)
作者单位
刘雪平 河南城建学院市政与环境工程学院 
梁 峰 河南城建学院市政与环境工程学院 
张 岩 河南城建学院市政与环境工程学院 
刘继红 河南省农业科学院农业质量标准与检测技术研究所 
王红旗 河南省农业科学院农业质量标准与检测技术研究所 
AuthorInstitution
LIU Xue-Ping Municipal and Environmental Engineering College, Henan University of Urban Construction 
LIANG Feng Municipal and Environmental Engineering College, Henan University of Urban Construction 
ZHANG Yan Municipal and Environmental Engineering College, Henan University of Urban Construction 
LIU Ji-Hong Institute of Quality Standard and Testing Technology for Agro-Products, Henan Academy of Agricultural Sciences 
WANG Hong-Qi Institute of Quality Standard and Testing Technology for Agro-Products, Henan Academy of Agricultural Sciences 
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中文摘要:
      目的 构建一种基于目标物诱导核酸适配体构象变换的电化学传感器一步法快速灵敏检测赭曲霉毒素A(ochratoxin A, OTA)的含量。方法 适配体一端标有巯基, 另一端标有羧基二茂铁, 通过Au-S共价作用将适配体固定到电极表面; 当加入目标分子OTA时, 引起构象变换, 使二茂铁远离电极表面, 电信号降低。结果 OTA与核酸适配体最佳作用时间为20 min。在0.1~100 ng/mL浓度范围内, 传感器产生的电信号和OTA浓度的对数呈线性关系, 相关系数R2为0.9908, 检测下限达0.08 ng/mL。在5、10和50 ng/mL 3个浓度加标水平下, OTA回收率为89.2%~106.9%。选用含10%异丙醇的PBS(pH 7.4)缓冲溶液清洗反应电极并连续使用8次, 测定OTA的相对标准偏差为4.2%, 说明该传感器可再生重复使用。结论 该传感器具有较高的灵敏度和选择性, 操作简单、样品消耗少、易实现阵列化检测和仪器微型化, 可用于OTA污染的农产品的检测。
英文摘要:
      Objective To construct a method of one-step electrochemical aptasensor based on the conformation transformation of aptamer induced by the target for the determination of ochratoxin A (OTA). Methods The aptamer with sulphur and carboxyl ferrocene at both terminals was covalently immobilized on the surface of the electrode by self-assembly. After adding the target molecular OTA, the conformation transformation would occur, causing ferrocene away from the electrode surface and reducing the electrical signal. Results The optimal reaction time between aptamer and OTA was 20 min. The developed electrochemical aptasensor had a good logarithmic linear relationship between the electrical signal produced by the sensor and OTA concentration in the range of 0.1~100 ng/mL, with the correlation coefficient of 0.9908. The limit of detection (LOD) was 0.08 ng/mL. The recoveries of OTA spiked at 3 levels of 5, 10, and 50 ng/mL were 89.2%~106.9%. When the electrode was cleaned by PBS buffer containing 10% isopropyl alcohol (pH 7.4) and used 8 times, the relative standard deviation of OTA was determined as 4.2%, which showed that the sensor could be renewable reuse. Conclusion The proposed aptasensor exhibits such advantages as high sensitivity and selectivity, simple operation, low sample consumption and compatibility with array format and miniaturization, which can be used for the determination of OTA contaminated agro-products.
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