电化学发光
发光
噻虫嗪
适体
检出限
材料科学
生物传感器
量子点
生物分子
分子
化学
纳米技术
光电子学
色谱法
有机化学
农学
遗传学
益达胺
杀虫剂
生物
作者
Shuhuai Li,Yan Deng,Chaohai Pang,Xionghui Ma,Yu‐Wei Wu,Wei Wang,Jianping Li,Zhixiang Xu,Lianming Zhang
标识
DOI:10.1016/j.snb.2023.134415
摘要
The performance of an electrochemiluminescent reagent directly affects the performance of its corresponding electrochemiluminescent (ECL) sensor. In this study, Fe/Zn-benzene-1,3,5-tricarboxylic acid metal–organic framework@C-dots (Fe/Zn-BTC@C-dots), which consist of a nano-loaded carbon quantum dot material with an excellent luminescence performance, were synthesised for the first time. Subsequently, they were used to modify the surface of a glassy carbon electrode, and combined with a single-chain thiamethoxam DNA aptamer to construct a biosensor. A novel method for the detection of thiamethoxam was established based on control of the excellent luminescence signal of the Fe/Zn-BTC@C-dots by specific recognition of the aptamer by the target molecule (a signal switch). Upon capturing thiamethoxam, the electrochemical luminescence intensity of the sensor was quenched. The ability of Fe/Zn-BTC to effectively catalyse and amplify the electrochemical luminescence of the C-dots significantly improved the sensitivity of the sensor, while the specific recognition of the target by the aptamer imparted the sensor with an excellent selection ability. Such an advanced approach is promising for the detection of thiamethoxam, with a linear range of 5–5000 × 10−11 mol/L and a sensitivity of 9.81 × 10−12 mol/L being achieved. Moreover, the sensor exhibited recovery rates of 90.5–109.3% upon the detection of thiamethoxam in actual samples.
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