生物分子
电化学发光
纳米颗粒
检出限
表面等离子共振
三磷酸腺苷
等离子体子
纳米结构
银纳米粒子
材料科学
蚀刻(微加工)
纳米技术
接受者
生物传感器
组合化学
光电子学
化学
物理
生物化学
图层(电子)
色谱法
凝聚态物理
作者
Yuanyuan Wang,Xianwen Kan
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2022-07-14
卷期号:5 (7): 9996-10002
被引量:5
标识
DOI:10.1021/acsanm.2c02415
摘要
Convenient and fast approaches for sensitive monitoring of different biomolecules are of vital importance for obtaining insights into biological processes and related diseases. Herein, silica nanospheres encapsulated with Ru(bpy)32+ (RuSiO2) were uniformly coated with silver nanoparticles (AgNPs) through the in-situ reduction method to form RuSiO2@Ag core–shell nanoparticles, which were employed to fabricate a versatile electrochemiluminescence (ECL) sensing system for the assay of glucose (Glu) and adenosine triphosphate (ATP) on the basis of ECL resonance energy transfer (ECL-RET). RuSiO2@Ag core–shell nanoparticles showed high RET efficiency due to the combination of the donor (RuSiO2)–acceptor (AgNPs) pair into one nanostructure, causing a significantly quenched ECL signal of RuSiO2. Afterward, the Glu oxidase immobilized on RuSiO2@Ag by DNA complementation naturally catalyzed the oxidation of Glu to produce H2O2, which then triggered the etching of AgNPs. Consequently, the remarkably recovered ECL signal was further used to specifically detect Glu and achieved a limit of detection of 0.15 μM. ATP was chosen as a model molecule to verify the detecting ability of the sensor and achieved femtomolar-level results. The versatile ECL sensing system based on enzymatic oxydate-triggered etching and RET strategies hold potential promise for the convenient and sensitive detection of multiple types of biomolecules.
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