发光体
烯醇化酶
电化学发光
检出限
猝灭(荧光)
材料科学
发光
化学
光化学
纳米技术
荧光
光电子学
生物
色谱法
免疫学
物理
光学
免疫组织化学
作者
Xinrong Shao,Jing Luo,Zhengxing Gong,Xingming Sun,Hongmin Ma,Dan Wu,Dawei Fan,Yuyang Li,Qin Wei,Huangxian Ju
标识
DOI:10.1016/j.snb.2022.132810
摘要
A quenching electrochemiluminescence (ECL) immunosensor for neuron-specific enolase (NSE) detection was constructed by the resonance energy transfer between Ag@Ce2Sn2O7 (energy donor) and Ag@Cu2O (energy acceptor). The novel luminophore, Ag@Ce2Sn2O7, was synthesized by complexing Ce2Sn2O7 nanocubes with Ag concave-convex nanospheres. It exhibits a stronger ECL emission and a lower potential required for the emissions than pure Ce2Sn2O7. The Ag@Cu2O core-shell structure is composed of a dense Ag core inside and a loose Cu2O shell that provide a large specific surface area and the protection for the independence and integrity of the Ag core. The UV-Vis absorption of Ag@Cu2O overlaps the ECL emission of Ag@Ce2Sn2O7, and thus it can act as a quencher to effectively quench the ECL signal of Ag@Ce2Sn2O7. The great application potentials of the immunosensor in the NSE detection is demonstrated with the good linearity in the wide concentration range of 25 fg/mL - 100 ng/mL, and the low detection limit of 8.6 fg/mL. Our work has provided a reference for the immunosensor development of other biomarkers.
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