化学
异质结
生物分析
生物传感器
极性(国际关系)
纳米技术
检出限
烯醇化酶
光电流
光电化学
选择性
半导体
光电子学
催化作用
电化学
电极
色谱法
材料科学
物理化学
生物化学
免疫组织化学
细胞
内科学
医学
作者
Feng‐Zao Chen,Xiao-Xue Fu,Xiaojie Yu,Yu-Hang Qiu,Shi‐Bin Ren,Yichao Wang,Deman Han,Weiwei Zhao
标识
DOI:10.1021/acs.analchem.3c01401
摘要
The sensitive detection of neuron-specific enolase (NSE) as a biomarker for lung cancer at an early stage is critical but has long been a challenge. The emergence of polarity-switchable photoelectrochemical (PEC) bioanalysis has opened up new avenues for developing highly sensitive NSE sensors. In this study, we present such a biosensor depending on the bioinduced AgI transition on MOF-on-MOF-derived semiconductor heterojunctions. Specifically, treatment of ZnO@In2O3@AgI by bioproduced H2S can in situ generate the ZnO@In2O3@In2S3@Ag2S heterojunction, with the photocurrent switching from the cathodic to anodic one due to the changes in the carrier transfer pathway. Linking an NSE-targeted sandwich immunorecognition with labeled alkaline phosphatase (ALP) catalyzed generation of H2S, such a phenomenon was correlated to NSE concentration with good performance in terms of selectivity and sensitivity and a low detection limit of 0.58 pg/mL. This study offered a new perspective on the use of MOF-on-MOF-derived heterostructures for advanced polarity-switchable PEC bioanalysis.
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