材料科学
生物传感器
等离子体子
纳米技术
多孔性
金属有机骨架
表面等离子共振
纳米结构
生物分子
光电子学
有机化学
纳米颗粒
复合材料
吸附
化学
作者
Xu Yan,Dandan Su,Hongxia Li,Xu Zhao,Xiaomin Liu,Fangmeng Liu,Peng Sun,Geyu Lu
标识
DOI:10.1002/adfm.202215192
摘要
Abstract Investigations on the utilization efficiency and bioactivity of the enzyme nanocarriers are critical for realizing sensitive biosensors. Herein, hierarchically porous enzyme@peptide‐directed metal–organic frameworks (enzyme@MOFs‐P) nanoarchitectures are constructed by implemented site‐selective epitaxial growth to create mesopore and defect structures. The expanded size of the pores provides suitable space for homogeneously accommodating enzymes and enhances interfacial contact with enzymes, as well as reducing steric hindrance of target recognition to boost the mass transfer process. Harnessing the enzyme‐mediated surface etching of gold nanostars, a robust enzyme@MOFs‐P‐based plasmonic immunosensor is constructed for the sensitive detection of imidacloprid pesticide. In conjunction with using a smartphone‐based homemade device and image‐processing algorithm, quantitative detection of imidacloprid is achieved with a half maximal inhibitory concentration of 0.02 ng mL −1 , which shows ≈1000‐fold improvement in sensitivity compared with that of a typical immunoassay. This work gives valuable insight into engineering size‐tunable nanostructures and the structure‐activity relationship of MOFs, guiding the construction of plasmonic biosensors for on‐site application.
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