化学
发色团
原位
水溶液中的金属离子
金属
灵敏度(控制系统)
沉积(地质)
光化学
纳米技术
组合化学
有机化学
古生物学
材料科学
电子工程
沉积物
生物
工程类
作者
Jiaren Song,Changdi Xu,Shen Zeng,Wanchao Zuo,Qing Yang,Qiannan Hu,Xiangming Meng,Jinjun Ye,Jianjun Dai,Yanmin Ju
标识
DOI:10.1021/acs.analchem.4c05781
摘要
Traditional lateral flow immunochromatography assays (LFIAs) have faced low sensitivity for trace detection due to the lack of colorimetric brightness. The current strategies to improve sensitivity commonly have the disadvantages of an uncontrollable enhancement process or high background interference, leading to huge obstacles for signal readout. Herein, an in situ metal ion-based chemical coordination amplification (MICCA) strategy has been reported. Metal ion clusters on metal–organic frameworks could coordinate with chromophores to produce colored complexes for visual signal enhancement. A Zr-based metal AIEgen framework (MAF) loaded with Prussian blue was chosen as the dual-mode signal tag for colorimetric and fluorescent readout. MAF could be employed as a grafting substrate to in situ deposit chromophores through the coordination with Zr4+ clusters and arsenazo III. The process of MICCA was in situ, controllable, and free of background interference. For target cancer biomarker alpha-fetoprotein (AFP), the limit of detection (LOD) by the naked eye was 25 ng/mL, and the LODs of MICCA and fluorescence were 5 ng/mL, which was 5-fold decreased. Significantly, MICCA-LFIA could effectively differentiate between AFP-positive and AFP-negative clinical serum samples. The quantitative results were highly consistent with clinical results (R2 = 0.9927). This work explored the application of metal ion-based chemical coordination reactions in signal amplification strategies and provided ideas for high-sensitivity LFIA development.
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