化学
免疫分析
电极
电化学
纳米技术
色谱法
抗体
免疫学
生物
物理化学
材料科学
作者
Xudong Ying,Wenxuan Fu,Lihang Zhu,Tao Sun,Min Qi,Lin Zhou,Ya-Feng Wang,Jing Wang,Bin Su,Jun Zhang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2024-06-24
卷期号:96 (26): 10630-10638
被引量:41
标识
DOI:10.1021/acs.analchem.4c01224
摘要
Paper-based lateral flow immunoassays (LFIAs) are cost-effective, portable, and simple methods for detection of diverse analytes, which however only provide qualitative or semiquantitative results and lack sufficient sensitivity. A combination of LFIA and electrochemical detection, namely, electrochemical lateral flow immunoassay (eLFIA), enables quantitative detection of analytes with high sensitivity, but the integration of external electrodes makes the system relatively expensive and unstable. Herein, the working, counter, and reference electrodes were prepared directly on the nitrocellulose membrane using screen printing, which remarkably simplified the structure of eLFIA and decreased the cost. Moreover, a horseradish peroxidase (HRP)-based electrochemical signal amplification strategy was used for further increasing the analytical sensitivity. HRP captured on the working electrode can catalyze the oxidation of tetramethylbenzidine (TMB) to form the TMB-TMBox precipitate on the electrode surface, which as an electrochemically active product can output an amplified current for quantification. We demonstrated that the eLFIA could detect low-abundant inflammatory biomarkers in human plasma samples with limits of detection of 0.17 and 0.54 pg mL–1 for interleukin-6 and C-reactive protein, respectively. Finally, a fully portable system was fabricated by integrating eLFIA with a flexible and wireless electrochemical workstation, realizing the point-of-care detection of interleukin-6.
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