生物传感器
光电流
材料科学
微电池
吞吐量
纳米技术
化学
光电子学
计算机科学
无线
电信
操作系统
作者
Min Liu,Danting He,Zhihong Liu,Chengguo Hu
标识
DOI:10.1016/j.bios.2023.115312
摘要
The high-throughput detection of multiple metabolites in saliva by electrochemical sensors is usually a challenge, which however is essential to the comprehensive evaluation of health status or screening of diseases. Here, a light-addressable and paper-based hydrogen peroxide (H2O2) photoelectrochemical (PEC) sensor for the high-throughput detection of multiple salivary metabolites is reported. This sensor has a unique solar microcell array structure with a silver nanowires/fullerene-Congo red (AgNWs/C60-CR) disc working electrode (WE) and a single-walled carbon nanotubes/platinum nanowires (SWCNTs/PtNWs) ring reference/counter electrode (RE/CE) in each microcell. Enzymes of different metabolites are immobilized on different separated microcells of a cover slide over the sensor, from which enzymatically produced H2O2 can react with p-hydroxyphenyl boric acid (4-HPBA) on the WE of the sensor to generate hydroquinone (HQ) for photocurrent responses. Based on this strategy, a disposable PEC sensor of saliva was developed, which allows the multiplexed detection of uric acid (UA), glucose (GLU) and lactate (LA) in diluted human saliva with high sensitivity and selectivity. Moreover, the detection throughput and application field of the sensor can be easily extended by connecting a series of sensors in parallel or varying the enzymes. The present work thus establishes a cost-effective approach to the scalable construction of versatile biosensing platforms with tunable throughput and varied analytes.
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