One-step construction of multiplexed enzymatic biosensors using light-addressable electrochemistry on a single silicon photoelectrode

• Published in: Biosensors & bioelectronics Vol. 253; p. 116194
• Main Authors: Yang, Qiaoyu, Liao, Jiaming, Feng, Luyao, Wang, Sen, Zhao, Zhibin, Wang, Jian, Bu, Yazhong, Zhuang, Jian, Zhang, De-Wen
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 01-06-2024
• Subjects: Hydrogel; Light-addressable electrochemistry; Metabolites detection; Multiplexed detection; Photocurrent; Silicon; Silicon; Photocurrent; Hydrogel; Metabolites detection; Multiplexed detection; Light-addressable electrochemistry
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2024.116194

The multiplexed detection of metabolites in parallel within a single biosensor plate is sufficiently valuable but also challenging. Herein, we combine the inherent light addressability of silicon with the high selectivity of enzymes, for the construction of multiplexed photoelectrochemical enzymatic biosensors. To conduct a stable electrochemistry and reagentless biosensing on silicon, a new strategy involving the immobilization of both redox mediators and enzymes using an amide bond-based hydrogel membrane was proposed. The membrane characterization results demonstrated a covalent coupling of ferrocene mediator to hydrogel, in which the mediator acted as not only a signal generator but also a renewable sacrifice agent. By adding corresponding enzymes on different spots of hydrogel membrane modified silicon and recording local photocurrents with a moveable light pointer, this biosensor setup was used successfully to detect multiple metabolites, such as lactate, glucose, and sarcosine, with good analytical performances. The limits of detection of glucose, sarcosine and lactate were found to be 179 μM, 16 μM, and 780 μM with the linear ranges of 0.5–2.5 mM, 0.3–1.5 mM, and 1.0–3.0 mM, respectively. We believe this proof-of-concept study provides a simple and rapid one-step immobilization approach for the fabrication of reagentless enzymatic assays with silicon-based light-addressable electrochemistry.
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