壳聚糖
碳纳米管
葡萄糖氧化酶
电子转移
黄素腺嘌呤二核苷酸
循环伏安法
吸附
生物传感器
电化学
脱氢酶
纳米技术
安培法
材料科学
固定化酶
化学
氧化还原
核化学
无机化学
酶
有机化学
电极
光化学
生物化学
物理化学
辅因子
作者
Won‐Yong Jeon,Han‐Sem Kim,Jang Hye-Won,Yesung Lee,Ueon Sang Shin,Hyug-Han Kim,Young‐Bong Choi
标识
DOI:10.1016/j.bej.2022.108589
摘要
Direct electron transfer (DET) glucose sensors are third-generation biosensors, which allow the enzyme to directly transfer electrons by glucose oxidation without a mediator. In previous studies, many researchers have focused on the glucose oxidase (GOx)-based DET glucose sensor; however, an efficient DET glucose sensor using flavin adenine dinucleotide (FAD)-glucose dehydrogenase (GDH) has not been developed. In the present study, we bound FAD-GDH and multi-walled carbon nanotubes (MWCNT), using chitosan (CS) compounds that support hydrogen bonding, van der Waals forces, and 3D structural adsorption. The GDH/CS-MWCNT-5 composite, which had a GDH concentration of 75 wt%, was physically adsorbed on screen-printed carbon electrodes (SPCEs), and cyclic voltammetry indicated that its oxidation and reduction peaks were at − 0.422 V and − 0.543 V (vs Ag/AgCl), respectively. In addition, the electrochemical results confirmed that the prepared GDH/CS-MWCNT/SPCEs were not affected by other interfering substances or oxygen at pH of 7. The GDH/CS-MWCNT/SPCEs displayed oxidation catalytic currents, which increased according to glucose concentrations across a range of 0–5.5 mM. Finally, the short-term stability of glucose, assessed for 10 days, was maintained at 80% of the GDH enzyme activity for 6 days, and it reduced to 50% of the initial activity for the remaining 4 days. Here, we illustrate the potential utility of the FAD-GDH-based DET method in continuous glucose monitoring sensors. Diagram of the GDH/CS-MWCNT fabrication process and glucose sensing • CS-MWCNTs were conjugated with FAD-GDH by hydrogen bonding. • CS-MWCNTs were optimized with GDH for DET glucose sensing. • GDH/CS-MWCNT showed good response with glucose under interfering substances.
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