Fabrication of bioresource-derived porous carbon-supported iron as an efficient oxidase mimic for dual-channel biosensing

M Wang, X Zhou, S Wang, X Xie, Y Wang… - Analytical …, 2021 - ACS Publications
M Wang, X Zhou, S Wang, X Xie, Y Wang, X Su
Analytical Chemistry, 2021ACS Publications
Herein, we designed a new strategy for fabricating a renewable bioresource-derived N-
doped hierarchical porous carbon-supported iron (Fe/NPC)-based oxidase mimic. The
obtained results suggested that Fe/NPC possessed a large specific surface area (1144
m2/g) and pore volume (0.62 cm3/g) to afford extensive Fe-Nx active sites. Taking
advantages of the remarkable oxidase-mimicking activity, outstanding stability, and
reusability of Fe/NPC, a novel dual-channel biosensing system was strategically fabricated …
Herein, we designed a new strategy for fabricating a renewable bioresource-derived N-doped hierarchical porous carbon-supported iron (Fe/NPC)-based oxidase mimic. The obtained results suggested that Fe/NPC possessed a large specific surface area (1144 m2/g) and pore volume (0.62 cm3/g) to afford extensive Fe-Nx active sites. Taking advantages of the remarkable oxidase-mimicking activity, outstanding stability, and reusability of Fe/NPC, a novel dual-channel biosensing system was strategically fabricated for sensitively determining acetylcholinesterase (AChE) through the integration of Fe/NPC and fluorescent silver nanoclusters (AgNCs) for the first time. The limits of detection for AChE can achieve as low as 0.0032 and 0.0073 U/L by the outputting fluorometric and colorimetric dual signals, respectively. Additionally, this dual-signal system was applied to analyze human erythrocyte AChE and its inhibitor with robust analytical performance. This work provides one sustainable and effective avenue to apply a bioresource for fabricating an Fe/NPC-based oxidase mimic with high catalytic performance and also gives new impetuses for developing novel biosensors by applying Fe/NPC-based enzyme mimics as substitutes for the natural enzyme.
ACS Publications
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