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The metal–organic frameworks (MOFs) are expected as ideal biomimetic enzymes for colorimetric glucose detection because of their large surface areas, well defined pore structures, tunable chemical composition, and multi-functional sites. However, the intrinsically chemical instability and low mimetic enzyme activity of MOFs hinder the application of them in imitating the enzyme reactions. In this work, we demonstrated a metal-MOF synergistic catalysis strategy, by loading Pt nanoparticles (Pt NPs) on MIL-88B-NH2 (Fe-MOF) to increase peroxidase-like activity for the detection of glucose. The induced electrons transfer from Pt atom to Fe atom accelerated the redox cycling of Fe3+/Fe2+, improved the overall efficiency of the peroxidase-like reaction, and enabled the efficient and robust colorimetric glucose detection, which was proved by both experiments and density functional theory (DFT) calculation. Additionally, the sensitivity and chemical stability of this synergistic effect strategy to detect the glucose are not affected by the complex external factors, which represented a great potential in fast, easy, sensitive, and specific recognition of clinical diabetes.

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Publication history
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Acknowledgements

Publication history

Received: 17 December 2020
Revised: 03 February 2021
Accepted: 20 February 2021
Published: 27 March 2021
Issue date: December 2021

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021

Acknowledgements

Acknowledgements

This work was supported by National Natural Science Foundation of China (Nos. 21705117, 21575115, 21904095, and 22004089), Program of Tianjin Science and Technology Major Project and Engineering (No. 19ZXYXSY00090), the Program for Chang Jiang Scholars and Innovative Research Team, Ministry of Education, China (No. IRT-16R61), Special Fund Project for the Central Government to Guide Local Science and Technology Development (2020), and the Applied Fundamental Research Fund of Sichuan Province (No. 2019YJ0169), and the new scholar fund of UESTC.

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