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Regulating relative nitrogen locations of bipyridine covalent organic frameworks with enhanced peroxidase-like activity for biosensing.

Created on 07 Sep 2026

Authors

Xueting Cao, Yan Zhang, Yuehua Guo, Lin Cui, Xianjuan Shen

Published in

Analytica chimica acta. Volume 1421. Pages 346035. Nov 01, 2026. Epub Jul 27, 2026.

Abstract

Since metal-based enzyme mimics can raise biosafety concerns due to potential toxicity accumulation, it is necessary to develop metal-free alternatives that exhibit high catalytic efficiency and enhanced selectivity. Herein, we report the development of bipyridine-bridged covalent organic frameworks (COFs) exhibiting peroxidase-like (POD-like) activity as intelligent artificial enzymes for biomarker detection. Their catalytic function is enabled by a facile strategy that modulates charge transfer within the framework through precise regulation of the nitrogen site in the bipyridine units. The nitrogen-modulated of charge transfer directionality intensified with increasing D-A contrast in Bpy-COF than PyIm-COF, resulting in a more efficient POD-like biocatalytic activity. The Bpy-COF exhibit favorable Michaelis-Menten kinetics than PyIm-COF. Moreover, the Bpy-COF show tunable biocatalytic detection capabilities, which outperform the recently reported state-of-the-art POD-mimics regarding biosensing efficiency. Remarkably, the Bpy-COF exhibits efficient measurement of α-glucosidase (α-Glu) with the extremely low limit of detection (LOD), facilitating its application in biomarker analysis. This work not only introduces a unique metal-free biocatalyst for highly sensitive and low-cost colorimetric assays but also provides valuable insights for developing advanced enzyme-mimicking COF materials through nitrogen-modulation strategies.

PMID:
42702453
Bibliographic data and abstract were imported from PubMed on 07 Sep 2026.

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