Rational design of cuprofullerene bipyridine nanozyme with high peroxidase-like activity for colorimetric sensing of bleomycin.

Anal Bioanal Chem

State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Science, Guangxi Normal University, Guilin, 541004, People's Republic of China.

Published: November 2024

The high catalytic activity of Cu-based nanozymes mainly depends on the efficient Fenton-like reaction of Cu/ HO, but Cu cannot exist stably. Trying to find a material that can stably support Cu while promoting the electron cycle of Cu/Cu still faces serious challenges. C is expected to be an ideal candidate to solve this problem due to its unique structure and rich physicochemical properties. Here, we designed and synthesized a C-doped Cu-based nanozyme (termed as C-Cu-Bpy) by loading high catalytic active site Cu onto C and coordinating with 2,2'-bipyridine (Bpy). The single crystal diffraction analysis and a series of auxiliary characterization technologies were used to demonstrate the successful preparation of C-Cu-Bpy. Significantly, the C-Cu-Bpy exhibited superior peroxidase-like activity during the catalytic oxidation of 3,3',5,5'-tetramethylbenzidine (TMB). Then, the catalytic mechanism of C-Cu-Bpy as peroxidase was elucidated in detail, mainly benefiting from the dual function of C. On the one hand, C acted as a carrier to directly support Cu, which has the ability to efficiently decompose HO to produce reactive oxygen species. The other was that C acted as an electron buffer, contributing to promoting the Cu/Cu cycle to facilitate the reaction. Furthermore, a colorimetric sensor for the quantitative analysis of bleomycin was established based on the principle of bleomycin specific inhibition of C-Cu-Bpy peroxidase-like activity, with satisfactory results in practical samples. This study provides a new strategy for the direct synthesis of Cu-based nanozymes with high catalytic performance.

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Source
http://dx.doi.org/10.1007/s00216-024-05234-8DOI Listing

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