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Polyoxometalate-based iron-organic complex nanozymes with peroxidase-like activities for colorimetric detection of hydrogen peroxide and ascorbic acid.

Authors :
Liu, Jingjing
Zhang, Yuan
Wang, Siyue
Zhao, Bo
Liu, Zhelin
Dong, Xiangting
Feng, Shouhua
Source :
Analytical & Bioanalytical Chemistry. Nov2024, Vol. 416 Issue 27, p6137-6148. 12p.
Publication Year :
2024

Abstract

As a new type of artificial enzyme, a nanozyme is an ideal substitute for natural enzymes and has been successfully applied in many fields. However, in the application of biomolecular detection, most nanozymes have the disadvantages of long reaction times or high detection limits, prompting researchers to search for new efficient nanozymes. In this work, the enzyme-like activities of three polyoxometalate-based iron-organic complexes ([Fe(bpp)2](Mo6O19), [Fe(bpp)2]2(Mo8O26)·2CH3OH, and [Fe(bpp)2]4H[Na(Mo8O26)]3), namely, FeMo6, Fe2Mo8, and Fe4Mo8Na, were analyzed. All three polyoxometalate-based iron-organic complexes were found to be capable of catalyzing hydrogen peroxide (H2O2) to oxidize 3,3′,5,5′-tetramethylbenzidine and o-phenylenediamine, resulting in visible color changes, further exhibiting peroxidase-like activity. Results showed that Fe4Mo8Na had more active sites due to its long chain structure, endowing more prominent peroxidase-like activity compared with Fe2Mo8 and FeMo6. A colorimetric sensing platform for H2O2 and ascorbic acid detection based on Fe4Mo8Na was established. The linear response range for H2O2 detection was 0.5–100 μM, and the detection limit was 0.143 μM. The linear response for ascorbic acid detection ranges from 0 to 750 μM with a detection limit of 1.07 μM. This study provides a new perspective for developing new nanozymes and expanding the sensing and detection application of nanozymes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16182642
Volume :
416
Issue :
27
Database :
Academic Search Index
Journal :
Analytical & Bioanalytical Chemistry
Publication Type :
Academic Journal
Accession number :
180498327
Full Text :
https://doi.org/10.1007/s00216-024-05440-4