Rationally Designed Cerium-Assembled Carbon Dot Phosphatase-Like Nanozyme Hydrogel in Tandem with 5,7-Dimethoxycoumarin for Sensitive, Selective, Wide-Range, Complementary Dual-Mode Biosensing of Paraoxon

The development of a sensitive, selective, and wide-range biosensor for paraoxon detection is critically demanded due to its high toxicity and environmental prevalence. While complementary multimode biosensing platforms offer enhanced performance like high sensitivity and a wide detection range by synergizing multiple detection strategies, their implementation remains challenging because of compromised reaction compatibility. To address this, an integrated complementary colorimetric/fluorescence dual-mode biosensing platform based on a rationally designed cerium-assembled carbon dot phosphatase-like nanozyme hydrogel (Ce-CD<sub>BM</sub>) in tandem with 5,7-dimethoxycoumarin (5,7-DMC) is presented for sensitive, selective, and wide-range detection of paraoxon. The Ce-CD<sub>BM</sub> nanoarchitecture, synthesized via cerium coordination with a carbon dot derived from 2-methylimidazole and 1,2,3,4-butanetetracarboxylic acid, exhibits dual functionalities: high phosphatase-like activity and amplified fluorescence quenching capability. Ce-CD<sub>BM</sub> enables specific hydrolysis of paraoxon to generate yellow 4-nitrophenol (4-NP), achieving colorimetric paraoxon detection with a limit of detection (LOD) of 1.2 μM. Simultaneously, the formation of a highly stable nonfluorescent ternary complex (5,7-DMC/4-NP/Ce-CD<sub>BM</sub>) facilitates the highly efficient static photoinduced electron transfer, significantly amplifying fluorescence quenching for ultrasensitive paraoxon detection with a LOD of 15.4 nM. This colorimetric/fluorescence dual-mode biosensing platform overcomes the intrinsic limitations of single-signal approaches by operating under identical hydrolysis conditions while expanding the dynamic range by 3 orders of magnitude. Furthermore, a smartphone-assisted portable platform was developed for on-site visual quantification of paraoxon in cauliflower and Chinese cabbage matrices, demonstrating recoveries of 99-114% with relative standard deviations below 5%. This work establishes a paradigm for designing compatible multimode biosensors through rational nanozyme engineering and synergistic signal amplification strategies.

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Publication Details

Journal
Analytical Chemistry
Published
2025-03-07
DOI
https://doi.org/10.1021/acs.analchem.4c06758
Citations
11
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
5.70

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article

Rationally Designed Cerium-Assembled Carbon Dot Phosphatase-Like Nanozyme Hydrogel in Tandem with 5,7-Dimethoxycoumarin for Sensitive, Selective, Wide-Range, Complementary Dual-Mode Biosensing of Paraoxon

Yong Wang, Yongnian Ni, Luohua Guo, Guotao Yi et al.
11 citations
Analytical Chemistry
Advanced Nanomaterials in Catalysis
5.70
article

Rationally Designed Cerium-Assembled Carbon Dot Phosphatase-Like Nanozyme Hydrogel in Tandem with 5,7-Dimethoxycoumarin for Sensitive, Selective, Wide-Range, Complementary Dual-Mode Biosensing of Paraoxon

Yong Wang, Yongnian Ni, Luohua Guo, Guotao Yi, Qianfen Zhuang, Pengjian Gong
article en
11 citations

Abstract

The development of a sensitive, selective, and wide-range biosensor for paraoxon detection is critically demanded due to its high toxicity and environmental prevalence. While complementary multimode biosensing platforms offer enhanced performance like high sensitivity and a wide detection range by synergizing multiple detection strategies, their implementation remains challenging because of compromised reaction compatibility. To address this, an integrated complementary colorimetric/fluorescence dual-mode biosensing platform based on a rationally designed cerium-assembled carbon dot phosphatase-like nanozyme hydrogel (Ce-CD<sub>BM</sub>) in tandem with 5,7-dimethoxycoumarin (5,7-DMC) is presented for sensitive, selective, and wide-range detection of paraoxon. The Ce-CD<sub>BM</sub> nanoarchitecture, synthesized via cerium coordination with a carbon dot derived from 2-methylimidazole and 1,2,3,4-butanetetracarboxylic acid, exhibits dual functionalities: high phosphatase-like activity and amplified fluorescence quenching capability. Ce-CD<sub>BM</sub> enables specific hydrolysis of paraoxon to generate yellow 4-nitrophenol (4-NP), achieving colorimetric paraoxon detection with a limit of detection (LOD) of 1.2 μM. Simultaneously, the formation of a highly stable nonfluorescent ternary complex (5,7-DMC/4-NP/Ce-CD<sub>BM</sub>) facilitates the highly efficient static photoinduced electron transfer, significantly amplifying fluorescence quenching for ultrasensitive paraoxon detection with a LOD of 15.4 nM. This colorimetric/fluorescence dual-mode biosensing platform overcomes the intrinsic limitations of single-signal approaches by operating under identical hydrolysis conditions while expanding the dynamic range by 3 orders of magnitude. Furthermore, a smartphone-assisted portable platform was developed for on-site visual quantification of paraoxon in cauliflower and Chinese cabbage matrices, demonstrating recoveries of 99-114% with relative standard deviations below 5%. This work establishes a paradigm for designing compatible multimode biosensors through rational nanozyme engineering and synergistic signal amplification strategies.

Analytical ChemistryVol. 97(10)
Jiangsu University (CN), Nanchang University (CN), CAS Key Laboratory of Urban Pollutant Conversion (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province
Openalex Percentile: Top 4%
Advanced Nanomaterials in Catalysis
5.70
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