Evidence map›Paper›PMID 42171811›Full record

ArticleMikrochimica acta2026

DNAzyme-responsive hydrogel platform integrating Au@Pt@4-MBN nanozyme for dual-mode Ochratoxin A detection.

Lihua Fan, Zongyuan Ou, Fan Li, Yiheng Shi, Di Wu, Yongning Wu, Guoliang Li

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In one paragraph

Article in Mikrochimica acta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Lihua FanSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China. afanlihua@163.com.
Zongyuan OuSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China.
Fan LiSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China.
Yiheng ShiSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China.
Di WuInstitute for Global Food Security, School of Biological Sciences, Queen's University Belfast, 19 Chlorine Gardens, Belfast, BT9 5DL, UK.
Yongning WuSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China.
Guoliang LiSchool of Food Science and Engineering, Shaanxi University of Science and Technology, Xi'an, Shaanxi, China. 61254368@163.com.

Funding

National Natural Science Foundation of China No.32302199National Natural Science Foundation of China No.32402263Scientific Research Program of the Shaanxi Provincial Education Department (No. 23JP009
6 · The paper itself

Abstract

Sensitive and reliable quantification of Ochratoxin A (OTA) in food is essential for ensuring food safety and protecting public health. In this study, a dual-mode colorimetric and Surface-Enhanced Raman Spectroscopy (SERS) biosensor was developed by integrating DNAzyme-responsive hydrogel and Au@Pt@4-MBN nanozyme for signal amplification. Upon introduction of OTA, a specific cascade reaction was triggered, activating the generated DNAzymes and leading to the disintegration of the hydrogel network and the subsequent release of encapsulated nanozymes. The extent of hydrogel disintegration exhibited a positive correlation with OTA concentration, enabling straightforward quantitative detection. The biosensor demonstrated excellent sensitivity, with detection limits of 0.0668 ng mL⁻¹ (colorimetric) and 0.0342 ng mL⁻¹(SERS). When applied to spiked corn samples, it achieved high recoveries of 98.70%-100.93% (colorimetric) and 95.6%-104.27% (SERS), confirming its reliability. The method also demonstrated high practical applicability for authentic non-spiked samples, with a positive detection rate of 10% that was consistent with the results of the national standard method. This robust platform offers significant potential for sensitive mycotoxin monitoring in food and environmental safety.

Indexed as

Biosensing TechniquesDNA, CatalyticHydrogelsMetal NanoparticlesOchratoxinsColorimetryFood ContaminationGoldLimit of DetectionPlatinumSpectrum Analysis, RamanZea maysDNA, CatalyticGoldHydrogelsochratoxin AOchratoxinsPlatinumColorimetric detectionDNA hydrogelDNAzymeNanozymeOTASERS

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.