Evidence map›Paper›PMID 41851510›Full record

ArticleAnalytical and bioanalytical chemistry2026

High-throughput microfluidic fluorescent aptasensor platform integrating dual carbon dots and Zn-TCPP for rapid detection of zearalenone.

Yanjun Yin, Hailin Shen, Jiayi Sun, Zhiguang Suo

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Article in Analytical and bioanalytical chemistry, 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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5 · Who and what money

Authors and funding

4 authors.

Yanjun YinSchool of Chemical Engineering and Materials, Changzhou Institute of Technology, Changzhou, 213032, China.
Hailin ShenSchool of Chemical Engineering and Materials, Changzhou Institute of Technology, Changzhou, 213032, China.
Jiayi SunCollege of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety and Nutrition, Henan University of Technology, Zhengzhou, 450001, China.
Zhiguang SuoCollege of Food Science and Technology, Henan Key Laboratory of Cereal and Oil Food Safety and Nutrition, Henan University of Technology, Zhengzhou, 450001, China. zg_suo@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zearalenone (ZEN) is a mycotoxin widely present in crops, posing a serious threat to human health. Therefore, it is of great significance to establish a rapid and accurate method for zearalenone detection. In this work, a microfluidic device was produced using 3D printing technology and employed to construct a high-throughput fluorescence analysis platform. The blue fluorescent carbon quantum dots (B-CDs) and green fluorescent carbon quantum dots (G-CDs) were synthesized and incorporated into separate detection areas to achieve different signal responses. The B-CDs-cDNA/Apt1 and G-CDs-Apt2 complexes are pre-positioned in this area. The two-dimensional layered nanomaterial Zn-TCPP is used as an efficient quencher, achieving specific quenching by its adsorption on single-stranded DNA. Finally, high-throughput rapid detection was achieved by identifying RGB values via a smartphone. Under optimal conditions, the detection range of the fluorescent aptasensor is 0.5-500 ng/mL, with a limit of detection of 1.325 pg/mL. Moreover, this high-throughput fluorescent aptasensor demonstrates excellent analytical performance in the detection of real samples. This work provides a novel strategy for the rapid detection of zearalenone.

Indexed as

Aptamers, NucleotideBiosensing TechniquesCarbon Quantum DotsFluorescent DyesLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesQuantum DotsZearalenoneCarbonHigh-Throughput Screening AssaysLimit of DetectionSpectrometry, FluorescenceZincAptamers, NucleotideCarbonFluorescent DyesZearalenoneZincCarbon quantum dotsMicrofluidic deviceRapid detectionZearalenoneZinc protoporphyrin

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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.