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Updated: Aug 14, 2026

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Published on: March 21, 2018
Fluorescent aptasensor for enrofloxacin detection based on APE1-assisted amplification and CsPbBr3@MSN nanocomposites
Huanhuan He1, Jing Feng1, Luna Guo1
1Key Laboratory of Optic-electric Sensing and Analytical Chemistry for Life Science, MOE; Shandong Key Laboratory of Biochemical Analysis; Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong; College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China. swl2016@qust.edu.cn.
None:
In this work, a fluorescent aptasensor was constructed for enrofloxacin (ENR) detection by combining the polyvalent aptamer (PA) structure, apurinic/apyrimidinic endonuclease 1 (APE1)-mediated signal amplification and mesoporous silica-encapsulated perovskite quantum dot (CsPbBr3@MSN) nanocomposites. With their multiple recognition sites, polyvalent aptamers bonded to ENR and released the trigger for the strand displacement reaction. Meanwhile, a highly sensitive FRET-based sensor was constructed using the CsPbBr3@MSN probe and gold nanoparticles (Au NPs). In the presence of the trigger and APE1, the fluorescence was recovered by separating the CsPbBr3@MSN probe and Au NPs via a cyclic strand displacement reaction. Coupled with the signal amplification strategy, this system achieved the linear detection of ENR in the range of 0.1 pg mL-1 to 50 ng mL-1 with a detection limit of 0.073 pg mL-1. This sensor offers a novel analytical strategy for detecting antibiotic residues and holds significant potential for applications in food safety monitoring and environmental analysis.
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