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Facile preparation of fluorescent water-soluble non-conjugated polymer dots and fabricating an acetylcholinesterase biosensor

Acetylcholinesterase (AChE) has been demonstrated as a crucial enzyme in the development and treatment of Alzheimer's disease (AD). The present work reported the preparation of high fluorescence emission, water-soluble, non-conjugated polymer dots (NCPDs) via Schiff base reaction, and its self-...

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Detalles Bibliográficos
Autores principales: Li, Cai-Hong, Wang, Wei-Feng, Stanislas, Nsanzamahoro, Yang, Jun-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982230/
https://www.ncbi.nlm.nih.gov/pubmed/35424765
http://dx.doi.org/10.1039/d1ra07854b
Descripción
Sumario:Acetylcholinesterase (AChE) has been demonstrated as a crucial enzyme in the development and treatment of Alzheimer's disease (AD). The present work reported the preparation of high fluorescence emission, water-soluble, non-conjugated polymer dots (NCPDs) via Schiff base reaction, and its self-assembly between hyperbranched poly(ethylenimine) (PEI) and pyrogallol in aqueous solutions. A one-pot method was introduced, which made the preparation process of the NCPDs more convenient, energy-efficient, and environmentally friendly. The mechanism of the inherent fluorescence of NCPDs and its fluorescence properties were investigated. This study, for the first time, explored the application of NCPDs to a nanoquencher biosensing system, discovering the reversible quenching effect of MnO(2) nanosheets for NCPDs. Furthermore, the quenching mechanism of MnO(2) for NCPDs was demonstrated to be an inner filter effect (IFE). The NCPDs–MnO(2) biosensing system showed a broader detection range from 12.3 to 3675 U L(−1) for AChE and the limit of detection (LOD) was as low as 4.9 U L(−1). The sensing system has been applied to screen AChE inhibitors, and the result of the positive drug was highly consistent with previous studies. The established method showed a promising prospect in screening for leading compounds in new drug discoveries for AD.