Published September 19, 2021 | Version v1
Journal article

DNA dendrimer–templated copper nanoparticles: self-assembly, aggregation-induced emission enhancement and sensing of lead ions

  • 1. Jiangnan University. State Key Lab of Food Science and Technology (China)
  • 2. Shenzhen Customs. Inspection and Quarantine Technology Centre (China)
  • 3. Jiangnan University. National Engineering Research Center for Functional Food (China)
  • 4. Jiangnan University. School of Food Science and Technology (China)
  • 5. Shanghai Jiaotong University. School of Agriculture and Biology (China)

Description

Copper nanomaterials based on DNA scaffold (DNA-Cu NMs) are becoming a novel fluorescent material, but it is still challenging to obtain highly fluorescent DNA-Cu NMs with excellent stability. In this work, we report a kind of copper nano-assemblies (Cu NASs) with aggregation-induced emission enhancement (AIEE) property using DNA dendrimers with sticky end as template. The sticky end of the DNA dendrimers induced the formation of much bigger Cu NASs with average size ranging from 131 to 264 nm, depending on the length of the DNA dendrimer sticky end from 6 bases to 27 bases. Compared with complete complementary DNA dendrimer, nearly 6-fold fluorescence enhancement was achieved using DNA dendrimer with 27 bases sticky end. Moreover, the DNA dendrimer-Cu NASs demonstrated excellent stability in serum and could be rapidly quenched by Pb2+ ions. Based on the above property, highly sensitive and selective fluorescent detection of Pb2+ ions was possible with a linear range of 2.0–100 nM and a detection limit of 0.75 nM. Due to the sensitive and rapid response to Pb2+ as well as excellent stability in complex matrix, the proposed fluorescent Cu NASs demonstrated high potential as an excellent fluorescent probe for Pb2+ in complex matrix. Graphical abstract:

Additional details

Identifiers

Publishing Information

Journal Title
Mikrochimica Acta
Journal Volume
188
Journal Issue
10
Journal Page Range
vp.
ISSN
0026-3672
CODEN
MIACAQ

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Copyright
Copyright (c) 2021 © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2021