Issue 52, 2020, Issue in Progress

Highly stable folic acid functionalized copper-nanocluster/silica nanoparticles for selective targeting of cancer cells

Abstract

In this paper, we present a novel strategy to construct folic acid functionalized conjugated Cu nanoclusters (CuNCs) and silica (SiO2) nanocomposites for targeted detection of cancer cells. First of all, BSA capped CuNCs were encapsulated into a SiO2 matrix. The resulting CuNCs@SiO2 nanoparticles showed bright red fluorescence with an enhanced photoluminescence quantum yield compared with free CuNCs, as well as improved stability in a complex biological environment owning to the protection of the SiO2 matrix. Upon attachment of folic acid via the poly-L-lysine conjugates (PLL-FA) on the surface of CuNCs@SiO2 driven by electrostatic interaction, the as-prepared CuNCs@SiO2/PLL-FA nanocomposites are capable of selectively recognizing folate receptor (FR) over-expressed cancer cells rather than FR-negative cells. The cell viability assay proved the low biotoxicity of CuNCs@SiO2/PLL-FA nanocomposites toward living cells and the in vitro cellular imaging assay results demonstrated their selective endocytosis of FR-positive cells (KB cells), bringing about red fluorescence labeling within the cells. Intriguingly, our strategy provides a novel route to synthesize functional CuNCs@SiO2/PLL-FA nanocomposites equipped with superior fluorescence properties, high stability against external stimuli and good biocompatibility, and have great application potential in bioimaging imaging and targeted cell detection.

Graphical abstract: Highly stable folic acid functionalized copper-nanocluster/silica nanoparticles for selective targeting of cancer cells

Supplementary files

Article information

Article type
Paper
Submitted
28 Jul 2020
Accepted
18 Aug 2020
First published
26 Aug 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 31463-31469

Highly stable folic acid functionalized copper-nanocluster/silica nanoparticles for selective targeting of cancer cells

X. Fang, Y. Huang, D. Yu, C. Shi and M. Liu, RSC Adv., 2020, 10, 31463 DOI: 10.1039/D0RA06523D

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