Issue 5, 2022

Efficient anchoring of CuO nanoparticles on Ugi four-component-functionalized graphene quantum dots: colloidal soluble nanoplatform with great photoluminescent and antibacterial properties

Abstract

In this work, the sustainable functionalization of graphene quantum dots (GQDs) obtained from citric acid via a novel, green, facile, and straightforward approach for effectively anchoring CuO nanoparticles (CuO NPs) and accordingly improving their colloidal solubility and antibacterial activity is reported. The GQDs were first synthesized through a green hydrothermal method and participated in a Ugi four-component reaction (Ugi-4CR) in water for carboxamide functionalization. Finally, in situ anchoring of CuO NPs was applied towards the Ugi-functionalized GQDs to synthesize the GQD-Ugi@CuO core–shell nanostructure. The constructed nanomaterials were characterized using XRD, FT-IR, NMR, TEM, DLS, UV-vis, and PL techniques. Significant antibacterial activity was observed for GQD-Ugi@CuO against both E. coli (MBC: 32 μg mL−1, MIC: 16 μg mL−1) and S. aureus (MBC: 64 μg mL−1, MIC: 32 μg mL−1) bacteria. The MTT assay reveals a good cytocompatibility for GQD-Ugi@CuO towards human skin fibroblast (HFF-1) cells. The results indicate that the synthesized GQD-Ugi@CuO has the potential to be employed as a safe photoluminescent nanoplatform with great antimicrobial activity.

Graphical abstract: Efficient anchoring of CuO nanoparticles on Ugi four-component-functionalized graphene quantum dots: colloidal soluble nanoplatform with great photoluminescent and antibacterial properties

Supplementary files

Article information

Article type
Paper
Submitted
15 Oct 2021
Accepted
13 Feb 2022
First published
14 Feb 2022

React. Chem. Eng., 2022,7, 1210-1218

Efficient anchoring of CuO nanoparticles on Ugi four-component-functionalized graphene quantum dots: colloidal soluble nanoplatform with great photoluminescent and antibacterial properties

S. Javanbakht, V. Khodkari, M. T. Nazeri and A. Shaabani, React. Chem. Eng., 2022, 7, 1210 DOI: 10.1039/D1RE00455G

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