Issue 62, 2017, Issue in Progress

Biofunctionalized zinc peroxide (ZnO2) nanoparticles as active oxygen sources and antibacterial agents

Abstract

Oxygen is one of the most important substances for physiological reactions and metabolisms in biological systems. Through the tailored design of oxygen-releasing materials it might be possible to control different biological processes. In this work we synthesized for the first time zinc peroxide nanoparticles with controlled sizes and biofunctionalized surfaces using a one-step reaction procedure. The zinc peroxide nanoparticles were obtained with tunable sizes (between 4.0 ± 1.2 nm and 9.4 ± 5.2 nm) and were decorated with glucose 1-phosphate (Glc-1P). The specific interaction of the phosphate function of Glc-1P with the nanoparticle surface was monitored by solid state 31P-NMR and zeta-potential measurements. Furthermore, using fluorescence measurements we demonstrated that anchored glucose molecules on the nanoparticle surface are accessible for specific interactions with lectins. It could be shown that these interactions strongly depend on the amount of Glc-1P attached to the nanoparticle surface. Additionally it was demonstrated that the oxygen release from biofunctionalized zinc peroxide nanoparticles could be tuned according to the chemical composition of the nanoparticles and the pH of the aqueous solution. The antibacterial efficiency of the synthesized nanoparticles against Enterococcus faecalis, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis and Prevotella intermedia was evaluated by determination of minimal bactericidal concentration (MIC).

Graphical abstract: Biofunctionalized zinc peroxide (ZnO2) nanoparticles as active oxygen sources and antibacterial agents

Supplementary files

Article information

Article type
Paper
Submitted
06 Jun 2017
Accepted
02 Aug 2017
First published
09 Aug 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 38998-39010

Biofunctionalized zinc peroxide (ZnO2) nanoparticles as active oxygen sources and antibacterial agents

C. Bergs, L. Brück, R. R. Rosencrantz, G. Conrads, L. Elling and A. Pich, RSC Adv., 2017, 7, 38998 DOI: 10.1039/C7RA06332F

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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