4.6 Article

Novel Structures of Functionalized Graphene Oxide with Hydrazide: Characterization and Bioevaluation of Antimicrobial and Cytocompatibility Features

Journal

COATINGS
Volume 12, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/coatings12010045

Keywords

hydrazide; graphene oxide; functionalization; antimicrobial activity; cytotoxicity activity

Funding

  1. Competitiveness Operational Programme (COP) A1.1.4. ID: P_37_798 MyeloAL-EDiaProT, MyeloAL Project [SMIS 106774, 149/26]
  2. project CNFIS-FDI-2021-0075-ProResearch: Quality, Performance, Excellenceconcepts for a stimulating and competitive environment in research (2021)

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Graphite was oxidized and activated for covalently linking hydrazides with graphene oxide. The obtained materials were characterized by various techniques, confirming the presence of specific functional groups. Raman spectroscopy was used to evaluate the disorder degree and crystallite size. The graphene oxide-hydrazide derivatives showed inferior antimicrobial activity, indicating the need for further optimization.
Graphite was oxidized to graphene oxide and activated by thionyl chloride, for further covalently linking three hydrazides with potential biological activity. The obtained materials were characterized by scanning electron microscopy with energy dispersive spectroscopy, Fourier-transform infrared and Raman spectroscopies. The presence of various functional groups specific to graphene oxide (GO) functionalized with different hydrazides was confirmed by spectral data. The ratio between D- and G-bands, observed in Raman spectra, allowed for an evaluation of the disorder degree and the mean crystallite size of the samples. The micrographs highlighted that the samples lead to the occurrence of disorders, probably caused by the sp(3) carbons, the formation of oxygen-containing functional groups in the basal planes, and by various structural defects. The new graphene oxide-hydrazide derivatives were tested for their antimicrobial and cytotoxicity activity. Their antimicrobial activity against planktonic and biofilm-embedded cells was inferior to that of free hydrazides, except for GO-3 against planktonic Escherichia coli and GO-2 against Pseudomonas aeruginosa biofilm, demonstrating that further optimization is needed to be able to exploit the huge potential of GO for developing potent antimicrobials.

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