EventsMOL2NET'19, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 5th ed.
Published
This submission belongs to the session 06. NANOMATJND-05: JSU-NDSU Nanotech. & Materials Science Workshop, Jackson & Fargo, USA, 2019 of the event MOL2NET'19, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 5th ed.
Published date
20 Jan, 2020
Citation
Ángel Serrano-Aroca, Belén Frígols, Beatriz Salesa, Miguel Martí, Carbon nanofibers: alternative weapons against multidrug-resistant pathogens, in Proceedings of MOL2NET'19, Conference on Molecular, Biomed., Comput. & Network Science and Engineering, 5th ed., 20 March–20 December 2019, MDPI: Basel, Switzerland, doi: 10.3390/mol2net-05-06776
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Carbon nanofibers: alternative weapons against multidrug-resistant pathogens

Belén Frígols 1
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1. Biomaterials and Bioengineering Lab, Centro de Investigación Traslacional San Alberto Magno, Universidad Católica de Valencia San Vicente Mártir, c/Guillem de Castro 94, 46001 Valencia, Spain
Abstract

Due to the current global health problem of antibiotic resistant recently announced by the World Health Organization, there is an imperious necessity of looking for new alternative antibacterial materials able to treat and impede multidrug-resistant infections which are cost-effective and non-toxic for human beings. In this regard, carbon nanofibers (CNFs) possess currently much lower cost than other carbon nanomaterials such as graphene oxide, and exhibit excellent chemical, mechanical and electric properties. Thus, here, we show the antibacterial activity of CNFs against a globally spreading multidrug-resistant pathogen, the methicillin-resistant Staphylococcus epidermidis (MRSE). This Gram-positive bacterium is becoming one of the most dangerous pathogens due to its abundance on skin. In this study, these hollow filamentous materials, in direct contact with cells showed no cytotoxicity for human keratinocyte HaCaT cells, which render them very promising for biomedical and bioengineering applications. The CNFs used in this work were characterized by Raman spectroscopy and observed by high-resolution transmission electron with energy-disperse X-ray spectroscopy.

Keywords
antibacterial activity
Staphylococcus epidermidis
multidrug-resistant bacteria
human keratinocyte HaCaT HaCaT cells
cytotoxicity
Manuscript
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