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Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide

A major issue of X-ray radiation therapy is that normal cells can be damaged, limiting the amount of X-rays that can be safely delivered to a tumor. This paper describes a new method based on graphene oxide (GO) to protect normal cells from oxidative damage by removing free radicals generated by X-r...

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Detalles Bibliográficos
Autores principales: Qiao, Yong, Zhang, Peipei, Wang, Chaoming, Ma, Liyuan, Su, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269382/
https://www.ncbi.nlm.nih.gov/pubmed/25530873
http://dx.doi.org/10.3390/nano4020522
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author Qiao, Yong
Zhang, Peipei
Wang, Chaoming
Ma, Liyuan
Su, Ming
author_facet Qiao, Yong
Zhang, Peipei
Wang, Chaoming
Ma, Liyuan
Su, Ming
author_sort Qiao, Yong
collection PubMed
description A major issue of X-ray radiation therapy is that normal cells can be damaged, limiting the amount of X-rays that can be safely delivered to a tumor. This paper describes a new method based on graphene oxide (GO) to protect normal cells from oxidative damage by removing free radicals generated by X-ray radiation using grapheme oxide (GO). A variety of techniques such as cytotoxicity, genotoxicity, oxidative assay, apoptosis, γ-H2AX expression, and micro-nucleus assay have been used to assess the protective effect of GO in cultured fibroblast cells. It is found that although GO at higher concentration (100 and 500 µg/mL) can cause cell death and DNA damage, it can effectively remove oxygen free radicals at a lower concentration of 10 µg/mL. The level of DNA damage and cell death is reduced by 48%, and 39%, respectively. Thus, low concentration GO can be used as an effective radio-protective agent in occupational and therapeutic settings.
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spelling pubmed-42693822014-12-17 Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide Qiao, Yong Zhang, Peipei Wang, Chaoming Ma, Liyuan Su, Ming Nanomaterials (Basel) Article A major issue of X-ray radiation therapy is that normal cells can be damaged, limiting the amount of X-rays that can be safely delivered to a tumor. This paper describes a new method based on graphene oxide (GO) to protect normal cells from oxidative damage by removing free radicals generated by X-ray radiation using grapheme oxide (GO). A variety of techniques such as cytotoxicity, genotoxicity, oxidative assay, apoptosis, γ-H2AX expression, and micro-nucleus assay have been used to assess the protective effect of GO in cultured fibroblast cells. It is found that although GO at higher concentration (100 and 500 µg/mL) can cause cell death and DNA damage, it can effectively remove oxygen free radicals at a lower concentration of 10 µg/mL. The level of DNA damage and cell death is reduced by 48%, and 39%, respectively. Thus, low concentration GO can be used as an effective radio-protective agent in occupational and therapeutic settings. MDPI 2014-06-24 /pmc/articles/PMC4269382/ /pubmed/25530873 http://dx.doi.org/10.3390/nano4020522 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Qiao, Yong
Zhang, Peipei
Wang, Chaoming
Ma, Liyuan
Su, Ming
Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title_full Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title_fullStr Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title_full_unstemmed Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title_short Reducing X-Ray Induced Oxidative Damages in Fibroblasts with Graphene Oxide
title_sort reducing x-ray induced oxidative damages in fibroblasts with graphene oxide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269382/
https://www.ncbi.nlm.nih.gov/pubmed/25530873
http://dx.doi.org/10.3390/nano4020522
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