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Biocompatibility of Graphene Oxide

Herein, we report the effects of graphene oxides on human fibroblast cells and mice with the aim of investigating graphene oxides' biocompatibility. The graphene oxides were prepared by the modified Hummers method and characterized by high-resolution transmission electron microscope and atomic...

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Autores principales: Wang, Kan, Ruan, Jing, Song, Hua, Zhang, Jiali, Wo, Yan, Guo, Shouwu, Cui, Daxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212228/
https://www.ncbi.nlm.nih.gov/pubmed/27502632
http://dx.doi.org/10.1007/s11671-010-9751-6
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author Wang, Kan
Ruan, Jing
Song, Hua
Zhang, Jiali
Wo, Yan
Guo, Shouwu
Cui, Daxiang
author_facet Wang, Kan
Ruan, Jing
Song, Hua
Zhang, Jiali
Wo, Yan
Guo, Shouwu
Cui, Daxiang
author_sort Wang, Kan
collection PubMed
description Herein, we report the effects of graphene oxides on human fibroblast cells and mice with the aim of investigating graphene oxides' biocompatibility. The graphene oxides were prepared by the modified Hummers method and characterized by high-resolution transmission electron microscope and atomic force microscopy. The human fibroblast cells were cultured with different doses of graphene oxides for day 1 to day 5. Thirty mice divided into three test groups (low, middle, high dose) and one control group were injected with 0.1, 0.25, and 0.4 mg graphene oxides, respectively, and were raised for 1 day, 7 days, and 30 days, respectively. Results showed that the water-soluble graphene oxides were successfully prepared; graphene oxides with dose less than 20 μg/mL did not exhibit toxicity to human fibroblast cells, and the dose of more than 50 μg/mL exhibits obvious cytotoxicity such as decreasing cell adhesion, inducing cell apoptosis, entering into lysosomes, mitochondrion, endoplasm, and cell nucleus. Graphene oxides under low dose (0.1 mg) and middle dose (0.25 mg) did not exhibit obvious toxicity to mice and under high dose (0.4 mg) exhibited chronic toxicity, such as 4/9 mice death and lung granuloma formation, mainly located in lung, liver, spleen, and kidney, almost could not be cleaned by kidney. In conclusion, graphene oxides exhibit dose-dependent toxicity to cells and animals, such as inducing cell apoptosis and lung granuloma formation, and cannot be cleaned by kidney. When graphene oxides are explored for in vivo applications in animal or human body, its biocompatibility must be considered.
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spelling pubmed-32122282011-11-09 Biocompatibility of Graphene Oxide Wang, Kan Ruan, Jing Song, Hua Zhang, Jiali Wo, Yan Guo, Shouwu Cui, Daxiang Nanoscale Res Lett Nano Express Herein, we report the effects of graphene oxides on human fibroblast cells and mice with the aim of investigating graphene oxides' biocompatibility. The graphene oxides were prepared by the modified Hummers method and characterized by high-resolution transmission electron microscope and atomic force microscopy. The human fibroblast cells were cultured with different doses of graphene oxides for day 1 to day 5. Thirty mice divided into three test groups (low, middle, high dose) and one control group were injected with 0.1, 0.25, and 0.4 mg graphene oxides, respectively, and were raised for 1 day, 7 days, and 30 days, respectively. Results showed that the water-soluble graphene oxides were successfully prepared; graphene oxides with dose less than 20 μg/mL did not exhibit toxicity to human fibroblast cells, and the dose of more than 50 μg/mL exhibits obvious cytotoxicity such as decreasing cell adhesion, inducing cell apoptosis, entering into lysosomes, mitochondrion, endoplasm, and cell nucleus. Graphene oxides under low dose (0.1 mg) and middle dose (0.25 mg) did not exhibit obvious toxicity to mice and under high dose (0.4 mg) exhibited chronic toxicity, such as 4/9 mice death and lung granuloma formation, mainly located in lung, liver, spleen, and kidney, almost could not be cleaned by kidney. In conclusion, graphene oxides exhibit dose-dependent toxicity to cells and animals, such as inducing cell apoptosis and lung granuloma formation, and cannot be cleaned by kidney. When graphene oxides are explored for in vivo applications in animal or human body, its biocompatibility must be considered. Springer 2010-08-21 /pmc/articles/PMC3212228/ /pubmed/27502632 http://dx.doi.org/10.1007/s11671-010-9751-6 Text en Copyright ©2010 Wang et al. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nano Express
Wang, Kan
Ruan, Jing
Song, Hua
Zhang, Jiali
Wo, Yan
Guo, Shouwu
Cui, Daxiang
Biocompatibility of Graphene Oxide
title Biocompatibility of Graphene Oxide
title_full Biocompatibility of Graphene Oxide
title_fullStr Biocompatibility of Graphene Oxide
title_full_unstemmed Biocompatibility of Graphene Oxide
title_short Biocompatibility of Graphene Oxide
title_sort biocompatibility of graphene oxide
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212228/
https://www.ncbi.nlm.nih.gov/pubmed/27502632
http://dx.doi.org/10.1007/s11671-010-9751-6
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