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Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate
Control of living cells on biocompatible materials or on modified substrates is important for the development of bio-applications, including biosensors and implant biomaterials. The topography and hydrophobicity of substrates highly affect cell adhesion, growth, and cell growth kinetics, which is of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031981/ https://www.ncbi.nlm.nih.gov/pubmed/27652886 http://dx.doi.org/10.1038/srep33835 |
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author | Jeong, Jin-Tak Choi, Mun-Ki Sim, Yumin Lim, Jung-Taek Kim, Gil-Sung Seong, Maeng-Je Hyung, Jung-Hwan Kim, Keun Soo Umar, Ahmad Lee, Sang-Kwon |
author_facet | Jeong, Jin-Tak Choi, Mun-Ki Sim, Yumin Lim, Jung-Taek Kim, Gil-Sung Seong, Maeng-Je Hyung, Jung-Hwan Kim, Keun Soo Umar, Ahmad Lee, Sang-Kwon |
author_sort | Jeong, Jin-Tak |
collection | PubMed |
description | Control of living cells on biocompatible materials or on modified substrates is important for the development of bio-applications, including biosensors and implant biomaterials. The topography and hydrophobicity of substrates highly affect cell adhesion, growth, and cell growth kinetics, which is of great importance in bio-applications. Herein, we investigate the adhesion, growth, and morphology of cultured breast cancer cells on a silicon substrate, on which graphene oxides (GO) was partially formed. By minimizing the size and amount of the GO-containing solution and the further annealing process, GO-coated Si samples were prepared which partially covered the Si substrates. The coverage of GO on Si samples decreases upon annealing. The behaviors of cells cultured on two samples have been observed, i.e. partially GO-coated Si (P-GO) and annealed partially GO-coated Si (Annealed p-GO), with a different coverage of GO. Indeed, the spreading area covered by the cells and the number of cells for a given culture period in the incubator were highly dependent on the hydrophobicity and the presence of oxygenated groups on GO and Si substrates, suggesting hydrophobicity-driven cell growth. Thus, the presented method can be used to control the cell growth via an appropriate surface modification. |
format | Online Article Text |
id | pubmed-5031981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50319812016-09-29 Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate Jeong, Jin-Tak Choi, Mun-Ki Sim, Yumin Lim, Jung-Taek Kim, Gil-Sung Seong, Maeng-Je Hyung, Jung-Hwan Kim, Keun Soo Umar, Ahmad Lee, Sang-Kwon Sci Rep Article Control of living cells on biocompatible materials or on modified substrates is important for the development of bio-applications, including biosensors and implant biomaterials. The topography and hydrophobicity of substrates highly affect cell adhesion, growth, and cell growth kinetics, which is of great importance in bio-applications. Herein, we investigate the adhesion, growth, and morphology of cultured breast cancer cells on a silicon substrate, on which graphene oxides (GO) was partially formed. By minimizing the size and amount of the GO-containing solution and the further annealing process, GO-coated Si samples were prepared which partially covered the Si substrates. The coverage of GO on Si samples decreases upon annealing. The behaviors of cells cultured on two samples have been observed, i.e. partially GO-coated Si (P-GO) and annealed partially GO-coated Si (Annealed p-GO), with a different coverage of GO. Indeed, the spreading area covered by the cells and the number of cells for a given culture period in the incubator were highly dependent on the hydrophobicity and the presence of oxygenated groups on GO and Si substrates, suggesting hydrophobicity-driven cell growth. Thus, the presented method can be used to control the cell growth via an appropriate surface modification. Nature Publishing Group 2016-09-22 /pmc/articles/PMC5031981/ /pubmed/27652886 http://dx.doi.org/10.1038/srep33835 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jeong, Jin-Tak Choi, Mun-Ki Sim, Yumin Lim, Jung-Taek Kim, Gil-Sung Seong, Maeng-Je Hyung, Jung-Hwan Kim, Keun Soo Umar, Ahmad Lee, Sang-Kwon Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title | Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title_full | Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title_fullStr | Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title_full_unstemmed | Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title_short | Effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
title_sort | effect of graphene oxide ratio on the cell adhesion and growth behavior on a graphene oxide-coated silicon substrate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031981/ https://www.ncbi.nlm.nih.gov/pubmed/27652886 http://dx.doi.org/10.1038/srep33835 |
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