Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells
Mohankandhasamy Ramasamy,1 Minakshi Das,1 Seong Soo A An,1 Dong Kee Yi2 1Division of Bionanotechnology, Gachon University, Seongnam, 2Department of Chemistry, Myongji University, Yongin, South Korea Abstract: The wide-scale applications of zinc oxide (ZnO) nanoparticles (NPs) in ­photocat...
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Dove Medical Press
2014
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oai:doaj.org-article:0c9a830d96154617958f13342b0f9db02021-12-02T00:12:17ZRole of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells1178-2013https://doaj.org/article/0c9a830d96154617958f13342b0f9db02014-08-01T00:00:00Zhttp://www.dovepress.com/role-of-surface-modification-in-zinc-oxide-nanoparticles-and-its-toxic-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013 Mohankandhasamy Ramasamy,1 Minakshi Das,1 Seong Soo A An,1 Dong Kee Yi2 1Division of Bionanotechnology, Gachon University, Seongnam, 2Department of Chemistry, Myongji University, Yongin, South Korea Abstract: The wide-scale applications of zinc oxide (ZnO) nanoparticles (NPs) in ­photocatalysts, gas sensors, and cosmetics may cause toxicity to humans and environments. Therefore, the aim of the present study was to reduce the toxicity of ZnO NPs by coating them with a silica (SiO2) layer, which could be used in human applications, such as cosmetic preparations. The sol–gel method was used to synthesize core ZnO with SiO2-shelled NPs (SiO2/ZnO NPs) with varying degrees of coating. Diverse studies were performed to analyze the toxicity of NPs against cells in a dose- and time-dependent manner. To ensure the decreased toxicity of the produced SiO2/ZnO NPs, cytotoxicity in membrane damage and/or intracellular reactive oxygen species (ROS) were assessed by employing 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, lactate dehydrogenase, 2',7'-dichlorofluorescin, and lipid peroxide estimations. The cores of ZnO NPs exhibited cytotoxicity over time, regardless of shell thickness. Nevertheless, the thicker SiO2/ZnO NPs revealed reduced enzyme leakage, decreased peroxide production, and less oxidative stress than their bare ZnO NPs or thinner SiO2/ZnO NPs. Therefore, thicker SiO2/ZnO NPs moderated the toxicity of ZnO NPs by restricting free radical formation and the release of zinc ions, and decreasing surface contact with cells. Keywords: zinc oxide, silica coating, photostability, human dermal fibroblast, membrane damage, oxidative stressRamasamy MDas MAn SSAYi DKDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2014, Iss Issue 1, Pp 3707-3718 (2014) |
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Medicine (General) R5-920 Ramasamy M Das M An SSA Yi DK Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
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Mohankandhasamy Ramasamy,1 Minakshi Das,1 Seong Soo A An,1 Dong Kee Yi2 1Division of Bionanotechnology, Gachon University, Seongnam, 2Department of Chemistry, Myongji University, Yongin, South Korea Abstract: The wide-scale applications of zinc oxide (ZnO) nanoparticles (NPs) in ­photocatalysts, gas sensors, and cosmetics may cause toxicity to humans and environments. Therefore, the aim of the present study was to reduce the toxicity of ZnO NPs by coating them with a silica (SiO2) layer, which could be used in human applications, such as cosmetic preparations. The sol–gel method was used to synthesize core ZnO with SiO2-shelled NPs (SiO2/ZnO NPs) with varying degrees of coating. Diverse studies were performed to analyze the toxicity of NPs against cells in a dose- and time-dependent manner. To ensure the decreased toxicity of the produced SiO2/ZnO NPs, cytotoxicity in membrane damage and/or intracellular reactive oxygen species (ROS) were assessed by employing 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, lactate dehydrogenase, 2',7'-dichlorofluorescin, and lipid peroxide estimations. The cores of ZnO NPs exhibited cytotoxicity over time, regardless of shell thickness. Nevertheless, the thicker SiO2/ZnO NPs revealed reduced enzyme leakage, decreased peroxide production, and less oxidative stress than their bare ZnO NPs or thinner SiO2/ZnO NPs. Therefore, thicker SiO2/ZnO NPs moderated the toxicity of ZnO NPs by restricting free radical formation and the release of zinc ions, and decreasing surface contact with cells. Keywords: zinc oxide, silica coating, photostability, human dermal fibroblast, membrane damage, oxidative stress |
format |
article |
author |
Ramasamy M Das M An SSA Yi DK |
author_facet |
Ramasamy M Das M An SSA Yi DK |
author_sort |
Ramasamy M |
title |
Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
title_short |
Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
title_full |
Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
title_fullStr |
Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
title_full_unstemmed |
Role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
title_sort |
role of surface modification in zinc oxide nanoparticles and its toxicity assessment toward human dermal fibroblast cells |
publisher |
Dove Medical Press |
publishDate |
2014 |
url |
https://doaj.org/article/0c9a830d96154617958f13342b0f9db0 |
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