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Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method

The purpose of this study is to prepare and evaluate the effect of synthesized titanium dioxide (TiO(2)) nanoparticles for their biocompatibility on physiological body fluids and the effect of cell toxicity to produce osteointegration when used as implantable materials. For the past few decades, the...

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Autores principales: Chellappa, M, Anjaneyulu, U, Manivasagam, Geetha, Vijayalakshmi, U
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599612/
https://www.ncbi.nlm.nih.gov/pubmed/26491305
http://dx.doi.org/10.2147/IJN.S79978
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author Chellappa, M
Anjaneyulu, U
Manivasagam, Geetha
Vijayalakshmi, U
author_facet Chellappa, M
Anjaneyulu, U
Manivasagam, Geetha
Vijayalakshmi, U
author_sort Chellappa, M
collection PubMed
description The purpose of this study is to prepare and evaluate the effect of synthesized titanium dioxide (TiO(2)) nanoparticles for their biocompatibility on physiological body fluids and the effect of cell toxicity to produce osteointegration when used as implantable materials. For the past few decades, the number of researches done to understand the importance of the biocompatibility of bioceramics, metals, and polymers and their effect on clinical settings of biomedical devices has increased. Hence, the total concept of biocompatibility encourages researchers to actively engage in the investigation of the most compatible materials in living systems by analyzing them using suitable physical, chemical, and biological (bioassay) methods. The ceramic material nano TiO(2) was prepared by sol-gel method and analyzed for its functional group and phase formation by Fourier transform infrared spectroscopy and powder X-ray diffraction. Furthermore, the particle size, shape, surface topography, and morphological behavior were analyzed by dynamic light scattering, zeta potential, scanning electron microscopy–energy dispersive X-ray analysis, and transmission electron microscopy analysis. In addition to this, the cytotoxicity and cytocompatibility were determined on MG63 cell lines with varying doses of concentrations such as 1 µg/mL, 10 µg/mL, 25 µg/mL, 50 µg/mL, and 100 µg/mL with different time periods such as 24 hours and 48 hours. The results have not shown any toxicity, whereas, it improved the cell viability/proliferation at various concentrations. Hence, these findings indicate that the nano TiO(2) material acts as a good implantable material when used in the biomedical field as a prime surface-modifying agent.
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spelling pubmed-45996122015-10-21 Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method Chellappa, M Anjaneyulu, U Manivasagam, Geetha Vijayalakshmi, U Int J Nanomedicine Original Research The purpose of this study is to prepare and evaluate the effect of synthesized titanium dioxide (TiO(2)) nanoparticles for their biocompatibility on physiological body fluids and the effect of cell toxicity to produce osteointegration when used as implantable materials. For the past few decades, the number of researches done to understand the importance of the biocompatibility of bioceramics, metals, and polymers and their effect on clinical settings of biomedical devices has increased. Hence, the total concept of biocompatibility encourages researchers to actively engage in the investigation of the most compatible materials in living systems by analyzing them using suitable physical, chemical, and biological (bioassay) methods. The ceramic material nano TiO(2) was prepared by sol-gel method and analyzed for its functional group and phase formation by Fourier transform infrared spectroscopy and powder X-ray diffraction. Furthermore, the particle size, shape, surface topography, and morphological behavior were analyzed by dynamic light scattering, zeta potential, scanning electron microscopy–energy dispersive X-ray analysis, and transmission electron microscopy analysis. In addition to this, the cytotoxicity and cytocompatibility were determined on MG63 cell lines with varying doses of concentrations such as 1 µg/mL, 10 µg/mL, 25 µg/mL, 50 µg/mL, and 100 µg/mL with different time periods such as 24 hours and 48 hours. The results have not shown any toxicity, whereas, it improved the cell viability/proliferation at various concentrations. Hence, these findings indicate that the nano TiO(2) material acts as a good implantable material when used in the biomedical field as a prime surface-modifying agent. Dove Medical Press 2015-10-01 /pmc/articles/PMC4599612/ /pubmed/26491305 http://dx.doi.org/10.2147/IJN.S79978 Text en © 2015 Chellappa et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Chellappa, M
Anjaneyulu, U
Manivasagam, Geetha
Vijayalakshmi, U
Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title_full Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title_fullStr Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title_full_unstemmed Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title_short Preparation and evaluation of the cytotoxic nature of TiO(2) nanoparticles by direct contact method
title_sort preparation and evaluation of the cytotoxic nature of tio(2) nanoparticles by direct contact method
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599612/
https://www.ncbi.nlm.nih.gov/pubmed/26491305
http://dx.doi.org/10.2147/IJN.S79978
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