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Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation

Application of ZnO nanoparticles in sunscreens exposes human skin with their adverse effects, which correlates to dissolution/translocation of free Zn(+2) ions. The possibility of decreasing solubility and therefore, reducing toxicity, by structural modifications have been discussed as a solution. T...

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Autores principales: Ghaderi-Shekhi Abadi, Parvaneh, Shirazi, Farshad H., Joshaghani, Mohammad, Moghimi, Hamid R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977415/
https://www.ncbi.nlm.nih.gov/pubmed/29854618
http://dx.doi.org/10.1016/j.toxrep.2018.03.001
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author Ghaderi-Shekhi Abadi, Parvaneh
Shirazi, Farshad H.
Joshaghani, Mohammad
Moghimi, Hamid R.
author_facet Ghaderi-Shekhi Abadi, Parvaneh
Shirazi, Farshad H.
Joshaghani, Mohammad
Moghimi, Hamid R.
author_sort Ghaderi-Shekhi Abadi, Parvaneh
collection PubMed
description Application of ZnO nanoparticles in sunscreens exposes human skin with their adverse effects, which correlates to dissolution/translocation of free Zn(+2) ions. The possibility of decreasing solubility and therefore, reducing toxicity, by structural modifications have been discussed as a solution. The present investigation has developed new metallic lattices of ZnO to reduce cytotoxicity of ZnO nanoparticles. Novel metal-promoted Zn-based nanocomposites ([Zn(O)/M], M = Mg, Al, Ca, Ti) were synthesized and their physicochemical properties and their cytotoxicity were evaluated. Solubility and release studies showed that modification of ZnO structure decreases release of Zn(+2) into culture medium. XRD and UV absorbance analyses showed that metallic-dopants percolate into crystalline lattice of ZnO. This phenomenon is basic reason for stability of Zn-based network. Cell culture studies and MTT assay on human skin cells (HFF-1) exposed to UVA radiation showed that the level of protection of [Zn(O)/M] compounds were more than of [ZnO]. Dichlorofluoroscein diacetate-ROS assay and Zn(+2) release experiments indicated that [Zn(O)/M] nanocomposites decreased the level of ROS generation and Zn(+2) release in compared to ZnO, indicating higher safety of nanocomposites. This study shows that the synthesized Zn-based nanocomposites have potential to be used as safer and more effective sunscreens than ZnO.
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spelling pubmed-59774152018-05-31 Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation Ghaderi-Shekhi Abadi, Parvaneh Shirazi, Farshad H. Joshaghani, Mohammad Moghimi, Hamid R. Toxicol Rep Article Application of ZnO nanoparticles in sunscreens exposes human skin with their adverse effects, which correlates to dissolution/translocation of free Zn(+2) ions. The possibility of decreasing solubility and therefore, reducing toxicity, by structural modifications have been discussed as a solution. The present investigation has developed new metallic lattices of ZnO to reduce cytotoxicity of ZnO nanoparticles. Novel metal-promoted Zn-based nanocomposites ([Zn(O)/M], M = Mg, Al, Ca, Ti) were synthesized and their physicochemical properties and their cytotoxicity were evaluated. Solubility and release studies showed that modification of ZnO structure decreases release of Zn(+2) into culture medium. XRD and UV absorbance analyses showed that metallic-dopants percolate into crystalline lattice of ZnO. This phenomenon is basic reason for stability of Zn-based network. Cell culture studies and MTT assay on human skin cells (HFF-1) exposed to UVA radiation showed that the level of protection of [Zn(O)/M] compounds were more than of [ZnO]. Dichlorofluoroscein diacetate-ROS assay and Zn(+2) release experiments indicated that [Zn(O)/M] nanocomposites decreased the level of ROS generation and Zn(+2) release in compared to ZnO, indicating higher safety of nanocomposites. This study shows that the synthesized Zn-based nanocomposites have potential to be used as safer and more effective sunscreens than ZnO. Elsevier 2018-03-06 /pmc/articles/PMC5977415/ /pubmed/29854618 http://dx.doi.org/10.1016/j.toxrep.2018.03.001 Text en © 2018 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ghaderi-Shekhi Abadi, Parvaneh
Shirazi, Farshad H.
Joshaghani, Mohammad
Moghimi, Hamid R.
Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title_full Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title_fullStr Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title_full_unstemmed Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title_short Influence of formulation of ZnO nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: An in vitro study on human skin cells exposed to UVA radiation
title_sort influence of formulation of zno nanoblokes containing metallic ions dopants on their cytotoxicity and protective factors: an in vitro study on human skin cells exposed to uva radiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5977415/
https://www.ncbi.nlm.nih.gov/pubmed/29854618
http://dx.doi.org/10.1016/j.toxrep.2018.03.001
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