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In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles
Over the last decade, magnetic iron oxide nanoparticles (IONPs) have drawn much attention for their potential biomedical applications. However, serious in vitro and in vivo safety concerns continue to exist. In this study, the effects of uncoated, Fe(m)O(n)-SiO(2) composite flake-like, and SiO(2)-Fe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245979/ https://www.ncbi.nlm.nih.gov/pubmed/28144141 http://dx.doi.org/10.2147/IJN.S122580 |
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author | Toropova, Yana G Golovkin, Alexey S Malashicheva, Anna B Korolev, Dmitry V Gorshkov, Andrey N Gareev, Kamil G Afonin, Michael V Galagudza, Michael M |
author_facet | Toropova, Yana G Golovkin, Alexey S Malashicheva, Anna B Korolev, Dmitry V Gorshkov, Andrey N Gareev, Kamil G Afonin, Michael V Galagudza, Michael M |
author_sort | Toropova, Yana G |
collection | PubMed |
description | Over the last decade, magnetic iron oxide nanoparticles (IONPs) have drawn much attention for their potential biomedical applications. However, serious in vitro and in vivo safety concerns continue to exist. In this study, the effects of uncoated, Fe(m)O(n)-SiO(2) composite flake-like, and SiO(2)-Fe(m)O(n) core-shell IONPs on cell viability, function, and morphology were tested 48 h postincubation in human umbilical vein endothelial cell culture. Cell viability and apoptosis/necrosis rate were determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and annexin V-phycoerythrin kit, respectively. Cell morphology was evaluated using bright-field microscopy and forward and lateral light scattering profiles obtained with flow cytometry analysis. All tested IONP types were used at three different doses, that is, 0.7, 7.0, and 70.0 μg. Dose-dependent changes in cell morphology, viability, and apoptosis rate were shown. At higher doses, all types of IONPs caused formation of binucleated cells suggesting impaired cytokinesis. Fe(m)O(n)-SiO(2) composite flake-like and SiO(2)-Fe(m)O(n) core-shell IONPs were characterized by similar profile of cytotoxicity, whereas bare IONPs were shown to be less toxic. The presence of either silica core or silica nanoflakes in composite IONPs can promote cytotoxic effects. |
format | Online Article Text |
id | pubmed-5245979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52459792017-01-31 In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles Toropova, Yana G Golovkin, Alexey S Malashicheva, Anna B Korolev, Dmitry V Gorshkov, Andrey N Gareev, Kamil G Afonin, Michael V Galagudza, Michael M Int J Nanomedicine Original Research Over the last decade, magnetic iron oxide nanoparticles (IONPs) have drawn much attention for their potential biomedical applications. However, serious in vitro and in vivo safety concerns continue to exist. In this study, the effects of uncoated, Fe(m)O(n)-SiO(2) composite flake-like, and SiO(2)-Fe(m)O(n) core-shell IONPs on cell viability, function, and morphology were tested 48 h postincubation in human umbilical vein endothelial cell culture. Cell viability and apoptosis/necrosis rate were determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and annexin V-phycoerythrin kit, respectively. Cell morphology was evaluated using bright-field microscopy and forward and lateral light scattering profiles obtained with flow cytometry analysis. All tested IONP types were used at three different doses, that is, 0.7, 7.0, and 70.0 μg. Dose-dependent changes in cell morphology, viability, and apoptosis rate were shown. At higher doses, all types of IONPs caused formation of binucleated cells suggesting impaired cytokinesis. Fe(m)O(n)-SiO(2) composite flake-like and SiO(2)-Fe(m)O(n) core-shell IONPs were characterized by similar profile of cytotoxicity, whereas bare IONPs were shown to be less toxic. The presence of either silica core or silica nanoflakes in composite IONPs can promote cytotoxic effects. Dove Medical Press 2017-01-13 /pmc/articles/PMC5245979/ /pubmed/28144141 http://dx.doi.org/10.2147/IJN.S122580 Text en © 2017 Toropova et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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 Toropova, Yana G Golovkin, Alexey S Malashicheva, Anna B Korolev, Dmitry V Gorshkov, Andrey N Gareev, Kamil G Afonin, Michael V Galagudza, Michael M In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title | In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title_full | In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title_fullStr | In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title_full_unstemmed | In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title_short | In vitro toxicity of Fe(m)O(n), Fe(m)O(n)-SiO(2) composite, and SiO(2)-Fe(m)O(n) core-shell magnetic nanoparticles |
title_sort | in vitro toxicity of fe(m)o(n), fe(m)o(n)-sio(2) composite, and sio(2)-fe(m)o(n) core-shell magnetic nanoparticles |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245979/ https://www.ncbi.nlm.nih.gov/pubmed/28144141 http://dx.doi.org/10.2147/IJN.S122580 |
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