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Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells

BACKGROUND: Radiosensitization using nanoparticles is proposed as a novel strategy for treatment of different cancers. Superparamagnetic iron oxide nanoparticles (SPIONs) have been reported to enhance effects of radiotherapy in several researches. OBJECTIVE: The objective of this research is to inve...

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Autores principales: S., Jafari, M., Cheki, M. B., Tavakoli, A., Zarrabi, K., Ghazikhanlu Sani, R., Afzalipour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036420/
https://www.ncbi.nlm.nih.gov/pubmed/32158708
http://dx.doi.org/10.31661/jbpe.v0i0.929
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author S., Jafari
M., Cheki
M. B., Tavakoli
A., Zarrabi
K., Ghazikhanlu Sani
R., Afzalipour
author_facet S., Jafari
M., Cheki
M. B., Tavakoli
A., Zarrabi
K., Ghazikhanlu Sani
R., Afzalipour
author_sort S., Jafari
collection PubMed
description BACKGROUND: Radiosensitization using nanoparticles is proposed as a novel strategy for treatment of different cancers. Superparamagnetic iron oxide nanoparticles (SPIONs) have been reported to enhance effects of radiotherapy in several researches. OBJECTIVE: The objective of this research is to investigate the radiosensitization properties of polyglycerol coated SPIONs (PG-SPIONs) on U87-MG cancer cells. MATERIAL AND METHODS: In this experimental study, polyglycerol coated SPIONs were synthesized by thermal decomposition method and characterized by FTIR, TEM and VSM analysis. Cellular uptake of nanoparticles by cells was examined via AAS. Cytotoxicity and radiosensitization of nanoparticles in combination with radiation were evaluated by MTT and colony assay, respectively. RESULTS: Mean size of nanoparticles was 17.9±2.85 nm. FTIR verified SPIONs coating by Polyglycerol and VSM showed that they have superparamagnetic behaviour. Viability significantly (P < 0.001) decreased at concentrations above 100µg/ml for SPIONs but not for PG-SPIONs (P > 0.05). Dose verification results by TLD for doses of 2 and 4 Gy were 2±0.19 and 4±0.12 Gy respectively. The combination index for all situations was less than 1 and the effect is antagonism. CONCLUSION: However, PG-SPIONs combination with 6 MV X-ray reduced survival of U87-MG cells compared to radiation alone but the effect is antagonism.
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spelling pubmed-70364202020-03-10 Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells S., Jafari M., Cheki M. B., Tavakoli A., Zarrabi K., Ghazikhanlu Sani R., Afzalipour J Biomed Phys Eng Original Article BACKGROUND: Radiosensitization using nanoparticles is proposed as a novel strategy for treatment of different cancers. Superparamagnetic iron oxide nanoparticles (SPIONs) have been reported to enhance effects of radiotherapy in several researches. OBJECTIVE: The objective of this research is to investigate the radiosensitization properties of polyglycerol coated SPIONs (PG-SPIONs) on U87-MG cancer cells. MATERIAL AND METHODS: In this experimental study, polyglycerol coated SPIONs were synthesized by thermal decomposition method and characterized by FTIR, TEM and VSM analysis. Cellular uptake of nanoparticles by cells was examined via AAS. Cytotoxicity and radiosensitization of nanoparticles in combination with radiation were evaluated by MTT and colony assay, respectively. RESULTS: Mean size of nanoparticles was 17.9±2.85 nm. FTIR verified SPIONs coating by Polyglycerol and VSM showed that they have superparamagnetic behaviour. Viability significantly (P < 0.001) decreased at concentrations above 100µg/ml for SPIONs but not for PG-SPIONs (P > 0.05). Dose verification results by TLD for doses of 2 and 4 Gy were 2±0.19 and 4±0.12 Gy respectively. The combination index for all situations was less than 1 and the effect is antagonism. CONCLUSION: However, PG-SPIONs combination with 6 MV X-ray reduced survival of U87-MG cells compared to radiation alone but the effect is antagonism. Shiraz University of Medical Sciences 2020-02-01 /pmc/articles/PMC7036420/ /pubmed/32158708 http://dx.doi.org/10.31661/jbpe.v0i0.929 Text en Copyright: © 2020: Journal of Biomedical Physics and Engineering https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 Unported License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
S., Jafari
M., Cheki
M. B., Tavakoli
A., Zarrabi
K., Ghazikhanlu Sani
R., Afzalipour
Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title_full Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title_fullStr Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title_full_unstemmed Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title_short Investigation of Combination Effect Between 6 MV X-Ray Radiation and Polyglycerol Coated Superparamagnetic Iron Oxide Nanoparticles on U87-MG Cancer Cells
title_sort investigation of combination effect between 6 mv x-ray radiation and polyglycerol coated superparamagnetic iron oxide nanoparticles on u87-mg cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036420/
https://www.ncbi.nlm.nih.gov/pubmed/32158708
http://dx.doi.org/10.31661/jbpe.v0i0.929
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