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SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay

A facile sol-gel route has been applied to synthesize hybrid silica-PVA-iron oxide nanocomposite materials. A step-by-step calcination (processing temperatures up to 400 °C) was applied in order to oxidize the organics together with the iron precursor. Transmission electron microscopy, X-ray diffrac...

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Autores principales: Putz, Ana-Maria, Ianăși, Cătălin, Dudás, Zoltán, Coricovac, Dorina, Watz, Claudia (Farcas), Len, Adél, Almásy, László, Sacarescu, Liviu, Dehelean, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038086/
https://www.ncbi.nlm.nih.gov/pubmed/32033018
http://dx.doi.org/10.3390/molecules25030653
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author Putz, Ana-Maria
Ianăși, Cătălin
Dudás, Zoltán
Coricovac, Dorina
Watz, Claudia (Farcas)
Len, Adél
Almásy, László
Sacarescu, Liviu
Dehelean, Cristina
author_facet Putz, Ana-Maria
Ianăși, Cătălin
Dudás, Zoltán
Coricovac, Dorina
Watz, Claudia (Farcas)
Len, Adél
Almásy, László
Sacarescu, Liviu
Dehelean, Cristina
author_sort Putz, Ana-Maria
collection PubMed
description A facile sol-gel route has been applied to synthesize hybrid silica-PVA-iron oxide nanocomposite materials. A step-by-step calcination (processing temperatures up to 400 °C) was applied in order to oxidize the organics together with the iron precursor. Transmission electron microscopy, X-ray diffraction, small angle neutron scattering, and nitrogen porosimetry were used to determine the temperature-induced morpho-textural modifications. In vitro cytotoxicity assay was conducted by monitoring the cell viability by the means of MTT assay to qualify the materials as MRI contrast agents or as drug carriers. Two cell lines were considered: the HaCaT (human keratinocyte cell line) and the A375 tumour cell line of human melanoma. Five concentrations of 10 µg/mL, 30 µg/mL, 50 µg/mL, 100 µg/mL, and 200 µg/mL were tested, while using DMSO (dimethylsulfoxid) and PBS (phosphate saline buffer) as solvents. The HaCaT and A375 cell lines were exposed to the prepared agent suspensions for 24 h. In the case of DMSO (dimethyl sulfoxide) suspensions, the effect on human keratinocytes migration and proliferation were also evaluated. The results indicate that only the concentrations of 100 μg/mL and 200 μg/mL of the nanocomposite in DMSO induced a slight decrease in the HaCaT cell viability. The PBS based in vitro assay showed that the nanocomposite did not present toxicity on the HaCaT cells, even at high doses (200 μg/mL agent).
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spelling pubmed-70380862020-03-10 SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay Putz, Ana-Maria Ianăși, Cătălin Dudás, Zoltán Coricovac, Dorina Watz, Claudia (Farcas) Len, Adél Almásy, László Sacarescu, Liviu Dehelean, Cristina Molecules Article A facile sol-gel route has been applied to synthesize hybrid silica-PVA-iron oxide nanocomposite materials. A step-by-step calcination (processing temperatures up to 400 °C) was applied in order to oxidize the organics together with the iron precursor. Transmission electron microscopy, X-ray diffraction, small angle neutron scattering, and nitrogen porosimetry were used to determine the temperature-induced morpho-textural modifications. In vitro cytotoxicity assay was conducted by monitoring the cell viability by the means of MTT assay to qualify the materials as MRI contrast agents or as drug carriers. Two cell lines were considered: the HaCaT (human keratinocyte cell line) and the A375 tumour cell line of human melanoma. Five concentrations of 10 µg/mL, 30 µg/mL, 50 µg/mL, 100 µg/mL, and 200 µg/mL were tested, while using DMSO (dimethylsulfoxid) and PBS (phosphate saline buffer) as solvents. The HaCaT and A375 cell lines were exposed to the prepared agent suspensions for 24 h. In the case of DMSO (dimethyl sulfoxide) suspensions, the effect on human keratinocytes migration and proliferation were also evaluated. The results indicate that only the concentrations of 100 μg/mL and 200 μg/mL of the nanocomposite in DMSO induced a slight decrease in the HaCaT cell viability. The PBS based in vitro assay showed that the nanocomposite did not present toxicity on the HaCaT cells, even at high doses (200 μg/mL agent). MDPI 2020-02-04 /pmc/articles/PMC7038086/ /pubmed/32033018 http://dx.doi.org/10.3390/molecules25030653 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Putz, Ana-Maria
Ianăși, Cătălin
Dudás, Zoltán
Coricovac, Dorina
Watz, Claudia (Farcas)
Len, Adél
Almásy, László
Sacarescu, Liviu
Dehelean, Cristina
SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title_full SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title_fullStr SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title_full_unstemmed SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title_short SiO(2)-PVA-Fe(acac)(3) Hybrid Based Superparamagnetic Nanocomposites for Nanomedicine: Morpho-textural Evaluation and In Vitro Cytotoxicity Assay
title_sort sio(2)-pva-fe(acac)(3) hybrid based superparamagnetic nanocomposites for nanomedicine: morpho-textural evaluation and in vitro cytotoxicity assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038086/
https://www.ncbi.nlm.nih.gov/pubmed/32033018
http://dx.doi.org/10.3390/molecules25030653
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