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Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds
Nowadays, there is an ever-increasing interest in the development of systems able to guide and influence cell activities for bone regeneration. In this context, we have explored for the first time the combination of type-I collagen and superparamagnetic iron oxide nanoparticles (SPIONs) to design ma...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778221/ https://www.ncbi.nlm.nih.gov/pubmed/35055200 http://dx.doi.org/10.3390/nano12020181 |
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author | Estévez, Manuel Montalbano, Giorgia Gallo-Cordova, Alvaro Ovejero, Jesús G. Izquierdo-Barba, Isabel González, Blanca Tomasina, Clarissa Moroni, Lorenzo Vallet-Regí, María Vitale-Brovarone, Chiara Fiorilli, Sonia |
author_facet | Estévez, Manuel Montalbano, Giorgia Gallo-Cordova, Alvaro Ovejero, Jesús G. Izquierdo-Barba, Isabel González, Blanca Tomasina, Clarissa Moroni, Lorenzo Vallet-Regí, María Vitale-Brovarone, Chiara Fiorilli, Sonia |
author_sort | Estévez, Manuel |
collection | PubMed |
description | Nowadays, there is an ever-increasing interest in the development of systems able to guide and influence cell activities for bone regeneration. In this context, we have explored for the first time the combination of type-I collagen and superparamagnetic iron oxide nanoparticles (SPIONs) to design magnetic and biocompatible electrospun scaffolds. For this purpose, SPIONs with a size of 12 nm were obtained by thermal decomposition and transferred to an aqueous medium via ligand exchange with dimercaptosuccinic acid (DMSA). The SPIONs were subsequently incorporated into type-I collagen solutions to prove the processability of the resulting hybrid formulation by means of electrospinning. The optimized method led to the fabrication of nanostructured scaffolds composed of randomly oriented collagen fibers ranging between 100 and 200 nm, where SPIONs resulted distributed and embedded into the collagen fibers. The SPIONs-containing electrospun structures proved to preserve the magnetic properties of the nanoparticles alone, making these matrices excellent candidates to explore the magnetic stimuli for biomedical applications. Furthermore, the biological assessment of these collagen scaffolds confirmed high viability, adhesion, and proliferation of both pre-osteoblastic MC3T3-E1 cells and human bone marrow-derived mesenchymal stem cells (hBM-MSCs). |
format | Online Article Text |
id | pubmed-8778221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87782212022-01-22 Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds Estévez, Manuel Montalbano, Giorgia Gallo-Cordova, Alvaro Ovejero, Jesús G. Izquierdo-Barba, Isabel González, Blanca Tomasina, Clarissa Moroni, Lorenzo Vallet-Regí, María Vitale-Brovarone, Chiara Fiorilli, Sonia Nanomaterials (Basel) Article Nowadays, there is an ever-increasing interest in the development of systems able to guide and influence cell activities for bone regeneration. In this context, we have explored for the first time the combination of type-I collagen and superparamagnetic iron oxide nanoparticles (SPIONs) to design magnetic and biocompatible electrospun scaffolds. For this purpose, SPIONs with a size of 12 nm were obtained by thermal decomposition and transferred to an aqueous medium via ligand exchange with dimercaptosuccinic acid (DMSA). The SPIONs were subsequently incorporated into type-I collagen solutions to prove the processability of the resulting hybrid formulation by means of electrospinning. The optimized method led to the fabrication of nanostructured scaffolds composed of randomly oriented collagen fibers ranging between 100 and 200 nm, where SPIONs resulted distributed and embedded into the collagen fibers. The SPIONs-containing electrospun structures proved to preserve the magnetic properties of the nanoparticles alone, making these matrices excellent candidates to explore the magnetic stimuli for biomedical applications. Furthermore, the biological assessment of these collagen scaffolds confirmed high viability, adhesion, and proliferation of both pre-osteoblastic MC3T3-E1 cells and human bone marrow-derived mesenchymal stem cells (hBM-MSCs). MDPI 2022-01-06 /pmc/articles/PMC8778221/ /pubmed/35055200 http://dx.doi.org/10.3390/nano12020181 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Estévez, Manuel Montalbano, Giorgia Gallo-Cordova, Alvaro Ovejero, Jesús G. Izquierdo-Barba, Isabel González, Blanca Tomasina, Clarissa Moroni, Lorenzo Vallet-Regí, María Vitale-Brovarone, Chiara Fiorilli, Sonia Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title | Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title_full | Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title_fullStr | Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title_full_unstemmed | Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title_short | Incorporation of Superparamagnetic Iron Oxide Nanoparticles into Collagen Formulation for 3D Electrospun Scaffolds |
title_sort | incorporation of superparamagnetic iron oxide nanoparticles into collagen formulation for 3d electrospun scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8778221/ https://www.ncbi.nlm.nih.gov/pubmed/35055200 http://dx.doi.org/10.3390/nano12020181 |
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