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Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration

Nanotechnology plays a key role in the development of innovative scaffolds for bone tissue engineering (BTE) allowing the incorporation of nanomaterials able to improve cell proliferation and differentiation. In this study, Mg-HA-Coll type I scaffolds (Mg-HA-based scaffolds) were nanofunctionalized...

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Autores principales: Calabrese, Giovanna, Petralia, Salvatore, Fabbi, Claudia, Forte, Stefano, Franco, Domenico, Guglielmino, Salvatore, Esposito, Emanuela, Cuzzocrea, Salvatore, Traina, Francesco, Conoci, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597806/
https://www.ncbi.nlm.nih.gov/pubmed/33149935
http://dx.doi.org/10.1093/rb/rbaa033
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author Calabrese, Giovanna
Petralia, Salvatore
Fabbi, Claudia
Forte, Stefano
Franco, Domenico
Guglielmino, Salvatore
Esposito, Emanuela
Cuzzocrea, Salvatore
Traina, Francesco
Conoci, Sabrina
author_facet Calabrese, Giovanna
Petralia, Salvatore
Fabbi, Claudia
Forte, Stefano
Franco, Domenico
Guglielmino, Salvatore
Esposito, Emanuela
Cuzzocrea, Salvatore
Traina, Francesco
Conoci, Sabrina
author_sort Calabrese, Giovanna
collection PubMed
description Nanotechnology plays a key role in the development of innovative scaffolds for bone tissue engineering (BTE) allowing the incorporation of nanomaterials able to improve cell proliferation and differentiation. In this study, Mg-HA-Coll type I scaffolds (Mg-HA-based scaffolds) were nanofunctionalized with gold nanorods (Au NRs), palladium nanoparticles (Pd NPs) and maghemite nanoparticles (MAG NPs). Nanofunctionalized Mg-HA-based scaffolds (NF-HA-Ss) were tested for their ability to promote both the proliferation and the differentiation of adipose-derived mesenchymal stem cells (hADSCs). Results clearly highlight that MAG nanofunctionalization substantially improves cell proliferation up to 70% compared with the control (Mg-HA-based scaffold), whereas both Au NRs and Pd NPs nanofunctionalization induce a cell growth inhibition of 94% and 89%, respectively. Similar evidences were found for the osteoinductive properties showing relevant calcium deposits (25% higher than the control) for MAG nanofunctionalization, while a decreasing of cell differentiation (20% lower than the control) for both Au NRs and Pd NPs derivatization. These results are in agreement with previous studies that found cytotoxic effects for both Pd NPs and Au NRs. The excellent improvement of both osteoconductivity and osteoinductivity of the MAG NF-HA-S could be attributed to the high intrinsic magnetic field of superparamagnetic MAG NPs. These findings may pave the way for the development of innovative nanostructured scaffolds for BTE.
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spelling pubmed-75978062020-11-03 Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration Calabrese, Giovanna Petralia, Salvatore Fabbi, Claudia Forte, Stefano Franco, Domenico Guglielmino, Salvatore Esposito, Emanuela Cuzzocrea, Salvatore Traina, Francesco Conoci, Sabrina Regen Biomater Research Articles Nanotechnology plays a key role in the development of innovative scaffolds for bone tissue engineering (BTE) allowing the incorporation of nanomaterials able to improve cell proliferation and differentiation. In this study, Mg-HA-Coll type I scaffolds (Mg-HA-based scaffolds) were nanofunctionalized with gold nanorods (Au NRs), palladium nanoparticles (Pd NPs) and maghemite nanoparticles (MAG NPs). Nanofunctionalized Mg-HA-based scaffolds (NF-HA-Ss) were tested for their ability to promote both the proliferation and the differentiation of adipose-derived mesenchymal stem cells (hADSCs). Results clearly highlight that MAG nanofunctionalization substantially improves cell proliferation up to 70% compared with the control (Mg-HA-based scaffold), whereas both Au NRs and Pd NPs nanofunctionalization induce a cell growth inhibition of 94% and 89%, respectively. Similar evidences were found for the osteoinductive properties showing relevant calcium deposits (25% higher than the control) for MAG nanofunctionalization, while a decreasing of cell differentiation (20% lower than the control) for both Au NRs and Pd NPs derivatization. These results are in agreement with previous studies that found cytotoxic effects for both Pd NPs and Au NRs. The excellent improvement of both osteoconductivity and osteoinductivity of the MAG NF-HA-S could be attributed to the high intrinsic magnetic field of superparamagnetic MAG NPs. These findings may pave the way for the development of innovative nanostructured scaffolds for BTE. Oxford University Press 2020-08-27 /pmc/articles/PMC7597806/ /pubmed/33149935 http://dx.doi.org/10.1093/rb/rbaa033 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Calabrese, Giovanna
Petralia, Salvatore
Fabbi, Claudia
Forte, Stefano
Franco, Domenico
Guglielmino, Salvatore
Esposito, Emanuela
Cuzzocrea, Salvatore
Traina, Francesco
Conoci, Sabrina
Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title_full Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title_fullStr Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title_full_unstemmed Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title_short Au, Pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
title_sort au, pd and maghemite nanofunctionalized hydroxyapatite scaffolds for bone regeneration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597806/
https://www.ncbi.nlm.nih.gov/pubmed/33149935
http://dx.doi.org/10.1093/rb/rbaa033
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