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Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds

The ability to produce constructs with a high control over the bulk geometry and internal architecture has situated 3D printing as an attractive fabrication technique for scaffolds. Various designs and inks are actively investigated to prepare scaffolds for different tissues. In this work, we prepar...

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Autores principales: Seyedsalehi, Amir, Daneshmandi, Leila, Barajaa, Mohammed, Riordan, John, Laurencin, Cato T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747749/
https://www.ncbi.nlm.nih.gov/pubmed/33335152
http://dx.doi.org/10.1038/s41598-020-78977-w
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author Seyedsalehi, Amir
Daneshmandi, Leila
Barajaa, Mohammed
Riordan, John
Laurencin, Cato T.
author_facet Seyedsalehi, Amir
Daneshmandi, Leila
Barajaa, Mohammed
Riordan, John
Laurencin, Cato T.
author_sort Seyedsalehi, Amir
collection PubMed
description The ability to produce constructs with a high control over the bulk geometry and internal architecture has situated 3D printing as an attractive fabrication technique for scaffolds. Various designs and inks are actively investigated to prepare scaffolds for different tissues. In this work, we prepared 3D printed composite scaffolds comprising polycaprolactone (PCL) and various amounts of reduced graphene oxide (rGO) at 0.5, 1, and 3 wt.%. We employed a two-step fabrication process to ensure an even mixture and distribution of the rGO sheets within the PCL matrix. The inks were prepared by creating composite PCL-rGO films through solvent evaporation casting that were subsequently fed into the 3D printer for extrusion. The resultant scaffolds were seamlessly integrated, and 3D printed with high fidelity and consistency across all groups. This, together with the homogeneous dispersion of the rGO sheets within the polymer matrix, significantly improved the compressive strength and stiffness by 185% and 150%, respectively, at 0.5 wt.% rGO inclusion. The in vitro response of the scaffolds was assessed using human adipose-derived stem cells. All scaffolds were cytocompatible and supported cell growth and viability. These mechanically reinforced and biologically compatible 3D printed PCL-rGO scaffolds are a promising platform for regenerative engineering applications.
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spelling pubmed-77477492020-12-22 Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds Seyedsalehi, Amir Daneshmandi, Leila Barajaa, Mohammed Riordan, John Laurencin, Cato T. Sci Rep Article The ability to produce constructs with a high control over the bulk geometry and internal architecture has situated 3D printing as an attractive fabrication technique for scaffolds. Various designs and inks are actively investigated to prepare scaffolds for different tissues. In this work, we prepared 3D printed composite scaffolds comprising polycaprolactone (PCL) and various amounts of reduced graphene oxide (rGO) at 0.5, 1, and 3 wt.%. We employed a two-step fabrication process to ensure an even mixture and distribution of the rGO sheets within the PCL matrix. The inks were prepared by creating composite PCL-rGO films through solvent evaporation casting that were subsequently fed into the 3D printer for extrusion. The resultant scaffolds were seamlessly integrated, and 3D printed with high fidelity and consistency across all groups. This, together with the homogeneous dispersion of the rGO sheets within the polymer matrix, significantly improved the compressive strength and stiffness by 185% and 150%, respectively, at 0.5 wt.% rGO inclusion. The in vitro response of the scaffolds was assessed using human adipose-derived stem cells. All scaffolds were cytocompatible and supported cell growth and viability. These mechanically reinforced and biologically compatible 3D printed PCL-rGO scaffolds are a promising platform for regenerative engineering applications. Nature Publishing Group UK 2020-12-17 /pmc/articles/PMC7747749/ /pubmed/33335152 http://dx.doi.org/10.1038/s41598-020-78977-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Seyedsalehi, Amir
Daneshmandi, Leila
Barajaa, Mohammed
Riordan, John
Laurencin, Cato T.
Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title_full Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title_fullStr Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title_full_unstemmed Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title_short Fabrication and characterization of mechanically competent 3D printed polycaprolactone-reduced graphene oxide scaffolds
title_sort fabrication and characterization of mechanically competent 3d printed polycaprolactone-reduced graphene oxide scaffolds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747749/
https://www.ncbi.nlm.nih.gov/pubmed/33335152
http://dx.doi.org/10.1038/s41598-020-78977-w
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