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A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration
Scaffolds with gradients of physico-chemical properties and controlled 3D architectures are crucial for engineering complex tissues. These can be produced using multi-material additive manufacturing (AM) techniques. However, they typically only achieve discrete gradients using separate printheads to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820014/ https://www.ncbi.nlm.nih.gov/pubmed/33479251 http://dx.doi.org/10.1038/s41467-020-20865-y |
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author | Sinha, Ravi Cámara-Torres, Maria Scopece, Paolo Verga Falzacappa, Emanuele Patelli, Alessandro Moroni, Lorenzo Mota, Carlos |
author_facet | Sinha, Ravi Cámara-Torres, Maria Scopece, Paolo Verga Falzacappa, Emanuele Patelli, Alessandro Moroni, Lorenzo Mota, Carlos |
author_sort | Sinha, Ravi |
collection | PubMed |
description | Scaffolds with gradients of physico-chemical properties and controlled 3D architectures are crucial for engineering complex tissues. These can be produced using multi-material additive manufacturing (AM) techniques. However, they typically only achieve discrete gradients using separate printheads to vary compositions. Achieving continuous composition gradients, to better mimic tissues, requires material dosing and mixing controls. No such AM solution exists for most biomaterials. Existing AM techniques also cannot selectively modify scaffold surfaces to locally stimulate cell adhesion. A hybrid AM solution to cover these needs is reported here. A dosing- and mixing-enabled, dual-material printhead and an atmospheric pressure plasma jet to selectively activate/coat scaffold filaments during manufacturing were combined on one platform. Continuous composition gradients in both 2D hydrogels and 3D thermoplastic scaffolds were fabricated. An improvement in mechanical properties of continuous gradients compared to discrete gradients in the 3D scaffolds, and the ability to selectively enhance cell adhesion were demonstrated. |
format | Online Article Text |
id | pubmed-7820014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78200142021-01-28 A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration Sinha, Ravi Cámara-Torres, Maria Scopece, Paolo Verga Falzacappa, Emanuele Patelli, Alessandro Moroni, Lorenzo Mota, Carlos Nat Commun Article Scaffolds with gradients of physico-chemical properties and controlled 3D architectures are crucial for engineering complex tissues. These can be produced using multi-material additive manufacturing (AM) techniques. However, they typically only achieve discrete gradients using separate printheads to vary compositions. Achieving continuous composition gradients, to better mimic tissues, requires material dosing and mixing controls. No such AM solution exists for most biomaterials. Existing AM techniques also cannot selectively modify scaffold surfaces to locally stimulate cell adhesion. A hybrid AM solution to cover these needs is reported here. A dosing- and mixing-enabled, dual-material printhead and an atmospheric pressure plasma jet to selectively activate/coat scaffold filaments during manufacturing were combined on one platform. Continuous composition gradients in both 2D hydrogels and 3D thermoplastic scaffolds were fabricated. An improvement in mechanical properties of continuous gradients compared to discrete gradients in the 3D scaffolds, and the ability to selectively enhance cell adhesion were demonstrated. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820014/ /pubmed/33479251 http://dx.doi.org/10.1038/s41467-020-20865-y Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sinha, Ravi Cámara-Torres, Maria Scopece, Paolo Verga Falzacappa, Emanuele Patelli, Alessandro Moroni, Lorenzo Mota, Carlos A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title | A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title_full | A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title_fullStr | A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title_full_unstemmed | A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title_short | A hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
title_sort | hybrid additive manufacturing platform to create bulk and surface composition gradients on scaffolds for tissue regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820014/ https://www.ncbi.nlm.nih.gov/pubmed/33479251 http://dx.doi.org/10.1038/s41467-020-20865-y |
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