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Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering
Conventional fabrication methods lack the ability to control both macro- and micro-structures of generated scaffolds. Three-dimensional printing is a solid free-form fabrication method that provides novel ways to create customized scaffolds with high precision and accuracy. In this study, an electri...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436361/ https://www.ncbi.nlm.nih.gov/pubmed/28553343 http://dx.doi.org/10.4103/1673-5374.205101 |
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author | Fu, Feng Qin, Zhe Xu, Chao Chen, Xu-yi Li, Rui-xin Wang, Li-na Peng, Ding-wei Sun, Hong-tao Tu, Yue Chen, Chong Zhang, Sai Zhao, Ming-liang Li, Xiao-hong |
author_facet | Fu, Feng Qin, Zhe Xu, Chao Chen, Xu-yi Li, Rui-xin Wang, Li-na Peng, Ding-wei Sun, Hong-tao Tu, Yue Chen, Chong Zhang, Sai Zhao, Ming-liang Li, Xiao-hong |
author_sort | Fu, Feng |
collection | PubMed |
description | Conventional fabrication methods lack the ability to control both macro- and micro-structures of generated scaffolds. Three-dimensional printing is a solid free-form fabrication method that provides novel ways to create customized scaffolds with high precision and accuracy. In this study, an electrically controlled cortical impactor was used to induce randomized brain tissue defects. The overall shape of scaffolds was designed using rat-specific anatomical data obtained from magnetic resonance imaging, and the internal structure was created by computer-aided design. As the result of limitations arising from insufficient resolution of the manufacturing process, we magnified the size of the cavity model prototype five-fold to successfully fabricate customized collagen-chitosan scaffolds using three-dimensional printing. Results demonstrated that scaffolds have three-dimensional porous structures, high porosity, highly specific surface areas, pore connectivity and good internal characteristics. Neural stem cells co-cultured with scaffolds showed good viability, indicating good biocompatibility and biodegradability. This technique may be a promising new strategy for regenerating complex damaged brain tissues, and helps pave the way toward personalized medicine. |
format | Online Article Text |
id | pubmed-5436361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54363612017-05-26 Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering Fu, Feng Qin, Zhe Xu, Chao Chen, Xu-yi Li, Rui-xin Wang, Li-na Peng, Ding-wei Sun, Hong-tao Tu, Yue Chen, Chong Zhang, Sai Zhao, Ming-liang Li, Xiao-hong Neural Regen Res Research Article Conventional fabrication methods lack the ability to control both macro- and micro-structures of generated scaffolds. Three-dimensional printing is a solid free-form fabrication method that provides novel ways to create customized scaffolds with high precision and accuracy. In this study, an electrically controlled cortical impactor was used to induce randomized brain tissue defects. The overall shape of scaffolds was designed using rat-specific anatomical data obtained from magnetic resonance imaging, and the internal structure was created by computer-aided design. As the result of limitations arising from insufficient resolution of the manufacturing process, we magnified the size of the cavity model prototype five-fold to successfully fabricate customized collagen-chitosan scaffolds using three-dimensional printing. Results demonstrated that scaffolds have three-dimensional porous structures, high porosity, highly specific surface areas, pore connectivity and good internal characteristics. Neural stem cells co-cultured with scaffolds showed good viability, indicating good biocompatibility and biodegradability. This technique may be a promising new strategy for regenerating complex damaged brain tissues, and helps pave the way toward personalized medicine. Medknow Publications & Media Pvt Ltd 2017-04 /pmc/articles/PMC5436361/ /pubmed/28553343 http://dx.doi.org/10.4103/1673-5374.205101 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Fu, Feng Qin, Zhe Xu, Chao Chen, Xu-yi Li, Rui-xin Wang, Li-na Peng, Ding-wei Sun, Hong-tao Tu, Yue Chen, Chong Zhang, Sai Zhao, Ming-liang Li, Xiao-hong Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title | Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title_full | Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title_fullStr | Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title_full_unstemmed | Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title_short | Magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
title_sort | magnetic resonance imaging-three-dimensional printing technology fabricates customized scaffolds for brain tissue engineering |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436361/ https://www.ncbi.nlm.nih.gov/pubmed/28553343 http://dx.doi.org/10.4103/1673-5374.205101 |
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