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Bioprinting Technologies and Bioinks for Vascular Model Establishment

Clinically, large diameter artery defects (diameter larger than 6 mm) can be substituted by unbiodegradable polymers, such as polytetrafluoroethylene. There are many problems in the construction of small diameter blood vessels (diameter between 1 and 3 mm) and microvessels (diameter less than 1 mm),...

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Autores principales: Kong, Zhiyuan, Wang, Xiaohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821327/
https://www.ncbi.nlm.nih.gov/pubmed/36614332
http://dx.doi.org/10.3390/ijms24010891
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author Kong, Zhiyuan
Wang, Xiaohong
author_facet Kong, Zhiyuan
Wang, Xiaohong
author_sort Kong, Zhiyuan
collection PubMed
description Clinically, large diameter artery defects (diameter larger than 6 mm) can be substituted by unbiodegradable polymers, such as polytetrafluoroethylene. There are many problems in the construction of small diameter blood vessels (diameter between 1 and 3 mm) and microvessels (diameter less than 1 mm), especially in the establishment of complex vascular models with multi-scale branched networks. Throughout history, the vascularization strategies have been divided into three major groups, including self-generated capillaries from implantation, pre-constructed vascular channels, and three-dimensional (3D) printed cell-laden hydrogels. The first group is based on the spontaneous angiogenesis behaviour of cells in the host tissues, which also lays the foundation of capillary angiogenesis in tissue engineering scaffolds. The second group is to vascularize the polymeric vessels (or scaffolds) with endothelial cells. It is hoped that the pre-constructed vessels can be connected with the vascular networks of host tissues with rapid blood perfusion. With the development of bioprinting technologies, various fabrication methods have been achieved to build hierarchical vascular networks with high-precision 3D control. In this review, the latest advances in 3D bioprinting of vascularized tissues/organs are discussed, including new printing techniques and researches on bioinks for promoting angiogenesis, especially coaxial printing, freeform reversible embedded in suspended hydrogel printing, and acoustic assisted printing technologies, and freeform reversible embedded in suspended hydrogel (flash) technology.
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spelling pubmed-98213272023-01-07 Bioprinting Technologies and Bioinks for Vascular Model Establishment Kong, Zhiyuan Wang, Xiaohong Int J Mol Sci Review Clinically, large diameter artery defects (diameter larger than 6 mm) can be substituted by unbiodegradable polymers, such as polytetrafluoroethylene. There are many problems in the construction of small diameter blood vessels (diameter between 1 and 3 mm) and microvessels (diameter less than 1 mm), especially in the establishment of complex vascular models with multi-scale branched networks. Throughout history, the vascularization strategies have been divided into three major groups, including self-generated capillaries from implantation, pre-constructed vascular channels, and three-dimensional (3D) printed cell-laden hydrogels. The first group is based on the spontaneous angiogenesis behaviour of cells in the host tissues, which also lays the foundation of capillary angiogenesis in tissue engineering scaffolds. The second group is to vascularize the polymeric vessels (or scaffolds) with endothelial cells. It is hoped that the pre-constructed vessels can be connected with the vascular networks of host tissues with rapid blood perfusion. With the development of bioprinting technologies, various fabrication methods have been achieved to build hierarchical vascular networks with high-precision 3D control. In this review, the latest advances in 3D bioprinting of vascularized tissues/organs are discussed, including new printing techniques and researches on bioinks for promoting angiogenesis, especially coaxial printing, freeform reversible embedded in suspended hydrogel printing, and acoustic assisted printing technologies, and freeform reversible embedded in suspended hydrogel (flash) technology. MDPI 2023-01-03 /pmc/articles/PMC9821327/ /pubmed/36614332 http://dx.doi.org/10.3390/ijms24010891 Text en © 2023 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 Review
Kong, Zhiyuan
Wang, Xiaohong
Bioprinting Technologies and Bioinks for Vascular Model Establishment
title Bioprinting Technologies and Bioinks for Vascular Model Establishment
title_full Bioprinting Technologies and Bioinks for Vascular Model Establishment
title_fullStr Bioprinting Technologies and Bioinks for Vascular Model Establishment
title_full_unstemmed Bioprinting Technologies and Bioinks for Vascular Model Establishment
title_short Bioprinting Technologies and Bioinks for Vascular Model Establishment
title_sort bioprinting technologies and bioinks for vascular model establishment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821327/
https://www.ncbi.nlm.nih.gov/pubmed/36614332
http://dx.doi.org/10.3390/ijms24010891
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