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Progress in scaffold‐free bioprinting for cardiovascular medicine

Biofabrication of tissue analogues is aspiring to become a disruptive technology capable to solve standing biomedical problems, from generation of improved tissue models for drug testing to alleviation of the shortage of organs for transplantation. Arguably, the most powerful tool of this revolution...

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Detalles Bibliográficos
Autor principal: Moldovan, Nicanor I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980192/
https://www.ncbi.nlm.nih.gov/pubmed/29536627
http://dx.doi.org/10.1111/jcmm.13598
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author Moldovan, Nicanor I.
author_facet Moldovan, Nicanor I.
author_sort Moldovan, Nicanor I.
collection PubMed
description Biofabrication of tissue analogues is aspiring to become a disruptive technology capable to solve standing biomedical problems, from generation of improved tissue models for drug testing to alleviation of the shortage of organs for transplantation. Arguably, the most powerful tool of this revolution is bioprinting, understood as the assembling of cells with biomaterials in three‐dimensional structures. It is less appreciated, however, that bioprinting is not a uniform methodology, but comprises a variety of approaches. These can be broadly classified in two categories, based on the use or not of supporting biomaterials (known as “scaffolds,” usually printable hydrogels also called “bioinks”). Importantly, several limitations of scaffold‐dependent bioprinting can be avoided by the “scaffold‐free” methods. In this overview, we comparatively present these approaches and highlight the rapidly evolving scaffold‐free bioprinting, as applied to cardiovascular tissue engineering.
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spelling pubmed-59801922018-06-07 Progress in scaffold‐free bioprinting for cardiovascular medicine Moldovan, Nicanor I. J Cell Mol Med Review Biofabrication of tissue analogues is aspiring to become a disruptive technology capable to solve standing biomedical problems, from generation of improved tissue models for drug testing to alleviation of the shortage of organs for transplantation. Arguably, the most powerful tool of this revolution is bioprinting, understood as the assembling of cells with biomaterials in three‐dimensional structures. It is less appreciated, however, that bioprinting is not a uniform methodology, but comprises a variety of approaches. These can be broadly classified in two categories, based on the use or not of supporting biomaterials (known as “scaffolds,” usually printable hydrogels also called “bioinks”). Importantly, several limitations of scaffold‐dependent bioprinting can be avoided by the “scaffold‐free” methods. In this overview, we comparatively present these approaches and highlight the rapidly evolving scaffold‐free bioprinting, as applied to cardiovascular tissue engineering. John Wiley and Sons Inc. 2018-03-13 2018-06 /pmc/articles/PMC5980192/ /pubmed/29536627 http://dx.doi.org/10.1111/jcmm.13598 Text en © 2018 The Author. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Moldovan, Nicanor I.
Progress in scaffold‐free bioprinting for cardiovascular medicine
title Progress in scaffold‐free bioprinting for cardiovascular medicine
title_full Progress in scaffold‐free bioprinting for cardiovascular medicine
title_fullStr Progress in scaffold‐free bioprinting for cardiovascular medicine
title_full_unstemmed Progress in scaffold‐free bioprinting for cardiovascular medicine
title_short Progress in scaffold‐free bioprinting for cardiovascular medicine
title_sort progress in scaffold‐free bioprinting for cardiovascular medicine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980192/
https://www.ncbi.nlm.nih.gov/pubmed/29536627
http://dx.doi.org/10.1111/jcmm.13598
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