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Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications
The aim of this study was the design of a 3D scaffold composed of poly(vinyl) alcohol (PVA) for cardiac tissue engineering (CTE) applications. The PVA scaffold was fabricated using a combination of gas foaming and freeze-drying processes that did not need any cross-linking agents. We obtained a bioc...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060459/ https://www.ncbi.nlm.nih.gov/pubmed/35520194 http://dx.doi.org/10.1039/c8ra08187e |
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author | Dattola, Elisabetta Parrotta, Elvira Immacolata Scalise, Stefania Perozziello, Gerardo Limongi, Tania Candeloro, Patrizio Coluccio, Maria Laura Maletta, Carmine Bruno, Luigi De Angelis, Maria Teresa Santamaria, Gianluca Mollace, Vincenzo Lamanna, Ernesto Di Fabrizio, Enzo Cuda, Giovanni |
author_facet | Dattola, Elisabetta Parrotta, Elvira Immacolata Scalise, Stefania Perozziello, Gerardo Limongi, Tania Candeloro, Patrizio Coluccio, Maria Laura Maletta, Carmine Bruno, Luigi De Angelis, Maria Teresa Santamaria, Gianluca Mollace, Vincenzo Lamanna, Ernesto Di Fabrizio, Enzo Cuda, Giovanni |
author_sort | Dattola, Elisabetta |
collection | PubMed |
description | The aim of this study was the design of a 3D scaffold composed of poly(vinyl) alcohol (PVA) for cardiac tissue engineering (CTE) applications. The PVA scaffold was fabricated using a combination of gas foaming and freeze-drying processes that did not need any cross-linking agents. We obtained a biocompatible porous matrix with excellent mechanical properties. We measured the stress–strain curves of the PVA scaffolds and we showed that the elastic behavior is similar to that of the extracellular matrix of muscles. The SEM observations revealed that the scaffolds possess micro pores having diameters ranging from 10 μm to 370 μm that fit to the dimensions of the cells. A further purpose of this study was to test scaffolds ability to support human induced pluripotent stem cells growth and differentiation into cardiomyocytes. As the proliferation tests show, the number of live stem cells on the scaffold after 12 days was increased with respect to the initial number of cells, revealing the cytocompatibility of the substrate. In addition, the differentiated cells on the PVA scaffolds expressed anti-troponin T, a marker specific of the cardiac sarcomere. We demonstrated the ability of the cardiomyocytes to pulse within the scaffolds. In conclusion, the developed scaffold show the potential to be used as a biomaterial for CTE applications. |
format | Online Article Text |
id | pubmed-9060459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90604592022-05-04 Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications Dattola, Elisabetta Parrotta, Elvira Immacolata Scalise, Stefania Perozziello, Gerardo Limongi, Tania Candeloro, Patrizio Coluccio, Maria Laura Maletta, Carmine Bruno, Luigi De Angelis, Maria Teresa Santamaria, Gianluca Mollace, Vincenzo Lamanna, Ernesto Di Fabrizio, Enzo Cuda, Giovanni RSC Adv Chemistry The aim of this study was the design of a 3D scaffold composed of poly(vinyl) alcohol (PVA) for cardiac tissue engineering (CTE) applications. The PVA scaffold was fabricated using a combination of gas foaming and freeze-drying processes that did not need any cross-linking agents. We obtained a biocompatible porous matrix with excellent mechanical properties. We measured the stress–strain curves of the PVA scaffolds and we showed that the elastic behavior is similar to that of the extracellular matrix of muscles. The SEM observations revealed that the scaffolds possess micro pores having diameters ranging from 10 μm to 370 μm that fit to the dimensions of the cells. A further purpose of this study was to test scaffolds ability to support human induced pluripotent stem cells growth and differentiation into cardiomyocytes. As the proliferation tests show, the number of live stem cells on the scaffold after 12 days was increased with respect to the initial number of cells, revealing the cytocompatibility of the substrate. In addition, the differentiated cells on the PVA scaffolds expressed anti-troponin T, a marker specific of the cardiac sarcomere. We demonstrated the ability of the cardiomyocytes to pulse within the scaffolds. In conclusion, the developed scaffold show the potential to be used as a biomaterial for CTE applications. The Royal Society of Chemistry 2019-02-14 /pmc/articles/PMC9060459/ /pubmed/35520194 http://dx.doi.org/10.1039/c8ra08187e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Dattola, Elisabetta Parrotta, Elvira Immacolata Scalise, Stefania Perozziello, Gerardo Limongi, Tania Candeloro, Patrizio Coluccio, Maria Laura Maletta, Carmine Bruno, Luigi De Angelis, Maria Teresa Santamaria, Gianluca Mollace, Vincenzo Lamanna, Ernesto Di Fabrizio, Enzo Cuda, Giovanni Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title | Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title_full | Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title_fullStr | Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title_full_unstemmed | Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title_short | Development of 3D PVA scaffolds for cardiac tissue engineering and cell screening applications |
title_sort | development of 3d pva scaffolds for cardiac tissue engineering and cell screening applications |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060459/ https://www.ncbi.nlm.nih.gov/pubmed/35520194 http://dx.doi.org/10.1039/c8ra08187e |
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