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Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization

Blood vessel reconstruction is still an elusive goal for the development of in vitro models as well as artificial vascular grafts. In this study, we used a novel photo-curable cytocompatible polyacrylate material (PA) for freeform generation of synthetic vessels. We applied stereolithography for the...

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Autores principales: Huber, Birgit, Engelhardt, Sascha, Meyer, Wolfdietrich, Krüger, Hartmut, Wenz, Annika, Schönhaar, Veronika, Tovar, Günter E. M., Kluger, Petra J., Borchers, Kirsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932468/
https://www.ncbi.nlm.nih.gov/pubmed/27104576
http://dx.doi.org/10.3390/jfb7020011
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author Huber, Birgit
Engelhardt, Sascha
Meyer, Wolfdietrich
Krüger, Hartmut
Wenz, Annika
Schönhaar, Veronika
Tovar, Günter E. M.
Kluger, Petra J.
Borchers, Kirsten
author_facet Huber, Birgit
Engelhardt, Sascha
Meyer, Wolfdietrich
Krüger, Hartmut
Wenz, Annika
Schönhaar, Veronika
Tovar, Günter E. M.
Kluger, Petra J.
Borchers, Kirsten
author_sort Huber, Birgit
collection PubMed
description Blood vessel reconstruction is still an elusive goal for the development of in vitro models as well as artificial vascular grafts. In this study, we used a novel photo-curable cytocompatible polyacrylate material (PA) for freeform generation of synthetic vessels. We applied stereolithography for the fabrication of arbitrary 3D tubular structures with total dimensions in the centimeter range, 300 µm wall thickness, inner diameters of 1 to 2 mm and defined pores with a constant diameter of approximately 100 µm or 200 µm. We established a rinsing protocol to remove remaining cytotoxic substances from the photo-cured PA and applied thio-modified heparin and RGDC-peptides to functionalize the PA surface for enhanced endothelial cell adhesion. A rotating seeding procedure was introduced to ensure homogenous endothelial monolayer formation at the inner luminal tube wall. We showed that endothelial cells stayed viable and adherent and aligned along the medium flow under fluid-flow conditions comparable to native capillaries. The combined technology approach comprising of freeform additive manufacturing (AM), biomimetic design, cytocompatible materials which are applicable to AM, and biofunctionalization of AM constructs has been introduced as BioRap(®) technology by the authors.
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spelling pubmed-49324682016-07-13 Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization Huber, Birgit Engelhardt, Sascha Meyer, Wolfdietrich Krüger, Hartmut Wenz, Annika Schönhaar, Veronika Tovar, Günter E. M. Kluger, Petra J. Borchers, Kirsten J Funct Biomater Article Blood vessel reconstruction is still an elusive goal for the development of in vitro models as well as artificial vascular grafts. In this study, we used a novel photo-curable cytocompatible polyacrylate material (PA) for freeform generation of synthetic vessels. We applied stereolithography for the fabrication of arbitrary 3D tubular structures with total dimensions in the centimeter range, 300 µm wall thickness, inner diameters of 1 to 2 mm and defined pores with a constant diameter of approximately 100 µm or 200 µm. We established a rinsing protocol to remove remaining cytotoxic substances from the photo-cured PA and applied thio-modified heparin and RGDC-peptides to functionalize the PA surface for enhanced endothelial cell adhesion. A rotating seeding procedure was introduced to ensure homogenous endothelial monolayer formation at the inner luminal tube wall. We showed that endothelial cells stayed viable and adherent and aligned along the medium flow under fluid-flow conditions comparable to native capillaries. The combined technology approach comprising of freeform additive manufacturing (AM), biomimetic design, cytocompatible materials which are applicable to AM, and biofunctionalization of AM constructs has been introduced as BioRap(®) technology by the authors. MDPI 2016-04-20 /pmc/articles/PMC4932468/ /pubmed/27104576 http://dx.doi.org/10.3390/jfb7020011 Text en © 2016 by the authors; 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huber, Birgit
Engelhardt, Sascha
Meyer, Wolfdietrich
Krüger, Hartmut
Wenz, Annika
Schönhaar, Veronika
Tovar, Günter E. M.
Kluger, Petra J.
Borchers, Kirsten
Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title_full Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title_fullStr Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title_full_unstemmed Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title_short Blood-Vessel Mimicking Structures by Stereolithographic Fabrication of Small Porous Tubes Using Cytocompatible Polyacrylate Elastomers, Biofunctionalization and Endothelialization
title_sort blood-vessel mimicking structures by stereolithographic fabrication of small porous tubes using cytocompatible polyacrylate elastomers, biofunctionalization and endothelialization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932468/
https://www.ncbi.nlm.nih.gov/pubmed/27104576
http://dx.doi.org/10.3390/jfb7020011
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