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Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering

Hydrogel optimisation for biofabrication considering shape stability/mechanical properties and cell response is challenging. One approach to tackle this issue is to combine different additive manufacturing techniques, e.g., hot-melt extruded thermoplastics together with bioplotted cell loaded hydrog...

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Autores principales: Zehnder, Tobias, Freund, Tim, Demir, Merve, Detsch, Rainer, Boccaccini, Aldo R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457208/
https://www.ncbi.nlm.nih.gov/pubmed/28774008
http://dx.doi.org/10.3390/ma9110887
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author Zehnder, Tobias
Freund, Tim
Demir, Merve
Detsch, Rainer
Boccaccini, Aldo R.
author_facet Zehnder, Tobias
Freund, Tim
Demir, Merve
Detsch, Rainer
Boccaccini, Aldo R.
author_sort Zehnder, Tobias
collection PubMed
description Hydrogel optimisation for biofabrication considering shape stability/mechanical properties and cell response is challenging. One approach to tackle this issue is to combine different additive manufacturing techniques, e.g., hot-melt extruded thermoplastics together with bioplotted cell loaded hydrogels in a sequential plotting process. This method enables the fabrication of 3D constructs mechanically supported by the thermoplastic structure and biologically functionalised by the hydrogel phase. In this study, polycaprolactone (PCL) and polyethylene glycol (PEG) blend (PCL-PEG) together with alginate dialdehyde gelatine hydrogel (ADA-GEL) loaded with stromal cell line (ST2) were investigated. PCL-PEG blends were evaluated concerning plotting properties to fabricate 3D scaffolds, namely miscibility, wetting behaviour and in terms of cell response. Scaffolds were characterised considering pore size, porosity, strut width, degradation behaviour and mechanical stability. Blends showed improved hydrophilicity and cell response with PEG blending increasing the degradation and decreasing the mechanical properties of the scaffolds. Hybrid constructs with PCL-PEG blend and ADA-GEL were fabricated. Cell viability, distribution, morphology and interaction of cells with the support structure were analysed. Increased degradation of the thermoplastic support structure and proliferation of the cells not only in the hydrogel, but also on the thermoplastic phase, indicates the potential of this novel material combination for biofabricating 3D tissue engineering scaffolds.
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spelling pubmed-54572082017-07-28 Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering Zehnder, Tobias Freund, Tim Demir, Merve Detsch, Rainer Boccaccini, Aldo R. Materials (Basel) Article Hydrogel optimisation for biofabrication considering shape stability/mechanical properties and cell response is challenging. One approach to tackle this issue is to combine different additive manufacturing techniques, e.g., hot-melt extruded thermoplastics together with bioplotted cell loaded hydrogels in a sequential plotting process. This method enables the fabrication of 3D constructs mechanically supported by the thermoplastic structure and biologically functionalised by the hydrogel phase. In this study, polycaprolactone (PCL) and polyethylene glycol (PEG) blend (PCL-PEG) together with alginate dialdehyde gelatine hydrogel (ADA-GEL) loaded with stromal cell line (ST2) were investigated. PCL-PEG blends were evaluated concerning plotting properties to fabricate 3D scaffolds, namely miscibility, wetting behaviour and in terms of cell response. Scaffolds were characterised considering pore size, porosity, strut width, degradation behaviour and mechanical stability. Blends showed improved hydrophilicity and cell response with PEG blending increasing the degradation and decreasing the mechanical properties of the scaffolds. Hybrid constructs with PCL-PEG blend and ADA-GEL were fabricated. Cell viability, distribution, morphology and interaction of cells with the support structure were analysed. Increased degradation of the thermoplastic support structure and proliferation of the cells not only in the hydrogel, but also on the thermoplastic phase, indicates the potential of this novel material combination for biofabricating 3D tissue engineering scaffolds. MDPI 2016-11-01 /pmc/articles/PMC5457208/ /pubmed/28774008 http://dx.doi.org/10.3390/ma9110887 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
Zehnder, Tobias
Freund, Tim
Demir, Merve
Detsch, Rainer
Boccaccini, Aldo R.
Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title_full Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title_fullStr Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title_full_unstemmed Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title_short Fabrication of Cell-Loaded Two-Phase 3D Constructs for Tissue Engineering
title_sort fabrication of cell-loaded two-phase 3d constructs for tissue engineering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457208/
https://www.ncbi.nlm.nih.gov/pubmed/28774008
http://dx.doi.org/10.3390/ma9110887
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