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1.
Ann Biomed Eng ; 45(1): 58-83, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27080376

RESUMO

Over the past decades, solid freeform fabrication (SFF) has emerged as the main technology for the production of scaffolds for tissue engineering applications as a result of the architectural versatility. However, certain limitations have also arisen, primarily associated with the available, rather limited range of materials suitable for processing. To overcome these limitations, several research groups have been exploring novel methodologies through which a construct, generated via SFF, is applied as a sacrificial mould for production of the final construct. The technique combines the benefits of SFF techniques in terms of controlled, patient-specific design with a large freedom in material selection associated with conventional scaffold production techniques. Consequently, well-defined 3D scaffolds can be generated in a straightforward manner from previously difficult to print and even "unprintable" materials due to thermomechanical properties that do not match the often strict temperature and pressure requirements for direct rapid prototyping. These include several biomaterials, thermally degradable materials, ceramics and composites. Since it can be combined with conventional pore forming techniques, indirect rapid prototyping (iRP) enables the creation of a hierarchical porosity in the final scaffold with micropores inside the struts. Consequently, scaffolds and implants for applications in both soft and hard tissue regeneration have been reported. In this review, an overview of different iRP strategies and materials are presented from the first reports of the approach at the turn of the century until now.


Assuntos
Materiais Biocompatíveis/química , Materiais Biocompatíveis/uso terapêutico , Impressão Tridimensional , Desenho de Prótese/métodos , Alicerces Teciduais/química , Animais , Humanos
2.
Macromol Biosci ; 16(12): 1883-1894, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27786417

RESUMO

In the present work, a photopolymerized urethane-based poly(ethylene glycol) hydrogel is applied as a porous scaffold material using indirect solid freeform fabrication (SFF). This approach combines the benefits of SFF with a large freedom in material selection and applicable concentration ranges. A sacrificial 3D poly(ε-caprolactone) structure is generated using fused deposition modeling and used as template to produce hydrogel scaffolds. By changing the template plotting parameters, the scaffold channel sizes vary from 280 to 360 µm, and the strut diameters from 340 to 400 µm. This enables the production of scaffolds with tunable mechanical properties, characterized by an average hardness ranging from 9 to 43 N and from 1 to 6 N for dry and hydrated scaffolds, respectively. Experiments using mouse calvaria preosteoblasts indicate that a gelatin methacrylamide coating of the scaffolds results in an increased cell adhesion and proliferation with improved cell morphology.


Assuntos
Materiais Biocompatíveis/química , Hidrogel de Polietilenoglicol-Dimetacrilato/química , Fotoquímica , Poliésteres/química , Alicerces Teciduais/química , Animais , Adesão Celular , Proliferação de Células , Células Cultivadas , Reagentes de Ligações Cruzadas/química , Reagentes de Ligações Cruzadas/efeitos da radiação , Fibroblastos/citologia , Fibroblastos/metabolismo , Hidrogel de Polietilenoglicol-Dimetacrilato/efeitos da radiação , Teste de Materiais , Camundongos , Porosidade , Crânio/citologia , Crânio/metabolismo , Raios Ultravioleta
3.
J Mater Sci Mater Med ; 26(10): 247, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26411443

RESUMO

The present work describes for the first time the production of self-supporting low gelatin density (<10 w/v%) porous scaffolds using methacrylamide-modified gelatin as an extracellular matrix mimicking component. As porous scaffolds starting from low gelatin concentrations cannot be realized with the conventional additive manufacturing techniques in the abscence of additives, we applied an indirect fused deposition modelling approach. To realize this, we have printed a sacrificial polyester scaffold which supported the hydrogel material during UV crosslinking, thereby preventing hydrogel structure collapse. After complete curing, the polyester scaffold was selectively dissolved leaving behind a porous, interconnective low density gelatin scaffold. Scaffold structural analysis indicated the success of the selected indirect additive manufacturing approach. Physico-chemical testing revealed scaffold properties (mechanical, degradation, swelling) to depend on the applied gelatin concentration and methacrylamide content. Preliminary biocompatibility studies revealed the cell-interactive and biocompatible properties of the materials developed.


Assuntos
Materiais Biocompatíveis/química , Gelatina/química , Alicerces Teciduais/química , Animais , Varredura Diferencial de Calorimetria , Bovinos , Linhagem Celular , Fibroblastos/citologia , Humanos , Hidrogéis , Teste de Materiais , Porosidade , Reologia , Propriedades de Superfície , Engenharia Tecidual/métodos
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