3D-printed alginate-peptide scaffolds for bone tissue engineering

A main challenge of Tissue engineering is to create sustainable scaffolds that provide optimal biological properties to mimic the extracellular matrix(ECM). The aim of this project is to develop RGD modified alginate bioinks for creating 3D-printed scaffolds for bone tissue engineering. To achieve t...

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Detalles Bibliográficos
Autor: Rosolek, Theo
Tipo de recurso: tesis de maestría
Fecha de publicación:2020
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/182354
Acceso en línea:https://hdl.handle.net/2117/182354
Access Level:acceso abierto
Palabra clave:Tissue engineering
Three-dimensional printing
Biomedical materials
Enginyeria de teixits
Impressió 3D
Teixits -- Bastides
Materials biomèdics
Àrees temàtiques de la UPC::Enginyeria biomèdica::Enginyeria de teixits
Àrees temàtiques de la UPC::Enginyeria dels materials
Descripción
Sumario:A main challenge of Tissue engineering is to create sustainable scaffolds that provide optimal biological properties to mimic the extracellular matrix(ECM). The aim of this project is to develop RGD modified alginate bioinks for creating 3D-printed scaffolds for bone tissue engineering. To achieve this purpose, a functionalisation protocol has been performed and improved and 2D biofilms have been elaborated. Then, physicochemical characterisation methods such as XPS and fluorescence confocal microscopy were carried out on films together with in vitro cell-based assays. After that, 3D filaments were created and biological characterisations once again carriedout. The amount of peptide being little, its presence with physical and chemical characterisation was hard to prove. However, successful biological results on biofilms spotlighted the presence of peptide and its homogeneous repartition in the hydrogel. It has also been detected that RGD functionalised films showed a great cell adhesion and spreading comparing to non-functionalised ones.Therefore, a better bioactivity was found after addition of RGD peptide sequences. However, filaments results being unreliable, further characterisation technics such as radiolabelling, radioactivity or biological assays with human cells have to be carried out to corroborate the results of this project.