Articolo in rivista, 2021, ENG, 10.3389/fbioe.2021.704185
Higuera G.A.; Ramos T.; Gloria A.; Ambrosio L.; Di Luca A.; Pechkov N.; de Wijn J.R.; van Blitterswijk C.A.; Moroni L.
Institute for BioMedical Technology and Technical Medicine (MIRA), Tissue Regeneration Department, University of Twente, Enschede, Netherlands; Institute of Ophthalmology, University College of London, London, United Kingdom; Institute of Polymers, Composites and Biomaterials, National Research Council of Italy, Naples, Italy; MERLN Institute for Technology-inspired Regenerative Medicine, Complex Tissue Regeneration Department, Maastricht University , Netherlands
The advantages of additive manufactured scaffolds, as custom-shaped structures with a completely interconnected and accessible pore network from the micro- to the macroscale, are nowadays well established in tissue engineering. Pore volume and architecture can be designed in a controlled fashion, resulting in a modulation of scaffold's mechanical properties and in an optimal nutrient perfusion determinant for cell survival. However, the success of an engineered tissue architecture is often linked to its surface properties as well. The aim of this study was to create a family of polymeric pastes comprised of poly(ethylene oxide therephthalate)/poly(butylene terephthalate) (PEOT/PBT) microspheres and of a second biocompatible polymeric phase acting as a binder. By combining microspheres with additive manufacturing technologies, we produced 3D scaffolds possessing a tailorable surface roughness, which resulted in improved cell adhesion and increased metabolic activity. Furthermore, these scaffolds may offer the potential to act as drug delivery systems to steer tissue regeneration.
Frontiers in Bioengineering and Biotechnology 9
microparticles, additive manufacturing, tissue engineering, polymers, mesenchymal stem cells, mechanical analysis
Ambrosio Luigi, Gloria Antonio
ID: 464575
Year: 2021
Type: Articolo in rivista
Creation: 2022-02-28 14:43:54.000
Last update: 2022-06-07 16:33:28.000
CNR authors
CNR institutes
External links
OAI-PMH: Dublin Core
OAI-PMH: Mods
OAI-PMH: RDF
DOI: 10.3389/fbioe.2021.704185
URL: http://www.scopus.com/record/display.url?eid=2-s2.0-85116040373&origin=inward
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:464575
DOI: 10.3389/fbioe.2021.704185
Scopus: 2-s2.0-85116040373