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Biodegradable composite porous poly(dl-lactide-co-glycolide) scaffold supports mesenchymal stem cell differentiation and calcium phosphate deposition.

Authors :
Casagrande S
Tiribuzi R
Cassetti E
Selmin F
Gervasi GL
Barberini L
Freddolini M
Ricci M
Schoubben A
Cerulli GG
Blasi P
Source :
Artificial cells, nanomedicine, and biotechnology [Artif Cells Nanomed Biotechnol] 2018; Vol. 46 (sup1), pp. 219-229. Date of Electronic Publication: 2017 Dec 21.
Publication Year :
2018

Abstract

In recent decades, tissue engineering strategies have been proposed for the treatment of musculoskeletal diseases and bone fractures to overcome the limitations of the traditional surgical approaches based on allografts and autografts. In this work we report the development of a composite porous poly(dl-lactide-co-glycolide) scaffold suitable for bone regeneration. Scaffolds were produced by thermal sintering of porous microparticles. Next, in order to improve cell adhesion to the scaffold and subsequent proliferation, the scaffolds were coated with the osteoconductive biopolymers chitosan and sodium alginate, in a process that exploited electrostatic interactions between the positively charged biopolymers and the negatively charged PLGA scaffold. The resulting scaffolds were characterized in terms of porosity, degradation rate, mechanical properties, biocompatibility and suitability for bone regeneration. They were found to have an overall porosity of ∼85% and a degradation half time of ∼2 weeks, considered suitable to support de novo bone matrix deposition from mesenchymal stem cells. Histology confirmed the ability of the scaffold to sustain adipose-derived mesenchymal stem cell adhesion, infiltration, proliferation and osteo-differentiation. Histological staining of calcium and microanalysis confirmed the presence of calcium phosphate in the scaffold sections.

Details

Language :
English
ISSN :
2169-141X
Volume :
46
Issue :
sup1
Database :
MEDLINE
Journal :
Artificial cells, nanomedicine, and biotechnology
Publication Type :
Academic Journal
Accession number :
29265950
Full Text :
https://doi.org/10.1080/21691401.2017.1417866