Designing bioactive materials for repairing or regenerating bone defects is an active area of research and discovery. Despite advances made in sol-gel-derived hybrid biomaterials design, three challenges remain: (i) the choice of biodegradable polymers that can form a homogeneous solution in the presence of water is very limited, (ii) low-temperature (below 50 °C) incorporation of calcium into the inorganic matrix while having molecular-level mixing has proven to be a difficult task, and (iii) incorporation of drug-loaded mesoporous nanoparticles into polymer-bioactive glass hybrid scaffolds has not been achieved. In this study, we developed bioactive biomaterials for bone repair/regeneration from an α-amino acid-derived biodegradable poly(ester amide) (PEA) and a tertiary bioglass (SiO-CaO-PO), where calcium was incorporated into the glass network at ambient temperature. Furthermore, drug-loaded functional mesoporous silica nanoparticles prepared by surfactant templating were successfully incorporated into PEA-bioglass porous scaffolds. The resulting homogenous single-phase materials showed deposition of hydroxyapatite on their surfaces, supported mesenchymal stem cell attachment and proliferation, and showed a sustained and slow release of a model compound. Taken together, these biomaterials have the potential to be used as a bifunctional platform for bone regeneration via ion release and biomolecule delivery.
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http://dx.doi.org/10.1021/acsabm.0c00257 | DOI Listing |
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