Reticulated åkermanite (Ca2MgSi2O7) 3D scaffolds were fabricated by direct ink writing of pastes based on a commercial silicone resin and fillers, such as calcium carbonate (CaCO3) and magnesium hydroxide (Mg(OH)2) microparticles, followed by heat treatment at 1100 °C in air. To form liquid phase upon firing and thus promote the ionic interdiffusion, borax (Na2B4O7·10H2O) or hydrated sodium phosphate (Na2HPO4·12H2O) were considered as alternative additives. Although leading to scaffolds with different strength-to-density ratio, the two additives did not lead to substantial differences in terms of biological response. All fabricated ceramics exhibited acellular in-vitro bioactivity upon immersion in simulated-body-fluid (SBF) as well as antibacterial activity against S. aureus and E. coli. Direct contact cell viability test, performed with a stromal-cell line from mouse bone marrow (ST-2 cells), indicated no cytotoxicity of both samples determined by the WST-8 assay.

Assessment of in-vitro bioactivity, biodegradability and antibacterial activity of polymer-derived 3D printed åkermanite scaffolds

Elsayed H.;Bernardo E.;
2023

Abstract

Reticulated åkermanite (Ca2MgSi2O7) 3D scaffolds were fabricated by direct ink writing of pastes based on a commercial silicone resin and fillers, such as calcium carbonate (CaCO3) and magnesium hydroxide (Mg(OH)2) microparticles, followed by heat treatment at 1100 °C in air. To form liquid phase upon firing and thus promote the ionic interdiffusion, borax (Na2B4O7·10H2O) or hydrated sodium phosphate (Na2HPO4·12H2O) were considered as alternative additives. Although leading to scaffolds with different strength-to-density ratio, the two additives did not lead to substantial differences in terms of biological response. All fabricated ceramics exhibited acellular in-vitro bioactivity upon immersion in simulated-body-fluid (SBF) as well as antibacterial activity against S. aureus and E. coli. Direct contact cell viability test, performed with a stromal-cell line from mouse bone marrow (ST-2 cells), indicated no cytotoxicity of both samples determined by the WST-8 assay.
2023
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3496157
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