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Updated: Dec 2, 2025

Biological Compatibility Profile on Biomaterials for Bone Regeneration
Published on: November 16, 2018
Development and evaluation of copper-containing mesoporous bioactive glasses for bone defects therapy
J Jiménez-Holguín1, S Sánchez-Salcedo1,2, M Vallet-Regí1,2
1Dpt. Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense de Madrid, UCM, Instituto de Investigación Hospital 12 de Octubre, imas12, 28040, Madrid, Spain.
Mesoporous bioactive glasses (MBGs) with copper oxide (CuO) show enhanced bone regeneration potential. The nitrate-based MBGs exhibit faster bioactive responses and release therapeutic ions, making them promising for bone defect treatments.
Area of Science:
- Biomaterials Science
- Materials Chemistry
- Biomedical Engineering
Background:
- Mesoporous bioactive glasses (MBGs) are investigated for bone defect treatment.
- Incorporating therapeutic oxides like copper oxide (CuO) enhances MBG biological activity.
Purpose of the Study:
- To synthesize and characterize MBGs with varying CuO content (0-5 mol-%) using different synthesis routes.
- To evaluate the influence of CuO and synthesis parameters on MBG properties and in vitro bioactivity.
Main Methods:
- Synthesis of two MBG series using chloride or nitrate precursors and catalysts.
- Characterization of nanoparticle size, structure, and ion release.
- In vitro bioactivity assessment using simulated body fluid (SBF) and cell culture media (MEM, THB).
Main Results:
- Nitrate-based MBGs showed larger metallic copper nanoparticles (>50 nm) and faster apatite layer formation in SBF.
- Chloride-based MBGs exhibited smaller calcium/copper phosphate nanoparticles (10-20 nm).
- All synthesized MBGs released therapeutic Ca2+ and Cu2+ ions within 24 hours in culture media.
Conclusions:
- MBGs synthesized using nitrate precursors demonstrate superior in vitro bioactivity and ion release profiles.
- These nitrate-based MBGs are proposed as excellent biomaterials for bone regeneration due to their rapid bioactivity and therapeutic ion release.
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