resumo
Mesoporous bioactive glasses (MBGs) with a compoisition of 85SiO(2)-10CaO-5P(2)O(5) (mol %) have been prepared through the evaporation-induced self-assembly (EISA) method, using P123 as a structure directing agent. For the first time, SiO2-CaO-P2O5 MBGs with identical composition and textural properties, but exhibiting different bicontinuous 3D-cubic and 2D-hexagonal structures, have been prepared. These materials allow us to discriminate file role of the structure Oil the bioactivity, from other parameters. To understand the role of each component on the mesostructure, local environment, and bioactive behavior, mesoporous 100SiO(2), 95SiO(2)-5P(2)O(5), and 90SiO(2)-10CaO (mol%) materials were also prepared under the same conditions. The results demonstrate that the joint presence of CaO and P2O5 results in amorphous calcium phosphate (ACP) clusters sited at the pore wall Surface. This heterogeneity highly improves the bioactive behavior of these materials, In addition, the presence of ACP clusters within the silica network leads to different mesoporous structures. The mesoporous order can be tuned through a rigorous control of the solvent evaporation temperature during the mesophase formation, resulting in p6mm, p6mm/Ia (3) over bard coexistence, and Ia (3) over bard phases for 20, 30, and 40 degrees C, respectively. Preliminary results indicate that, in the case of identical composition and textural properties, the mesoporous Structure does not have influence on the apatite formation, although initial ionic exchange is slightly enhanced for 3D cubic bicontinuous structures.
palavras-chave
BONE TISSUE REGENERATION; SOL-GEL GLASSES; IN-VITRO; DRUG-DELIVERY; MEDICAL APPLICATIONS; SILICA; CAO-P2O5-SIO2; SURFACTANT; BEHAVIOR; POWDERS
categoria
Chemistry; Materials Science
autores
Garcia, A; Cicuendez, M; Izquierdo-Barba, I; Arcos, D; Vallet-Regi, M
nossos autores
Monica Cicuéndez Maroto
Bolseiro de pós-DoutoramentoGrupos
agradecimentos
This work was supported by the Spanish CICYT (through Project No. MAT2008-00736) and by the Communidad Autonoma de Madrid (through Project No. S-0505/MAT/0324). We also thank to the CAI Electron Microscopy Center, CAI Nuclear Magnetic Resonance and Fernando Conde (CAI X-ray Diffraction), Universidad Complutense de Madrid, for their valuable technical assistance.