By employing 31P multiple-quantum coherence-based solid-state nuclear magnetic resonance spectroscopy, we present the first comprehensive experimental assessment of the nature of the orthophosphate-ion distributions in silicate-based bioactive glasses (BGs). Results are provided both from melt-prepared BG and evaporation-induced self-assembly-derived mesoporous bioactive glass (MBG) structures of distinct compositions. The phosphate species are randomly dispersed in melt-derived BGs (comprising 44-55 mol % SiO 2) of the Na2O-CaO-SiO2-P2O 5 system, whereas a Si-rich (86 mol % SiO2) and Ca-poor ordered MBG structure exhibits nanometer-sized amorphous calcium phosphate clusters, conservatively estimated to comprise at least nine orthophosphate groups. A Ca-richer MBG (58 mol % SiO2) reveals a less pronounced phosphate clustering. We rationalize the variable structural role of P in these amorphous biomaterials. © 2013 American Chemical Society.
CITATION STYLE
Mathew, R., Turdean-Ionescu, C., Stevensson, B., Izquierdo-Barba, I., García, A., Arcos, D., … Edén, M. (2013). Direct probing of the phosphate-ion distribution in bioactive silicate glasses by solid-state NMR: Evidence for transitions between random/clustered scenarios. Chemistry of Materials, 25(9), 1877–1885. https://doi.org/10.1021/cm400487a
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