AI Article Synopsis

  • The study focuses on the synthesis of nanostructured calcium phosphates, specifically nanohydroxyapatite (HAP) with varying silicon content, through aqueous precipitation and calcination.
  • The materials were characterized using various techniques, including XRD and FTIR, which confirmed the presence of HAP and β-TCP phases, alongside nanocrystalline features, and highlighted changes due to silicon and calcination temperatures.
  • The scaffolds created from these materials showed improved cell adhesion and proliferation in human osteoblast cultures, indicating their potential for use in bone reconstruction applications.

Article Abstract

Nanostructured calcium phosphates, such as nanohydroxyapatite (HAP) and HAP with silicon content (HAP-Si) of 0.47wt.% (1% SiO2), 2.34wt.% (5% SiO2) and 4.67wt.% (10% SiO2) in the final product, were synthesized by aqueous precipitation, freeze dried and then calcined at 650, 950 and 1150°C. The obtained materials were investigated by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectrometry, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM) imaging. From the analysis of the XRD patterns, the HAP and β-tricalcium phosphate (β-TCP) phases were identified and their amounts in the samples were estimated. The size of HAP and β-TCP crystallites was estimated to be in the nanocrystalline domain. FTIR spectra showed the presence of characteristic vibrations for P-O, H-O and Si-O groups and their modification with Si content and calcination temperature. TEM, SEM and AFM images also revealed the morphology of the particles and of their aggregates. These materials have been used to manufacture scaffolds which were tested for their influence on adhesion and proliferation of cells, in human osteoblast culture, considering their further use in bone reconstruction. It was found that an appropriate addition of silicon in nanocalcium phosphate scaffolds leads to an enhanced adhesion and proliferation of cells in osteoblasts in vitro.

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http://dx.doi.org/10.1016/j.msec.2013.12.027DOI Listing

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