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      Effects of incorporation of hydroxyapatite and fluoroapatite nanobioceramics into conventional glass ionomer cements (GIC).

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          Abstract

          Hydroxyapatite (HA) has excellent biological behavior, and its composition and crystal structure are similar to the apatite in the human dental structure and skeletal system; a number of researchers have attempted to evaluate the effect of the addition of HA powders to restorative dental materials. In this study, nanohydroxy and fluoroapatite were synthesized using an ethanol based sol-gel technique. The synthesized nanoceramic particles were incorporated into commercial glass ionomer powder (Fuji II GC) and were characterized using Fourier transform infrared and Raman spectroscopy, X-ray diffraction and scanning electron microscopy. Compressive, diametral tensile and biaxial flexural strengths of the modified glass ionomer cements were evaluated. The effect of nanohydroxyapatite and fluoroapatite on the bond strength of glass ionomer cement to dentin was also investigated. Results showed that after 1 and 7 days of setting, the nanohydroxyapatite/fluoroapatite added cements exhibited higher compressive strength (177-179MPa), higher diametral tensile strength (19-20MPa) and higher biaxial flexural strength (26-28MPa) as compared with the control group (160MPa in CS, 14MPa in DTS and 18MPa in biaxial flexural strength). The experimental cements also exhibited higher bond strength to dentin after 7 and 30 days of storage in distilled water. It was concluded that glass ionomer cements containing nanobioceramics are promising restorative dental materials with both improved mechanical properties and improved bond strength to dentin.

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          Author and article information

          Journal
          Acta Biomater
          Acta biomaterialia
          1742-7061
          1742-7061
          Mar 2008
          : 4
          : 2
          Affiliations
          [1 ] Department of Materials, Interdisciplinary Research Centre in Biomedical Materials, Queen Mary University of London, Mile End Road, London E1 4NS, UK.
          Article
          S1742-7061(07)00121-3
          10.1016/j.actbio.2007.07.011
          17921077
          b8fe40f2-bccc-4ff1-a2f4-1d6605d2a0ef
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