This project intends to develop restorative dental nanomaterial composites that are light-curable and show minimal shrinkage. Such nanocomposites are improved via employing 2,2-bis[4(2-hydroxy-3-methacryloylpropyloxy) phenyl] propane (Bis-GMA) with the unsaturated monomers bisphenol A dimethacrylate, N,N-dimethylacetamide (DMA), ethylene glycol (EG), and methacrylic acid (MAA) and loading them with SiO2, ZrO2, or hydroxyapatite (HA) as nanofillers of 10–30 nm. The first step was to create and characterize these novel dental materials. 1,6-hexanediol methacrylate (HDOMA) was used as a cross-linking agent. The composites based on Bis-GMA and HDOMA with a mass ratio of 40/20 were loaded with 2.5, 5.0, 7.5, 10.0, 12.5, and 15.0 wt.% of the fillers mentioned above. Photopolymerization was induced by a system of photoinitiation based on Camphorquinone/2- (Diethyl amino) ethyl acrylate (CQ/DMAEMA). The nanofillers were treated with 3-(methacryloyloxy) propyltrimethoxysilane (MPTMS) at a ratio of 1.5, 2.5, as well as 3.5%wt. compared to the filler) and a silane coupling agent to increase bonding between the phases and reduce the tendency of agglomerations. SEM images displayed the adhesion between the matrix and the three functionalized nanofillers. FTIR was used to prove the functionalization of the nanofillers by silanization with MPTMS. According to the polymer matrix, two different series of dental nanocomposites were obtained. The compressive strength of dental nanocomposites treated with 2.5 wt.% MPTMS was considerably more significant than those treated with 1.5 and 3.5%wt. MPTMS. Compressive strength (CS) and volumetric shrinkage (VS) were examined as examples of physicochemical properties. This improved nanocomposite was tested for its suitability as a dental restorative material and found to have low shrinkage and high strength.
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