Methods: A hybrid resin composite preheated to three different temperatures (37°C, 54°C and 68°C) was cured using a high intensity light emitting diode (LED) curing unit. The light source was used in 40-and 20-second continuous mode as well as soft start mode. The resin composite was monitored for PGSS during curing and 10 minutes following light irradiation using strain gauges. DC was measured using FTIR spectrometer. The results were analyzed using two-way ANOVA followed by the Duncan's Multiple Range Test for pairwise comparisons. The significance level was set at p≤ ≤0.05. Results: Preheating of the resin composite significantly increased its PGSS and DC. The soft start groups revealed significantly lower PGSS values compared to the 20-and 40-second groups without altering the DC.Conclusions: Preheating of resin composite prior to curing increased its DC but also increased its PGSS. The soft-start mode decreased the PGSS of resin composite without altering the DC. INTRODUCTIONOne of the recent innovations in resin composite application involves preheating of resin composite material before insertion into the cavity.1 Preheating of resin DI El-Korashy Clinical RelevanceThe preheating of resin composite prior to curing yielded a better degree of conversion but had a negative impact on the induced post-gel shrinkage strain; soft-start mode is recommended, as it reduces the post-gel shrinkage strain without affecting the degree of conversion.

This work is focused on integrating nanotechnology with bone tissue engineering (BTE) to fabricate a bilayer scaffold with enhanced biological, physical and mechanical properties, using polycaprolactone (PCL) and gelatin (Gt) as the base nanofibrous layer, followed by the deposition of a bioactive glass (BG) nanofibrous layer via the electrospinning technique. Electrospun scaffolds were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy. Surface area and porosity were evaluated using the nitrogen adsorption method and mercury intrusion porosimetry. Moreover, scaffold swelling rate, degradation rate and in vitro bioactivity were examined in simulated body fluid (SBF) for up to 14 days. Mechanical properties of the prepared scaffolds were evaluated. Cell cytotoxicity was assessed using MRC-5 cells. Analyses showed successful formation of bead-free uniform fibers and the incorporation of BG nanoparticles within fibers. The bilayer scaffold showed enhanced surface area and total pore volume in comparison to the composite single layer scaffold. Moreover, a hydroxyapatite-like layer with a Ca/P molar ratio of 1.4 was formed after 14 days of immersion in SBF. Furthermore, its swelling and degradation rates were significantly higher than those of pure PCL scaffold. The bilayer’s tensile strength was four times higher than that of PCL/Gt scaffold with greatly enhanced elongation. Cytotoxicity test revealed the bilayer’s biocompatibility. Overall analyses showed that the incorporation of BG within a bilayer scaffold enhances the scaffold’s properties in comparison to those of a composite single layer scaffold, and offers potential avenues for development in the field of BTE.

Objectives To evaluate the polymerization efficiency of a matrix-modified bulk-fill composite, and compare it to a conventional composite which has a similar filler system. The degree of conversion (DC%) and monomer elution were measured over different storage periods. Additionally, fillers' content was examined. Materials and Methods Cylindrical specimens were prepared, in bulk and incrementally, from Filtek Bulk Fill (B) and Filtek Supreme XTE (S) composites using a Teflon mold, for each test ( n = 6). Using attenuated total reflection method of Fourier transformation infrared spectroscopy, DC% was measured after 24 hours, 7 days, and 30 days. Using high-performance liquid chromatography, elution of hydroxyethyl methacrylate, triethylene glycol dimethacrylate, urethane dimethacrylate, and bisphenol-A glycidyl dimethacrylate was measured after 24 hours, 7 days and 30 days. Filler content was examined by scanning electron microscopy (SEM). Data were analyzed using 2-way mixed-model analysis of variance (α = 0.05). Results There was no significant difference in DC% over different storage periods between B-bulk and S-incremental. Higher monomer elution was detected significantly from S than B. The elution quantity and rate varied significantly over storage periods and between different monomers. SEM images showed differences in fillers' sizes and agglomeration between both materials. Conclusions Matrix-modified bulk-fill composites could be packed and cured in bulk with polymerization efficiency similar to conventional composites.

This study compared two resin composites with similar filler systems and different matrix compositions. The depth of cure (DoC), polymerization shrinkage, and marginal leakage were evaluated. A Filtek Bulk Fill resin composite (FB) and a Filtek Supreme resin composite (FS) were used. For the DoC and polymerization shrinkage, cylindrical specimens with different thicknesses were prepared. The DoC was attributed to the bottom/top ratios of Vickers microhardness numbers. For polymerization shrinkage, each specimen was firstly scanned using micro-computed tomography (µCT) then cured for 20 s, then for 10 s, and then for 10 s, and they were rescanned between each curing time. Data were processed using the Mimics software. For marginal leakage, standardized 5 mm cavities were prepared in 90 molars. After etching and bonding, materials were packed according to groups: FB-bulk, FB-incremental, and FS-incremental, which were cured for 20, 30, and 40 s, respectively. After thermo-cycling, teeth were stored in 1% methylene blue dye for 24 h and then sectioned and observed for dye penetration. The results showed insignificant differences in the shrinkage and leakage between the different packing techniques and curing times of both materials. In conclusion, the introduction of a novel matrix into resin composite composition enabled bulk-filling in one layer up to 5 mm deep while keeping a tolerable polymerization shrinkage.

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