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Purpose: The objective of this study was to evaluate the physical and mechanical properties of a short fiber-reinforced resin composite: everX-Posterior and compare it with two bulk-fill composites, namely, Filtek Bulk-fill and Beautifil-Bulk, which are intended for large posterior restorations. Methods: Investigated properties were flexural strength, flexural modulus, surface roughness, volumetric shrinkage and depth of cure. Scanning electron microscopy images of each specimen after the flexural test were used for cross-sectional comparison. Results were analyzed using ANOVA following Tukey post-hoc test. Results: Flexural strength of everX-Posterior was comparable with two other resin composites, showing higher flexural modulus. EverX-Posterior showed the highest surface roughness after polishing and the lowest volumetric shrinkage (2.29%) among all composites used in this study. Data also showed that the everX-Posterior depth of cure was 4.24 mm, which was the highest among the three groups. Conclusion: Based on the results of this study, it was concluded that everX-Posterior as a short fiber-reinforced composite showed improvements and satisfactory performance in mechanical and physical properties, which make it a reliable base material candidate for large posterior restorations., Journal of Oral Science, 63(2), pp. 148-151; 2021

Recently, ferroptosis has gained scientists’ attention as an iron-related regulated necrosis. However, not many reports have investigated the effect of ferroptosis on bone. Therefore, with the present study, we assessed the effect of ferroptosis inhibition using ferrostatin-1 on the MC3T3-E1 pre-osteoblast cell. Cell images, cell viability, alkaline phosphatase activity test, alizarin red staining, and RUNX2 gene expression using real-time PCR were applied to investigate the effects of ferrostatin and erastin on MC3T3-E1 osteoblast cells. Erastin was used as a well-known ferroptosis inducer reagent. Erastin with different concentrations ranging from 0 to 50 µmol/L was used for inducing cell death. The 25 µmol/L erastin led to controllable partial cell death on osteoblast cells. Ferrostatin-1 with 0 to 40 µmol/L was used for cell doping and cell death inhibition effect. Ferrostatin-1 also displayed a recovery effect on the samples, which had already received the partially artificial cell death by erastin. Cell differentiation, alizarin red staining, and RUNX2 gene expression confirmed the promotion of the bone formation ability effect of ferrostatin-1 on osteoblast cells. The objective of this study was to assess ferrostatin-1’s effect on the MC3T3-E1 osteoblast cell line based on its ferroptosis inhibitory property., International Journal of Molecular Sciences, 22(22), art. no. 12259; 2021

This study prepared glass ionomer cement (GIC) containing nanoporous silica (NPS) (GIC-NPS) at 5 wt% concentrations using 3 types of NPS with different pore and particle sizes and evaluated the differences in their cationic ion capture/release abilities and mechanical properties. The cationic water-soluble dye was used as cationic ion. The test GIC-NPS complexes captured dyes by immersion in 1 wt% dye solutions. All the GIC-NPS complexes released dyes for 28 d, and the amount of dye released from the complexes increased with decreasing pore size; however, the particle size of NPS did not affect the amount of dye released. Additionally, GIC-NPS was able to recharge the dye, and the amount of released the dye by the complexes after recharge was almost identical to the amount released on the first charge. Although not significantly different, the compressive strength of GIC-NPS was slightly greater than that of GIC without NPS regardless of the type of NPS. These results suggest that the degree of capture and release of cationic molecules, such as drugs, can be controlled by optimizing the pore size of NPS without sacrificing its mechanical strength when its content is 5 wt%.

This study aimed to evaluate the bonding performance of a new one-step self-etching adhesive system containing a novel hydrophilic amide monomer. Clearfil Universal Bond Quick (CUB) and Clearfil Megabond 2 (CMB) were used as the one-step and two-step adhesive systems, respectively. Flat dentin surfaces of human premolars were exposed using #600 SiC (silicon carbide) and bonded with the respective adhesives of each system. The teeth were sectioned to obtain beams (1 mm x 1 mm) after 24 h of water storage. The mean bond strength and standard deviations (MPa) on an occlusal surface were as follows: CUB: 45.9 +/- 19.7 and CMB: 67.9 +/- 25.3. The values for cervical ones were CUB: 56.0 +/- 20.3 and CMB: 67.6 +/- 16.0, respectively. In both conditions, the microtensile bond strength (mu TBS) value was lower than that of CMB. As seen during the microscopic observation, no adhesive failure was observed after mu TBS testing because CUB formed a firm and tight adhesive interface.

Metal ion elution, including Cr and Ni from dental orthodontic stainless steel, accounts for some allergies. In this study, a self-assembled monolayer (SAM) on a wire surface is proposed for suppressing such elution. This method involves modifying the stainless steel surface using phosphonic acid containing a long alkyl chain. The uncoated and coated wires are immersed in different acidic solutions, and the supernatant is analyzed by inductively coupled plasma mass spectrometry after 1-4 weeks. The results reveal that Cr and Ni ion elution is significantly suppressed by SAM modification. These findings will help in minimizing potential allergens from dental orthodontics., Coatings, 10(4), art.no.367; 2020

This study aimed to evaluate the bonding performance of a new one-step self-etching adhesive system containing a novel hydrophilic amide monomer. Clearfil Universal Bond Quick (CUB) and Clearfil Megabond 2 (CMB) were used as the one-step and two-step adhesive systems, respectively. Flat dentin surfaces of human premolars were exposed using #600 SiC (silicon carbide) and bonded with the respective adhesives of each system. The teeth were sectioned to obtain beams (1 mm x 1 mm) after 24 h of water storage. The mean bond strength and standard deviations (MPa) on an occlusal surface were as follows: CUB: 45.9 +/- 19.7 and CMB: 67.9 +/- 25.3. The values for cervical ones were CUB: 56.0 +/- 20.3 and CMB: 67.6 +/- 16.0, respectively. In both conditions, the microtensile bond strength (mu TBS) value was lower than that of CMB. As seen during the microscopic observation, no adhesive failure was observed after mu TBS testing because CUB formed a firm and tight adhesive interface.

The aim of this study was to evaluate calcium charge and release of conventional glass-ionomer cement (GIC) containing nanoporous silica (NPS). Experimental specimens were divided into two groups: the control (GIC containing no NPS) and GIC-NPS (GIC containing 10 wt % NPS). The specimens were immersed in calcium chloride solutions of 5 wt % calcium concentration for 24 h at 37 degrees C, whereupon the calcium ion release of the specimens was measured. The calcium ion release behavior of GIC-NPS after immersion in the calcium solution was significantly greater than that of the control. Scanning electron microscopy and electron-dispersive X-ray spectroscopy results indicated that calcium penetrated inside the GIC-NPS specimen, while the calcium was primarily localized on the surface of the control specimen. It was demonstrated that NPS markedly improved the calcium charge and release property of GIC.

Herein, we report a method for Ag nanoparticle preparation using hydrogen peroxide as a reducing agent. Ag nanoparticles were synthesized using silver(i) nitrate as a silver precursor, aqueous NH3 as a pH adjustor, and poly(vinyl pyrrolidone) (PVP) as a dispersant. The PVP concentration, the reaction temperature, the pH of the reaction solution, and the silver precursor all have a great influence on the size of the Ag nanoparticles. These parameters affected the reduction speed of the Ag+ ions and the aggregation of Ag nanoparticles. Ag nanoparticles of uniform shape were obtained under optimized conditions. In this work, we discuss a Ag nanoparticle growth mechanism based on La Mer's model, and aggregation control using PVP. This is a promising Ag nanoparticle preparation method with a low environmental load. Antibacterial tests using the obtained Ag nanoparticles were also carried out.

The aim of this study was to evaluate calcium charge and release of conventional glass-ionomer cement (GIC) containing nanoporous silica (NPS). Experimental specimens were divided into two groups: the control (GIC containing no NPS) and GIC-NPS (GIC containing 10 wt % NPS). The specimens were immersed in calcium chloride solutions of 5 wt % calcium concentration for 24 h at 37 degrees C, whereupon the calcium ion release of the specimens was measured. The calcium ion release behavior of GIC-NPS after immersion in the calcium solution was significantly greater than that of the control. Scanning electron microscopy and electron-dispersive X-ray spectroscopy results indicated that calcium penetrated inside the GIC-NPS specimen, while the calcium was primarily localized on the surface of the control specimen. It was demonstrated that NPS markedly improved the calcium charge and release property of GIC.