No abstract

This study evaluated the cytotoxicity of methacrylate‐based resins containing dimethyl sulfoxide (DMSO). DMSO was incorporated into hydrophobic (R2) and hydrophilic (R5) resins at weight concentrations of 0, 0.01, 0.1, 1, 5, or 10 w/w %. Resin discs (n = 10/group) were prepared. Human gingival fibroblasts (HGF‐1) were exposed to resin eluates for 24 h. Furthermore, dentin barrier test was performed using 3‐D cultures of odontoblast‐like cells (SV40 transfected pulp derived cells) with dentin slices of 400 µm thickness (n = 8). After acid etching of dentin, DMSO‐modified resins were applied into the cavity part of the device and light‐cured for 20 s. Cell viability (%) was assessed by MTT and analyzed spectrometrically. Data were analyzed by ANOVA and Tukey test (α = 0.05). Resin eluates showed statistically significantly lower % cell viability for all neat and DMSO‐modified resins than seen for the negative control. Moreover, DMSO‐R5 eluates resulted in significantly lower % cell viability than DMSO‐R2 emulates. The dentin barrier test showed that DMSO‐R2 did not result in significantly lower % cell viability, whereas incorporation of 1‐10 w/w % DMSO into R5 resulted in significantly lower % of cell viability. Incorporating DMSO into hydrophilic self‐etching resins may increase cytotoxicity. The biocompatibility is not influenced by the addition of DMSO into hydrophobic resin.

This study investigates the effect of ions released from S-PRG fillers on host-derived enzymatic degradation of dentin collagen matrices. Dentin beams (n=80) were demineralized and distributed to eight groups following baseline dry mass and total MMP activity assessments. Each group treated with boron, fluoride, sodium, silicone, strontium, aluminium, or S-PRG eluate solutions for 5 min. Untreated beams served as control. After pre-treatment, MMP activity was reassessed, beams were incubated in complete medium for 1 week, dry mass was reassessed. Incubation media were analyzed for MMP and cathepsin-K-mediated degradation fragments. Data were analyzed with ANOVA and Tukey's test. All pretreatment groups showed significant reduction in total MMP activity (p<0.05) that was sustainable after incubation in all groups except for boron and silicone groups (p<0.05). Cathepsin-K activity did not differ between control or treatment groups. The results indicated that ions released from S-PRG fillers have the potential to partly inhibit MMP-mediated endogenous enzymatic activity.

This study presents an exploratory investigation into the mechanical and thermal properties of a modified adhesive (high adhesive, Sikadur®-330) when mixed with fly ash or a combination of fly ash and fine-sand at various ratios, as well as the adhesive's performance under high temperatures of 250℃. A series of physical tests, including compressive strength, consistency, modulus of rupture, density, and ultrasonic pulse velocity, were conducted alongside thermal assessments, such as final and initial shrinkage, linear expansion coefficient, and heat of reaction measurements. The results demonstrate that the incorporation of fly ash and fine-sand significantly enhances the adhesive's thermal properties by reducing both final and initial shrinkage, minimizing the linear expansion coefficient, and attenuating the heat of reaction. Furthermore, the mechanical properties of the adhesive were observed to improve upon exposure to high temperatures of 250℃. The addition of fine-sand and fly ash to the adhesive not only reduced costs but also led to a notable increase in the modulus of rupture and compressive strength. Consequently, the optimal ratio of adhesive, sand, and fly ash was determined to be 1:1:1 by weight, considering improvements in mechanical and thermal properties, cost reduction, and preserved workability.