The specimens were randomly divided into four groups (n = 10), and restored with Cu–Al cast dowel-and-cores cemented with one of four options: conventional glass ionomer cement (GI); resin-modified glass ionomer cement (GR); dual-cure resin cement (RC); or zinc-phosphate cement (ZP). Sequentially, fracture resistance of the specimens was tested with a tangential load at a 135° angle with a 0.5 mm/min
crosshead speed. Data were analyzed using one-way analysis HSP tumor of variance (ANOVA) and the Fisher test. Two-dimensional finite element analysis (2D-FEA) was then performed with representative models of each group simulating a 100 μm cement layer. Results were analyzed based on von Mises stress distribution criteria. Results: The mean fracture resistance values were (in N): RC, 838.2 ± 135.9; GI, 772.4 ± 169.8; GR, 613.4 ± 157.5; ZP, 643.6 ± 106.7. FEA revealed that RC and GR presented lower stress values than ZP and GI. The higher stress concentration was coincident with more catastrophic failures, and PXD101 molecular weight consequently, with lower fracture resistance values. Conclusions: The
type of cement influenced fracture resistance, failure mode, and stress distribution on teeth restored with cast dowel-and-cores. “
“Dentures are often colonized with a variety of microorganisms, including Candida albicans, that contribute to denture stomatitis. Several in vitro models have been previously established to study denture-related microbial colonization and evaluate treatment efficacy of denture cleansers; however, those models typically fail to appreciate the complex topology and heterogeneity of denture surfaces and lack effective ways to accurately measure microbial colonization. The purpose
of this study was to study microbial colonization with a new model system based on real dentures, to more realistically mimic in vivo conditions. Scanning electron microscopy was used to observe G protein-coupled receptor kinase topological structures among surfaces from different parts of the denture. Employing C. albicans as a model microorganism, we established microbial colonization on different denture surfaces. Moreover, we applied a modified MTT (3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide) colorimetric assay to quantify C. albicans colonization on dentures without the necessity of biofilm removal and to evaluate treatment efficacy of denture cleansers. There were significant variations in topological structures among surfaces from different parts of the denture, with the unpolished side having the highest amounts of indentations and pores. The distinct denture surfaces support microbial colonization differently, with the unpolished side containing the highest level of microbial colonization and biofilm formation.
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