RESUMEN
Objectives: The purpose of this study is to evaluate the effect of the palatal metal collar height on the fracture resistance of metal-ceramic crowns. Materials and Methods: A maxillary premolar typodont tooth was prepared and scanned to fabricate 48 metal analogs. The analogs were then scanned to fabricate metal copings divided into 4 groups according to palatal metal collar height as follows; (C0): 0 mm, (C1): 1.0 mm, (C2): 1.5 mm, and (C3): 2.0 mm. After a standard application of pressed ceramic, each crown was cemented onto its corresponding metal tooth analog. The crown-analog assembly was subjected to a sequence of thermal stressing for 5,000 cycles. A universal testing machine applied controlled loads to the crowns until fracture. Examination under a stereomicroscope determined the failure mode. A scanning electron microscope (SEM) was used to examine fracture. Load to failure data was analyzed using ANOVA followed by Tukey HSD (P ≤ 0.05). Results: ANOVA statistics revealed that groups with a palatal metal collar presented significantly higher failure loads when compared to the collarless group (P < 0.0001). Difference in failure loads between 1.5-mm and 2.0-mm palatal metal collar height were not statistically significant (P = 0.935). There were no significant differences detected among the groups in terms of failure mode. Conclusions: The height of the palatal metal collar has an effect on the fracture resistance of the metal-ceramic crowns. Clinical Relevance. The incorporation of a palatal collar with a predetermined height is essential to reduce the mechanical failure of metal-ceramic crowns.
RESUMEN
This study assessed the dose-dependent effect on the cytotoxicity of BioRoot RCS (BR) and Endosequence BC (BC) sealers in human bone marrow mesenchymal stem cells (hMSCs) compared to those of the AH Plus sealer. Cells were exposed to different dilutions of extracts from freshly prepared sealers (1:2, 1:8, 1:32). Unexposed cells acted as the negative control. Cytotoxicity was evaluated by an alamar blue assay. Cell morphology was analyzed by using scanning electron microscopy after exposure to the different sealers' extracts. Statistical analysis was performed using a one-way analysis of variance and the Bonferroni post hoc test (p < 0.05). The cytotoxicities of BC and BR were less than that of AH Plus. In the presence of 1:2 BR, the cell proliferation was significantly lower than the control. At 1:8 and 1:32 concentrations, both the tricalcium silicate sealers led to similar cellular proliferation. Cells in BC and BR sealers' extracts spread better than those in AH Plus extract.