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Aim: To evaluate whether the bioceramic materials Bio‐C Pulpo (Bio‐C, Angelus) and mineral trioxide aggregate (MTA) Repair HP (MTA‐HP, Angelus) induce fibroblast proliferation and release of interleukin‐10 (IL‐10), an anti‐inflammatory cytokine, stimulating connective tissue remodelling. The tissue response of Bio‐C and MTA‐HP was compared with the White MTA (WMTA; Angelus) since studies have demonstrated that WMTA induces tissue repair. Methodology: Bio‐C, MTA‐HP and WMTA were inserted into polyethylene tubes and implanted in the subcutaneous tissue of Holtzman rats for 7, 15, 30 and 60 days. As a control group (CG), empty tubes were implanted subcutaneously. The number of fibroblasts (FB), Ki‐67‐, fibroblast growth factor‐1‐ (FGF‐1) and IL‐10‐immunolabelled cells and collagen content in the capsules was obtained. The data were subjected to two‐way anova followed by Tukey's test (p ≤.05). Results: At 7 days, significant differences in the number of FB were not detected amongst Bio‐C, MTA‐HP and WMTA groups (p ˃.05). The capsules of all groups exhibited a significant increase in the number of FB and content of collagen over time. From 7 to 60 days, a significant reduction in the number of FGF‐1‐ and Ki‐67‐immunolabelled cells was seen in the capsules of all specimens. In all periods, no significant difference in the number of FGF‐1‐immunolabelled cells was detected between Bio‐C and CG specimens. At 60 days, significant differences in the immunoexpression of FGF‐1 were not observed amongst the groups. At 7 and 15 days, the highest immunoexpression for Ki‐67 was present in Bio‐C specimens whilst, after 30 and 60 days, no significant difference was observed amongst the bioceramic materials. At 7 days, few IL‐10 immunolabelled cells were present in the capsules of all specimens whereas, at 60 days, a significant increase in the IL‐10‐immunostaining was present in all groups. At 60 days, the Bio‐C, MTA‐HP and WMTA groups showed a greater number of IL‐10‐immunolabelled cells than in the CG specimens (p <.0001). Conclusions: Bio‐C, MTA‐HP and WMTA stimulate fibroblast proliferation, leading to the formation of collagen‐rich capsules. FGF‐1 and IL‐10 may mediate the remodelling of capsules around Bio‐C, MTA‐HP and WMTA bioceramic materials. [ABSTRACT FROM AUTHOR]

Aim: To evaluate the tissue reaction of a tricalcium silicate‐based repair material associated with 30% calcium tungstate (TCS + CaWO4) in comparison to Bio‐C Repair (Bio‐C; Angelus) and to MTA Repair HP (MTA HP; Angelus). Methodology: Polyethylene tubes filled with one of the materials or left empty (control group, CG) were implanted into the subcutaneous tissues of rats for 7, 15, 30 and 60 days (n = 32/group). The capsule thickness, number of inflammatory cells, collagen content, interleukin‐6 (IL‐6), osteocalcin (OCN), von Kossa reaction and analysis under polarized light were evaluated. The data were subjected to generalized linear models for repeated measures, except the OCN. OCN data were submitted to Kruskal–Wallis and Dunn's post hoc test and Friedman followed by Nemenyi's test at significance level of 5%. Results: At all time points, significant differences in the number of inflammatory cells were not observed between TCS + CaWO4 and Bio‐C, whereas, at 15, 30 and 60 days, no significant difference was detected between TCS + CaWO4 and MTA HP. At all periods, significant differences were not detected in the number of fibroblasts in TCS + CaWO4 versus MTA HP, and, at 60 days, no significant difference was demonstrated between these groups and CG. Significant differences in the immunoexpression of IL‐6 were not detected amongst bioceramic materials at all periods. From 7 to 60 days, significant reduction in the number of inflammatory cells, number of IL‐6‐immunopositive cells and in the capsule thickness was accompanied by significant increase in the collagen in all groups. OCN‐immunolabelled cells, von Kossa‐positive structures and amorphous calcite deposits were observed around all materials, whereas, in the CG, these structures were not seen. Conclusions: These findings indicate that the experimental material (TCS + CaWO4) is biocompatible and has a bioactive potential, similar to the MTA HP and Bio‐C Repair, and suggest its use as a root repair material. [ABSTRACT FROM AUTHOR]

Copyright of Universidade Estadual Paulista. Revista de Odontologia is the property of Universidade Estadual Paulista. Revista de Odontologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Universidade Estadual Paulista. Revista de Odontologia is the property of Universidade Estadual Paulista. Revista de Odontologia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Objective: This study aimed to evaluate the fracture strength and failure modes of different core techniques in teeth with simulated coronal destruction. Materials and methods: Forty teeth were endodontically prepared and the specimens were divided into four experimental groups (n = 10) according to the core composition: Filtek One Bulk Fill‐FOBF, Filtek Z350 XT‐FZ350 (standard group), Filtek Bulk Fill Flow‐FBFF, and LuxaCore Z‐LCZ. CAD/CAM Monolithic zirconia crowns were obtained and cemented with RelyX U200. After storage in distilled water at 37°C for 48 h, the specimens were subjected to thermal cycling and to compressive strength mechanical tests. Statistical analyses (α = 0.05) were performed by non‐parametric Kruskal–Wallis, Dunn post hoc, and Fisher's exact tests. Results: No significant differences (p > 0.05) were observed among FOBF, FZ350, and FBFF (mean ranks = 20.30, 12.20, and 23.20, respectively). LCZ (mean rank = 26.30) produced results similar to those of FOBF and FBFF (p > 0.05) and higher than those of FZ350 (p = 0.042). The most frequent type of failure was irreparable, regardless of the experimental condition. The lowest percentages of reparable fractures were produced by FOBF group (10%). Conclusions: The use of bulk fill materials, including the "core‐and‐post" LCZ dual‐cure resin composite, did not impair the fracture strength of endodontically treated teeth with coronal destruction. Clinical significance: Resin composite bulk fill materials that can be used as a core‐and‐post cementation in an only stage are interesting, since they enable clinicians to work with one only material, and avoid several materials interfaces, technical sensitivity, and longer chair‐time due to multistep procedures. [ABSTRACT FROM AUTHOR]

This study evaluated the physicochemical and biological properties of novel reparative materials composed of pure tricalcium silicate (Ca3SiO5), Ca3SiO5 doped with fluoride ions (Ca3SiO5‐F) and their association with ZrO2 (Ca3SiO5 + ZrO2, Ca3SiO5‐F + ZrO2), in comparison with Biodentine (BIO). Setting time radiopacity, pH, solubility, and dimensional change were evaluated based on ISO 6876 Standard. Volumetric change and flow/filling were assessed by microcomputed tomography (micro‐CT). Biological properties were evaluated by the MTT assay 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide), Neutral Red (NR), cell migration, alkaline phosphatase activity (ALP), and Alizarin Red Staining (ARS) assays. Statistical analysis was performed by ANOVA, Tukey, or Bonferroni tests (α =.05). Ca3SiO5‐F + ZrO2 had higher radiopacity, shorter setting time, and lower solubility and volumetric loss than BIO (p <.05). Ca3SiO5‐F + ZrO2 had flow and filling capacity similar to BIO (p >.05). All the cements evaluated had an alkaline pH. Ca3SiO5‐F + ZrO2 demonstrated cell viability similar to negative control (p >.05), increase in ALP activity in 7 days, mineralized nodule production in 21 days and repair capacity according to cell migration. In conclusion, Ca3SiO5‐F + ZrO2 had adequate setting time, radiopacity, solubility, and dimensional change. This material presented low volumetric change besides flow and filling capacity in micro‐CT assessment. In addition, Ca3SiO5‐F + ZrO2 was biocompatible and bioactive, suggesting its use as reparative material. [ABSTRACT FROM AUTHOR]