Biological assessment of a new ready-to-use hydraulic sealer

被引:6
作者
Benetti, Francine [1 ,2 ]
Gomes-Filho, Joao Eduardo [2 ]
de Azevedo-Queiroz, India Olinta [2 ]
Carminatti, Marina [2 ]
Conti, Leticia Citelli [2 ]
dos Reis-Prado, Alexandre Henrique
Penha de Oliveira, Sandra Helena [3 ]
Ervolino, Edilson [3 ]
Dezan-Junior, Eloi [2 ]
Angelo Cintra, Luciano Tavares [2 ]
机构
[1] Univ Fed Minas Gerais, Sch Dent, Dept Restorat Dent, Belo Horizonte, MG, Brazil
[2] Sao Paulo State Univ UNESP, Sch Dent, Dept Prevent & Restorat Dent, R Jose Bonifacio 1193, BR-SP160150 Aracatuba, SP, Brazil
[3] Sao Paulo State Univ UNESP, Sch Dent, Dept Basic Sci, Aracatuba, SP, Brazil
关键词
Biocompatibility; Cytotoxicity; Hydraulic sealer; Mineral trioxide aggregate; Tenascin; MINERAL TRIOXIDE AGGREGATE; IMMUNOHISTOCHEMICAL EXPRESSION; ENDODONTIC SEALER; TISSUE REACTION; MTA FILLAPEX; CALCIUM; CYTOTOXICITY; BIOCOMPATIBILITY; TENASCIN; FIBRONECTIN;
D O I
10.5395/rde.2021.46.e21
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: This study compared the cytotoxicity, biocompatibility, and tenascin immunolabeling of a new ready-to-use hydraulic sealer (Bio-C Sealer) with MTA-Fillapex and white MTA-Angelus. Materials and Methods: L929 fibroblasts were cultivated and exposed to undiluted and diluted material extracts. Polyethylene tubes with or without (the control) the materials were implanted into the dorsa of rats. At 7 days and 30 days, the rats were euthanized, and the specimens were prepared for analysis; inflammation and immunolabeling were measured, and statistical analysis was performed (p < 0.05). Results: MTA-Fillapex exhibited greater cytotoxicity than the other materials at all time points (p < 0.05). The undiluted Bio-C Sealer exhibited greater cytocompatibility at 6 and 48 hours than white MTA-Angelus, with higher cell viability than in the control (p < 0.05). White MTA-Angelus displayed higher cell viability than the control at 24 hours, and the one-half dilution displayed similar results at both 6 and 48 hours (p < 0.05). At 7 days and 30 days, the groups exhibited moderate inflammation with thick fibrous capsules and mild inflammation with thin fibrous capsules, respectively (p > 0.05). At 7 days, moderate to strong immunolabeling was observed (p > 0.05). After 30 days, the control and MTA-Fillapex groups exhibited strong immunolabeling, the white MTA-Angelus group exhibited moderate immunolabeling (p > 0.05), and the Bio-C Sealer group exhibited low-to-moderate immunolabeling, differing significantly from the control (p < 0.05). Conclusions: Bio-C Sealer and white MTA-Angelus exhibited greater cytocompatibility than MTA-Fillapex; all materials displayed adequate biocompatibility and induced tenascin immunolabeling.
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页数:12
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