Optimal Cytocompatibility of a Bioceramic Nanoparticulate Cement in Primary Human Mesenchymal Cells

被引:101
作者
De-Deus, Gustavo [1 ]
Canabarro, Antonio [2 ]
Alves, Gutemberg [3 ]
Linhares, Adriana [3 ]
Senne, Maria Isabel [4 ]
Granjeiro, Jose Mauro [3 ]
机构
[1] Univ Veiga de Almeida, Dept Endodont, Rio De Janeiro, Brazil
[2] Univ Veiga de Almeida, Dept Periodontol, Rio De Janeiro, Brazil
[3] Univ Fed Fluminense, Inst Biol, Cellular Therapy Ctr, Clin Res Unity, BR-24220000 Niteroi, RJ, Brazil
[4] Univ Estado Rio De Janeiro, Dept Endodont, Rio De Janeiro, Brazil
关键词
BioAggregate; biocompatibility; cytotoxicity; mineral trioxide aggregate; root-end filling model; stem cells; MINERAL TRIOXIDE AGGREGATE; PERIODONTAL-LIGAMENT FIBROBLASTS; PORTLAND-CEMENT; STEM-CELLS; CYTOTOXICITY; MTA; OSTEOBLASTS; MODEL; LINES; PULP;
D O I
10.1016/j.joen.2009.06.022
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: The aim of this study was to evaluate and compare the cytotoxic effects of BioAggregate (Innovative BioCaramix Inc, Vancouver, BC, Canada), a novel bioceramic nanoparticulate cement, on human mesenchymal cells. White Pro-Root MTA (Dentsply, Tulsa Dental, Tulsa, OK) was used as a reference for comparison. Methods: Fifty-six human maxillary incisor teeth were submitted to a step-back flaring technique and prepared for cytotoxicity assay in an in situ root-end filling experimental model. After retro filling, each root containing MTA, BioAggregate, or empty root canals (control) was exposed to culture media for 24, 48, or 72 hours, providing several extraction media. Mesenchymal cells were incubated with each extract medium for 24 hours, and toxicity was evaluated by three different parameters of cell survival and integrity on the same sample: XTT, neutral red, and crystal violet dye elution. Results: No statistically significant differences between MTA and BioAggregate were found in all the experimental periods (p > 0.05). Conclusion: DiaRoot BioAggregate displayed in vitro compatibility similar to MTA. (J Endod 2009,35:1387-1390)
引用
收藏
页码:1387 / 1390
页数:4
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