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ENDODONTIA MODERNA OBJETIVANDO RESULTADOS CLÍNICOS

ENDODONTIA MODERNA OBJETIVANDO RESULTADOS CLÍNICOS
EEC

quinta-feira, 18 de abril de 2013

JOE april 2013 - In Vitro Cytotoxicity Evaluation of a Novel Root Repair Material


In Vitro Cytotoxicity Evaluation of a Novel Root
Repair Material
Hui-min Zhou, PhD,*† Ya Shen, DDS, PhD,† Zhe-jun Wang, DDS, PhD,†‡ Li Li, PhD,* Yu-feng Zheng, PhD,*§ Lari Ha€kkinen, DDS, PhD,jj and Markus Haapasalo, DDS, PhD†

Abstract
Introduction: This study examined the effect of a new bioactive dentin substitute material (Biodentine) on the viability of human gingival fibroblasts. 

Methods: Bio- dentine, White ProRoot mineral trioxide aggregate (MTA), and glass ionomer cement were evaluated. Human gingival fibroblasts were incubated for 1, 3, and 7 days both in the extracts from immersion of set materials in culture medium and directly on the surface of the set materials immersed in culture medium. Fibro- blasts cultured in Dulbecco modified Eagle medium were used as a control group. Cytotoxicity was evaluated by flow cytometry, and the adhesion of human gingival fibroblasts to the surface of the set materials was as- sessed by using scanning electron microscopy. The data of cell cytotoxicity were analyzed statistically by using a one-way analysis of variance test at a signifi- cance level of P < .05. 

Results: Cells exposed to extracts from Biodentine and MTA showed the highest viabilities at all extract concentrations, whereas cells exposed to glass ionomer cement extracts displayed the lowest viabilities (P < .05). There was no significant difference in cell viabilities between Biodentine and MTA during the entire experimental period (P > .05). Human gingival fibroblasts in contact with Biodentine and MTA attached to and spread over the material surface after an overnight culture and increased in numbers after 3 and 7 days of culture. 

Conclusions: Biodentine caused gingival fibroblast reaction similar to that by MTA. Both materials were less cytotoxic than glass ionomer cement. (J Endod 2013;39:478–483)

Key Words
Biocompatibility, Biodentine, calcium silicate–based materials, cell adhesion, cytotoxicity, flow cytometry, glass ionomer, human gingival fibroblast, MTA

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