Cytotoxicity and genotoxicity of calcium silicate-based cements on an osteoblast lineage

被引:8
|
作者
Gomes-Cornelio, Ana Livia [1 ]
Rodrigues, Elisandra Marcia [1 ]
Mestieri, Leticia Boldrin [1 ]
Rodrigues Sanzovo Falcoski, Thais de Oliveira [2 ]
Soares, Christiane Pienna [2 ]
Guerreiro-Tanomaru, Juliane Maria [1 ]
Rossa Junior, Carlos [3 ]
Tanomaru-Filho, Mario [1 ]
机构
[1] Univ Estadual Paulista UNESP, Araraquara Sch Dent, Dept Restorat Dent, Araraquara, SP, Brazil
[2] Univ Estadual Paulista UNESP, Dept Clin Anal, Sch Pharmaceut Sci, Araraquara, SP, Brazil
[3] Univ Estadual Paulista UNESP, Dept Diag & Surg, Araraquara Sch Dent, Araraquara, SP, Brazil
来源
BRAZILIAN ORAL RESEARCH | 2016年 / 30卷 / 01期
基金
巴西圣保罗研究基金会;
关键词
Cytotoxicity; Immunologic; Mutagenicity Tests; Calcium Compounds; MINERAL TRIOXIDE AGGREGATE; PORTLAND-CEMENT; IN-VITRO; PHYSICOCHEMICAL PROPERTIES; SEALING ABILITY; BIOCOMPATIBILITY; MTA; DIFFERENTIATION; PROLIFERATION; APOPTOSIS;
D O I
10.1590/1807-3107BOR-2016.vol30.0048
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Several calcium silicate-based biomaterials have been developed in recent years, in addition to Mineral Trioxide Aggregate (MTA). The aim of this study was to evaluate the cytotoxicity, genotoxicity and apoptosis/necrosis in human osteoblast cells (SAOS-2) of pure calcium silicate-based cements (CSC) and modified formulations: modified calcium silicate-based cements (CSCM) and three resin-based calcium silicate cements (CSCR1) (CSCR 2) (CSCR3). The following tests were performed after 24 hours of cement extract exposure: methyl-thiazolyl tetrazolium (MTT), apoptosis/necrosis assay and comet assay. The negative control (CT-) was performed with untreated cells, and the positive control (CT+) used hydrogen peroxide. The data for MTT and apoptosis were submitted to analysis of variance and Bonferroni's posttest (p < 0.05), and the data for the comet assay analysis, to the Kruskal-Wallis and Dunn tests (p < 0.05). The MTT test showed no significant difference among the materials in 2 mg/mL and 10 mg/mL concentrations. CSCR3 showed lower cell viability at 10 mg/mL. Only CSC showed lower cell viability at 50 mg/mL. CSCR1, CSCR2 and CSCR3 showed a higher percentage of initial apoptosis than the control in the apoptosis test, after 24 hours exposure. The same cements showed no genotoxicity in the concentration of 2 mg/mL, with the comet assay. CSC and CSCR2 were also not genotoxic at 10 mg/mL. All experimental materials showed viability with MTT. CSC and CSCR2 presented a better response to apoptosis and genotoxicity evaluation in the 10 mg/mL concentration, and demonstrated a considerable potential for use as reparative materials.
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页数:10
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