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首页> 外文期刊>Brazilian Dental Journal >Cytotoxic effects of White-MTA and MTA-Bio cements on odontoblast-like cells (MDPC-23)
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Cytotoxic effects of White-MTA and MTA-Bio cements on odontoblast-like cells (MDPC-23)

机译:White-MTA和MTA-Bio水泥对成牙本质细胞样细胞(MDPC-23)的细胞毒性作用

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This study evaluated the cytotoxic effects of 2 mineral trioxide aggregate (MTA) cements - White-MTA-Angelus and a new formulation, MTA-Bio - on odontoblast-like cell (MDPC-23) cultures. Twenty-four disc-shaped (2 mm diameter x 2 mm thick) specimens were fabricated from each material and immersed individually in wells containing 1 mL of DMEM culture medium for either 24 h or 7 days to obtain extracts, giving rise to 4 groups of 12 specimens each: G1 - White-MTA/24 h; G2 - White-MTA/7 days; G3 - MTA-Bio/24 h; and G4 - MTA-Bio/7 days. Plain culture medium (DMEM) was used as a negative control (G5). Cells at 30,000 cells/cm2 concentration were seeded in the wells of 24-well plates and incubated in a humidified incubator with 5% CO2 and 95% air at 37oC for 72 h. After this period, the culture medium of each well was replaced by 1 mL of extract (or plain DMEM in the control group) and the cells were incubated for additional 2 h. Cell metabolism was evaluated by the MTT assay and the data were analyzed statistically by ANOVA and Tukey's test (α=0.05). Cell morphology and the surface of representative MTA specimens of each group were examined by scanning electron microscopy. There was no statistically significant difference (p>0.05) between G1 and G2 or between G3 and G4. No significant difference (p>0.05) was found between the experimental and control groups either. Similar cell organization and morphology were observed in all groups, regardless of the storage periods. However, the number of cells observed in the experimental groups decreased compared to the control group. MTA-Bio presented irregular surface with more porosities than White-MTA. In conclusion, White-MTA and MTA-Bio presented low cytotoxic effects on odontoblast-like cell (MDPC-23) cultures.
机译:这项研究评估了2种三氧化二矿骨料(MTA)水泥-White-MTA-Angelus和一种新配方MTA-Bio-对成牙本质细胞样细胞(MDPC-23)培养的细胞毒性作用。用每种材料制作二十四个盘状(直径2毫米x厚度2毫米)的标本,并分别浸入含有1 mL DMEM培养基的孔中24 h或7天,以获取提取物,产生4组每个12个样本:G1-白色-MTA / 24小时; G2-白色-MTA / 7天; G3-MTA-Bio / 24小时;和G4-MTA-Bio / 7天。普通培养基(DMEM)用作阴性对照(G5)。将浓度为30,000个细胞/ cm2的细胞接种在24孔板的孔中,并在37°C的5%CO2和95%空气的潮湿培养箱中孵育72小时。在此期间之后,将每个孔的培养基替换为1 mL提取物(或对照组中的普通DMEM),并将细胞再孵育2小时。通过MTT分析评估细胞代谢,并通过ANOVA和Tukey检验(α= 0.05)对数据进行统计学分析。通过扫描电子显微镜检查每组的代表性MTA样品的细胞形态和表面。 G1和G2之间或G3和G4之间没有统计学上的显着差异(p> 0.05)。实验组和对照组之间也没有发现显着差异(p> 0.05)。无论储存时间长短,所有组均观察到相似的细胞组织和形态。但是,与对照组相比,实验组中观察到的细胞数量减少了。 MTA-Bio的不规则表面比White-MTA的孔隙率更高。总之,White-MTA和MTA-Bio对成牙本质细胞样细胞(MDPC-23)培养的细胞毒性较低。

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