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Effect of curing regime on the cytotoxicity of resin-modified glass-ionomer lining cements applied to an odontoblast-cell line

机译:固化方式对成牙本质细胞系中树脂改性的玻璃离聚物衬里水泥细胞毒性的影响

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Objective. The aim of this in vitro study was to evaluate the cytotoxicity of resin-modified glass-ionomer lining cements submitted to different curing regimes and applied to an immortalized odontoblast-cell line (MDPC-23). Methods. Forty round-shaped specimens of each experimental material (Fuji Lining LC and Vitrebond) were prepared. They were light-cured for the manufacturers' recommended time (MRT = 30s), under-cured (0.5 MRT = 15s), over-cured (1.5 MRT = 45s) or allowed to dark cure (0 MRT). Sterilized filter papers soaked with either 5 μL of PBS or HEMA were used as negative and positive control, respectively. After placing the specimens individually in wells of 24-well dishes, odontoblast-like cells MDPC-23 (30,000 cells/cm~2) were plated in each well and incubated for 72h in a humidified incubator at 37℃ with 5% CO_2 and 95% air. The cytotoxicity was evaluated by the cell metabolism (MTT assay) and cell morphology (SEM). Results. Fuji Lining LC was less cytotoxic than Vitrebond (p < 0.05) in all the experimental conditions. However, the cytotoxicity of Fuji Lining LC was noticeably increased in the absence of light-curing while the same was not observed for Vitrebond. The length of light-curing (15, 30 or 45 s) did not influence the toxicity of both lining materials when they were applied on the odontoblast-cell line MDPC-23. Significance. The light-activation plays an important role in reducing the cytotoxicity of Fuji Lining LC. Following the manufacturer' recommendation regarding the light-curing regime may prevent toxic effect to the pulp cells.
机译:目的。这项体外研究的目的是评估提交至不同固化方案并应用于永生化成牙本质细胞系(MDPC-23)的树脂改性玻璃离聚物衬里水泥的细胞毒性。方法。每种实验材料(Fuji Lining LC和Vitrebond)准备了40个圆形样品。将它们在制造商建议的时间里进行光固化(MRT = 30s),固化不足(0.5 MRT = 15s),固化过度(1.5 MRT = 45s)或进行暗固化(0 MRT)。分别用5μLPBS或HEMA浸泡的灭菌滤纸用作阴性和阳性对照。将标本分别放入24孔培养皿的孔中后,将成牙本质细胞样细胞MDPC-23(30,000细胞/ cm〜2)铺在每个孔中,并在37℃,5%CO_2和95的加湿培养箱中孵育72h。 %空气。通过细胞代谢(MTT测定)和细胞形态(SEM)评估细胞毒性。结果。在所有实验条件下,Fuji Lining LC的细胞毒性均比Vitrebond(p <0.05)小。但是,在没有光固化的情况下,Fuji Lining LC的细胞毒性显着增加,而对于Vitrebond则没有观察到。当将两种内衬材料应用于成牙细胞细胞系MDPC-23时,光固化的时间(15、30或45 s)不会影响两种内衬材料的毒性。意义。光活化在降低Fuji Lining LC的细胞毒性中起重要作用。遵循制造商关于光固化方案的建议,可以防止对果肉细胞的毒性作用。

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