Antonella Castellanos Caroprese, Alexa Nicolle Chinchilla Navarrete, Sandra Janeth Gutiérrez Prieto, Jean Carlos Villamil, Octavio Alejandro Castañeda Uribe, Juan Carlos Salcedo Reyes, And Henry Alberto Méndez Pinzón
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引用次数: 0
摘要
关于粘接剂对牙髓组织的细胞毒性作用的研究尚无定论。为了指出这些材料在临床使用中是否安全,我们使用实验装置模拟了牙髓与粘接剂的体内暴露,在该实验装置中,人牙髓干细胞(hDPSC)通过牙本质屏障暴露于两种粘接剂(自酸洗粘接剂和两步粘接剂)的作用下。通过 MTT 检测协议和荧光显微镜评估了这些细胞的细胞毒性效应,并将其结果与单个 hDPSC 的拉曼光谱结果进行了对比。总体而言,综合使用所有技术均未观察到明显的细胞毒性效应,在牙本质屏障厚度至少为 1 毫米的情况下,细胞存活率接近 90%。此外,拉曼光谱还能检测到一些暴露于两步粘接剂的牙髓细胞的 DNA 结构损伤,这表明该技术可被视为一种补充工具,具有评估细胞存活率以外的细胞毒性的潜力。
Cytotoxic effects on human dental pulp stem Cells after exposure to adhesive bonding agents.
Studies regarding cytotoxic effects attributed to the use of adhesive bonding agents on pulp tissue are not conclusive. To point out whether these materials are safe for clinical use, in vivo exposure of dental pulp to adhesive bonding agents was simulated using an experimental setup in which Human Dental Pulp Stem Cells (hDPSC) are exposed to the action of two kinds of adhesives: self-etching adhesives and two-step bonding agents through a dentine barrier. Cytotoxic effects on these cells were evaluated by MTT assay protocol and fluorescence microscopy, and their results were contrasted to those obtained through Raman spectra taken on single hDPSCs. Overall, no significant cytotoxic effects were observed by combining all the techniques, and cell viability close to 90% was achieved for a dentine barrier of at least 1 mm thick. Moreover, Raman spectroscopy was able to detect structural DNA damage in some dental pulp cells when exposed to two-step bonding agents, suggesting that this technique could be considered a complementary tool with the potential to evaluate cell toxicity beyond cell viability.