Trindade F Z, Ribeiro A P D, Sacono N T, Oliveira C F, Lessa F C R, Hebling J, Costa C A S
Departments of Dental Materials and Prosthodontics, Araraquara School of Dentistry, São Paulo State University, Araraquara, SP, Brazil.
Int Endod J. 2009 Jun;42(6):516-24. doi: 10.1111/j.1365-2591.2009.01544.x.
To evaluate the trans-enamel and trans-dentinal cytotoxic effects of a 35% H(2)O(2) bleaching gel on an odontoblast-like cell lines (MDPC-23) after consecutive applications.
Fifteen enamel/dentine discs were obtained from bovine central incisor teeth and placed individually in artificial pulp chambers. Three groups (n = 5 discs) were formed according to the following enamel treatments: G1: 35% H(2)O(2) bleaching gel (15 min); G2: 35% H(2)O(2) bleaching gel (15 min) + halogen light (20 s); G3: control (no treatment). After repeating the treatments three consecutive times, the extracts (culture medium + gel components that had diffused through enamel/dentine discs) in contact with the dentine were collected and applied to previously cultured MDPC-23 cells (50 000 cells cm(-2)) for 24 h. Cell metabolism was evaluated by the MTT assay and data were analysed statistically (alpha = 5%; Kruskal-Wallis and Mann-Whitney U-test). Cell morphology was analysed by scanning electron microscopy.
Cell metabolism decreased by 92.03% and 82.47% in G1 and G2 respectively. G1 and G2 differed significantly (P < 0.05) from G3. Regardless of halogen light activation, the application of the bleaching gel on the cultured odontoblast-like cells caused significantly more severe cytotoxic effects than those observed in the nontreated control group. In addition, significant morphological cell alterations were observed in G1 and G2.
After three consecutive applications of a 35% H(2)O(2) bleaching agent, the diffusion of the gel components through enamel and dentine caused severe toxic effects to cultured pulp cells.
评估35%过氧化氢漂白凝胶连续应用后对成牙本质细胞样细胞系(MDPC - 23)的穿釉质和穿牙本质细胞毒性作用。
从牛的中切牙获取15个釉质/牙本质盘,并分别置于人工牙髓腔中。根据以下釉质处理方式分为三组(每组n = 5个盘):G1:35%过氧化氢漂白凝胶(15分钟);G2:35%过氧化氢漂白凝胶(15分钟)+卤素灯照射(20秒);G3:对照组(未处理)。连续重复处理三次后,收集与牙本质接触的提取物(培养基+通过釉质/牙本质盘扩散的凝胶成分),并将其应用于先前培养的MDPC - 23细胞(50000个细胞/cm²)24小时。通过MTT法评估细胞代谢,并对数据进行统计学分析(α = 5%;Kruskal - Wallis检验和Mann - Whitney U检验)。通过扫描电子显微镜分析细胞形态。
G1组和G2组细胞代谢分别下降了92.03%和82.47%。G1组和G2组与G3组有显著差异(P < 0.05)。无论是否有卤素灯激活,在培养的成牙本质细胞样细胞上应用漂白凝胶所产生的细胞毒性作用比未处理的对照组明显更严重。此外,在G1组和G2组中观察到明显的细胞形态改变。
35%过氧化氢漂白剂连续应用三次后,凝胶成分通过釉质和牙本质的扩散对培养的牙髓细胞产生了严重的毒性作用。