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研究当前牙本质粘结剂对人牙髓细胞的细胞毒性作用。

Investigation of the cytotoxic effect of current dentine bonding agents on human dental pulp cells.

机构信息

Faculty of Dentistry, Department of Pedodontics, Istanbul University, İstanbul, Turkey.

Private Pediatric Dentist, İstanbul, Turkey.

出版信息

BMC Oral Health. 2024 Oct 10;24(1):1207. doi: 10.1186/s12903-024-04985-1.

Abstract

BACKGROUND

An ideal aesthetic restorative material should be attached to the tooth tissues by adhesion, have a smooth surface as possible, should not cause toxic reactions in the pulp and discoloration and microleakage. This study aims at comparatively assess the cytotoxicity of current adhesive systems on human dental pulp cells.

MATERIALS AND METHODS

The adequate density of human pulp cells was observed from the ready cell line. The passaging was performed and the 3rd passage cells were selected. Adhesive systems and MTA were used on the cultures. Trypan blue staining was conducted on the cells at the 1st, 2nd, 3rd days and a count of live and dead cells using a light microscope. The dead cells whose membrane integrity was impaired by staining with trypan blue and the viability rate was determined using live and dead cell numbers. Data analysis was performed using IBM SPSS Statistics 22.

RESULTS

A significant difference in vialibity rates between adhesive systems was observed on the first day. No significant statistical differences were observed on the 2nd and 3rd days (p < 0.05).

CONCLUSION

Futurabond M showed similar biocompatibility with MTA on human pulp cells and it can be applied in cavities with 1-1.5 mm hard tissue between pulp and dentine.

摘要

背景

理想的美学修复材料应通过黏附附着在牙齿组织上,表面尽可能光滑,不应在牙髓中引起毒性反应、变色和微渗漏。本研究旨在比较评估当前几种黏接系统对人牙髓细胞的细胞毒性。

材料与方法

从现成的细胞系中观察到足够密度的人牙髓细胞。进行传代,选择第 3 代细胞。将黏接系统和 MTA 应用于培养物上。在第 1、2、3 天使用台盼蓝染色对细胞进行染色,并使用相差显微镜对活细胞和死细胞进行计数。使用 IBM SPSS Statistics 22 进行数据分析。

结果

第 1 天,黏接系统之间的存活率有显著差异。第 2 和第 3 天无显著统计学差异(p < 0.05)。

结论

Futurabond M 对人牙髓细胞具有与 MTA 相似的生物相容性,可应用于牙髓和牙本质之间有 1-1.5mm 硬组织的窝洞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4571/11468065/6c55cdc5fe46/12903_2024_4985_Fig1_HTML.jpg

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