吉林大学学报(医学版) ›› 2021, Vol. 47 ›› Issue (5): 1116-1123.doi: 10.13481/j.1671-587X.20210506

• 基础研究 • 上一篇    下一篇

肉桂醛抗菌粘接剂的制备及其抗菌性能评价

王晗,田子璐,朱轩言,杨宇斌,朱松()   

  1. 吉林大学口腔医院修复科,吉林 长春 130021
  • 收稿日期:2020-12-29 出版日期:2021-09-28 发布日期:2021-10-26
  • 通讯作者: 朱松 E-mail:zhusong1965@163.com
  • 作者简介:王 晗(1994-),女,吉林省松原市人,在读硕士研究生,主要从事口腔修复材料方面的研究。
  • 基金资助:
    国家自然科学基金项目(82071163)

Preparation of cinnamaldehyde antibacterial adhesive and evaluation on its antibacterial property

Han WANG,Zilu TIAN,Xuanyan ZHU,Yubin YANG,Song ZHU()   

  1. Department of Prosthodontics,Stomatology Hospital,Jilin University,Changchun 130021,China
  • Received:2020-12-29 Online:2021-09-28 Published:2021-10-26
  • Contact: Song ZHU E-mail:zhusong1965@163.com

摘要: 目的

制备一种含肉桂醛的抗菌牙本质粘接剂,并对粘接剂的抗菌性能、体外细胞毒性和即刻粘接性能进行评价。

方法

选择变异链球菌进行实验。以微量肉汤稀释法测定肉桂醛的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)。将肉桂醛以质量分数2%、4%、6%和8%的比例加入商品粘接剂Single Bond 2(SB2)中均匀混合制备抗菌粘接剂,以SB2作为对照组,制备试件。试件与细菌共培养,平板菌落计数法测定试件表面细菌黏附数量并计算抗菌率;对试件表面黏附的细菌进行细菌活/死细菌染色实验,观察试件表面黏附细菌状态。试件与细胞培养液共同孵育24 h制备浸提液,采用MTT法测定粘接剂的体外细胞毒性,评价其细胞毒性等级。在此基础上,选取有明显抗菌性能的实验组,采用微拉伸实验测定粘接剂的微拉伸强度,评价其即刻粘接性能。

结果

肉桂醛的MIC和MBC均为250 mg·L-1,肉桂醛具有良好的抗菌效果。肉桂醛的质量分数为4%、6%和8%时,粘接剂的抗菌率均高于99%。体外细胞毒性实验,在相同的稀释倍数下,与对照组比较,抗菌粘接剂的细胞毒性等级均未升高。微拉伸实验,依据抗菌实验的结果,选取质量分数4%、6%和8%肉桂醛组进行实验,与对照组比较,质量分数4%、6%和8%肉桂醛组微拉伸强度差异无统计学意义(P>0.05)。

结论

肉桂醛具有良好的抗菌性能;在商品粘接剂SB2中,肉桂醛的质量分数高于4%时,抗菌粘接剂具有明显的抗菌性能,其体外细胞毒性和即刻粘接性能未受影响。

关键词: 肉桂醛, 粘接剂, 抗菌性能, 体外细胞毒性, 微拉伸强度

Abstract: Objective

To prepare a antibacterial dentin adhesive containing cinnamaldehyde, and to evaluate the antibacterial properties, in vitro cytotoxicity and instant adhesive properties of the adhesive.

Methods

The Streptococcus mutans were selected for experiment. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of cinnamaldehyde were determined by the micro broth dilution method. Cinnamaldehyde was added to the commercial adhesive Single Bond 2(SB2) in the mass fractions of 2%, 4%, 6%, and 8% to prepare the antibacterial adhesive. The commercial adhesive SB2 was used as control groups; the specimens were prepared and they were co-cultured with the bacteria. The plate colony counting method was used to determine the number of bacteria attached to the surface of the specimens and the antibacterial rates were calculated; the bacteria attached to the surface of the specimens were subjected to live/dead bacterial staining experiments to observe the state of bacteria attached to the surface of the specimens. The adhesive was incubated with the cell culture solution for 24 h to prepare the extract. The MTT method was used to determine the in vitro cytotoxicity of the adhesive and its cytotoxicity level was evaluated. On this basis, an experimental group with significant antibacterial properties was selected, and the micro-tensile test was used to measure the micro-tensile strength of the adhesive and evaluate its immediate adhesive performance.

Results

The MIC and MBC of cinnamaldehyde were both 250 mg·L-1, and cinnamaldehyde had a good antibacterial effect; when the mass fractions of cinnamaldehyde were 4%, 6% and 8%, the antibacterial rates of the adhesive were all higher than 99%. In the in vitro cytotoxicity experiment, under the same dilution ratio, compared with control group, the cytotoxicity level of the antimicrobial adhesive did not change significantly. According to the results of the antibacterial experiment, 4%, 6%, and 8% cinnamaldehyde groups were selected for the micro-tensile experiment. Compared with control group,the micro-tensile strengths in 4%,6% and 8% cinnamaldehyde groups had no statistically significant differences(P>0.05).

Conclusion

Cinnamaldehyde has good antibacterial properties; when the mass fraction of cinnamaldehyde in the commercial adhesive SB2 is higher than 4%, the antibacterial adhesive has significant antibacterial properties, and its in vitro cytotoxicity and immediate bonding properties are not affected.

Key words: cinnamaldehyde, adhesive, antibacterial property, in vitro cytotoxicity, micro-tensile strength

中图分类号: 

  • R783.1