Antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers on oral pathogens
Antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers on oral pathogens
复制标题
两种新型交联抗菌单体对口腔病原体的抗菌活性和细胞毒性
DOI:
10.1016/j.archoralbio.2010.10.011
复制
发表时间:
2011-04-01
影响因子:
3
通讯作者:
Chen, Ji-hua
中科院分区:
文献类型:
--
作者:
Huang, Li;Xiao, Yu-hong;Chen, Ji-hua
Objectives: The antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers, 2-methacryloxylethyl dodecyl methyl ammonium bromide (MAE-DB) and 2-methacryloxylethyl hexadecyl methyl ammonium bromide (MAE-HB) were tested in this study.Design: The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of unpolymerized MAE-DB and MAE-HB against eight strains of oral bacteria were tested using a broth dilution test. Time-kill determinations were performed to examine the kinetics of unpolymerized MAE-DB and MAE-HB against Streptococcus mutans UA159 and Streptococcus sanguinis ATCC6715. Bacterial morphology was observed using a field emission scanning electron microscope (Fe-SEM). The cytotoxicity of unpolymerized two new monomers and Bis-GMA on the human gingival fibroblast cell line H2620 was assessed using a methyl thiazolyl tetrazolium assay.Results: Unpolymerized MAE-DB and MAE-HB showed strong bactericidal activity against oral bacteria. The MBC value of MAE-DB ranged from 12.2 to 24.4 mu g/ml and the MBC value of MAE-HB ranged from 6.2 to 48.8 mu g/ml. Time-kill determinations indicated that unpolymerized MAE-DB and MAE-HB had rapid killing effects against S. mutans UA159 and S. sanguinis ATCC6715 at the concentration of 4x MBC. The Fe-SEM observation showed that MAE-DB and MAE-HB could disturb the integrity of bacteria and cause lysis of bacterial cells. The median lethal concentration values on human gingival fibroblast for both monomers were between 10 and 20 mu g/ml, and greater than that of Bis-GMA.Conclusions: Unpolymerized MAE-DB and MAE-HB monomers had strong bactericidal activity against eight strains of oral bacteria. Their cytotoxicities were less than that of Bis-GMA. (C) 2010 Elsevier Ltd. All rights reserved.