Effect of pH on Galla chinensis extract's stability and anti-caries properties in vitro

被引:33
作者
Huang, Xuelian [1 ,2 ,4 ,5 ]
Cheng, Lei [1 ,2 ]
Exterkate, R. A. M. [4 ,5 ]
Liu, Mingdong [3 ]
Zhou, Xuedong [1 ,2 ]
Li, Jiyao [1 ,2 ]
ten Cate, J. M. [4 ,5 ]
机构
[1] Sichuan Univ, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
[2] Sichuan Univ, W China Sch Stomatol, Chengdu 610064, Peoples R China
[3] Sichuan Univ, W China Sch Preclin & Forens Med, Dept Analyt Toxicol, Chengdu 610064, Peoples R China
[4] Free Univ Amsterdam, Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Ctr Dent Amsterdam ACTA, Dept Cariol Endodontol Pedodontol, Amsterdam, Netherlands
基金
中国国家自然科学基金;
关键词
Dental caries; Galla chinensis; Polyphenol; Stability; Demineralization; Polymicrobial biofilms; GREEN TEA CATECHINS; ENAMEL; REMINERALIZATION; FLUORIDE; DEMINERALIZATION; POLYPHENOLS; MICROCOSM; BIOFILMS; LESIONS; GROWTH;
D O I
10.1016/j.archoralbio.2012.04.007
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: Considering that Galla chinensis extract (GCE) solution has a low pH, which might dissolve dental enamel, we investigated the effects of elevation of pH on GCE stability, and on its anti-caries properties. Designs: Stability of GCE solutions, either in H2O (PH less than 4.0) or when buffered at pH 5.5, 7.0 and 10.0, was assessed from UV-VIS spectra. Inhibition of enamel demineralization Was determined in a pH-cycling set up, comprising treatments with either GCE solutions or negative control buffers and acid and neutral buffer immersions. Demineralization was assessed by calcium in the acetate buffers. To determine antimicrobial properties, polymicrobial biofilms were formed after saliva inoculation on glass surfaces which were treated after 48 h. Treatment output parameters were lactic acid formation and viability, the latter by colony forming unit (CFU) counts. Results: At pH 7.0 and higher GCE solutions changed colour and absorption spectra in UV-VIS, indicative of chemical changes. Regarding enamel demineralization, significant inhibitions (P < 0.05) were found for all GCE treatments when compared with corresponding controls. In polymicrobial biofilms, GCE reduced the acid production, compared with the negative controls (P < 0.05). However, this difference was only significant at the lower pH values. Conclusions: GCE solutions were unstable under neutral and alkaline conditions. pH did not significantly influence the inhibiting effect of GCE on enamel demineralization. However, GCE was not effective on polymicrobial biofilms at alkaline pH (8.5). To avoid enamel damage due to acidic treatment, GCE solutions should be used at about pH 5.5. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1093 / 1099
页数:7
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