A new model for nanoscale enamel dissolution

被引:68
|
作者
Wang, LJ
Tang, RK
Bonstein, T
Orme, CA
Bush, PJ
Nancollas, GH
机构
[1] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Sch Dent Med, Buffalo, NY 14260 USA
[3] Lawrence Livermore Natl Lab, Livermore, CA 94550 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2005年 / 109卷 / 02期
关键词
D O I
10.1021/jp046451d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dissolution kinetics of human tooth enamel surfaces was investigated using nanomolar-sensitive constant composition (CC) and in situ atomic force microscopy (AFM) under simulated caries formation conditions (relative undersaturation with respect to hydroxyapatite = 0.902, pH = 4.5). Scanning electron microscopic (SEM) examination of the resulting etched enamel surfaces showed that deminerzalization, initiated at core/wall interfaces of rods, developed anisotropically along the c-axes. After an initial rapid removal of surface polishing artifacts, the dissolution rate decreased as the reaction proceeded in accordance with our recently proposed crystal dissolution model, resulting in hollow enamel cores and nanosized remaining crystallites, resistant to further dissolution. Generally, dissolution of minerals is regarded as a spontaneous reaction in which all the solid phase can be dissolved in undersaturated solutions However, the dissolution of some biominerals may be suppressed when the crystallites approach nanometer size. This studs shows that CC demineralization of enamel in acidic medium follows this new model that can be used to mimic carious lesion formation. In dissolution studies, nanosized enamel crystallites exhibit a remarkable degree of self-preservation in the fluctuating physiological milieu.
引用
收藏
页码:999 / 1005
页数:7
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