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人类牙齿矿物质的溶解性特性与龋齿的发病机制

Solubility properties of human tooth mineral and pathogenesis of dental caries.

作者信息

Aoba T

机构信息

Department of Pathology, The Nippon Dental University, Tokyo, Japan.

出版信息

Oral Dis. 2004 Sep;10(5):249-57. doi: 10.1111/j.1601-0825.2004.01030.x.

Abstract

Dental research over the last century has advanced our understanding of the etiology and pathogenesis of caries lesions. Increasing knowledge of the dynamic demineralization/remineralization processes has led to the current consensus that bacteria-mediated tooth destruction can be arrested or even to some degree reversed by adopting fluoride and other preventive measures without using restorative materials. Our experimental approach provided new insight into the stoichiometries and solubility properties of human enamel and dentin mineral. The determination of the solubility product constant on the basis of the stoichiometric model (Ca)5.x(Mg)q(Na)u(HPO4)v(CO3)w(PO4)3.y(OH,F)1.z, verifies the difference in their solubility properties, supporting the phase transformation between tooth mineral and calcium phosphates in a wide range of fluid compositions as found in the oral environment. Further refinement of the stoichiometry and solubility parameters is essential to assess quantitatively the driving force for de- and remineralization of enamel and dentin in the oral fluid environment. Prediction of the effects of a combination of inhibitors and accelerator(s) on remineralization kinetics is also required. In order to develop devices efficient for optimizing remineralization in the lesion body, it is a critical question how, and to what extent, fluoride can compensate for the activity of any inhibitors in the mineralizing media.

摘要

过去一个世纪的牙科研究增进了我们对龋损病因和发病机制的理解。对动态脱矿/再矿化过程的了解不断增加,使得目前人们达成共识:通过采取氟化物及其他预防措施,不使用修复材料,细菌介导的牙齿破坏可以得到阻止,甚至在一定程度上得以逆转。我们的实验方法为人类牙釉质和牙本质矿物质的化学计量和溶解性提供了新的见解。基于化学计量模型(Ca)5.x(Mg)q(Na)u(HPO4)v(CO3)w(PO4)3.y(OH,F)1.z确定溶度积常数,验证了它们溶解性的差异,支持了牙齿矿物质与磷酸钙在口腔环境中多种流体成分下的相变。进一步完善化学计量和溶解度参数对于定量评估口腔液体环境中牙釉质和牙本质脱矿和再矿化的驱动力至关重要。还需要预测抑制剂和促进剂组合对再矿化动力学的影响。为了开发能够有效优化病变体内再矿化的装置,氟化物如何以及在多大程度上能够补偿矿化介质中任何抑制剂的活性是一个关键问题。

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