QUANTITATION OF ENAMEL DEMINERALIZATION MECHANISMS
牙釉质脱矿机制的定量
基本信息
- 批准号:6497911
- 负责人:
- 金额:$ 21.38万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1982
- 资助国家:美国
- 起止时间:1982-11-01 至 2006-01-31
- 项目状态:已结题
- 来源:
- 关键词:X ray crystallography acidity /alkalinity apatites calcification calcium carbonates chemical kinetics chemical synthesis crystallization dentin fluoride ion human tissue hydroxyapatites infrared spectrometry minerals precipitation scanning electron microscopy solubility statistics /biometry stoichiometry strontium temperature tooth enamel
项目摘要
DESCRIPTION (Adapted from the Investigator's Abstract): The long term
objectives of the proposed research are to gain a better understanding of the
mechanisms of dental caries and to provide rational bases for improved
preventive or therapeutic regimens. The Principal Investigator proposes to do
basic studies of the anomalous solubility behavior of carbonated apatites
(CAPs) and human dental enamel (HE) with the general objective of establishing
how the solubility depends on the composition of the mineral phase, the
crystallinity of the mineral phase, an the composition of the external
dissolution medium. The studies will rely heavily on the metastable equilibrium
solubility (MES) distribution paradigm and the surface complex hypothesis
developed just prior to the beginning of the past project period. The MES and
the surface complex concepts have dictated entirely new approaches to both
experimental design and data interpretation and have provided the framework for
understanding the interrelationship between mineral composition, mineral
crystallinity, solution composition and the observed solubility of biominerals
and synthetic apatites. There are four specific aims. Aim 1 proposes studies to
establish for the CAPs the quantitative relationships between the magnitude of
the MES, the CAP crystallinity (especially crystallite microstrain), and
carbonate content, and the stoichiometry of the MES governing surface complex.
In Aim 2, studies are proposed to quantitatively establish the influence of
solution foreign ions (strontium and fluoride) on the magnitude of the MES and
the stoichiometry of the MES governing surface complex. In Aim 3, studies are
proposed to quantitatively establish the possible crystal lattice effects of
these foreign ions on the magnitude of the MES. Aim 4 proposes to establish the
relevance of the findings in the CAP studies (above) to the solubility behavior
of HE. Two major experimental breakthroughs of the past project period make it
possible for accomplishing these aims. The first of these is a procedure of
relatively high accuracy for deducing the dissolution driving force function
(and therefore the stoichiometry of the MES governing surface complete) from
analysis of the MES distribution data obtained as a function of several
independent variables (e.g., buffer pH, solution common ions, and solution
foreign ions). The other is a procedure for separating and quantifying the
contributions of crystallite size and microstrain to CAP crystallinity using
X-ray diffraction data and the Rietveld method of whole-pattern-fitting
structure-refinement. Taken together, these two methods permit addressing the
questions associated with each of the Specific Aims.
描述(改编自研究者摘要):长期
拟议研究的目标是更好地了解
探讨龋病的发病机制,为龋病的防治提供理论依据。
预防或治疗方案。主要研究者建议
碳磷灰石溶解度异常行为的基础研究
(CAP)和人牙釉质(HE)的总体目标是建立
溶解度如何取决于矿物相的组成,
矿物相的结晶度,以及外部
溶出介质这些研究将在很大程度上依赖于亚稳平衡
溶解度(MES)分布范式和表面络合物假说
就在上一个项目期开始之前开发的。MES和
表面复杂的概念已经决定了全新的方法,
实验设计和数据解释,并提供了框架,
了解矿物成分、矿物
结晶度、溶液组成和观察到的生物矿物溶解度
和合成磷灰石。有四个具体目标。目标1建议开展研究,
为CAP建立数量关系,
MES、CAP结晶度(尤其是微晶微应变),以及
碳酸盐含量和MES控制表面络合物的化学计量。
在目标2中,建议进行研究,以定量确定
溶液外来离子(锶和氟化物)对MES的影响,
MES控制表面复合物的化学计量。在目标3中,
建议定量建立可能的晶格效应,
这些外来离子对MES的影响。目标4建议建立
CAP研究(上文)中的发现与溶解度行为的相关性
他的。过去项目期间的两大实验突破使其成为
有可能实现这些目标。其中第一个是一个程序,
推导溶解驱动力函数的精度较高
(and因此,MES调节表面的化学计量完成),
分析作为几个函数获得的MES分布数据,
独立变量(例如,缓冲液pH值、溶液常见离子和溶液
外来离子)。另一个是分离和定量的程序,
微晶尺寸和微应变对CAP结晶度的贡献,
X射线衍射数据和Rietveld全谱拟合方法
结构细化总之,这两种方法允许解决
与每个具体目标相关的问题。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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William I Higuchi其他文献
William I Higuchi的其他文献
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{{ truncateString('William I Higuchi', 18)}}的其他基金
Novel Method for the Ocular Iontophoretic Delivery of Avastin and Lucentis
眼部电离子导入阿瓦斯汀和雷珠单抗的新方法
- 批准号:
7927575 - 财政年份:2010
- 资助金额:
$ 21.38万 - 项目类别:
TRANSDERMAL IONTOPHORESIS AND POLYPEPTIDE DELIVERY
透皮离子电渗疗法和多肽输送
- 批准号:
2608906 - 财政年份:1989
- 资助金额:
$ 21.38万 - 项目类别:
TRANSDERMAL IONTOPHORESIS AND POLYPEPTIDE DELIVERY
透皮离子电渗疗法和多肽输送
- 批准号:
2022341 - 财政年份:1989
- 资助金额:
$ 21.38万 - 项目类别:
TRANSDERMAL IONTOPHORESIS AND POLYPEPTIDE DELIVERY
透皮离子电渗疗法和多肽输送
- 批准号:
2181850 - 财政年份:1989
- 资助金额:
$ 21.38万 - 项目类别:














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