Dentin Structure, Demineralization and Remineralization

牙本质结构、脱矿和再矿化

基本信息

  • 批准号:
    8373473
  • 负责人:
  • 金额:
    $ 49.73万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2006
  • 资助国家:
    美国
  • 起止时间:
    2006-07-15 至 2017-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Current trends in conservative and minimally invasive dentistry (MID) emphasize the reversal and repair of the active caries process as a first step to restoring the diseased tissue. Enamel remineralization is an accepted phenomenon with established mechanisms, but dentin remineralization strategies are at an early stage of development. Results from the prior period have shown substantial recovery of the hydrated carious tissues mechanical properties, which we have termed "functional remineralization." If functional remineralization can be clinically achieved, it would become a key strategy in MID with the eventual outcome of improved oral health care and lower costs. In support of this goal, , new knowledge on basic biomineralization mechanisms has emerged, and has inspired new approaches that achieve appropriate remineralization within collagen fibrils (intrafibrillar) and between the fibrils (extrafibrillar) to improve the functional remineralization of carious dentin structures. We propose to continue the UCSF-Univ. of Florida collaboration established in the prior period, which will include: Aim 1 a) enhancing the polymer-induced liquid-precursor (PILP) process that has successfully mineralized a variety of collagen matrices, and shown significant functional remineralization of artificial caries lesions. b) extending PILP by potential synergisti approaches including other polyanionic polymers and constant composition methods. c) studying the structure of carious dentin zones to determine their role in limitations of the remineralization process. d) defining microstructural variations in normal and functionally remineralized dentin. Aim 2 evaluates dentin collagen mineralization in model systems including mouse models that lack critical non-collagenous proteins to gain insight into mineralization mechanisms of the collagen scaffold. Aim 3 a) applies the improvements from Aims 1 and insights from Aim 2 to applications in two in vitro models of natural human caries that progressively move towards clinical application. Aim 4 establishes that functional remineralization as indicated by AFM-based nanoindentation testing of hydrated tissue also reflects properties at clinically relevant sizes by use of 4-point bending tests combined with Micro X- ray Computed Tomography. To carry out this work we have established a talented team of SF Bay area investigators from UCSF, LBNL and SSRL, as well as our Florida collaborators who developed the PILP process. The proposed studies will build on our progress and translate the emerging understanding of mechanisms in biomineralization so that we can optimize remineralization kinetics and restoration of dentin caries and move toward a clinically relevant delivery system. Establishing methods to functionally remineralize dentin caries thereby restoring the mechanical properties of the hydrated tissue will minimize conventional restorative treatment and maximize conservation of tooth structure. PUBLIC HEALTH RELEVANCE: Dental caries (tooth decay) is the most common infectious disease and untreated disease ranges from about 20% in children 2-5 years to 26% in adults age 20-64 (http://www.cdc.gov/nchs/FASTATS/dental.htm). Although enamel caries may be remineralized in its early stages, once caries has reached the dentin, the tissue that forms the bulk of the tooth, standard conservative treatments require restoration (drill and fill). This projct develops methods to functionally remineralize dentin caries, restoring the mechanical properties of the hydrated tissue and thereby minimizing conventional restorative treatment and maximizing conservation of tooth structure.
描述(由申请人提供):目前保守和微创牙科(MID)的趋势强调逆转和修复活动性蛀牙过程是恢复病变组织的第一步。牙釉质再矿化是一种公认的现象,其机制已建立,但牙本质再矿化策略尚处于早期发展阶段。前一阶段的结果表明,水化后的龋齿组织的机械性能得到了实质性的恢复,我们称之为“功能性再矿化”。如果功能性再矿化可以在临床上实现,它将成为MID的关键策略,最终结果是改善口腔保健和降低成本。为了支持这一目标,关于基本生物矿化机制的新知识已经出现,并激发了在胶原原纤维(纤维内)和原纤维(纤维外)内实现适当再矿化的新方法,以改善各种牙本质结构的功能性再矿化。我们建议继续ucsf - university。目标1a)增强聚合物诱导的液体前体(PILP)过程,该过程已经成功矿化了多种胶原基质,并显示出人工龋齿病变的显著功能再矿化。b)通过潜在的协同作用方法扩展PILP,包括其他聚阴离子聚合物和恒定组成方法。C)研究龋齿区的结构,以确定它们在再矿化过程中的限制作用。D)定义正常和功能再矿化牙本质的微观结构变化。目的2评估模型系统中牙本质胶原矿化,包括缺乏关键非胶原蛋白的小鼠模型,以深入了解胶原支架的矿化机制。目标3a)将目标1的改进和目标2的见解应用于自然人类龋齿的两种体外模型,逐步走向临床应用。目的4表明,通过使用4点弯曲试验结合微X射线计算机断层扫描,水化组织的基于afm的纳米压痕测试表明的功能性再矿化也反映了临床相关尺寸的特性。为了开展这项工作,我们建立了一个由来自加州大学旧金山分校、LBNL和SSRL的SF海湾地区研究人员组成的天才团队,以及我们开发了PILP过程的佛罗里达合作者。提出的研究将以我们的进展为基础,转化对生物矿化机制的新理解,以便我们能够优化再矿化动力学和牙本质龋的修复,并朝着临床相关的输送系统迈进。建立功能性牙本质龋再矿化的方法,从而恢复水化组织的力学性能,将最大限度地减少传统的修复治疗,最大限度地保护牙齿结构。

项目成果

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LAURIE B GOWER其他文献

LAURIE B GOWER的其他文献

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{{ truncateString('LAURIE B GOWER', 18)}}的其他基金

An In Vitro Model for Studying the Role of Acidic Proteins in Randalls Plaque and
研究酸性蛋白在兰德尔斑块和斑块中作用的体外模型
  • 批准号:
    8295711
  • 财政年份:
    2012
  • 资助金额:
    $ 49.73万
  • 项目类别:
An In Vitro Model for Studying the Role of Acidic Proteins in Randalls Plaque and
研究酸性蛋白在兰德尔斑块和斑块中作用的体外模型
  • 批准号:
    8462971
  • 财政年份:
    2012
  • 资助金额:
    $ 49.73万
  • 项目类别:
An In Vitro Model for Studying the Role of Acidic Proteins in Randalls Plaque and
研究酸性蛋白在兰德尔斑块和斑块中作用的体外模型
  • 批准号:
    8661765
  • 财政年份:
    2012
  • 资助金额:
    $ 49.73万
  • 项目类别:
Dentin Structure, Demineralization and Remineralization
牙本质结构、脱矿和再矿化
  • 批准号:
    8853852
  • 财政年份:
    2006
  • 资助金额:
    $ 49.73万
  • 项目类别:
Dentin Structure, Demineralization and Remineralization
牙本质结构、脱矿和再矿化
  • 批准号:
    8674977
  • 财政年份:
    2006
  • 资助金额:
    $ 49.73万
  • 项目类别:
Dentin Structure, Demineralization and Remineralization
牙本质结构、脱矿和再矿化
  • 批准号:
    8525385
  • 财政年份:
    2006
  • 资助金额:
    $ 49.73万
  • 项目类别:
Role of Biopolymers and Lipids in Kidney Stone Formation
生物聚合物和脂质在肾结石形成中的作用
  • 批准号:
    6341432
  • 财政年份:
    2001
  • 资助金额:
    $ 49.73万
  • 项目类别:
Role of Biopolymers and Lipids in Kidney Stone Formation
生物聚合物和脂质在肾结石形成中的作用
  • 批准号:
    6517941
  • 财政年份:
    2001
  • 资助金额:
    $ 49.73万
  • 项目类别:
Role of Biopolymers and Lipids in Kidney Stone Formation
生物聚合物和脂质在肾结石形成中的作用
  • 批准号:
    6604974
  • 财政年份:
    2001
  • 资助金额:
    $ 49.73万
  • 项目类别:
Role of Biopolymers and Lipids in Kidney Stone Formation
生物聚合物和脂质在肾结石形成中的作用
  • 批准号:
    6766962
  • 财政年份:
    2001
  • 资助金额:
    $ 49.73万
  • 项目类别:

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