EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
基本信息
- 批准号:6697114
- 负责人:
- 金额:$ 20.81万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-02-01 至 2006-01-31
- 项目状态:已结题
- 来源:
- 关键词:X ray crystallographybiomaterial interface interactionbiomaterialscalcium ioncell differentiationcell proliferationdental implantsfibronectinsflow cytometryhydroxyapatitesinfrared spectrometryinterferometrylaboratory rabbitlaboratory ratmedical implant sciencenucleic acid probesoligonucleotidesosteoblastsosteogenesisosteopontinphosphatespolymerase chain reactiontitanium
项目摘要
DESCRIPTION (Verbatim from the Applicant): The goal of this research is to gain
a better understanding of the biological basis for successful orthopaedic and
dental implant therapy by elucidating the early phenomena that govern
osseointegration. In this proposal, the effect of sputtered hydroxyapatite (HA)
crystallinity on early bone cell activity in vitro and in vivo will be
investigated under highly controlled and defined conditions. Our overall
hypothesis is that, under conditions where other variables are controlled, the
degree of crystallinity of the HA surface directly affects early bone cell
activity in vitro and the rate of development of osseointegration in vivo. The
objective of this study is to correlate the effect of characterized HA
crystallinity to dissolution and protein adsorption, bone cell response in
vitro and early cell activities in vivo. In this proposal, Aim 1 will be to
determine the relationship between crystalline content of well-characterized HA
surfaces and 1) the adsorption of specific extracellular matrix proteins,
fibronectin and osteopontin, and 2) the rate of dissolution of the surface. The
HA and Ti coatings will be produced using sputter coating. The rationale for
using the sputtering technology is due to the high coating-metal adhesion
strength compared to plasma spraying. Protein adsorption and dissolution of the
coatings will be measured over time. Aim 2 will determine the extent to which
the crystalline content of HA surfaces effects osteoblast proliferation,
differentiation, and metabolism in vitro. It is hypothesized in this aim that
because osteoblast proliferation and differentiation may be affected by either
the adsorption of specific extracellular matrix proteins, fibronectin and
osteopontin, or the rate of dissolution of the surface, or both; metabolic
activity leading to mineral formation will vary with the crystalline content of
the HA surface. Implicit in this hypothesis is there exists an optimal
crystalline content of an HA surface for the promotion of bone formation
activity. Aim 3 will evaluate the extent to which the crystalline content of HA
surfaces affects osseointegration in vivo. Early bone activity will be
evaluated using histology, mechanical strength and immunohistochemistry in this
aim. Data generated from this study will provide information on the early
maturation of bone cells in the presence of implant biomaterials and will
provide a correlation between biomaterial properties and bone cell responses in
vitro and in vivo. Additionally, information generated will contribute to the
development of an ideal implant surface, thereby reducing long-term implant
failures.
描述(申请人逐字记录):本研究的目标是获得
更好地了解成功矫形外科和
通过阐明控制牙种植体治疗的早期现象
骨整合。在该提案中,溅射羟基磷灰石(HA)的效果
结晶度对体外和体内早期骨细胞活性的影响
在高度控制和明确的条件下进行研究。我们的整体
假设是,在控制其他变量的条件下,
HA表面的结晶度直接影响早期骨细胞
体外活性和体内骨整合的发育速率。这
本研究的目的是关联特征化 HA 的效果
结晶度溶解和蛋白质吸附,骨细胞反应
体外和体内早期细胞活动。在本提案中,目标 1 是
确定表征良好的 HA 晶体含量之间的关系
表面和 1) 特定细胞外基质蛋白的吸附,
纤连蛋白和骨桥蛋白,2) 表面溶解速率。这
HA 和 Ti 涂层将使用溅射涂层生产。理由
使用溅射技术是由于涂层与金属的附着力高
与等离子喷涂相比的强度。蛋白质的吸附和溶解
涂层将随着时间的推移进行测量。目标 2 将确定在多大程度上
HA表面的结晶含量影响成骨细胞增殖,
体外分化和代谢。在此目标中假设
因为成骨细胞的增殖和分化可能受到以下任一因素的影响
特定细胞外基质蛋白、纤连蛋白和
骨桥蛋白,或表面溶解速率,或两者;新陈代谢的
导致矿物形成的活性将随晶体含量的变化而变化
HA 表面。这个假设隐含的是存在一个最优的
HA 表面的结晶含量可促进骨形成
活动。目标 3 将评估 HA 结晶含量的程度
表面影响体内骨整合。早期骨骼活动将
使用组织学、机械强度和免疫组织化学进行评估
目的。这项研究产生的数据将提供有关早期研究的信息
骨细胞在植入生物材料存在的情况下成熟,并将
提供生物材料特性和骨细胞反应之间的相关性
体外和体内。此外,生成的信息将有助于
形成理想的种植体表面,从而减少长期种植
失败。
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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{{ truncateString('JOO L. ONG', 18)}}的其他基金
Sacrificial templated grafts to encourage bone healing through mechanotransduction
牺牲模板移植物通过机械传导促进骨愈合
- 批准号:
10811305 - 财政年份:2023
- 资助金额:
$ 20.81万 - 项目类别:
EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
- 批准号:
7285398 - 财政年份:2001
- 资助金额:
$ 20.81万 - 项目类别:
EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
- 批准号:
6863766 - 财政年份:2001
- 资助金额:
$ 20.81万 - 项目类别:
EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
- 批准号:
6259343 - 财政年份:2001
- 资助金额:
$ 20.81万 - 项目类别:
EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
- 批准号:
6497421 - 财政年份:2001
- 资助金额:
$ 20.81万 - 项目类别:
EARLY BONE FORMATION AT BONE BIOMATERIAL INTERFACE
骨生物材料界面的早期骨形成
- 批准号:
6628107 - 财政年份:2001
- 资助金额:
$ 20.81万 - 项目类别:
HA AND TI COATINGS ON BONE/IMPLANT INTERACTIONS
HA 和 TI 涂层对骨/种植体相互作用的影响
- 批准号:
2897156 - 财政年份:1998
- 资助金额:
$ 20.81万 - 项目类别:
HA AND TI COATINGS ON BONE/IMPLANT INTERACTIONS
HA 和 TI 涂层对骨/种植体相互作用的影响
- 批准号:
2703647 - 财政年份:1998
- 资助金额:
$ 20.81万 - 项目类别:














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