I-Corps: Development of a bioengineered organic matrix for enhanced bone regeneration

I-Corps:开发生物工程有机基质以增强骨再生

基本信息

  • 批准号:
    1462613
  • 负责人:
  • 金额:
    $ 5万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-11-01 至 2016-04-30
  • 项目状态:
    已结题

项目摘要

Currently, synthetic bone substitutes are poorly designed materials that do not effectively induce new bone formation. Use of these products increases risk of delayed bone healing. Bone matrix proteins (BMPs) stimulate new bone formation, but are expensive and are known to cause adverse effects in patients, as documented recently by the FDA. The team has developed a cost-effective, organic biomaterial for enhanced bone mineralization and orthopedic regeneration. Through the use of an innovative, materials design approach employing the aforementioned bone proteins, this project aims at commercializing a new class of hybrid organic matrices that can significantly enhance the growth of new bone tissue. The development of the bone substitute seeks to shift paradigms in orthopedic regenerative medicine. The success of this work will usher in a new class of bioengineered matrices that safely induce new bone formation and prevent occurrence of non-unions. An increased efficacy in bone grafting procedures will directly translate to lowered hospitals costs and better patient outcomes.Non-collagenous proteins (NCPs) osteocalcin (OC) and osteopontin (OPN) are building blocks of bone, and are released by cells into the extracellular environment during the mineralization process, where they are incorporated into the matrix due to their affinity for bone mineral. OC and OPN are considered powerful regulators of bone matrix quality, strongly influencing mechanical integrity of bone. NCPs function as link proteins connecting the collagen and mineral phases of bone matrix together, and as regulators of bone mineral properties. The self-healing potential of NCPs due, to their interactions with both, the mineral and collagen phases in bone matrix, makes them ideal candidates to explore in the field of orthopedic regeneration. By providing the body with these building blocks of bone, the team seeks to achieve enhanced mineralization and accelerated bone regeneration. The team is fabricating and characterizing collagen-based matrices containing NCPs that now need to be characterized and tested for efficacy through in vitro and in vivo studies. Preliminary conversations with clinicians and angel investors, have led the team to believe that a successful test of efficacy will be a significant milestone in the commercialization of its innovation.
目前,合成骨替代材料设计不良,不能有效诱导新骨形成。使用这些产品会增加骨愈合延迟的风险。正如 FDA 最近记录的那样,骨基质蛋白 (BMP) 会刺激新骨形成,但价格昂贵,而且已知会对患者造成不良影响。该团队开发了一种具有成本效益的有机生物材料,用于增强骨矿化和骨科再生。通过采用上述骨蛋白的创新材料设计方法,该项目旨在将新型混合有机基质商业化,该基质可以显着促进新骨组织的生长。 骨替代品的开发旨在改变骨科再生医学的范式。这项工作的成功将带来一类新型生物工程基质,可以安全地诱导新骨形成并防止骨不连的发生。骨移植手术效率的提高将直接转化为降低医院成本和改善患者预后。非胶原蛋白 (NCP)、骨钙素 (OC) 和骨桥蛋白 (OPN) 是骨的组成部分,在矿化过程中被细胞释放到细胞外环境中,由于它们对骨矿物质的亲和力,它们被纳入基质中。 OC 和 OPN 被认为是骨基质质量的强大调节剂,强烈影响骨的机械完整性。 NCP 充当将骨基质的胶原蛋白和矿物质相连接在一起的连接蛋白,并作为骨矿物质特性的调节剂。 由于 NCP 与骨基质中的矿物质和胶原相相互作用,NCP 具有自愈潜力,使其成为骨科再生领域探索的理想候选者。通过为身体提供这些骨骼构建块,该团队力求实现增强矿化和加速骨骼再生。 该团队正在制造和表征含有 NCP 的胶原蛋白基质,现在需要通过体外和体内研究来表征和测试其功效。 与临床医生和天使投资者的初步对话使团队相信,成功的功效测试将成为其创新商业化的一个重要里程碑。

项目成果

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Deepak Vashishth其他文献

Advanced glycation and glycoxidation end products in bone
骨中的晚期糖基化终末产物和糖氧化终末产物
  • DOI:
    10.1016/j.bone.2023.116880
  • 发表时间:
    2023-11-01
  • 期刊:
  • 影响因子:
    3.600
  • 作者:
    Bowen Wang;Deepak Vashishth
  • 通讯作者:
    Deepak Vashishth
Influence of phase angle between axial and torsional loadings on fatigue fractures of bone.
轴向和扭转载荷之间的相位角对骨疲劳断裂的影响。
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    2.4
  • 作者:
    W. T. George;Deepak Vashishth
  • 通讯作者:
    Deepak Vashishth
A tribute to Robert L. Spilker
Stress fracture of bone under physiological multiaxial cyclic loading: Activity-based predictive models
  • DOI:
    10.1016/j.bone.2024.117279
  • 发表时间:
    2025-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Winson T. George;Shayom Debopadhaya;Samuel J. Stephen;Bryan A. Botti;David B. Burr;Deepak Vashishth
  • 通讯作者:
    Deepak Vashishth
Trabecular Shear Stresses Predict In Vivo Linear Microcrack Density but not Diffuse Damage in Human Vertebral Cancellous Bone
  • DOI:
    10.1114/1.1569264
  • 发表时间:
    2003-06-01
  • 期刊:
  • 影响因子:
    5.400
  • 作者:
    Yener N. Yeni;Fu J. Hou;Traci Ciarelli;Deepak Vashishth;David P. Fyhrie
  • 通讯作者:
    David P. Fyhrie

Deepak Vashishth的其他文献

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{{ truncateString('Deepak Vashishth', 18)}}的其他基金

A New Self-healing Mechanism and its Impact on Multiscale Biomechanics of Bone
一种新的自愈机制及其对骨多尺度生物力学的影响
  • 批准号:
    1363526
  • 财政年份:
    2014
  • 资助金额:
    $ 5万
  • 项目类别:
    Standard Grant

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