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Degradation of vascular devices (de-vasc): a combined engineering and biological approach

Degradation of vascular devices (de-vasc): a combined engineering and biological approach
血管装置的降解(de-vasc):工程和生物学相结合的方法
批准号:
EP/P009662/1
负责人:
Michael Bryant
金额:
$12.87万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2017
资助国家:
英国
项目状态:
已结题
起止时间:
2017 至 --

项目摘要

项目成果

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中文摘要
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英文摘要
The PI has established a multi-disciplinary team of engineers and biologists with the view to develop novel methodologies to understand the metal-vascular biology interface that is established during stent or graft placement using core underpinning engineering and biological sciences. Expandable metallic structures (typically Co-based or NiTi alloys), known as 'stents', are commonly used to treat Peripheral Arterial Occlusive Diseases (PAOD), a thickening of the artery wall as a result of proliferation of intimal-smooth-muscle cells and Abdominal Aortic Aneurysms (AAA), a weakening of the aorta. PAOD and AAA are commonly treated with braided or a series of overlapping stents resulting in multiple metal-metal contacts being established in-vivo. A thorough understanding of the degradation processes and their role on the remodeling of the vasculature does not exist. This project will fuse contemporary tribocorrosion methods with unique patient specific cell cultures (ie cells obtained from a human donor undergoing vascular intervention) to quantify the synergy between mechanical, corrosion and biological approaches. Novel surface science approaches will then be explored, using the developed methodologies, with the view to further understand and increase the bio-compatibility of future implanted devices. The framework established as part of this grant will bridge the current gap in bio-compatibility testing.The development of an instrument combining mechanical and corrosive processes with clinically relevant biology (all of which are present and interacting in-vivo) will provide an alternative to simplistic static cell culture and complex animal models. This has the potential to significantly reduce R&D costs through more effective screening of prospective technologies as well as reducing the need for animal testing.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1016/j.biotri.2020.100122
发表时间: 2020-06
期刊: Biotribology
影响因子: --
作者: [Emily R. Clark;Karen E. Hemmings;S. Greco;A. Neville;K. Porter;M. Bryant]
通讯作者: Emily R. Clark;Karen E. Hemmings;S. Greco;A. Neville;K. Porter;M. Bryant
DOI: 10.1016/j.biotri.2019.100093
发表时间: 2019-06
期刊: Biotribology
影响因子: --
作者: [Emily R. Clark;K. Porter;M. Bryant]
通讯作者: Emily R. Clark;K. Porter;M. Bryant
CPS: Synergy: Collaborative Research: Hybrid Continuous-Discrete Computers for Cyber-Physical Systems
  • 批准号:
    1239136
  • 项目类别:
    Standard Grant
  • 资助金额:
    $21.0万
  • 财政年份:
    2012
  • 负责人:
    Michael Bryant
  • 依托单位:
Manufacturing and Reliability of Three-Dimensional Micro-Mechanical Actuators
  • 批准号:
    0115527
  • 项目类别:
    Standard Grant
  • 资助金额:
    $18.5万
  • 财政年份:
    2001
  • 负责人:
    Michael Bryant
  • 依托单位:
Tribology Issues in Biology and Medicine, a Workshop (June 2001, Chicago, Illinois)
  • 批准号:
    0112199
  • 项目类别:
    Standard Grant
  • 资助金额:
    $6.0万
  • 财政年份:
    2001
  • 负责人:
    Michael Bryant
  • 依托单位:
U.S.-Korea Cooperative Research on Improving Friction Brakes by Eliminating Tribological Problems and Reducing Wear
  • 批准号:
    9731221
  • 项目类别:
    Standard Grant
  • 资助金额:
    $1.34万
  • 财政年份:
    1998
  • 负责人:
    Michael Bryant
  • 依托单位:
国内基金
海外基金
环境抗雄激素干预AR/TGFB1I1致尿道下裂血管内皮细胞发育异常的机制及其“预警信号”在早期诊断中的价值
  • 批准号:
    82371605
  • 项目类别:
    面上项目
  • 资助金额:
    46.00万元
  • 批准年份:
    2023
  • 负责人:
    蒋君涛
  • 依托单位:
尾加压素II介导血管外膜氧化应激促进血管重构的作用研究
  • 批准号:
    81141003
  • 项目类别:
    专项基金项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2011
  • 负责人:
    丁文惠
  • 依托单位:
核素靶向示踪肿瘤新生血管作用位点研究
  • 批准号:
    81071183
  • 项目类别:
    面上项目
  • 资助金额:
    32.0万元
  • 批准年份:
    2010
  • 负责人:
    王荣福
  • 依托单位:
硫化氢通过核转录因子-kB信号途径调节高血压大鼠血管平滑肌细胞增殖的研究
  • 批准号:
    81070212
  • 项目类别:
    面上项目
  • 资助金额:
    33.0万元
  • 批准年份:
    2010
  • 负责人:
    金红芳
  • 依托单位: