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3DSTAR

Highly porous collagen scaffolds for building 3D vascular networks: structure and property relationships

Total Cost €

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EC-Contrib. €

0

Partnership

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 3DSTAR project word cloud

Explore the words cloud of the 3DSTAR project. It provides you a very rough idea of what is the project "3DSTAR" about.

vascular    fluid    imaging    collagen    sizes    excellence    dry    quantified    suitable    customised    contribution    cells    strain    anisotropic    mechanical    size    diffusion    organization    vasculature    germany    perfusion    drying    hierarchical    architecture    investigation    organisation    view    young    measured    shape    assays    tomography    significance    encompassing    resistance    blood    tests    function    systematic    photon    permeability    surprisingly    engineered    cell    vessels    pressure    hypoxia    small    native    characterisation    self    constant    conventional    experimentation    functional    histology    respectively    endothelial    original    modulus    varied    lab    scaffolds    removal    variety    ray    gradient    mimicking    inter    microscopy    isotropic    pore    disciplinary    founding    vitro    scaffold    culture    hydrated    mainz    expertissues    interconnectivity    time    nutrient    biochemical    single    vs    repair    ratios    3d    confocal    network    structure    static    dried    structures    co    property    freeze    maturation    flow    waste   

Project "3DSTAR" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website https://www-memti.eng.cam.ac.uk/people/Sasha
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-11-14   to  2018-11-13

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 195˙454.00

Map

 Project objective

This proposal concerns with the development of functional 3D hierarchical vasculature within engineered freeze-dried collagen scaffolds. The main objective is to investigate the contribution of scaffold’s pore architecture (size, shape and interconnectivity) and culture conditions, such as cell ratios in co-culture, perfusion vs. static culture and hypoxia, on the self-organisation of endothelial cells into vascular-like structures. A comprehensive 2-year, highly inter-disciplinary programme is planned encompassing processing, scaffold structure characterisation, structure-property investigation and systematic in vitro experimentation. The in vitro work will be carried out in collaboration with the REPAIR-lab in Mainz, Germany - a founding member of the European Commission Network of Excellence EXPERTISSUES. Freeze-drying process parameters will be varied to produce isotropic and anisotropic scaffolds, with pore sizes mimicking native small blood vessels. The pore architecture, in both dry and hydrated states, will be quantified via X-ray tomography and 2-photon confocal microscopy, respectively, using original methodologies. The Young’s modulus and resistance to fluid flow (permeability) of scaffolds will be measured as a function of pore architecture characteristics. A customised set-up allowing low strain measurements of Young’s modulus will be used to establish whether conventional mechanical testing is suitable. Fluid permeability will be measured by applying a constant pressure gradient. Rather surprisingly in view of permeability’s significance in nutrient diffusion and waste removal, there is only a single study on permeability. Vascular organization, maturation and functionality of optimised scaffolds will be studied as a function of pore architecture, using state-of-the-art microscopy, real-time imaging, perfusion tests, histology and a variety of biochemical assays.

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The information about "3DSTAR" are provided by the European Opendata Portal: CORDIS opendata.

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