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BONDS TERMINATED

Bilayered ON-Demand Scaffolds: On-Demand Delivery from induced Pluripotent Stem Cell Derived Scaffolds for Diabetic Foot Ulcers

Total Cost €

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EC-Contrib. €

0

Partnership

0

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 BONDS project word cloud

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

adult    coordinated    platform    heal    matrix    dfu    healing    appropriate    mechanical    biomimetic    scaffolds    ultrasound    platelet    clinical    pi    undergo    biomaterial    treatment    dfus    diabetics    mimic    technologies    alginate    builds    layer    designed    repair    model    functionalised    pdna    foot    stem    lower    made    guide    genes    fibroblasts    confirm    pluripotent    tested    interspersed    cell    size    epidermis    dna    ulcers    innovative    mostly    bonds    devastatingly    native    gt    porous    powerful    pore    dermis    ips    fibroblast    diabetic    recalcitrant    keratinocytes    leg    combines    consist    angiogenic    drug    gene    grown    bilayered    environment    never    disruptive    directions    grow    first    amputation    cells    ppdgf    demand    adapting    wounds    skin    angiogenesis    dermal    timed    direct    lab    vivo    uncoordinated    microparticles    sips    structure    film    platforms    material    keratinisation    releasing    scaffold    million    chronic    source    pro    plasmid    diverse    epidermal   

Project "BONDS" data sheet

The following table provides information about the project.

Coordinator
ROYAL COLLEGE OF SURGEONS IN IRELAND 

Organization address
address: Saint Stephen's Green 123
city: DUBLIN
postcode: 2
website: www.rcsi.ie

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 Ireland [IE]
 Total cost 1˙372˙135 €
 EC max contribution 1˙372˙135 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2017
 Duration (year-month-day) from 2017-10-01   to  2022-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ROYAL COLLEGE OF SURGEONS IN IRELAND IE (DUBLIN) coordinator 1˙372˙135.00

Map

 Project objective

This program’s goal is to develop a scaffold using a new biomaterial source that is functionalised with on-demand delivery of genes for coordinated healing of diabetic foot ulcers (DFUs). DFUs are chronic wounds that are often recalcitrant to treatment, which devastatingly results in lower leg amputation. This project builds on the PI’s experience growing matrix from induced-pluripotent stem cell derived (iPS)-fibroblasts and in developing on-demand drug delivery technologies. The aim of this project is to first develop a SiPS: a scaffold from iPS-fibroblast grown matrix, which has never been tested as a source material for scaffolds. iPS-fibroblasts grow a more pro-repair and angiogenic matrix than (non-iPS) adult fibroblasts. The SiPS structure will be bilayered to mimic native skin: dermis made mostly by fibroblasts and epidermis made by keratinocytes. The dermal layer will consist of a porous scaffold with optimised pore size and mechanical properties and the epidermal layer will be film-like, optimised for keratinisation. Second, the SiPS will be functionalised with delivery of plasmid-DNA (platelet derived growth factor gene, pPDGF) to direct angiogenesis on-demand. As DFUs undergo uncoordinated healing, timed pPDGF delivery will guide them through angiogenesis and healing. To achieve this, alginate microparticles, designed to respond to ultrasound by releasing pPDGF, will be interspersed throughout the SiPS. This BONDS will be tested in an in vivo pre-clinical DFU model to confirm its ability to heal wounds by providing cells with the appropriate biomimetic scaffold environment and timed directions for healing. With >100 million current diabetics expected to get a DFU, the BONDS would have a powerful clinical impact. This research program combines a disruptive technology, the SiPS, with a new platform for on-demand delivery of pDNA to heal DFUs. The PI will build his lab around these innovative platforms, adapting them for treatment of diverse complex wounds.

 Publications

year authors and title journal last update
List of publications.
2019 Ronaldo J. F. C. do Amaral, Noora M. A. Zayed, Elena I. Pascu, Brenton Cavanagh, Chris Hobbs, Francesco Santarella, Christopher R. Simpson, Ciara M. Murphy, Rukmani Sridharan, Arlyng González-Vázquez, Barry O\'Sullivan, Fergal J. O\'Brien, Cathal J. Kearney
Functionalising Collagen-Based Scaffolds With Platelet-Rich Plasma for Enhanced Skin Wound Healing Potential
published pages: , ISSN: 2296-4185, DOI: 10.3389/fbioe.2019.00371
Frontiers in Bioengineering and Biotechnology 7 2020-03-05
2019 Niusha Nikravesh, Owen G. Davies, Ioannis Azoidis, Richard J. A. Moakes, Lucia Marani, Mark Turner, Cathal J. Kearney, Neil M. Eisenstein, Liam M. Grover, Sophie C. Cox
Physical Structuring of Injectable Polymeric Systems to Controllably Deliver Nanosized Extracellular Vesicles
published pages: 1801604, ISSN: 2192-2640, DOI: 10.1002/adhm.201801604
Advanced Healthcare Materials 8/9 2020-01-28
2018 Ronaldo Jose Farias Correa Amaral, Brenton Cavanagh, Fergal Joseph O\'Brien, Cathal John Kearney
Platelet‐derived growth factor stabilises vascularisation in collagen‐glycosaminoglycan scaffolds in vitro
published pages: , ISSN: 1932-6254, DOI: 10.1002/term.2789
Journal of Tissue Engineering and Regenerative Medicine 2020-01-28

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