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NOVACHIP SIGNED

Novel vascular-like BBB-on-a-chip

Total Cost €

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EC-Contrib. €

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Partnership

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 NOVACHIP project word cloud

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

bioprinting    pathophysiology    blood    biomechanical    scalable    3d    mri    therapies    matrix    disorders    native    acute    predict    quantifying    model    incorporate    grow    self    tissue    made    starting    exhibit    reports    there    technique    drugs    vivo    novachip    chip    practical    biologically    ecm    evident    fabrication    functional    animal    human    variety    industry    20    neurological    magnetic    found    properly    assembly    shown    strofunscaff    capillaries    drug    designed    off    compare    erc    biological    plaques    pharmaceutical    diseases    models    capacity    cells    imaging    kidney    preparation    brain    toxicity    alzheimer    structural    indicate    resemble    rat    overcome    thanks    constitutes    nephrotoxicity    ad    resonance    combines    reduce    companies    proposes    relevance    microfluidic    patients    biomarkers    screening    bbb    linked    break    permeability    inability    complications    disease    molecules    sizes    safer    vessels    vessel    components    risk    treatments    obstacle    ineffective    fluidic    stiffness    endothelialized    grant    patent    barrier    commercially    vitro    personalized    poc    limited    recreating    generating    extracellular    geometries   

Project "NOVACHIP" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF NOTTINGHAM 

Organization address
address: University Park
city: NOTTINGHAM
postcode: NG7 2RD
website: www.nottingham.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]
 Total cost 149˙951 €
 EC max contribution 149˙951 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-PoC
 Funding Scheme ERC-POC
 Starting year 2020
 Duration (year-month-day) from 2020-11-01   to  2022-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF NOTTINGHAM UK (NOTTINGHAM) coordinator 149˙951.00

Map

 Project objective

There is great need to develop safer and more biologically relevant models for drug screening. Recent reports indicate that up to 20% of acute kidney complications can be linked to drug-induced nephrotoxicity and more than 40 molecules found to reduce Alzheimer’s Disease (AD)-related plaques in animal models were shown to be ineffective in AD patients. It is increasingly evident that both in vitro and in vivo models being used to develop drugs have a limited capacity to predict the pathophysiology of human disease, personalized response, and off-target drug toxicity. The inability to properly test drugs and treatments to diseases such as AD constitutes a risk for pharmaceutical companies and a major obstacle to overcome. This ERC PoC proposal aims to establish a practical microfluidic fabrication process capable of recreating structural and biomechanical features of native blood vessels. Specifically, we aim to develop a scalable 3D Blood-Brain-Barrier in vitro model (BBB-on-a-chip) able to provide a higher level of biological relevance than current in vitro models. The development of such a system would represent a major break-through for the pharmaceutical industry generating therapies for a variety of neurological disorders. Thanks to the ERC Starting Grant STROFUNSCAFF, we have developed a simple fabrication process that combines bioprinting and self-assembly to grow functional fluidic devices with endothelialized vessel-like capillaries (patent application in preparation). NOVACHIP proposes to a) build scalable microfluidic devices made from capillaries that incorporate relevant cells and extracellular matrix (ECM) components, exhibit tissue-like stiffness, and can be designed with specific sizes and geometries to better resemble the native BBB and b) compare it to a commercially available in vitro model as well as c) an established rat model by quantifying permeability of specific imaging biomarkers for Magnetic Resonance Imaging (MRI) technique.

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