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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.

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

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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