Opendata, web and dolomites

ExoSonic SIGNED

A microfluidic chip for non-invasive, early detection of pancreatic cancer – liquid biopsy

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ExoSonic project word cloud

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

cutting    detect    suggesting    microfluidic    laboratories    possessing    leverages    decades    disease    fabrication       stage    components    window    edge    2030    diagnostics    utilisation    sentence    ultralow    vesicles    technically    inefficient    elapses    detecting    therapies    fourth    predicted    unprecedented    inability    beginning    particles    pancreatic    isolated    patient    hospital    poor    inaccessible    paving    chamber    diagnosis    rate    death    powerful    blood    exosomes    clinical    initial    module    precision    mortality    constraints    extremely    uk    tiny    lack    exosome    microfabrication    regarded    device    sized    plan    emerged    resolution    opportunity    circulating    chip    nanometre    screening    harness    first    separation    biomarker    sensitivity    cancer    shed    bloodstream    biomarkers    isolation    era    changed    specificity    facilities    invasive    resource    detection    incorporate    technological    settings    figure    tumour    concerned    commercialisation    survival   

Project "ExoSonic" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.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˙997 €
 EC max contribution 149˙996 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-PoC
 Funding Scheme ERC-POC
 Starting year 2018
 Duration (year-month-day) from 2018-02-01   to  2019-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 149˙996.00

Map

 Project objective

Pancreatic cancer is the fourth-leading cause of cancer related mortality and is predicted to be the second leading cause of cancer death by 2030. Widely regarded as a death sentence, the 5-year survival rate is only 3% in the UK and this figure has not changed over the past four decades due to lack of specific therapies and inability to detect it early. Several years often elapses from the beginning of the disease to the patient’s diagnosis, suggesting a window of opportunity for early detection. Recently, tiny nanometre-sized vesicles (exosomes) shed by the tumour in the bloodstream, have emerged as powerful circulating biomarkers possessing extremely high sensitivity and specificity, thus paving the way for a new era of non-invasive cancer diagnostics. However, currently the process of exosome isolation and detection is not only highly inefficient, but also technically challenging and inaccessible to hospital laboratories, clinical facilities and resource-poor settings. To address technological constraints of exosome utilisation, we are developing a microfluidic device that leverages cutting-edge microfabrication technology to enable isolation and detection of tumour exosomes from the blood for screening and detecting early-stage pancreatic cancer with unprecedented precision. This chip will have two components, a separation module where exosomes will be isolated from all other blood particles, and a detection chamber that will incorporate technology to achieve ultralow resolution. The first stage of development will be concerned with the fabrication of all components necessary to harness the sensitivity of the exosome biomarker. Following initial testing, we plan to take steps towards commercialisation of the device.

 Publications

year authors and title journal last update
List of publications.
2019 Alistair Rice, Armando del Rio Hernandez
The mutational landscape of pancreatic and liver cancers, as represented by circulating tumour DNA
published pages: , ISSN: 2234-943X, DOI: 10.3389/fonc.2019.00952
Frontiers in Oncology 2020-03-30
2018 Carlos Matellan, Armando E. del Río Hernández
Cost-effective rapid prototyping and assembly of poly(methyl methacrylate) microfluidic devices
published pages: , ISSN: 2045-2322, DOI: 10.1038/s41598-018-25202-4
Scientific Reports 8/1 2020-03-30
2018 Tyler Lieberthal
Bioengineering and biomechanical approaches for pancreatic cancer
published pages: , ISSN: , DOI:
2020-03-30
2019 Deana Kwong Hong Tsang, Tyler Lieberthal, Clare Watts. Iain E. Dunlop, Sami Ramadan, Armando Del Rio Hernandez, Norbert Klein
Chemically Functionalised Graphene FET Biosensor for the Label-free Sensing of Exosomes
published pages: , ISSN: 2045-2322, DOI: 10.1038/s41598-019-50412-9
Scientific Reports 2020-03-30

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "EXOSONIC" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.1.)

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

AST (2019)

Automatic System Testing

Read More  

CellProbe (2019)

CellProbe: Microfluidic probe for simultaneous tagging and extraction of single cells

Read More