Opendata, web and dolomites

SPeNTa-Brain SIGNED

Synthetic Peptidic Nanovesicles for Targeting Paediatric Brain tumours

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SPeNTa-Brain project word cloud

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

immunotherapy    assemble    loaded    paediatric    synergistic    rop    selectivity    time    barrier    ligands    accounting    reaching    overcome    strategies    yielding    biodegradable    activate    polymersomes    vesicles    central    methodology    fight    cancer    diffuse    cns    amphiphiles    blood    ring    nanovesicles    brain    cancers    invasive    super    polypeptide    treatment    scalable    combinations    chemo    deadliest    tumour    incurable    nervous    amphiphilic    block    25    limitation    solid    immuno    selective    pathologies    receptor    critical    anticancer    polypeptides    resistance    agents    children    functionalised    clinically    join    metastases    drug    wise    trojan    innovative    cross    reproducible    therapy    primary    combination    bottleneck    solutions    tumours    death    polymerisation    acting    self    synthesise    glioma    active    lies    immune    chemotherapy    situation    ncas    bbb    horses    first    aqueous    difficulty    opening    modulators    transcytosis    stages    carboxyanhydrides    synthetic    binding    nanometric    crossing   

Project "SPeNTa-Brain" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY COLLEGE LONDON 

Organization address
address: GOWER STREET
city: LONDON
postcode: WC1E 6BT
website: n.a.

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 183˙454 €
 EC max contribution 183˙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-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE LONDON UK (LONDON) coordinator 183˙454.00

Map

 Project objective

Brain tumours are the most common solid tumours in children, accounting for about 25% of all primary paediatric tumours. The situation is particularly critical for the deadliest brain tumour: glioma, being the leading cause of cancer-related death in children. The main bottleneck for the treatment of central nervous system (CNS) pathologies, including brain tumours (at early stages), as well as brain metastases, lies in the difficulty to cross the blood brain barrier (BBB). In this proposal, I aim to overcome such limitation with the use of super-selective targeted and fully biodegradable polypeptide-based polymersomes, carrying relevant drug combinations for the treatment of paediatric glioma. I propose a step-wise and bottom-up approach to synthesise biodegradable polymersomes from amphiphilic block-polypeptides obtained via the scalable and reproducible methodology of Ring Opening Polymerisation (ROP) of N-Carboxyanhydrides (NCAs). The polypeptide amphiphiles are expected to self-assemble in aqueous solutions yielding nanometric vesicles. These synthetic vesicles will be functionalised with selected BBB receptor ligands in order to approach the super-selectivity concept aiming for active targeting and transcytosis to the brain acting as the so-called “Trojan Horses”. Finally, the super-selective nanovesicles will be loaded with synergistic and clinically relevant combination therapy using anticancer agents and immuno-modulators in order to approach paediatric glioma treatment. I will join for the first time, the use of fully biodegradable polymersomes based on polypeptides, super-selective binding strategies for BBB crossing and the use of chemotherapy immunotherapy. Overall, I will develop an innovative therapy, capable of reaching the brain in a non-invasive way, being able to diffuse and target the brain tumour, overcome chemo-resistance and activate the immune system to fight these tumours, being the future end-users, children with incurable cancers.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "SPENTA-BRAIN" 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 "SPENTA-BRAIN" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

STIMOS (2019)

Stimulation of Multiple Organoids Simultaneously

Read More  

MarshFlux (2020)

The effect of future global climate and land-use change on greenhouse gas fluxes and microbial processes in salt marshes

Read More  

VINCI (2020)

The Value of Information and Choice to Improve Control.

Read More