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.

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

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.)

OSeaIce (2019)

Two-way interactions between ocean heat transport and Arctic sea ice

Read More  

ACES (2019)

Antarctic Cyclones: Expression in Sea Ice

Read More  

FarGo (2019)

'Farming God's Way': Cultivation and religious practice in contemporary South Africa

Read More