PATHCHOOSER

"Innovative, mechanistic-based strategies for delivery of therapeutic macromolecules across cellular and biological barriers"

 Coordinatore UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN 

 Organization address address: BELFIELD
city: DUBLIN
postcode: 4

contact info
Titolo: Mr.
Nome: Donal
Cognome: Doolan
Email: send email
Telefono: 35317161656
Fax: +353 1 716 1216

 Nazionalità Coordinatore Ireland [IE]
 Totale costo 3˙036˙614 €
 EC contributo 3˙036˙614 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-ITN
 Funding Scheme MC-ITN
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-10-01   -   2017-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN

 Organization address address: BELFIELD
city: DUBLIN
postcode: 4

contact info
Titolo: Mr.
Nome: Donal
Cognome: Doolan
Email: send email
Telefono: 35317161656
Fax: +353 1 716 1216

IE (DUBLIN) coordinator 788˙281.75
2    E.P.O.S. IASIS RESEARCH AND DEVELOPMENT LTD

 Organization address address: KOSTI PALAMA 34 ASPELIA DIAM 5
city: LEFKOSIA
postcode: 1096

contact info
Titolo: Dr.
Nome: Andreani
Cognome: Odysseos
Email: send email
Telefono: +357 22 894501

CY (LEFKOSIA) participant 378˙437.40
3    KING'S COLLEGE LONDON

 Organization address address: Strand
city: LONDON
postcode: WC2R 2LS

contact info
Titolo: Mr.
Nome: Paul
Cognome: Labbett
Email: send email
Telefono: +44 20 7848 8184

UK (LONDON) participant 289˙456.62
4    THE UNIVERSITY OF MANCHESTER

 Organization address address: OXFORD ROAD
city: MANCHESTER
postcode: M13 9PL

contact info
Titolo: Ms.
Nome: Claire
Cognome: Faichnie
Email: send email
Telefono: +44 161 2751413

UK (MANCHESTER) participant 285˙056.62
5    UNIVERSITY OF BRISTOL

 Organization address address: TYNDALL AVENUE SENATE HOUSE
city: BRISTOL
postcode: BS8 1TH

contact info
Titolo: Mrs.
Nome: Elodie
Cognome: Mahieu-Wedande
Email: send email
Telefono: 441173000000

UK (BRISTOL) participant 285˙056.62
6    SYDDANSK UNIVERSITET

 Organization address address: CAMPUSVEJ 55
city: ODENSE M
postcode: 5230

contact info
Titolo: Prof.
Nome: Jan
Cognome: Mollenhauer
Email: send email
Telefono: +45 6550 3970

DK (ODENSE M) participant 284˙579.47
7    AvantiCell Science Ltd

 Organization address address: GIBBSYARD BUILDING
city: AYR
postcode: KA6 5HW

contact info
Titolo: Dr.
Nome: Joanna
Cognome: Oliver
Email: send email
Telefono: 441293000000
Fax: 441293000000

UK (AYR) participant 281˙607.70
8    HELMHOLTZ-ZENTRUM FUER INFEKTIONSFORSCHUNG GMBH

 Organization address address: Inhoffenstrasse 7
city: BRAUNSCHWEIG
postcode: 38124

contact info
Titolo: Dr.
Nome: Michael
Cognome: Straetz
Email: send email
Telefono: +49 531 61812020
Fax: +49 531 61812299

DE (BRAUNSCHWEIG) participant 222˙068.88
9    MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Dr.
Nome: Birgit
Cognome: Knepper-Nicolai
Email: send email
Telefono: +49 351 210 2772
Fax: +49 351 210 1089

DE (MUENCHEN) participant 222˙068.88

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

regulatory    disciplinary    biological    diseases    efficient    barrier    therapeutic    strategies    crossing    limited    pathchooser    itn    significant   

 Obiettivo del progetto (Objective)

'Nanomedicine offers capability to significantly change the course of treatment for life-threatening diseases. Many of the most significant current therapeutic targets, to be viable in practice, require the efficient crossing of at least one biological barrier. However, the efficient and controlled crossing of the undamaged barrier is difficult. The range of small molecules that can successfully do so (via diffusive or other non-specific processes) is limited in size and physiochemical properties, greatly restricting the therapeutic strategies that may be applied. In practice, after several decades of limited success, there is a broad consensus that new multi-disciplinary, multi-sectoral strategies are required. Key needs include detailed design and understanding of the bionano-interafce, re-assessment of in vitro models used to assess transport across barriers, and building regulatory considerations into the design phase of nanocarriers. The overarching premises of the PathChooser ITN are that (i) significant advances can only be made by a more detailed mechanistic understanding of key fundamental endocytotic, transcytotic, and other cellular processes, especially biological barrier crossing; (ii) elucidating the Mode of Action / mechanism of successful delivery systems (beyond current level) will ensure more rapid regulatory and general acceptance of such medicines. Paramount in this is the design and characterization of the in situ interface between the carrier system and the uptake and signalling machinery. (iii) inter-disciplinary knowledge from a range of scientific disciplines is required to launch a genuine attack on the therapeutic challenge. The PathChooser ITN program of research and training will equip the next generation of translational scientists with the tools to develop therapies for a range of currently intractable (e.g. hidden in the brain) and economically unviable diseases (e.g. orphan diseases affecting a limited population).'

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