NANOGEND

Novel Thermoresponsive Organic Nanogels for Topical Gene Delivery of RNA-Based Drugs

 Coordinatore QUEEN MARY UNIVERSITY OF LONDON 

 Organization address address: 327 MILE END ROAD
city: LONDON
postcode: E1 4NS

contact info
Titolo: Dr.
Nome: Marina
Cognome: Resmini
Email: send email
Telefono: +44 20 7882 3268

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 209˙033 €
 EC contributo 209˙033 €
 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-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-07-01   -   2014-10-07

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    QUEEN MARY UNIVERSITY OF LONDON

 Organization address address: 327 MILE END ROAD
city: LONDON
postcode: E1 4NS

contact info
Titolo: Dr.
Nome: Marina
Cognome: Resmini
Email: send email
Telefono: +44 20 7882 3268

UK (LONDON) coordinator 209˙033.40

Mappa


 Word cloud

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

vitro    thermoresponsive    molecular    cross    permeation    model    drug    skin    imprinting    inflammatory    diseases    group    nanogels   

 Obiettivo del progetto (Objective)

'The scientific aim of this project is to develop and characterize a selected set of novel intelligent nanogels, designed to be able to cross the Stratum Corneum of the skin, and to study their suitability as drug delivery systems in inflammatory skin diseases. Ultrasmall nanogels will be synthesized using high dilution radical polymerization, a technique well established in the host’s laboratory, which allows the control of the particle size and polydispersity. Three different groups of nanogels will be prepared: 1) fluorescent nanogels 2) molecular imprinting nanogels 3) thermoresponsive nanogels. The first group will be used to study the distribution and localization of nanogels in normal human skin model reproduced in vitro by organotype cell co-culture. The second group will be used to evaluate the molecular imprinting approach as a tool to obtain very selective delivery system with high recognition characteristics. This has not been studied before and will provide a unique approach, when coupled with high permeation characteristics. The last group, the thermoresponsive nanogels, will combine good permeation with ability to release the drug following a change in temperature and will be compared with more traditional systems. The project will explore the use of each nanogels set to complex and deliver (a) small anti-inflammatory drugs, and (b) large molecules, in particular siRNA, given the strong expertise of the applicant in this area and the emerging interest for these new therapeutics in topical administration. Penetration and pharmacological effects of the drug-nanogels complexes will be assessed in pathological skin in vitro model by the improvement of the disease phenotype. The most significant novelty of the project will be the development of new organic polymeric nanogels able to cross the SC of the skin, providing a new non-invasive gene delivery technology system, that could bring very important applications in dermathology as well as in other fields.'

Introduzione (Teaser)

The outer layer of skin presents a formidable barrier to drug delivery for skin cancer, diseases and infections. A new nanogel promises the way forward.

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