STIRENA

Dual stimuli-responsive nanoparticles as novel topical drug delivery systems

 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 221˙606 €
 EC contributo 221˙606 €
 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-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-06-01   -   2015-05-31

 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 221˙606.40

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drug    multifunctional    materials    poly    nanoparticles    stimuli    temperature    skin    ph    responsive   

 Obiettivo del progetto (Objective)

'This project aims to develop new stimuli-responsive nanoparticles (SRN’s) reacting to changes in temperature and pH, and to evaluate their applications for both topical and transdermal drug delivery. New multifunctional materials, thermoresponsive as well as nanogels and dual pH-Tm responsive materials, using a combination of poly(N-isopropylacrylamide), poly(2-oxazolines) and chitosan will be synthesized and characterized. The main objective of this project will be to develop stimuli responsive nanoparticles based on the new multifunctional materials and evaluate their use as drug delivery nano-systems for skin application. Different techniques such as coprecipitation, oil/water solvent evaporation and high dilution radical polymerization will be used to generate nanoparticle with different physicochemical characteristics. Their clinical potential will be evaluated using preclinical in vitro skin models. The stimuli responsive nanoparticles proposed in this project may be characterized as an innovative approach to the development of new multifunctional skin delivery systems allowing the drug to be released, only when the tissue itself give the appropriate message, in terms of temperature and/or pH response.'

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