POP SILICA

Towards Biodegradable Nanoparticles: Hybrid Organic Mesoporous Silica

 Coordinatore UNIVERSITE DE STRASBOURG 

 Organization address address: rue Blaise Pascal 4
city: Strasbourg
postcode: 67070

contact info
Titolo: Mrs.
Nome: Sandrine
Cognome: Schott-Carrière
Email: send email
Telefono: +33 368851124

 Nazionalità Coordinatore France [FR]
 Totale costo 97˙023 €
 EC contributo 97˙023 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-03-01   -   2015-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE STRASBOURG

 Organization address address: rue Blaise Pascal 4
city: Strasbourg
postcode: 67070

contact info
Titolo: Mrs.
Nome: Sandrine
Cognome: Schott-Carrière
Email: send email
Telefono: +33 368851124

FR (Strasbourg) coordinator 97˙023.30

Mappa


 Word cloud

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

medical    theranostic    diagnostic    translation    therapeutic    tools    msinps    biodegradability    nano    function    clinical   

 Obiettivo del progetto (Objective)

'Despite their great potential, full exploitation of mesoporous silica nanoparticles (MSiNPs) as in-vivo multi-functional theranostic agents is still held back by the lack of a controlled and complete biodegradability. Indeed removal of nano-medical tools from the biologic system after the accomplishment of their diagnostic or therapeutic function still remains a pivotal, yet unresolved issue impeding their clinical translation. A most desirable design for improving the properties of nano-medical tools would hence involve their ability to hierarchically self-degrade into renally clearable products after carrying out their function. Thus, the ambitious aim of this project targets the synthesis of novel, specific, hybrid MSiNPs-based theranostic tools, able to perform their beneficial action and subsequently fragment in smaller pieces allowing easy execration via renal system. In this way, thanks to the combination of the intrinsic biocompatibility of MSiNPs, their ease of functionalization and the newly conferred enhanced biodegradability, a superior material adaptable to a wide range of diagnostic and therapeutic applications, with great promise for clinical translation, will be achieved.'

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