MRLI

A combined approach to smart imaging agents- using heterometallic lanthanide complexes as diagnostics

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Linda
Cognome: Polik
Email: send email
Telefono: +44(0)1865289811
Fax: +44(0)1865289801

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 177˙740 €
 EC contributo 177˙740 €
 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-2007-2-1-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-04-01   -   2009-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Linda
Cognome: Polik
Email: send email
Telefono: +44(0)1865289811
Fax: +44(0)1865289801

UK (OXFORD) coordinator 0.00

Mappa


 Word cloud

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

contrast    prepare    imaging    multimodal    lanthanide    complexes    agents   

 Obiettivo del progetto (Objective)

'This proposal aims to develop new contrast agents, derived from heterobinuclear lanthanide complexes, for use in imaging. These will combine the interesting properties of gadolinium complexes used in magnetic resonance imaging with those of luminescent lanthanide ions used in time-resolved micrscopy and assay applications. Our aims are fourfold, namely: To develop synthetic strategies which allow us to prepare heterometallic complexes suitable for multimodal imaging, using multi-component reactions or approaches involving diazo coupling to access these complexes; To develop methods by which nucleotide or PNA recognition domains are used to facilitate rapid transport of imaging components and programmed self-assembly of the multimodal imaging edifice at the target site; To develop switchable multi-modal agents, whose properties are altered by chemical or electrochemical change; and To prepare and study a range of multimodal imaging agents that can be targeted to cell surface receptors, and which have sufficiently high relaxivity to provide meaningful MRI contrast at low concentrations.'

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