RAMAN

Gold Nanoprisms as Raman Signal Amplifiers for Bioimaging of Lung Cancer

 Coordinatore DUBLIN INSTITUTE OF TECHNOLOGY 

 Organization address address: RATHMINES ROAD LOWER 143-149
city: DUBLIN
postcode: 6

contact info
Titolo: Prof.
Nome: Brian
Cognome: O' Neill
Email: send email
Telefono: +353 1 4023370

 Nazionalità Coordinatore Ireland [IE]
 Totale costo 254˙637 €
 EC contributo 254˙637 €
 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) 2013-04-01   -   2015-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    DUBLIN INSTITUTE OF TECHNOLOGY

 Organization address address: RATHMINES ROAD LOWER 143-149
city: DUBLIN
postcode: 6

contact info
Titolo: Prof.
Nome: Brian
Cognome: O' Neill
Email: send email
Telefono: +353 1 4023370

IE (DUBLIN) coordinator 254˙637.80

Mappa


 Word cloud

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

screening    pegylated    probing    cancer    spectroscopy    biomolecules    disease    sensitivity    spontaneous    signal    detection    raman    wavelength    vivo    gold    nm    aunprs    sers    surface    tissue    rapid   

 Obiettivo del progetto (Objective)

'Raman spectroscopy is a powerful tool for probing biochemical changes in situ at tissue level. The vibrational profile can provide invaluable molecular details for medical diagnosis and disease prognosis. Important technological as well as health and safety considerations, however, limits its clinical application, as spontaneous Raman is a relatively weak effect and high laser powers are required for rapid screening. Surface-enhanced Raman scattering (SERS) makes is possible to probe single molecules adsorbed onto a silver or gold nanoparticle, greatly enhancing the sensitivity of spontaneous Raman and therefore potentially significantly reducing screening times. However, the SERS sensitivity from spherical gold nanoparticles is still insufficient to detect trace biomolecules and/or the interaction between biomolecules, which may be overcome through using novel shape nanomaterials as SERS substrates for the improvement of the bio-detection limit. Recently, Pegylated gold nanoprisms (AuNPrs) have been successfully employed as signal amplifiers in multimodal in vivo imaging of cancer cells, and therefore pose a great potential for Raman spectroscopy as well. Excellent biocompatibility properties are known for Pegylated AuNPrs, with side lengths of 120nm and thicknesses of 10nm. They absorb strongly at a wavelength of 830 nm, with co-efficients of up to 37 µg.mL-1•OD-1, a wavelength within the tissue transparency window, promising deep penetration in vivo This project will explore the optimisation of Pegylated AuNPrs for surface enhancement of the Raman signal (SERS)of their local cellular environment for probing disease in vitro and ulimately in vivo. Lung cancer is the most common cause of death from cancer in the EU and is therefore chosen as a model for the development of a Raman based rapid screening technique for early detection of disease.'

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