NANOSMARTS

Smart nondimensional biosensors for detection of tumor cells and cytotoxic amyloids intermediates

 Coordinatore Ukraine National Pirogov Memorial Medical University 

 Organization address address: Pirogov Street 56
city: Vinnitsa
postcode: 21018

contact info
Titolo: Dr.
Nome: Andriy
Cognome: Tkach
Email: send email
Telefono: -570754
Fax: -670585

 Nazionalità Coordinatore Ukraine [UA]
 Totale costo 15˙000 €
 EC contributo 15˙000 €
 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-2007-4-2-IIF
 Funding Scheme MC-IIFR
 Anno di inizio 0
 Periodo (anno-mese-giorno) 0000-00-00   -   0000-00-00

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    Ukraine National Pirogov Memorial Medical University

 Organization address address: Pirogov Street 56
city: Vinnitsa
postcode: 21018

contact info
Titolo: Dr.
Nome: Andriy
Cognome: Tkach
Email: send email
Telefono: -570754
Fax: -670585

UA (Vinnitsa) coordinator 15˙000.00

Mappa


 Word cloud

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

glioma    folding    fluorescent    dual    qds    drug    dyes    aggregation    binding    diseases    nanoparticles    tumor    protein    probes    neurodegenerative    emission    proteins    smaller    biosensors    assays    egfr    distinguish    nm    cells    conjugated    silicon   

 Obiettivo del progetto (Objective)

'This project integrates the development of (a) bioconjugated silicon nanoparticles (NPs) as new, < 3nm, fluorescent probes and (b) dual-emission band fluorescent biosensors for protein conformation investigations to be applied in diagnostic procedures related to tumor biology and neurodegenerative diseases. Epidermal growth factor receptor (EGFR) is an important therapeutic target in a variety of tumors, particularly malignant gliomas where mutation and/or amplification of EGFR is often observed. The laboratory has demonstrated in a pilot study the specific binding of biomolecules conjugated to Quantum Dots to patient-derived glioma spheroids. High wavelength emitting QDs are necessary to distinguish binding from tissue autofluorescence but such QDs are large (~40 nm) and do not penetrate deeply into tissues or access cellular junctions. The project will develop smaller, more inert, and less toxic conjugated silicon nanoparticles that can ultimately be used for the detection of residual glioma cells in patients after surgical resection. Additionally, more complex composite nanoparticles that selectively internalize in the tumor cells will be investigated as vehicles for drug delivery or selective killing. The aggregation of proteins and peptides is a fundamental feature of neurodegenerative diseases such as Alzheimer’s, Parkinson’s and spongiform encephalopathies. It is not clear whether the fibrillar aggregates or smaller forms of the implicated proteins are the cause of cytotoxicity. Both in vitro assays and in vivo studies are hampered by the lack of probes that can distinguish and quantitate early stages of the aggregation phenomenon. This project will develop fluorescent biosensors for protein folding on the basis of environment sensitive ratiometric dyes that exhibit dual emission. Such dyes are prospective tools for a development of facile and rapid assays for protein folding for application in diagnostics and drug screening assays.'

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