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NanoFEITH SIGNED

Nanoparticles for Fluorescence-Enhanced Imaging and Therapy of Breast Cancer

Total Cost €

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EC-Contrib. €

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Partnership

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 NanoFEITH project word cloud

Explore the words cloud of the NanoFEITH project. It provides you a very rough idea of what is the project "NanoFEITH" about.

breast    signals    au    advantages    dyes    women    platforms    nir    multimodal    therapeutic    diagnosis    zn    bearing    sensitivity    sizes    resolution    site    fluorescence    minimize    ph    passive    strategy    tumours    nps    toward    systemic    infrared    vivo    near    responsive    training    tumour    collaborations    host    vital    surface    metal    ion    complement    mef    optical    mortality    first    nanobipyramids    photothermal    international    therapy    multidisciplinary    core    combined    bc    techniques    materials    accumulation    efficacy    gold    combining    ineffective    translation    drug    lids    tips    detection    worldwide    enhanced    complementary    cell    biodistribution    dramatically    vitro    mitigating    promise    vs    enhancement    chemotherapeutic    theranostic    personalized    elongated    coating    computational    clinical    resistant    expertise    spatial    professional    skills    cultures    limited    combine    maturity    nanotechnology    treating    time    coordinated    fluorescent    nanoparticles    3d    nanomedicine    sharp    imaging    np    biocompatibility    carrier    active    cancer    death    treatment    paving    offers    insights    modalities    tunable    science    release   

Project "NanoFEITH" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF CYPRUS 

Organization address
address: KALLIPOLEOS STREET 75
city: NICOSIA
postcode: 1678
website: www.ucy.ac.cy

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Cyprus [CY]
 Total cost 151˙648 €
 EC max contribution 151˙648 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-06-01   to  2020-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF CYPRUS CY (NICOSIA) coordinator 151˙648.00

Map

 Project objective

Breast cancer (BC) represents a leading cause of cancer-related death in women worldwide, in large part due to ineffective detection and treatment. Nanotechnology offers new promise in mitigating BC mortality, by combining therapy with early diagnosis in “theranostic” nanoparticles (NPs). Here, a multidisciplinary approach is proposed to develop and evaluate novel theranostic NPs, which for the first time combine near infrared (NIR) metal-enhanced fluorescence (MEF) imaging with multimodal cancer treatment. MEF is a promising strategy for dramatically improving the low fluorescent signals of available NIR dyes, but limited MEF platforms for in vivo applications have been developed. Here, elongated gold (Au) NPs (nanobipyramids) with two sharp tips and tunable sizes/optical properties are expected to provide distinct advantages, including large fluorescence enhancement and increased tumour accumulation, thus enabling real-time in vivo imaging with high sensitivity and spatial resolution. Furthermore, BC photothermal therapy by the Au core will be combined with a chemotherapeutic drug-carrier surface coating, bearing pH-responsive lids to allow controlled drug and Zn ion release at the tumour site. Coordinated use of these modalities is expected to minimize systemic side effects, improve therapeutic efficacy and be useful in treating drug resistant tumours. Several complementary techniques, including computational modelling, 3D in vitro cell cultures, in vivo testing and advanced 3D imaging will be combined to characterize NP biodistribution, biocompatibility and passive vs. active tumour targeting. These will provide vital insights for the – still challenging – clinical translation of NPs in general, paving the way toward personalized nanomedicine. The proposed research/training will complement the Applicant’s skills in materials science with the Host’s expertise in cancer drug delivery to enhance his professional maturity and promote international collaborations.

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