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MULTIFUNSOME TERMINATED

Anti-EGFR Monoclonal Antibody Conjugated Thermoresponsive Liposome for Triple Negative Breast Cancer Thermo-Chemotherapy

Total Cost €

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EC-Contrib. €

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Partnership

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 MULTIFUNSOME project word cloud

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

aggressive    cells    sensitive    breast    proposes    chemical    egfr    fellowship    co    enhanced    core    subtypes    options    histological    therapeutic    induce    influence    critical    minimize    magnetic    efficiency    thermoresponsive    synergistically    monoclonal    nano    thermo    multifunsome    poorer    concurrent    thermal    multidisciplinary    superparamagnetic    intracellularly    effectiveness    anti    membrane    heating    spio    size    multicore    limited    potentially    prognosis    encapsulation    subtype    cargo    content    triple    liposomes    conjugating    serve    drug    readily    drugs    spios    liposome    epidermal    conjugated    liposomal    hyperthermia    overexpressing    nanoparticles    chemotherapy    treatment    area    alternating    negative    tnbc    oxide    expertise    internalization    death    release    formulation    training    iron    manipulated    trigger    collaborations    efficacious    therapy    permeability    combining    receptor    effect    simultaneously    lipid    dose    efficient    generate    women    cancer    impacts    physical    mh    maximize    antibody    fellow    anticancer   

Project "MULTIFUNSOME" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

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 United Kingdom [UK]
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-09-01   to  2019-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 195˙454.00

Map

 Project objective

In Europe, breast cancer is by far the most important cause of cancer death among women. In particular, triple negative breast cancer (TNBC) is an aggressive histological subtype with limited treatment options and associated with poorer prognosis than other breast cancer subtypes. MULTIFUNSOME proposes the use of an anti-Epidermal Growth Factor Receptor (EGFR) monoclonal antibody-conjugated thermoresponsive liposome to deliver simultaneously an anticancer drug and superparamagnetic iron oxide nanoparticles (SPIO) to TNBC cells for thermo-chemotherapy. We will investigate: 1) the effect of combining anti-EGFR targeting and magnetic hyperthermia (MH) on TNBC in such thermo-chemotherapy and 2) how chemical-physical properties of the SPIOs and liposomes influence the therapeutic activity of the formulation. By conjugating anti-EGFR monoclonal antibody to a liposomal delivery system for targeting, drug and SPIO internalization into EGFR overexpressing TNBC cells will be greatly enhanced. SPIO co-encapsulation in the drug nano-cargo will induce a thermal dose to the TNBC cells when an alternating magnetic field is applied. MH will make TNBC cells more sensitive to chemotherapy and trigger the release of drugs intracellularly by enhancing the lipid membrane permeability. As a result, the effectiveness of chemotherapy could be synergistically enhanced by the concurrent application of MH and chemotherapy. The core size of SPIO will serve as a design parameter that can be readily manipulated to maximize the heating efficient of the multicore SPIO so as to minimize the necessary iron oxide content and maximize the drug encapsulation efficiency. The fellowship program will include a comprehensive training which will help the fellow to develop a unique multidisciplinary expertise. Furthermore, the project will generate important knowledge, impacts and collaborations in the European Research Area and could potentially address the critical need for a more efficacious TNBC therapy.

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The information about "MULTIFUNSOME" are provided by the European Opendata Portal: CORDIS opendata.

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