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SCoTMOF SIGNED

Combined Chemo- and Radiotherapies by Controlling the Surface Chemistry of Truncated Metal Organic Framework Nanoparticles

Total Cost €

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EC-Contrib. €

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Partnership

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 SCoTMOF project word cloud

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

selective    prepare    trapping    clean    imaging    disease    capacities    promise    efficient    unprecedented    emerged    chemistries    multidisciplinary    dramatic    chemistry    syntheses    medicines    75    units    release    drug    patients    incorporation    vitro    carriers    cargo    responsive    technological    drugs    porous    self    cancers    pi    generate    tissues    joints    entirely    ones    fundamental    mechanisms    supramolecular    expertise    stimuli    efficiency    therapeutic    medicinal    considerable    materials    synthetic    world    concerted    vivo    amenability    assembly    treatments    effort    diseased    sirna    chance    rapid    theranostic    organic    linkers    derivatives    mitigate    aptamers    peptides    body    metal    pet    separations    death    comprised    toxic    molecular    mofs    treatment    location    alternative    vectors    populations    mof    nanoparticulate    chelates    biotargeting    frameworks    age    functionalization    experiences    incorporated    site    surface    released    avenues    breakthroughs    microwave    biosciences    catalysis    radionuclides    storage    streamlining    transport    installation    sophisticated    30   

Project "SCoTMOF" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITY OF GLASGOW 

Organization address
address: UNIVERSITY AVENUE
city: GLASGOW
postcode: G12 8QQ
website: www.gla.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]
 Project website http://www.forganlab.com
 Total cost 1˙493˙777 €
 EC max contribution 1˙493˙777 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-STG
 Funding Scheme ERC-STG
 Starting year 2016
 Duration (year-month-day) from 2016-09-01   to  2021-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITY OF GLASGOW UK (GLASGOW) coordinator 1˙493˙777.00

Map

 Project objective

Cancers are the leading cause of death in the developed world, with populations facing a 30% chance of developing the disease by the age of 75. As part of a concerted effort to open up new treatments and improve patients’ experiences with existing ones, the concept of drug delivery – using non-toxic carriers to transport medicines directly to the location of disease – has emerged. Metal-organic frameworks (MOFs), porous materials comprised of organic linkers and metal joints, show considerable promise as drug delivery vectors due to their high storage capacities, amenability to functionalization and the ability to prepare entirely non-toxic nanoparticulate derivatives. This proposal will use the PI’s expertise in advanced MOF synthetic methods to facilitate dramatic technological breakthroughs through unprecedented control of MOF self-assembly and surface chemistry. Management of MOF surface chemistry will allow installation of stimuli responsive release mechanisms and offer control over the trapping and release of cargo within MOFs, ensuring drugs are released only at the site of disease in the body. Surface incorporation of sophisticated biotargeting units such as peptides and aptamers will facilitate selective uptake of the MOFs by diseased tissues only. Rapid clean microwave syntheses will allow metal radionuclides to be incorporated for PET imaging, offering a novel alternative to traditional chelates. Comprehensive in vitro and in vivo testing will ensure that this multidisciplinary streamlining of materials, supramolecular and medicinal chemistries with the biosciences will generate highly efficient theranostic devices, offering more efficient, targeted drug delivery to improve treatment efficiency, mitigate side effects and open up new therapeutic avenues such as siRNA delivery. The fundamental advances required to generate these novel materials will also impact across the many applications of MOFs, from molecular storage and separations to catalysis.

 Publications

year authors and title journal last update
List of publications.
2019 Dominic Bara, Claire Wilson, Max Mörtel, Marat M. Khusniyarov, Sanliang Ling, Ben Slater, Stephen Sproules, Ross S. Forgan
Kinetic Control of Interpenetration in Fe–Biphenyl-4,4′-dicarboxylate Metal–Organic Frameworks by Coordination and Oxidation Modulation
published pages: , ISSN: 0002-7863, DOI: 10.1021/jacs.9b03269
Journal of the American Chemical Society 2019-06-06
2018 Isabel Abánades Lázaro, Sandra Abánades Lázaro, Ross S. Forgan
Enhancing anticancer cytotoxicity through bimodal drug delivery from ultrasmall Zr MOF nanoparticles
published pages: 2792-2795, ISSN: 1359-7345, DOI: 10.1039/c7cc09739e
Chemical Communications 54/22 2019-06-06
2019 Isabel Abánades Lázaro, Ross S. Forgan
Application of zirconium MOFs in drug delivery and biomedicine
published pages: 230-259, ISSN: 0010-8545, DOI: 10.1016/j.ccr.2018.09.009
Coordination Chemistry Reviews 380 2019-06-06
2018 Isabel Abánades Lázaro, Salame Haddad, Jose M. Rodrigo-Muñoz, Ross J. Marshall, Beatriz Sastre, Victoria del Pozo, David Fairen-Jimenez, Ross S. Forgan
Surface-Functionalization of Zr-Fumarate MOF for Selective Cytotoxicity and Immune System Compatibility in Nanoscale Drug Delivery
published pages: 31146-31157, ISSN: 1944-8244, DOI: 10.1021/acsami.8b11652
ACS Applied Materials & Interfaces 10/37 2019-06-06

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