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Light4Sight SIGNED

Light-activated carriers for the controlled delivery of therapeutic peptides in posterior segment eye diseases

Total Cost €

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EC-Contrib. €

0

Partnership

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 Light4Sight project word cloud

Explore the words cloud of the Light4Sight project. It provides you a very rough idea of what is the project "Light4Sight" about.

frequent    glaucoma    biopharmaceuticals    adverse    peptides    diseases    visible    protein    global    injections    ocular    risk    biopharmaceutical    quality    ophthalmic    life    35    sensitive    patient    benefits    providers    patients    concentration    demand    drug    degeneration    nanocarriers    placing    age    light    avoiding    reducing    irradiation    half    rapid    consisting    consequently    vision    treatments    match    evades    site    ways    minimizes    acceptable    administration    diabetic    loading    assembling    billion    retinopathy    activated    self    eye    burst    systemic    sales    platform    suspended    light4sight    treatment    pose       clearance    burden    dose    2016    doses    repeated    population    intraocular    peptide    barriers    ing    invasive    macular    therapeutic    complete    injection    suffering    topical    treat    2025    intravitreal    vitreous    drugs    hydrogel    protects    alternative    market    lifestyle    toxicity    therapy    innovative    primarily    aged    posterior    provides    supramolecular    vitreoretinal    healthcare    moderate    chronic    injected    release    reduces    incorporating    exceeded   

Project "Light4Sight" data sheet

The following table provides information about the project.

Coordinator
QUEEN MARY UNIVERSITY OF LONDON 

Organization address
address: 327 MILE END ROAD
city: LONDON
postcode: E1 4NS
website: http://www.qmul.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 224˙933 €
 EC max contribution 224˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-11-01   to  2021-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    QUEEN MARY UNIVERSITY OF LONDON UK (LONDON) coordinator 224˙933.00

Map

 Project objective

In 2016, the global sales of biopharmaceutical drugs (protein, peptides) in ophthalmic applications exceeded $8 billion and is estimated to increase to $35.7 billion by 2025. The growth of the ophthalmic drug market is primarily driven by an increasing aged population suffering from age- and lifestyle-related diseases such as macular degeneration, diabetic retinopathy, glaucoma, among others. These diseases cause moderate or complete vision loss, resulting in significant reduction in quality of life. Consequently, innovative approaches for the effective delivery of biopharmaceuticals for the treatment of chronic intraocular diseases are required. Currently, intravitreal injection of drugs is the most acceptable and effective method to treat vitreoretinal diseases. By placing the drug in the posterior eye, it evades the ocular barriers common in topical and systemic delivery, allowing higher drug doses to reach the target site. However, treatments require frequent injections to maintain adequate intraocular concentration, which are invasive, increase the risk of adverse effects and pose significant treatment burden on patients and healthcare providers. Thus, alternative ways to deliver these drugs that require less frequent administration need to be developed. Light4Sight aims to develop a novel delivery platform consisting of self-assembling nanocarriers incorporating therapeutic peptides and suspended within a light-sensitive supramolecular hydrogel. The hydrogel can be injected in the vitreous and release of nanocarriers be activated through the irradiation of visible light. This approach provides several benefits: 1) minimizes the use of repeated injections reducing treatment burden; 2) reduces burst release of the nanocarriers avoiding potential dose related toxicity; 3) on-demand release to match patient needs; 4) allows high drug loading for long-term therapy; 5) protects peptide drugs from rapid clearance in the vitreous increasing their half-life.

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The information about "LIGHT4SIGHT" are provided by the European Opendata Portal: CORDIS opendata.

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