OTHOx | Spatiotemporal control of singlet oxygen release from supramolecular hydrogels to improve cancer therapy

Summary
This research aims to develop novel supramolecular hydrogels and study their application as singlet oxygen (1O2) carriers. In medicine, 1O2 generated in-vivo through photochemistry has been used to treat a variety of ailments including bacterial infections, acne, and several types of cancer. Though promising, this approach suffers from drawbacks such as diminished effectiveness in hypoxic conditions, both native and induced and lack of control over the total concentration and dosage of active 1O2. Recently, endoperoxides (EPO) have been identified as a potential solution for those, as they are self-contained sources of 1O2 produced ex-situ. However, they still do not allow for precise spatiotemporal control of 1O2 release, which is desirable to maximize for effectiveness of the treatment. Grafting EPOs on solid supports has been explored as a solution, but the state-of-the-art materials rely on complicated supports with low EPO loadings and thermal release mechanisms. Herein, we propose a new strategy for spatiotemporal control of 1O2 through the unprecedented use of hydrogels as EPO carriers. Hydrogels offer an easy to control and stable, but not persistent matrix in which the main component is water. The OTHO (oxotriphenylhexanoate) hydrogels enjoy unparalleled modularity, due to their highly robust and selective multicomponent one-pot synthesis. Thus, we will synthesize a range of OTHOs containing EPO units and perform detailed studies by rheology, solid-state NMR, small-angle x-ray and neutron scattering and electron microscopy to understand the properties and behavior of the resulting hydrogels. The biocompatibility and cytotoxic profile of the materials will be investigated against yeast cells expressing human disease markers. This will pave the way for a new breed of supramolecular pharmacology materials for 1O2 therapy against cancer.
Unfold all
/
Fold all
More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/101152118
Start date: 01-09-2024
End date: 31-08-2026
Total budget - Public funding: - 206 887,00 Euro
Cordis data

Original description

This research aims to develop novel supramolecular hydrogels and study their application as singlet oxygen (1O2) carriers. In medicine, 1O2 generated in-vivo through photochemistry has been used to treat a variety of ailments including bacterial infections, acne, and several types of cancer. Though promising, this approach suffers from drawbacks such as diminished effectiveness in hypoxic conditions, both native and induced and lack of control over the total concentration and dosage of active 1O2. Recently, endoperoxides (EPO) have been identified as a potential solution for those, as they are self-contained sources of 1O2 produced ex-situ. However, they still do not allow for precise spatiotemporal control of 1O2 release, which is desirable to maximize for effectiveness of the treatment. Grafting EPOs on solid supports has been explored as a solution, but the state-of-the-art materials rely on complicated supports with low EPO loadings and thermal release mechanisms. Herein, we propose a new strategy for spatiotemporal control of 1O2 through the unprecedented use of hydrogels as EPO carriers. Hydrogels offer an easy to control and stable, but not persistent matrix in which the main component is water. The OTHO (oxotriphenylhexanoate) hydrogels enjoy unparalleled modularity, due to their highly robust and selective multicomponent one-pot synthesis. Thus, we will synthesize a range of OTHOs containing EPO units and perform detailed studies by rheology, solid-state NMR, small-angle x-ray and neutron scattering and electron microscopy to understand the properties and behavior of the resulting hydrogels. The biocompatibility and cytotoxic profile of the materials will be investigated against yeast cells expressing human disease markers. This will pave the way for a new breed of supramolecular pharmacology materials for 1O2 therapy against cancer.

Status

SIGNED

Call topic

HORIZON-MSCA-2023-PF-01-01

Update Date

22-11-2024
Images
No images available.
Geographical location(s)
Structured mapping
Unfold all
/
Fold all
Horizon Europe
HORIZON.1 Excellent Science
HORIZON.1.2 Marie Skłodowska-Curie Actions (MSCA)
HORIZON.1.2.0 Cross-cutting call topics
HORIZON-MSCA-2023-PF-01
HORIZON-MSCA-2023-PF-01-01 MSCA Postdoctoral Fellowships 2023