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Active H2020 European Commission

Nano bio-responsive systems designed to avoid staphylococcal colonization of implant interfaces

€279.3K EUR

Funder European Commission
Recipient Organization Universitaet Innsbruck
Country Austria
Start Date Apr 01, 2022
End Date Jul 31, 2026
Duration 1,582 days
Number of Grantees 1
Roles Coordinator
Data Source European Commission
Grant ID 101025065
Grant Description

Antimicrobial resistance (AMR) is responsible for 25,000 deaths per year in the EU and costs EUR 1.5 billion annually.

Methicillin-sensitive Staphylococcus aureus (MSSA), Methicillin-resistant S. aureus (MRSA) and S. epidermidis remain a serious problem in the treatment of periprosthetic joint infection (PJI). After surgery, bacteria may attach to the surface of prosthetic joints to form biofilms.

The fate of an available surface can be conceptualized as a race between tissue cell integration and bacterial adhesion to that same surface.

If the race is won by tissue, then the surface is occupied and defended and is thus less available for bacterial colonization.

The integration of the synthetic routes for smart molecular coatings doped with anti-staphylococcal agents that promote tissue growth, their biological responses and biointerface interactions into functional nano bio-responsive systems (NanoBioRS) able to avoid PJI is an unexplored opportunity for innovation.

In order to tackle PJI and to contribute to avoid the development and spread of antimicrobial resistance, NanoBioRS aims to engineer smart coatings equipped with three frontlines: (i) Increased adhesiveness of their interface to favour tissue cell integration. (ii) Smart responses to eradicate MSSA, MRSA and S. epidermidis using antimicrobials that are not prompt to resistance development. (iii) Means of avoiding biofilm and horizontal gene transfer (HGT) of AMR.

Thiol-modified polymers, surface-tethered stimuli-responsive polymer brushes and antimicrobial/antifouling agents will render coatings with eukaryotic cell adhesive, smart bacterial contact-kill and anti-biofilm properties, respectively. Endonucleases will be used to avoid biofilm and HGT of AMR. Implant surfaces will be modified with NanoBioRS.

Nanoscale characterization will allow for the understanding of biointerface interactions taking place during eukaryotic cell colonization and bacterial invasion of implants.

All Grantees

Universitaet Innsbruck

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