Eosin Y derivatives for visible light-mediated free-radical polymerization: Applications in 3D-photoprinting and bacterial photodynamic inactivation

This study reports the design and the subsequent use of mono-allylated (EY-MA) and di-allylated (EY-DA) derivatives of eosin Y (EY) as highly efficient visible light-sensitive photosensitizers (PS) of bio-based H-donor molecules (cysteamine (Cys) or N-acetyl-L-cysteine (NAC)) and an electron donor (N-methyldiethanolamine, MDEA) for free-radical and thiol-acrylate polymerizations of a biobased monomer derived from soybean oil (SOA) upon exposure to visible light. High final acrylate conversions for SOA polymerization (up to 80 %) evidence the efficient photoinitiating properties of the eosin derivatives systems under irradiation with light emitting diodes (LEDs) centred at 405, 455 and 505 nm, and outperform those obtained with EY and other common photosensitizers such as camphorquinone or benzophenone. As described by fluorescence and phosphorescence analyses, laser flash photolysis (LFP) and electron paramagnetic resonance spin-trapping (EPR-ST) experiments, EY-MA and EY-DA can react via a proton/proton-coupled electron transfer reaction with Cys (or NAC) and MDEA respectively. The efficient singlet oxygen generation of the EY-MA-based materials upon exposure to visible light leads to excellent antibacterial properties, against both Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli). A 3-log decrease of E. coli adhesion on the surface of the materials is observed and 100 % adhesion inhibition of S. aureus is also demonstrated. The co-polymerization of the eosin-derived PS with the polymer matrix ensures sustainable antibacterial properties against both bacteria strains upon visible light exposure as it prevents their leakage out of the polymer network. Finally, finely complex 3D structures are successfully obtained by a 3D-photoprinting technology with the investigated EY-MAbased formulation using LED@405 nm.