Abstract
This study focuses on the structure-response relationship of symmetrically substituted phenothiazinium dyes. Four hydrophilic derivatives with the ability of additional hydrogen bonding (5, 6) or additional electrostatic interaction (3, 4) were synthesized, photophysically characterized and compared to the parent compound methylene blue (MB, 1) and a lipophilic derivative (2) without additional ...
Abstract
This study focuses on the structure-response relationship of symmetrically substituted phenothiazinium dyes. Four hydrophilic derivatives with the ability of additional hydrogen bonding (5, 6) or additional electrostatic interaction (3, 4) were synthesized, photophysically characterized and compared to the parent compound methylene blue (MB, 1) and a lipophilic derivative (2) without additional coordination sites. Derivative 5 was most effective against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli reaching a maximum photodynamic efficacy of >5log(10) steps (>= 99.999%) of bacteria killing in 10 minutes (5 mu M, 30 J cm(-2)) without inherent dark toxicity after one single treatment with the incoherent light source PDT1200 (lambda(max) = 660 nm, 50 mW cm(-2)). Interestingly, one derivative with two additional primary positive charges (3) showed selective killing of Escherichia coli (5 mu M, 30 J cm(-2), 4log(10) steps inactivation (>= 99.99%)) and no antimicrobial effect on Staphylococcus aureus. This might allow the development of a new generation of photosensitizers with higher antimicrobial efficacy and selectivity for future applications.
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