Incorporation of cationic groups
into polymers represents one of
the most widely used strategies to prepare antibacterial materials.
Sulfonium, as a typical cationic moiety, displays potent antibacterial
efficacy in the form of small molecules, however, has long underperformed
in polymeric systems. Herein, we developed a series of alternating
polysulfoniums, where the hydrophobicity of each alternating unit
can be accurately tuned by altering the monomer precursors. Excellent
antibacterial activity against a broad spectrum of clinically relevant
bacteria, including Methicillin-resistant Staphylococcus
aureus, can be obtained in the optimal compositions
with minimum bactericidal concentrations in the range of 1.25–10
μg/mL, as well as negligible hemolytic effect at polymer concentrations
even up to 10000 μg/mL. Bacteria do not readily develop resistance
to polysulfoniums due to the antibacterial action is possibly the
membrane disrupting mechanism. This work demonstrates sulfonium-based
polymers with well-defined sequences can function as a promising candidate
to combat drug-resistant bacterial infection.