An efficient formulation based on cationic porphyrins to photoinactivate

Antibiotic resistance is an increasingly serious worldwide problem that needs to be addressed with alternative tools. Antimicrobial photodynamic therapy seems a promising approach but in some cases the synthesis of highly efficient photosensitizers requires laborious processes burdened by extensive chromatographic purifications. In this study, we evaluate the suitability of a formulation ( ) containing porphyrins bearing different charges, obtained during the synthesis of the highly efficient photosensitizer 5,10,15-tris(1-methylpyridinium-4-yl)-20-(pentafluorophenyl)porphyrin tri-iodide. was equally effective in the photoinactivation of and (reductions >5 log) as the best stand-alone photosensitizer. The effective reduction of bacteria with provided promising indications supporting its use, leading to a substantial decrease in costs and production time.