摘要： Novel water soluble Zn(II)phthalocyanines (ZnPc) peripherally substituted with 4-dimethylaminopyridine (DMAP) units (ZnPc 1-2) and the corresponding quaternized derivatives (ZnPc 1a-2a) were synthesized and their photodynamic inactivation (PDI) efficiency against a Gram-negative bacterium, a recombinant bioluminescent Escherichia coli strain either in planktonic and biofilm form was investigated. The analysis of the photophysical properties revealed that the increase in the number of DMAP units on ZnPc shifted the absorption and emission band in aqueous media to red. The presence of multi-positive charges on ZnPc derivatives prevented aggregation and enhances the solubility in aqueous medium. The quaternized derivatives ZnPc 1a and 2a displayed good stability and promising efficacy to generate singlet oxygen (1O2). The affinity of the amphiphilic ZnPc 1-2 and quaternized ZnPc 1a-2a to planktonic bacterial cells corresponded to an average uptake of ~106 PS molecules.CFU-1. The PDI assays conducted with planktonic cells and biofilms of E. coli show that irradiation with red or white light (150 mW.cm-2) in the presence of 20 μM of ZnPc derivatives caused an effective inactivation. ZnPc 1a and ZnPc 2a exhibited the highest inactivation efficiency, particularly of the planktonic form, causing 5 log (99.99%) reductions in bioluminescence. The inactivation factor for biofilms was 99% (2 log). ZnPc 1a and ZnPc 2a can be regarded as promising photosensitizers for the photodynamic inactivation of Gram-negative bacteria.