| Literature DB >> 33721278 |
Maximiliano L Agazzi1, Javier E Durantini2, Ezequiel D Quiroga1, M Gabriela Alvarez1, Edgardo N Durantini3.
Abstract
A novel amphiphilic photosensitizing agent based on a tricationic fullerene C60 (DMC603+) was efficiently synthesized from its non-charged analogue MMC60. These fullerenes presented strong UV absorptions, with a broad range of less intense absorption up to 710 nm. Both compounds showed low fluorescence emission and were able to photosensitize the production of reactive oxygen species. Furthermore, photodecomposition of L-tryptophan sensitized by both fullerenes indicated an involvement of type II pathway. DMC603+ was an effective agent to produce the photodynamic inactivation (PDI) of Staphylococcus aureus, Escherichia coli and Candida albicans. Mechanistic insight indicated that the photodynamic action sensitized by DMC603+ was mainly mediated by both photoprocesses in bacteria, while a greater preponderance of the type II pathway was found in C. albicans. In presence of potassium iodide, a potentiation of PDI was observed due to the formation of reactive iodine species. Therefore, the amphiphilic DMC603+ can be used as an effective potential broad-spectrum antimicrobial photosensitizer.Entities:
Keywords: Fulleropyrrolidine; Iodide; Microorganisms; Photodynamic inactivation; Photosensitizer
Mesh:
Substances:
Year: 2021 PMID: 33721278 DOI: 10.1007/s43630-021-00021-1
Source DB: PubMed Journal: Photochem Photobiol Sci ISSN: 1474-905X Impact factor: 3.982