Agazzi Maximiliano L, Durantini Javier E, Gsponer Natalia S, Durantini Andrés M, Bertolotti Sonia G, Durantini Edgardo N
IDAS-CONICET, Departamento de Química Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, Ruta Nacional 36 Km 601, X5804BYA, Río Cuarto, Córdoba, Argentina.
IITEMA-CONICET, Departamento de Química Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, Ruta Nacional 36 Km 601, X5804BYA, Río Cuarto, Córdoba, Argentina.
Chemphyschem. 2019 May 3;20(9):1110-1125. doi: 10.1002/cphc.201900181. Epub 2019 Apr 10.
A covalently linked BODIPY-fullerene C dyad (BDP-C ) was synthesized as a two-segment structure, which consists of a visible light-harvesting antenna attached to an energy or electron acceptor moiety. This structure was designed to improve the photodynamic action of fullerene C to inactivate bacteria. The absorption spectrum of BDP-C was found to be a superposition of the spectra of its constitutional moieties, whereas the fluorescence emission of the BODIPY unit was strongly quenched by the fullerene C . Spectroscopic, calculations, and redox studies indicate a competence between photoinduced energy and electron transfer. Protonating the dimethylaminophenyl substituent through addition of an acidic medium led to a substantial increase in the fluorescence emission, triplet excited state formation, and singlet molecular oxygen production. At physiological pH, photosensitized inactivation of Staphylococcus aureus mediated by 1 μM BDP-C exhibited a 4.5 log decrease of cell survival (>99.997 %) after 15 min irradiation. A similar result was obtained with Escherichia coli using 30 min irradiation. Moreover, proton-activated photodynamic action of BDP-C turned this dyad into a highly effective photosensitizer to eradicate E. coli. Therefore, BDP-C is an interesting photosensitizing structure in which the light-harvesting antenna effect of the BODIPY unit combined with the protonation of dimethylaminophenyl group can be used to improve the photoinactivation of bacteria.
合成了一种共价连接的硼二吡咯-富勒烯C二元体(BDP-C),其具有两段结构,由连接到能量或电子受体部分的可见光捕获天线组成。设计这种结构是为了增强富勒烯C的光动力作用以灭活细菌。发现BDP-C的吸收光谱是其组成部分光谱的叠加,而硼二吡咯单元的荧光发射被富勒烯C强烈猝灭。光谱、计算和氧化还原研究表明光诱导能量和电子转移之间存在竞争。通过添加酸性介质使二甲基氨基苯基取代基质子化导致荧光发射、三重态激发态形成和单线态分子氧产生大幅增加。在生理pH值下,1 μM BDP-C介导的金黄色葡萄球菌的光致敏失活在照射15分钟后细胞存活率降低了4.5个对数(>99.997%)。使用大肠杆菌照射30分钟也获得了类似结果。此外,BDP-C的质子活化光动力作用使该二元体成为根除大肠杆菌的高效光敏剂。因此,BDP-C是一种有趣的光敏结构,其中硼二吡咯单元的光捕获天线效应与二甲基氨基苯基的质子化相结合可用于改善细菌的光灭活作用。