Cationic thiazolothiazole derivatives - A new class of photosensitizing agents against Staphylococcus aureus

被引:0
|
作者
Cerqueira, Ana F. R. [1 ]
Perez, Maria E.
Gsponer, Natalia S. [2 ]
Neves, Maria G. P. M. S. [1 ]
Parola, A. Jorge [3 ]
Durantini, Edgardo N. [2 ]
Tome, Augusto C. [1 ]
机构
[1] Univ Aveiro, Dept Chem, LAQV REQUIMTE, P-3810193 Aveiro, Portugal
[2] Univ Nacl Rio Cuarto, IDAS CONICET, Fac Ciencias Exactas Fis Quim & Nat, Dept Quim, Ruta Nacl 36 Km 601,X5804BYA, Rio Cuarto, Cordoba, Argentina
[3] Univ Nova Lisboa, NOVA Sch Sci & Technol, Dept Chem, LAQV REQUIMTE,FCT NOVA, P-2829516 Caparica, Portugal
关键词
Thiazolothiazole; Photosensitizer; Photoinactivation; Microorganism; Biofilm; PHOTODYNAMIC INACTIVATION; SOLAR-CELLS; BACTERIA; FLUORESCENCE; SEMICONDUCTORS; EFFICIENCY; MOLECULES; ENERGY; CORE; DYES;
D O I
10.1016/j.jphotochem.2024.115849
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The assessment of thiazolothiazoles (TzTz) as photosensitizers in photodynamic inactivation (PDI) experiments is reported for the first time. Mono and dicationic TzTz derivatives were synthesized, and their photosensitizing ability was assessed on Staphylococcus aureus cells, both in suspension or attached to a surface, and using white light. The biological results showed that the photodynamic efficiency of these derivatives is dependent on the TzTz structure and irradiation time. The best results were obtained with the monocationic derivative TPATzTzPyMe & thorn; that allowed to reach a value over 7 log (99.9999 %) cell inactivation after white light irradiation for 30 min. Furthermore, TPATzTzPyMe & thorn; also revealed to be effective on the inactivation of S. aureus adhered to surfaces, a good indication of its potential to prevent biofilm formation. TPATzTzPyMe & thorn; was also effective against Escherichia coli , with a reduction in cell viability of 5.7 log after irradiation for 30 min.
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页数:7
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