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Antimicrobial photodynamic activity and cytocompatibility of Au(25)(Capt)(18) clusters photoexcited by blue LED light irradiation
Antimicrobial photodynamic therapy (aPDT) has beneficial effects in dental treatment. We applied captopril-protected gold (Au(25)(Capt)(18)) clusters as a novel photosensitizer for aPDT. Photoexcited Au clusters under light irradiation generated singlet oxygen ((1)O(2)). Accordingly, the antimicrobi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388257/ https://www.ncbi.nlm.nih.gov/pubmed/28435253 http://dx.doi.org/10.2147/IJN.S131602 |
Sumario: | Antimicrobial photodynamic therapy (aPDT) has beneficial effects in dental treatment. We applied captopril-protected gold (Au(25)(Capt)(18)) clusters as a novel photosensitizer for aPDT. Photoexcited Au clusters under light irradiation generated singlet oxygen ((1)O(2)). Accordingly, the antimicrobial and cytotoxic effects of Au(25)(Capt)(18) clusters under dental blue light-emitting diode (LED) irradiation were evaluated. (1)O(2) generation of Au(25)(Capt)(18) clusters under blue LED irradiation (420–460 nm) was detected by a methotrexate (MTX) probe. The antimicrobial effects of photoexcited Au clusters (0, 5, 50, and 500 μg/mL) on oral bacterial cells, such as Streptococcus mutans, Aggregatibacter actinomycetemcomitans, and Porphyromonas gingivalis, were assessed by morphological observations and bacterial growth experiments. Cytotoxicity testing of Au clusters and blue LED irradiation was then performed against NIH3T3 and MC3T3-E1 cells. In addition, the biological performance of Au clusters (500 μg/mL) was compared to an organic dye photosensitizer, methylene blue (MB; 10 and 100 μg/mL). We confirmed the (1)O(2) generation ability of Au(25)(Capt)(18) clusters through the fluorescence spectra of oxidized MTX. Successful application of photoexcited Au clusters to aPDT was demonstrated by dose-dependent decreases in the turbidity of oral bacterial cells. Morphological observation revealed that application of Au clusters stimulated destruction of bacterial cell walls and inhibited biofilm formation. Aggregation of Au clusters around bacterial cells was fluorescently observed. However, photoexcited Au clusters did not negatively affect the adhesion, spreading, and proliferation of mammalian cells, particularly at lower doses. In addition, application of Au clusters demonstrated significantly better cytocompatibility compared to MB. We found that a combination of Au(25)(Capt)(18) clusters and blue LED irradiation exhibited good antimicrobial effects through (1)O(2) generation and biosafe characteristics, which is desirable for aPDT in dentistry. |
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