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Mechanistic insight into the photodynamic effect mediated by porphyrin-fullerene C(60) dyads in solution and in Staphylococcus aureus cells
The photodynamic action mechanism sensitized by a non-charged porphyrin-fullerene C(60) dyad (TCP-C(60)) and its tetracationic analogue (TCP-C(60)(4+)) was investigated in solution and in Staphylococcus aureus cells. The ability of both dyads to form a photoinduced charge-separated state was evidenc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081455/ https://www.ncbi.nlm.nih.gov/pubmed/35540123 http://dx.doi.org/10.1039/c8ra04562c |
Sumario: | The photodynamic action mechanism sensitized by a non-charged porphyrin-fullerene C(60) dyad (TCP-C(60)) and its tetracationic analogue (TCP-C(60)(4+)) was investigated in solution and in Staphylococcus aureus cells. The ability of both dyads to form a photoinduced charge-separated state was evidenced by the reduction of methyl viologen in N,N-dimethylformamide (DMF). Moreover, the formation of superoxide anion radicals induced by these dyads was detected by the reduction of nitro blue tetrazolium. Also, photosensitized decomposition of l-tryptophan (Trp) was investigated in the presence of reactive oxygen species (ROS) scavengers. The addition of β-carotene and sodium azide had a slight effect on reaction rate. However, photooxidation of Trp mediated by TCP-C(60) was negligible in the presence of d-mannitol, while no protection was found using TCP-C(60)(4+). In a polar medium, these dyads mainly act by a contribution of type I pathway with low generation of singlet molecular oxygen, O(2)((1)Δ(g)). In S. aureus cell suspensions, an aerobic atmosphere was required for the photokilling of this bacterium. The photocytotoxicity induced by TCP-C(60) was increased in D(2)O with respect to water, while a small effect was found using TCP-C(60)(4+). Furthermore, photoinactivation of microbial cells was negligible in the presence of sodium azide. The addition of d-mannitol did not affect the photoinactivation induced by TCP-C(60). In contrast, S. aureus cells were protected by d-mannitol when TCP-C(60)(4+) was used as a photosensitizer. Also, generation of O(2)((1)Δ(g)) in the S. aureus cells was higher for TCP-C(60) than TCP-C(60)(4+). Therefore, TCP-C(60) appears to act in microbial cells mainly through the mediation of O(2)((1)Δ(g)). Although, a contribution of the type I mechanism was found for cell death induced by TCP-C(60)(4+). Therefore, these dyads with high capacity to produce photoinduced charge-separated state represent interesting photosensitizers to inactivate microorganisms by type I or type II mechanisms. In particular, TCP-C(60) may be located in a non-polar microenvironment in the cells favoring a type II pathway, while a contribution of the type I mechanism was produced using the cationic TCP-C(60)(4+). |
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