RESUMEN
Excited-state chemistry relies on the communication between molecules, making it a crucial aspect of the field. One important question that arises is whether intermolecular communication and its rate can be modified when a molecule is confined. To explore the interaction in such systems, we investigated the ground and excited states of 4'-N,N-diethylaminoflavonol (DEA3HF) in an octa acid-based (OA) confined medium and in ethanolic solution, both in the presence of Rhodamine 6G (R6G). Despite the observed spectral overlap between the flavonol emission and the R6G absorption, as well as the fluorescence quenching of the flavonol in the presence of R6G, the almost constant fluorescence lifetime at different amounts of R6G discards the presence of FRET in the studied systems. Steady-state and time-resolved fluorescence indicate the formation of an emissive complex between the proton transfer dye encapsulated within water-soluble supramolecular host octa acid (DEA3HF@(OA)2) and R6G. A similar result was observed between DEA3HF:R6G in ethanolic solution. The respective Stern-Volmer plots corroborate with these observations, suggesting a static quenching mechanism for both systems.
Asunto(s)
Éteres Cíclicos , Rodaminas/química , Análisis Espectral/métodosRESUMEN
Monomeric zinc phthalocyanine has been studied as a promising active photosensitizer in photodynamic therapy against cancer, in which its aggregate form is non-active. This paper aimed to describe the monomer/aggregates equilibrium of zinc phthalocyanine in binary water/DMSO mixtures. To reach this aim theoretical calculation, electronic absorption, static and time-resolved fluorescence, and resonance light scattering was used. Zinc phthalocyanine shows a complex water dependence behavior in the mixture. At least three distinct steps were observed: (i) until 30% water zinc phthalocyanine is essentially in the monomeric form, changing to (ii) small slipped cofacial-aggregates around 30% to 40% water and finally to (iii) a staircase arrangement of large aggregates at higher water percent. The staircase arrangement is driven by the intermolecular coordination between the pyrrolic nitrogen lone-pairs and the central metal zinc. The water-Zn coordination governs the fluorescence quenching by a static mechanism. These results have direct relevance in the better understanding on the behavior of zinc phthalocyanine in vivo and when incorporated in drug delivery systems for clinical applications in photodynamic therapy.
Asunto(s)
Complejos de Coordinación/química , Indoles/química , Modelos Moleculares , Fármacos Fotosensibilizantes/química , Zinc/química , Complejos de Coordinación/farmacocinética , Complejos de Coordinación/farmacología , Sistemas de Liberación de Medicamentos , Humanos , Indoles/farmacocinética , Indoles/farmacología , Isoindoles , Fotoquimioterapia , Fármacos Fotosensibilizantes/farmacocinética , Fármacos Fotosensibilizantes/farmacología , Zinc/farmacocinética , Zinc/farmacologíaRESUMEN
Abstract This paper presents a study of the fluorescence quenching of 1-hydroxypyrene-3,6,8-trisulfonic acid (HPTS) in the presence of single-walled carbon nanotubes (SWCNT) using a fluorescence method. To investigate the quenching mechanism (dynamic or static) of HPTS, Stern-Volmer plots of single walled carbon nanotubes at different temperatures were used. The positive deviation from linearity in Stern-Volmer plots suggests that single walled carbon nanotubes follow a static quenching mechanism evidenced by the formation of a stable ground state complex. The results presented here help us to clarify the quenching mechanism in the interaction of a pyrene derived dye and carbon nanotubes. This study will open new possibilities in the use of the conjugate formed by SWCNTs and HPTS in the fabrication of a biosensor based on intracellular fluorescent probes.
Resumen Este artículo presenta el estudio de la desactivación de florescencia del ácido 1-hidroxipyreno-3,6,8-trisulfónico (HPTS) en presencia de nanotubos de carbono de pared única (SWCNT). Para investigar el mecanismo de desactivación (dinámico o estático) del HPTS se evaluaron nanotubos de carbono de pared única a diferentes temperaturas y se analizaron por medio de gráficas Stern-Volmer. La desviación positiva de la linealidad en las gráficas Stern-Volmer sugiere que los nanotubos de carbono de pared única actúan por medio de un mecanismo de desactivación estático, que se evidencia también por la formación de un complejo estable en estado fundamental. Los resultados presentados aquí nos ayudan a aclarar el mecanismo de desactivación de fluorescencia cuando tiene lugar la interacción entre un colorante derivado del pireno y nanotubos de carbono. Este estudio abre nuevas posibilidades para el uso de conjugados formados por SWCNT y HPTS en la fabricación de un biosensor basado en sondas fluorescentes intracelulares.
Resumo Este artigo apresentao estudo da diminuicao da fluorescência do ácido 1-hidroxipireno-3,6,8-trisulfônico (HPTS) em presença de nanotubos de carbono de parede simples (SWCNT). Para investigar o mecanismo da desativação (dinâmico ou estático) do HPTS se avaliaram nanotubos de parede simples em diferentes temperaturas e se analisaram por meio de gráficos Stern-Volmer. O desvio positivo de linearidade nos gráficos Stern-Volmer sugere que os nanotubos de carbono de parede simples atuam por meio de um mecanismo de desativação estática, que também se evidencia pela formação de um complexo estável fundamental. Os resultados apresentados aqui nos ajudam a aclarar o mecanismo de desativação de fluorescência quando ocorre a interação entre um corante derivado do pireno e nanotubos de carbono. Este estudo abre novas possibilidades para o uso de conjugados formados por SWCNT e HPTS na fabricação de um biosensor baseado em sondas fluorescentes intracelulares.