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Preparation and photodynamic antibacterial/anticancer effects of ultralong-lifetime room-temperature phosphorescent N-doped carbon dots

Room-temperature phosphorescent (RTP) N-doped carbon-dots (CNDs) featuring eco-friendliness, low cost and high biocompatibility, are ideal photodynamic antibacterial and anticancer nanomaterials. However, the existing CNDs are limited by low singlet oxygen ((1)O(2)) quantum yield, which has become a...

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Detalles Bibliográficos
Autores principales: Miao, Yanming, Zhang, Xinhao, Li, Jinyao, Yang, Wenli, Huang, Xiaomin, Lv, Jinzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285010/
https://www.ncbi.nlm.nih.gov/pubmed/35919183
http://dx.doi.org/10.1039/d2ra02251f
Descripción
Sumario:Room-temperature phosphorescent (RTP) N-doped carbon-dots (CNDs) featuring eco-friendliness, low cost and high biocompatibility, are ideal photodynamic antibacterial and anticancer nanomaterials. However, the existing CNDs are limited by low singlet oxygen ((1)O(2)) quantum yield, which has become a bottleneck in the development of CNDs. One basic reason is the short T(1)-state exciton lifetime of CNDs. Herein, triethylenetetramine hexaacetic acid was used to synthesize CNDs via a one-step hydrothermal method. CNDs are characterized with low toxicity, high biocompatibility and ultralong-lifetime RTP (URTP). In addition to the URTP (average lifetime 414 ms) under solid conditions, CNDs even had URTP (average lifetime 320 ms) in a water environment. The ultralong T(1) exciton lifetime largely extends the collision time between T(1) state excitons and O(2) and prolongs the energy transfer time, not only improving the quantum yield (0.63) of singlet oxygen ((1)O(2)) in solution, but also facilitating the photodynamic antibacterial and anticancer effects.