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1.
Anal Chem ; 89(7): 4077-4084, 2017 04 04.
Artículo en Inglés | MEDLINE | ID: mdl-28281746

RESUMEN

Ascorbic acid (AA), as one of the most important vitamins, participates in various physiological reactions in the human body and is implicated with many diseases. Therefore, the development of effective methods for monitoring the AA level in living systems is of great significance. Up to date, various technologies have been developed for the detection of AA. However, few methods can realize the direct detection of endogenous AA in living cells. In this work, we for the first time reported that near-infrared (NIR) graphene quantum dots (GQD) possessed good two-photon fluorescence properties with a NIR emission at 660 nm upon exciting with 810 nm femtosecond pulses and a two-photon (TP) excitation action cross-section (δΦ) of 25.12 GM. They were then employed to construct a TP nanoprobe for detection and bioimaging of endogenous AA in living cells. In this nanosystem, NIR GQDs (NGs), which exhibited lower fluorescence background in living system to afford improved fluorescence imaging resolution, were acted as fluorescence reporters. Also CoOOH nanoflakes were chosen as fluorescence quenchers by forming on the surface of NGs. Once AA was introduced, CoOOH was reduced to Co2+, which resulted in a "turn-on" fluorescence signal of NGs. The proposed nanoprobe demonstrated high sensitivity toward AA, with the observed LOD of 270 nM. It also showed high selectivity to AA with excellent photostability. Moreover, the nanoprobe was successfully used for TP imaging of endogenous AA in living cells as well as deep tissue imaging.


Asunto(s)
Ácido Ascórbico/análisis , Colorantes Fluorescentes/química , Grafito/química , Nanopartículas/química , Imagen Óptica , Fotones , Puntos Cuánticos/química , Células HeLa , Humanos , Tamaño de la Partícula , Propiedades de Superficie
2.
Anal Chem ; 88(3): 1639-46, 2016 Feb 02.
Artículo en Inglés | MEDLINE | ID: mdl-26744211

RESUMEN

Upconversion nanoparticles (UCNPs) possess several unique features, but they suffer from surface quenching effects caused by the interaction between the UCNPs and fluorophore. Thus, the use of UCNPs for target-induced emission changes for biosensing and bioimaging has been challenging. In this work, fluorophore and UCNPs are effectively separated by a silica transition layer with a thickness of about 4 nm to diminish the surface quenching effect of the UCNPs, allowing a universal and efficient luminescence resonance energy transfer (LRET) ratiometric upconversion luminescence nanoplatform for biosensing applications. A pH-sensitive fluorescein derivative and Hg(2+)-sensitive rhodamine B were chosen as fluoroionphores to construct the LRET nanoprobes. Both showed satisfactory target-triggered ratiometric upconversion luminescence responses in both solution and live cells, indicating that this strategy may find wide applications in the design of nanoprobes for various biorelated targets.


Asunto(s)
Técnicas Biosensibles/métodos , Luminiscencia , Mediciones Luminiscentes/métodos , Nanopartículas/análisis , Nanopartículas/química , Fluoresceínas/análisis , Fluoresceínas/química , Células HeLa , Humanos , Concentración de Iones de Hidrógeno , Mediciones Luminiscentes/instrumentación , Mercurio/análisis , Tamaño de la Partícula , Rodaminas/análisis , Rodaminas/química , Propiedades de Superficie , Células Tumorales Cultivadas
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