Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Nanoscale Adv ; 6(3): 925-933, 2024 Jan 30.
Artículo en Inglés | MEDLINE | ID: mdl-38298589

RESUMEN

To achieve a high quantum yield (QY) of nanomaterials suitable for optical applications, we improved the optical properties of AgIn5S8 (AIS) quantum dots (QDs) by employing an alloyed-core/inner-shell/outer-shell (ZAIS/ZIS/ZnS) structure. We also investigated the mechanism of optical transitions to clarify the improvement of QYs. In AIS, the low-energy absorption near the band edge region is attributed to the weakly allowed band gap transition, which gains oscillator strength through state intermixing and electron-phonon coupling. The main photoluminescence is also ascribed to the weakly allowed band gap transition with characteristics of self-trapped excitonic emission. With alloying/shelling processes, the weakly allowed transition is enhanced by the evolution of the electronic structures in the alloyed core, which improves the band gap emission. In shelled structures, the nonradiative process is reduced by the reconstructed lattice and passivated surface, ultimately leading to a high QY of 85% in ZAIS/ZIS/ZnS. These findings provide new insights into the optical transitions of AIS because they challenge previous conclusions. In addition, our work elucidates the mechanism behind the enhancement of QY accomplished through alloying/shelling processes, providing strategies to optimize nontoxic QDs for various applications using a green chemistry approach.

2.
Nanoscale Adv ; 4(5): 1351-1358, 2022 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-36133688

RESUMEN

Three types of carbon dots (CDs) are synthesized from isomers of phenylenediamine to develop multicolor nanomaterials with low toxicity, high stability, and high quantum yield. The distinctive electronic structures of CDs lead to the characteristic optical transitions, such as three colors of blue, green, and red, which are primarily attributed to the difference in configurations, despite the similar basic structures of conjugated systems. The excitation-independent emission and the single exponential decay of CDs indicate the single chromophore-like nature in each type of CD. In addition, the two-photon luminescence of CDs exhibits a comparable shape and time profile to the typical photoluminescence with high photostability. Although the surface-related defect states are observed by intragap excitation, the contribution of defect states is barely observed in the emission profile upon band gap excitation. Consequently, the controllability of optical transitions in CDs enhances the potential of tunable multicolor nanomaterials for various applications as alternatives to quantum dots containing toxic elements.

3.
J Biomol Screen ; 19(10): 1383-90, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25245988

RESUMEN

Recently, dual-specificity phosphatase 16 (DUSP16) emerged as a promising therapeutic target protein for the development of anti-atherosclerosis and anticancer medicines. The present study was undertaken to identify the novel inhibitors of DUSP16 based on the structure-based virtual screening. We have been able to find seven novel inhibitors of DUSP16 through the drug design protocol involving homology modeling of the target protein, docking simulations between DUSP16 and its putative inhibitors with the modified scoring function, and in vitro enzyme assay. These inhibitors revealed good potency, with IC50 values ranging from 1 to 22 µM, and they were also screened computationally for having desirable physicochemical properties as drug candidates. Therefore, they deserve consideration for further development by structure-activity relationship studies to optimize the inhibitory activity against DUSP16. Structural features relevant to the stabilization of the newly identified inhibitors in the active site of DUSP16 are addressed in detail.


Asunto(s)
Fosfatasas de Especificidad Dual/antagonistas & inhibidores , Fosfatasas de Especificidad Dual/química , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Fosfatasas de la Proteína Quinasa Activada por Mitógenos/antagonistas & inhibidores , Fosfatasas de la Proteína Quinasa Activada por Mitógenos/química , Dominio Catalítico , Diseño de Fármacos , Fosfatasas de Especificidad Dual/metabolismo , Inhibidores Enzimáticos/metabolismo , Concentración 50 Inhibidora , Fosfatasas de la Proteína Quinasa Activada por Mitógenos/metabolismo , Modelos Moleculares , Simulación del Acoplamiento Molecular , Homología Estructural de Proteína , Relación Estructura-Actividad , Interfaz Usuario-Computador
4.
IEEE Trans Biomed Eng ; 49(3): 269-73, 2002 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11876292

RESUMEN

The interrelationship of cilia and the order of wave directions are important factors that determine the effectiveness of cilia to transport materials in mucociliary systems of the respiratory tract. The interrelationship of cilia and the directional disorder of ciliary metachronal wave were analyzed using digital microscopic images. The degree of synchronization between ciliary beats was determined by the correlation factor between two different spots. To find out the uniphase directions of beating cilia, principal axes of inertia were applied to the two-dimensional correlation map calculated from sequential ciliary images. The standard deviation of determined wave directions in a region of interest (ROI) was defined as a measure of metachronal wave disorder. The pooled mean of metachronal wave disorder was 23.4 +/- 8.79 degrees in ROIs of 8 microm x 8 microm and 25.4 +/- 6.46 degrees in 32 microm x 24 microm from the sphenoid sinus mucosa of five normal subjects. Our result shows that there is a considerable variation in metachronal wave directions of cilia beating on the epithelium.


Asunto(s)
Cilios/fisiología , Mucosa Nasal/fisiología , Humanos , Procesamiento de Imagen Asistido por Computador , Grabación en Video
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA