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1.
Nanoscale ; 15(30): 12481-12491, 2023 Aug 03.
Artículo en Inglés | MEDLINE | ID: mdl-37401670

RESUMEN

Binary nanoparticle superlattices (BNSLs) are one of the important classes of nanomaterial architectures for a wide range of potential applications because they can provide synergistically enhanced properties depending on the morphology and spatial arrangement of nanoparticles (NPs). However, although many studies have been conducted on the fabrication of BNSLs, there are still several challenges in achieving BNSLs with a three-dimensional lattice due to their complicated synthesis, hindering their practical applications. Herein, we report the fabrication of temperature-sensitive BNSLs in complexes of gold nanoparticles (AuNPs), Brij 58 surfactant, and water via a two-step evaporation method. The surfactant was utilized for two different purposes, i.e., surface modification of the AuNPs to control their interfacial energy and as a template material for the formation of the superlattice. Depending on the size and concentration of the AuNPs, the mixture of AuNPs and surfactant self-assembled into three types of BNSLs, including CaF2, AlB2, and NaZn13, which were sensitive to temperature. This study is the first demonstration of the temperature- and particle size-dependent control of BNSLs in the bulk state without the covalent functionalization of NPs via a simple two-step solvent evaporation method.

2.
Sci Rep ; 12(1): 4548, 2022 Mar 16.
Artículo en Inglés | MEDLINE | ID: mdl-35296763

RESUMEN

The two-dimensional (2D) assembly of gold nanoparticles (AuNPs) in a confined geometry is a rare phenomenon that has not been experimentally verified for complex systems. In this study, this process was investigated in detail using two types of block copolymers with hydrophobic and hydrophilic blocks and a series of AuNPs of three different sizes protected by hydrophobic ligands. In aqueous solutions, the selected block copolymers self-assembled into vesicular nanostructures with a hydrophobic domain in the wall, which functions as a confined geometrical space for hydrophobic AuNPs (i.e., it exerts a confinement effect and restricts the movement of AuNPs). Small-angle X-ray scattering studies revealed that AuNPs of different sizes assembled differently in the same confined geometry of the vesicular wall. In addition, optimal conditions for the formation of a regular NP array in the hydrophobic domain were determined. The AuNPs successfully self-assembled into a regular 2D lattice structure, forming a shell around the vesicle, when their size matched the thickness of the hydrophobic domain of the vesicular nanostructure. This study provides guidelines for the fabrication of nanoparticle arrays with controlled structures, which could enhance the functionality of materials and their physical properties.

3.
Phytother Res ; 26(2): 239-45, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21647997

RESUMEN

The objective of this study was to determine the antiinflammatory effects of Polygoni Rhizoma (PR), an Oriental medicinal herb, in interleukin 1 beta (IL-1ß) and lipopolysaccharide (LPS)-stimulated RAW264.7 mouse macrophage cells. PR significantly reduced the production of pro-inflammatory cytokines such as IL-6, tumor necrosis factor alpha (TNF-α) and pro-inflammatory mediators such as inducible nitric oxide synthase (iNOS), nitric oxide (NO), cyclooxygenase 2 (COX-2) and prostaglandin E2 (PGE2) even at a concentration of 1 µg/mL in the cells. In addition, PR inhibited the transcriptional activity of NF-κB as well as the degradation and phosphorylation of inhibitory kappa B alpha (IκBα). Furthermore, PR suppressed the phosphorylation of extracellular signal regulated kinase 1/2 (ERK1/2), p38 and c-Jun N-terminal kinase 1/2 (JNK1/2) in IL-1ß and LPS-treated RAW264.7. The results suggest that PR exerts an antiinflammatory property by inhibiting iNOS, COX-2, TNF-α and IL-6 production in association with inactivation of the NF-κB and MAPK signaling pathways in RAW 264.7 cells.


Asunto(s)
Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Macrófagos/efectos de los fármacos , Proteínas Quinasas Activadas por Mitógenos/antagonistas & inhibidores , FN-kappa B/antagonistas & inhibidores , Extractos Vegetales/farmacología , Polygonum/química , Animales , Línea Celular , Ciclooxigenasa 2/metabolismo , Dinoprostona/metabolismo , Inflamación/tratamiento farmacológico , Interleucina-6/metabolismo , Macrófagos/metabolismo , Ratones , Óxido Nítrico/metabolismo , Óxido Nítrico Sintasa de Tipo II/metabolismo , Factor de Necrosis Tumoral alfa/metabolismo
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