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1.
Nanotechnology ; 21(20): 205201, 2010 May 21.
Artículo en Inglés | MEDLINE | ID: mdl-20413842

RESUMEN

We demonstrate the surface plasmon-enhanced blue light-emitting diodes (LEDs) using Ag nanoparticles embedded in p-GaN. A large increase in optical output power of 38% is achieved at an injection current of 20 mA due to an improved internal quantum efficiency of the LEDs. The enhancement of optical output power is dependent on the density of the Ag nanoparticles. This improvement can be attributed to an increase in the spontaneous emission rate through resonance coupling between the excitons in multiple quantum wells and localized surface plasmons in Ag nanoparticles embedded in p-GaN.


Asunto(s)
Galio/química , Nanopartículas del Metal/química , Plata/química , Resonancia por Plasmón de Superficie/métodos , Diseño de Equipo , Luz , Microscopía de Fuerza Atómica/métodos , Nanotecnología/métodos , Óptica y Fotónica
2.
J Med Food ; 10(3): 479-85, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17887942

RESUMEN

Antioxidant properties of brown seaweed (Sargassum siliquastrum) extracts were evaluated using various antioxidant measurements, i.e., inhibitory effect on thiobarbituric acid-reactive substances (TBARS), 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging, metal chelating effect, reducing power effect, and total phenolic compounds. When the extraction solvents n-hexane, chloroform, ethanol, and water were compared, the water extract showed the highest yield in extracted mass. Total phenolic compounds were the highest in the ethanol extract, with 127.4 mg/g. The TBARS inhibition of chloroform and ethanol extracts at 10 mg/mL was 90.9% and 80.9%, respectively. DPPH radical scavenging capacity was more than 90% in all extracts at 1 mg/mL. The chloroform extract exhibited the highest metal ion chelating ability of 69.6% at 10 mg/mL. The reducing power was found to be the highest in the ethanol extract at 10 mg/mL, showing an effect similar to ascorbic acid. Thus, the ethanol extract of S. siliquastrum has potential as a natural antioxidant.


Asunto(s)
Antioxidantes/farmacología , Sargassum/química , Antioxidantes/análisis , Antioxidantes/aislamiento & purificación , Compuestos de Bifenilo , Cloroformo , Etanol , Hexanos , Quelantes del Hierro , Oxidación-Reducción , Fenoles/análisis , Picratos , Solventes , Sustancias Reactivas al Ácido Tiobarbitúrico , Agua
3.
Cancer Res ; 71(23): 7216-25, 2011 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-21987726

RESUMEN

Occult metastases are a major cause of cancer mortality, even among patients undergoing curative resection. Therefore, practical strategies to target the growth and persistence of already established metastases would provide an important advance in cancer treatment. Here, we assessed the potential of protein therapy using a cell permeable NM23-H1 metastasis suppressor protein. Hydrophobic transduction domains developed from a screen of 1,500 signaling peptide sequences enhanced the uptake of the NM23 protein by cultured cells and systemic delivery to animal tissues. The cell-permeable (CP)-NM23 inhibited metastasis-associated phenotypes in tumor cell lines, blocked the establishment of lung metastases, and cleared already established pulmonary metastases, significantly prolonging the survival of tumor-bearing animals. Therefore, these results establish the potential use of cell-permeable metastasis suppressors as adjuvant therapy against disseminated cancers.


Asunto(s)
Neoplasias Pulmonares/tratamiento farmacológico , Nucleósido Difosfato Quinasas NM23/farmacología , Secuencia de Aminoácidos , Animales , Línea Celular Tumoral , Movimiento Celular/efectos de los fármacos , Movimiento Celular/fisiología , Péptidos de Penetración Celular/genética , Péptidos de Penetración Celular/farmacocinética , Péptidos de Penetración Celular/farmacología , Progresión de la Enfermedad , Femenino , Células HCT116 , Humanos , Neoplasias Pulmonares/enzimología , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/patología , Ratones , Ratones Endogámicos BALB C , Quinasas de Proteína Quinasa Activadas por Mitógenos/antagonistas & inhibidores , Quinasas de Proteína Quinasa Activadas por Mitógenos/metabolismo , Datos de Secuencia Molecular , Terapia Molecular Dirigida/métodos , Células 3T3 NIH , Nucleósido Difosfato Quinasas NM23/genética , Nucleósido Difosfato Quinasas NM23/farmacocinética , Metástasis de la Neoplasia , Señales de Clasificación de Proteína , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/farmacocinética , Proteínas Recombinantes de Fusión/farmacología , Ensayos Antitumor por Modelo de Xenoinjerto
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