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1.
ACS Appl Mater Interfaces ; 11(1): 655-665, 2019 Jan 09.
Artigo em Inglês | MEDLINE | ID: mdl-30525401

RESUMO

Thinning CIGSe absorber layer to less than 500 nm is desirable for reducing the cost per unit watt of photovoltaic-generated electricity, and also, the semitransparent solar cell based on such a thin absorber can be used in bifacial and superstrate configurations if the back electrode is transparent. In this study, a WO x layer is inserted between Cu(In,Ga)Se2 (CIGSe) absorber and tin-doped indium oxide back-contact to enhance the hole collection at the back electrode. A WO x interlayer with a thickness of 6 nm is found to be optimum because it causes a ∼38% relative increase in the fill factor of a ∼450 nm thick CIGSe-based device compared to the reference device without a WO x interlayer. While fixing the thickness of CIGSe, increasing the WO x interlayer thickness to ≥6 nm results in decreases of solar cell parameters primarily because of the emergence of a GaO x interfacial layer at the CIGSe/WO x junction.

2.
J Nanosci Nanotechnol ; 14(12): 9189-93, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25971035

RESUMO

In this study, the coating of synthesized carbon nanowalls (CNWs) with various metal layers (Ni, Cu, and W) was investigated. CNWs were synthesized by microwave plasma enhanced chemical vapor deposition (PECVD) with a methane (CH4) and hydrogen (H2) gas mixture on a p-type Si wafer, and then coated with metal films (Ni, Cu, and W) using an RF magnetron sputtering system with four-inch targets. Different sputtering times (5, 10, 20, and 30 min) were established to obtain different thicknesses of the metal layers with which the CNWs were coated. Field emission scanning electron microscopy (FE-SEM) was used to examine the cross-sectional and planar conditions of the CNWs, and energy dispersive spectroscopy (EDS) was used to analyze the CNW elements. The FE-SEM analysis of the cross-sectional and planar images confirmed that the metal layers were synthesized to a depth of 0.5 µm from the surfaces of the CNWs, and to a greater depth at the ends of the CNWs, irrespective of the deposition time and the metal species. The resistivity of the as-deposited CNWs appeared as 4.18 x 10(-3) Ω cm; that of the metal-coated CNWs was slightly lower; and that of the Ni-coated CNWs was the lowest (1.74 x 10(-3) Ω cm). The mobility of the metal-coated CNWs was almost unchanged, and that of the as-deposited CNWs was 1.23 x 10(3) cm2 V(-1) s(-1).

3.
Am J Chin Med ; 40(6): 1257-70, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23227796

RESUMO

Allergic inflammatory diseases such as food allergy, asthma, sinusitis, and atopic dermatitis are increasing worldwide. In this study, we investigated the effects of aqueous extract of Mosla chinensis Max. (AMC) on mast cell-mediated allergic inflammation and studied the possible mechanism of this action. AMC inhibited compound 48/80-induced systemic and immunoglobulin E (IgE)-mediated local anaphylaxis. AMC reduced intracellular calcium levels and downstream histamine release from rat peritoneal mast cells activated by compound 48/80 or IgE. In addition, AMC decreased gene expression and secretion of proinflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-6 and IL-8 in human mast cells. The inhibitory effect of AMC on cytokine expression was nuclear factor (NF)-κB dependent. Our results indicate that AMC inhibits mast cell-mediated allergic inflammatory reaction by suppressing histamine release and expression of proinflammatory cytokines and the involvement of calcium and NF-κB in these effects. AMC might be a possible therapeutic candidate for allergic inflammatory disorders.


Assuntos
Hipersensibilidade/prevenção & controle , Inflamação/prevenção & controle , Lamiaceae/química , Mastócitos/efeitos dos fármacos , Extratos Vegetais/farmacologia , Animais , Western Blotting , Citocinas/metabolismo , Ensaio de Imunoadsorção Enzimática , Liberação de Histamina/efeitos dos fármacos , Hipersensibilidade/imunologia , Hipersensibilidade/metabolismo , Inflamação/imunologia , Mediadores da Inflamação/metabolismo , Masculino , Mastócitos/metabolismo , Camundongos , Camundongos Endogâmicos ICR , Ratos , Ratos Sprague-Dawley
4.
Int J Mol Med ; 29(2): 303-10, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22075758

RESUMO

In this study, we investigated the effect of a water extract of the ripe fruits of Rubus coreanus Miq. (Rosaceae) (RFRC) on mast cell-mediated allergic inflammation and studied the possible mechanism of action. Mast cell-mediated allergic disease is involved in many diseases such as anaphylaxis, rhinitis, asthma and atopic dermatitis. RFRC dose-dependently inhibited compound 48/80-induced systemic anaphylaxis and serum histamine release in mice. RFRC reduced the immunoglobulin E (IgE)-mediated local allergic reaction, passive cutaneous anaphylaxis. RFRC attenuated histamine release from rat peritoneal mast cells and human mast cells by the reduction of intracellular calcium. RFRC decreased the phorbol 12-myristate 13-acetate (PMA) and the calcium ionophore A23187 (PMACI)-stimulated expression and secretion of pro-inflammatory cytokines in human mast cells. The inhibitory effect of RFRC on cytokine production was nuclear factor (NF)-κB- and mitogen-activated protein kinase (MAPK)-dependent. In addition, RFRC suppressed the activation of caspase-1. Our findings provide evidence that RFRC inhibits mast cell-derived allergic inflammatory reactions, and for the involvement of calcium, NF-κB, MAPKs and caspase-1 in these effects. Furthermore, in vivo and in vitro anti-allergic inflammatory effects of RFRC provide affirmative proof of a possible therapeutic application of this agent in allergic inflammatory diseases.


Assuntos
Anafilaxia/imunologia , Frutas/química , Mastócitos/efeitos dos fármacos , Mastócitos/imunologia , Extratos Vegetais/farmacologia , Rosaceae/química , Anafilaxia/induzido quimicamente , Animais , Cálcio/metabolismo , Caspase 1/metabolismo , Linhagem Celular , Modelos Animais de Doenças , Ativação Enzimática/efeitos dos fármacos , Expressão Gênica/efeitos dos fármacos , Liberação de Histamina/efeitos dos fármacos , Humanos , Inflamação/imunologia , Mediadores da Inflamação/metabolismo , Masculino , Camundongos , Proteínas Quinases Ativadas por Mitógeno/metabolismo , NF-kappa B/metabolismo , Ratos , Ratos Sprague-Dawley , p-Metoxi-N-metilfenetilamina/efeitos adversos
5.
Exp Biol Med (Maywood) ; 236(9): 1070-7, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21807818

RESUMO

Mast cell-mediated allergic reaction is involved in many diseases such as asthma and allergic rhinitis. Therefore, discovery of drugs for the prevention or treatment of allergic disease is an important topic in human health. In this study, we evaluated the effects of water extract of Elsholtzia ciliata (Thunb.) Hyland (Labiatae) (WEEC) on mast cell-mediated allergic inflammation and studied the possible mechanisms of action. WEEC inhibited compound 48/80-induced systemic and immunoglobulin E-mediated local anaphylaxis, and serum histamine release in mice. WEEC reduced intracellular calcium levels and downstream histamine release from human mast cells (HMC-1) activated with phorbol 12-myristate 13-acetate and calcium ionophore A23187. In addition, WEEC decreased gene expression and secretion of proinflammatory cytokines such as tumor necrosis factor-α, interleukin (IL)-1ß and IL-6 in HMC-1. The inhibitory effect of WEEC on cytokine expression was nuclear factor (NF)-κB and p38 mitogen-activated protein kinase (MAPK) dependent. Our results indicate that WEEC inhibits mast cell-mediated allergic inflammatory reactions by suppressing histamine release and proinflammatory cytokine expression, and involvement of calcium, NF-κB and p38 MAPK in these effects.


Assuntos
Cálcio/fisiologia , Hipersensibilidade/tratamento farmacológico , Lamiaceae , Mastócitos/efeitos dos fármacos , NF-kappa B/fisiologia , Extratos Vegetais/farmacologia , Proteínas Quinases p38 Ativadas por Mitógeno/fisiologia , Animais , Cálcio/sangue , Liberação de Histamina/efeitos dos fármacos , Hipersensibilidade/fisiopatologia , Inflamação/tratamento farmacológico , Inflamação/fisiopatologia , Masculino , Mastócitos/fisiologia , Camundongos , Camundongos Endogâmicos ICR , NF-kappa B/efeitos dos fármacos , Anafilaxia Cutânea Passiva/efeitos dos fármacos , Ratos , Ratos Sprague-Dawley , p-Metoxi-N-metilfenetilamina/farmacologia , Proteínas Quinases p38 Ativadas por Mitógeno/efeitos dos fármacos
6.
Food Chem Toxicol ; 48(10): 2797-802, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20633593

RESUMO

Mast cell-mediated allergic symptoms are involved in many diseases, such as asthma and sinusitis. In this study, we investigated the effect of ethanol extract of fruits of Prunus persica (L) Batsch (FPP) on the mast cell-mediated allergic inflammation and studied the possible mechanism of action. FPP dose-dependently inhibited compound 48/80-induced systemic anaphylaxis and immunoglobulin E-mediated local allergic reactions. Histamine releasing from mast cells was reduced by FPP, which was mediated by modulation of intracellular calcium. In addition, FPP attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated expression and secretion of pro-inflammatory cytokines in human mast cells. The inhibitory effect of FPP on pro-inflammatory cytokines was nuclear factor (NF)-kappaB dependent. Our findings provide evidence that FPP inhibits mast cell-derived allergic inflammation and involvement of calcium and NF-kappaB in these effects.


Assuntos
Antialérgicos/farmacologia , Anti-Inflamatórios/farmacologia , Sinalização do Cálcio/efeitos dos fármacos , NF-kappa B/metabolismo , Prunus/química , Anafilaxia/imunologia , Anafilaxia/prevenção & controle , Animais , Western Blotting , Cálcio/metabolismo , Citocinas/biossíntese , Liberação de Histamina/efeitos dos fármacos , Indicadores e Reagentes , Interleucina-8/metabolismo , Masculino , Mastócitos/efeitos dos fármacos , Mastócitos/metabolismo , Camundongos , Camundongos Endogâmicos ICR , Anafilaxia Cutânea Passiva/efeitos dos fármacos , Extratos Vegetais/farmacologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Necrose Tumoral alfa/metabolismo , p-Metoxi-N-metilfenetilamina/farmacologia
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