Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Métodos Terapêuticos e Terapias MTCI
Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Int J Nanomedicine ; 9: 3631-43, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25120361

RESUMO

Although the health effects of zinc oxide nanoparticles (ZnONPs) on the respiratory system have been reported, the fate, potential toxicity, and mechanisms in biological cells of these particles, as related to particle size and surface characteristics, have not been well elucidated. To determine the physicochemical properties of ZnONPs that govern cytotoxicity, we investigated the effects of size, electronic properties, zinc concentration, and pH on cell viability using human alveolar-basal epithelial A549 cells as a model. We observed that a 2-hour or longer exposure to ZnONPs induced changes in cell viability. The alteration in cell viability was associated with the zeta potentials and pH values of the ZnONPs. Proteomic profiling of A549 exposed to ZnONPs for 2 and 4 hours was used to determine the biological mechanisms of ZnONP toxicity. p53-pathway activation was the core mechanism regulating cell viability in response to particle size. Activation of the Wnt and TGFß signaling pathways was also important in the cellular response to ZnONPs of different sizes. The cadherin and Wnt signaling pathways were important cellular mechanisms triggered by surface differences. These results suggested that the size and surface characteristics of ZnONPs might play an important role in their observed cytotoxicity. This approach facilitates the design of more comprehensive systems for the evaluation of nanoparticles.


Assuntos
Óxido de Alumínio , Sobrevivência Celular/efeitos dos fármacos , Nanopartículas Metálicas , Proteoma/efeitos dos fármacos , Óxido de Zinco , Óxido de Alumínio/química , Óxido de Alumínio/toxicidade , Linhagem Celular , Humanos , Nanopartículas Metálicas/química , Nanopartículas Metálicas/toxicidade , Proteínas/análise , Proteínas/química , Proteínas/classificação , Proteoma/análise , Proteoma/química , Óxido de Zinco/química , Óxido de Zinco/toxicidade
2.
J Med Food ; 15(6): 520-6, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22468646

RESUMO

Soybean fermentation broth (SFB) exhibits potent antibacterial activity against different species of bacteria in in vitro assays and animal models. Four isoflavone compounds-daidzin, genistin, genistein, and daidzein-of SFB were analyzed and quantified by high-performance liquid chromatography. In the in vitro test, daidzin and daidzein had more potent antibacterial activity than genistin. The minimum inhibition concentration values for these bacteria of SFB ranged from 1.25% to 5%, and the minimum bactericidal concentration values of strains ranged from 2.5% to 10%, depending on the species or strain. Vancomycin-resistant Entercoccus faecalis (VRE) strains were also tested for susceptibility to SFB in two species of animal model: the Sprague-Dawley rat and the BALB/c mouse. SFB-fed Sprague-Dawley rats showed excellent elimination efficiency against VRE, close to 99% compared with the phosphate-buffered saline-fed control group. In the BALB/c mouse model, SFB antibacterial activity was 65-80% against VRE compared with the control. In conclusion, SFB contains natural antibacterial substances such as daidzin, genistin, and daidzein that inhibit bacterial growth.


Assuntos
Antibacterianos/uso terapêutico , Enterococcus faecalis/efeitos dos fármacos , Glycine max/química , Infecções por Bactérias Gram-Positivas/tratamento farmacológico , Isoflavonas/uso terapêutico , Leite de Soja/farmacologia , Resistência a Vancomicina/efeitos dos fármacos , Animais , Antibacterianos/farmacologia , Modelos Animais de Doenças , Fermentação , Infecções por Bactérias Gram-Positivas/microbiologia , Isoflavonas/análise , Isoflavonas/farmacologia , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Testes de Sensibilidade Microbiana , Ratos , Ratos Sprague-Dawley
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA