188 resultados para BD
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PhD Thesis in Bioengineering
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PhD thesis in Bioengineering
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Doctoral Thesis (PhD Programm on Molecular and Environmental Biology)
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Stents são estruturas entrançadas utilizadas no tratamento de doenças cardiovasculares, uma vez que previnem ou impedem a constrição do fluxo sanguíneo. A sua forma tubular é essencial para que consiga atingir a sua finalidade e manter o normal fluxo sanguíneo nos vasos sanguíneos. Neste trabalho foram desenvolvidos stents fibrosos entrançados, à base de poliéster (PES), poliamida (PA) e polipropileno (PP). Além disso, as propriedades mecânicas, que são influenciadas pelo ângulo de entrançamento e o diâmetro do mandril, foram testadas e discutidas. Este trabalho mostra que os stents fibrosos apresentam propriedades mecânicas adequadas e elevado potencial de mercado
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Tese de Doutoramento em Ciências da Educação - Especialidade em Filosofia da Educação
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Tese de Doutoramento - Leaders for Technical Industries (LTI) - MIT Portugal
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The MAP-i Doctoral Program of the Universities of Minho, Aveiro and Porto
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Tese de Doutoramento em Ciências da Literatura - Especialidade em Teoria da Literatura
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The MAP-i Doctoral Program of the Universities of Minho, Aveiro and Porto.
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Tese de Doutoramento em Estudos da Criança (área de especialização em Comunicação Visual e Expressão Plástica)
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Tese de Doutoramento em Engenharia Química e Biológica.
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Tese de Doutoramento em Ciências da Educação (Área de Conhecimento: Educação ambiental e para a Sustentabilidade)
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Staphylococcus epidermidis is a biofilm - forming bacterium and a leading etiological agent of nosocomial infections. The ability to establish biofilms on indwelling medical devices is a key virulence factor for this bacterium. Still, the influence of poly - N - acetyl glucosamine (PNAG), the major component of the extracellular biofilm matrix, in the host immune response has been scarcely studied. Here, t h is influence was assessed in mice challenged i.p. with PNAG - p roducing (WT) and isogenic - mutant lacking PNAG (M10) bacteria grown in biofilm - inducing conditions. Faster bacterial clearance was observed in the mice infected with WT bacteria than in M10 - infected counterparts , which w as accompanied by earlier neutrophil recruitment and higher IL - 6 production. Interestingly, in the WT - infected mice, but not in those infected with M10 , elevated serum IL - 10 was detected . To further study the effe ct of PNAG in the immune response, mice were primed with WT or M10 biofilm bacteria and subsequently infected with WT biofilm - released cells. WT - primed mice presented a higher frequency of splenic IFN - γ + and IL - 17 + CD4 + T cells, and more severe liver patho logy than M10 - primed counterparts. Nevertheless, T reg cells obtained from the WT - primed mice presented a higher suppressive function than those obtained from M10 - primed mice. This effect was abrogated when IL - 10 - deficient mice were similarly primed and infected indicating that PNAG promotes the differentiati on of highly suppressive T reg cells by a mechanism dependent on IL - 10. Altogether, these results provide evidence help ing explain ing the coexistence of inflammation and bacterial persistence often observed in biofilm - originated S. epidermidis infections
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Efficient liposome disruption inside the cells is a key for success with any type of drug delivery system. The efficacy of drug delivery is currently evaluated by direct visualization of labeled liposomes internalized by cells, not addressing objectively the release and distribution of the drug. Here, we propose a novel method to easily assess liposome disruption and drug release into the cytoplasm. We propose the encapsulation of the cationic dye Hoechst 34,580 to detect an increase in blue fluorescence due to its specific binding to negatively charged DNA. For that, the dye needs to be released inside the cell and translocated to the nucleus. The present approach correlates the intensity of detected fluorescent dye with liposome disruption and consequently assesses drug delivery within the cells.
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Tese de Doutoramento em Ciências da Comunicação (área de especialização em Sociologia da Comunicação e da Informação).