Micro-infiltration et rétention des scellants : évaluation de trois protocoles de mise en place

Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.

Micro-infiltration et rétention des scellants : évaluation de trois protocoles de mise en place

Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.

Restauração directa de classes II em pré-molares com compósitos

Tese de Doutoramento apresentada à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Doutor em em Biotecnologia e Saúde, Epidemiologia e Saúde Pública.

Selamento coronário em Endodontia

Introdução: A Endodontia é a especialidade da Medicina Dentária responsável pelo estudo e tratamento da câmara pulpar, de todo o sistema de canais radiculares e dos tecidos periapicais, bem como das doenças que os afetam. O selamento da porção coronária dos dentes alvo de tratamento endodôntico apresenta-se como um critério determinante no sucesso ou insucesso do tratamento. São vários os fatores que podem proporcionar um correto selamento coronário evitando assim a microinfiltração de microorganismos no sistema de canais radiculares. Entre estes fatores destacam-se o tratamento pré-endodôntico, a correta e eficaz instrumentação e desinfeção dos canais radiculares, a aplicação de materiais de selamento imediato, o número de sessões em que é concluído o tratamento e ainda a restauração provisória e definitiva do dente tratado endodonticamente. Objetivos: A elaboração deste trabalho de revisão teve como principais objetivos aprofundar o conhecimento sobre o selamento coronário tendo em conta as consequências deste processo no prognóstico de dentes alvo de tratamento endodôntico, bem como, os meios a utilizar pelo clínico para prevenir a microinfiltração através da porção coronária e os materiais mais indicados para que o selamento seja alcançado. Materiais e Métodos: Foi realizada uma pesquisa bibliográfica de artigos científicos disponíveis nas bases de dados eletrónicas MEDLINE/Pubmed, Science Direct, Scielo e B-on. As palavras-chave utilizadas nesta pesquisa foram: Coronal Seal, Coronal Microleakage, Coronal Leakage, Temporary Restauration, Temporary Filling Materials, Restauration in Endodontics, Post and Core Restauration, Restorative Materials. Esta pesquisa foi realizada entre Março de 2016 e Maio do mesmo ano e dela resultou a seleção de 132 artigos publicados entre 1985 e 2016, primeiramente pela leitura do titulo e do abstract. Após a leitura completa dos artigos excluíram-se 94 por não se terem considerado relevantes para a elaboração desta revisão bibliográfica, obtendo-se um total de 38 artigos utilizados. Foi também realizada uma pesquisa bibliográfica na biblioteca da Universidade Fernando Pessoa, na secção dedicada à Endodontia, da qual resultou a seleção dos manuais que se encontram descritos pormenorizadamente na bibliografia. Conclusão: O Médico Dentista deve estar sensibilizado para as implicações que o selamento coronário tem para o sucesso do tratamento endodôntico, uma vez que este pode afetar o resultado de todo o tratamento.

Dermal fibroblast infiltration of poly(ε-caprolactone) scaffolds fabricated by melt electrospinning in a direct writing mode

Melt electrospinning in a direct writing mode is a recent additive manufacturing approach to fabricate porous scaffolds for tissue engineering applications. In this study, we describe porous and cell-invasive poly (ε-caprolactone) scaffolds fabricated by combining melt electrospinning and a programmable x–y stage. Fibers were 7.5 ± 1.6 µm in diameter and separated by interfiber distances ranging from 8 to 133 µm, with an average of 46 ± 22 µm. Micro-computed tomography revealed that the resulting scaffolds had a highly porous (87%), three-dimensional structure. Due to the high porosity and interconnectivity of the scaffolds, a top-seeding method was adequate to achieve fibroblast penetration, with cells present throughout and underneath the scaffold. This was confirmed histologically, whereby a 3D fibroblast-scaffold construct with full cellular penetration was produced after 14 days in vitro. Immunohistochemistry was used to confirm the presence and even distribution of the key dermal extracellular matrix proteins, collagen type I and fibronectin. These results show that melt electrospinning in a direct writing mode can produce cell invasive scaffolds, using simple top-seeding approaches.

In vitro assessment of surface congruency and integration of chondrocytes at adjacent edges of micro-fabricated clefts on cartilage

Osteochondral grafts are common treatment options for joint focal defects due to their excellent functionality. However, the difficulty is matching the topography of host and graft(s) surfaces flush to one another. Incongruence could lead to disintegration particularly when the gap reaches subchondoral region. The aim of this study is therefore to investigate cell response to gap geometry when forming cartilage-cartilage bridge at the interface. The question is what would be the characteristics of such a gap if the cells could bridge across to fuse the edges? To answer this, osteochondral plugs devoid of host cells were prepared through enzymatic decellularization and artificial clefts of different sizes were created on the cartilage surface using laser ablation. High density pellets of heterologous chondrocytes were seeded on the defects and cultured with chondrogenic differentiation media for 35 days. The results showed that the behavior of chondrocytes was a function of gap topography. Depending on the distance of the edges two types of responses were generated. Resident cells surrounding distant edges demonstrated superficial attachment to one side whereas clefts of 150 to 250 µm width experienced cell migration and anchorage across the interface. The infiltration of chondrocytes into the gaps provided extra space for their proliferation and laying matrix; as the result faster filling of the initial void space was observed. On the other hand, distant and fit edges created an incomplete healing response due to the limited ability of differentiated chondrocytes to migrate and incorporate within the interface. It seems that the initial condition of the defects and the curvature profile of the adjacent edges were the prime determinants of the quality of repair; however, further studies to reveal the underlying mechanisms of cells adapting to and modifying the new environment would be of particular interest.

Protease-activated receptor 2 mediates eosinophil infiltration and hyperreactivity in allergic inflammation of the airway

Trypsin and mast cell tryptase can signal to epithelial cells, myocytes, and nerve fibers of the respiratory tract by cleaving proteinase-activated receptor 2 (PAR2). Since tryptase inhibitors are under development to treat asthma, a precise understanding of the contribution of PAR2 to airway inflammation is required. We examined the role of PAR2 in allergic inflammation of the airway by comparing OVA-sensitized and -challenged mice lacking or overexpressing PAR2. In wild-type mice, immunoreactive PAR2 was detected in airway epithelial cells and myocytes, and intranasal administration of a PAR2 agonist stimulated macrophage infiltration into bronchoalveolar lavage fluid. OVA challenge of immunized wild-type mice stimulated infiltration of leukocytes into bronchoalveolar lavage and induced airway hyperreactivity to inhaled methacholine. Compared with wild-type animals, eosinophil infiltration was inhibited by 73% in mice lacking PAR2 and increased by 88% in mice overexpressing PAR2. Similarly, compared with wild-type animals, airway hyperreactivity to inhaled methacholine (40 micro g/ml) was diminished 38% in mice lacking PAR2 and increased by 52% in mice overexpressing PAR2. PAR2 deletion also reduced IgE levels to OVA sensitization by 4-fold compared with those of wild-type animals. Thus, PAR2 contributes to the development of immunity and to allergic inflammation of the airway. Our results support the proposal that tryptase inhibitors and PAR2 antagonists may be useful therapies for inflammatory airway disease.

The physicochemical characterization and in vivo response of micro/nanoporous bioactive ceramic particulate bone graft materials

In this study, the physicochemical characteristics of calcium phosphate based bioactive ceramics of different compositions and blends presenting similar micro/nanoporosity and micrometer scale surface texture were characterized and evaluated in an in vivo model. Prior to the animal experiment, the porosity, surface area, particle size distribution, phase quantification, and dissolution of the materials tested were evaluated. The bone regenerative properties of the materials were evaluated using a rabbit calvaria model. After 2, 4, and 8 weeks, the animals were sacrificed and all samples were subjected to histologic observation and histomorphometric analysis. The material characterization showed that all materials tested presented variation in particle size, porosity and composition with different degrees of HA/TCP/lower stoichiometry phase ratios. Histologically, the calvarial defects presented temporal bone filling suggesting that all material groups were biocompatible and osteoconductive. Among the different materials tested, there were significant differences found in the amount of bone formation as a function of time. At 8 weeks, the micro/nanoporous material presenting similar to 55,TCP:45%,HA composition ratio presented higher amounts of new bone regeneration relative to other blends and a decrease in the amount of soft tissue infiltration. (C) 2014 Elsevier B.V. All rights reserved.