No description available.

<p>   </p> <p>Subcutaneous injection is a biotherapeutic drug delivery method that is currently growing due to low cost, better patient compliance, minimally invasive, and the convenience that it can be done at home. Common injection sites for subcutaneous injection include the upper outer arms, abdomen, buttocks, and upper outer thigh. Heterogeneity of the tissue exists between and within each of these locations. The subcutaneous tissue space is made up of adipose tissue, proteins, collagen, and blood vessels and each of these components has an impact on the mass transport of the injected biotherapeutics and how they are absorbed into the vascular system and then distributed to the body. The current methods used to model the subcutaneous tissue space are either very expensive and not feasible for multiple repetitions, cannot incorporate fibrillar proteins or cellular components, or model a more homogeneous tissue space. These limitations do not allow for these models to accurately represent the subcutaneous tissue space. The engineering objective for this project was to develop a platform with tunable matrix architecture and biochemical composition for evaluating mass transport. This project utilizes collagen and the primary matrix due to the large abundance of collagen in the body.  We explored the effects that a change in polymerization temperature of the collagen and collagen concentration had on the fiber architecture and pore diameter. The results showed that higher polymerization temperatures of the collagen gels resulted in smaller fiber and pore diameters and an increase in concentration resulted in an increase in fiber volume fraction and a decrease in pore diameter. Fibronectin (FN) and hyaluronic acid (HA) were added to the collagen gels to analyze the impact on the structure of collagen gels with a change in polymerization temperature and collagen concentration. The addition of FN did not strongly alter the collagen fiber architecture between polymerization temperatures and collagen concentrations. Through staining and imaging, we saw an aggregation of FN around the collagen fibrils due to their opposing charges causing them to bind. The addition of HA had moderate impact on collagen fiber architecture across all polymerization temperatures and between collagen concentrations. The collagen + FN gels were used for the mass transport study. The results showed that there was little to no difference between the recovery rates of macromolecules of different charges and size between the collagen and collagen + FN gels, indicating that the transport of molecules through both of the collagen gels was impacted by a steric effect rather than an effect in charge.</p> <p>  </p>

This master thesis introduces FGSSNet, a novel multi-headed feature-guided semantic segmentation (FGSS) architecture designed to improve the generalization ability of segmentation models on floorplans by injecting domain-specific information into the latent space, guiding the segmentation process. FGSSNet features a U-Net segmentation backbone with a jointly trained reconstruction head attached to the U-Net decoder, tasked with reconstructing the injected feature maps, forcing their utilization throughout the decoding process. A multi-headed dedicated feature extractor is used to extract the domain-specific feature maps used by the FGSSNet while also predicting the wall width used for our novel dynamic scaling algorithm, designed to ensure spatial consistency between the training and real-world floorplans. The results show that the reconstruction head proved redundant, diverting the networks attention away from the segmentation task, ultimately hindering its performance. Instead, the ablated reconstruction head model, FGSSNet-NoRec, showed increased performance by utilizing the injected features freely, showcasing their importance. FGSSNet-NoRec slightly improves the IoU performance of comparable U-Net models by achieving 79.3 wall IoU(%) on a preprocessed CubiCasa5K dataset while showing an average IoU increase of 3.0 (5.3%) units on the more challenging real-world floorplans, displaying a superior generalization performance by leveraging the injected domain-specific information.

No description available.

The diploma thesis deals with the social stigma of injecting users of illegal addictive substances, specifically it deals with the social stigmas that may occur in connection with the use of addictive substances. Social stigma can result in barriers to the use of social services by injecting drug users. The diploma thesis deals with the obstacles that injecting users of illegal addictive substances encounter when using social services. The work tries to identify, map, and describe these obstacles. The theoretical part of the thesis describes the topic of the social environment, addictive substances, addiction, methods of working with users of addictive substances and obstacles associated with the use of social services and other services. The main chapters deal with theoretical topics related to the topic and title of the diploma thesis. The subchapters then elaborate the main topics in more detail. The empirical part of the work was realized through a qualitative survey, specifically through semi-structured interviews. The research sample was a set of contact center clients in the Ústí Region. The main goal of this work is to identify and describe the obstacles that injecting users of illegal addictive substances encounter when using social services. The other sub-objectives were as follows: to...

<div>In contrast to traditional steel and aluminum, short fiber reinforced polymer composites (SFRCs) provide promising alternatives in material selection for automotive and aerospace applications due to their potential to decrease weight while maintaining excellent mechanical properties. However, uncertainties about the influence of complex microstructures and defects on mechanical response have prevented widespread adoption of material models for</div><div>SFRCs. In order to build confidence in models’ predictions requires deepened insight into the heterogenous damage mechanisms. Therefore, this research takes a micro-mechanics standpoint of assessing the damage behavior of SFRCs, particularly micro-void nucleation at the fiber tips, by passing information of microstructural attributes within neighborhoods of incipient damage and non-damage sites, into a framework that establishes correlations between the microstructural information and damage. To achieve this, in-situ x-ray tomography of the gauge sections of two cylindrical injection molded dog-bone specimens, composed of E-glass fibers in a polypropylene matrix, was conducted while the specimens were monotonically loaded until failure. This was followed by (i) the development of microstructural characterization frameworks for segmenting fiber and porosity features in 3D images, (ii) the development of a digital volume correlation informed damage detection framework that confines search spaces of potential damage sites, and (iii) the use of a Gaussian process classification framework to explore the dependency of micro-void nucleation on neighboring microstructural defects by ranking each of their contributions. Specifically, the analysis considered microstructural metrics related to the closest fiber, the closest pore, and the local stiffness, and the results demonstrated that less stiff resin rich areas were more relevant for micro-void nucleation than clustered fiber tips, T-intersections of fibers, or varying porosity volumes. This analysis provides a ranking of microstructural metrics that induce microvoid nucleation, which can be helpful for modelers to validate their predictions on proclivity of damage initiation in the presence of wide distributions of microstructural features and</div><div>manufacturing defects. </div>

La majorité des personnes utilisatrices de drogues par injection (PUDI) contracteront le virus de l’hépatite C (VHC), les mettant à risque accru de complications hépatiques graves et parfois mortelles. Les comportements les plus risqués pour l’acquisition du VHC incluent le partage de matériel d’injection et l’injection à haute fréquence. Un facteur jusqu’ici négligé dans l’évaluation du risque de VHC est l’aspect dynamique de l’injection, c.-à-d. la manière dont elle varie dans le temps, incluant l’effet des périodes sans injection et celui des changements dans la fréquence d’injection. On reconnaît également l’effet délétère que l’instabilité résidentielle peut avoir sur le risque de VHC, bien que les mécanismes sous-jacents soient mal compris. Cette thèse s’intéresse à l’effet des variations temporelles de l’injection sur le risque de VHC, et à la manière dont la fréquence d’injection évolue en concomitance avec les conditions résidentielles dans le temps, afin d’aider au développement de nouvelles stratégies de prévention du VHC. Les données ont été recueillies entre mars 2011 et juin 2016 dans la Hepatitis Cohort, une cohorte de PUDI suivies trimestriellement à Montréal, au Québec. Une première analyse a évalué l’effet des périodes sans injection de trois mois ou moins sur le risque de VHC sur 916 personnes-années de suivi, par régression de Cox (N=372). Celle-ci suggère que les PUDI présentant des périodes sans injection courtes (3/3 mois sans injection) et sporadiques (1/3 ou 2/3 mois sans injection) sont respectivement 76% et 44% moins à risque de VHC que celles s’injectant de manière persistante (0/3 mois sans injection). Une deuxième analyse a utilisé la modélisation de trajectoires fondée sur le groupement pour identifier cinq types distincts de trajectoires de fréquence d’injection suivies sur une année, lesquels ont ensuite été comparés en termes d’incidence du VHC sur des périodes de suivi allant de 71 à 355 personnes-années (N=386). Les résultats suggèrent que les PUDI dont la fréquence reste élevée (injection fréquente) ou change dans le temps (croissante, décroissante) sont à plus haut risque de VHC que celles s’injectant à basse fréquence (sporadique, peu fréquente). Une dernière analyse a identifié trois types de trajectoires de stabilité résidentielle suivies sur un an (persistance, déclin, amélioration; N=386), lesquels ont été évalués en association avec les trajectoires de fréquence d’injection suivies simultanément. Les résultats suggèrent qu’il existe un lien entre l’amélioration des conditions résidentielles et la diminution de la fréquence d’injection, mais aussi que la probabilité d’injection à fréquence croissante est plus élevée chez les PUDI maintenant des conditions résidentielles stables que celles chez qui elles s’améliorent. Collectivement, les résultats ont de nombreuses implications en termes de prévention du VHC. Cliniquement, l’instabilité de la fréquence d’injection semble être un facteur de risque à monitorer régulièrement. En termes de santé publique, les interventions favorisant l’engagement dans des périodes sans injection ou le maintien d’une basse fréquence d’injection pourraient être prometteuses. Enfin, les stratégies visant l’amélioration des conditions résidentielles pourraient éventuellement aider les PUDI à réduire leur fréquence d’injection, mais être insuffisantes pour maintenir celle-ci à basse fréquence une fois la stabilité atteinte. / The majority of people who inject drugs (PWID) will become infected with hepatitis C virus (HCV), placing them at risk of serious and sometimes fatal liver complications. Injecting behaviours with higher risk of HCV transmission include injecting equipment sharing and high frequency injecting. One factor that has been overlooked when assessing HCV acquisition risk is the dynamic aspect of drug injecting, i.e., how drug injecting varies over time, including the role of injecting cessation episodes and that of changes in injecting frequency. Moreover, there is growing recognition of the deleterious effect unstable housing can have on HCV acquisition risk, although the underlying mechanisms are not yet fully understood. This thesis examines how temporal variations in drug injecting relate to HCV acquisition risk and further explores how housing conditions and injecting frequency evolve together over time, for the purposes of contributing to the development of novel HCV prevention strategies. Data were collected between March 2011 and June 2016 in the Hepatitis Cohort, a prospective cohort study of PWID interviewed and tested for HCV infection at three-monthly intervals in Montréal, Québec. A first analysis examined the effect of injecting cessation episodes of three months or less on the risk of contracting HCV during 916 person-years of follow-up, using Cox regression (N=372). Results suggest that PWID with short injecting cessation episodes (3/3 months without injecting) or sporadic injecting cessation episodes (1/3 or 2/3 months without injecting) are 76% and 44% less at risk of contracting HCV than those with persistent injecting (0/3 months without injecting), respectively. A second analysis used group-based trajectory modeling to identify five distinct types of one-year injecting frequency trajectories and compared these in terms of HCV incidence over follow-up periods ranging from 71 to 355 person-years (N=386). Findings suggest that PWID injecting with consistently high frequencies (frequent) or time-varying frequencies (increasing, decreasing) are at greater HCV acquisition risk compared with those maintaining low injecting frequencies (sporadic, infrequent). Finally, a third analysis identified three types of one-year housing stability trajectories (sustained, declining, improving) and examined their associations with concomitant injecting frequency trajectories (N=386). Findings suggest an association between improving housing stability and decreasing injecting frequency, but also a higher probability of increasing injecting frequency among PWID who maintain housing stability compared to those that improve it. Collectively, these findings have numerous implications for HCV prevention. Clinically, instability in injecting frequency appears to be a risk factor that should be monitored regularly. From a public health perspective, interventions that promote engagement in injecting cessation episodes or maintenance of low injecting frequency may be promising. Finally, strategies aimed to improve housing stability may help PWID to decrease their injecting frequency but may not be sufficient to help them maintain low injecting frequencies once housing stability is achieved.