Despite the effort to optimize soft contact lens performance, almost half of the 140 million contact lens wearers worldwide experience symptoms of ocular dryness and discomfort, especially towards the end of the day. These symptoms are attributed to reduced compatibility between the contact lens and the ocular surface and are the main reason for contact lens discontinuation. As the interactions of the contact lens-eye interface are dynamic, the surface properties play a key role in improving ocular compatibility, comfort and overall performance of contact lenses. One promising method to reduce adverse interfacial interactions between the contact lens and the ocular surface is to modify the contact lens surface with a biomimetic layer inspired by the ocular surface and the tear film. Hyaluronic acid (HA) is a non-sulfated glycosaminoglycan naturally found in the ocular environment providing ocular hydration and lubrication. Proteoglycan 4 (PRG4), a mucin-like glycoprotein naturally produced at the ocular surface contributes to natural lubrication during blinking and to tear film stability. Surface modification with HA or PRG4 has been shown to result in improved wetting, lubricating and antifouling properties. Moreover, HA and PRG4 have been previously found to interact and synergistically reduce friction further. In the current work, novel HA and PRG4-grafted soft contact lens surfaces were prepared, and the impact of the surface tethered layer on important contact lens properties was assessed. Furthermore, the potential synergistic effect between HA and rhPRG4 on the examined properties was evaluated. Surface immobilization of HA on model conventional (pHEMA) and silicone (pHEMA-co-TRIS) hydrogel contact lenses was achieved by thiol-ene “click” chemistry, while full-length recombinant human PRG4 (rhPRG4) was surface grafted via carbonyldiimidazole (CDI) linking chemistry respectively. The chemical structure after each modification step was determined by attenuated total reflectance FTIR (FTIR-ATR) and X-ray photoelectron spectroscopy (XPS) analyses. HA-grafted model soft contact lenses were characterized by improved surface wettability, antifouling and water retentive properties, while a decreasing trend in boundary friction was observed but only for the HA-grafted pHEMA-co-TRIS materials. Surface-tethering of rhPRG4 was found to effectively enhance the surface wettability and boundary lubricating properties of pHEMA-co-TRIS hydrogels only, whereas both rhPRG4-grafted pHEMA and pHEMA-co-TRIS materials exhibited lower protein sorption and dehydration rate. Overall, the surface immobilization processes followed herein did not alter the optical transparency of the model soft contact lenses or their in vitro compatibility with human corneal epithelial cells. Finally, there was evidence that HA and rhPRG4 synergistically interacted, further improving the contact lens properties. However, the degree of HA/rhPRG4 synergy was found to be dependent on the configuration of the formed HA/rhPRG4 complex as well as the composition of the substrate hydrogel material, with the noted improvement being more significant for the model silicone hydrogels. This is the first study to examine surface grafted full-length rhPRG4 and the effect of this modification on contact lens properties. Moreover, the study is the first to investigate the interactions between covalently tethered rhPRG4 and solutions containing HA. The results of this thesis demonstrate that HA and rhPRG4 are good candidates for the development of novel biomimetic surfaces, especially for silicone hydrogel contact lenses. The potential for using these compounds in synergy was also demonstrated, with wetting solutions of HA showing promise for modifying rhPRG4 modified materials to improve symptoms of discomfort. These naturally occurring ocular agents have the potential to improve the management of ocular dryness and discomfort, thus optimizing the overall soft contact lens performance. / Thesis / Doctor of Philosophy (PhD)

No / Three-dimensional (3D) representations of com- plex geometric shapes, especially when they are recon- structed from magnetic resonance imaging (MRI) and com- puted tomography (CT) data, often result in large polygon meshes which require substantial storage for their handling, and normally have only one fixed level of detail (LOD). This can often be an obstacle for efficient data exchange and interactive work with such objects. We propose to re- place such large polygon meshes with a relatively small set of coefficients of the patchwise partial differential equation (PDE) function representation. With this model, the approx- imations of the original shapes can be rendered with any desired resolution at interactive rates. Our approach can di- rectly work with any common 3D reconstruction pipeline, which we demonstrate by applying it to a large reconstructed medical data set with irregular geometry.

Yes / Titanium alloy Ti-6Al-4V is known for both its excellent mechanical properties and its low surface hardness. This study explores a two-step process for depositing a hard nanocrystalline coating onto the surface of the Ti-alloy, followed by surface melting, which embeds hard nanoparticles into a thin surface layer of the alloy. The treated surface layer was studied using X-ray diffraction, scanning electron microscopy, and Vicker's micro-hardness testing. The results of the study show that the surface of the Ti-6Al-4V alloy can be successfully hardened by embedding nanosized Al2O3 particles into the surface using gas tungsten arc welding to melt the surface of the material. Surface melting the Ti-6Al-4V alloy with a 50A welding current produced the maximum microhardness of 701 HV0.2kg. The micro-hardness of the treated surface layer decreased with the increasing size of the nanoparticles, while the roughness of the surface increased with the increasing welding current. The heat input into the surface during the surface melting process resulted in the formation of various intermetallic compounds capable of further increasing the hardness of the Ti-6Al-4V surface.

A study of the stability of bicontinuous nanoporous metals is presented. Atomic scale simulations are used to probe the dominant mechanisms of geometric relaxation in these materials. A method is presented for generating model bicontinuous metal / void structures for use in atomistic simulations of bicontinuous nanoporous solids. The structures are generated with periodic boundary conditions using a phase-field model to simulate the spinodal decomposition of an ideal system. One phase in the model is then associated with the pore volume while the other phase is associated with the metal ligaments. Small angle neutron scattering was used to quantitatively compare experimental samples to those generated by the phase field method. EAM results using model structures with experimentally accessible length scales are presented which demonstrate the potential of such simulations in understanding the behavior of nanoporous metals. Simulated relaxations of these structures, as well as the relaxation of model spherical clusters, indicate that the surface relaxation effect dominates the overall dimensional relaxation of np-metals post processing. Capillary effects play a secondary role in the overall relaxation. The simulation results presented also identify a maximum surface area to volume ratio necessary to maintain mechanical stability beyond which the pore structure collapses. / Ph. D.

The aerodynamic flow and fluctuating surface pressure of a plane, turbulent, two-dimensional wall jet flow into still air over smooth and rough surfaces has been investigated in a recently constructed wall jet wind tunnel testing facility. The facility has been shown to produce a wall jet flow with Reynolds numbers based on the momentum thickness, Re<SUB>&delta</SUB> = &deltaU<SUB>m</SUB>/&nu, of between 395 and 1100 and nozzle exit Reynolds numbers, Re<SUB>j</SUB> = U<SUB>m</SUB>b/&nu, of between 16000 and 45000. The wall jet flow properties (&delta, &delta<SUP>*</SUP>, &theta, y<SUB>1/2</SUB>, U<SUB>m</SUB>, u<SUP>*</SUP>, etc.) were measured and characterized over a wide range of initial flow conditions and measurement locations relative to the wall jet source. These flow properties were measured for flow over a smooth flow surface and for flow over roughness patches of finite extent. The patches used in the current study varied in length from 305 mm to 914 mm (between 24 and 72 times the nozzle height, b) and were placed so that the leading edge of the patch was fixed at 1257 mm (x/b = 99) downstream of the wall jet source. These roughness patches were of a random sand grain roughness type and the roughness grain size was varied throughout this experiment. The tests covered roughness Reynolds numbers (k<SUP>+</SUP>) ranging from less than 2 to over 158 (covering the entire range of rough wall flow regimes from hydrodynamically smooth to fully rough). For the wall jet flows over 305 mm long patches of roughness, the displacement and momentum thicknesses were found to vary noticeably with the roughness grain size, but the maximum velocity, mixing layer length scale, y<SUB>/2</SUB>, and the boundary layer thickness were not seen to vary in a consistent, determinable way. Velocity spectra taken at a range of initial flow conditions and at several distinct heights above the flow surface showed a limited scaling dependency on the skin friction velocity near the flow surface. The spectral density of the surface pressure of the wall jet flow, which is not believed to have been previously investigated for smooth or rough surfaces, showed distinct differences with that seen in a conventional boundary layer flow, especially at low frequencies. This difference is believed to be due to the presence of a mixing layer in the wall jet flow. Both the spectral shape and level were heavily affected by the variation in roughness grain size. This effect was most notable in overlap region of the spectrum. Attempts to scale the wall jet surface pressure spectra using outer and inner variables were successful for the smooth wall flows. The scaling of the rough wall jet flow surface pressure proved to be much more difficult, and conventional scaling techniques used for ordinary turbulent boundary layer surface pressure spectra were not able to account for the changes in roughness present during the current study. An empirical scaling scheme was proposed, but was only marginally effective at scaling the rough wall surface pressure. / Ph. D.

The self-assembly blends of cellulose propionate (CP) and fluorine (F)-containing cellulose derivatives was examined on a model system of solvent cast films. The F-containing derivatives were either high molecular weight statistical cellulose esters with a number of F-containing substituent evenly distributed along the backbone (F-esters), or F-terminated CP-segments with exactly one F-containing endgroup. The F-esters were synthesized in a homogeneous phase and identified by 19F-NMR. Thermal analysis showed improved thermal stability of the F-esters when compared to F-free derivatives. 1-monohydroxy functionalized CP-segments were synthesized by HBr depolymerization using either a commercially available CP with residual OH-groups or a perpropionylated CP (CTP). The hydrolysis using the commercial CP yielded only segments of a minimum DP of 50 and the Mark-Houwink constant declined from 1 to 0.6. The results indicate that in the presence of free hydroxyls branches are formed by transglycosidation. The hydrolysis from perpropionylated CP resulted in segments with a minimum DP of 7, which is in accordance to previous studies. F-terminated CP segments were synthesized by coupling of the appropriate F-containing alcohol to the CP segment via toluene diisocyanate. Solutions containing F-terminated CP-segments showed typical critical micelle behavior. The critical micelle concentration depended on the molecular weight of the CP segment and the type of F-containing endgroup. The micelles are thought to consist of a core of the F-endgroups and a corona made-up of CP. Films containing the oligomers cast from micellar solution revealed a linear decrease in wetting force according to the blend composition of the oligomer, i.e. behavior according to the rule of mixing. This indicated the absence of surface segregation of the F-endgroup and it is explained with the fact that the micellar structure is retained in the solid state, suppressing surface segregation. The solid state micelles were visualized as dome-like protrusions by height image atomic force microscopy. In systems blended with CP the distance between the protrusions was found to increase with increasing CP content which was explained by a dilution process. Films containing F-esters were characterized by wetting force measurements and x-ray photoelectron spectroscopy (XPS). The wetting force decreased dramatically at low blend content of the F-ester and at the same time an F surface-concentration higher then expected from the blend composition was found by XPS. This indicated self-assembly by surface segregation of the F-containing species during film formation. The extent of surface segregation was found to depend on the type of the F-ester group as well as on the blend concentration of the F-ester. Dynamic wetting force measurements revealed hysteresis in films containing either F-esters or F-terminated CP segments. The hysteresis was found to be both kinetic (water sorption and reorganization) and thermodynamic (surface roughness and surface coverage with F-moieties) in nature. Consecutive force loops revealed an increase in the wetting force (advancing and receding) with increasing loop number, indicating the increased hydrophobicity of the surface. The force increase was determined to be due to water sorption as well as due to surface reorganization. An increase in the size of the F-groups signified a decrease in reorganization rate due to a decreased mobility of the group. The process of reorganization was fully reversible, a behavior which is congruent with the definition of smart behavior. / Ph. D.

Metallic nanoparticles (NPs) are exploited for their ability to interact with organic compounds and to increase significantly the fluorescence intensity and the photostability of many fluorescent dye molecules. Metal enhanced fluorescence (MEF) is therefore widely investigated for biosensing applications. When used in immunoassays, silver island films (SIFs) could augment the fluorescence intensity of fluorescein by a factor of seventeen; SIFs were also able to double or triple the emission intensity of cyanine dyes which are commonly used in (deoxyribonucleic acid) DNA microarrays. The emission intensity of indocyanine green — widely used as a contrast agent in medical imaging — was about twenty times higher in the proximity of SIFs. This enhancement phenomenon — due to the surface plasmon polaritons associated with the metallic NPs — can be explained by energy transfer from the metal NPs to the fluorescent dye molecules or by a modified local electromagnetic field experienced by the fluorophores in the vicinity of metal surfaces. Our research focused on the optical characterization of colloidal gold-silver alloy NPs containing different ratios of gold and silver (Au_1.00-Ag_0.00, Au_0.75-Ag_0.25, Au_0.50-Ag_0.50, and Au_0.25-Ag_0.75), as well as their interaction with three fluorophores: rose bengal, rhodamine B, and fluorescein sodium. Depending upon the dye quantum yield and its concentration in solution, enhancement or quenching of fluorescence was obtained. Thus, a three to five times increase in fluorescence intensity was observed in a 2.0 mM solution of rose bengal with all nanoalloys, a slight enhancement of fluorescence (1.2 – 1.6 times) was noticed in a 0.13 mM solution of rhodamine B with all four types of NPs, and fluorescence quenching occurred in all the fluorescein-NP solutions regardless of the dye concentration. / Master of Science

Yes / Bezier curves and surfaces are two very useful tools in Geometric Modeling, with many applications. In this paper, we will offer a new method to provide approximations of regular curves and surfaces by Bezier ones, with the corresponding examples.

Depuis la préhistoire, plusieurs matériaux ont été utilisés pour fabriquer des instruments et des appareils de santé. Au cours des dernières décennies, avec l’apparition du terme « biomatériau », les matériaux ont été conçus pour contrôler des réactions biologiques spécifiques, pour augmenter la durée de vie des biodispositifs et la qualité de vie des patients dans le monde. Cependant, indépendamment de la nature du matériau, ou au sens strict du biomatériau, et de la fonction remplie, ils sont susceptibles aux phénomènes de surface causés par son environnement. Certains phénomènes intéressants incluent l’action des protéines, des électrolytes et des cellules sur les surfaces métalliques. Ces interactions peuvent entraîner le développement de complications telles que la formation de thrombus, la corrosion et la calcification, qui affecteront le fonctionnement des dispositifs, et la contamination bactérienne qui peut transformer la surface en vecteur de propagation de maladies. Des recherches ont exploité des stratégies de modification de surface pour minimiser ou éviter ces complications. Ces approches demandent du temps et des efforts pour développer une surface efficace pour chaque cas. Sur cette base, l’objectif principal de ce travail était de concevoir et de développer des revêtements à base de chitosane à utiliser dans le revêtement de surfaces métalliques et de dispositifs utilisés dans le système de santé et de modifier ces surfaces pour moduler la réponse biologique. Pour atteindre cet objectif, le projet de recherche a été divisé en trois parties. La première était le greffage du chitosane utilisant de la dopamine comme ancre. La deuxième était le développement d’un greffage original en une étape remplaçant la dopamine par l’acide caféique. La dernière était la modification du revêtement de chitosane pour moduler la réponse biologique de la surface. À chaque étape, les surfaces revêtues ont été caractérisées par analyses biologiques et physico-chimiques. Les résultats ont démontré que la méthodologie développée produisait des revêtements de chitosane qui possédait des réponses biologiques et des performances physico-chimiques favorables et qui pouvait être modifiés pour améliorer ou conférer la propriété souhaitée. De plus, cette méthodologie permet de produire une plateforme capable d’être appliquée sur une large gamme de complications en raison de sa modulabilité. Cela représente une diminution de la consommation de temps pour créer une nouvelle surface à partir du zéro pour chaque situation. / Since prehistoric times, several materials have been used to make health instruments and devices. In recent decades, with the appearance of the term "biomaterial", materials have been designed to control specific biological reactions, to increase the lifespan of biodevices and the quality of life of patients around the world. However, regardless of the nature of the material, or in the strict sense of the biomaterial, and the function fulfilled, they are susceptible to the surface phenomena caused by its environment. These phenomena include the action of proteins, electrolytes, and cells on metal surfaces. These interactions can lead to the development of complications such as thrombus formation,corrosion, and calcification, which will affect the functioning of the devices, and bacterial contamination, which can transform the surface into a vector for the spread of disease. Researches were made on the use of surface modification strategies to minimize or avoid these complications. These approaches require time and effort to develop an effective surface for each case. On this basis, the main objective of this work was to design and develop chitosan-based coatings to coat metallic surfaces and devices used in the health care system and to modify these surfaces to modulate the biological response. To accomplish this objective, the research project was divided into three parts. The first was the grafting of chitosan using dopamine as an anchor. The second was the development of an original one step graft replacing dopamine with caffeic acid. The last was the modification of the chitosan coating to modulate the biological response of the surface. At each stage, the coated surfaces were characterized by biological and physicochemical analyzes. The results obtained showed that the developed methodology produced chitosan coatings that had favorable biological responses and physicochemical performances, and that it could be modified to improve or confer the desired property. Besides, this methodology makes it possible to produce a platform able to be applied to many complications due to its modularity. It represents a reduction in the consumption of time to create a new surface from scratch for each situation.

Published Article / The development of innovative products and their realisation by means of advanced manufacturing methods and process combinations is more becoming a key issue in international competitiveness. The industrial production is subsequently influenced ever more by the possibilities that Rapid Technologies -Rapid Modelling and Reverse Engineering, Rapid Prototyping and Tooling, Rapid Manufacturing can offer. Reverse Engineering (RE) is the process of digitising a physical object to obtain computerised data for further development as opposed to manufacturing a product from a digital model, e.g. CNC machining. This paper reflects experiences gained in the use of RE approaches for industrial applications, comparing specifically the use of tactile methods and digitising techniques based on photogrammetry principles. Process capabilities and the internal process chain are scrutinised. Practical case studies are presented and discussed with an emphasis on project lead times and dimensional accuracy obtained. Particular attention is paid to challenges related to surface recreation and manufacture of tooling for various components. The purpose of the paper is therefore to highlight the capabilities and wide range of applications for Reverse Engineering, while at the same time outlining pitfalls and limitations of this remarkable technology.