Les travaux réalisés au cours de cette thèse concernent trois différentes techniques de formulation innovantes qui ont été étudiées en tant que procédés robustes et efficaces pour l’élaboration de polymères fonctionnels à architecture contrôlée ou bien de films minces réticulés. La première stratégie exploite le caractère orthogonal de la click chemistry la plus connue: la cycloaddition catalysée par le cuivre(I) entre un azoture et un alcyne (CuAAC). Nous avons développé deux stratégies monotopes tandem complémentaires alliant CuAAC et Polymérisation Radicalaire Contrôlée (PRC) afin d’obtenir efficacement des architectures complexes en une seule étape. La deuxième stratégie concerne l’utilisation de la chimie thiol-ène en tant que click chemistry pour la fonctionnalisation de polymères et la réalisation d’architectures bien définies. Une série de polymères portant des insaturations ont été synthétisés par des techniques de polymérisation contrôlée dans le but d’étudier et de comparer l’efficacité des couplages thiol-ène initiés thermiquement ou hotochimiquement. Dans cette étude, l’orthogonalité de la chimie thiol-ène avec la CuAAC a également été étudiée. La troisième stratégie est inspirée des récentes techniques d’élaboration de matériaux réticulés/fonctionnalisés par couplage des azotures avec des insaturations. Nous avons développé une nouvelle stratégie d’élaboration efficace de matériaux massifs et de films minces de PDMS réticulés par utilisation d’un diazoture comme agent réticulant. Cette étude est réalisée en combinant des expertises en rhéologie, chimie et en couches minces. / This thesis focuses on three different and innovative techniques studied as efficient and robust processes to elaborate functional polymers with controlled architecture or crosslinked materials and thin films. The first strategy exploits the orthogonal property of a famous click chemistry: the Copper (I)-catalyzed Azide–Alkyne Cycloaddition (CuAAC). We developed two complementary strategies based on the one-pot tandem combination of CuAAC and Controlled Radical Polymerisation techniques (CRP) to efficiently elaborate complex polymer architectures. The second strategy is focused on the thiol-ene chemistry as a click chemistry and its use for the functionalisation of polymers in order to obtain well defined architectures. A series of alkenefunctional polymers were synthesized by controlled polymerization techniques in order to investigate and compare the efficiency and orthogonality of both photochemically and thermally initiated thiol-ene click coupling reactions. Orthogonality of thiol-ene chemistry with CuAAC was also studied. The third strategy is inspired of new processes developed to perform crosslinked/functionalised materials by azide-ene couplings. We investigate a new strategy for the elaboration of crosslinked PDMS in bulk or in thin films with the use of a diazide as coupling agent. This last study combines analyses in rheology, chemistry and in thin layer.

L’objectif de ce travail a été d’introduire des groupements fonctionnels au sein de chaînes polymère silicone pour former des assemblages supramoléculaires, dans le but de former de nouveaux matériaux. Tout d’abord, une étude approfondie de la bibliographie a permis de cerner les avantages et limitations de la réaction d’aza-Michael appliquée aux silicones. Cette étude a aussi permis d’acquérir de solides connaissances générales sur la réaction d’aza-Michael appliquée à des composés organiques aminé et de soulever des points peu ou pas traités tels que la sélectivité et la réversibilité de la réaction. Afin de comprendre et contrôler cette réaction, une étude modèle impliquant un PDMS aminé simple et l’acrylate de butyle a été réalisée. Plusieurs paramètres tels que la présence de solvants polaires protiques, de catalyseurs, ou une température élevée permettent de promouvoir la réaction. Des données cinétiques ont également mis en relief la possibilité de contrôler la sélectivité de la réaction sur un groupement amine primaire (mono- ou di-addition). Un composé 100% mono-adduit et un composé 100% di-adduit ont ainsi été synthétisé en choisissant soigneusement les paramètres expérimentaux. La réaction d’aza-Michael a ensuité été appliquée à un accepteur de Michael moins réactif, l’acide acrylique. Ce composé a la particularité de réagir instantanément et exothermiquement avec les amines par réaction acido-basique. Un déplacement de l’équilibre chimique de la réaction acido-basique vers la formation d’adduits de Michael a été rendu possible, générant ainsi des groupements zwitterioniques. Une étude approfondie de la réaction avec des amines organiques et des oligomères/polymères siliciés et aminés a été réalisée afin de déterminer la structure exacte des groupements fonctionnels obtenus et d’évaluer les propriétés visco-élastiques de tels produits. La dernière partie de ce projet a été focalisée sur l’étude et la caractérisation de ces matériaux silicones supramoléculaires s’échelonnant du liquide visco-élastique à l’élastomère silicone thermoplastique. / This PhD thesis was focused on the incorporation of functional groups onto the siloxane polymer backbone such that supramolecular assemblies are formed, in order to prepare new supramolecular silicone materials. First, an in-depth review of the aza-Michael reaction applied to silicon-containing compounds was realized, highlighting the whole potential of this addition reaction. The aza-Michael reaction applied to organic amines was thoroughly analyzed in order to emphasize some open issues such as selectivity or retro-aza-Michael reaction. In order to understand and master the aza-Michael reaction, a model reaction involving a bis-(3-aminopropyl)-terminated PDMS and butylacrylate was then fully investigated. Operating parameters such as protic polar solvents, catalysts or temperature allow promoting the reaction rate. Kinetic data showed that the selectivity towards the main formation of mono- or di-adduct can be controlled by carefully selecting the solvent nature and content. The syntheses of 100% mono- and 100% di-adduct compounds was succesfully achieved. The aza-Michael reaction was then applied to a less reactive Michael acceptor, i.e. acrylic acid. This unsaturated organic acid reacts instantaneously with amines by acid-base reaction leading to the formation of ionic pairs. This acid-base equilibrium is then shifted in the forward direction allowing the synthesis of zwitterionic groups by aza-Michael. The aza-Michael reaction of this peculiar Michael acceptor was thoroughly investigated both with simple organic amines and aminosilicone oligomers and polymers in order to elucidate the structures and to evaluate the rheological properties. Finally, supramolecular silicone materials bearing zwitterionic-like groups were prepared leading to supramolecular materials with properties ranging from visco-elastic liquids to thermoplastic silicone elastomers.

[pt] Estima-se que 50 por cento das reservas mundiais de petróleo e gás sejam mantidas em reservatórios carbonáticos naturalmente fraturados. Um dos maiores desafios neste tipo de formações é a sua heterogeneidade. Além da presença de fraturas que conectam longitudinalmente o meio poroso, vugs em diferentes escalas e distribuições estão espalhados por toda a matriz porosa. Essas cavidades tornam as características do escoamento de fluidos significativamente diferentes daquelas dos reservatórios convencionais de estrutura porosa homogênea, e trazem a necessidade de avaliar propriedades petrofísicas equivalentes para o meio heterogêneo. Neste estudo, uma abordagem microfluídica é usada para determinar as curvas de permeabilidade relativa de água e óleo e os perfis de distribuição das fases em micromodelos 2D de meios porosos vugulares. Experimentos de injeção simultânea de água-óleo em estado estacionário foram realizados a diferentes fluxos fracionários de água, monitorando a dinâmica da queda de pressão e visualizando o deslocamento de fluidos na escala de poros. A aquisição de imagens em tempo real por microscopia de fluorescência permitiu examinar a evolução da saturação das fases. A comparação direta entre as curvas de permeabilidade relativa dos meios porosos vugulares com aquela da matriz porosa mostrou que a incorporação de vugs leva a (i) maior permeabilidade absoluta equivalente, especialmente com cavidades mais longas e em maior número, (ii) aumento da ocupação de óleo na matriz porosa, devido à invasão de água menos eficiente, e (iii) maior permeabilidade relativa à água, que flui preferencialmente pelo espaço vugular. Esses resultados são consistentes com a natureza molhável ao óleo dos micromodelos, uma vez que os vugs oferecem menor resistência capilar ao fluxo da fase não molhante. Nossa abordagem microfluídica de baixo custo provavelmente nos permitirá estudar sistematicamente configurações mais complexas de meios porosos heterogêneos / [en] It is estimated that 50 percent of world s oil and gas reserves are held in naturally fractured carbonate reservoirs. One of the biggest challenges in this type of formation is its heterogeneous nature. Besides the presence of fractures that longitudinally connect the porous medium, vugs at different scales and distributions are scattered throughout the porous matrix. These cavities cause fluid flow characteristics to significantly differ from those of conventional homogeneous pore structure reservoirs and bring the need to evaluate equivalent petrophysical properties of the heterogeneous medium. In this study, a microfluidic approach is used to determine the water and oil relative permeability curves and phase distribution profiles in 2D micromodels of vugular porous media. Steady-state water-oil injection experiments were performed in these devices at different fractional flows, while monitoring the dynamics of the pressure drop and visualizing the fluid displacement at the pore scale. Live-image acquisition through fluorescence microscopy made it possible to examine the evolution of the saturation of water and oil phases. The direct comparison between the relative permeability curves of well-characterized vugular porous media and their porous matrix showed that the incorporation of vugs leads to (i) higher equivalent absolute permeability, especially with longer cavities and higher vug density, (ii) increased oil occupancy in the porous matrix, due to less efficient water invasion into the porous matrix, and (iii) higher relative permeability to water, which flows preferentially through the vugular space. These results are consistent with the oil-wet nature of micromodels, since the vugs are offering less capillary resistance to the flow of the non-wetting phase. Our low-cost microfluidic approach will likely allow us to systematically study more complex vugular-fractured systems.

Master of Science / Department of Mechanical and Nuclear Engineering / Kevin B. Lease / This research was intended to measure the interfacial shear strength between fiber/ matrix systems and to investigate the relation between structure-mechanical properties and performance of fiber/matrix systems. This work conducted a systematic study on model fiber/matrix systems to enhance the fundamental understanding on how variation of polymeric compositions (and hence, different structures), different curing conditions, and fiber surface treatments influence the interactions between the fiber and matrix. In order to measure the interfacial shear strength of fiber/matrix systems, the microdroplet technique was used. In this technique a polymer droplet was deposited on a fiber in the liquid state. Once the droplet was cured a shear force was applied to the droplet in order to detach the droplet from the fiber. The amount of the force needed to de-bond the droplet was directly related to the strength of the bonds formed between the fiber and matrix during the curing process. In addition, the micro-droplet technique was used to evaluate effects of different crosslinker ratio of fiber/ matrix system and also to see if different curing conditions affect the interfacial shear strength of fiber/ matrix system. Surface treatment was also conducted to evaluate its effects on the interfacial shear strength of the fiber/ matrix system using microdroplet technique. The interfacial shear strength of fiber/ matrix system increased along with the increase of crosslinker ratio to a limiting value, and it decreased as long as the crosslinker ratio increased. Curing condition also caused the interfacial shear strength of fiber/ matrix system to increase when it was cured at higher temperature. Fiber surface treatment exhibited a significant effect to the interfacial shear strength as well as the fiber/ matrix contact angle measurement.

The main objective of this thesis is to present a simple and robust hands-on technology for the fabrication of a microfluidic chip in a laboratory. The purpose of this new technology is to replace the existing PDMS based microfluidic chip used for optical trapping of diverse single nano particles. It also lists the different fabrication methods attempted and the successful integration of this chip to the optical trap system which is used to study binding at the single molecular level. Microfluidics is a quickly growing field which deals with manipulating the fluids in channels whose dimensions are few tens of micrometers. Its potential has a major impact on fields like chemical analysis and synthesis techniques, biological analysis and separation techniques, and optics and information technology. One of the main application of these microfluidic chips is in optofluidics, which is the emerging field of integrated photonics with fluidics. This provides freedom to both fields and permits the realization of optical and fluidic property. It requires small volumes of fluids and connections and eventually performs better than conventional methods of robotic fluid handling. Here, the microfluidic chip is targeted for optical trapping with double nano-hole aperture to trap a single protein. The double nanoholes integrated with this microfluidic chip show that stable trapping can be achieved below flow rates of few μL/min. This has provided many possibilities of co-trapping of proteins and study their interactions. / Graduate

Profound sensorineural hearing loss is at the present time a major worldwide health concern, affecting over 5% of the worlds' population. Through cochlear implants (CI), treatment of sensorineural hearing loss now offers the possibility to restore hearing function through electrical stimulation of auditory nerves. Treatment is based on the surgical implantation of a thin, flexible array of microelectrodes into the cochlea. Nevertheless, availability of the treatment is limited due to high costs, and surgical insertion is associated with a high risk of trauma to the fragile soft tissue of the cochlea. At the heart of this thesis lies the proposition that these two problems may be addressed by the development of a novel type of cochlear implant founded on batch-producible, stretchable printed circuit board (PCB) technology. As an alternative to conventional cochlear implant fabrication, this thesis presents a fabrication process based on batch-producible stretchable PCB, featuring liquid alloy microchannels in place of solid metallic wire conductors. A series of proof-of-concept prototypes were designed, fabricated and evaluated. According to results obtained from evaluation of the prototypes, certain steps in the fabrication process were later revisited and improved upon. Preliminary prototype fabrication yielded batches of thin flexible cone-shaped electrode arrays designed for in-vivo evaluation in guinea-pig cochleae. In-vitro evaluation in 3D-printed cochlea models revealed that the prototypes were sufficiently thin and compliant for insertion 23 mm deep into a human cochlea and 4-6 mm into a guinea-pig cochlea, comparable to commercially available counterparts. Characterization of prototype test devices by optical microscopy, optical interferometry and resistance measurements revealed a high inherent variability in the developed fabrication process. In order to ensure consistently adequate quality, further improvement must be done. In particular, results of this work suggest that the deposition of liquid alloy involved in stretchable PCB fabrication should be automated to minimize uncertainty in the deposited liquid alloy thickness and thus enable further miniaturization of the stretchable PCB. Future efforts to successfully produce and integrate electrodes from soft materials, e.g. conductive polymer, liquid alloy or conductive hydrogels are highly recommended to further reduce implant stiffness.

Dans l'optique de développement de matériaux performants avec une approche respectueuse de l'environnement, l'obtention de copolymères à blocs de type hard-soft avec une forte proportion de polydiméthylsiloxane (PDMS) en utilisant le procédé d'extrusion est une étape vers des élastomères thermoplastiques d'intérêt. Afin de s'affranchir de la faible réactivité des extrémités de chaînes des longues macromolécules, la voie originale mise en avant consiste en la réalisation de copolymères ayant une partie centrale PDMS courte puis en l'allongement de celle-ci selon les propriétés visées. L'étape critique d'allongement est effectuée à l'aide de bases phosphazènes comme agents de polymérisation de décaméthylcyclopentasiloxane (D5). Dans un premier temps, une approche chemio-rhéologique de la polymérisation du D5 à l'aide de ces superbases a été réalisée. L'acquisition des données intrinsèques de cette réaction permet de mettre au point la modélisation de l'évolution de viscosité du système en cours de réaction, vérifiant ainsi sa compatibilité avec l'utilisation de l'extrusion réactive. Dans un second temps, l'utilisation d'une architecture modèle de PDMS fonctionnalisé en bout de chaîne par des groupements chimiques volumineux de type naphtyl valide l'hypothèse d'allongement du chaînon central par insertion de D5 selon cette catalyse. Finalement, cette approche a été appliquée à des architectures macromoléculaires de type poly(styrène-b-diméthylsiloxane-b-styrène). Dans ce cas, les résultats sont, à cette heure, moins probants. Ceci est potentiellement dû à l'aspect procédé de nos manipulations. Cette dernière observation révèle l'intérêt de l'extrusion dans ce type de synthèse.

Ce travail de thèse présente la conception et la réalisation de dispositifs microfluidiques en PDMS (Polydiméthylsiloxane) pour l'intégration d'analyses biologiques. Dans un premier temps, des outils microfluidiques sont construits et améliorés dans ce but: une méthode de pompage passif et de mise en oeuvre du PDMS a fait l'objet d'un dépôt de brevet. Les micro-pompes, éléments clés d'une intégration poussée, sont étudiées expérimentalement et théoriquement, menant à un modèle prédictif basé sur une équivalence électrique. Ce travail a été publié dans \textit{Journal of Applied Physics}. La dispersion hydrodynamique, diluant les échantillons lors de leur transport est caractérisée. De cette analyse, une nouvelle méthode de génération de gradients de concentration est conçue et testée expérimentalement. Fort de ces développements, une plate-forme microfluidique originale intégrant des puces à ADN est fabriquée en une version de laboratoire et une version portable. Grâce à ce dispositif, les connaissances de la réaction d'hybridation sur une surface, base des puces à ADN, sont complétées par des mesures comparées de courbes de fusion et un modèle de couplage réaction-diffusion-advection est étendu expérimentalement au cas des puces à ADN. Finalement dans le cadre d'une collaboration avec l'IGH (Institut de Génétique Humaine) de Montpellier, deux méthodes originales de dosage d'allèles pour la trisomie 21 sont testées et des expériences sur des échantillons biologiques sont en cours de préparation. En conclusion, cette thèse a donné lieu au dépôt d'un brevet et à la publication deux articles. Elle aura abouti à la mise en oeuvre de méthodes et approches originales basées sur la technologie microfluidique, appliquées à différents domaines (dispersion, pompage, puce à ADN).

Precise control of stem cell fate is a fundamental issue in the use of human embryonic stem (hES) cells in the context of cell therapy We examined three ways in which the microenvironment can be controlled to alter hES cell behavior, providing insight into the best conditions for maintenance of pluripotency and neural differentiation in developmental and therapeutic studies. We first examined the effects of polydimethylsiloxane (PDMS) growth surfaces on hES cell survival and maintenance of pluripotency. Lightly cured, untreated PDMS was shown to be a poor growth surface for hES cells. Some of the adverse effects caused by PDMS could be mitigated with increased curing or UV treatment of the surface, but neither modification provided a growth surface that supported pluripotent hES cells as well as polystyrene. This work provides a basis for further optimizing PDMS for hES cell culture, moving towards the use of microdevices in establishing precise control over stem cell fate. The second study explored the use of an easily constructed diffusion-based device to grow hES cells in culture on a defined, physiologic oxygen (O₂) gradient. We observed greater hES cell survival and higher levels of pluripotency markers in the lower O₂ regions of the gradient. The greatest benefit was observed at O₂ levels below 5%, narrowing the potential optimal range of O₂ for the maintenance of pluripotent hES cells. Finally, we developed a small molecule-mediated adherent and feeder-free neural differentiation protocol that reduced the cost and time scale for in vitro differentiation of neural precursors and functional neurons from human pluripotent cells. hES cell-derived neural precursors transplanted into a murine model of focal ischemic stroke survived, improved neurogenesis, and differentiated into neurons. Transplant also led to a more consistent and measurable sensory recovery after stroke as compared to untransplanted controls. This protocol represents a potentially translatable method for the generation of CNS progenitors from human pluripotent stem cells.

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