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Interest in microemulsions as potential platforms for polymerization stems from the wide range of phase behaviour dependant morphologies and domain sizes that can be generated in a low viscosity environment. By introducing polymerizable components into the oil and aqueous phases of a microemulsion, we may essentially create a low viscosity, low interfacial tension, bicontinuous template with nanostructured morphologies and narrow domain size distributions analogous to those generated through conventional interpenetrating polymer network (IPN) synthesis and spinodal decomposition. The main objective of this dissertation is to test the application of bicontinuous microemulsion templates to the formulation and polymerization of a silicone-hydrogel IPN. In addition, the project expands on the classical definition of IPNs to a scale of entanglement at the level of groups of polymer chains, as opposed to molecular or chain-level entanglement. This study is divided into two main parts. In the first part, silicone microemulsions were developed and characterized according to the Hydrophilic-Lipophilic Difference (HLD) framework. The hydrophobicity of silicone oils, the characteristic curvature of silicone surfactants and the co-surfactant contribution of methacrylic acid (MAA) and hydroxyethyl methacrylate (HEMA) were quantified. These findings led to the successful formulation of bicontinuous microemulsions (μEs) containing silicone oil, silicone alkyl polyether and reactive monomers in aqueous solution. Ternary phase diagrams of these systems revealed the potential for silicone-containing polymer composites with bicontinuous morphologies. In the second part of this study, the formulation and simultaneous polymerization of polydimethylsiloxane-poly(methacrylic acid – hydroxyethyl methacrylate), (PDMS-P(MAA-HEMA) IPNs from bicontinuous microemulsions was demonstrated. Laser scanning confocal microscopy (LSCM) on swollen polymers highlights aqueous pathways, and indicates the formation of bicontinuous morphologies with domain sizes at equilibrium swelling ranging from ~100 nm to 1 μm. Incorporating polymerizable surfactants into the microemulsion aided in stabilizing the initial microemulsion structure during polymerization. The process developed demonstrates a simple, single-step polymerization approach to forming IPNs from low viscosity microemulsion templates, and could potentially be extended to a variety of hydrophilic and hydrophobic monomers.

Interest in microemulsions as potential platforms for polymerization stems from the wide range of phase behaviour dependant morphologies and domain sizes that can be generated in a low viscosity environment. By introducing polymerizable components into the oil and aqueous phases of a microemulsion, we may essentially create a low viscosity, low interfacial tension, bicontinuous template with nanostructured morphologies and narrow domain size distributions analogous to those generated through conventional interpenetrating polymer network (IPN) synthesis and spinodal decomposition. The main objective of this dissertation is to test the application of bicontinuous microemulsion templates to the formulation and polymerization of a silicone-hydrogel IPN. In addition, the project expands on the classical definition of IPNs to a scale of entanglement at the level of groups of polymer chains, as opposed to molecular or chain-level entanglement. This study is divided into two main parts. In the first part, silicone microemulsions were developed and characterized according to the Hydrophilic-Lipophilic Difference (HLD) framework. The hydrophobicity of silicone oils, the characteristic curvature of silicone surfactants and the co-surfactant contribution of methacrylic acid (MAA) and hydroxyethyl methacrylate (HEMA) were quantified. These findings led to the successful formulation of bicontinuous microemulsions (μEs) containing silicone oil, silicone alkyl polyether and reactive monomers in aqueous solution. Ternary phase diagrams of these systems revealed the potential for silicone-containing polymer composites with bicontinuous morphologies. In the second part of this study, the formulation and simultaneous polymerization of polydimethylsiloxane-poly(methacrylic acid – hydroxyethyl methacrylate), (PDMS-P(MAA-HEMA) IPNs from bicontinuous microemulsions was demonstrated. Laser scanning confocal microscopy (LSCM) on swollen polymers highlights aqueous pathways, and indicates the formation of bicontinuous morphologies with domain sizes at equilibrium swelling ranging from ~100 nm to 1 μm. Incorporating polymerizable surfactants into the microemulsion aided in stabilizing the initial microemulsion structure during polymerization. The process developed demonstrates a simple, single-step polymerization approach to forming IPNs from low viscosity microemulsion templates, and could potentially be extended to a variety of hydrophilic and hydrophobic monomers.

Silicone hydrogels are receiving considerable interest due to their important biomedical application areas such as contact lenses and wound dressings. The applications of such materials are usually in the hydrated state, as hydrogels. However, manufacturing and molding processes are mostly carried out in the organically solvated state, as organogels. This thesis investigates the effects of some of the manufacturing parameters such as curing time and thermal processing on thermal, mechanical, viscoelastic and adhesive/cohesive fracture properties of silicone semi-interpenetrating polymer network organogels. Curing time may affect the extent of reaction and the crosslink density of a gel network. In order to investigate the effect of this parameter, materials were photo-cured for different times within the range of 150s to 1800s. Gel content, uniaxial tensile, dynamic mechanical, adhesive fracture and cohesive fracture properties were obtained as a function of photo-curing time and results were correlated with each other in order to have a better understanding of the effects on the material properties. Additionally, thermal properties of the gels were studied in detail. Crystallization and melting behavior of one of the solvents in the organogel were investigated by differential scanning calorimetry and thermal optical microscopy. Correlation between the thermal properties of the solvent and the gel network structure was shown. Dynamic mechanical analysis experiments were performed to investigate the effect of solvent crystallization on the mechanical properties. Finally, the effect of thermal processing parameters such as the heating  rate and the minimum cooling temperatures on the crystallization and the thermo-mechanical properties were studied. / Master of Science

The unique compressive, optical, and biocompatible properties of silicone hydrogels allow them to be used in a wide variety of applications in the biomedical field. However, the relatively weak mechanical behavior, as well as the highly deformable nature of these elastomeric materials, presents a myriad of challenges when attempting to understand their constitutive and fracture properties in order to improve hydrogel manufacturing and performance in applications. In this thesis, a series of experimental techniques were developed or adapted from common engineering approaches in order to investigate the effects of rate and temperature on the viscoelastic constitutive and fracture behavior of two solvated semi-interpenetrating polymer network silicone hydrogel systems. Viscoelastic characterization of these material systems was performed by implementing a series of uniaxial tension and dynamic mechanical analysis shear tests in order to generate relevant master curves and corresponding thermal shift factors of such properties as shear relaxation modulus, dynamic moduli, and the loss factor. Concurrently, the cohesive fracture properties were studied by utilizing a "semi-infinite" strip geometry under constrained tension in which thin pre-cracked sheets of these cured hydrogels were exposed to several different loading conditions. Fracture tests were performed over a relevant range of temperatures and crosshead rates to determine and generate a master curve of the subcritical strain energy release rate. Experimental methods utilizing high-speed camera images and digital image correlation to monitor viscoelastic strain recovery in the wake of a propagating crack were explored. The results from this thesis may prove useful in an investigation of the interfacial fracture of these hydrogel systems on several different polymer substrates associated with an industrial manufacturing problem. / Master of Science

Lignocellulosic biomass is believed to serve a prominent role in tomorrow’s sustainable energy and material development. Among the polysaccharide fractions of lignocellulosic biomass, the potential of hemicelluloses as a valuable material resource is increasingly recognized. Thanks to their hydrophilic structure, hemicelluloses are suitable substrates for hydrogel design. The work summarized in this thesis aims to develop feasible strategies for the conversion of O-acetyl galactoglucomannan (AcGGM), an ample hemicellulose in softwood, into hydrogels. Within this framework, four synthetic pathways targeting the formation of crosslinked hydrogel networks from pure or unrefined AcGGM fractions were developed.   Aqueous AcGGM-rich and lignin-containing side-stream process liquors of forest industry, known as softwood hydrolysates (SWHs) were formulated into highly swellable hydrogels by: i) allyl-functionalization of AcGGM chains of crude SWH to obtain a viable precursor for hydrogel synthesis via free-radical crosslinking, ii) directly incorporating unmodified SWH fractions into semi-interpenetrating polymer networks (semi-IPNs). SWH hydrogels and semi-IPNs were characterized with appreciable maximum swelling ratios of Qeq = 170 and Qeq = 225, respectively.   Rapid crosslinking of AcGGM through thiol-click chemistry was addressed by first imparting thiol functionality onto pure AcGGM chains in a one-pot procedure. The thiolated AcGGM proved to be a suitable substrate for the synthesis of hemicellulose hydrogels via thiol-ene and thiol Michael addition reactions. Finally, sequential full IPNs were developed by subjecting single network hydrogels of pure AcGGM to a second network formation. IPNs obtained through either free radical crosslinking or thiol-ene crosslinking exhibited higher shear storage moduli than their single network counterparts. / <p>QC 20161102</p>

La peau est un organe à l'architecture complexe qui assure plusieurs rôles essentiels dont celui de barrière contre les agressions extérieures. De plus, il est capable de se régénérer grâce un processus hautement régulé: la cicatrisation. Des biomatériaux, synthétisés à partir de macromolécules d'origine naturelle et/ou synthétique, ont été développés pour servir de pansements, de support de culture cutanée ou de substitut cutané.L'originalité de notre étude a été de mimer, non pas la matrice extracellulaire dermique, mais le réseau de fibrine, temporaire, qui apparait lors de la cicatrisation. Au cours de travaux précédents, il a été démontré qu'il était possible de renforcer mécaniquement un réseau de fibrine, à concentration physiologique, en l'associant, dans une architecture de réseaux interpénétrés de polymères (RIP), avec un réseau de polyoxyde d'éthylène (POE). Durant mes travaux, la non toxicité de ces matériaux envers des cellules modèles a été démontrée. Puis, la composition du matériau a été optimisée pour augmenter son module de stockage jusqu'à un facteur 100 par rapport à celui du gel de fibrine. Ensuite, grâce à la synthèse d'alcool polyvinylique méthacrylate (PVAm) pour le remplacement du POE, un matériau présentant mêmes qualités, mais plus facilement stockable à l'état déshydraté et complètement réhydratable, a pu être obtenu. Nous nous sommes ensuite attachés à rendre ce nouveau matériau biodégradable. L'introduction de sérum albumine bovine méthacrylate (BSAm) copolymérisée avec le PVAm (co-réseau) dans une architecture RIP avec un réseau de fibrine a permis de synthétiser un matériau hydride présentant l'ensemble des propriétés précédemment décrites et dégradable par des enzymes. Ce matériau a été testé en contact avec des populations cellulaires fibroblastiques. Il a pu être démontré, qu'en plus d'être non cytotoxique, ce matériau pouvait être totalement colonisé par ces cellules. Pour finir, l'encapsulation de cellules à l'intérieur de cette matrice et leur prolifération ont pu être observées. En conclusion, les matériaux synthétisés lors de ces travaux, c'est-à-dire des RIPs associant un réseau de fibrine à la concentration physiologique et un réseau de polymère synthétique, possèdent les propriétés nécessaires pour être utilisés en tant que pansements et supports de culture pour la régénération cutanée. De plus, la possibilité d'encapsuler des fibroblastes dans le RIP à base de coréseaux de PVAm et BSAm en fait un substitut cutané potentiel.Mots clefs : hydrogel, réseaux interpénétrés de polymères, fibrine, POE, PVA, BSA, encapsulation cellulaire, fibroblaste, médecine régénérative, peau. / The skin is an organ with a complex architecture that provides several key roles including barrier against external aggressions. In addition, it has the ability to regenerate itself by following a highly regulated process,: the wound healing. Biomaterials, synthesized by using macromolecules from natural and/or synthetic origin, have been developed to serve as wound dressing, cell culture support or skin substitute.The originality of our study was to not mimic the dermal extracellular matrix, but mimic the the fibrin scaffold, the temporary matrix who appears during the healing process. In previous work, it was shown that it was possible to mechanically reinforce a fibrin scaffold at physiological concentration by associating into interpenetrating polymer network (IPN) architecture with a polyethylene oxide (PEO) network. In my work, the non-toxicity of these materials was proved with model cells. Then, the material composition has been optimized to increase the storage modulus by 100 in comparison of the fibrin scaffold. Then, through the synthesis of polyvinyl alcohol methacrylate (PVAm) to replace the POE, a material with the same properties, but more easily stored in a dehydrated state (more ductile) and completely rehydratable could be obtained. We then attached to make this new biodegradable material. The use of bovin serum albumin methacrylate (BSAm) copolymerized with PVAm(conetwork) into IPN architecture with a fibrin scaffold performs to synthesize a hybrid material with all the properties described above and degradable by enzymes. This material has been tested in contact with human fibroblast. It has been demonstrated that in addition to be non-cytotoxic, this material could be completely colonized by these cells. Finally, the encapsulation of cells in the bulk of this matrix and their proliferation inside were observed.In conclusion, the materials synthesized in this work, IPN containing a fibrin scaffold at physiological concentration and a synthetic polymer network, have sufficient properties to be used as wound dressings or cells culture support for skin regeneration. In addition, the ability to encapsulate fibroblasts in material based on conetwork of PVAm and BSAM makes it suitable for a skin substitute application.Key words: hydrogel, Interpenetrating Polymer Network, fibrin, POE, PVA, BSA, entrapping, fibroblast, tissue engineering, skin.

Le but de ces travaux de thèse sera l’élaboration de microactionneurs à base de polymère conducteur électronique PCE .Dans un premier temps, l’objectif sera la synthèse des matrices hôtes à base de réseaux interpénétrés de polymères (RIPs) POE/PTHF et POE/NBR en visant une diminution de l’épaisseur finale (avec PEDOT) de 5 à 10 µm. Ensuite nous procéderons à l’Elaboration d’actionneurs se déformant en flexion et en torsion afin de mimer les mouvements des ailes d’insectes. Deux voix de synthèse des PCE seront utilisées, la voie chimique qui consiste en la synthèse de RIPs ou encore par voie électrochimique avec la formation d’un système tricouche qui permettra un bien meilleur contrôle de leurs propriétés. / The purpose of thesis is the Design of electronic conducting polymer based microactuators by microsystem process. First, the objective will be the synthesis of Interpenetrating Polymers Networks (IPNs) POE/PTHF and POE/NBR, aiming a decrease of the final thickness (with PEDOT) until 5 – 10 µm. Then, we proceed with the development of actuators deforming in bending and twisting to the movements of insects wings. Two different synthesis methods will be used, chemical process based on synthesis of Interpenetrating Polymers Networks, or electrochemical process enabling a much better control of their properties.

Choosing the right solvent is critical for many industrial applications. A useful property for selection of solvents is their solubility parameters. This concept of solubility parameters is central to this thesis and has been used in two different case studies of material treatment applications. Silicone rubber (crosslinked poly(dimethyl siloxane), PDMS) has many favorable material properties making it useful in biomedical devices. However, a limiting aspect of its material properties is a hydrophobic surface. The aim of this work was to prepare a hydrophilic PDMS material while retaining the transparency of the material. To do this, PDMS was combined with a hydrophilic polymer, polyvinylpyrrolidone (PVP) in an interpenetrating polymer network (IPN). A two-step IPN synthesis method was developed and it was found that the solvent used for polymerization of PVP had a significant influence on the water-wettability and the transparency of the PVP/PDMS IPN. Several different analytical techniques were used for determining the degree of phase separation in the PVP/PDMS IPN. It was found, by using microscopy techniques, that the PVP phase domains varied between 200 nm up to a few micrometers, and the size of the phase domains was correlated to the solvent used for polymerization of the IPN. The second topic for which solvent effects were explored was for the use of mesoporous silica particles as potential drug delivery devices. In the present work a drug molecule, ibuprofen, was loaded into mesoporous silica particles using different solvents, and in addition adsorption isotherms were established in each solvent. The maximum loading of ibuprofen in the mesoporous material was achieved when using a nonpolar solvent, in particular liquid carbon dioxide was successfully used. One of the advantages of using liquid carbon dioxide is that no solvent residues are left in the final material, which is important for pharmaceutical applications. Furthermore, it was concluded that ibuprofen was stored in an X-ray amorphous form in the mesoporous particles. Release studies in water showed a rapid release of ibuprofen from the mesoporous silica particles, while the dissolution of samples with crystalline ibuprofen was slower. This was verified to be an effect of a larger exposed ibuprofen area in the ibuprofen-loaded mesoporous silica particles, and it was concluded that the intrinsic dissolution rate for the samples were identical.

Biodegradable hydrogels have become very promising materials for a number of biomedical applications, including tissue engineering and drug delivery. For optimal tissue engineering design, the mechanical properties of hydrogels should match those of native tissues as closely as possible because these properties are known to affect the behavior and function of cells seeded in the hydrogels. At the same time, high water-contents, large mesh sizes and well-tuned degradation rates are favorable for the controlled release of growth factors and for adequate transport of nutrients through the hydrogel during tissue regeneration. With these factors in mind, the goal of this research was to develop and investigate the behavior of injectable, biodegradable hydrogels with enhanced stiffness properties that persist even at high degrees of swelling. In order to do this, degradable functionalities were incorporated into photo-crosslinkable poly(ethylene glycol) and poly(acrylic acid) hydrogels, and these two components were used to make a series of double-network hydrogels. Synthesis of the precursor macromers, photopolymerization of the hydrogels, and structural parameters of the hydrogels were analyzed. The composition and the molecular weight between crosslinks (Mc) of the hydrogel components were varied, and the degradation, swelling, thermal and mechanical properties of the hydrogels were characterized over various time scales. These properties were compared to corresponding properties of the component single-network hydrogels.