Implantable medical devices face numerous complications when interfacing with soft tissue, and are plagued by negative responses from host tissue. One such class devices are percutaneous osseointegrated prosthetics (POP). POP consist of a bone anchored titanium post that extrudes through the skin and attaches to an external prosthetic. Compared to the traditional socket interface, POPs offer better stability, limb functionality, and osseoperception for both upper and lower prosthetic limbs. Although the POP surgery technique is well established, the main disadvantage to this technology remains the titanium (Ti) - skin interface. Some of the complications that can arise include epithelial downgrowth, mechanical tearing, and infection. Various types of coatings, surface structure, and antibiotic release technologies have been used to coat Ti in an effort to mitigate POP's associated obstacles, but these methods have failed to translate into published clinical studies and mainstream medical use. One potential solution may be to mimic an interface already found in the human body, the fingernail-skin interface, which is infection-free and mechanically stable. The same keratins that make up the cortex of human hair fibers are found in the fingernail. These cortical human hair keratins can be extracted and purified, and fingernail-specific dimeric complexes coated onto Ti surfaces using silane coupling chemistry. Keratin has been used in other studies for its cell adhesion and differentiation properties, and it has been suggested that the Leu-Asp-Val (LDV) amino acid motif is the primary site responsible for cellular attachment. In the present work, keratins extracted from human hair fibers and recombinant keratin nanomaterials (KN) were used to create biomimetic coatings on silanized Ti surfaces. These coatings were characterized and investigated for surface topography, elemental composition, cell adhesion motifs, and cell adhesion. Both keratin substrates showed the ability to create uniform coatings that retain a protein conformation that exhibits cell adhesion motifs. The coatings exhibit the ability to support cell adhesion of both epithelial and connective tissue cells. Application of fluid shear stress was used to test the mechanical adhesion strength of cells on keratin coatings. The structure, biochemical stability and sustained cellular adhesion of these coatings support keratin's capacity to provide a stable interface between POPs and skin. Side-by-side studies of extracted and recombinant keratins reveals that the recombinant form of these materials may provide distinct advantages for their use in POP devices. Overall, this study confirmed that a uniform, silane-coupled keratin coating was feasible. We demonstrated the substrates contain a biological function in terms of cellular adhesion and phenotypic changes in skin-relevant cells. These results support the biomimetic function of keratin on silanized Ti, which may provide a suitable coating to translate percutaneous medical device coating applications toward clinical use. / Ph. D.

No description available.

Many of the materials used today for cardiovascular implants exhibit good bulk mechanical properties but fail to provide desirable surface properties for reducing thrombogenicity and promoting tissue integration. In fact, biological responses at the blood-material interface, including non-specific protein adsorption, coagulation, and platelet adhesion and activation significantly limit the use of currently available materials in many blood contacting applications. As our understanding of the biological responses to foreign materials has grown, so too has the potential for creating 'bioactive' materials capable of inducing and directing beneficial cellular processes. One promising technique for circumventing undesirable blood-biomaterial interactions involves seeding vascular endothelial cells (ECs) onto synthetic vascular grafts as a means of exploiting the physiological anticoagulant characteristics of the endothelium. Methods for improving cell retention on these constructs include immobilization of cell recognition motifs on the biomaterial surface in order to improve interactions between cells and the synthetic substrate. However, there remains the need to better understand the interactions between surface bound ligands and cells, and the role of linker molecule chemistry on ligand bioactivity and cellular response. In the current work, a novel method was optimized for modifying poly (dimethylsiloxane) (PDMS) with cell adhesion peptides tethered via a heterobifunctional allyl-, NSC-terminated polyethylene oxide (PEO) linker molecule. These novel surfaces combine the protein repellant property of PEO with the cell binding property of cell adhesion peptides. It was found that surfaces modified in this manner reduced protein adsorption to PDMS while increasing cell adhesion. Therefore the use of a generic PEO linker molecule was shown to be a very promising method of reducing non-specific protein interactions while maintaining ligand bioactivity. Silicone surfaces were also modified with diaminobutane (DAB) dendrimers in an attempt to increase the surface capacity for attachment of biomolecules and to compare the effect of surface peptide density with ligand mobility. Grafting cell adhesion peptides via surface bound dendrimers was found to increase the surface peptide density when compared to peptides grafted via the PEO spacer alone. However, cell adhesion was not significantly improved on the dendrimer-peptide modified surfaces compared to PDMS controls. This observation provides evidence that the properties of the linker molecule used for attachment of cell adhesion peptides to a biomaterial surface may be a critical factor in determining peptide bioactivity. In this case the peptides bound to the surface via the highly mobile linear PEO linker showed increased cell adhesion when compared to peptides linked via the rigid, highly branched dendrimer. It is therefore hypothesized that ligand mobility on a biomaterial surface may significantly influence ligand-cell receptor interactions to an even greater extent than surface peptide density. / Thesis / Master of Applied Science (MASc)

Patch clamping is considered the gold standard in measuring the bioelectrical activity of a cell. It is used to detect and measure ion transport through ion channels located throughout a cell membrane. Ion movement is crucial to cell viability and cell-to-cell communication. Pharmaceutical companies increasingly target ion channels because of their significance in disease and to help design better targeted drugs. However, the traditional method of patch clamping is cumbersome and is being replaced by planar high throughput screening (HTS) systems. These systems are reaching their limits due to materials and cost of processing; cell handling methods and small varieties of applicable cell types are also issues to be addressed. In this work, the core components of a new kind of planar patch clamping device have been designed and developed, after analysis of currently available HTS systems. This design approaches patch clamping using polymers to overcome some of the limitations in current systems, specifically cell handling and positioning, by using a simple modification technique to provide distinct attractive areas for cell binding. This uniquely allows the culture of both single cells and cell networks to increase the range of cell types that can be measured and circumvents challenges from using suction to pull cells onto measurement holes. The components of the design are a 10 x 10 array of small holes drilled in a polymer then aligned modifications for precise cell placement are added and a planar electrode array for individual addressing of each cell. A study of methods to produce a leak-tight seal required between microfluidic chambers was done. Cell adhesion parameters for the modification techniques were established. The principle viability of this approach was confirmed using the modification technique to culture cells over holes and measure their resistance using a rig developed for this work.

Concentrating quaternary (positive) charge at polymer surfaces is important for applications including layer-by-layer polyelectrolyte deposition and antimicrobial coatings. Prior techniques to introduce quaternary charge to the surface involve grafting of quaternary ammonium moieties to a substrate or using polyurethanes with modified hard segments however there are impracticalities involved with these techniques. In the case of the materials discussed, the quaternary charge is introduced via polyurethane based polymer surface modifiers (PSMs) with quaternized soft segments. The particular advantage to this method is that it utilizes the intrinsic phase separation between the hard and soft segments of polyurethanes. This phase separation results in the surface concentration of the soft segments. Another advantage is that unlike grafting, where modification has to take place after device fabrication, these PSMs can be incorporated with the matrix material during device fabrication. The soft segments of these quaternized polyurethanes are produced via ring opening copolymerization of oxetane monomers which possess either a trifluoroethoxy (3FOx) side chains or a quaternary ammonium side chain (C12). These soft segments are subsequently reacted with 4,4’-(methylene bis (p-cyclohexyl isocyanate)), HMDI and butanediol (BD) to form the PSM. It was initially intended to increase the concentration of quaternary ammonium charge by increasing PSM soft segment molecular weight. Unexpectedly, produced blends with surface microscale phase separation. This observation prompted further investigation of the effect of PSM soft segment molecular weight on phase separation in PSM-base polyurethane blends and the subsequent effects of this phase separation on the biocidal activity. Analysis of the surface morphology via tapping mode atomic force microscopy (TMAFM) and scanning electron microscopy (SEM) revealed varying complexities in surface morphology as a function of the PSM soft segment molecular weight and initial annealing temperature. Many of these features include what are described as nanodots (100-300 nm), micropits (0.5-2 um) and micropeaks (1-10 um). It was also observed that surface morphology continued to coarsen with time and that the larger features were typically observed in blends containing PSMs with low molecular weight soft segments. This appearance of surface morphological feature correlates with decreased biocidal activity of the PSM blends, that is, the PSM blends exhibit little to no activity upon development of phase separated features. A model has been developed for phase separation and concomitant reduction of surface quaternary charge. This model points the way to future work that will stabilize surface charge and provide durability of surface modification.

To create functional surfaces for soft materials, such as polyurethanes, our approach is to use a semifluorinated surface modifier as minor component to the matrix material. The surface modifier, driving by reduction in surface energy, surface-concentrates to form a functionalized surface layer at the air-polymer interface. In our previous studies, linear PTMO-based polyurethanes were used as the matrix material. These systems undergo slow surface phase separation at room temperature due to the thermodynamically immiscibility of the soft blocks. In this study, chemically crosslinked matrix was developed to provides a steric hindrance to constrain the mobility of surface modifier and to form a kinetically stable surface. The physical property and morphology of base crosslinked matrix has been characterized using DSC, UTT, DMA and AFM. The surface morphology of surface modified crosslinked matrix has been characterized using AFM, DCA and XPS.

The goal of this research is to cover a broad set of scientific investigations of elastomeric materials based on polydimethylsiloxane (PDMS) and poly((3,3,3-trifluoroethoxymethyl)methyloxetane) diol. The scope of study covers five areas, well correlated with each other. The first study investigates the near surface morphology of condensation cured PDMS as a function of increasing the amount of siliceous phase. The appearance, disappearance and reappearance of untreated fumed silica nanoparticles at the PDMS near surface and their correlation with the volume fraction of siliceous phase have been studied. This research with PDMS nanocomposites has led to the development of an alternative route for improving mechanical strength of PDMS elastomers, conventionally known to have weak mechanical properties. The second study involves synthesis of a triblock copolymer comprising of four mutually immiscible phases, namely, soft segments comprising of fluorous and silicone domains, a diisocyanate hard segment and a glassy siliceous phase. Structure-property relationship has been established with an investigation of the interesting surface and bulk morphology. The highly improved mechanical strength of these soft materials is noteworthy. The dominance of silicone soft block at the triblock near surface has led to the third study which investigates their potential non-adhesive or abhesive characteristic in both a laboratory scale and in a marine environment. The peak removal stress and the removal energy associated with the detachment of a rigid object from the surface of these triblock copolymers have been measured. Results obtained from laboratory scale experiments have been verified by static immersion tests performed in the marine environment, involving the removal of adhered soft and hard fouling organisms. Gaining insights on the characteristics of an easy release surface, namely low surface energy and a low near surface modulus, a new way for controlling the near surface composition for elastomeric coatings have been developed. This technique involves an elastomer end-capped with a siliceous crosslinking agent and a tough, linear polyurethane. The basic concept behind the hybrid compositions is to develop a coating suitable for foul release applications, having a low energy surface, low surface modulus but good bulk mechanical strength. Henceforth, the fourth study deals with synthesis and characterization of the hybrid polymers over a wide range of composition and investigates their foul release characteristic in laborartory scale experiments. In our final study, attempts have been made in generating a silicone coating with antimicrobial property. A quaternary alkylammonium in different weight percents have been incorporated into a conventional, condensation cured polydimethylsiloxane (PDMS) elastomer. Antimicrobial assay has been performed on these modified silicone coatings to assess their biocidal activity against strains of Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa. Surface accessibility of quaternary charges has been quantified by measuring the streaming potential of a modified coating. An effort has been made in improving the mechanical strength of the weak PDMS elastomers by adding treated fumed silica nanoparticles as reinforcements. The effect of adding fillers on the mechanical property (tensile), surface concentration of quaternary charge and on the biocidal activity of a representative sample has been investigated.

<p>A Polyvinylchloride surface was modified by coating a biocompatible, hydrophilic and antibacterial polymer by a mild surface modification method. The surface was first activated and then functionalized, followed by coating with polymer. The surface functionality was evaluated using cell adhesion, bacterial adhesion and bacterial viability for polymers with antibacterial properties. 3T3 mouse fibroblast cells were used for cell adhesion, Pseudomonas aeruginosa, Escherichia coli, and Staphylococcus aureus were used for bacterial adhesion in the first study, Pseudomonas aeruginosa and Staphylococcus aureus were used for bacterial adhesion and antibacterial activity in the second study.</p><p></p><p><br></p><p>Chapter 2 reports how we synthesized, immobilized and evaluated a novel hydrophilic polymer with anti-fouling properties onto surface of polyvinylchloride via an effective and mild surface coating technique. The polyvinylchloride surface was first activated by azidation as well as amination, and then tethering a newly synthesized hydrophilic and biocompatible polyvinylpyrrolidone having pendent reactive succinimide functionality onto the surface. Results show that the coated hydrophilic polymer significantly reduced the 3T3 fibroblast cell adhesion as well as the adhesion of the three bacterial species. </p><p><br></p><p>Chapter 3 reports how we prepared, immobilized and evaluated an antibacterial and anti-fouling polymer onto polyvinylchloride surface following an efficient and simple method of surface modification. The surface coated with a terpolymer constructed with N-vinylpyrrolidone, 3,4-Dichloro-5-hydroxy-2(5H)-furanone derivative and succinimide residue was evaluated with cell adhesion, bacterial adhesion and bacterial viability. Surface adhesion was evaluated with 3T3 mouse fibroblast cells and two bacterial species. Also, antibacterial activity was evaluated by bacterial viability assay with the two bacterial species. Results showed that the polymer-modified polyvinylchloride surface exhibited significantly decreased 3T3 fibroblast cell adhesion and bacterial adhesion. Furthermore, the modified polyvinylchloride surfaces exhibited significant antibacterial functions by inhibiting bacterial growth with bactericidal activity.</p><p><br></p><p>Altogether, we have successfully modified the surface of polyvinylchloride using a novel efficient and mild surface coating technique. The first hydrophilic polymer-coated polyvinylchloride surface significantly reduced cell adhesion as well as adhesion of three bacterial species. The second hydrophilic and antibacterial polymer-coated polyvinylchloride surface demonstrated significant antibacterial functions by inhibiting bacterial growth and killing bacteria in addition to significantly reduced 3T3 fibroblasts and bacterial adhesions.</p>

Neste trabalho, filmes híbridos produzidos pela técnica da automontagem eletrostática camada-por-camada foram preparados usando-se Polioxometalatos do tipo Keggin, ácido fosfotúngstico (HPW) e o complexo monolacunar K(TPA)4[PW11O39Mn(OH2)] alternados via um polímero catiônico, poli(cloreto de alilamônio) (PAH). O filme que continha uma pré-camada de adsorção de PDMS, juntamente com 5 bicamadas de PAH e HPW apresentou um melhor comportamento eletroquímico em filmes formados sobre óxido de índio e estanho (ITO). Em função disso, este filme foi caracterizado através de Espectroscopias de Absorção na região do Ultra-Violeta Visível (UV-vis), de Absorção-Reflexão na Região do Infra-vermelho (FT-IRRAS) e de Ressonância de Plásmons de Superfície (SPR). Foi constatado por FT-IRRAS que parte da camada de PDMS está se difundindo para a superfície quando as bicamadas de PAH e HPW vão sendo preparadas. Imagens de Microscopia Eletrônica de Varredura com Emissão de Campo (MEV-EC) confirmam esta hipótese. Espectroscopia de SPR indicou que tanto a adsorção de PAH quanto a de HPW ocorrem em tempos curtos. Experimentos de Voltametria Cíclica com [Fe(CN)6]3-mostraram que este filme é poroso. Resultados de Espectroscopia de Fotoelétrons Excitados por Raios X (XPS) comprovaram que PDMS protege o substrato contra corrosão. Esse mesmo filme pôde ser utilizado numa aplicação de caráter ambiental. Ele foi capaz de detectar melamina e atrazina em concentrações 4.10-8 mol.L-1 e 1.10-6 mol.L-1 respectivamente. Filmes contendo 5 bicamadas de PAH e K(TPA)4[PW11O39Mn(OH2)] mostraram comportamentos similares referentes à queda da eletroatividade para arquiteturas iniciadas com PAH e PDMS. O filme com 5 bicamadas de PAH e K(TPA)4[PW11O39Mn(OH2)] iniciado com PAH não mostrou comportamento eletrocatalítico para a oxidação de triazinas. / In this work, self-assembled hybrid layer-by-layer films were prepared using Keggin type polyoxometalates, phosphotungstic acid (HPW) and the monolacunary complex K(TPA)4[PW11O39Mn(OH2)] alternated by a cationic polymer, poly(allylamine hydrochloride) (PAH). The film containing 5 bilayers of PAH and HPW deposited on a PDMS cushion exhibited better electrochemical behavior onto indium tin oxide (ITO) electrodes. So, this film was characterized by UV-vis spectroscopy, Fourier transformed infrared reflection adsorption spectroscopy (FT-IRRAS) and Surface Plasmon Resonance Spectroscopy (SPR). FT-IRRAS results showed that PDMS is going to the top of the bilayers of PAH and HPW when the film is prepared. Images of the Scanning Electronic Microscopy with field emission guns (FEG-SEM) confirm this fact. SPR spectroscopy results showed adsorption times of PAH and HPW short. Cyclic Voltammetry experiments with [Fe(CN)6]3- for the film confirm that it is porous. X-Ray Photoelectron spectroscopy (XPS) proved that in this film PDMS is present and it is responsible by protection against corrosion of substrate. This film can be used for environmental application. It was able to detect melamine and atrazine in concentrations of 4.10-8 and 1.10-6 mol.L-1 respectively. Films containing 5 bilayers of PAH and K(TPA)4[PW11O39Mn(OH2)] exhibited similar electrochemical behaviors for the decrease in the electroactivity for cushions of PAH and PDMS. The film with 5 bilayers of PAH and K(TPA)4[PW11O39Mn(OH2)] with PAH cushion does not exhibited electrocatalytic behavior for oxidation of triazines.

"The design and development of chemically modified surfaces for bioanalytical applications is presented. Chemical surface modification is demonstrated to be a method to control surface properties on the molecular level by selecting the appropriate substrate, linking chemistry, and terminal group functionality. These systems utilize spontaneous interactions between individual molecules that allow them to self-assemble into larger, supramolecular constructs with a predictable structure and a high degree of order. Applications investigated in this thesis include: surface patterning, switchable surface wettability, and biological sensor devices that combine surface based molecular recognition, electrochemical detection methods, and microfluidics. A multilayered approach to complex surface patterning is described that combines self-assembly, photolabile protecting groups, and multilayered films. A photolabile protecting group has been incorporated into molecular level films that when cleaved leaves a reactive surface site that can be further functionalized. Surface patterns are created by using a photomask and then further functionalizing the irradiated area through covalent coupling. Fluorophores were attached to the deprotected regions, providing visual evidence of surface patterning. This approach is universal to bind moieties containing free amine groups at defined regions across a surface, allowing for the development of films with complex chemical and physico-chemical properties. Systems with photoswitchable wettability were developed by fabricating multilayered films that include a photoisomerizable moiety, cis-/trans- dicarboxystilbene. When this functionality was incorporated into a multilayered film using non-covalent interactions, irradiation with light of the appropriate wavelength resulted in a conformational change that consequently changed the hydrophobicity of the substrate. Methods were investigated to increase the reversibility of the photoswitching process by creating surface space between the stilbene ligands. Utilizing mixed monolayers for spacing resulted in complete isomerization for one cycle, while the use of SAMs with photolabile groups produced surfaces that underwent isomerization for three complete cycles. A microfluidic device platform for ion sensing applications has been developed. The platform contains components to deliver small volumes of analyte to a surface based microelectrode array and measure changes in analyte concentration electrochemically in an analogous method to that used in conventional electrochemical cells. Crown ether derivatives that bind alkali metal ions have been synthesized and tested as ionophores for a multi-analyte device of this type, and the sensing platform was demonstrated to measure physiological relevant concentrations of potassium ions. Advantages of this design include: high sensitivity (uM to mM), small sample volumes (less than 0.1 mL), multi-analyte capabilities (multiple working electrodes), continuous monitoring (a flow through system), and the ability to be calibrated (the system is reusable). The self-assembled systems described here are platform technologies that can be combined and used in molecular level devices. Current and future work includes: photopatterning of gold and glass substrates for directed cell adhesion and growth, the design and synthesis of selective ion sensors for biological samples, multi-analyte detection in microfluidic devices, and incorporating optical as well as electrochemical transduction methods into sensor devices to allow for greater sensitivity and self-calibration."