Hepatitis C virus (HCV) causes a significant health problem worldwide due to the lack of effective vaccines. It has been recognized that a rapid, vigorous, and broadly targeted cell-mediated immune response (Th1-like) is often associated with the clearance of HCV infections. DNA vaccines represent a promising means for HCV vaccination because they tend to induce a Th1-biased cell-mediated response in the host cell. Currently, the delivery of DNA vaccine for HCV in large animals as well as in humans is not as effective as in small animals. Nano delivery systems would be a promising approach to overcome this problem. Carbon nanotubes (CNTs) have been extensively studied for delivering drugs, proteins, peptides, and nucleic acids including plasmid DNA to cells and organs with varying degrees of success, but few of them have been applied to DNA vaccine for HCV.<p> This thesis presents a study of using functionalized CNTs (f-CNTs) to improve the efficacy of plasmid DNA vaccine delivery for HCV. First, CNTs were functionalized via 1,3-dipolar cycloaddition reaction with the appropriate amino acids and aldehydes. NMR and TEM results suggested that the CNTs were successfully functionalized and became soluble in water. Then plasmid DNAs which encode green fluorescence protein reporter gene, luciferase reporter gene, and HCV core protein, respectively, were delivered into human hepatoma cells via calcium phosphate precipitation method, f-CNT delivery system, and a combination of f-CNT and calcium phosphate method, respectively. The result showed that f-CNTs, in combination with the calcium phosphate method, significantly enhanced the gene expression in human hepatoma cells.<p> Consequently, this study concludes that the f-CNT can significantly enhance gene expression in liver cells conferred by a plasmid DNA when combined with calcium phosphate precipitation method. Even though the mechanisms of this enhancement await further investigation, the results of this thesis may have important implications in developing DNA vaccines for infectious diseases in general and for hepatitis C in particular.

Basic physics teaches us that the frictional force (lateral force) needed to move objects on surfaces are proportional to load (normal force) – Amonton’s Laws. In tribology, this force is proportional to contact area, whereas Amonton is just a special case for contact area scaling with load. Such established laws do not seem to apply to small drops on flat, smooth surfaces in which frictional forces have an inverse relation to contact area and have time component prior to movement. Such phenomena can be explained by Shanahan-deGennes were intermolecular forces are considered for a deformed surface. Graphene is a special case where no time component is observed and frictional forces are attributed to its chemical homogeneity and stability. In the second part of this thesis, graphene is considered as nanofiller to build up polymer nanocomposites via Layer by Layer (LbL). Graphene Nanoribbons derived from multi-walled carbon nanotubes (MWCNT) offers a special case for thermoplastic polyurethane nanocomposites in that of thermally activated twisting morphology influences nanocomposite properties. Finally an electric field driven transdermal hydrogel drug delivery device has been demonstrated by just using CNTs, polyvinyl-borax gel and a CNT membrane

Hepatitis C virus (HCV) causes a significant health problem worldwide due to the lack of effective vaccines. It has been recognized that a rapid, vigorous, and broadly targeted cell-mediated immune response (Th1-like) is often associated with the clearance of HCV infections. DNA vaccines represent a promising means for HCV vaccination because they tend to induce a Th1-biased cell-mediated response in the host cell. Currently, the delivery of DNA vaccine for HCV in large animals as well as in humans is not as effective as in small animals. Nano delivery systems would be a promising approach to overcome this problem. Carbon nanotubes (CNTs) have been extensively studied for delivering drugs, proteins, peptides, and nucleic acids including plasmid DNA to cells and organs with varying degrees of success, but few of them have been applied to DNA vaccine for HCV.<p> This thesis presents a study of using functionalized CNTs (f-CNTs) to improve the efficacy of plasmid DNA vaccine delivery for HCV. First, CNTs were functionalized via 1,3-dipolar cycloaddition reaction with the appropriate amino acids and aldehydes. NMR and TEM results suggested that the CNTs were successfully functionalized and became soluble in water. Then plasmid DNAs which encode green fluorescence protein reporter gene, luciferase reporter gene, and HCV core protein, respectively, were delivered into human hepatoma cells via calcium phosphate precipitation method, f-CNT delivery system, and a combination of f-CNT and calcium phosphate method, respectively. The result showed that f-CNTs, in combination with the calcium phosphate method, significantly enhanced the gene expression in human hepatoma cells.<p> Consequently, this study concludes that the f-CNT can significantly enhance gene expression in liver cells conferred by a plasmid DNA when combined with calcium phosphate precipitation method. Even though the mechanisms of this enhancement await further investigation, the results of this thesis may have important implications in developing DNA vaccines for infectious diseases in general and for hepatitis C in particular.

The study presented in this thesis was aimed to gain the fundamental knowledge regarding the mechanism of H2S measurement in sera by using carbon nanotubes (CNT) and fluorescence response. Characterization techniques such as Raman spectroscopy, X-ray absorption spectroscopy (XAS) and confocal laser scanning microscopy (CLSM) were employed to achieve this goal. The model system used for this study was composed of H2S, distilled water, two major serum proteins (albumin and globulin), serum, hemoglobin, and CNT. The results of this study showed that: (1) Two major serum proteins (albumin and globulin) are physically adsorbed on the sidewall of the CNTs; while H2S is adsorbed on the defect site of the CNTs. (2) Presence of the proteins on the CNTs did not affect the CNTs adsorption of H2S. (3) Using CLSM with the incident wavelength of 514 nm and the emission wavelength of 530 to 580 nm to acquire the fluorescence response of the H2S adsorbed on the CNTs is a reliable approach to measure H2S in sera. (4) Single-wall carbon nanotubes (SWNTs) outperform multi-wall carbon nanotubes (MWNTs) in measurement sensitivity. (5) Presence of hemoglobin in a H2S solution did not affect the measurement of H2S with CNTs and CLMS. The study described in this thesis has provided new knowledge of the interaction behaviors of CNTs with H2S and major proteins in sera along with the mechanism which governs these behaviors. Such knowledge is very useful to further advance the CNT approach to sensing H2S in sera and water solution and to further extend the approach to sensing H2S in other mammalian tissues such as blood.

Multi-walled carbon nanotubes (MWNTs) are a nanofiller that has desirable multifunctional properties. They have been shown to offer improved mechanical, thermal, and electrical properties in composites. Research has been studying their incorporation into polymer composites. Polyamide 12 is a polyamide of interest that has been manufactured to have lower moisture absorption and higher ductility than other commercial polyamides such as 6 and 6,6 at room temperature. In these studies, MWNTs have been incorporated into polyamide 12 at different weight loadings and using MWNTs with differing outer diameters. The composites were melt processed and characterized using differential scanning calorimetry (DSC) to understand the effects of MWNTs on the crystallization behavior of polyamide 12. A melt peak splitting behavior was observed in the polyamide 12 and composite samples when the specimens were not allowed to fully anneal. Total crystallinity in the samples remained the same between the polyamide 12 and composites when the samples were fully annealed. Total crystallinity increased by 1 to 4 percent in the composites over the polyamide 12 when samples were not fully annealed. The addition of MWNTs to the polyamide 12 system increased the amount of crystallization contained in the lower temperature melting peak. An increase in MWNT concentration resulted in an increase in the crystallinity contained in the lower temperature peak. The addition of smaller diameter MWNTs resulted in a further increase in the lower temperature peak when the outer diameter was below a critical size.

This thesis examines the value of using dispersed conductive fillers as a stress/strain sensing material. The effect of the intrinsic conductivity of the filler on the ability to be effective and the influence of filler concentration on the conductivity are also examined. To meet these objectives, nanocomposites of polyvinylidene fluoride (PVDF) with carbon nanofibers (CNFs) and carbon nanotubes (CNTs) were prepared by melt-blending using a twin screw extruder. Since PVDF has a potential to be piezoresistive based on the type of crystalline phase, the effect of CNFs on PVDF crystallinity, crystalline phase, quasi static and dynamic mechanical property was studied concurrently with piezoresponse. Three time dependencies were examined for PVDF/CNTs nanocomposites: quasi-static, transient and cyclic fatigue. The transient response of the strain with time showed viscoelastic behavior and was modeled by the 4-element Burger model. Under quasi-static loading the resistance showed negative pressure coefficient below yield but changed to a positive pressure coefficient after yield. Under cyclic load, the stress-time and resistance-time were synchronous but the resistance peak value decreased with increasing cycles, which was attributed to charge storage in the nanocomposite. The outcomes of this thesis indicate that a new piezoresponsive system based on filled polymers is a viable technology for structural health monitoring.

This work investigates the material properties and production parameters of carbon infiltrated carbon nanotube structures (CI-CNT's). The impact of non homogeneous infiltration and the porosity of cross section regions, coupled with changes in designed geometry, in this case beam width, on the density and modulus of elasticity are compared. Three potential geometric models of beam cross section are proposed and evaluated. 3-point bending, SEM images, and numerical optimization are used to assess the validity of each model and the implications they have for future CI-CNT material applications. Carbon capping near exterior beam surfaces is observed and determined to be a contributing factor to variations in material properties correlated with changes in designed geometry and infiltration parameters (temperature, time, and hydrogen flow rate). Unexpected relationships between beam width and elastic modulus are partially explained by modeling the carbon-capped beams as C-shaped structural members consisting of a graphitic carbon shell of varying porosity and thickness and uninfiltrated carbon nanotube internal regions with a near negligible stiffness. Findings of previous works on the effects of infiltration parameters and carbon capping on materials properties are confirmed and expanded. Flange and web thickness and porosity of the graphitic carbon shell are identified as potential design parameters for pursuing tunable material properties in high precision geometry MEMS and compliant mechanism applications.

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