Theses and Dissertations from UMD

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New submissions to the thesis/dissertation collections are added automatically as they are received from the Graduate School. Currently, the Graduate School deposits all theses and dissertations from a given semester after the official graduation date. This means that there may be up to a 4 month delay in the appearance of a give thesis/dissertation in DRUM

More information is available at Theses and Dissertations at University of Maryland Libraries.

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    PREPARATION OF A NANOSUSPENSION OF THE PHOTOSENSITIZER VERTEPORFIN FOR PHOTODYNAMIC AND LIGHT-INDEPENDENT THERAPY IN GLIOBLASTOMA
    (2024) Quinlan, John Andrew; Huang, Huang-Chiao; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Photodynamic therapy (PDT) using verteporfin (VP) has treated ocular disease for over 20 years, but recent interest in VP’s light-independent properties has reignited interest in the drug, particularly in glioblastoma (GBM) (NCT04590664). Separate efforts to apply PDT to GBM using 5-aminolevulinic acid (5-ALA)-induced protoporphyrin IX (PpIX) have also garnered attention (NCT03048240), but, unfortunately, clinical trials using 5-ALA-induced PpIX-PDT have yet to yield a survival benefit. Previous studies have shown VP to be a superior PDT agent than 5-ALA-induced PpIX. Our lab has shown that 690 nm light activates VP up to 2 cm into the brain, while 635 nm light only activates PpIX at depths <1 cm into the brain. Additionally, VP is a more effective photosensitizer than PpIX because it has a higher singlet oxygen yield and is active in the vasculature as well as target tumor cells. However, the hydrophobicity of VP limits effective delivery of the drug to the brain for treatment of GBM.In this context, this thesis aims to re-evaluate the delivery method for VP. VP traditionally requires lipids for delivery as Visudyne. Recent shortages of Visudyne and potential drawbacks of liposomal carriers motivated our development of a carrier-free nanosuspension of VP, termed NanoVP. Previous work has shown that cellular uptake of VP is greater when delivered as NanoVP rather than liposomal VP, resulting in improved cell killing after light activation. This thesis builds on this previous work by (1) evaluating synthesis and storage parameters for NanoVP, (2) determining the pharmacokinetics, biodistribution, and brain bioavailability of NanoVP, and (3) evaluating the potential efficacy of NanoVP as a PDT and a chemotherapy agent, and by supporting development of a zebrafish model of the blood-brain barrier (BBB) for mechanistic studies of improved drug delivery to the brain.
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    3D ENGINEERING OF VIRUS-BASED PROTEIN NANOTUBES AND RODS: A TOOLKIT FOR GENERATING NOVEL NANOSTRUCTURED MATERIALS
    (2018) Brown, Adam Degen; Culver, James N; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Technological innovation at the nanometer scale has the potential to improve a wide range of applications, including energy storage, sensing of environmental and medical signals, and targeted drug delivery. A key challenge in this area is the ability to create complex structures at the nanometer scale. Difficulties in meeting this challenge using traditional fabrication methods have prompted interest in biological processes, which provide inspiration for complex structural organization at nanometer to micrometer length scales from self-assembling components produced inexpensively from common materials. From that perspective, a system of targeted modifications to the primary amino acid structure of Tobacco mosaic virus (TMV) capsid protein (CP) has been developed that induces new self-assembling behaviors to produce nanometer-scale particles with novel architectures. TMV CPs contain several negatively charged carboxylate residues which interact repulsively with those of adjacent CP subunits to destabilize the assembled TMV particle. Here, the replacement of these negatively charged carboxylate residues with neutrally charged or positively charged residues results in the spontaneous assembly of bacterially expressed CP into TMV virus-like particles (VLPs) with a range of environmental stabilities and morphologies and which can be engineered to attach perpendicularly to surfaces and to display functional molecular patterns such as target-binding peptide chains or chemical groups for attachment of functional targets. In addition, the distinct electrostatic surface charges of these CP variants enable the higher-level coassembly of TMV and VLP into continuous rod-shaped nanoparticles with longitudinally segregated distribution of functionalities and surface properties. Furthermore, the unique, novel, environmentally responsive assembly and disassembly behaviors of the modified CPs are shown to act as simple mechanisms to control the fabrication of these hierarchically structured functional nanoparticles.
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    Immobilized Seed-mediated Growth of Two Dimensional Arrays of Shaped Metallic Nanocrystals
    (2017) Perez Cardenas, Maria Teresa; Nie, Zhihong; Chemistry; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Acknowledging that the optical properties of noble metal nanocrystals (NMNCs) are largely determined by their size, composition, and shape, the demand for NMNCs with controlled shapes is expected to increase. To expand the property discovery and application development of polyhedral NMNCs, it is pivotal to understand the key factors involve in the nucleation and growth processes of NMNCs for better control over the crystal facets. Furthermore, to implement polyhedral NMNCs into functional devices for applications in such as chemical sensors, photovoltaics, and catalysis, it is essential to design cost-effective methods to assemble NMNCs into two-dimensional arrays with controlled orientation and particle distance. This dissertation describes the stability and interaction of molecular species formed during the reduction of gold metal precursor, as well as factors that influence the formation of nanocrystals with different shapes. Our study suggests that during the Au reduction step, an intermediate complex is formed. Over time the complex degrades decreasing the concentration of gold ions and subsequently slowing down or inhibiting the nucleation; thereby, affecting the reproducibility of synthetic methods. My findings will provide guidance for the development of more simple, reliable methods to control the shapes of the nanocrystals. Additionally, I developed an immobilized seed-mediated growth strategy for the fabrication of two-dimensional arrays of mono- and bi-metallic polyhedral nanocrystals with well-defined shapes and orientations on a substrate. This method relies on the controlled solution-phase deposition of gold and palladium metals on a selectively exposed surface of self-assembled seed nanoparticles that are immobilized on a substrate through collapsed polymer brushes. The synthetic approach I developed presents an important addition to current tools for the fabrication of substrate-supported functional nanocrystals as new materials and devices.
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    Development of Nanoparticle-Based Intracellular Dual Sensing and Actuation Modalities
    (2017) Field, Lauren D.; White, Ian M; Medintz, Igor L; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    The integration of therapeutics with diagnostic agents, or theranostics, is vital for the development of novel and effective disease treatments. To effectively design new and efficient theranostic materials, a thorough understanding of the carrier ensemble, the interactions within the construct components, and the surrounding environment is required. This dissertation focuses on the development of new strategies to produce an effective ‘toolbox’ of nanoscale theranostics, namely through the use of a central NP scaffold and the visualization technique of Förster Resonance Energy Transfer (FRET). The NP scaffold used throughout this work, the semiconductor quantum dot (QD), is ideal for visualizing sensing modalities due to their high quantum yield (QY), tunable, narrow and symmetric emission profiles with broad, far-UV excitation, and resistance to photobleaching - making them optimal FRET donors. We first examined the intracellular assembly of QDs to proteins by injecting 545 nm emitting QDs, coated with various capping ligands, into cells transfected to express mCherry at two distinct intracellular locations: the cytosol and the plasma membrane. We found that the small, zwitterionic capping ligand CL4 and the cytosolically located mCherry protein assembled into the most efficient FRET complexes. We used this knowledge to design and implement a novel intracellular actuation modality for drug delivery that used a 520 nm emitting QD with the carrier maltose binding protein appended to the surface and carrying drug or dye conjugated to a maltose analog, -cyclodextrin in the binding pocket. Rather than relying on intracellular environmental changes or external stimuli to actuate release, the addition of the innocuous sugar maltose to the medium induced cargo actuation and could be visualized via FRET. Finally, the same methods were implemented to develop a novel pH sensor to report on the extracellular changes that occur in tumor development where the physiological pH is lowered dramatically. Using a 464 nm QD scaffold conjugated to pH-responsive FITC, we successfully monitored changes in extracellular pH and accurately determined unknown pH values. With the work in this thesis, we believe we have contributed greatly to the advancement and development NPs for the design and implementation of sensing and actuation complexes.
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    PHYSICAL CHARACTERIZATION OF DNA CONDENSED WITH CATIONIC AGENTS
    (2016) Salgado, Eddy; Briber, Robert M; Material Science and Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Gene therapy using non viral vectors remains a challenging problem of maximizing efficiency while minimizing risks due to the multiple biological hurdles for a carrier agent to deliver its genetic cargo. The precise connection between the physical properties of the vectors and their transfection behaviors remains to be fully realized. We have used atomic force microscopy as well as dynamic light scattering and zeta potential measurements in order to image and characterize DNA complexes with polyethylenimine (PEI), histidine-lysine (HK) peptide, and triethylenetetramine (TETA)-functionalized gold nanoparticles. The resulting complex structures are analyzed as a function of amine to phosphate (N/P) ratios and as a function of sample preparation protocols. This work aims to not only characterize these specific complexes, but to aid in the general understanding of complex formation and how it relates to transfection observations to promote a more rational design of future gene delivery agents.
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    Characterization of Quantum Vortex Dynamics in Superfluid Helium
    (2015) Meichle, David P.; Lathrop, Daniel P; Physics; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Liquid helium obtains superfluid properties when cooled below the Lambda transition temperature of 2.17 K. A superfluid, which is a partial Bose Einstein condensate, has many exotic properties including free flow without friction, and ballistic instead of diffusive heat transport. A superfluid is also uniquely characterized by the presence of quantized vortices, dynamical line-like topological phase defects around which all circulation in the flow is constrained. Two vortices can undergo a violent process called reconnection when they approach, cross, and retract having exchanged tails. With a numerical examination of a local, linearized solution near reconnection we discovered a dynamically unstable stationary solution to the Gross-Pitaevskii equation, which was relaxed to a fully non-linear solution using imaginary time propagation. This investigation explored vortex reconnection in the context of the changing topology of the order parameter, a complex field governing the superfluid dynamics at zero temperature. The dynamics of the vortices can be studied experimentally by dispersing tracer particles into a superfluid flow and recording their motions with movie cameras. The pioneering work of Bewley et al. provided the first visualization technique using frozen gases to create tracer particles. Using this technique, we experimentally observed for the first time the excitation of helical traveling waves on a vortex core called Kelvin waves. Kelvin waves are thought to be a central mechanism for dissipation in this inviscid fluid, as they provide an efficient cascade mechanism for transferring energy from large to microscopic length scales. We examined the Kelvin waves in detail, and compared their dynamics in fully self-similar non-dimensional coordinates to theoretical predictions. Additionally, two experimental advances are presented. A newly invented technique for reliably dispersing robust, nanometer-scale fluorescent tracer particles directly into the superfluid is described. A detailed numerical investigation of the particle-vortex interactions provides novel calculations of the force trapping particles on vortices, and a scaling was found suggesting that smaller particles may remain bound to the vortices at much higher speeds than larger particles. Lastly, a new stereographic imaging system has been developed, allowing for the world-first three-dimensional reconstruction of individual particles and vortex filament trajectories. Preliminary data, including the first three-dimensional observation of a vortex reconnection are presented.
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    Novel Interactions of Liquid Crystals with Coated Nanoparticles
    (2013) Taylor, Jefferson; Martinez-Miranda, Luz J; Material Science and Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Functionalized nanoparticles have a wide range of applications in liquid crystal systems, including displays, photovoltaics, and drug delivery. We need to understand the interactions between the nanoparticles and the liquid crystal molecules in order to utilize them fully and safely. We investigate the short-range interaction of coated nanoparticles with a liquid crystal membrane or bulk sample through the use of atomic force microscopy (AFM) and X-ray scattering techniques. We identify the role the functionalization plays in the phase behavior of the liquid crystal both as a thin film and in bulk. Our research produced three results. We identify differing behavior in thin film samples of liquid crystal and coated nanoparticles dependent upon particle functionalization using AFM. Using X-ray scattering we measure the alignment and smectic layer formation in the presence of coated nanoparticles, even above the smectic-A to nematic transition temperature. We find evidence of a "halo" that forms around coated nanoparticles, particularly with longer coating molecules.
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    Research and Development of Liquid Phase Epitaxy Grown Iron Garnet Thin Films Utilizing Plasmon Resonances for Enhancement of Magneto-Optic Effects
    (2013) Lang, Garrett Seth; Mayergoyz, Isaak D; Electrical Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Plasmon resonance induced Faraday rotation enhancement in garnet films offers the promise for development of compact and higher performance polarization dependent optical devices. Enhancement of Faraday rotation has been achieved utilizing strong localized electric fields induced by the excitation of plasmon resonances in gold nanoparticles deposited on or in garnets. Experimental results are presented that reveal strong Faraday rotation enhancement in bismuth-doped garnet films with gold nanoparticles incorporated in or on the epitaxial films. The strength of the enhancement is governed by the thickness of the garnet films, the dimensions and separations of the nanoparticle assemblies, and the relative ratio between the height of the nanoparticles and the thickness of the films. For samples with embedded nanoparticles, there have been noticeable effects on the magnetic properties of the films due to the presence of the embedded gold nanoparticles. The embedding of nanoparticles in the films can be practically utilized to control the local anisotropy of the films. Special efforts have been made to improve the growth process and produce sub-micron thick films with thicknesses around 200nm to ensure that the induced electric fields are uniformly spread over the thickness of the films. At this thickness, nanoparticles have been incorporated on the surface of the liquid phase epitaxy grown garnet films rather than embedded in the films due to the low growth rate necessary to grow these films. New techniques have been developed to improve the accuracy of Faraday rotation enhancement measurements. Faraday rotation enhancement as high as 110% has been observed for samples with nanoparticle assemblies incorporated on the surfaces of the films but the enhancement depends on a number of factors and can be substantially lower. Stronger enhancement can be obtained by increasing the nanoparticle height to film thickness ratio as well as increasing the relative spacing between nanoparticles.
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    Electrospray-Differential Mobility Analysis of Bionanoparticles
    (2012) Guha, Suvajyoti; Zachariah, Michael R; Mechanical Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    The growth of the multibillion dollar bionanoparticle industry has spurred the development of new physical characterization methods. One such method, electrospray-differential mobility analysis (ES-DMA) constitutes an electrospray for aerosolization of bionanoparticles (such as viruses, gold-nanoparticles, proteins, nanoparticle-protein complexes) and an ion mobility method that operates at atmospheric conditions, and separates bionanoparticles spatially. This dissertation identifies some relevant "problem" areas for ES-DMA by reviewing selected applications. Some such problems are: proteins while passing through ES capillaries are found to interact with it and thus produce time dependent size distributions. Further, it is thought that adsorbed proteins may subsequently desorb and influence size distributions with the ES-DMA which may concomitantly affect quantification of aggregates. These artifacts are studied systematically and it is demonstrated that ES-DMA can quantify adsorption-desorption of complex protein mixtures at high shear rates. Further, it is shown that desorbing proteins do not have a significant effect on size distributions. Another artifact of the ES takes place during the aersolization process. Two units (called monomers) of a bionanoparticle may get encapsulated in the same ES droplet and upon drying of the droplet create artificial dimers thus affecting quantification with ES-DMA. Assuming Poisson distribution, this thesis provides a systematic approach that can be undertaken to eliminate this artifact. A third artifact arises from the low sensitivity of the DMA to size increase. When a ligand (for e.g. protein) adsorbs to a bionanoparticle it creates an increase in the size of the later, which can be used to quantify the amount of ligand adsorbed per bionanoparticle. As ligands can change conformations upon adsorption, using ES-DMA for such applications may be flawed. This issue has been identified and a solution has been provided by integrating a mass analyzer after the ES-DMA. After correcting for these artifacts, this dissertation delves into characterization of different types of bionanoparticles and demonstrates that ES-DMA has several advantages over other traditional techniques such as transmission electron microscopy, size exclusion chromatography, analytical ultracentrifugation, dynamic light scattering and plaque assay and thus has immense potential to become a process analytical technique in biomanufacturing environments.
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    SPECTROSCOPIC ENHANCEMENT FROM NOBLE METALLIC NANOPARTICLES
    (2011) Tsai, Shu-Ju; Phaneuf, Raymond J.; Material Science and Engineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    Resonant coupling of localized surface plasmon resonances (LSPRs) in noble metallic nanostructures to incident radiation and the related subject of localized behavior of electromagnetic waves are currently of great interest due to their potential application to sensors, biochemical assays, optical transmission, and photovoltaic devices. My thesis research is made up of two related parts. In part one I examined enhanced fluorescence in dye molecules in proximity to Ag nanostructures. In part two I studied the effect of Au nanostructure arrays on the performance of poly(3-hexylthiophene-2,5-diyl) : [6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PCBM) bulk heterojunction (BHJ) organic solar cells (OSCs). Nanostructures were fabricated by two different methods: e-beam lithography (top down) and spray pyrolysis (bottom up). Using e-beam lithography, we produced arrays of nanostructures with well defined shapes, sizes, and spacings. By systematically varying these topographical parameters, we measured their effect on nanometer-sized metallic structure-enhanced fluorescence (nMEF) and on absorption and external quantum efficiency (EQE) in OSC devices as a function of optical wavelength. In analyzing experimental results, we carried out numerical simulations of the local electric field under incident light, across plasmonic resonances. The comparison between the calculated local field squared and measured fluorescence/EQE provides physical insight on the configuration- dependence of these two processes. Our results indicate that local field enhancement near nanostructures is dominant in nMEF, and that the local field is strongly affected by the substrate and device architectures. For the OSCs, both measurements and calculations show that absorbance within the active layer is enhanced only in a narrow band of wavelengths (~640-720 nm) where the active layer is not very absorbing for our prototype nanopillar-patterned devices. The peak enhancement for 180 nm wide Au nanopillars was approximately 60% at 675nm. The corresponding resonance involves both localized surface plasmon excitation and multiple reflections/diffraction within the cavity formed by the electrodes. Finally, we explore the role of the size of the nanostructures in such a device on the optical absorption in the OSC active layer. We find that small Au nanopillars produce strong internal absorption resulting in Joule heating, and suppressing the desired enhancement in EQE in OSC devices.