published_or_final_version / abstract / Chemistry / Doctoral / Doctor of Philosophy

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

published_or_final_version / Chemistry / Master / Master of Philosophy

No description available.

Therapeutic efficacy of drugs depends on their ability to reach the treatment target. Drugs that exert their effect within cells are constrained by an inability to cross the cell membrane. Methods are being developed to overcome this barrier including biochemical and biophysical strategies. The application of ultrasound with microbubbles increases the permeability of cell membranes allowing molecules, which otherwise would be excluded, to enter the intracellular space of cells; a phenomenon known as sonoporation. This thesis describes studies aimed at improving our understanding of the mechanism underpinning sonoporation and of the exposure parameters affecting sonoporation efficiency. Cancer cells (KHT-C) in suspension were exposed to ultrasound and microbubbles – total of 97 exposure conditions. The effects on cells were assessed through uptake of cell-impermeable molecules (10 kDa to 2 MDa FITC-dextran), cell viability and microscopic observations of the plasma membrane using flow cytometry, colony assay and electron microscopy techniques. Sonoporation was a result of the interaction of ultrasound and microbubbles with the cell membrane. Disruptions (30-100 nm) were generated on the cell membrane allowing cell impermeable molecules to cross the membrane. Molecules up to 2 MDa in size were delivered at high efficiency (~70% permeabilisation). Sonoporation was short lived; cells re-established their barrier function within one minute, which allowed compounds to remain inside the cell. Following uptake, cells remained viable; ~50% of sonoporated cells proliferated. Sonoporation efficiency depended on ultrasound and microbubble exposure conditions. Microbubble disruption was a necessary but insufficient indicator of ultrasound-induced permeabilisation. The exposure conditions can be tailored to achieve a desired effect; cell permeability of ~70% with ~25% cell death versus permeability of ~35% with ~2% cell death. In addition, sonoporation depended on position in the cell cycle. Cells in later stages were more prone to being permeabilised and killed by ultrasound and microbubbles. This study indicated that sonoporation can be controlled through exposure parameters and that molecular size may not be a limiting factor. However, the transient nature may necessitate that the drug be in close vicinity to target cells in sonoporation-mediated therapies. Future work will extend the investigation into in vivo models.

Class of 2010 Abstract / OBJECTIVES: The purpose of this study was to determine the incidence of contrast induced nephropathy (CIN) for patients receiving a pre-hydration regimen to prevent CIN. METHODS: This was a descriptive retrospective chart review study. Charts were reviewed from Banner Boswell Medical Center and a nephrologist’s office in Sun City, Arizona. RESULTS: There were a total of 12 patients included in the study. The population after completetion of chart reviews consisted of 6 male patients and 6 female patients. The age range of the patients included was 54-90 years old. CIN occurred in zero of the twelve patients. Half of the 12 patients had a decrease in serum creatinine ranging from 0.1- 0.6 mg/dL, 24-48 hours post-diagnostic procedure. CONCLUSIONS: There was no incidence of CIN after the 12 patients received the specific protocol. This study demonstrates the potential for this regimen as a pre-hydration option for individuals undergoing procedures in which radiocontrast is necessitated. A prospective observational study with a larger sample size would be warranted to determine the safety and efficacy of the protocol and increase the validity of the results of this descriptive study.

In my paintings and mixed media works, I incorporate rough textures and vibrant, high contrast colors. I find beauty and intrigue in the gnarled roots of a tree; the crumbling plaster on a wall; and the wrinkled, roughened hands of my grandmother. To explore these types of surfaces, the materials are distorted by twisting, ripping, and pulling the pieces apart. For instance, canvas is layered and stitched together in an uneven manner with knots and lumps added to the distressed surface. I view these distorted, strained surfaces as different forces in my life that push or pull me in varied directions. This metaphor helps me to express myself through formal elements. I approach my compositions gesturally and intuitively by letting them evolve during my process. As a compositional device, I sometimes use a gridded infrastructure or multi-piece presentation. This underlying framework allows me to organize my presentation as I apply marks and manipulate surfaces. I use complementary color palettes that are bright and vibrant. These palettes have a virile quality that emanates a strong sense of purpose and commands attention from the viewer.

In this thesis, we demonstrate in-situ scanning electron microscopy techniques for both electron beam lithography (EBL) and in-situ one dimensional nano materials electrical characterization. A precise voltage contrast image positioning for in-situ EBL to integrate nanowires into suspended structures for nanoswitch fabrication has been developed. The in-situ EBL eliminates the stage movement error and field stitching error by preventing any movements of the stage during the nanolithography process; hence, a high precision laser stage and alignment marks on the substrate are not needed, which simplifies the traditional EBL process. The ZnO piezoelectronics is also studied using nano-manipulators in scanning electron microscope. Methods to improve the contact have been demonstrated and the contacts between probe tips and the nanowires are found to have significant impact on the measurement results.

For several years, we have been developing vortex phase masks based on sub-wavelength gratings, known as Annular Groove Phase Masks. Etched onto diamond substrates, these AGPMs are currently designed to be used in the thermal infrared (ranging from 3 to 13 pm). Our AGPMs were first installed on VLT/NACO and VLT/VISIR in 2012, followed by LBT/LMIRCam in 2013 and Keck/NIRC2 in 2015. In this paper, we review the development, commissioning, on-sky performance, and early scientific results of these new coronagraphic modes and report on the lessons learned. We conclude with perspectives for future developments and applications.

Objetivo: Avaliar a Função de Sensibilidade ao Contraste de Luminância Espacial e Temporal, estudar o desenvolvimento destas funções, a contribuição das vias de processamento paralelo para as funções de Sensibilidade ao Contraste e seu respectivo desenvolvimento e, por fim, determinar valores normativos destas funções visando uma aplicabilidade clínica.Método A avaliação psicofísica de sensibilidade ao contraste de luminância espacial e temporal foi realizada em 112 sujeitos divididos em três grupos:GrupoI ( idade média =9,14±2,7 anos),Grupo II ( idade média=23,7 ± 3,4 anos) e Grupo III ( idade média=41,8± 5,5 anos) com o programa PSYCHO for Windows Versão 2.36 (Cambridge Research Systems, CRS-Ltd, UK) acoplado a um microcomputador PC XTC -600. . Os estímulos foram apresentados em um monitor Sony Triniton de 19 polegadas GFD420 (Sony Corporation, USA) com resolução espacial de 800X600 e resolução temporal de 69 Hz Os estímulos eram comandados pela placa gráfica VSG 2/4 (Cambridge Research Systems, CRS-Ltd, UK).Resultados A avaliação psicofísica para a sensibilidade ao contraste espacial e temporal mostraram que esta função já está desenvolvida e em pleno funcionamento em crianças (6 anos) ocorrendo um declínio para as frequências espaciais de 2,0cpg;8,3cpg e 14,5cpg para os grupos II e III.Para a frequência temporal de 2,5Hz o declínio ocorre nos Grupos II e III e para a frequência temporal de 5,0 Hz nas idades mais avançadas(GIII). Para o estudo da contribuição das vias de processamento paralelo (magnocelular e parvocelular) podemos notar uma maior sensibilidade ao contraste para decremento de luz do que para incremento de luz, porém não foi possível determinar a real contribuição dessas vias para a função de sensibilidade ao contraste. Conclusão Avaliamos com sucesso a Sensibilidade ao Contraste Espacial e Temporal para todas as faixas etárias e, assim, conseguimos ter acesso ao desenvolvimento desta função, entre as idades de 6 e 57 anos. Valores normativos para as tais funções foram estabelecidos por metodologia nãoparamétrica.. O estudo da contribuição das vias magnocelular e parvocelular não pode ser conclusivo, porém os achados mostraram uma maior sensibilidade para o decremente de luz o que corrobora com a literatura / Purpose: To analyze the spatial and temporal luminance contrast sensitivity function, to study the development of these functions, the contribution of the parallel processing pathways and to determine the normative values of these functions to order a clinical applicability normative. Methods the psychophysical evaluation of the spatial and temporal luminance contrast sensitivity was performed in 112 subjects divided into three groups: Group I (mean age =9.14±2.7 years), Group II (mean age=23.7 ± 3.4 years) and Group III (mean age=41.8± 5.5 years) with the PSYCHO for Windows Version 2.36 (Cambridge Research Systems, CRS-Ltd, UK) connect to the microcomputer PC XTC -600. The stimuli was showed in a monitor Sony Triniton de 19 inches GFD420 (Sony Corporation, USA) with spatial resolution of the 800X600 and temporal resolution of the 69 Hz. The stimuli was made by the graphics card VSG 2/4 (Cambridge Research Systems, CRS-Ltd, UK).Results The psychophysics evaluation to spatial and temporal contrast sensitivity showed that this function is already developed and full operation in children (6 years old) with a decline to spatial frequencies of 2.0cpg;8.3cpg and 14.5 cpg to the groups II and III. For the temporal frequency of 2.5Hz the decline occur to the groups II and III .and to the temporal frequency of 5.0 Hz the decline occur to the advantage ages(GIII). For the study of the parallel processing pathways (magnocellular e parvocellular) we can see bigger contrast sensitivity to decrement than to increment of light. It was not possible determine the real contribution of these pathways to the contrast sensitivity function. Conclusion We evaluated in a successful way the spatial and temporal contrast sensitivity to all age range and so we could access the development of this function between the ages from 6 to 57 years old. Normatives values to this function were established for non parametric methodology. The study of the contribution of the parvocellular and magnocellular pathways is not conclusive, but the results showed a bigger sensibility to decrement than to increment of light that was similar to the literature