A mathematical model for polymer gel dosimeters was extended to simulate the effects of radiation depth doses of various radiation beams on the mass of polymer formed. The influences of monomer diffusion and temperature variation were investigated and predicted by the model. Simulation results indicate that both diffusion and temperature effects are most noticeable at the depth of maximum dose. Diffusion effects are larger for steep depth-dose curves with large dose gradients, while temperature effects are larger for extensive depth-dose curves that deliver high doses of radiation to a greater depth. Based on simulation results, involving a maximum dose of 5 Gy, the amount of additional polymer formed due to diffusion is small, ranging from 0.1 % for 15 MV x-ray photons to 2.6 % for Co60 γ-radiation. This small amount of additional polymer should not cause significant problems for the accuracy of depth-dose calibration curves, particularly if the depth of maximum dose is avoided. Inaccuracies caused by temperature effects are expected to be smaller than those caused by diffusion. Experimental studies were undertaken to improve the radiation dose response using x-ray Computed Tomography (CT). A new polymer gel dosimeter recipe with enhanced dose response was achieved by using a large quantity of N-isopropyl acrylamide (NIPAM) (15 wt%) to help dissolve the N,N’-methylene bisacrylamide (Bis) crosslinker. The solubility of Bis was substantially increased, allowing for large quantities of dissolved NIPAM and Bis in the system. The new dosimeter exhibits an enhanced dose sensitivity and dose resolution for x-ray CT imaging, which holds promise for clinical applications. The dose resolution of approximately 0.1 Gy, for up to absorbed doses of 50 Gy, for the new recipe is superior to that for previous dosimeter formulations developed for x-ray CT. / Thesis (Master, Chemical Engineering) -- Queen's University, 2010-12-21 18:10:28.37

No description available.

Fractured reservoirs have always been considered poor candidates for enhanced oil recovery. This can be attributed to the complexities involved in understanding and predicting performance in these reservoirs. In a fractured system, the high permeability fracture forms the preferred pathway for the injected fluids, and a large amount of oil that is stored in the matrix is bypassed. Hence, a good understanding of multiphase fluid flow in fractures is required to reduce oil bypass and increase recovery from these reservoirs. This research investigates the effect of heterogeneity and injection rates on oil bypass and also the various techniques used for the improvement of sweep efficiency in heterogeneous systems. Several coreflood experiments were performed using homogeneous and heterogeneous cores and a 4th generation X-Ray CT scanner was used to visualize heterogeneity and fluid flow in the core. Porosity and saturation measurements were made during the course of the experiment. The experimental results indicate that injection rates play a very important role in affecting the recovery process, more so in the presence of fractures. At high injection rates, faster breakthrough of CO2 and higher oil bypass were observed than at low injection rates. But very low injection rates are not attractive from an economic point of view. Hence water viscosified with a polymer was injected directly into the fracture to divert CO2 flow into the matrix and delay breakthrough, similar to the WAG process. Although the breakthrough time reduced considerably, water ??leak off?? into the matrix was very high. To counter this problem, a cross-linked gel was used in the fracture for conformance control. The gel was found to overcome ??leak off?? problems and effectively divert CO2 flow into the matrix. This experimental research will serve to increase the understanding of fluid flow and conformance control methods in fractured reservoirs.

Excess water production is a major economic and environmental problem for the oil and gas industry. The cost of processing excess water runs into billions of dollars. Polymer gel technology has been successfully used in controlling water influx without damaging hydrocarbon production in conventional naturally fractured or hydraulically fractured reservoirs. However, there has been no systematic investigation on effectiveness and placement conditions of polymer gels for shutting off water flow from fractures with narrow apertures in shale and tight gas reservoirs. The existing polymer gels, like those based on Chromium(III) Acetate, as a crosslinker will exert very high extrusion pressure to effectively penetrate the narrow aperture fractures present in shale and tight gas reservoirs. This gives rise to a need for a new polymer gel system that can be used for selectively shutting off water flow from narrow aperture fractures in shale and tight gas reservoirs. The new gel system will have a longer gelation time than the existing polymer gels; this ensures minimum crosslinking of the gel by the time it reaches bottom hole. The gelant solution will be pumped at low pressure so that, it penetrates only pre-existing fractures in the formation with ease. This study for the first time focuses on developing an environmentally benign polymer gel system based on high molecular weight HPAM, as a base polymer and a commercial grade PEI as an organic crosslinker. Gel samples of different concentration ratios of the polymer and crosslinker were prepared and classified under Sydansk code of gel strength to find optimum concentration ratios that gave good gels. The gel system was characterized using Brookfield DV-III Ultra Rheometer and Fann-35 Viscometer.

X-ray computed tomography (CT) polymer gel dosimetry (PGD) is an attractive tool for three-dimensional (3D) radiation therapy (RT) treatment verification due to the availability of CT scanners in RT clinics. Nevertheless, wide-spread use of the technique has been hindered by low signal-to-noise CT images largely resulting from gel formulations with low radiation sensitivity. However, a new gel recipe with enhanced dose sensitivity was recently introduced that shows great promise for use with CT readout. This dissertation describes development of an CT PGD system for 3D verification of RT treatments using the new gel formulation. The work is divided into three studies: gel characterization, commissioning of a multislice CT scanner and investigation of a dose rate dependence observed during gel characterization. The first component of this work examines the dosimetric properties of the new gel formulation. The response of the gel is found to be stable between 15 - 36 hours post-irradiation and excellent batch reproducibility is seen for doses between 0 - 28 Gy. A dose rate dependence is found for gels irradiated between 100 - 600 MU/min, indicating machine dose rate must be consistent for calibration and test irradiations to avoid dosimetric error. An example clinical application is also presented using an IMRT treatment verification that demonstrates the potential of the system for use in modern RT. The second component of this work focuses on commissioning a multislice CT scanner for CT PGD. A new slice-by-slice background subtraction technique is introduced to account for the anode heel effect. Additional investigations show recommendations for optimizing image quality in CT PGD using a single slice machine also apply to multislice scanners. In addition, the consistency of CT numbers across the multislice detector array is found to be excellent for all slice thicknesses. Further work is performed to assess the tube load characteristics of the scanner and develop a scanning protocol for imaging large gel volumes. Finally, images acquired throughout the volume of an unirradiated active gel show variations in CT data across each image on the order of 7 HU. However, these variations are not expected to greatly influence gel measurements as they are consistent throughout the gel volume. The third component of this work examines the dose rate dependence found during gel characterization. Studies using gel vials and 1 L cylinders indicate the response of the gel does not depend on changes in mean dose rate on the order of seconds to minutes. However, the machine dose rate remains, indicating variations in dose rate on the order of milliseconds influence the response of the gel. An attempt is made to mitigate the effect by increasing the concentration of antioxidant in the gel system but results in reduced overall response. Further work is performed to determine if self-crosslinking of one of the gel components contributes to the observed machine dose rate dependence. In summary, this dissertation has significantly advanced the field of gel dosimetry by providing a prototype CT PGD system with enhanced dose resolution for complex RT treatment verification. / Graduate / 0992 / 0495 / 0756 / holly.johnston@utsouthwestern.edu

Kyoto University (京都大学) / 0048 / 新制・課程博士 / 博士(工学) / 甲第13789号 / 工博第2893号 / 新制||工||1427(附属図書館) / 26005 / UT51-2008-C705 / 京都大学大学院工学研究科材料化学専攻 / (主査)教授 瀧川 敏算, 教授 木村 俊作, 教授 田中 文彦 / 学位規則第4条第1項該当

Was vor einigen Jahren undenkbar erschien, könnte zukünftig möglich sein: Krankes Gewebe mit Gesundem ersetzen, das in vitro mit modernsten Biofabrikationstechniken hergestellt wird. Dabei werden bisherige Grenzen überschritten: Während lichtbasierte Biodruckverfahren wie die Zwei-Photonen-Polymerisation Auflösungen bis in den Nanometerbereich erzielen, ermöglicht der Volumetrische Biodruck (VB) den Druck zentimetergroßer Konstrukte in wenigen Sekunden. Diese Geschwindigkeiten erweisen sich unter Biodruckverfahren als konkurrenzlos und werden erreicht, da das Bioharz nicht konsekutiv, sondern zugleich vernetzt wird. Einschränkend gilt bislang nur der Mangel an geeigneten Bioharzen für den VB. Daher beschäftigt sich vorliegende Arbeit mit der Charakterisierung und Modifikation eines dafür geeigneten Bioharzes: Gelatine-Methacrylat (GelMA). Dank seiner Zusammensetzung ähnelt das etablierte Hydrogelsystem der Extratrazellularmatrix: Der Gelatine-Anteil ermöglicht Biokompatibilität und Bioaktivität durch zelladhäsive sowie degradierbare Aminosäure-Sequenzen. Zugleich können durch photovernetzbare Methacryloyl-Substituenten Konstrukte mit einer Formstabilität bei 37 °C erzeugt werden. Zunächst wurde das Bioharz zellbiologisch charakterisiert, indem mit der embryonalen Mausfibroblasten-Zelllinie NIH-3T3 beladene GelMA-Zylinder gegossen, photopolymerisiert und kultiviert wurden. Im Verlauf einer Woche wurde die Zytokompatibilität der Gele anhand der Proliferationsfähigkeit (PicoGreen-Assay), des Metabolismus (CCK-8-Assay) und der Vitalität (Live/Dead-Assay) der Zellen beurteilt. Dabei wurden Polymerkonzentrationen von 6 – 8 % sowie GelMA-Harze zweier verschiedener Molekulargewichte verglichen. Alle hergestellten Gele erwiesen sich als zytokompatibel, 6 % ige Gele ließen im Inneren jedoch zusätzlich eine beginnende Zellspreizung zu und ein niedriges GelMA-Molekulargewicht verstärkte die gemessene Proliferation. Die sich anschließende mechanische und physikalische Charakterisierung belegte, dass höher konzentrierte Gele einen größeren E-Modul aufwiesen und damit steifer waren. Eine Modifikation der Gele mit Fibronektin beeinflusste die Zellverträglichkeit weder positiv noch negativ und die Zugabe von Kollagen war wegen Entmischungseffekten nicht bewertbar. Es liegt die Vermutung nah, dass eine weitere Reduktion der Polymerkonzentration und damit Verringerung der Gelsteifigkeit der Schlüssel für mehr Zellspreizung und -wachstum ist. Da jedoch die Druckbarkeit des Bioharzes die weitere Senkung des GelMA-Gehalts limitiert, sollten zunächst Methoden entwickelt werden, welche die Netzwerkdichte des GelMAs anderweitig herabsetzen. / What seemed unthinkable a few years ago could be possible in the future: replacing diseased tissue with healthy tissue produced in vitro using the latest biofabrication techniques. Previous limits are being exceeded: While light-based bioprinting processes such as two-photon polymerization achieve resolutions down to the nanometer range, volumetric bioprinting (VB) makes it possible to print centimeter-sized constructs in just a few seconds. These speeds are unrivaled among bioprinting processes and are achieved because the bioresin is not cross-linked consecutively but simultaneously. The only limitation to date is the lack of suitable bioresins for VB. Therefore, the present work deals with the characterization and modification of a suitable bioresin: gelatine methacrylate (GelMA). Thanks to its composition, the established hydrogel system is similar to the extracellular matrix: The gelatine component enables biocompatibility and bioactivity through cell-adhesive as well as degradable amino acid sequences. At the same time, photo-crosslinkable methacryloyl substituents can be used to produce constructs with dimensional stability at 37 °C. First, the bioresin was characterized cell biologically by casting, photopolymerizing and culturing GelMA cylinders loaded with the embryonic mouse fibroblast cell line NIH-3T3. Over the course of a week, the cytocompatibility of the gels was assessed based on proliferation capacity (PicoGreen assay), metabolism (CCK-8 assay) and viability (Live/Dead assay) of the cells. Polymer concentrations of 6 - 8 % and GelMA resins of two different molecular weights were compared. All gels produced were found to be cytocompatible, however, 6 % gels additionally allowed incipient cell spreading inside and a low GelMA molecular weight increased the measured proliferation. The subsequent mechanical and physical characterization showed that gels with higher concentration had a higher modulus of elasticity and were therefore stiffer. Modifications of the gels with fibronectin had neither a positive nor negative effect on cell compatibility and the addition of collagen could not be evaluated due to segregation effects. It is reasonable to assume that further reduction in polymer concentration and thus a reduction in gel stiffness is the key to more cell spreading and growth. However, since the printability of the bioresin limits further reduction of the GelMA content, methods should first be developed to reduce the network density of the GelMA in other ways.

Dosimetry is a vital component of treatment planning in radiation therapy. Methods of radiation dosimetry currently include the use of: ionization chambers, thermoluminescent dosimeters (TLDs), solid-state detectors and radiographic film. However, these methods are inherently either 1D or 2D and their use involves the perturbation of the radiation beam. Although the dose distribution within tissues following radiation therapy treatments can be modeled using computerized treatment planning systems, a need exists for a dosimeter that can accurately measure dose distributions directly and produce 3D dose maps. Some radiation therapy and brachytherapy treatments require mapping the dose distributions in high-resolution (typically < 1 mm). A dosimetry technique that is capable of producing high resolution 3D dose maps of the absorbed dose distribution within tissues is required. Gel dosimetry is inherently a 3D integrating dosimeter that offers high spatial resolution, precision and accuracy. Polymer gel dosimetry is founded on the basis that monomers dissolved in the gel matrix polymerize due to the presence of free radicals produced by the radiolysis of water molecules. The amount of polymerization that occurs within a polymer gel dosimeter can be correlated to the absorbed dose. The gel matrix maintains the spatial integrity of the polymers and hence a dose distribution can be determined by imaging the irradiated polymer gel dosimeter using an imaging modality such as MRI, x-ray computed tomography (CT), ultrasound, optical CT or vibrational spectroscopy. Polymer gel dosimeters, however, suffer from oxygen contamination. Oxygen inhibits the polymerization reaction and hence polymer gel dosimeters must be manufactured, irradiated and scanned in hypoxic environments. Normoxic polymer gel dosimeters incorporate an anti-oxidant into the formulation that binds the oxygen present in the gel and allows the dosimeter to be made under normal atmospheric conditions. The first part of this study was to provide a comprehensive investigation into various formulations of polymer and normoxic polymer gel dosimeters. Several parameters were used to characterize and assess the performance of each formulation of polymer gel dosimeter including: spatial resolution and stability, temporal stability of the R2-dose response, optimal R2-dose response for changes in concentration of constituents and the effects of oxygen infiltration. This work enabled optimal formulations to be determined that would provide greater dose sensitivity. Further work was done to investigate the chemical kinetics that take place within normoxic polymer gel dosimeters from manufacture to post-irradiation. This study explored the functions that each of the constituent chemicals plays in a polymer gel dosimeter. Although normoxic polymer gel dosimeters exhibit very similar characteristics to polyacrylamide polymer gel dosimeters, one important difference between them was found to be a decrease in R2-dose sensitivity over time in the normoxic polymer gel dosimeter compared to an increase in the polyacrylamide polymer gel dosimeters. From an investigation into the function of anti-oxidants in normoxic polymer gel dosimeters, alternatives were proposed. Several alternative anti-oxidants were explored in this study that found that whilst some were reasonably effective, tetrakis (hydroxymethyl) phosphonium chloride (THPC) had the highest reaction rate. THPC was found not only to be an aggressive scavenger of oxygen, but also to increase the dose sensitivity of the gel. Hence, a formulation of normoxic polymer gel dosimeter was proposed, called MAGAT, that comprised: methacrylic acid, gelatin, hydroquinone and THPC. This formulation was examined in a similar fashion to the studies of the other formulations of polymer and normoxic polymer gel dosiemeters. The gel was found to exhibit spatial and temporal stability and an optimal formulation was proposed based on the R2-dose response. Applications such as IVBT require high-resolution dosimetry. Combined with high-resolution MRI, polymer gel dosimetry has potential as a high-resolution 3D integrated dosimeter. Thus, the second component of this study was to commission a micro-imaging MR spectrometer for use with normoxic polymer gel dosimeters and investigate artifacts related to imaging in high-resolutions. Using high-resolution MRI requires high gradient strengths that, combined with the Brownian motion of water molecules, was found to produce an attenuation of the MR signal and hence lead to a variation in the measured R2. The variation in measured R2 was found to be dependent on both the timing and amplitude of pulses in the pulse sequence used during scanning. Software was designed and coded that could accurately determine the amount of variation in measured R2 based on the pulse sequence applied to a phantom. Using this software, it is possible to correct for differences between scans using different imaging parameters or pulse sequences. A normoxic polymer gel dosimeter was irradiated using typical brachytherapy delivery and the resulting dose distributions compared with dose points predicted by the computerized treatment planning system.The R2-dose response was determined and used to convert the R2 maps of the phantoms to dose maps. The phantoms and calibration vials were imaged with an in-plane resolution of 0.1055 mm/pixel and a slice thickness of 2 mm. With such a relatively large slice thickness compared to the in-plane resolution, partial volume effects were significant, especially in the region immediately adjacent the source where high dose gradients typically exist. Estimates of the partial volume effects at various distances within the phantom were determined using a mathematical model based on dose points from the treatment planning system. The normalized and adjusted dose profiles showed very good agreement with the dose points predicted by the treatment planning system.

The polymer gels especially hydrogels have a very special structure and useful features such as unusual volume phase transition, compatibility with biological systems, and sensitivity to environmental stimuli (temperature, pH value, electric field, light and more), which lead to many potential applications in physical and biochemical fields. This research includes: (1) the theoretical and experimental studies of polymer gels on swelling kinetics, spinodal decomposition, and solution convection in gel matrix; (2) applications of polymer gels in wound dressing, tissue-simulating optical phantom and gel display. The kinetics of gel swelling has been theoretically analyzed by considering coupled motions of both solvent and polymer network. Analytical solutions of the solvent and the network movement are derived from collective diffusion equations for a long cylindrical and a large disk gel. Kinetics of spinodal decomposition of N-isopropylacrylamide (NIPA) polymer gel is investigated using turbidity and ultrasonic techniques. By probing movement of domains, a possible time-dependent gel structure in the spinodal decomposition region is presented. Theoretical studies of solution convection in gel matrix have been done and more analysis on dimensionless parameters is provided. To enhance the drug uptake and release capacity of silicone rubber (SR), NIPA hydrogel particles have been incorporated into a SR membrane. This SR/NIPA composite gel has promising attributes for wound dressing and other uses. Tissue-simulating optical phantom has been synthesized and studied using NIPA solution trapped inside a hydrogel. Polymer gels with engineered surface patterns were implemented. NIPA gel deposited on the surface of an acrylamide gel can be used as responsive gel display. A dynamically measurement technique of local shear modulus and swelling ratio of gel is presented based on an engineered periodic surface pattern as square array.

A presença de material de alto número atômico adjacente ao tecido mole aumenta localmente a dose absorvida pelo tecido quando submetido à radiação. Este efeito ocorre devido aos fotoelétrons ejetados do material de alto número atômico. Dosímetros de gel polimérico com partículas de ouro foram utilizados para investigar este efeito. Foram realizados cálculos analíticos para estimar o aumento de dose e simulações com o método de Monte Carlo. A irradiação de amostras de gel polimérico (GP) puro e com 0,005 gAu/gGP utilizando um feixe de raios X produzido por um potencial de 150 kV filtrado com 4 mmAl e 5 mmCu resultou em uma dose absorvida pelas amostras com ouro aproximadamente 20% maior que a dose absorvida pelas amostras de gel polimérico puro. Os cálculos analíticos e a simulação com o método de Monte Carlo resultaram em um aumento de aproximadamente 30% na dose absorvida. / The presence of high-Z material adjacent to soft tissue, when submitted to irradiation, enhances locally the absorbed dose in these soft tissues. Such effect occurs due to the outscattering of photoelectrons from the high-Z material. Polymer gel dosimeters have been used to investigate this effect. Analytic calculations to estimate the dose enhancement and Monte Carlo simulations have been performed. Samples containing polymer gel (PG) with 0.005 gAu/gPG and pure polymer gel have been irradiated using an X-rays beam produced by 150 kV, filtered with 4 mm Al and 5 mm Cu, which resulted in an approximately 20% higher absorbed dose in the samples with gold in comparison to those with pure polymer gel. The analytic calculations and the Monte Carlo simulation resulted in a dose enhancement factor of approximately 30%.