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
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Item The Novel Use of Nitroxide Antioxidants as Free Radical Scavengers in Ultra-High Molecular Weight Polyethylene (UHMWPE) for Total Joint Replacements(2010) Chumakov, Marina Konstantinovna; Al-Sheikhly, Mohamad; Bioengineering; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)Ultra-high molecular weight polyethylene (UHMWPE) has been the standard load-bearing material used in total joint replacements since the 1960s. However, oxidative degradation can lead to premature aging and wear of UHMWPE, requiring implant revision. The novel use of nitroxide antioxidants to prevent oxidation in UHMWPE was proposed and the resulting structure and property changes were evaluated in this work. Standard sterilization and crosslinking methods of Co-60 gamma or high energy electron beam radiation produce alkyl free radicals on the polymer chain. Alkyl radicals react to form bimolecular crosslinks and long-lived allyl radicals at high dose rates; at low dose rates they tend to react with oxygen to form peroxyl radicals. The peroxyl radicals further interact with the polymer chain producing hydroperoxides and more free radicals, leading to oxidative degradation. As an alternative to post-irradiation remelting, which allows radical recombination but reduces fatigue strength, antioxidants can be introduced into UHMWPE to scavenge residual radicals. Nitroxides are stable organic compounds that have a strong paramagnetic signal and are very efficient in preventing lipid peroxidation and in providing radioprotection in biological tissues. The nitroxides used are 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and 4-hydroxy-TEMPO (Tempol). Through radical-radical interactions, radiolytically-produced alkyl radicals in UHMWPE are scavenged by the nitroxide radical. This is demonstrated through Electron Paramagnetic Resonance (EPR) spectroscopy where the paramagnetic nitroxide signal decays as it interacts with carbon-centered radicals in UHMWPE. Pulse radiolysis kinetics studies also show that alkyl radicals in UHMWPE preferentially react with nitroxides in the absence of oxygen. Controlled infiltration of UHMWPE with nitroxides is also observed using EPR. The resulting crosslink densities were investigated using Thermomechanical Analysis. It was observed that the addition of nitroxides after irradiation does not alter the crosslink density. Tensile testing of crosslinked and nitroxide-doped UHMWPE demonstrates increased ultimate tensile strength and toughness and the material exhibits an increase in crystallinity. Additionally, accelerated aging of specimens containing trace levels of nitroxide show very low oxidation levels when placed in an aggressive oxygen environment. Consequently, low concentrations of nitroxides diffused into UHMWPE after crosslinking produce an oxidation-resistant and highly crosslinked material for improved implant performance.Item A Novel Pre-fluorescent Nitroxide Probe for the Highly Sensitive Determination of Peroxyl and Other Radical Oxidants(2009) Jia, Min; Blough, Neil V; Chemistry; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)ABSTRACT Peroxyl and other radical oxidants react with stable cyclic nitroxides, such as the piperidinyl and pyrrolidinyl nitroxides to form initially the one electron oxidation product, the oxoammonium cation. For most of the nitroxides studied thus far, the oxoammonium cation can in part be regenerated to the nitroxide through reduction by solution constituents. The reaction mechanisms, however, remain a matter of debate. Further, the highly-sensitive, quantitative determination of peroxyl and other radical oxidants has yet to be achieved, posing a major hurdle to a further understanding of the impact of peroxyl radicals in many biological and environmental processes. A unique, amino-pyrrolidinyl nitroxide, 3-amino-2,2,5,5,-tetramethyl-1-pyrrolidinyloxy (3-ap) is shown to undergo an irreversible reaction with peroxyl radicals and other radical oxidants to generate a diamagnetic product. When a fluorophore, fluorescamine is covalently linked through the amino group on the nitroxide, the resulting compound (3-apf, or I) has very low fluorescence quantum yield. Upon reaction with peroxyl and other radical oxidants, the quantum yield of the product increases dramatically (~100 fold), and thus 3-ap or 3-apf can be used as a highly sensitive and versatile probe to determine oxidant production optically, either by monitoring the changes in fluorescence intensity using a spectrofluorometer, by HPLC analysis with fluorescence detection, or by a combination of both approaches. By changing the [O2]/[nitroxide] ratio, it is shown that peroxyl radicals can be detected and quantified preferentially in the presence of other radical oxidants, such as *NO2 and CO3*-. When decreasing the [O2]/[nitroxide] ratio, the oxidation product decreases, with a concomitant increase of the alkoxylamine product resulting from reaction of 3-ap (3-apf) with carbon centered radicals. Preliminary studies suggest that the reactions of 3-ap and 3-apf with peroxyl radical produce different final products. High resolution mass spectrometry and NMR studies indicate that 3-ap is oxidized to form a cyclic peroxide structure, while 3-apf is oxidized to form a cyclic -NH-O- structure, with this difference resulting possibly from the presence of the fluorescamine moiety in 3-apf. Detection of photochemically produced peroxyl radicals is achieved by employing 3-amino-2,2,5,5,-tetramethyl-1-pyrrolidinyloxy (3-ap) alone, followed by derivatization with fluorescamine, while detection of thermally-generated peroxyl radicals employs 3-apf. Preliminary applications include the detection of peroxyl radicals generated thermally in soybean phosphatidylcholine liposomes by 3-apf and produced photochemically in tap water by 3-ap.