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An investigation of structure activity relationships for aryl nitrenium stability and mutagenicity for amino polyaromatic hydrocarbons /Yeatts, Karin Beatrice, January 1990 (has links)
Thesis (M.S.)--Virginia Polytechnic Institute and State University, 1990. / Vita. Abstract. Includes bibliographical references (leaves 68-73). Also available via the Internet.
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The distribution of organic bases in reverse phase liquid chromatography : a study of mechanismsJayasinghe, Dudley Shelton 05 September 1989 (has links)
The distribution of hydrophobic ionogenic organic compounds
(HIOC's) between aqueous and nonaqueous phases has been
investigated. The HIOC's are aniline and methyl substituted
anilines. The aqueous phases are methanol-water mixed solvents with
varying pH and ionic strength. The nonaqueous phases are silica and
alkyl derivatized silica with ethyl- (C-2), octyl- (C-8), and
octadecyl- (C-18) silanes.
A gas-liquid equilibration method has been developed to
determine the Henry's law constants and the activity coefficients of
methyl anilines in methanol-water mixed solvents. The logarithm of
the Henry's law constants vary quadratically with the volume fraction
of methanol.
The chromatographic study has been performed to investigate the
effect of three mobile phase factors, fraction of methanol, pH, and
ionic strength, on the retention of methyl anilines on different
stationary phases.
The logarithm of mass distribution ratios, log k's, of methyl
anilines vary linearly with the volume fraction of methanol. The
ratios of H / k' of methyl anilines increase with increase in
methanol in the mobile phase, indicating an increase in the activity
coefficients in the stationary phases. This observation is found to
be true for different methyl anilines in different stationary phases.
A partition model is presented to describe the effect of pH and
ionic strength on the retention of HIOC's in the mobile phase. The
variation in log k' among neutral and ionic methyl anilines can be
explained by linear free energy relationships. Equations are
established to predict retention of neutral or ionized methyl
anilines from their octanol-water partition coefficients at any
methanol content in the mobile phase. Acid dissociation constants of
methyl anilines determined from the dependence of log k' on pH are in
close agrement with those determined by potentiometric titrations.
The effect of ionic strength on the retention of both neutral and
ionic species of methyl anilines is negligible. That is, the
contribution from electrostatic energy and salting out effect are not
significant.
The chromatographic study is extended to study the retention of
methyl anilines on silica as a function of pH and methanol at a
constant ionic strength. The dependence of retention on pH is
qualitatively interpreted from an ion exchange reaction between the
dissociated silanol groups in the surface and the ionized methyl
anilines. The effect of methanol on the retention of methyl anilines
and of pyridine on silica is described by a quadratic relationship
between the log k' and volume fraction of methanol. / Graduation date: 1990
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Food mutagens : factors that modulate their metabolic activationAyrton, Andrew David January 1989 (has links)
No description available.
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The solid-matrix luminescence of heterocyclic aromatic amines in sugar glassesHubbard, Sara E. January 2008 (has links)
Thesis (Ph.D.)--University of Wyoming, 2008. / Title from PDF title page (viewed on August, 3 2009). Includes bibliographical references (p. 131-139).
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Modulation of genotoxic responses by environmental agentsWagner, Elizabeth Diane January 1999 (has links)
A metabolite of a widely used pesticide, paraoxon, exerted a dramatic mutagenic synergistic effect in Salmonella typhimurium with a number of mammalian-activated or plant-activated aromatic amines and heterocyclic amines. The mutagenic synergy required an activated an aromatic amine, and was not attributable to the generation of new mutagenic products or to the modification of the stability of the activated aromatic amine products. Paraoxon modulated the genotoxic potency of dietaiy heterocyclic amines in human cells. The results of this study raise the concern of the environmental effects of organophosphorus ester insecticides. A clone of the Chinese hamster ovary cell line, AS52, was isolated, characterised and analysed under identical treatment conditions with the mutagens 2-acetoxy-acetylaminofluorene (2AAAF), ethyl methanesulphonate (EMS), and UV radiation. The genetic endpoints included acute DNA damage detected in the alkaline single cell gel electrophoresis (SCGE) assay, whole cell clastogenicity detected with laser beam flow cytometry and forward mutation at a target gene. There were statistically significant increases in DNA damage and forward mutation with all three mutagens. Statistically significant increases in chromosome damage were observed with 2AAAF and EMS but not with UV. A non-uniform distribution of DNA damage throughout the genome was indicated with the chemical mutagens in the SCGE assay. Another type of modulation in genotoxic response was investigated whereby numerous commercial soybean processing products and by-products were analysed for their antimutagenic and antigenotoxic activities. Antimutagenic activity was detected in a soybean processing by-product, soybean molasses and in an ethanol extract, fraction PCC. PCC protected mammalian cells against direct DNA damage, clastogenic damage and point mutation induced by 2AAAF. A fraction of PCC, PCC100 was an effective antimutagen in mammalian cells and in human lymphocytes. Analytical chemical studies identified the compounds responsible for the antimutagenic activity as the soyasaponins I, III and V.
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Multinuclear magnetic resonance studies on the metabolism model of fluoroaromatic xenobioticsTugnait, Meera January 1994 (has links)
No description available.
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Methods for assessment of exposure to aromatic amines/isocyanates by air monitoring and biomarkersBrunmark, Per. January 1994 (has links)
Thesis (doctoral)--Lund University, 1994.
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Methods for assessment of exposure to aromatic amines/isocyanates by air monitoring and biomarkersBrunmark, Per. January 1994 (has links)
Thesis (doctoral)--Lund University, 1994.
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Regulation of subcellular localization of the aryl hydrocarbon receptor (AHR)Richter, Catherine Ann, January 2000 (has links)
Thesis (Ph. D.)--University of Missouri--Columbia, 2000. / Typescript. Vita. Includes bibliographical references (leaves 113-122). Also available on the Internet.
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Strategies to reduce arylamine drug toxicity in people with AIDS /Winter, Helen Rayma, January 1998 (has links)
Thesis (Ph. D.)--University of Washington, 1998. / Vita. Includes bibliographical references (leaves [134]-149).
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