Poly(p-phenylenebenzobisimidazole), PBI, is a rigid-rod polymer with a fully conjugated backbone having superior mechanical properties, thermo-oxi- dative and solvent stabilities. The stabilities cause processing difficulties and in terms limit its applications in critical technologies, such as conducting polymers, nonlinear optics, and solid polyelectrolytes. In this study, a chemical derivative of PBI, poly[1,7-dihydrobenzo[1,2- d:4,5-d¡¦]diimidazo-2,6-diyl[2-(2-sulfo)-p-phenylene]], sPBI, was synthesized by polycondensation reaction of 1,2,4,5-tetraaminobenzene tetrahydrochloride with 2-sulfoterephthalic acid in poly(phosphoric acid). Isolated sPBI was measured in 30oC methanesulfonic acid for an intrinsic viscosity as high as 10.5 dL/g. sPBI polymer was then reacted with 1,3-propanesultone in dimethylsulfoxide containing sodium hydride for water-soluble rigid-rod polyelectrolyte, poly[1,7- dipropylsulfobenzo-[1,2-d:4,5-d¡¦]diimidazo-2,6-diyl-[2,(2-sulfo)-p-phenylene]], sPBI-PS(Na+). sPBI-PS(Na+) was further converted to sPBI-PS(Li+) with hydrochloride and followed with lithium hydroxide. Various analyses were applied to ascertain chemical structure, purities and thermal properties of synthesized monomers and polymers. sPBI-PS(Li+) aqueous solutions were doped individually with lithium salts of LiI, LiBF4, and LiCF3SO3 at concentrations up to 1.7¡Ñ10-5 wt./wt., which were cast into freestanding films of 10-25 £gm in thickness. Direct-current conductivity measured at room- temperature parallel to the film surface was as large as 9.74¡Ñ10-5 S/cm. The ionic nature of the conductivity was revealed by constant-voltage depletion measurements. X-ray scattering results suggested that the cast film was in-plane isotropic but out-of-the plane anisotropic with the rigid-rod backbone lying in the plane of the film.

This thesis focuses on the characterization of soluble iron in ambient/urban and source emission aerosols, primarily focusing on the sources and atmospheric processes contributing to iron solubility. Multiple techniques, including bulk and single particle measurements, were used to investigate the complex chemistry of iron solubility. A technique was developed and validated (PILS-LWCC), allowing for 12-minute measurements of water-soluble ferrous iron (WS_Fe(II)) in aerosols with a limit of detection of 4.6 ng m-3 and 12% relative uncertainty. The PILS-LWCC was deployed at several urban field sites (Atlanta, GA and Dearborn, MI) and a biomass burning event to determine major sources and atmospheric processes of WS_Fe(II) in aerosols. PILS-LWCC measurements suggest that industrial and biomass burning are sources of WS_Fe(II). In addition, acid-processing mechanisms also appeared to influence WS_Fe(II) concentrations, based on a strong correlation between WS_Fe(II) and SO42- (r2 = 0.76) as well as apparent aerosol acidity (r2 =0.78) during a field campaign in Atlanta, GA. Synchrotron-based techniques, such as X-ray Absorption Near-Edge Structure (XANES) spectroscopy and micro X-ray fluorescence measurements, were also used to identify the chemical composition (redox state and phase) and mixing state (two properties that may influence iron solubility) of source emission and ambient single iron-containing particles. These single particle measurements were used in conjunction with bulk iron solubility to assess the influence of chemical composition and mixing state on iron solubility. Single particle (synchrotron-based) and bulk iron solubility measurements suggested that iron solubility is not primarily driven by chemical composition in source emission and ambient particles. Differences in iron solubility, however, were related to single particle sulfur content in ambient and source emission aerosols, suggesting that similar sources/atmospheric processes control iron solubility in these samples. The relationship between iron solubility and sulfur content corresponded well with bulk ground-based measurements of ambient aerosol using the PILS-LWCC. Combined single particle and bulk online measurements provide compelling evidence that atmospheric acid processing, involving sulfur-containing acids (H2SO4), is an important formation route of soluble iron in ambient urban aerosols. The results of this thesis provide valuable information to further understanding the controls of iron solubility in atmospheric aerosols.

Traumatic brain injury (TBI) has become an increasingly unmet clinical need due to intense military conflicts worldwide. Directly impacted brain cells suffer massive death, with neighboring cells succumbing to progressive neurodegeneration accompanied by inflammatory and other secondary cell death events. Subsequent neurodegenerative events may extend to normal areas beyond the core of injury, thereby exacerbating the central nervous system’s inflammatory response to TBI. Recently CD-36 (cluster of differentiation 36/fatty acid translocase (FAT), a class B scavenger receptor of modified low-density lipoproteins (mLDLs) in macrophages, has been implicated in lipid metabolism, atherosclerosis, oxidative stress, and tissue injury in cerebral ischemia, and in certain neurodegenerative diseases. Accordingly, we proposed that CD-36 has a pivotal role in the neuroinflammatory cascade that further contributes to the pathology of TBI. First, we explored the neuroinflammatory role of CD-36 after acute and chronic stages of TBI. Second, we employed a neuroinflammatory model to test the therapeutic effect of the soluble receptor of advanced end-glycation product (sRAGE); previously shown to abrogate increased CD-36 expression in stroke. Third, we further examined ameliorating TBI related inflammation as a therapeutic pathway by combination of stem cell therapy and sRAGE. At acute stages of TBI, we observed brain co-localization of CD-36, monocyte chemoattractant protein 1 (MCP-1) and ionized calcium-binding adapter molecule 1 (Iba-1) on impacted cortical areas, significant increases of CD-36 and MCP-1 positive cells in the ipsilateral vs. contralateral hemispheres of TBI animals in acute, but no significant increases of Iba-1 expressing cells over time. In early acute stages of TBI immunoblotting showed overexpression of CD-36 in brain cortex when comparing ipsilateral and contralateral hemispheres vs. sham. Spleen CD-36 protein expression at acute post-TBI stages showed no significant difference between TBI and sham groups. In addition, immunohistochemistry revealed minimal CD-36 detection on the cortical area of impact on our chronic group. Spleen immunohistochemistry also showed co-localization of CD-36 and MCP-1 in the red pulp of spleen in acute stages of TBI animals when compared to sham. Ongoing ischemic and hyperlipidemic rodent models suggest that infiltrating monocytes/macrophages from the periphery are the major source of CD-36 in the post-ischemic brain. Likewise, CD-36 expressing monocytes in the spleen after TBI may suggest its role in peripheral immune response, which may exacerbates the inflammatory response after TBI. Therefore, CD-36 may play a key role as a pathological link between inflammation and TBI. Our results suggest an intimate involvement of CD-36 mediated inflammation in TBI, providing novel insights into the understanding of disease neuroinflammation and as a potent therapeutic target for TBI treatment. The critical timing (i.e., 24-48 hours) of CD-36 expression (from downregulation to upregulation) may signal the transition of functional effects of this immune response from pro-survival to cell death. This observed dynamic CD-36 expression also suggests the therapeutic window for TBI. The detection of CD-36 expression in brain areas proximal, as well as distal, to the site of impacted injury suggests its role in both acute and progressive evolution of TBI. CD-36 neuroinflammatory role has clinical relevance for treating patients who have suffered any TBI condition at acute and chronic stages.

The Bio J-FIL process has been demonstrated to be a viable method for manufacturing nanoscale, polymeric drug carriers. The process allows for precise control of the size and shape of the drug carriers. While the original process is sufficient for research scale projects, reliability issues have prevented it from being scalable to levels that could potentially be used for mass-production of the drug carriers. In this thesis, a detailed root cause analysis has been conducted to determine the cause of the reliability issues limiting the Bio JFIL process. A series of experiments with varying substrate and imprint fluid combinations were conducted to pinpoint the cause of imprint failure in the Bio J-FIL process. Upon determining the cause of failure, an alternative imprint process was investigated that sought to increase the variety of materials used in the process by utilizing an intermediary layer. This process is referred to in this thesis as the Bio JFIL-I process. The results using Bio JFIL-I indicated increased reliability over the standard Bio J-FIL process. Further refinement of the Bio JFIL-I process could also address additional issues with the Bio J-FIL process unrelated to process reliability. The Bio JFIL-I approach presented in this thesis is complementary to other approaches that have been recently pursued in the literature which are discussed in the thesis. / text

The number of newly developed chemical entities exhibiting poor water solubility has increased dramatically in recent years. In many cases this intrinsic property results in poor or erratic dissolution in biological fluids. Improving aqueous solubility of these compounds, even temporarily, can have a significant impact on in vivo performance. Single phase amorphous solid dispersions of a drug and polymer have emerged as a technique to not only increase the level of drug supersaturation but also maintain these levels for extended periods of time. Hot-melt extrusion (HME) has become the preferred processing technique to prepare systems such as these but has a number of limitations that prevent the successful formulation of many drug substances. Within this dissertation, the use of concentration enhancing polymers was investigated in parallel with a thorough evaluation of a novel fusion-based processing technique, KinetiSol® Dispersing (KSD), to prepare single phase amorphous solid dispersions that could not be successfully prepared by HME. Studies showed that the KSD technique is suitable for rendering thermally labile and high melting point drug substances amorphous through a combination of frictional and shearing energy. Compounds such as these were shown to degrade during HME processing due to relatively long residence times and low shear forces. Similarly, the KSD process was shown to successfully process solid dispersion compositions containing a high viscosity polymer with significantly lower levels of polymer degradation than obtained by HME processing. In the final study, KSD processing was used to prepare solid dispersions containing the hydrophilic polymer Soluplus[superscript TM] and methods were evaluated to formulate a tablet with rapid tablet disintegration characteristics, a requirement for sufficient dissolution enhancement. Combined, the studies demonstrated the effectiveness of combining proper polymer selection and formulation approaches with a suitable processing technique to form solid dispersion systems that provide rapid and extended durations of supersaturation. / text

D. Tech. Chemical, Metallurgical and Materials Engineering / Aims to develop a thermoplastic matrix-based composite with a view to identifying the most suitable combinations of locally available natural fibres and matrices, which meet some basic requirements (e.g., fire and moisture resistance) for the structural and non-structural materials utilised in the building and construction industries.This general goal is divided into three distinct aims: 1. Examine the chemical surface modification of natural fibres (flax, hemp, pineapple and sisal) using water glass (WG). The study investigates the effect of WG treatment on the mechanical and thermooxidative properties of natural fibres. 2. To produce untreated and WG-treated short sisal/polypropylene (with or without maleic anhydride-grafted-polypropylene) compounds using the injection moulding process. The study also investigates the failure behaviour of the composites produced by the tensile-acoustic emission technique as well as the thermal and water absorption characteristics thereof. 3. To produce untreated and WG-treated nonwoven sisal/polypropylene (with or without maleated polypropylene) composites by using the compression moulding process. The study also investigated the fire resistance characteristics of composite materials.

Cancer remains a global pandemic and is rapidly overtaking other diseases as the no.1 killer in developing nations. Photodynamic therapy (PDT) has been advanced as a minimally invasive cancer therapy. In addition, the emergence of harmful microbes with increasing resistance to drugs has prompted the employment of photodynamic antimicrobial chemotherapy (PACT) as a promising alternative to combat antibiotic resistance. In PDT and PACT, a photosensitizer (dye/drug) upon activation by light transfers energy to molecular oxygen producing singlet oxygen which kills cells. There is increased attention and research into more selective and non-aggregated photosensitizers that will better PDT in treating cancer. This research work is focused on design and synthesis of non-aggregated asymmetric phthalocyanines (dyes) tagged with mitochondrial targeting vehicles to maximize selectivity and photo-killing of tumor cells. Chapter 1 presents a brief review of the current status of PDT and treatment of cancer. The three components of PDT namely, light, oxygen and the photosensitizer, are briefly discussed giving a concise overview of the development of each of them in bettering PDT as an alternative to cancer therapy. Chapter 2 outlines the design, synthesis and characterization of two non-aggregated symmetric ZnPc isomers that have improved water solubility due to incorporation of triethylene glycol groups. The extension of the max absorption to near-IR via non-peripheral substitution on the Pc macrocycle is reported, while comparing the photophysical characteristics of both isomers. Chapter 3 details the improved selectivity of photosensitizers by conjugating ZnPcs to rhodamine B, a delocalized lipophilic cation, which targets the mitochondria of the cell. This conjugation achieved 70% more cell death suggesting that incorporation of rhodamine improved cellular uptake and localization of the photosensitizers which is crucial. Chapters 4 and 5 cover the design, synthesis, characterization, and photodynamic therapy evaluation of ZnPc and phosphorous phthalocyanines. Introduction of phosphorous as an electron deficient central atom promoted a 42 nm bathochromic shift relative to the corresponding ZnPc isomer. Additionally, the effect of peripheral and non-peripheral substitution on phototoxicity of these new compounds is studied and reported. Chapter 5 also gives concluding remarks, and future directions of this work.

Thrombospondin-1 (TSP-1) binding to its membrane receptor CD47 results in an inhibtion of the nitric oxide (NO) receptor soluble guanylate cyclase (sGC) and a decrease in intracellular cGMP levels. This causes physiologic effects such as vasoconstriction and a rise in blood pressure. The mechanism by which TSP-1 binds to CD47 at the membrane to decrease sGC activity is largely unknown. CD47 can physically associate with a number of binding partners, including α(v)β₃ and vascular endothelial growth factor receptor 2 (VEGFR2). Binding of a C-terminal fragment of TSP-1 called E3CaG1 to CD47 leads to a rise in intracellular calcium ([Ca²⁺](i)), which decreases sGC activity via a phosphorylation event. Binding of E3CaG1 is also known to disrupt the interaction between CD47 and VEGFR2, leading to a decrease in endothelial nitric-oxide synthase (eNOS) activity and cGMP levels through an Akt signaling pathway. However, it is not known whether other membrane proteins associated with CD47 are required for E3CaG1 binding and a subsequent [Ca²⁺](i) increase. Plasmon-waveguide resonance (PWR) spectroscopy was employed to elucidate the mechanism of TSP-1 inhibition of sGC activity through membrane complexes involving CD47. Using PWR, I found E3CaG1 can bind specifically to CD47 within native Jurkat membranes with picomolar and nanomolar dissociation constants (K(d)), suggesting multiple CD47 complexes are present. Among these complexes, CD47/VEGFR2 was found to bind E3CaG1 with a picomolar K(d)and CD47/α(v)β₃ was found to bind E3CaG1 with a nanomolar K(d). In addition, the presence of an anti-VEGFR2 antibody inhibited the E3CaG1-induced calcium response, which suggested CD47 in complex with VEGFR2 was responsible for TSP-1 reduction of sGC activity. I show that when both CD47 and VEGFR2 are returned to a HEK 293T cell line that does not contain these receptors, an increase in [Ca²⁺](i) upon E3CaG1 binding is restored. Interestingly, E3CaG1 was also found to bind to VEGFR2 in complex with the integrin α(v)β₃ on CD47-null cell lines and their derivations, causing a decrease in [Ca²⁺](i) levels. Therefore, the third type 2 repeat and C-terminal domains of TSP-1 can cause both increases and decreases in calcium based upon the availability of protein complexes to which it binds.

La tesis consta de 4 proyectos: dos estudios de intervención, aleatorizados, paralelos y controlados, uno sobre los efectos de productos del cacao y otro sobre los de fibra soluble, Plantago ovata husk (Po-husk), sobre biomarcadores de enfermedad cardiovascular (ECV) en sujetos hipercolesterolémicos. El tercero es la identificación de compuestos fenólicos del aceite de oliva virgen (AOV) en plasma humano (en ayunas y en fase postprandial) y el cuarto, el desarrollo de una aplicación informática para implementar los criterios CONSORT.Los productos del cacao y Po-husk reducen las concentraciones plasmáticas de c-LDL y ejercen efectos beneficiosos sobre otros biomarcadores de ECV.Además se han detectado hasta 10 compuestos fenólicos del AOV, incluido el 3,4-DHPEA-EDA, en plasma humano postprandrial.Finalmente, la incorporación de productos del cacao o Po-husk o el AOV o su combinación a una dieta cardiosaludable se adecuará al perfil de biomarcadores de riesgo de ECV de cada paciente. / The thesis is based on 4 projects: 2 randomised, controlled, interventional studies, one of the cocoa cream products and the other of the soluble fibre (Plantago ovata husk (Po-husk) on biomarkers of CVD. Third, the virgin olive oil (VOO) phenolic compounds identification in fasting and postprandial human plasma, and fourth, designed a technology application to facilitate the implementation of criteria CONSORT statement.The cocoa cream products and Po-husk reduced in plasma LDL-c and also, had beneficial effects on other CVD biomarkers and risk factors.Also, had been detected until 10 phenolic compounds from VOO, including 3,4-DHPEA-EDA, in human postprandial plasma.Finally, applying cocoa products or Po-husk or VOO or in combination in a cardio-protective diet warrants consideration as individualised therapeutic measures based on the individual's CVD risk factor profile.

A novel method for determination of tetrabromobisphenol-A (TBBPA), was developed using gas chromatography-negative ion chemical ionization-mass spectrom- etry (GC-NCI-MS). Samples of municipal wastewater treatment plant (WWTP) influent were analyzed for TBBPA. Levels ranged from 1 to 41 ng/L, with an average of 20 ± 14 ng/L. Matrix effects were shown to be 30 ± 17 % in the influent and -30 ± 11 % in membrane permeate. The method limit of quantitation was 0.1 ng/L TBBPA. Sorption of TBBPA to fresh mixed-liquor suspended solids (MLSS) from a membrane bioreactor (MBR) were studied. In a kinetic study, sorption was found to be essentially complete after 12 hours of exposure to MLSS. Log Koc and log Kd were measured at 4.7 ± 0.8 and 1.9 ± 0.8 respectively (n = 22). These values were much higher than modelled estimates based on Kow (p ≥ 0.05), and higher than modelled estimates based on Kow and pKa (p ≥ 0.05). Data was successfully modelled using the Freundlich isotherm, having a Kf value of 8.5 and an n value of 1.7. TBBPA adsorbed to borosilicate glassware, with a wall-loss coefficient (Kw) of 0.15 ± 0.1 (n ≥ 3). TBBPA levels in WWTP influent varied from 13 to 29 ng/L while effluent concentrations varied from 0 to 2.2 ng/L over the same period. Three pilot-scale membrane bioreactors (MBRs) removed less TBBPA during the same time period, though MBR removal was also significant (p ≥ 0.05). Increasing MBR sludge residence time (SRT) increased removal at the 86 % confidence interval (p = 0.14). A nitrifying MABR was shown to remove TBBPA significantly when spiked with ammonia and TBBPA (p ≥ 0.05), showing that nitrifying bacteria can degrade TBBPA. An MABR hollow fibre was found to adsorb TBBPA. Various soluble microbial products (SMP) were studied from MBRs fed munici- pal influent. Using current measurement practices, SMP were shown to be sensitive to matrix effects. Use of the standard addition technique (SA) can compensate for this. Measurements using SA showed SMP degrades rapidly during storage in the fridge and due to freezing. SA was also used to compare commonly used SMP extraction techniques, and showed that extraction method influences recovery.