The vitamin D metabolite 1,25(OH)2D3 has long been known to inhibit growth of prostate cancer cells and this mainly through a VDR-mediated pathway controlling target gene expression, resulting in cell cycle arrest, apoptosis and differentiation. Another major way in which 1,25(OH)2D3 inhibits cell growth in prostate cancer is via membrane-initiated steroid signalling, which triggers activation of signal cascades upon steroid binding to a receptor complex, leading to induction of genes regulating cell growth, proliferation and apoptosis. The main prostate cancer inhibiting membrane-initiated route is the TGFβ signalling pathway, elicited by the protein TGFβ. In this experiment the activating effects of 1,25(OH)2D3 on TGFβ in prostate cancer cells, as well as two other important proteins downstream in this cascade, Smad2 and 3, were investigated. PC-3 cells were incubated for 3, 5, 10, 30 and 60 minutes as well as 38 hours both together with 1,25(OH)2D3 of the concentrations 10-10 and 10-7 M and without. As the downstream cascade protein JNK is a known activator of Smad2/3, this procedure was also repeated with a JNK inhibitor. An ELISA assay scanning for activated TGFβ was then performed on supernatants from the cells treated without JNK inhibitor. In addition, a Western Blot scanning for activated Smad2 and 3 was performed on supernatants from all groups of treatment. The analysis of the result values showed that 10-10 M 1,25(OH)2D3 significantly lowered the content of active TGFβ in PC-3 cells within 3 and 5 minutes. Unfortunately the Western Blot was unsuccessful and needs therefore be repeated.

The vitamin D metabolite 1,25(OH)2D3 has long been known to inhibit growth of prostate cancer cells and this has been attributed to a VDR-mediated pathway controlling target gene expression, resulting in cell cycle arrest, apoptosis and differentiation. New research has shown that another vitamin D metabolite, 24,25(OH)2D3, inhibits proliferation of prostate cancer cells as well, more specifically, cells of the line LNCaP. It is not clear exactly how 24,25(OH)2D3 exerts this cancer growth inhibition but it has been shown that it is to some extent regulated via G protein coupled signalling pathways. Catalase is a haem-containing redox enzyme found in the majority of animal cells, plant cells and aerobic microorganisms. This enzyme is very important because it prevents excessive accumulation of the strongly oxidizing agent H2O2 which otherwise can do damage to the cells. Because of this preventive effect of catalase, important cellular processes which generate H2O2 as by-product can proceed safely. Biochemical analysis of catalase has shown that it binds endogenously to 24,25(OH)2D3. The fact that 24,25(OH)2D3 has anti-proliferative effects on prostate cancer cells combined with the fact that it binds to catalase generates the hypothesis that this binding interferes with the essential task of catalase to keep the cell free from accumulation of destructive H2O2, and by means of this interference induces apoptosis. Finding out about the cancer growth inhibiting mechanism behind each vitamin D metabolite is important and may be a lead in the search for a new, better treatment of prostate cancer. The specific aim of this project was to study if and in what way 24,25(OH)2D3 affects the enzymatic activity of catalase in LNCaP cells and to do this with dose and time responses in focus. In this experiment LNCaP cells were incubated for 48 hours together with 24,25(OH)2D3 in five different concentrations, then a catalase assay was performed on the cells including fluorescence-mediated measuring of catalase activity in both treated and untreated cells. The analysis of the result values showed that regardless of dose or time, 24,25(OH)2D3 has no statistically significant effect on catalase activity in cells of the line LNCaP.

The vitamin D metabolite 1,25(OH)2D3 has long been known to inhibit growth of prostate cancer cells and this has been attributed to a VDR-mediated pathway controlling target gene expression, resulting in cell cycle arrest, apoptosis and differentiation. New research has shown that another vitamin D metabolite, 24,25(OH)2D3, inhibits proliferation of prostate cancer cells as well, more specifically, cells of the line LNCaP. It is not clear exactly how 24,25(OH)2D3 exerts this cancer growth inhibition but it has been shown that it is to some extent regulated via G protein coupled signalling pathways. Catalase is a haem-containing redox enzyme found in the majority of animal cells, plant cells and aerobic microorganisms. This enzyme is very important because it prevents excessive accumulation of the strongly oxidizing agent H2O2 which otherwise can do damage to the cells. Because of this preventive effect of catalase, important cellular processes which generate H2O2 as by-product can proceed safely. Biochemical analysis of catalase has shown that it binds endogenously to 24,25(OH)2D3. The fact that 24,25(OH)2D3 has anti-proliferative effects on prostate cancer cells combined with the fact that it binds to catalase generates the hypothesis that this binding interferes with the essential task of catalase to keep the cell free from accumulation of destructive H2O2, and by means of this interference induces apoptosis. Finding out about the cancer growth inhibiting mechanism behind each vitamin D metabolite is important and may be a lead in the search for a new, better treatment of prostate cancer. This is a follow-up to an earlier study, and the specific aim of this project was to find out if and in what way 24,25(OH)2D3 affects the enzymatic activity of catalase in LNCaP cells during long-term treatment (up to 48 hours). In this experiment LNCaP cells were incubated for 48 hours together with 24,25(OH)2D3 of the concentration 10-8 M, then a catalase assay was performed on the cells including fluorescence-mediated measuring of catalase activity in both treated and untreated cells. The analysis of the result values showed that despite of the rather high dose used, 24,25(OH)2D3 has no statistically significant effect on catalase activity in cells of the line LNCaP, regardless of time.

Cette thèse a pour objet l'analyse de la cinétique de la conversion de l'acétaldéhyde, CH₃CHO, à des concentrations initiales inférieures ou égale à 5000 ppm dans un mélange de gaz à base d'azote et contenant jusqu'à 20% d'oxygène, à température ambiante. L'étude a été réalisée en utilisant trois réacteurs mettant en œuvre des décharges de qualités spatiales différentes. Il s'agit d'un réacteur (UV510) à décharge pré-ionisée (photo-déclenchée) par rayonnement UV produisant un plasma homogène, et de deux réacteurs à décharge à barrière diélectrique (DBD), de géométrie plane (plan-plan) et de géométrie cylindrique (tige-tube) alimentés par impulsion HT et produisant des plasmas non homogènes à faible (plan) ou forte (cylindre) filamentation ; un diagnostic d'imagerie rapide (ns) de la DBD de géométrie plane montre que le plasma peut être considéré quasi-homogène. En s'appuyant sur une modélisation 0D auto-cohérente de la décharge photo-déclenchée, l'étude de la cinétique du mélange N₂/CH₃CHO montre l'importance des états métastables de la molécule d'azote, triplet A³Σu⁺, et singlets (groupe a' ¹∑⁻u, a ¹∏g, et w ¹Δu) dans la dissociation de l'acétaldéhyde. Un coefficient minimum de 6.5×10⁻¹¹ cm³.s⁻¹ est estimé pour le quenching des singlets par l'acétaldéhyde. Le coefficient du triplet est estimé entre 4.2×10⁻¹¹ cm³.s⁻¹ et 6.5×10⁻¹¹ cm³.s⁻¹. Cette dissociation produit des radicaux (CH₃, CH₃CO, HCO, H, O) et des molécules (CH₄, CH₂CO, C₂H₄, C₂H₂, H₂, CO). Ainsi les sous-produits majoritaires mesurés à la fin de la post décharge temporelle sont le méthane, le dihydrogène, le monoxyde de carbone et l'éthane. Les minoritaires sont l'acétylène, l'éthène, l'acétone et l'acétonitrile. Dans les mélanges contenant de l'oxygène, l'importance de la dissociation de CH₃CHO par quenching des états métastables de N₂ diminue au profit des processus d'oxydation par le radical hydroxyle, OH, et l'oxygène atomique, O (³P). La mesure résolue en temps du radical OH dans la post-décharge du réacteur UV510 montre une très forte réactivité de ce radical avec les sous-produits de conversion de l'acétaldéhyde. Une densité maximum de OH égale à 3.5×10¹⁴ cm⁻³ a été mesurée pour 10 % d'oxygène et 5000 ppm d'acétaldéhyde. Le schéma cinétique adopté pour ces mélanges donne, par la modélisation auto-cohérente, une valeur de densité plus élevée. Toutefois, la conversion de l'acétaldéhyde dans N₂/O₂/CH₃CHO est bien expliquée par le modèle, de même que les concentrations produites de méthane et d'éthane. Enfin, la comparaison de l'efficacité énergétique des trois réacteurs étudiés montre que l'homogénéité de la décharge favorise, pour des milieux pauvres en oxygène (moins de 2 %), la conversion de l'acétaldéhyde.

This research deals with the synthesis and characterization (transmission electron microscopy and optical spectroscopy) of composite nanocondensates produced by pulse laser ablation (PLA) on Zn, Zn-Cu and Cu-Au targets in liquid or vacuum. First, wurtzite-type (W)-ZnO and

<p>The vitamin D metabolite 1,25(OH)2D3 has long been known to inhibit growth of prostate cancer cells and this has been attributed to a VDR-mediated pathway controlling target gene expression, resulting in cell cycle arrest, apoptosis and differentiation. New research has shown that another vitamin D metabolite, 24,25(OH)2D3, inhibits proliferation of prostate cancer cells as well, more specifically, cells of the line LNCaP. It is not clear exactly how 24,25(OH)2D3 exerts this cancer growth inhibition but it has been shown that it is to some extent regulated via G protein coupled signalling pathways. Catalase is a haem-containing redox enzyme found in the majority of animal cells, plant cells and aerobic microorganisms. This enzyme is very important because it prevents excessive accumulation of the strongly oxidizing agent H2O2 which otherwise can do damage to the cells. Because of this preventive effect of catalase, important cellular processes which generate H2O2 as by-product can proceed safely. Biochemical analysis of catalase has shown that it binds endogenously to 24,25(OH)2D3. The fact that 24,25(OH)2D3 has anti-proliferative effects on prostate cancer cells combined with the fact that it binds to catalase generates the hypothesis that this binding interferes with the essential task of catalase to keep the cell free from accumulation of destructive H2O2, and by means of this interference induces apoptosis. Finding out about the cancer growth inhibiting mechanism behind each vitamin D metabolite is important and may be a lead in the search for a new, better treatment of prostate cancer. The specific aim of this project was to study if and in what way 24,25(OH)2D3 affects the enzymatic activity of catalase in LNCaP cells and to do this with dose and time responses in focus. In this experiment LNCaP cells were incubated for 48 hours together with 24,25(OH)2D3 in five different concentrations, then a catalase assay was performed on the cells including fluorescence-mediated measuring of catalase activity in both treated and untreated cells. The analysis of the result values showed that regardless of dose or time, 24,25(OH)2D3 has no statistically significant effect on catalase activity in cells of the line LNCaP.</p>

<p>The vitamin D metabolite 1,25(OH)2D3 has long been known to inhibit growth of prostate cancer cells and this has been attributed to a VDR-mediated pathway controlling target gene expression, resulting in cell cycle arrest, apoptosis and differentiation. New research has shown that another vitamin D metabolite, 24,25(OH)2D3, inhibits proliferation of prostate cancer cells as well, more specifically, cells of the line LNCaP. It is not clear exactly how 24,25(OH)2D3 exerts this cancer growth inhibition but it has been shown that it is to some extent regulated via G protein coupled signalling pathways. Catalase is a haem-containing redox enzyme found in the majority of animal cells, plant cells and aerobic microorganisms. This enzyme is very important because it prevents excessive accumulation of the strongly oxidizing agent H2O2 which otherwise can do damage to the cells. Because of this preventive effect of catalase, important cellular processes which generate H2O2 as by-product can proceed safely. Biochemical analysis of catalase has shown that it binds endogenously to 24,25(OH)2D3. The fact that 24,25(OH)2D3 has anti-proliferative effects on prostate cancer cells combined with the fact that it binds to catalase generates the hypothesis that this binding interferes with the essential task of catalase to keep the cell free from accumulation of destructive H2O2, and by means of this interference induces apoptosis. Finding out about the cancer growth inhibiting mechanism behind each vitamin D metabolite is important and may be a lead in the search for a new, better treatment of prostate cancer. This is a follow-up to an earlier study, and the specific aim of this project was to find out if and in what way 24,25(OH)2D3 affects the enzymatic activity of catalase in LNCaP cells during long-term treatment (up to 48 hours). In this experiment LNCaP cells were incubated for 48 hours together with 24,25(OH)2D3 of the concentration 10-8 M, then a catalase assay was performed on the cells including fluorescence-mediated measuring of catalase activity in both treated and untreated cells. The analysis of the result values showed that despite of the rather high dose used, 24,25(OH)2D3 has no statistically significant effect on catalase activity in cells of the line LNCaP, regardless of time.</p>

Jusqu'à récemment, la plupart des applications des arcs électriques mettaient en oeuvre les propriétés du coeur de la colonne, un effort particulier a donc été effectué pour développer des méthodes de caractérisation de ces zones dont la température moyenne est de l'ordre de 10000 K. Avec le développement de la plasma-chimie, le diagnostic des zones périphériques d'arcs et des décharges hors équilibre est devenu un enjeu primordial. Les méthodes de mesure classiques sont mal adaptées pour cette tâche ; le but du travail présenté dans cette thèse se résume donc au développement et à la validation de techniques de diagnostic adaptées à ces zones, dont la température cinétique n'excède pas 8000 K. Deux méthodes innovantes basées sur l'indice de réfraction, l'ombroscopie quantitative et la déflectométrie moirée, ont été étudiées en détails. Les résultats théoriques ainsi que le traitement des données obtenues ont été validés sur un jet de plasma laminaire d'argon, un modèle parfait de zone périphérique. Pour sonder les décharges hors équilibre, l'utilisation du spectre UV de OH a été aussi envisagée. À cette occasion, un programme de simulation de spectre moléculaire a été développé. L'étude des spectres synthétiques obtenus a permis de mettre au point des méthodes de mesure simples de la température rotationnelle et vibrationnelle pour une large gamme de résolution. Une des méthodes développées a été mise en œuvre sur une décharge à faible intensité de courant. On montre que les résultats obtenus par spectroscopie moléculaire sur le radical OH sont très proches de ceux obtenus à l'aide d'une simulation.

The ignition process is a critical consideration for combustion devices. External energy transfer to the combustor is required for ignition in common combustion systems. There are many ways to deposit energy into the flow but a standard method is a spark discharge because it is simple, compact, and reliable. Sparks can be categorized as either inductive or capacitive sparks that use a coil or an electrical resonance circuit with capacitor, respectively, to amplify the voltage. The creation of a successful ignition event depends on the spark energy deposited into the flow, the initial composition, pressure, temperature, turbulence level of flow etc. The deposited energy by the spark into the flow is critical for estimation of initial energy available for ignition of the mixture. Therefore, the electrical characteristics of the sparks were investigated under various flow conditions. Then measurements of deposited energy into the flow were conducted using a very accurate experimental procedure that was developed in this research. The results showed considerable electric energy losses to the electrodes for the relatively long, inductive sparks. However, the short, capacitive spark deposits electric energy into the flow with minimal loss (above 90% deposition efficiency). In addition, the characteristics of inductive spark are affected by flow velocity and by the existence of a flame. However, variations in the flow conditions do not affect the characteristics of the capacitive spark such as voltage-current time trace and energy deposition efficiency. Two ignition systems using above mentioned two spark types were developed. First, the capacitive spark energy was directly deposited into the premixed flow. Most researchers have not concentrated on the early initiation process but on the flame growth. Therefore, the generated kernel formed by the energy deposition was observed and characterized using optical methods, immediately following the spark. In addition, the mixing effect for this ignition kernel with surrounding gas was simulated using a numerical method. Based on the time trace of the OH* chemiluminescence, the reaction starts with the discharge and it is continuous until combustion begins. This means that in the presence of a high density spark in premixed flow, there exists no traditional delay as defined by other researchers for auto ignition. A simple Radical Jet Generator (RJG) was developed that is able to ignite and stabilize a flame in a high-speed flow. The inductive spark initiates the combustion in the RJG chamber. The RJG then injects the partially-burned products carrying large amounts of heat and radicals into a rapidly moving flammable main stream. Then it ignites and stabilizes a flame. The RJG requires low levels of electrical power as long as the flow velocity is relatively low since most of the radicals are produced by the incomplete combustion in its chamber. The importance of radicals was analyzed by RJG experiments and numerical methods. The reaction zone for RJG using a rich mixture was located both inside and outside of the RJG chamber. Therefore, the RJG using a rich mixture performed better in the ignition and stabilization of combustion in the main flow. According to an analysis using the CHEMKIM simulation software combined with the San Diego chemical mechanism, the RJG jet resulting from a rich mixture contains more radicals and intermediates than that produced by a lean mixture for the same sensible enthalpy. In addition, the burned gas contains less radicals and intermediates than the partially burned gas. If the RJG is operating with a high speed main flow, the flow rate through the RJG chamber must be increased to allow the radical jet to penetrate well into the rapid flow due to their higher injection velocity. Unfortunately, this leads to unsteady combustion in the RJG, which results in the pulsation of the radical jet. This reduces the number of radicals injected into the main flow. To investigate this operating condition, special attention was focused on four possible factors: unburned reactant pockets caused by motion of the spark channel, spark frequency, flame propagation speed and ignition delay. It was shown that the unsteadiness is affected by the flame speed and ignition delay because the frequency of pulsation in the chamber is highly dependent on the equivalence ratio. In addition, the interaction between the RJG operation and the combustion dynamics in the main combustor was documented. The acoustic pressure oscillations in the main combustor were suppressed when the RJG jet was turned on because the reaction region is relocated by the operation of the RJG.

Flame chemiluminescence has received increasing attention for its potential sensor and diagnostic applications in combustors. A number of studies have used flame chemiluminescence to monitor flame status, and combustor performance. While most of these studies have been empirical in nature, chemiluminescence modeling has the potential to provide a better understanding of the chemiluminescence processes and their dependence on various combustion operating conditions. The primary objective of this research was to identify and validate the important chemiluminescence reaction mechanisms for OH*, CH* and CO2*. To this end, measurements were performed at various operating conditions, primarily in laminar, premixed flames, fueled with methane, syngas (H2/CO) and Jet-A. The results are compared to 1-d laminar flame simulations employing the chemiluminescence mechanisms. The secondary objective was to use the experiments and validated chemiluminescence reaction mechanisms to evaluate the usefulness of flame chemiluminescence as a combustion diagnostic, particularly for heat release rate and equivalence ratio. The validation studies were able to identify specific mechanisms for OH*, CH* and CO2* that produced excellent agreement with the experimental data in most cases. The mechanisms were able to predict the variation of the chemiluminescence signals with equivalence ratio but not with pressure and reactant preheat. The possible reasons causing this disagreement could be due to the inaccuracies in the basic chemical mechanism used in the simulations, lack of accurate quenching data (for CH*), thermal excitation (for OH*) and radiative trapping (for OH* and CO2*) and interference from the emissions of other species (such as HCO and H2O), for CO2*. Regarding the utility of chemiluminescence for sensing, a number of observations can be made. In syngas-air flames, CO2* is a reasonable heat release rate marker, at least for very lean conditions. OH* shows some advantage in atmospheric-pressure methane and Jet-A flames in general, while CH* is advantageous at high pressure and very lean conditions at atmospheric pressure. The CO2*/OH* intensity ratio is not useful for sensing equivalence ratio in syngas flames, except maybe at very lean conditions. However, the CH*/OH* signal ratio is a promising approach for sensing equivalence ratio at low or very high pressure conditions in hydrocarbon flames. Thermal excitation and self-absorption processes for OH* chemiluminescence can become important for combustors operating at high pressure, high preheat and near stoichiometric conditions. Background subtracted chemiluminescence signals are recommended for sensing purposes.