Demands for using electrical resistivity techniques (surface and bulk resistivity) as an alternative to the rapid chloride penetrability test (RCPT) have been growing, for example by a number of transportation agencies in North America, to give an indication of the relative penetrability of concrete. While resistivity measurements may reflect the quality of pore structure in the cementitious matrix, their accuracy might be affected by a multitude of parameters including the concentration of ionic species in the pore solution, particularly when supplementary cementitious materials (SCMs) are incorporated in the binder. Hence, a systematic investigation on the resistivity of concrete and its corresponding physical penetrability is warranted. Zinc sacrificial anodes are considered an effective and economical method to prevent the electrochemical corrosion of steel bars by providing cathodic current to bars, which can provide corrosion protection at low galvanic current densities in the range of 0.2 to 2 mA/m2. Sacrificial anodes are commonly used in RC structures particularly in bridge decks to mitigate a critical phenomenon that occurs in the original concrete beside the repaired patches, which is known as the ‘halo effect’. One of the key factors affecting the efficacy of zinc anodes is the resistivity of concrete or cementitious repair material in which these anodes are embedded. There is a general notion that the higher the electrical resistivity of concrete or repair material, the less likely that zinc anodes produce the target galvanic current for optimum protection of steel bars. However, no systematic data are available on the maximum allowable electrical resistivity of repair materials/concretes beyond which zinc anodes cannot properly function to prevent corrosion. In the first part of this thesis, a tripartite relationship (nomogram) to correlate surface resistivity with penetrability (migration coefficient) and porosity of concrete using a wide range ii of concrete mixtures, taking into account the effect of key mixture design parameters (water-to-binder ratio, air-entrainment, SCMs and type of cement) was established. Relationships between surface and bulk resistivity as well as migration coefficient and porosity of concrete were also introduced. In addition, a penetrability classification of concrete based on the corresponding ranges of surface resistivity, migration coefficient and porosity has been proposed. The nomogram and penetrability classification provided reasonable assessment for the condition of field cores extracted from newly constructed and aging concrete pavement. In the second part of this thesis, the functionality of zinc anodes at mitigating patch accelerated corrosion (halo effect) in repaired concrete was explored. Concrete slabs were cast to simulate the patch repair configuration in the field, and the main parameters in this study were changing the resistivity of the repair section in the slabs (5,000, 15,000, 25,000, 50,000 and 100,000 Ω-cm), and anode spacing (25, 100, and 250 mm) inside the repair patch. Analysis of current and potential data shows a high level of effectiveness of the anodes at controlling corrosion in this slab configuration up to 52 weeks under a wetting-drying exposure. / February 2017

Phonon transport analysis in nano- and micro-porous materials is critical to their energy-related applications. Assuming diffusive phonon scattering by pore edges, the lattice thermal conductivity can be predicted by modifying the bulk phonon mean free paths with the characteristic length of the nanoporous structure, i.e., the phonon mean free path (Lambda(pore)) for the pore-edge scattering of phonons. In previous studies (Jean et al., 2014), a Monte Carlo (MC) technique have been employed to extract geometry determined Lambda(pore) for nanoporous bulk materials with selected periods and porosities. In other studies (Minnich and Chen, 2007; Machrafi and Lebon, 2015), simple expressions have been proposed to compute Lambda(pore). However, some divergence can often be found between lattice thermal conductivities predicted by phonon MC simulations and by analytical models using Lambda(pore). In this work, the effective Lambda(pore) values are extracted by matching the frequency-dependent phonon MC simulations with the analytical model for nanoporous bulk Si. The obtained Lambda(pore) values are usually smaller than their analytical expressions. These new values are further confirmed by frequency-dependent phonon MC simulations on nano porous bulk Ge. By normalizing the volumetric surface area A and Lambda(pore) with the period length p, the same curve can be used for bulk materials with aligned cubic or spherical pores up to dimensionless p.A of 1.5. Available experimental data for nanoporous Si materials are further analyzed with new Lambda(pore) values. In practice, the proposed model can be employed for the thermal analysis of various nanoporous materials and thus replace the time-consuming phonon MC simulations.

The study of multiphase flow in porous media is highly relevant to many problems of great scientific importance, such as CO2 storage and enhanced oil recovery. Even though significant progress has been made in these areas, many challenges still remain. For instance, the leakage of stored CO2 may occur due to the capillary trapping failure of cap rock. Approximately 70% of oil cannot be easily recovered from underground, because the oil is held in tight porous rocks. Although CO2 storage and enhanced oil recovery are engineering processes at a geological scale, they are predominantly controlled by the transport and displacement of CO2 and reservoir fluids in aquifers and reservoirs, which are further controlled by wetting and fluid properties at pore scale. This work focuses on experimental investigations of pore-scale wetting and displacement of fluids and CO2 in porous core samples. Pore wetting, which has been measured based on contact angle, is a principal control on multiphase flow through porous media. However, contact angle measurement on other than flat surfaces still remains a challenge. In order to indicate the wetting in a small pore, a new pore contact angle measurement technique is developed in this study to directly measure the contact angles of fluids and CO2 in micron-sized pores. The equilibrium and dynamic contact angles of various liquids are directly measured in single glass capillaries, by studying the effects of surface tension, viscosity and chemical structure. The pore contact angles are compared with the contact angles on a planar substrate. The pore contact angle of a confined liquid in a glass capillary differs from the contact angle measured on a flat glass surface in an open space. Surface tension is not the only dominant factor affecting contact angle. The static contact angle in a glass pore also varies with liquid chemical structure. Viscosity and surface tension can significantly affect the dynamic pore contact angle. A new empirical correlation is developed based on our experimental data to describe dynamic pore wetting. The CO2-fluid contact angle in porous media is an important factor affecting the feasibility of long-term permanent CO2 storage. It determines CO2 flow and distribution in reservoirs or aquifers, and thus ultimately finally the storage capacity. CO2-fluid contact angles were measured in small water-wet pores and oil-wet pores, investigating the effect of CO2 phase (gas/liquid/supercritical). The CO2 phase significantly affects the CO2-fluid contact angle in an oil-wet pore. Supercritical CO2-fluid contact angles are larger than gas CO2-fluid contact angles, but are smaller than liquid CO2-fluid contact angles. However, this significant CO2 phase effect on contact angle was not observed in a water-wet pore. Another key issue considered in this study is two-phase flow displacement in porous media. This strongly relates to the important macroscopic parameters for multiphase flow transport in porous media, such as capillary pressure and relative permeability. Here CO2-water displacements are studied by conducting CO2 flooding experiments in a sandstone core sample, considering the effects of CO2 phase, pressure and CO2 injection rate. The capillary pressure-saturation curve, water production behaviour and relative permeability are investigated for gas CO2-water, liquid CO2-water and supercritical CO2-water displacements in porous media. The pressure-dependant drainage capillary pressures are obtained as a result of CO2-water interfacial tension. Various water production behaviours are obtained for gas CO2-water and liquid CO2-water displacements, mainly due to the effect of CO2 dissolution. The significant irregular capillary pressure-saturation curves and water production behaviors can be observed for the supercritical CO2-water displacements. The water and CO2 relative permeabilities for CO2-water displacements in a porous media are then predicted.

This master thesis provides an overview of the paper machine with focus on the forming section. The forming section is the first part in the paper machine where the paper pulp is injected through a head box. The paper pulp contains about 99.5% of water and 0.5% fiber. The water as content is reduced by vacuum and gravity. The problem to be studied in this project is related to external rewetting. This is water going back to the paper web from the forming fabric after the dewatering zone. The dewatering is based on vacuum slots under the forming fabric. The vacuum slots absorb water from the soaked paper pulp through the forming fabric. External rewetting causes problem, hence the paper will have a higher dry content when leaving the forming section. The paper should have as low dry content as possible in the end of the forming section. Three different forming fabrics from Albany International were chosen for the project. The structures of the forming fabrics were two different double layers and one plain weave. The performance of the fabrics was studied by 4 different methods. The methods used were 2 different wicking tests, a vacuum dewatering trial and one foulard test. Also micro tomography was done to understand the structure of each design. The main test was a foulard test where the aim was to see in what way the rewetting got affected by different pores sizes. The results showed higher water content for the paper that was on top of the forming fabric with the larger pores.

No description available.

Dans cette thèse, des simulations PN de séchage sont comparées à des données expérimentales obtenues dans le séchage d´un réseau de micro-fluidique 2D représentatif dans du SiO2 soumis à des conditions thermiques variables dans le but d’identifier les phénomènes physiques à l´échelle des pores qui sont les plus influents. A partir de cette étude, un PN efficace non-isotherme est développé. Ce modèle incorpore i) les phénomènes associés à la dépendendence en température de l´invasion à l´échelle des pores, c´est à dire l´invasion capillaire sous effet thermique et le flux de vapeur ainsi que ii) le transport secondaire induit par d´épais films liquides observé dans les expériences de microfluidique. Cette étude prouve clairement que le comportement macroscopique du séchage est fondamentalement dirigé par le gradient de température imposé sur le PN ainsi que par le transport capillaire secondaire. En accord avec la littérature, les schémas d´invasion que l´on trouve dans l´invasion percolatrice avec l´évaporation progressive d´amas individuels sont observés dans le séchage à variation de température locale négligeable;des gradients où la température diminue à partir de la surface (gradient de température négatif)peut stabiliser le front de séchage, qui évolue entre la phase gazeuse invasive et la phase liquide qui recule, alors qu´une température qui augmente à partir de la surface (gradient de température positif) amène à la déstabilisation de la phase liquide avec une percée prématurée de la branche gazeuse et l’initiation d´un deuxième front de séchage qui migre dans la direction opposé de celle du front de séchage original. Une attention particulière est prêtée aux régimes distincts que l´on trouve dans le second cas (gradient positif) parce qu´ils sont associés à différents procédés d´invasion à l´échelle des pores. Plus précisément, la dépendance en température de la tension de surface établit l´ordre d´invasion tant que la phase liquide est connectée au groupe liquide principal (que l´on trouve généralement pendant la première période de séchage). En revanche,l´étude détaillée des mécanismes de transfert de la vapeur met l´accent sur le fait que la diffusion de la vapeur à travers la région partiellement saturée peut contrôler les distributions des phases gazeuses et liquides à l´échelle des pores pendant la période de séchage lorsque la phase liquide est déconnectée en petits groupes. Cela est aussi lié à la croissance des amas induite par la condensation partielle de la vapeur. Cette thèse montre et discute en détail que cet effet ne dépend pas seulement de la direction et magnitude du gradient de température pour une distribution de tailles de pores donnée mais qu’en plus le taux d´évaporation influence le mécanisme de croissances des amas. Cela indique que la migration du liquide pendant la phase de séchage de milieux poreux peut être contrôlé par l’interaction des gradients thermiques et du taux de séchage. En somme, l´étude du séchage sous effet thermique des réseaux de pores 2D révèle des phénomènes complexes à l´échelle des pores, généralement aussi anticipés dans le séchage des milieux poreux réels. Cela mène au développement d´un modèle mathématique efficace au niveau des pores basés sur des découvertes expérimentales. Cette thèse démontre la manière dont ce modèle peut être appliqué afin de comprendre et développer des procédés de séchage modernes basés sur la simulation du transfert de masse sous effet thermique à l´échelle des pores / In this thesis, PN simulations of drying are compared with experimentally obtained data fromdrying of a representative 2D microfluidic network in SiO2 under varying thermal conditions withthe aim to identify governing physical pore scale effects. Gravity and viscous effects aredisregarded in this thesis. Instead drying with slight local temperature variation and drying withimposed thermal gradients are studied. Based on this investigation, a powerful non-isothermalPNM is developed. This model incorporates i) the phenomena associated with the temperaturedependency of pore scale invasion, namely thermally affected capillary invasion and vapor flow aswell as ii) the secondary effects induced by wetting liquid films of different morphology. This studyclearly evidences that the macroscopic drying behavior is fundamentally dictated by thetemperature gradient imposed on the PN and moreover by the secondary capillary invasion aswell. In agreement with literature, invasion patterns as in invasion percolation with progressiveevaporation of single clusters are observed in drying with negligible local temperature variation;gradients with temperature decreasing from the surface (negative temperature gradient) canstabilize the drying front, evolving between the invading gas phase and the receding liquid phase,whereas temperature increasing from the surface (positive temperature gradient) leads todestabilization of the liquid phase with early breakthrough of a gas branch and initiation of asecond invasion front migrating in opposite direction to the evaporation front receding from theopen surface of the PN. Special attention is paid on the distinct drying regimes found in thesituation of a positive gradient because they are associated with different pore scale invasionprocesses. More precisely, temperature dependency of surface tension dictates the order ofinvasion as long as the liquid phase is connected in a main liquid cluster (usually found during thefirst period of drying). In contrast to this, detailed study of the vapor transfer mechanismsemphasizes that vapor diffusion through the partially saturated region can control the pore leveldistributions of liquid and gas phase during the period of drying when the liquid phase isdisconnected into small clusters. This is also related to the cluster growth induced by partialcondensation of vapor. It is shown and discussed in detail in this thesis that this effect not onlydepends on direction and height of the temperature gradient for a given pore size distribution butthat moreover the overall evaporation rate influences the cluster growth mechanism. This indicatesthat liquid migration during drying of porous media might be controlled by the interplay of thermalgradients and drying rate. In summary, the study of thermally affected drying of the 2-dimensionalPN reveals complex pore scale mechanisms, usually also expected in drying of real porous media.This leads to the development of a strong mathematical pore scale model based on experimentalfindings. It is demonstrated how this model might be applied to understand and develop moderndrying processes based on the simulation of thermally affected pore scale mass transfer

"Porous materials have been a focus of researchers for their applications as molecular storage, molecular sensing, catalysis, asymmetric synthesis and host materials. Metal-organic frameworks (MOFs) represent a promising new class of porous crystalline solids because they exhibit large pore volumes, high surface areas, permanent porosity, high thermal stability, and feature open channels with tunable dimensions and topology. We are currently investigating the design, synthesis, and structures of a new family of MOFs derived from transition metals complexes of 4-(imidazole-1-yl)benzoic acids. Here we present our effort in continuing design and synthesis MOFs composed of 4-(imidazole-1-yl)benzoic acids to expand our knowledge about 4-(imidazole-1-yl)benzoic acid MOF family. A series of ligands are synthesized and Cu MOF-3N, 4, 5 and Cd MOF-3 were synthesized, structure determination found out metal-ligand complex follows our proposal, while Cu MOF-4,5 exhibit porous framework structure via absolute structure determination. Sorption behavior is a key focus in MOF application because the great potential applications MOF bears. Here we carry out a fundamental study about MOF texture and selectivity on MOF-5 and Cd MOF-2. Non-polar polyaromatic hydrocarbons such as naphthalene, phenanthrene, and pyrene, polar molecules such as 2-naphthol, ibuprofen were selected to test our hypothesis that sorption is influenced by the degree of tight fitting, and guest-host interaction such as van der waals and hydrogen bonding. By determining Langmuir isotherms of selected guest molecules, we are able to demonstrate our hypothesis that tighter the fit of the guest molecule and the pores, the higher the amount it would sorb. The sorption difference of non-polar and polar molecules suggest hydrogen bonding is not involved in guest sorption and the dominating force of sorption is hydrophobic interaction. Polymorphism is an interesting phenomenon that bears great value in pharmaceutical industry. Here we report the first case for MOF to serve as a heterogeneous surface that induced nucleation of indomethacin. It is also a first report of this polymorph form of indomethacin. PXRD, DSC, TGA, NMR are conducted as our initial investigation effort. This polymorph exhibits exceptionally thermal stability and low solubility, indicating an unusual tight binding between indomethacin and ethanol solvate. "

Pneumolysin, a protein toxin, represents one of the major virulence factors of Streptococcus pneumoniae. This pathogen causes bacterial meningitis with especially high disease rates in young children, elderly people and immunosuppressed patients. The protein toxin belongs to the family of cholesterol-dependent cytolysins, which require membrane cholesterol in order to bind and to be activated. Upon activation, monomers assemble in a circle and undergo conformational change. This conformational change leads to the formation of a pore, which eventually leads to cell lysis. This knowledge was obtained by studies that used a higher concentration compared to the concentration of pneumolysin found in the cerebrospinal fluid of meningitis patients. Thus, a much lower concentration of pneumolysin was used in this work in order to investigate effects of this toxin on primary mouse astrocytes. Previously, a small GTPase activation, possibly leading to cytoskeletal changes, was found in a human neuroblastoma cell line. This led to the hypothesis that pneumolysin can lead to similar cytoskeletal changes in primary cells. The aim of this work was to investigate and characterise the effects of pneumolysin on primary mouse astrocytes in terms of a possible pore formation, cellular trafficking and immunological responses. Firstly, the importance of pore-formation on cytoskeletal changes was to be investigated. In order to tackle this question, wild-type pneumolysin and two mutant variants were used. One variant was generated by exchanging one amino acid in the cholesterol recognising region, the second variant was generated by deleting two amino acids in a protein domain that is essential for oligomerisation. These variants should be incapable of forming a pore and were compared to the wild-type in terms of lytic capacities, membrane binding, membrane depolarisation, pore-formation in artificial membranes (planar lipid bilayer) and effects on the cytoskeleton. These investigations resulted in the finding that the pore-formation is required for inducing cell lysis, membrane depolarisation and cytoskeletal changes in astrocytes. The variants were not able to form a pore in planar lipid bilayer and did not cause cell lysis and membrane depolarisation. However, they bound to the cell membrane to the same extent as the wild-type toxin. Thus, the pore-formation, but not the membrane binding was the cause for these changes. Secondly, the effect of pneumolysin on cellular trafficking was investigated. Here, the variants showed no effect, but the wild-type led to an increase in overall endocytotic events and was itself internalised into the cell. In order to characterise a possible mechanism for internalisation, a GFP-tagged version of pneumolysin was used. Several fluorescence-labelled markers for different endocytotic pathways were used in a co-staining approach with pneumolysin. Furthermore, inhibitors for two key-players in classical endocytotic pathways, dynamin and myosin II, were used in order to investigate classical endocytotic pathways and their possible involvement in toxin internalisation. The second finding of this work is that pneumolysin is taken up into the cell via dynamin- and caveolin-independent pinocytosis, which could transfer the toxin to caveosomes. From there, the fate of the toxin remains unknown. Additionally, pneumolysin leads to an overall increase in endocytotic events. This observation led to the third aim of this work. If the toxin increases the overall rate of endocytosis, the question arises whether toxin internalisation favours bacterial tissue penetration of the host or whether it serves as a defence mechanism of the cell in order to degrade the protein. Thus, several proinflammatory cytokines were investigated, as previous studies describe an effect of pneumolysin on cytokine production. Surprisingly, only interleukin 6-production was increased after toxin-treatment and no effect of endocytotic inhibitors on the interleukin 6-production was observed. The conclusion from this finding is that pneumolysin leads to an increase of interleukin 6, which would not depend on the endocytotic uptake of pneumolysin. The production of interleukin 6 would enhance the production of acute phase proteins, T-cell activation, growth and differentiation. On the one hand, this activation could serve pathogen clearance from infected tissue. On the other hand, the production of interleukin 6 could promote a further penetration of pathogen into host tissue. This question should be further investigated. / Das Protein-Toxin Pneumolysin ist einer der entscheidenden Virulenzfaktoren von Streptococcus pneumoniae. Dieses Protein-Toxin gehört zur Familie der cholesterinabhängigen Zytolysine, die Membrancholesterol für ihre Aktivierung und Bindung benötigen. Nach der Membranbindung ordnen sich die Toxinmonomere kreisförmig an und ändern ihre Konformation, wodurch eine Pore entsteht, die dann zu einer Lyse der Zelle führt. Vor kurzem wurde nach Pneumolysinbehandlung in einer humanen Neuroblastomzelllinie eine Aktivierung kleiner GTPasen gefunden, die für zytoskelettale Veränderungen entscheidend sind (z.B. Zellbewegungen). Deshalb wurde die Hypothese aufgestellt, dass Pneumolysin diese zytoskelettalen Veränderungen auch in primären neuronalen Zellen auslösen könnte. Das Ziel dieser Arbeit war, die Effekte von Pneumolysin auf primäre Mausastrozyten im Hinblick auf Porenbildung, zelluläre Transportprozesse und immunologische Antworten zu untersuchen. Im ersten Teil wird die Bedeutung der Porenbildung auf zytoskelettale Veränderungen untersucht. Hierbei wurden lytische Fähigkeiten, Membranbindung, Membrandepolarisation, Porenbildung im künstlichen Bilayer und Effekte auf das Zytoskelett untersucht. Sowohl der Wildtyp als auch die Varianten zeigten die gleiche Stärke an Membranbindung. Diese Untersuchungen weisen darauf hin, dass die Porenbildung für die Zell-Lyse, Membrandepolarisation und zytoskelettale Veränderungen in Mausastrozyten wichtig ist und führt zu der Schlussfolgerung, dass nicht die Membranbindung, sondern die Porenbildung entscheidend für die beobachteten zytoskelettalen Veränderungen ist. Im zweiten Teil dieser Arbeit wurde der Effekt des Pneumolysin auf zelluläre Transportprozesse untersucht. Erneut zeigten die Pneumolysinvarianten keine Wirkung, während der Wildtyp die Gesamtrate der Endozytose erhöhte. Weiterhin wurde nur der Wildtyp internalisiert. Um einen möglichen Mechanismus für die Internalisierung des Toxins vorschlagen zu können, wurde Pneumolysin als GFP-markiertes Toxin genutzt. Weiterhin wurden einige Marker für unterschiedliche endozytotische Transportprozesse genutzt um eine Ko-lokalisation mit Pneumolysin-GFP zu ermöglichen. Des Weiteren wurden Inhibitoren für zwei Schlüsselproteine endozytotischer Vorgänge, Dynamin und Myosin II, genutzt. Die Ergebnisse dieser Untersuchungen zeigten, dass Pneumolysin wahrscheinlich durch dynamin- und caveolin-unabhängige Pinozytose in die Zelle aufgenommen wird. Dieser Mechanismus führt zu der Bildung von Caveosomen, deren weiterer Transport, und somit das Schicksal des internalisierten Toxins, bis heute noch nicht aufgeklärt ist. Die Beobachtung, dass Pneumolysin die Gesamtrate an Endozytose erhöht, führte zum dritten Teil dieser Arbeit. Wenn das Toxin die Gesamtrate an Endozytose erhöht, stellt sich die Frage, ob dieser Vorgang der Zerstörung des Toxins – also einer Abwehr der Zelle – dient, oder ob diese Internalisierung eine Strategie des Pathogens ist, um tiefer in das Wirtsgewebe einzudringen. Aktuelle Studien belegen, dass Pneumolysin einen Einfluss auf inflammatorische Antworten des Immunsystems hat. Aus diesem Grund wurden unterschiedliche proinflammatorische Zytokine untersucht. Überraschenderweise zeigte sich nur eine Erhöhung des Interleukin 6 nach der Toxinbehandlung. Weiterhin hatten die Endozytoseinhibitoren keinen Effekt auf die Produktion dieses proinflammatorischen Zytokins. Pneumolysin führt also zu einem Anstieg der Interleukin 6 Produktion, diese Produktion ist jedoch unabhängig von der Internalisierung dieses Toxins. Die Produktion dieses Interleukins würde zur Produktion der Akute-Phase Proteine, der Aktivierung der T-Zell Antwort, zu Wachstum und Zelldifferenzierung führen. Einerseits könnte diese Aktivierung die Infektion durch das Pathogen bekämpfen. Andererseits könnte S. pneumoniae die erhöhte Produktion durch PLY an Interleukin 6 nutzen um weiter in das Wirtsgewebe vordringen zu können. Diese Frage sollte noch durch weitere Experimente untersucht werden.

The ability to produce toxins is spread among a huge variety of bacterial strains. A very prominent class of bacterial protein toxins is the family of binary AB toxins sharing a common mode of intoxication. A pore forming component B binds and translocates an enzymatic component A into the cytosol of target cells exhibiting a fatal mode of action. These components are supposed to be not toxic themselves but both required for cell toxicity. Anthrax toxin produced by the Gram-positive bacteria Bacillus anthracis is the best studied binary toxin especially since its use as a biological weapon in the context of the attacks of 9/11 in 2001. In contrast to other binary toxins, Anthrax toxin possesses two different enzymatic components, edema factor (EF), a calcium- and calmodulin-dependent adenylat-cyclase and lethal factor (LF), a zinc-dependent metalloprotease. Protective antigen (PA) is the pore-forming component responsible for binding and translocation. Clostridium botulinum possesses in addition to the well known botulinum toxin (Botox) a variety of other toxins, such as the binary C2 toxin. C2 toxin is composed of the binding and translocation moiety C2II and the enzymatic moiety C2I acting as an actin-ADP-ribosyltransferase. In this study, the mode of translocation and the binding kinetics to the enzymatic component were studied in a biophysical experimental setup. In chapter 2, the binding of the N-terminal fractions EFN and LFN to the PA channel are analyzed in artificial bilayer membranes revealing lower binding affinity compared to full-length EF and LF. Other biophysical properties like voltage-dependency and ionic-strength dependency are not influenced. The results suggest that additional forces are involved in the binding process, than those concerning the N-terminus exclusively, as it was supposed previously. As the treatment of an Anthrax infection with antibiotics is often medicated very late due to the lack of early symptoms, tools to prevent intoxication are required. 4-aminoquinolones like chloroquine are known to block the PA channel, thereby inhibiting intoxication but they also lead to severe side-effects. In chapter 3 new promising agents are described that bind to PA in artificial bilayer systems, elucidating common motives and features which are necessary for binding to PA in general. The possible interaction of Anthrax and C2 toxin is investigated by measuring the binding of one enzymatic component to the respective other toxin’s pore (chapter 4). Interestingly, in vitro experiments using the black lipid bilayer assay show that PA is able to bind to C2I resulting in half saturation constants in the nanomolar range. Furthermore, in vivo this combination of toxin components exhibits cell toxicity in human cell lines. This is first-time evidence that a heterologous toxin combination is functional in in vitro and in vivo systems. In contrast, C2II is able to bind to EF as well as to LF in vitro, whereas in in vivo studies almost no toxic effect is detected. In the case of PA, an N-terminal His6-tag attached to the enzymatic subunit increased the binding affinity (chapter 5). A His6-tag attached to not related proteins also led to high binding affinities, providing the possibility to establish PA as a general cargo protein. In chapter 6 a set of different molecules and proteins is summarized, which are either related or not related to binary toxins, PA is able to bind. In first line, the presence of positive charges is found to be responsible for binding to PA which is in accordance to the fact that PA is highly cation selective. Furthermore, we present evidence that different cationic electrolytes serve as a binding partner to the PA channel. In the last decade another toxin has aroused public attention as it was found to be responsible for a rising number of nosocomial infections: Clostridium difficile CDT toxin. The mode of action of the enzymatic subunit CDTa is similar to C2I of C2 toxin, acting as an ADP-ribosylating toxin. The channel forming and binding properties of CDT toxin are studied in artificial bilayer membranes (chapter 7). We found that two different types of channels are formed by the B component CDTb. The first channel is similar to that of iota toxin’s Ib of Clostridium perfringens with comparable single channel conductance, selectivity and binding properties to the enzymatic subunit CDTa. The formation of this type of channel is cholesterol-dependent, whereas in the absence of cholesterol another kind of channel is observed. This channel has a single channel conductance which is rather high compared to all other binary toxin channels known so far, it is anion selective and does not show any binding affinity to the enzymatic component CDTa. The results reveal completely new insights in channel formation properties and the flexibility of a pore-forming component. Additionally, these findings suggest further possibilities of toxicity of the pore forming component itself which is not known for any other binary toxin yet. Therefore, the pathogenic role of this feature has to be studied in detail. / Die Fähigkeit, Toxine zu produzieren, ist unter verschiedensten Bakterienstämmen sehr verbreitet. Zu diesen Toxinen zählt auch die Familie der binären AB-Toxine, die hauptsächlich von Bakterien der Gattung Bacillus und Clostridium gebildet werden. Charakteristisch für diese bakteriellen Proteintoxine ist der Wirkungsmechanismus der Zellintoxikation. Eine porenformende Untereinheit B bindet eine enzymatische Untereinheit A und transportiert diese in das Zytosol von Zielzellen, die dort tödliche Wirkung entfalten. Es wird angenommen, dass die einzelnen Komponenten an sich nicht toxisch sind, sondern nur in Kombination Zellvergiftung auslösen. Anthrax-Toxin, das von dem Gram-positiven Bakterium Bacillus anthracis produziert wird, ist das bekannteste und am besten untersuchte binäre Toxin, besonders seit es im Jahr 2001 als Biowaffe eingesetzt wurde. Im Gegensatz zu anderen binären Toxinen besitzt das Anthrax-Toxin zwei enzymatische Komponenten: Edema Factor (EF), eine kalzium- und calmodulinabhängige Adenylatzyklase, und Lethal Factor (LF), eine zinkabhängige Metalloprotease. Protective Antigen (PA) ist die porenformende Komponente, die für die Binding und die Translokation der enzymatischen Untereinheiten verantwortlich ist. Clostridium botulinum produziert neben dem bekannten Botulinumtoxin (Botox) eine Reihe weiterer Toxine, unter anderem das binäre C2 Toxin. Dieses besteht aus der Binde- und Translokationskomponente C2II und der enzymatischen Komponente C2I, die als ADP-Ribosyltransferase fungiert. Im Rahmen der vorliegenden Arbeit werden der Translokationsmechanismus und die kinetischen Bindeeigenschaften dieser Toxine biophysikalisch untersucht. In Kapitel 2 wird die Bindung der N-terminalen Fragmente EFN und LFN an den PA-Kanal in künstlichen Lipidmembranen analysiert. Obwohl die Spannungs- und Ionenstärkeabhängigkeit unverändert sind, weisen die verkürzten Proteine deutlich geringe Bindeaffinitäten zu PA im Vergleich zu den vollständigen Proteinen auf. Die Ergebnisse zeigen, dass, anders als bisher angenommen, weitere Kräfte als die zwischen dem N-Terminus und dem PA-Kanal eine Rolle für die Bindung der enzymatischen Komponente spielen. Da bei einer Anthraxinfektion häufig keine frühen Symptome sichtbar sind, erfolgt die Behandlung mit Antibiotika in der Regel relativ spät. Daher werden neue Wirkstoffe benötigt, um einer Intoxikation vorzubeugen. Es ist bekannt, dass 4-Aminoquinolone, wie zum Beispiel Chloroquin, in der Lage sind, die PA-Pore zu blockieren und somit eine Zellvergiftung zu verhindern, allerdings haben diese Wirkstoffe starke Nebenwirkungen. In Kapitel 3 werden neue, vielversprechende Wirkstoffe beschrieben, die an PA binden können und Aufklärung darüber geben, welche Eigenschaften für die Bindung an PA im Allgemeinen verantwortlich sind. Des Weiteren wird untersucht, ob eine Kreuzreaktion zwischen den Komponenten des Anthrax- und C2-Toxins möglich ist (Kapitel 4). Dazu wird die Bindung einer enzymatischen Komponente an die Pore des entsprechenden anderen Toxins gemessen. Interessanterweise ergeben in vitro Experimente an künstlichen Lipidmembranen, dass PA an C2I bindet und in vivo Vergiftungen an humanen Zelllinien auslöst. Damit wird zum ersten Mal gezeigt, dass eine heterologe Toxinkombination sowohl in vitro als auch in vivo funktionell ist. C2II hingegen ist zwar in der Lage, EF und LF zu binden, die Transportrate in Zielzellen ist jedoch sehr gering. Im Fall von PA bewirkt ein N-terminaler His6-tag, der an die enzymtischen Einheiten gekoppelt ist, eine Erhöhung der Bindeaffinität, beschrieben in Kapitel 5. Dies ist sowohl für nah verwandte Proteine der Fall als auch für Proteine, die nicht im Zusammenhang mit binären Toxinen stehen. Somit eröffnet sich die Möglichkeit, PA als universelles Transportprotein zu nutzen. In Kapitel 6 werden verschiedene Moleküle und Proteine beschrieben, die in der Lage sind, an PA zu binden. Vor allem positive Ladungen scheinen für die Bindung an PA-Kanäle verantwortlich zu sein, was mit der Tatsache, dass PA stark kationenselektiv ist, im Einklang steht. Des Weiteren wird zum ersten Mal beschrieben, dass verschiedene Kationen selbst als Bindepartner fungieren können. Seit einigen Jahren ist ein weiteres Toxin in den Fokus der Öffentlichkeit gerückt, da es zunehmend für nosokomiale Infektionen verantwortlich gemacht wird: CDT-Toxin von Clostridium difficile. Wie das C2-Toxin besitzt CDT-Toxin ADP-Ribosyltransferaseaktivität, was zu irreversiblen Schäden des Aktin- Zytoskeletts und somit zum Zelltod führt. Die biophysikalischen Eigenschaften, betreffend Porenbildung und Bindeaffinität des CDT-Toxins werden in Kapitel 7 beschrieben. Wir zeigen, dass die B Komponente CDTb fähig ist, zwei unterschiedliche Kanäle zu bilden. Einer dieser Kanäle ist dem des Iota-Toxins von Clostridium perfringens ähnlich, die Einzelkanalleitfähigkeit, Selektivität und Bindeeigenschaften sind vergleichbar. Die Bildung dieses Kanals ist abhängig von Cholesterin, wohingegen in Abwesenheit von Cholesterin überwiegend ein anderer Kanal geformt wird. Dieser zeigt eine für einen binären Toxinkanal ungewöhnlich hohe Einzelkanalleitfähigkeit, der Kanal ist anionselektiv und weist keinerlei Bindeaffinität zu der enzymatischen Komponente CDTa auf. Die Ergebnisse offenbaren neue Einblicke in die Formierung von Toxinkanälen und deuten darauf hin, dass dieses Toxin durch die Flexibilität der Kanalbildung möglicherweise zusätzliche Fähigkeiten besitzt, Zellintoxikation auszulösen. Dennoch ist die physiologische und pathogene Rolle dieser Eigenschaft noch weitestgehend ungeklärt und bedarf intensiver Untersuchung.

<p>In this thesis, the strength-enhancing mechanisms of dry binders in direct compression were studied. The systems investigated were binary mixtures containing various compounds and binders. Among the binders used were a series of different molecular weights of polyethylene glycol. The proposed simplified tablet model describing the fracture path in a tablet during strength testing offers an explanation for the increase in tablet strength caused by the binder. The model and results in this thesis indicate that fractures will usually propagate around the tablet particles and through the interparticulate voids during tablet strength testing.</p><p>One important characteristic of the binder is its ability to be effectively and evenly distributed through the interparticulate voids in a compound tablet. Characteristics such as high plasticity, low elasticity and a small particle size were associated with a more even distribution and a consequent pronounced effect on pore structure and marked improvement in tablet strength. The strength of tablets containing less plastic binders was governed more by the compactibility of the binder. The tablet porosity, bonding mechanisms and volume reduction mechanisms of the compound also influenced the effect of the binder. For example, the plasticity and particle size of the binder had the most significant effects on tablet strength when the tablet porosity of the com-pound was relatively low. A combination of the plasticity and the compactibility of the binder determined the strength of tablets when the tablet of a compound was more porous. The positive effect of a binder on pore structure and tablet strength resulted in an increase in the disintegration time. Although addition of a superdisintegrant generally improved the disintegration time, the effect was decreased when the formulation included more deformable binders.</p><p>The choice of a suitable binder for a tablet formulation requires extensive knowledge of the relative importance of binder properties for enhancing the strength of the tablet and also of the interactions between the various materials constituting a tablet. Thus, the increased knowledge of the functionality of a binder obtained in this thesis enables a more rational approach to tablet formulation.</p>