The thermodynamic properties of bioactive peptides determine how they interact with cellular assemblies. Ultrasonic velocity and density measurements were used to analyse the volumetric properties in aqueous solution of 3 different materials: KCl, bioactive peptides (from hemp seed and dairy proteins), and liposomes (cell membrane models), as well as the interaction between peptides and liposomes. Serial dilutions of the three different materials showed linear relationships between density and concentration and between ultrasonic velocity and concentration. The apparent specific volume and apparent specific compressibility in solution of all materials showed concentration dependence as a result of increased electrostriction as solutions were diluted. The experimental ultrasonic velocities of liposome-dairy peptide mixes were higher than the theoretical additive value, due to interactions between liposomes and peptides. My research demonstrates the benefits of precise volumetric assessments in biological assays.

Molecular Dynamics (MD) simulations were used in conjunction with the Kirkwood-Buff (KB) theory to compute partial molar volume (PMV) for solutes of various chemical natures. Simulations performed with only the Lennard-Jones (LJ) potential yield PMV for solutes which coincide with the cavity volumes derived from calculations with scaled particle theory (SPT). Whereas, simulations carried out with only the repulsive LJ term produced PMV of solutes closer to their excluded volumes. We also determined the thermal volume, VT, which represents the volume of the effective void created around solutes of varying cavity sizes and applied the spherical approximation of solute geometry to evaluate the thickness of the thermal volume, . Our results reveal an increase in the thickness of thermal volume, , with an increase in the size of the solute. Our theoretical results are in good agreement with the reported empirical schemes for parsing PMV data on small solutes.

This work presents the design, theory, and measurement of a phase-reconfigurable reflectarray (RA) element for beamforming applications enabled by fluidic networks and colloidal dispersions. The element is a linearly polarized microstrip patch antenna loaded with a Coaxial Stub Microfluidic Impedance Transformer (COSMIX). Specifically, adjusting the concentration of highly dielectric particulate in the dispersion provides localized permittivity manipulation within the COSMIX. This results in variable impedance load on the patch and ultimately continuous, low-loss phase control of a signal reflected from the patch. Different aspects of design, modeling, and measurement are discussed for a proof-of-concept prototype and three further iterations. Initial measurements with manual injections of materials into a fabricated proof-of-concept demonstrate up to 200 degrees of phase shift and a return loss of less than 1.2 dB at the operating frequency of 3 GHz. The next design iteration addresses fabrication challenges as well the general cumbersomeness of the proof-of-concept by replacing the static material delivery system with a dynamic closed-loop fluidic network. It also makes use of a design procedure to maximize the phase sensitivity. Measurements demonstrate progressive phase shifts through dilution of the system reservoir; however, the initial measurements with this system are not in line with simulated predictions. Investigations suggest the primary culprit to be inaccurate material data. The dielectric constant of the particulate (colloidal BSTO) was overrated and the loss tangent of the fluid medium (a silicone-based oil) was underrated. After accounting for these issues the measurement a second measurement with the system demonstrates 270 degrees of phase shift with return loss of 9 dB. The next design iteration examines a trade-off between phase sensitivity and reduced losses. The design also features modifications to the fluidic system to allow for layered fabrication in the GND plane as well integration with a 2-port coaxial measurement cell. Attempted measurements discover the fluidic system cannot flow the higher concentrations of nanoparticles necessary for phase shifting. A final design iteration addresses this challenge by expanding and repositioning inlets to the fluidic system. Free space reflection measurements with this element initially demonstrate phase shifting until a buildup of nanoparticles form within the COSMIX.

No description available.

No description available.

The thermodynamic properties of bioactive peptides determine how they interact with cellular assemblies. Ultrasonic velocity and density measurements were used to analyse the volumetric properties in aqueous solution of 3 different materials: KCl, bioactive peptides (from hemp seed and dairy proteins), and liposomes (cell membrane models), as well as the interaction between peptides and liposomes. Serial dilutions of the three different materials showed linear relationships between density and concentration and between ultrasonic velocity and concentration. The apparent specific volume and apparent specific compressibility in solution of all materials showed concentration dependence as a result of increased electrostriction as solutions were diluted. The experimental ultrasonic velocities of liposome-dairy peptide mixes were higher than the theoretical additive value, due to interactions between liposomes and peptides. My research demonstrates the benefits of precise volumetric assessments in biological assays.

Outlined is a new approach to the problem of surfacing particle-based fluid simulations. The key idea is to construct a surface that is as smooth as possible while remaining faithful to the particle locations. We describe a mesh-based algorithm that expresses the surface in terms of a constrained optimization problem. Our algorithm incorporates a secondary contribution in Marching Tiles, a generalization of the Marching Cubes isosurfacing algorithm. Marching Tiles provides guarantees on the minimum vertex valence, making the surface mesh more amenable to numerical operators such as the Bilaplacian.

Obstructive sleep apnoea (OSA) is a common respiratory disorder characterised by repetitive periods of upper airway (UA) collapse during sleep. OSA is more common in males and the obese but the reasons why remain poorly understood. Abdominal obesity, particularly common in males, is likely to indirectly modulate the amount of tension (tracheal traction) exerted on the UA by the trachea and other intrathoracic structures, potentially leading to increased UA collapsibility. Other factors such as lung volume changes with obesity, altered drive to UA muscles and exaggerated arousal responses are also likely to contribute to UA instability. An investigation of these potential contributing factors forms the basis of this thesis. In the first study, the effect of external abdominal compression on UA collapsibility during sleep was investigated in a group of obese male OSA patients. A large pneumatic cuff wrapped around the abdomen was inflated to increase intra-abdominal pressure, aiming to produce an upward force on the diaphragm, designed to reduce axial tension on the UA. Abdominal compression increased end-expiratory gastric (PGA) and end-expiratory transdiaphragmatic (PDI) pressure by ~50% and produced a significant rise in UA collapsibility compared to the cuff deflated condition. These data support that increased intra-abdominal pressure has a negative effect on UA function during sleep. This effect may help explain why obesity is the leading risk factor for OSA and why OSA affects men more than women, given that abdominal obesity is particularly common in obese males. In the second study, differences in minimum expiratory (tonic) diaphragm activity during wakefulness were compared between 8 obese OSA patients and 8 healthyweight controls. Changes in tonic diaphragm activity and lung volume following sleep onset were also compared between the two groups. There was no evidence of increased tonic diaphragmatic activity during wakefulness in obese OSA patients to support significant diaphragmatic compensation for abdominal compressive effects of obesity. There were small decrements in lung volume following sleep onset in both groups (<70 ml), with significantly greater lung volume and diaphragmatic EMG decrements when sleep onsets were immediately followed by respiratory events. While lung volume decrements at sleep onset were relatively small, this does not discount that UA function is not more sensitive to effects of reduced lung volume in obese OSA patients. To more closely investigate the potential interactive effects of obesity on physiological variables likely influencing UA function, the third study investigated the temporal relationships between a comprehensive range of relevant physiological variables leading into and following the termination of obstructive apnoeas during sleep in 6 obese OSA patients. Prior to UA obstruction, diaphragm and genioglossus muscle activity decreased, while UA resistance increased. Lung volume and end-expiratory PGA and end-expiratory PDI also fell during this period, consistent with diaphragm ascent. There was a substantial increase in ventilation, muscle activity and lung volume immediately following the termination of obstructive events. Respiratory events and arousals occurred in close temporal proximity prior to and following obstructive apnoeas, supporting that cyclical respiratory events and arousals may both help to perpetuate further events. The results from this study support that there is a ‘global’ loss in respiratory drive to UA dilator and pump muscles precipitating obstructive respiratory events. The associated decreases in UA dilator muscle activity and lung volume may therefore both contribute to the propensity for the UA to obstruct. In summary, increased intra-abdominal pressure was shown to negatively impact UA airway collapsibility during sleep. A decrease in lung volume at sleep onset and prior to UA obstruction further support that lung volume decrement, coincident with a decline in overall respiratory drive, potentially contributes to the propensity for airway obstruction. Further studies are needed to elucidate the relative contribution of relatively small changes in lung volume versus changes in respiratory and UA muscle activity per se on UA patency in OSA patients. / Thesis (Ph.D.) -- University of Adelaide, School of Medical Sciences, 2010

Diss. (sammanfattning) Umeå : Sveriges lantbruksuniv. / Härtill 6 uppsatser.

Thesis (M.S.)--Ohio University, June, 1995. / Title from PDF t.p.