2,285 research outputs found

    Analytical miniaturization and nanotechnologies

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    The boundary layer of VW Hyi in quiescence

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    In this letter, we suggest that the missing boundary layer luminosity of dwarf novae in quiescence is released mainly in the ultraviolet (UV) as the second component commonly identified in the far ultraviolet (FUV) as the "accretion belt". We present the well-studied SU UMa-type system VW Hyi in detail as a prototype for such a scenario. We consider detailed multiwavelength observations and in particular the recent FUSE observations of VW Hyi which confirm the presence of a second component (the "accretion belt") in the FUV spectrum of VW Hyi in quiescence. The temperature (50,000K) and rotational velocity (> 3,000km/s) of this second FUV component are entirely consistent with the optically thick region (tau = 1) located just at the outer edge of optically thin boundary layer in the simulations of Popham (1999). This second component contributes 20% of the FUV flux, therefore implying a boundary layer luminosity: LBL=2×(0.2×LUV+LXray)=0.6×LdiscL_{BL} = 2 \times (0.2 \times L_{UV} + L_{X-ray}) = 0.6 \times L_{disc}, while the theory (Klu\'zniak 1987) predicts, for the rotation rate of VW Hyi's WD, LBL0.77LdiscL_{BL} \approx 0.77 L_{disc}. The remaining accretion energy (<0.1Lacc<0.1 L_{acc}) is apparently advected into the star as expected for optically thin advection dominated boundary layers. This scenario is consistent with the recent simultaneous X-ray and UV observations of VW Hyi by (Pandel, C\'ordova & Howell 2003), from which we deduced here that the alpha viscosity parameter in the boundary layer region must be as small as α0.004\alpha \approx 0.004.Comment: 4 page

    Initial Results from a Stacked Ring Apparatus for Simulation of a Soil Profile

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    A stack of 48 rings, lined with a latex membrane, is used to confine a column of soil 12 inches high by 12 inches in diameter (300 mm x 300 mm). Both dry and saturated columns of fine sand are shaken at their base, at a centrifugal acceleration of 35.5 g. Measurements of the settlement of the surface, horizontal displacement and pore pressures show that the columns of soil are behaving essentially (although not exactly) as one-dimensional shear beams

    Development and comparison of an esophageal Doppler monitoring-based treatment algorithm with a heart rate and blood pressure-based treatment algorithm for goal-directed fluid therapy in anesthetized dogs: A pilot study

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    The objective of this pilot study was to determine the feasibility of a study comparing the efficacy of an esophageal Doppler monitor (EDM)-based fluid therapy algorithm with a heart rate (HR)- and mean arterial blood pressure (MAP)-based algorithm in reducing hypotension and fluid load in anesthetized dogs. Client-owned dogs undergoing general anesthesia for surgical procedures were randomized to two groups. An EDM probe for monitoring blood flow in the descending aorta was placed in each dog before receiving a crystalloid bolus (5 mL/kg) over 5 min. Fluids were repeated in case of fluid responsiveness defined by increasing Velocity Time Integral (VTI) ≥ 10% in group EDM and by decreasing HR ≥ 5 beats/min and/or increasing MAP ≥ 3 mmHg in group standard. The feasibility outcomes included the proportion of dogs completing the study and the clinical applicability of the algorithms. The clinical outcomes were the total administered fluid volume and the duration of hypotension defined as MAP &lt; 60 mmHg. Data was compared between groups with Mann-Whitney U-test. p &lt; 0.05 were deemed significant. Of 25 dogs screened, 14 completed the study (56%). There were no differences in the proportion of recorded time spent in hypotension in group standard [2 (0–39)% (median (range))] and EDM [0 (0–63) %, p = 1], or the total volume of fluids [standard 8 (5–14) mL/kg/h, EDM 11 (4–20) mL/kg/h, p = 0.3]. This study declined the feasibility of a study comparing the impact of two newly developed fluid therapy algorithms on hypotension and fluid load in their current form. Clinical outcome analyses were underpowered and no differences in treatment efficacy between the groups could be determined. The conclusions drawn from this pilot study provide important information for future study designs

    Photonic crystal resonator integrated in a microfluidic system

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    We report on a novel optofluidic system consisting of a silica-based 1D photonic crystal, integrated planar waveguides and electrically insulated fluidic channels. An array of pillars in a microfluidic channel designed for electrochromatography is used as a resonator for on-column label-free refractive index detection. The resonator was fabricated in a silicon oxynitride platform, to support electroosmotic flow, and operated at 1.55 microns. Different aqueous solutions of ethanol with refractive indices ranging from n = 1.3330 to 1.3616 were pumped into the column/resonator and the transmission spectra were recorded. Linear shifts of the resonant wavelengths yielded a maximum sensitivity of 480 nm/RIU and a minimum difference of 0.007 RIU was measured

    Evaluation of the Effect of Induced Endotoxemia on ROTEM S® and Platelet Parameters in Beagle Dogs Anaesthetized with Sevoflurane

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    Endotoxemia is thought to induce severe changes in coagulation status. In this study, blood samples from six beagle dogs receiving 1 mg/kg E. coli lipopolysaccharide (LPS) intravenously were analyzed to describe the concurrent changes in platelet count, platelet function assessed with impedance thromboaggregometry, thromboelastometry and d-dimers during artificially induced endotoxemia and its therapy with fluids and vasopressors at five timepoints (baseline, after LPS and 30 mL/kg Ringer’s acetate, during noradrenaline ± dexmedetomidine infusion, after a second fluid bolus and a second time after vasopressors). Results were analyzed for changes over time with the Friedman test, and statistical significance was set at p < 0.05. We found decreased platelet count and function and changes in all platelet-associated rotational thromboelastometry (ROTEM) variables indicating hypocoagulability, as well as increases in d-dimers indicating fibrinolysis within one hour of intravenous administration of LPS, with partial recovery of values after treatment and over time. The fast changes in platelet count, platelet function and ROTEM variables reflect the large impact of endotoxemia on the coagulation system and support repeated evaluation during the progress of endotoxemic diseases. The partial recovery of the variables after initiation of fluid and vasopressor therapy may reflect the positive impact of the currently suggested therapeutic interventions during septic shock in dogs

    Direct monitoring of calcium-triggered phase transitions in cubosomes using small-angle X-ray scattering combined with microfluidics

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    This article introduces a simple microfluidic device that can be combined with synchrotron small-angle X-ray scattering (SAXS) for monitoring dynamic structural transitions. The microfluidic device is a thiol-ene-based system equipped with 125 μm-thick polystyrene windows, which are suitable for X-ray experiments. The device was prepared by soft lithography using elastomeric molds followed by a simple UV-initiated curing step to polymerize the chip material and simultaneously seal the device with the polystyrene windows. The microfluidic device was successfully used to explore the dynamics of the structural transitions of phytantriol/dioleoylphosphatidylglycerol-based cubosomes on exposure to a buffer containing calcium ions. The resulting SAXS data were resolved in the time frame between 0.5 and 5.5 s, and a calcium-triggered structural transition from an internal inverted-type cubic phase of symmetry Im3m to an internal inverted-type cubic phase of symmetry Pn3m was detected. The combination of microfluidics with X-ray techniques opens the door to the investigation of early dynamic structural transitions, which is not possible with conventional techniques such as glass flow cells. The combination of microfluidics with X-ray techniques can be used for investigating protein unfolding, for monitoring the formation of nanoparticles in real time, and for other biomedical and pharmaceutical investigations. A combination of microfluidics with X-ray techniques has been used to perform dynamic structural studies on nanoparticulate formulations
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