On the effect of surfactants on drop coalescence at liquid/liquid interfaces

In this work the effect of surfactants on the coalescence of a drop with a flat aqueous-organic interface was experimentally investigated. A high speed Particle Image Velocimetry (PIV) system was used to obtain velocity profiles and kinetic energy per unit mass distribution inside the coalescing droplets. Different mass ratios of surfactant to oil below the CMC value, up to ϕ = 5 × 10−4, of a non-ionic surfactant dissolved in the organic phase were studied. It was found that an increase in the surfactant concentration promoted the deformation of the interface before the film that separated the drop from the interface ruptured. A high surfactant concentration also increased the time needed for film rupture. When rupture occurred, two counter-rotating vortices formed inside the droplet on either side of the rupture point, which moved upwards with time. The propagation of the vortices inside the droplet was faster for low surfactant concentrations, while the intensities of the two counter-rotating vortices significantly decreased for increasing surfactant concentration. At the early stages of coalescence after film rupture, the kinetic energy per unit mass was mainly distributed near the bottom part of the droplet, while at later stages it was distributed near the upper part of the droplet

Isotropic reconstruction of 3D fluorescence microscopy images using convolutional neural networks

Fluorescence microscopy images usually show severe anisotropy in axial versus lateral resolution. This hampers downstream processing, i.e. the automatic extraction of quantitative biological data. While deconvolution methods and other techniques to address this problem exist, they are either time consuming to apply or limited in their ability to remove anisotropy. We propose a method to recover isotropic resolution from readily acquired anisotropic data. We achieve this using a convolutional neural network that is trained end-to-end from the same anisotropic body of data we later apply the network to. The network effectively learns to restore the full isotropic resolution by restoring the image under a trained, sample specific image prior. We apply our method to $3$ synthetic and $3$ real datasets and show that our results improve on results from deconvolution and state-of-the-art super-resolution techniques. Finally, we demonstrate that a standard 3D segmentation pipeline performs on the output of our network with comparable accuracy as on the full isotropic data

An experimental study on the drop/interface partial coalescence with surfactants

This paper presents investigations on the partial coalescence of an aqueous drop with an organicaqueous interface with and without surfactants. The organic phase was different silicone oils and the aqueous phase was a glycerol-water solution at different concentrations. It is found that when the surfactant Span 80 is introduced into the organic phase, the partial coalescence region is reduced in the Oh-Bo coalescence map. The range of the inertio-capillary regime reduces when surfactants are present, while the drop size ratio decreases with increasing surfactant concentration. The velocity fields inside the aqueous drop were studied with high speed particle image velocimetry for the first time. In the surfactant-free system, it was found that the inward motion of the fluids at the upper part of the drop favours the generation of a liquid cylinder at the early stages of coalescence. The pressure gradient created by the downward stream at the bottom of the liquid cylinder drives the pinch-off of the secondary drop. When surfactants are present, the rupture of the film between the drop and the interface occurs at an off-axis location. The liquid cylinder formed in this case is not symmetric and does not lead to pinch-off. It is also found that the vortices inside the droplet have little impact on the partial coalescence

Adaptation Accelerating Sampling-based Bayesian Inference in Attractor Neural Networks

The brain performs probabilistic Bayesian inference to interpret the external world. The sampling-based view assumes that the brain represents the stimulus posterior distribution via samples of stochastic neuronal responses. Although the idea of sampling-based inference is appealing, it faces a critical challenge of whether stochastic sampling is fast enough to match the rapid computation of the brain. In this study, we explore how latent feature sampling can be accelerated in neural circuits. Specifically, we consider a canonical neural circuit model called continuous attractor neural networks (CANNs) and investigate how sampling-based inference of latent continuous variables is accelerated in CANNs. Intriguingly, we find that by including noisy adaptation in the neuronal dynamics, the CANN is able to speed up the sampling process significantly. We theoretically derive that the CANN with noisy adaptation implements the efficient sampling method called Hamiltonian dynamics with friction, where noisy adaption effectively plays the role of momentum. We theoretically analyze the sampling performances of the network and derive the condition when the acceleration has the maximum effect. Simulation results validate our theoretical analyses. We further extend the model to coupled CANNs and demonstrate that noisy adaptation accelerates the sampling of the posterior distribution of multivariate stimuli. We hope that this study enhances our understanding of how Bayesian inference is realized in the brain

Laser induced fluorescence studies on the distribution of surfactants during drop/interface coalescence

The spatiotemporal distribution of fluorescent surfactants on the merging interfaces during the coalescence of an aqueous drop with an organic/aqueous flat interface was studied experimentally with high-speed laser induced fluorescence. The aqueous phase was a 46% glycerol solution, while the organic phase was a 5 cSt silicone oil. A fluorescently tagged surfactant was used at a concentration of 0.001 mol/m3 in the aqueous phase. To vary the concentration of surfactants on the interfaces, the drop and the flat interface were left to stand for different times before the coalescence experiments (different interface ages). It was found that when a drop rested on the interface, the surfactants adsorbed on the interfaces were swept outwards by the draining liquid film between the drop and the flat interface and reached a peak value at 0.75Rh away from the centre of the film, where Rh is the horizontal drop radius. After the film rupture, the concentration of the surfactants at the tip of the meniscus increased. Once the film had retracted, the concentration of the surfactants peaked at the meniscus at the bottom of the drop. As the liquid in the drop started to merge with its homophase, the drop formed a cylinder from the upward capillary waves on the drop surface. The surfactant concentration was found to be low at the top of the liquid cylinder as the interface was stretched by the convergence of the capillary waves. Subsequently, the cylinder began to shrink and the top part of the drop acquired a high surfactant concentration

Theoretical study of the insulating oxides and nitrides: SiO2, GeO2, Al2O3, Si3N4, and Ge3N4

An extensive theoretical study is performed for wide bandgap crystalline oxides and nitrides, namely, SiO_{2}, GeO_{2}, Al_{2}O_{3}, Si_{3}N_{4}, and Ge_{3}N_{4}. Their important polymorphs are considered which are for SiO_{2}: $\alpha$-quartz, $\alpha$- and $\beta$-cristobalite and stishovite, for GeO_{2}: $\alpha$-quartz, and rutile, for Al_{2}O_{3}: $\alpha$-phase, for Si_{3}N_{4} and Ge_{3}N_{4}: $\alpha$- and $\beta$-phases. This work constitutes a comprehensive account of both electronic structure and the elastic properties of these important insulating oxides and nitrides obtained with high accuracy based on density functional theory within the local density approximation. Two different norm-conserving \textit{ab initio} pseudopotentials have been tested which agree in all respects with the only exception arising for the elastic properties of rutile GeO_{2}. The agreement with experimental values, when available, are seen to be highly satisfactory. The uniformity and the well convergence of this approach enables an unbiased assessment of important physical parameters within each material and among different insulating oxide and nitrides. The computed static electric susceptibilities are observed to display a strong correlation with their mass densities. There is a marked discrepancy between the considered oxides and nitrides with the latter having sudden increase of density of states away from the respective band edges. This is expected to give rise to excessive carrier scattering which can practically preclude bulk impact ionization process in Si_{3}N_{4} and Ge_{3}N_{4}.Comment: Published version, 10 pages, 8 figure

Risk of second primary cancer in men with breast cancer

INTRODUCTION: A retrospective registry-based cohort study was conducted to examine the risk of second primary cancer following the occurrence of breast cancer in males. METHODS: Data obtained from the California Cancer Registry in the period 1988 to 2003 included 1,926 men aged 85 years and younger diagnosed with a first primary breast cancer. Person-year analysis was applied to determine the risk of second primary cancers after the occurrence of a first primary breast cancer. The effects of age, race, and time since the first breast cancer diagnosis were assessed. RESULTS: Of the 1,926 male breast cancer cases, 221 (11.5%) developed a second primary cancer. Men with first incidence of breast cancer have a significantly higher risk of second cancer (standardized incidence ratio (SIR) = 1.16, 95% confidence interval (CI) = 1.01–1.32). The risk of a second site-specific cancer is elevated for breast cancer (SIR = 52.12, 95% CI = 31.83–80.49), cutaneous melanoma (SIR = 2.98, 95% CI = 1.63–5.00) and stomach cancer (SIR = 2.11, 95% CI = 1.01–3.88). There is a general tendency towards higher risks of second malignancies among younger men compared to older men and the risk increased with the passage of time. CONCLUSION: Male breast cancer patients should be monitored carefully for the occurrence of second primary cancers, especially a second primary breast cancer

Activity and expression of urokinase-type plasminogen activator and matrix metalloproteinases in human colorectal cancer

BACKGROUND: Matrix metalloproteinase-2 (MMP-2), matrix metalloproteinase-9 (MMP-9), and urokinase-type plasminogen activator (uPA) are involved in colorectal cancer invasion and metastasis. There is still debate whether the activity of MMP-2 and MMP-9 differs between tumors located in the colon and rectum. We designed this study to determine any differences in the expression of MMP-2, MMP-9 and uPA system between colon and rectal cancer tissues. METHODS: Cancer tissue samples were obtained from colon carcinoma (n = 12) and rectal carcinomas (n = 10). MMP-2 and MMP-9 levels were examined using gelatin zymography and Western blotting; their endogenous inhibitors, tissue inhibitor of metalloproteinase-2 (TIMP-2) and tissue inhibitor of metalloproteinase-1 (TIMP-1), were assessed by Western blotting. uPA, uPAR and PAI-1 were examined using enzyme-linked immunosorbent assay (ELISA). The activity of uPA was assessed by casein-plasminogen zymography. RESULTS: In both colon and rectal tumors, MMP-2, MMP-9 and TIMP-1 protein levels were higher than in corresponding paired normal mucosa, while TIMP-2 level in tumors was significantly lower than in normal mucosa. The enzyme activities or protein levels of MMP-2, MMP-9 and their endogenous inhibitors did not reach a statistically significant difference between colon and rectal cancer compared with their normal mucosa. In rectal tumors, there was an increased activity of uPA compared with the activity in colon tumors (P = 0.0266), however urokinase-type plasminogen activator receptor (uPAR) and plasminogen activator inhibitor-1 (PAI-1) showed no significant difference between colon and rectal cancer tissues. CONCLUSION: These findings suggest that uPA may be expressed differentially in colon and rectal cancers, however, the activities or protein levels of MMP-2, MMP-9, TIMP-1, TIMP-2, PAI-1 and uPAR are not affected by tumor location in the colon or the rectum

A clinical evaluation of amlexanox oral adhesive pellicles in the treatment of recurrent aphthous stomatitis and comparison with amlexanox oral tablets: a randomized, placebo controlled, blinded, multicenter clinical trial

<p>Abstract</p> <p>Background</p> <p>Amlexanox has been developed as a 5 percent topical oral paste for the treatment of patients with recurrent aphthous stomatitis (RAS) in most European countries. However, it is not yet available in China and has not been generally accepted in clinical treatment. The aim of this study was to explore the effectiveness of amlexanox oral adhesive pellicles in the treatment of minor recurrent aphthous ulcers, and compare the results with those of amlexanox oral adhesive tablets in order to analyse the difference between the two dosage forms of amlexanox.</p> <p>Methods</p> <p>We performed a randomized, blinded, placebo-controlled, parallel, multicenter clinical study. A total of 216 patients with minor recurrent aphthous ulcers (MiRAU) were recruited and randomized to amlexanox pellicles or placebo pellicles. Pellicles were consecutively applied four times per day, for five days. The size and pain level of ulcers were measured and recorded on treatment days 0, 4 and 6. Finally, the results were compared with those of our previous 104 cases treated with amlexanox tablets.</p> <p>Results</p> <p>Amlexanox oral adhesive pellicles significantly reduced ulcer size (P= 0.017 for day 4, P=0.038 for day 6) and alleviated ulcer pain (P=0.021 for day 4, P=0.036 for day 6). No significant difference was observed in the treatment effectiveness between the pellicle and tablet form of amlexanox.</p> <p>Conclusions</p> <p>Amlexanox oral adhesive pellicles are as effective and safe as amlexanox oral adhesive tablets in the treatment of MiRAU for this Chinese cohort. However, pellicles seem to be more comfortable to use when compared with the dosage form of tablets. Therefore, in clinical practice, amlexanox oral adhesive pellicles may be a better choice for RAS patients.</p> <p>Trials registration</p> <p>Nederlands Trial Register NTR1727.</p