DelayDroid: an instrumented approach to reducing tail-time energy of Android apps

Mobile devices with 3G/4G networking often waste energy in the so-called “tail time” during which the radio is kept on even though no communication is occurring. Prior work has proposed policies to reduce this energy waste by batching network requests. However, this work is challenging to apply in practice due to a lack of mechanisms. In response, we have developed DelayDroid, a framework that allows a developer to add the needed policy to existing, unmodified Android applications (apps) with no human effort as well as no SDK/OS changes. This allows such prior work (as well as our own policies) to be readily deployed and evaluated. The DelayDroid compile-time uses static analysis and bytecode refactoring to identify method calls that send network requests and modify such calls to detour them to the DelayDroid run-time. The run-time then applies a policy to batch them, avoiding the tail time energy waste. DelayDroid also includes a cross-app communication mechanism that supports policies that optimize across multiple apps running together, and we propose a policy that does so. We evaluated the correctness and universality of the DelayDroid mechanisms on 14 popular Android apps chosen from the Google App Store. To evaluate our proposed policy, we studied three DelayDroid-enabled apps (weather forecasting, email client, and news client) running together, finding that the DelayDroid mechanisms combined with our policy can reduce 3G/4G tail time energy waste by 36%.     

Electrocatalytic Determination of Glucose in a Ringer''s Solution by Pulse-Voltammetry

Improvement of the electrocatalytic method of glucose determination was achieved by applying the pulse voltammetry technique. This technique, compared. to previously applied cyclic voltammetry, enhances selectivity of a platinum-black working electrode for glucose measurement. A low catalytic load working electrode has been used which is less susceptible to poisoning and has longer term stability. With cyclic voltammetry previously applied, those electrodes were limited by their narrow concentration range for glucose detection. By applying a pulsing technique, these electrodes exhibit linearity up to a glucose concentration 200 mg/dl with correlation coefficients greater than 0.9. The pulse voltammetry diminishes interference by low molecular weight serum components such as serum urea. Concentrations from 20. to 40 mg/di had an interference of 4 percent compared to 40 percent with cyclic voltammetry. Further investigations are carried on to adopt pulse voltammetry for direct measurements of glucose in body fluids.     

Simultaneous absorption of two gases reacting between themselves in a liquid—II: Approximate solutions

An attempt has been made to analyse the hitherto existing approximate solutions of nonlinear differential equations representing a mass balance of two gases which react between themselves in an inert liquid. New approximate analytical solutions of the problem have been obtained and compared with the numerical and the existing approximate solutions in order to show the best approximations and the most convenient mathematical formulas for calculating the concentration profiles and the enhancement factors.     

Removal of arsenic(III) and arsenic(V) from sulfuric acid solution by liquid–liquid extraction

Extraction of arsenic(III) and arsenic(V) from sulfuric acid solution was studied. Cyanex^® 923, Cyanex^® 925, dialkyldithiophosphinic acids (Cyanex^® 301), hydrophobic glycol (2‐ethylhexane‐1,3‐diol), and hydroxamic acids were used as extractants. The efficiency of extraction depended on extractant, diluent, valency of arsenic, and sulfuric acid concentration. Acidic reagents extracted As(III) better than As(V), while the opposite order of extraction efficiency was observed for the solvating extractants. The use of an aromatic diluent (toluene) was preferred. Toluene was found to be a better diluent for the Cyanex^® 923 and Cyanex^® 925 than Exxsol D 220/230 and octane. In the case of neo‐decanohydroxamic acids, the type of diluent had no significant effect on extraction of arsenic. The extraction of both As(III) and As(V) increased when the concentration of the sulfuric acid in the feed increased. The co‐extraction of sulfuric acid was observed. The extraction with hydroxamic acids was significantly slower in comparison to the extraction with other reagents. Extractant: arsenic species: sulfuric acid molar ratios were determined and they confirmed the composition of extracted species. Copyright © 2003 Society of Chemical Industry     

The Influence of Novel,Biocompatible, and Bioresorbable Poly(3-hydroxyoctanoate) Dressings on Wound Healing in Mice

The human body’s natural protective barrier, the skin, is exposed daily to minor or major mechanical trauma, which can compromise its integrity. Therefore, the search for new dressing materials that can offer new functionalisation is fully justified. In this work, the development of two new types of dressings based on poly(3-hydroxyoctanoate) (P(3HO)) is presented. One of the groups was supplemented with conjugates of an anti-inflammatory substance (diclofenac) that was covalently linked to oligomers of hydroxycarboxylic acids (Oli-dicP(3HO)). The novel dressings were prepared using the solvent casting/particulate leaching technique. To our knowledge, this is the first paper in which P(3HO)-based dressings were used in mice wound treatment. The results of our research confirm that dressings based on P(3HO) are safe, do not induce an inflammatory response, reduce the expression of pro-inflammatory cytokines, provide adequate wound moisture, support angiogenesis, and, thanks to their hydrophobic characteristics, provide an ideal protective barrier. Newly designed dressings containing Oli-dicP(3HO) can promote tissue regeneration by partially reducing the inflammation at the injury site. To conclude, the presented materials might be potential candidates as excellent dressings for wound treatment.     

Oligomerization of Human Cystatin C—An Amyloidogenic Protein: An Analysis of Small Oligomeric Subspecies

Human cystatin C (HCC), an amyloidogenic protein, forms dimers and higher oligomers (trimers, tetramers and donut like large oligomers) via a domain-swapping mechanism. The aim of this study was the characterization of the HCC oligomeric states observed within the pH range from 2.2 to 10.0 and also in conditions promoting oligomerization. The HCC oligomeric forms obtained in different conditions were characterized using size exclusion chromatography, dynamic light scattering and small-angle X-ray scattering. The marked ability of HCC to form tetramers at low pH (2.3 or 3.0) and dimers at pH 4.0–5.0 was observed. HCC remains monomeric at pH levels above 6.0. Based on the SAXS data, the structure of the HCC tetramer was proposed. Changes in the environment (from acid to neutral) induced a breakdown of the HCC tetramers to dimers. The tetrameric forms of human cystatin C are formed by the association of the dimers without a domain-swapping mechanism. These observations were confirmed by their dissociation to dimers at pH 7.4.     

Congo Red as a Supramolecular Carrier System for Doxorubicin: An Approach to Understanding the Mechanism of Action

The uptake and distribution of doxorubicin in the MCF7 line of breast-cancer cells were monitored by Raman measurements. It was demonstrated that bioavailability of doxorubicin can be significantly enhanced by applying Congo red. To understand the mechanism of doxorubicin delivery by Congo red supramolecular carriers, additional monolayer measurements and molecular dynamics simulations on model membranes were undertaken. Acting as molecular scissors, Congo red particles cut doxorubicin aggregates and incorporated them into small-sized Congo red clusters. The mixed doxorubicin/Congo red clusters were adsorbed to the hydrophilic part of the model membrane. Such behavior promoted transfer through the membrane.