Quantifying the Impact of Biopics on Wikipedia Articles

Wikipedia is known for its extensive and comprehensive knowledge of multifarious topics. These topics are maintained as articles along with a history of versions of these articles, these versions are also known as revisions. Revisions are the results of edits made by various users. Here, the authors analyze biographical Wikipedia articles, mainly biographies that have a movie based on them re- leased after the year 2010. The authors look at the impact of the movie release on its corresponding biography article on Wikipedia by looking at various metrics of each revision in a Wikipedia article and analyze how the revisions closer to the movie’s release date compare with the rest of the revisions. The results show that quality and content in Wikipedia articles increases significantly during the release time frame of corresponding biopics. The authors believe their work will stimulate more research in the direction of understanding Wikipedia’s relationship with its allied portals.

Quantifying the Impact of Biopics on Wikipedia Articles

Wikipedia is known for its extensive and comprehensive knowledge of multifarious topics. These topics are maintained as articles along with a history of versions of these articles, these versions are also known as revisions. Revisions are the results of edits made by various users. Here, the authors analyze biographical Wikipedia articles, mainly biographies that have a movie based on them re- leased after the year 2010. The authors look at the impact of the movie release on its corresponding biography article on Wikipedia by looking at various metrics of each revision in a Wikipedia article and analyze how the revisions closer to the movie’s release date compare with the rest of the revisions. The results show that quality and content in Wikipedia articles increases significantly during the release time frame of corresponding biopics. The authors believe their work will stimulate more research in the direction of understanding Wikipedia’s relationship with its allied portals.

Regulation of the intermittent release of giant unilamellar vesicles under osmotic pressure

Osmotic pressure can break the fluid balance between intracellular and extracellular solutions. In hypo-osmotic solution, water molecules, which transfer into the cell and burst, are driven by the concentrations difference of solute across the semi-permeable membrane. The complicated dynamic processes of the intermittent burst have been previously observed. However, the underlying physical mechanism has yet to be thoroughly explored and analyzed. Here, the intermittent release of inclusion in giant unilamellar vesicles was investigated quantitatively, applying the combination of experimental and theoretical methods in the hypo-osmotic medium. Experimentally, we adopted highly sensitive EMCCD to acquire intermittent dynamic images. Notably, the component of the vesicle phospholipids affected the stretch velocity, and the prepared solution of the vesicle adjusted the release time. Theoretically, we chose equations numerical simulations to quantify the dynamic process in phases and explored the influence of physical parameters such as bilayer permeability and solution viscosity on the process. It was concluded that the time taken to achieve the balance of giant unilamellar vesicles was highly dependent on the structure of the lipid molecular. The pore lifetime was strongly related with the internal solution environment of giant unilamellar vesicles. The vesicle prepared in viscous solution accessed visualized long-lived pore. Furthermore, the line tension was measured quantitatively by the release velocity of inclusion, which was in the same order of magnitude as the theoretical simulation. In all, the experimental values well matched the theoretical values. Our investigation clarified the physical regulatory mechanism of intermittent pore formation and inclusion release, which had an important reference for the development of novel technologies such as gene therapy based on transmembrane transport as well as controlled drug delivery based on liposomes.

Effects of Pressure and Coal Rank on the Oxy-Fuel Combustion of Pulverized Coal

Pressurized oxy-fuel combustion technology is the second generation of oxy-fuel combustion technology and has low energy consumption and low cost. In this research, a visual pressurized flat-flame reaction system was designed. A particle-tracking image pyrometer (PTIP) system based on a high-speed camera and an SLR camera was proposed. Combining the experimental system and data-processing method developed, the ignition and combustion characteristics of a single coal particle between 69 and 133 μm in size were investigated. The results indicated that at atmospheric pressure, the ignition delay time of ShanXi (SX) anthracite coal was longer than that of ShenHua (SH) bituminous coal, while that of PRB sub-bituminous coal was the shortest. As the pressure rose, the ignition delay time of the PRB sub-bituminous coal and SX anthracite coal showed a continuous increasing trend, while the ignition delay time of SH bituminous coal showed a trend of first increasing and then decreasing. Moreover, pressure also affects the pyrolysis process of coal. As the pressure increases, it became more difficult to release the volatiles produced by coal pyrolysis, which reduced the release rate of volatiles during the ignition stage, and prolonged the release time and burning duration time of volatiles.

The Interactions and Release Kinetics of Sodium Hyaluronate Implemented in Nonionic and Anionic Polymeric Hydrogels, Studied by Immunoenzymatic ELISA Test

Hyaluronan is a natural polymer that was introduced to wound therapy. Formulations based on synthetic polymers such as methylcellulose (MC) and polyacrylic acid (PA) containing hyaluronan (HA) were proposed for the development of prospective wound-healing preparations. The formulations of different carrier concentrations containing a fixed amount of HA were prepared, and their viscosity was measured. The HA release was evaluated by employing the apparatus paddle over a disc. The hydrogels were introduced to the donor chamber, and HA was released to the pH = 7.4 buffer. The amount of HA released was obtained using the ELISA test. The release was analyzed on the basis of different kinetic models: zero-, first-, and second-order kinetics, as well as Higuchi and Korsmeyer–Peppas equations. The release rate constants and the half release time were calculated from these equations. According to the value of the coefficient of the determination, the best model describing the observed process was selected. The comparison between the dissolution profiles was carried out by calculating the difference factor f1 and the similarity factor f2. The interaction between the hydrogel components was investigated by Fourier-transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC) measurements. The study revealed that the zero-order equation best described the release of HA from the formulations studied. The FTIR research and the DSC study showed the intermolecular interaction between HA chains in MC-based compositions, as well as between HA and the synthetic polymer in the PA-based formulations. The study revealed that the formulation with a higher concentration of synthetic polymer may prolong the release of HA. The obtained results indicated that the proposed hydrogels have potential for wound healing and may accelerate skin regeneration.

“Smart” Polylactic Acid Films with Ceftriaxone Loaded Microchamber Arrays for Personalized Antibiotic Therapy

Bacterial infections are a severe medical problem, especially in traumatology, orthopedics, and surgery. The local use of antibiotics-elution materials has made it possible to increase the effectiveness of acute infections treatment. However, the infection prevention problem remains unresolved. Here, we demonstrate the fabrication of polylactic acid (PLA) “smart” films with microchamber arrays. These microchambers contain ceftriaxone as a payload in concentrations ranging from 12 ± 1 μg/cm2 to 38 ± 8 μg/cm2, depending on the patterned film thickness formed by the different PLA concentrations in chloroform. In addition, the release profile of the antibiotic can be prolonged up to 72 h in saline. At the same time, on the surface of agar plates, the antibiotic release time increases up to 96 h, which has been confirmed by the growth suppression of the Staphylococcus aureus bacteria. The efficient loading and optimal release rate are obtained for patterned films formed by the 1.5 wt % PLA in chloroform. The films produced from 1.5 and 2 wt % PLA solutions (thickness—0.42 ± 0.12 and 0.68 ± 0.16 µm, respectively) show an accelerated ceftriaxone release upon the trigger of the therapeutic ultrasound, which impacted as an expansion of the bacterial growth inhibition zone around the samples. Combining prolonged drug elution with the on-demand release ability of large cargo amount opens up new approaches for personalized and custom-tunable antibacterial therapy.

A Combinatorial 2-Approximation Algorithm for the Parallel-Machine Scheduling with Release Times and Submodular Penalties

In this paper, we consider parallel-machine scheduling with release times and submodular penalties (P|rj,reject|Cmax+π(R)), in which each job can be accepted and processed on one of m identical parallel machines or rejected, but a penalty must paid if a job is rejected. Each job has a release time and a processing time, and the job can not be processed before its release time. The objective of P|rj,reject|Cmax+π(R) is to minimize the makespan of the accepted jobs plus the penalty of the rejected jobs, where the penalty is determined by a submodular function. This problem generalizes a multiprocessor scheduling problem with rejection, the parallel-machine scheduling with submodular penalties, and the single machine scheduling problem with release dates and submodular rejection penalties. In this paper, inspired by the primal-dual method, we present a combinatorial 2-approximation algorithm to P|rj,reject|Cmax+π(R). This ratio coincides with the best known ratio for the parallel-machine scheduling with submodular penalties and the single machine scheduling problem with release dates and submodular rejection penalties.

An overview of Natural Superdisintegrants

The oral route is the most convenient route of administration for various drugs. It is viewed as the most convenient, most secure, and economical route for patients. Fast disintegrating tablets are popular these days as they disintegrate in the mouth within a few seconds without the use of water. The burdens of regularly used medications in pediatric and geriatric patients have been overwhelmed by quick-dissolving tablets. Natural superdisintegrants have been used for fast-dissolving tablets because they are biodegradable, chemically inert, non-harmful, more affordable, and generally accessible. Natural polymer improves the properties of the tablet as it is commonly used as diluents and binders. Natural super disintegrants decrease the release time and give healthful results to the patients. Most polymers are obtained from nature, they are cost-effective, non-toxic, and non-irritants. Disintegration is the most important step for releasing the drug from the tablet matrix to decrease the disintegration time. In this, drug and polymers come in contact with water, it swells, hydrate, and react chemically to release the drug in the mouth and gastrointestinal tract. Superdisintegrants are those substances that encourage the quick breaking down with a lesser amount contrasted with disintegrants. The quick disintegrants tablets are set up by utilizing suitable polymers which rely on the Physico-chemical properties of drugs and excipients, for example, drug and polymer compatibility, hardness and thickness of tablet, nature of drug and excipients, PH of drug and release parameters of drug formulation. Superdisintegrants are the vehicles added to tablet formulation to advance the breaking of tablets and capsules into small microparticles in aqueous media resulting in to increase in the surface area and promote quick drug release. The disintegrants have a significant capacity to oppose the efficacy of tablet binders and compression forces to form the tablet. Commonly there are three methods to incorporate disintegrants into the tablet: A. Inner addition, B. External expansion, C. Internal, and external addition. Most of the regularly based tablets are those expected to be swallow, disintegrate and release medicaments in the gastrointestinal tract but over a while tablets are manufactured to deliver medicaments in the mouth and gastrointestinal tract within few seconds of swallowing. It has been demonstrated that characteristic polymers are more effective than synthetic polymers. Some research is going to develop safe and effective medication with super disintegrating agents that can be dissolved rapidly to treat the disease.

Kepadatan populasi dan waktu efektif pelepasan tungau predator Neoseiulus longispinosus Evans untuk pengendalian Tetranychus kanzawai Kishida

Kanzawa spider mite, Tetranychus kanzawai Kishida (Tetranychidae) is one of the most important pest mite in Indonesia. This mite is known as the pest of many crops, including cassava. Neoseiulus longispinosus Evans (Phytoseiidae) is a predatory mite commonly found on plant infested by kanzawa spider mite. This predatory mite has high potential to be developed as biological control agent of T. kanzawai. The aim of this research is to elucidate the effective density and release time of N. longispinosus to control T. kanzawai on cassava. The research was conducted in the greenhouse, using cassava of Mentega cultivar. T. kanzawai were introduced into the cassava plants two weeks after planting, with density 5 female adults/plants. N. longispinosus were introduced 1, 2, and 3 weeks after T. kanzawai introduction with predator:prey ratio of 0:5, 1:5, 2:5, dan 3:5, respectively. Population of T. kanzawai and N. longispinosus, and also plant damage were observed at 6 weeks after planting. N. longispinosus could suppress T. kanzawai population and the highest suppression occurred at the interaction between 3:5 ratio and the release time at one week after T. kanzawai infestation. There was no significant effect of N. longispinosus release at various release ratio and time on attack intensity of T. kanzawai.

Formation mechanism of carbide slag composite sustained-alkalinity-release particles for the source control of acid mine drainage

Acid mine drainage (AMD) has caused serious and long-lasting damage to the environment in many countries. Preventing AMD formation at the source is considered the most direct and effective method of remediation. Carbide slag, an industrial waste, is a potential AMD treatment material due to its strong alkalinity. However, applying carbide slag at the source carries difficulties due to its rapid release of alkalinity. This is the first attempt to mix carbide slag with bentonite to prepare sustained-alkalinity-release particles for source control of AMD. The size of Ca(OH)2 crystallites is decreased from 267 to 211 nm, and the reduced part forms calcium silicate hydrate gel (C–S–H) between the carbide slag and bentonite. C–S–H encapsulated on the surface of the carbide slag, increasing the mechanical strength of the particles, and achieving slow release of alkalinity. The suggested optimum preparation conditions for the particles are as follows: bentonite-to-carbide slag mass ratio of 3:7, Na2CO3 dose of 10 wt%, and calcination temperature of 500 °C for 1 h. The particles can remove 105 mg/g Cu2+ within 12 h, and the loss rate is only 7.4%. The alkalinity release time of the particles is 4 times greater than that of carbide slag.