Aetiology and Pathogenesis of Cutaneous Melanoma: Current Concepts and Advances

Melanoma develops from malignant transformations of the pigment-producing melanocytes. If located in the basal layer of the skin epidermis, melanoma is referred to as cutaneous, which is more frequent. However, as melanocytes are be found in the eyes, ears, gastrointestinal tract, genitalia, urinary system, and meninges, cases of mucosal melanoma or other types (e.g., ocular) may occur. The incidence and morbidity of cutaneous melanoma (cM) are constantly increasing worldwide. Australia and New Zealand are world leaders in this regard with a morbidity rate of 54/100,000 and a mortality rate of 5.6/100,000 for 2015. The aim of this review is to consolidate and present the data related to the aetiology and pathogenesis of cutaneous melanoma, thus rendering them easier to understand. In this article we will discuss these problems and the possible impacts on treatment for this disease.     

On the use of ball milling to develop PHBV–graphene nanocomposites (I)—Morphology,thermal properties,and thermal stability

In the first part of this work, novel nanocomposites based on poly (3‐hydroxybutyrate co‐3‐hydroxyvalerate) (PHBV) and functionalized graphene nanosheets (FGS) were prepared through ball milling. As revealed by morphological characterization, this blending methodology was able to allow proper nanofiller dispersion and distribution into the matrix. Thermal properties were studied under non‐isothermal and isothermal conditions and the addition of FGS into PHBV matrix, although no changes in crystallization mechanism were observed, it modified the crystallization kinetics leading to increased crystallinity. Thermal stability analysis revealed that FGS affected the mechanism of oxidative thermal degradation and had no effect on thermal degradation by pyrolysis. Furthermore, an analysis of isothermal degradation kinetics showed that FGS speeded up the degradation rate. The Sestak‐Berggren model was used as a model to explain the isothermal degradation behavior of the obtained materials in good agreement with the experimental data. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42101.     

Progress on large area n‐type silicon solar cells with front laser doping and a rear emitter

We report on the progress of imec's n‐type passivated emitter, rear totally diffused rear junction silicon solar cells. Selective laser doping has been introduced in the flow, allowing the implementation of a shallow diffused front surface field and a reduction of the recombination current in the contact area. Simplifications have been implemented towards a more industrial annealing sequence, by replacing expensive forming gas annealing steps with a belt furnace annealing. By applying these improvements, together with an advanced texturing process and emitter passivation by atomic layer deposition of Al₂O₃, 22.5% efficient cells (three busbars) have been realized on commercial 156 · 156 mm² Czochralski‐Si. This result has been independently confirmed by ISE CalLab. Copyright © 2016 John Wiley & Sons, Ltd.     

Attaching Different Kinds of Proteinaceous Nanospheres to a Variety of Fabrics Using Ultrasound Radiation

The application of a rapid, non-destructive, cost-effective technique such as ultrasonic emulsification for the coating of different textiles was explored. The technical benefits for this research were the generation of multifunctional materials and their combinations through environmentally friendly processing technologies. We have shown for the first time that ultrasonic waves can be used to coat proteinaceous micro- and nanospheres (PM) of BSA (Bovine Serum Albumin) protein and casein on the surface of cotton and polyester (PE) fabrics. The creation and the anchoring of the microbubbles to the fabrics were performed by a one-step reaction, and the process is usually stopped after 3 min. The PM of bovine serum albumin (BSA) bonded to cotton and polyester fabrics has shown stability for ∼9 months. The PMs were shown to be attached more strongly to the polyester than to the cotton, and sustained stronger washing conditions on PE. The diameter of the BSA and the casein spheres on cotton was in the range of 0.8–1.0 μm, while on the PE it varied between 60 and 120 nm.     

Design of an aquatic biomonitoring network for an environmental specimen bank

The aim of the present study was to establish an aquatic biomonitoring network for the Galician Environmental Specimen Bank (BEAG) (NW Spain). For this, a sampling system was designed that comprised of 121 points distributed throughout Galician rivers, from which samples of water and of three species of bryophytes were collected. The results obtained allowed selection of 74 sampling points and 2 species (Fontinalis antipyretica Hedw. and F. squamosa Hedw.) as the most suitable for use in future BEAG sampling surveys. The two species selected showed a strong similarity in their capacity to accumulate the 17 elements determined (Al, As, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, Pb, Se and Zn), as well as in their ecological preferences. Furthermore, the levels of contamination of epicontinental waters were lower than those observed in previous surveys.     

Browning Inhibition in Fresh-cut'Fuji'Apple Slices by Natural Antibrowning Agents

ABSTRACT Response surface methodology was used to study the effect of antibrowning agents (4‐hexylresorci‐nol, glutathione, N‐acetylcysteine, and ascorbic acid) and storage time (14 d) on the color of minimally processed Fuji apples. The selected color parameters were L*,a*, b*, hue angle (h*), and color difference (ΔE*). Storage time had a significant effect on all the studied color parameters (P± 0.05). 4‐hexylresorcinol showed the most effective individual effect on keeping constant a*values (P± 0.0001). Besides, the interaction of N‐acetylcysteine/ glutathione was found to have a significant effect (P± 0.05) on maintaining a* values over time. On the other hand, individual treatment with N‐acetylcysteine in concentrations higher than 0.75% w/v may be used to preserve a*and h*.According to the F‐test, 4‐hexylresorcinol and N‐acetylcysteine (P± 0.05) displayed a significant individual effect on ΔE*, indicating that ΔE* decreased when increasing the concentration of these antibrowning agents. Nevertheless, color difference went down when 4‐hexylresorcinol concentration increased up to 0.5%, but higher concentrations of this agent led to an increase in ΔE* that indicates browning.     

Cucurbiturils as Versatile Receptors for Redox Active Substrates

Research on the chemistry of cucurbit[n]uril (CBn) hosts has picked up and maintained an impressive pace in the last decade, primarily due to the isolation of hosts with relatively larger cavity sizes, such as CB7 and CB8. This review article summarizes our involvement in this research effort, with particular emphasis on the binding of redox active guests by the CB7 and CB8 hosts. The binding of 4,4′-bipyridinium (viologen) derivatives was the starting point of our CB research. While methylviologen is encapsulated by CB7, forming a highly symmetric inclusion complex, more hydrophobic viologens are bound by inclusion of one of the terminal N-substituents inside the host cavity. Cationic ferrocene derivatives reach extremely high binding affinities with CB7. Binding by CB8 offers additional possibilities, since this host may accommodate two aromatic units inside its cavity, which can be utilized to exert redox control on the assembly of suitably dendronized guests. From a purely electrochemical standpoint, CB7-included viologens maintain their voltammetric reversibility, but CB7-included ferrocene residues experience a pronounced attenuation of their electron transfer kinetics. We have also applied these binding and electrochemical properties to the design and preparation of switchable, CB-based pseudorotaxanes.     

Effect of the sintering additive content on the protective passive oxidation behaviour of pressureless liquid-phase-sintered SiC

The long-term oxidation behaviour in air of pressureless liquid-phase-sintered SiC was investigated as a function of the sintering-additive content (a mixture of Y₂O₃ and Al₂O₃ in the 3:5 molar ratio) at oxidizing temperatures in the interval 1100–1300 °C. It is shown that oxidation under these mild conditions is always passive, and with formation of protective oxide scales. However, the oxidation kinetics cannot be described appropriately by the parabolic-rate law. Instead, due to the gradual crystallization of the oxide scales during oxidation, it is more complex, exhibiting two different stretches given respectively by the arctan- and parabolic-rate laws. Furthermore, it was found that the rate-limiting mechanism of the initial arctan oxidation is the outward diffusion of metal cations from the secondary intergranular phase into the oxide scale, with the activation energy of the oxidation being very high and decreasing from 545 to 432 kJ/mol with increasing sintering-additive content from 5 to 20 wt%. The rate-limiting mechanism of the subsequent parabolic oxidation is however the inward diffusion of oxygen through the multicomponent oxide scale, with the activation energy being lower than before and also decreasing from 345 to 205 kJ/mol as the sintering-additive content increases from 5 to 20 wt%. It is also shown that the oxidation resistance decreases with increasing sintering-additive content, but that while the decrease is moderate up to 10 wt%, it is very marked for greater contents.