Self-Assembling Properties and Recovery Effects on Damaged Skin Cells of Chemically Synthesized Mannosylerythritol Lipids

Mannosylerythritol lipids (MELs), which are one of the representative sugar-based biosurfactants (BSs) produced by microorganisms, have attracted much attention in various fields in the sustainable development goals (SDGs) era. However, they are inseparable mixtures with respect to the chain length of the fatty acids. In this study, self-assembling properties and structure-activity relationship (SAR) studies of recovery effects on damaged skin cells using chemically synthesized MELs were investigated. It was revealed, for the first time, that synthetic and homogeneous MELs exhibited significant self-assembling properties to form droplets or giant vesicles. In addition, a small difference in the length of the fatty acid chains of the MELs significantly affected their recovery effects on the damaged skin cells. MELs with medium or longer length alkyl chains exhibited much higher recovery effects than that of C18-ceramide NP.     

Metastatic Voyage of Ovarian Cancer Cells in Ascites with the Assistance of Various Cellular Components

Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy and has a unique metastatic route using ascites, known as the transcoelomic root. However, studies on ascites and contained cellular components have not yet been sufficiently clarified. In this review, we focus on the significance of accumulating ascites, contained EOC cells in the form of spheroids, and interaction with non-malignant host cells. To become resistant against anoikis, EOC cells form spheroids in ascites, where epithelial-to-mesenchymal transition stimulated by transforming growth factor-β can be a key pathway. As spheroids form, EOC cells are also gaining the ability to attach and invade the peritoneum to induce intraperitoneal metastasis, as well as resistance to conventional chemotherapy. Recently, accumulating evidence suggests that EOC spheroids in ascites are composed of not only cancer cells, but also non-malignant cells existing with higher abundance than EOC cells in ascites, including macrophages, mesothelial cells, and lymphocytes. Moreover, hetero-cellular spheroids are demonstrated to form more aggregated spheroids and have higher adhesion ability for the mesothelial layer. To improve the poor prognosis, we need to elucidate the mechanisms of spheroid formation and interactions with non-malignant cells in ascites that are a unique tumor microenvironment for EOC.     

Synthesis of Dense Lead Titanate Ceramics with Submicrometer Grains by Spark Plasma Sintering

Dense PbTiO₃ ceramics consisting of submicrometer-sized grains were prepared using the spark-plasma-sintering (SPS) method. Hydrothermally prepared PbTiO₃ (0.1 μm) was used as a starting powder. The powder was densified to ≳98% of the theoretical X-ray density by the SPS process. The average grain size of the spark-plasma-sintered ceramics (SPS ceramics) was ≲1 μm, even after sintering at 900°–1100°C, because of the short sintering period (1–3 min). The measured permittivity of the SPS ceramics showed almost no frequency dependence over the range 10¹–10⁶ Hz, mainly because pores were absent from the ceramics. The coercive field of the SPS ceramics was somewhat higher than that of conventionally sintered ceramics, which could be attributed to the small-grained microstructures of the SPS ceramics.     

Formation of needle‐like lepidocrocite fine particles by oxidation of an aqueous suspension of ferrous hydroxide in a bubble column

Fine particles of needle‐like lepidocrocite (γ‐FeOOH) were synthesized by the oxidation of aqueous suspensions of ferrous hydroxide using a bubble column with draft tube at a constant temperature ranging from 20°C to 30°C. The oxidation steps leading to green rust (an intermediate) and lepidocrocite (final product), termed Step I and II, respectively, could be described apparently as first order, with respect to oxygen, and zero order, with respect to total ferrous species. When the concentration of oxygen in the feed stream was varied under a constant gas velocity, the mean size based on the major axis of needle‐like particle decreased from 0.60 to 0.35 μm with increasing oxidation rate. When the gas velocity was varied under a constant oxygen concentration, the particle size was almost independent of the oxidation rate and was equal to ca. 0.6 μm. By the addition of a small amount of sodium dihydrogenphosphate (NaH₂PO₄), the major axis could be reduced to 0.2 μm with the minor axis and the oxidation rate almost unchanged.     

H2O-tolerant monolithic catalysts for preferential oxidation of carbon monoxide in the presence of hydrogen

Pt–Fe/mordenite (4 wt% Pt–0.5 wt% Fe) powder catalysts were wash-coated onto ceramic straight-channel monoliths by using silica- and/or alumina-sol as a binder, and were evaluated for the preferential oxidation of carbon monoxide (PROX) in a hydrogen-rich gas. In a synthetic reformate gas (1% CO, 1% O₂, 5% H₂O, 20% CO₂, and balance H₂), the CO concentration was reduced to less than 20 ppm at temperatures ranging from 100 to 130 °C. After a certain period of the PROX reaction, condensation of H₂O in the pores of the mordenite-support occurred over the monolithic catalyst, which was wash-coated with alumina-sol, in the lower temperature range (100–120 °C), resulting in a rapid increase in CO concentration. The monolithic catalyst wash-coated with silica-sol, however, showed an excellent tolerance against H₂O condensation and offered a stable catalytic performance, maintaining a CO concentration of ca. 20 ppm for 200 h. The H₂O-tolerant characteristic was attributed to the relatively small adsorption amount of H₂O over the silica-modified monolithic catalyst.     

Photocatalytic Inactivation of Legionella Pneumophila and an Aerobic Bacteria Consortium in Water over TiO2/SiO2 Fibres in a Continuous Reactor

A continuous photoreactor, working in a total recycle mode and irradiated by a low-pressure Hg lamp, has been used to study the bactericidal effect of a photocatalyst, formed by TiO₂ embedded in SiO₂ fibres, on Legionella pneumophila and a consortium of common gram-negative aerobic bacteria: (Escherichia coli, Klebsiella sp., Pseudomona sp. and Proteus sp.) in water. The kinetic modeling of the inactivation process, carried out with the measured values of viable bacteria concentration at the outlet of photoreactor, evidenced that for each pass inside the photoreactor the ratio between the outlet and inlet cell concentrations was of order of 0.01 for the inactivation of L. pneumophila. For the other aerobic bacteria, which are usually taken as reference in photocatalytic bacteria inactivation studies, this ratio was of order of 0.3 for the first hour of illumination, while upon prolonged irradiation (up to 9 h) this ratio increased to 0.7. Several factors inducing this latter decrease of efficiency are possible, as e.g. competition for photocatalytic attack between microorganisms and organic compounds released by damaged bacteria or photoinduced alteration of a small fraction of still viable bacteria making them less interactive with the photocatalyst. The inactivation mechanism normally proposed for common bacteria involves an initial attack of the photogenerated radicals to the outer membrane; the consequent membrane dispersion allows the radicals to damage the cytoplasmic membrane. The higher lethality of the photocatalytic method observed towards Legionella: (in comparison to the other aerobic bacteria) is explained considering that the radicals attack the Legionella secretion system, which is adapted for high virulence and would become activated for and through adhesion to the TiO₂ surface. This attack would then be able to inactivate L. pneumophila without dispersing the outer membrane. Apart from this, the water flow through the catalyst fibres can facilitate the bacteria transport towards the anatase surface, and additionally the generated shear stress may help adhesion, at least for some bacteria as E. coli, contributing further to improve the photokilling efficiency; both factors may contribute to the efficiency of this photoreactor configuration.     

铝合金局部加压凝固及流动数值模拟的研究

局部加压方法是压铸中用于消除铸件厚壁处缩孔缺陷的一种新工艺.本研究通过实验模型测量了不同加压条件下铸件的冷却曲线,分析了局部加压引起的凝固变化.考虑局部加压引起的补缩流动,通过适时修改网格文件、初始和边界条件的方法,模拟了局部加压过程中铝合金的凝固及流动变化,并与实验结果进行了对比,二者基本吻合.     

The effect of thickness on the steady-state creep properties of freestanding aluminum nano-films

To clarify the effects of film thickness on the creep properties of nano-films we conducted tensile creep experiments on freestanding aluminum films with thickness values in the range ～100–800 nm at room temperature. The nano-films showed typical creep behavior comprising transient, steady-state, and accelerated creep stages. The steady-state creep exponents of the 100–800 nm thick specimens were 0.84–2.7 in the stress range 30–120 MPa, which are close to the value for diffusion creep (1). Creep deformation clearly shows a thickness effect: the steady-state creep rate increases as the thickness decreases from 800 to 400 nm, shows a peak in the range 400–200 nm, and then decreases in the 200–100 nm thickness range. The creep experiments under a small stress of 1 MPa show a negative strain rate, indicating the presence of a driving force to reduce the surface area due to surface tension. The explanation for the thickness effect is as follows. Since the ratio of surface and grain boundary area to volume increases with decreasing thickness, diffusion creep along these paths is enhanced, resulting in an increase in the creep rate. As the thickness decreases to 200–100 nm, however, the surface tension effect to reduce the surface area becomes dominant, decreasing the creep rate. In addition, the creep rate of the nano-films is about two or three orders of magnitude smaller than that of the bulk material dominated by the dislocation creep mechanism.     

Marked Effect of Mo and Fe Addition Upon Liquid Phase Methanol Reforming with Water Over Al2O3 Supported Pt Catalysts

Successively impregnated Pt–Mo/Al₂O₃ and Pt–Fe/Al₂O₃ catalysts exhibited large enhancement effect in H₂ formation rate of liquid phase methanol reforming. Added Mo oxide forms monolayer on Al₂O₃ and facilitates the higher dispersion of Pt particles. In the case of Fe, formation of some surface bimetallic clusters between Pt and Fe was confirmed by XAS analysis, which causes the enhancement effect of H₂ formation in MeOH–H₂O reaction.     

Designed RNAs with Two Peptide‐Binding Units as Artificial Templates for Native Chemical Ligation of RNA‐Binding Peptides

The template effect plays important roles not only in modern synthetic and enzymatic catalysis but also in the ancient “RNA‐polypeptide (RNP) world,” which has been postulated to be a crucial stage in the origin of life. To mimic primitive template catalysis of peptide ligations by RNAs, we previously reported the design and synthesis of a ternary RNP complex in which the ligation of two peptides was significantly facilitated by a template RNA with two peptide‐binding units. However, RNA molecules also promoted the ligation reaction in a nonspecific manner through electrostatic interactions between RNA and basic peptides. In this study, we suppressed this effect by reducing the length of the original template derived from the Tetrahymena intron RNA. This modification, however, decreased the template ability for the specific reaction. As an alternative RNA that was as effective as the original template, we found that a self‐dimerizing RNA was a promising template for peptide ligation without a nonspecific effect.