Influence of Particle Size on the Distributions of Liposomes to Atherosclerotic Lesions in Mice

ABSTRACT

In order to confirm the efficacy of liposomes as a drug carrier for atherosclerotic therapy, the influence of particle size on the distribution of liposomes to atherosclerotic lesions in mice was investigated. In brief, liposomes of three different particle sizes (500, 200, and 70 nm) were prepared, and the uptake of liposomes by the macrophages and foam cells in vitro and the biodistributions of liposomes administered intravenously to atherogenic mice in vivo were examined. The uptake by the macrophages and foam cells increased with the increase in particle size. Although the elimination rate from the blood circulation and the hepatic and splenic distribution increased with the increase in particle size in atherogenic mice, the aortic distribution was independent of the particle size. The aortic distribution of 200 nm liposomes was the highest in comparison with the other sizes. Surprisingly, the aortic distribution of liposomes in vivo did not correspond with the uptake by macrophages and foam cells in vitro. These results suggest that there is an optimal size for the distribution of liposomes to atherosclerotic lesions.     

Nondestructive Quantitative Evaluation of Porosity Volume Distribution in Aluminum Alloy Die Castings by Fractal Analysis

The nondestructive and three-dimensional quantitative evaluation of porosity in aluminum alloy die castings is proposed to identify whether the predominant cause of pore formation is shrinkage or entrapped gas. The validity of this method of evaluation was shown by comparing two different regions with different ratios of pores formed by shrinkage and gas. It was shown that the proposed evaluation can be used as a quantitative indication of porosity.     

Overall Adsorption Isotherm of Natural Organic Matter

Adsorption equilibrium data in lumped water quality indices obtained for diluted solutions of a peat water and effluents from a wastewater treatment were analyzed using the ideal adsorbed solution theory with the Freundlich equation. The use of the same value for Freundlich exponent 1∕n in the ideal adsorbed solution theory resulted in a straightforward and less computationally demanding expression to describe an overall batch adsorption isotherm. A fictive component approach, assuming a logarithmic normal distribution of Freundlich K and a nonadsorbable fraction, adequately described and predicted the overall isotherms for different initial concentrations of diluted solutions presented as a lumped water quality index. The parameters in the distributed fictive component approach were independently sensitive to each portion of an isotherm curvature. Preferential adsorption of the smaller molecular weight (MW) components was observed by a size-exclusion high-performance liquid chromatography. Two-dimensional distribution analysis of organics in terms of Freundlich K and MW revealed a weak tendency of the adsorptive strength to decrease with the increase of the MW.     

The separation of fission-product rare elements toward bridging the nuclear and soft energy systems

Based on the present state of the art of the separation technology, recycling of fission-product rare elements (FRE) in the FBR spent fuel is discussed. The rad.-waste fractionation is in accordance with the present society's trend toward zero-emission, and the mean of salt-free method utilizing electrochemistry agrees with the principles of the newly established green chemistry. A catalytic electrolytic extraction method is proposed to separate the target, radioactive but potentially strategic elements, Pd, Ru, Rh, Re (Tc), Te and Se dissolved in the HLLW. It avoids secondary waste arising. This method is particularly feasible for the separation of Pd where cyclic reaction of metal cations such as Pd(II) or Fe(II), acting as promoters or mediators and already contained in HLLW, accelerates the electrochemical deposition of Ru, Rh and Re. Elemental separation not only offers alternative material resources to meet expanding demands for catalysts in Fuel Cell/Soft Energy system but is also the first step for transmutation or other selective strategies for waste management of long-lived fission products (LLFP).     

Zone drawn NEW-TPI thermoplastic polyimide and its blends with Xydar liquid crystalline polymer

In this work we report the effects of single stage zone drawing on the properties of NEW-TPI thermoplastic polyimide homopolymer, and its blends with Amoco's Xydar liquid crystalline polymer. Zone drawing was performed first on homopolymer NEW-TPI films to determine the effect of load weight, heater speed, and drawing temperature on the attainable draw ratio. Degree of crystallinity and chain orientation increase as the draw ratio increases for NEW-TPI. Blends of NEW-TPI/Xydar compositions 90/10 and 70/30 were studied next. In blends, the Xydar component is not molecularly dispersed, and is initially preferentially oriented along the machine direction during the film processing stage. Xydar acts as a nucleation site and lowers the temperature for crystallization of the NEW-TPI from the rubbery amorphous state. Zone drawing was performed either parallel or perpendicular to Xydar's initial preferred orientation direction. Blends with lower Xydar fraction could be zone-drawn to higher ratios. Zone drawing perpendicular to Xydar's initial orientation direction also resulted in increased draw ratio. Dynamic mechanical properties of the zone drawn materials were studied. In homopolymer NEW-TPI, dynamic modulus increased by a factor of two to 4.0 GPa in zone drawn films, largely as a result of the formation of oriented crystallites. In the blends, the modulus parallel to Xydar's initial orientation direction was greater than that in the transverse direction. Depending upon composition and test direction, zone drawing increased the dynamic moduli of the blends from 1.5 up to 2.7 times, in the temperature range from 150°C to 300°C.     

Synthesis of non-equilibrium phases in immiscible metals mechanically mixed by high pressure torsion

The structural changes in mechanically mixed metals of immiscible combinations of elements caused by bulk mechanical alloying (MA) through the use of high pressure torsion (HPT) were investigated in Ag–Ni and Nb–Zr systems. There was no alloying between Ag and Ni on atomic scale even after 100 rotations of HPT. On the other hand, the β-Zr phase started to appear after HPT 2 rotations in the Nb–Zr system, even though β-Zr is a high temperature phase. Further, Nb and Zr were completely mixed to form a bcc structured single phase after HPT 100 rotations. The sequence of alloying in the Nb–Zr system during HPT was discussed. These results clearly suggest that non-equilibrium phases can form in the Nb–Zr system by bulk MA by the use of HPT.     

Enhancement of the hydrophobicity and oleophobicity of a polyurethane coating using a fluorine-free polyfarnesene-based polyol

The development of hydrophobic and oleophobic surfaces on materials has attracted significant attention in various research fields. Fluoropolymers, which possess low surface energy and are both highly hydrophobic and oleophobic in nature, are widely used to enhance the liquid repellency of materials. However, during fluoropolymer manufacture, fluorine-containing compounds are released into the environment; thus, alternatives to fluoropolymers are required for maintaining environmental safety and realizing a sustainable society. Notably, the development of such alternative materials has been limited. Thus, we herein report the application of a novel polyurethane (PU) coating synthesized from bio-based raw materials. The prepared hydrogenated polyfarnesene PU (HHPF PU), which possesses an amorphous bottlebrush-like polyalkyl structure, was found to exhibit higher hydrophobicity and oleophobicity than polytetrafluoroethylene (PTFE), which is a typical low-surface-energy material. The water and n-hexadecane contact angles of the HHPF PU were determined to be 119° and 68°, respectively, whereas those of PTFE were 108° and 46°, respectively. In addition, the density depth profile of the PU thin film was confirmed through x-ray reflectometry. This study provides a novel approach for enhancing the hydrophobicity and oleophobicity of materials using bottlebrush-like polyalkyl structure instead of fluorine.     

The motion capturing of female divers under water and the trial production of motion viewers for developing a virtual diving experience learning system

The virtual diving experience learning system of “Ama”, Japanese traditional female divers, has been developed to simulate how divers move in a virtual space using the diving interface and utilizing an accelerometer and a gyroscope. This interface not only detects the diving motion but also outputs the movement. Diving motion is shown in the ways of hand motion while standing. Although this makes it possible for a learner to understand the divers’ actions more clearly, this system’s difficulty is in visualizing a divers’ actions including their hands or bodies. Therefore, our study focuses on developing the operation system to reproduce actual ways of Amas’ diving with a virtual human body in a virtual space. First, the motion capture was done in an underwater condition. In the next process, the virtual human body was created. Finally, with the motion viewer, the more vivid actions of the Ama were successfully reproduced much more than in previous attempts. Using this system, the effectiveness of the Amas’ movement learning was confirmed, because a learner practices Amas’ movement.     

Characterization of C-S-H from Highly Reactive β-Dicalcium Silicate Prepared from Hillebrandite

β-dicalcium silicate synthesized by thermal dissociation of hydrothermally prepared hillebrandite (Ca₂(SiO₃)(OH)₂) exhibits extremely high hydration activity. Characterization of the hydrates obtained and investigation of the hydration mechanism was carried out with the aid of trimethylsilylation analysis, ²⁹Si magic angle spinning nuclear magnetic resonance, transmission electron microscopy selected area electron diffraction, and XRD. The silicate anion structure of C-S-H consisted mainly of a dimer and a single-chain polymer. Polymerization advances with increasing curing temperature and curing time. The C-S-H has an oriented fibrous structure and exhibits a 0.73-nm dreierketten in the longitudinal direction. On heating, the C-S-H dissociates to form β-C₂S. The temperature at which βC₂S begins to form decreases with increasing chain length of the C-S-H or as the Ca/Si ratio becomes higher. The high activity of β-C₂S is due to its large specific surface area and the fact that the hydration is chemical-reaction-rate-controlled until its completion. As a result, the hydration progresses in situ and C-S-H with a high Ca/Si ratio is formed.