Synthesis of polypyridine-graft-PEG copolymer for protein repellent and stable interface

Polypyridine grafted with poly(ethylene glycol) (Py-g-PEG) have been synthesized. Radical copolymerization of methyl-terminated PEG macromonomer with 4-pyridylmethyl methacrylate homogeneously proceeded and the obtained copolymer spontaneously adsorbs from aqueous solution onto gold surfaces, where the pyridine parts act as the multipoint anchor to the surface and the PEG parts provide the strong steric repulsion between the chains. As a result, the highly protein repellent and stable surface was constructed through multipoint pyridine attachment as compared with singlepoint pyridine attachment. Py-g-PEGs thus synthesized are promising material to functionalize metal and semiconductor material and to self-assemble into micelle in biotechnological and biomedical field.     

Mechanical properties of As-cast and directionally solidified Nb-Mo-W-Ti-Si <Emphasis Type="Italic">in-situ</Emphasis> composites at high temperatures

To improve the high-temperature strength of Nb-Mo-Ti-Si in-situ composites, alloying with W and a directional solidification technique were employed. The alloy composition of Nb-xMo-10Ti-18Si (x=10 or 20) was used as the base, and Nb was further replaced by 0, 5, 10 and 15 mol pct W. For samples without W, the as-cast microstructure was a eutectic mixture of fine Nb solid solution (Nb _SS ) and (Nb, Me)₅ Si₃ silicide (Me = Mo, W, or Ti), while large primary Nb _SS particles appeared besides the eutectic mixture as a result of replacing Nb by W. The directionally solidified samples consisted of coarse Nb _SS and (Nb,Me)₅ Si₃ silicides, and the microstructure showed a slight orientation in the direction of growth. The maximum compressive ductility (ɛ _max) at room temperature decreased with increasing W content and was in the range of 0.8 to 2.3 pct, in contrast to the Vickers hardness (HV), which increased with W content. The 0.2 pct yield compressive strength (σ _0.2) and the specific 0.2 pct yield compressive strength (σ _0.2S ) (σ _0.2 divided by the density of sample) at elevated temperatures were markedly improved by the W addition. The directionally solidified samples always showed higher σ _0.2 and σ _0.2S values than the as-cast samples. At elevated temperatures, the directionally solidified sample with 10 mol pct Mo and 15 mol pct W had the highest σ _0.2 and σ _0.2S values; even at 1770 K, σ _0.2 was as high as 650 MPa. The directionally solidified materials alloyed with W exhibited excellent compressive creep performance. The sample with 10 mol pct Mo and 15 mol pct W had a minimum creep rate of 1.4×10⁻⁷s⁻¹ and retained steady creep deformation at 1670 K and an initial stress of 200 MPa. Under compression, the damage and failure of these in-situ composites were dominated by decohesion of interfaces between the Nb _SS and silicide matrix.     

Micro-patterned nanofibrous biomaterials

Nanofibrous materials made from bioabsorbable and biocompatible polymers have promising applications as tissue-engineered scaffolds. Genetic analysis of human umbilical vein endothelial cells (HUVEC) that attached to Poly(glycolide) (PGA) nanofibrous materials prepared via electrospinning methods demonstrated high expression of Integrin v and VEGF receptor genes, which are known angiogenesis markers. In order to improve the function of the PGA nanofibrous materials for tissue engineering applications, we used a micro-patterned template instead of a flat collector in the electrospinning process. "Micro-patterned nanofibrous material" demonstrated uniformly sized dents with diameters of 200 micrometers and depths of 36 micrometers. The dents were regularly spaced, with a 250 micrometer space between two dents. These sizes are similar to that of the template. We will discuss further applications of this designable micro-patterned nanofibrous biomaterial.     

Prospective Validation of High-Shear Wet Granulation Process by Wet Granule Sieving Method. II. Utility of Wet Granule Sieving Method

The general utility of a method for determination of high-shear wet granulation end point by monitoring the wet granule particle size distribution was evaluated. Wet granulation was conducted in a 25-liter high-shear mixer using four model drugs with different solubilities and particle sizes (ethenzamide, unmilled and milled acetaminophen, and antipyrine). For each drug formulation, its wet granule particle size fraction and target range for granulation end point determination were selected based on the tablet characteristics that are known to be influenced by the wet granulation process. Granules manufactured under different conditions (i.e., different main and chopper blade speeds and binder supplying rate) but manufactured to the same granulation end point determined by the selected fraction and range showed very similar granule characteristics and subsequently very similar tabler characteristics. From the fact that there was a good correlation between the wet and dry-sized granule particle size distributions even if the drying method was changed from fluid-bed drying to vacuum drying, the general application of the end point determining method was verified. Further, the method was shown to be sensitive to the critical granulation parameters for granulation progression and to be very capable of determining the granulation extent. Thus, it was suggested that the method is applicable to various drugs and formulations for determination of wet granulation end point.     

Effects of tungsten addition on tensile properties of a refractory Nb−18Si−10Ti−10Mo−<Emphasis Type="Italic">x</Emphasis>W (<Emphasis Type="Italic">x</Emphasis>=0,5, 10 and 15 mol.%)<Emphasis Type="Italic">in-situ</Emphasis> Composites at 1670 K

To investigate the effect of tungsten addition on mechanical properties, we prepared refractory (62−x)Nb−18Si−10Mo−10Ti−xW (x=0, 5, 10 and 15 mol.%)in-situ composites by the conventional arc-casting technique, and then explored the microstructure, hardness and elastic modulus at ambient temperature and tensile properties at 1670 K. The microstructure consists of relatively fine (Nb, Mo, W, Ti)₅Si₃ silicide and a Nb solid solution matrix, and the fine eutectic microstructure becomes predominant at a Si content of around 18 mol.%. The hardness of (Nb, Mo, W, Ti)₅Si₃ silicide in a W-free sample is 1680 GPa, and goes up to 1980 GPa in a W 15 mol.% sample. The hardness, however, of Nb solid solution does not exhibit a remarkable difference when the nominal W content is increased. The elastic modulus shows a similar tendency to the hardness. The optimum tensile properties of the composites investigated are achieved at W 5 mol.% sample, which exhibits a relatively good ultimate strength of 230 MPa and an excellent balance of yield strength of 215 MPa, and an elongation of 3.7%. The SEM fractography generally indicates a ductile fracture in the W-free sample, and a cleavage rupture in W-impregnated ones.     

Application of 3-D models to computer vision

A flexible computer vision is described which is able to recognize 3-D objects if their models are given. The models can be built in a CAD process using a geometric modeler GEOMAP. Three cases are studied: surface normals are available, a part of surface normals are available, and range data is available. In order to perform efficient matching, three methods are proposed for those cases: use of EGI representation, use of relative angles between surface normals, and use of kernels.     

Sc(OTf)3-catalyzed Cyclooligomerization of 2,4-Dialkoxybenzyl Alcohols. Formation of Resorcin[n]arene Peralkyl Ethers

Summary The cyclooligomerization of 2,4-dialkoxybenzyl alcohols 3 catalyzed by Sc(OTf)₃ in CH₃CN under high dilution conditions produced a series of resorcin[n]arene peralkyl ethers containing four to nine resorcinol units. When the reactions were conducted at 50°C, the cyclic tetramers 4, which are thermodynamically favored products, are selectively formed in good yields. It is noteworthy that the reaction of 2,4-dimethoxybenzyl alcohol 3d at 0°C produced the corresponding cyclic octamer 8d as the major product. In other cases, such as the selective formation of a cyclic octamer could not be observed. This selective formation of 8d is due to a combination of the reversibility of the oligomerization in the presence of 3d and the insolubility of the octamer in the reaction medium. The conformational analysis of these cyclic oligomers was done by variable temperature ¹H NMR spectroscopy.     

Direct measurement of energetic electron flow in Q-shu University experiment with steady-state spherical tokamak

In magnetized plasmas, the presence of a significant number of energetic electrons has been observed but quantitative characteristics of these electrons are proving difficult to investigate. A Langmuir probe offers a means to provide quantitative measurement of these energetic electrons that takes into account electron emissions (secondary electron emission and electron reflection) from the probe tips and sheath expansion around the probe tips caused by a considerable negative potential. In this paper, these effects are experimentally confirmed and an analytical means to measure energetic electron characteristics are proposed. An analysis of plasmas produced by a high frequency wave is then applied leading to the successful detection of an asymmetric flow of energetic electrons. The estimated electron temperature and current density were approximately 4-5 keV and 2-3 kA/m(2).     

Purification and identification of a novel and four known serine proteinase inhibitors secreted by human glioblastoma cells

Our previous studies have shown that some human cancer cell lines produce pancreatic trypsinogen, plasminogen, and tissue-type kallikrein. To understand the regulatory mechanism of these proteinases, serine proteinase inhibitors secreted by human glioblastoma cell line T98G were analyzed by gelatin reverse zymography with trypsin. The serum-free conditioned medium of T98G cells showed more than ten trypsin inhibitor bands ranging from 16 to 150 kDa in the reverse zymography. Major trypsin inhibitors were purified by trypsin-affinity chromatography. Analysis of their N-terminal amino acid sequences demonstrated that the purified inhibitors were identical to the secreted forms of amyloid protein precursors (APPs), tissue factor pathway inhibitor (TFPI), placental protein 5 (PP5)/TFPI-2, and secretory leukocyte proteinase inhibitor (SLPI). In addition, a novel 25-kDa trypsin-binding protein, tentatively named p25TI, was identified. p25TI showed weak inhibitory activity against trypsin in reverse zymography as compared with the other inhibitors. The secretion of multiple forms of serine proteinase inhibitors by human cancer cells raises the possibility that they might be involved in the abnormal growth of cancer cells.     

Reinforcement effects of MWCNT and VGCF in bulk composites and interlayer of CFRP laminates

The reinforcement effects of two nanofillers, i.e., multi-walled carbon nanotube (MWCNT) and vapor grown carbon fiber (VGCF), which are used at the interface of conventional CFRP laminates, and in epoxy bulk composites, have been investigated. When using the two nanofillers at the interface between two conventional CFRP sublaminates, the Mode-I interlaminar tensile strength and fracture toughness of CFRP laminates are improved significantly. The performance of VGCF is better than that of MWCNT in this case. For epoxy bulk composites, the two nanofillers play a similar role of good reinforcement in Young’s modulus and tensile strength. However, the Mode-I fracture toughness of epoxy/MWCNT is much better than that of epoxy/VGCF.