Immunohistochemical quantitation for extracellular matrix proteins in rats with glomerulonephritis induced by monoclonal anti-Thy-1.1 antibody

During clot retraction, platelets interact with fibrin resulting in marked reduction of clot volume. Altered fibrin structure has been reported to affect clot retraction as measured by serum expression. This study was performed to test whether such altered retraction was the result of increased resistance to network collapse or due to decreased force development by platelets. Altered fibrin structure was documented as variation of fibre mass/length ratios (mu) and shifts in clot elastic modulus. The force developed by platelets during clotting was measured directly. Increasing the fibrinogen concentration led to thinner fibre formation (decreased mu), and a linear increase in gel elastic modulus. Over a fibrinogen concentration range of 100 to 400 mg/dl, force development was minimally affected. Force development and clot elastic modulus increased in a linear fashion with increasing platelet concentration. Increasing the calcium concentration from 5 to 20 mM caused a 160% increase in fibrin fibre size (mu), and a 52% decline in clot modulus. Force developed at 1200 s declined by 17%. At 15 mg/ml, dextran and hydroxyethyl starch (HES) also increased mu, and decreased clot modulus; however, both agents markedly reduced force development. Increasing ionic strength or the addition of IgG decreased mu and increased gel elastic modulus. Force development increased modestly with increased ionic strength, did not change with addition of IgG in saline and declined with addition of IgG in maltose. This study indicates that force development is primarily dependent on platelet function while clot modulus depends on both fibrin structure and platelet function.(ABSTRACT TRUNCATED AT 250 WORDS)     

Measurement and correlation of mutual diffusion coefficients for styrene-butadiene rubber(SBR)-n-nonane systems

The mutual diffusion coefficients for styrene-butadiene rubber(SBR)-n-nonane systems were measured using a sorption apparatus with a quartz spring at 100 and 130°C for mass fractions of n-nonane ranging from 0 to 0.16. The mutual diffusion coefficients were correlated with good agreement by the free-volume theory.     

Apatite-forming ability of alginate fibers treated with calcium hydroxide solution

Calcium alginate fibers were prepared by extruding an aqueous sodium alginate solution into an aqueous calcium chloride solution. The fibers were treated with a saturated aqueous calcium hydroxide solution for various periods and their apatite-forming ability was examined in a simulated body fluid (SBF). The calcium alginate fibers were treated with the aqueous calcium hydroxide solution for periods longer than five days formed apatite on their surfaces in SBF, and their apatite-forming ability improved with increasing calcium hydroxide treatment time. The amount of calcium ions released from the fibers also increased with increasing calcium hydroxide treatment time, resulting in acceleration of nucleation and growth of apatite on the fiber surfaces. The resultant apatite-alginate fiber composite is expected to be useful as a flexible bioactive bone-repairing material.     

Reconstruction of a high-resolution image on a compound-eye image-capturing system

The authors have proposed an architecture for a compact image-capturing system called TOMBO (thin observation module by bound optics), which uses compound-eye imaging for a compact hardware configuration [Appl. Opt. 40, 1806 (2001)]. The captured compound image is decomposed into a set of unit images, then the pixels in the unit images are processed with digital processing to retrieve the target image. A new method for high-resolution image reconstruction, called a pixel rearrange method, is proposed. The relation between the target object and the captured signals is estimated and utilized to rearrange the original pixel information. Experimental results show the effectiveness of the proposed method. In the experimental TOMBO system, the resolution obtained is four times higher than that of the unit image that did not undergo reconstruction processing.     

Membranes prepared from keratin–polyacrylonitrile graft copolymers

Graft copolymerization of acrylonitrile onto a soluble wool keratin derivative was studied with the reduced and carboxymethylated low-sulfur protein fraction from wool. Copolymerization was carried out under a variety of conditions with a redox system of (NH₄)₂S₂O₈–Na₂SO₃ in 60% (w/w) aqueous ZnCl₂ solution at 10°C. Monomer conversions higher than 90% were obtained by the stepwise addition of initiator. The graft products were successfully separated into grafted copolymer and homopolyacrylonitrile (PAN) by fractional precipitation or solvent extraction with DMF. Grafted PAN were isolated by acid hydrolysis of the keratin backbone. Characterization of grafted and homo-PAN was carried out by IR spectroscopy, amino acid endgroup analysis, and viscometry. On the basis of the results, effects of polymerization conditions on grafting parameters were discussed. Membranes were prepared from 60% aqueous ZnCl₂ solution by using ice-cold water as the regenerating medium. All the membranes formed from the graft products were transparent. Observation by scanning electron microscopy showed that the surface consisted of rather spherical keratin domains regularly distributed in the PAN matrix. Selective hydrolysis of the keratin domains allowed a new type of porous PAN membrane to be obtained, with the inner walls of the pores being charged with amino acid residues attached to PAN chains as the endgroup.     

Scattering and mode conversion of guided modes by an arbitrary cross-sectional cylindrical object in an optical slab waveguide

The scattering and mode conversion of guided modes caused by a cylindrical scatterer of arbitrary cross section embedded in, or placed on, a dielectric slab waveguide are investigated theoretically. The method employed for the analysis is the surface current integral equation technique. The total scattered power, mode-conversion coefficients, and scattering patterns for the typical numerical examples are shown.     

Helmholtz-Type Equations of State for Hydrocarbon Refrigerant Mixtures of Propane/n-Butane, Propane/Isobutane, n-Butane/Isobutane, and Propane/n-Butane/Isobutane

Highly accurate thermodynamic property models for binary and ternary hydrocarbon mixtures containing propane, n-butane, and isobutane have been developed. In the present model, reliable equations of state explicit in Helmholtz free energy for these three hydrocarbons that have already been developed by the present authors have been adapted. The excess term used to represent the contribution of mixing was optimized for each binary mixture by using the available experimental thermodynamic property data including PTx, isochoric heat capacity, and saturation properties (bubble-point pressures, mole fractions in the vapor phase, and saturated vapor- and liquid-densities) as input data. A generalized correction for the three binary mixtures, besides the ideal mixing, consists of only four terms in its functional form, the structure of which was determined by simultaneous optimization to the input data for the three binary mixtures by employing a stepwise regression analysis. The bank of terms, that is a matrix of candidate terms applied for the regression, was carefully prepared through detailed observation of the nonideal mixing representation of the experimental data of the three binary mixtures. No additional adjustable parameters were used in the present model for the ternary propane/n-butane/isobutane mixture. Based on comparisons with the available experimental data and values from the developed equations of state, the present models for the three binary and the ternary hydrocarbon mixtures accurately represent most of the reliable experimental data. In addition, the graphical tests of the derived thermodynamic properties show that the models, including that for the ternary mixture, provide a physically sound representation of all the thermodynamic properties over the entire fluid phase.     

Strong induction of phytochelatin synthesis by zinc in marine green alga, Dunaliella tertiolecta

Synthesis of phytochelatins (PCs), heavy-metal-sequestering peptides, in the marine green alga, Dunaliella tertiolecta, was evaluated under various conditions of exposure to heavy metals. To investigate the effect of heavy metals on both PC synthesis and their upstream biosynthetic reactions, an ion-pair-HPLC system was developed in this study, by which PCs and their biosynthetic intermediates, cysteine (Cys), gamma-glutamylcysteine (gammaEC) and glutathione (GSH), could be determined simultaneously with high sensitivity. When the cells were exposed to Zn2+, the level of PCs was maximal at 200 microM and significantly higher than that obtained after exposure to 400 microM Cd2+, which is the strongest inducer of PC synthesis in higher plants in vivo and in vitro as well as in microalgae. The predominant PC subtype was PC4, followed by PC3 and PC5, whereas PC2, which is generally abundant in higher plants, has the lowest level among PC2 to PC5. These results suggest that the characteristics of PC synthase in D. tertiolecta including the requirement of heavy metals for its catalysis and substrate specificity towards GSH and PC(n) are considerably different from those in higher plants and other algae. While PC synthesis proceeded in the heavy-metal-treated cells, the level of GSH did not appreciably change. To maintain the same size of the GSH pool, GSH must be newly synthesized to balance the amount consumed for PC synthesis.     

Ion-beam processing of single crystal diamond using SOG mask

Various ion-beam etching characteristics of diamond and selectivity between diamond and spin-on-glass (SOG) were examined. The maximum selectivity of diamond and SOG was 12.7 in oxygen reactive ion-beam etching process at 100 V acceleration voltage. Using this etching condition and dot-shaped SOG mask, conical diamond field electron emitter arrays with 30 nm curvature radius, 2.58 μm base radius and 5.86 μm height were fabricated.