Ultramicro determination of organic halogens using sealed tube dry combustion method

A sealed tube dry combustion method that is simple, accurate, and precise for ultramicro determination of halogens in organic compounds has been developed. Samples below 1 mg are heated at 580 °C for 1 h in an electric furnace. After the combustion and absorption of the gaseous halogen, the interior of the tube is rinsed. Subsequent titration is carried out potentiometrically with silver nitrate and yielded standard deviations of 0.21% for chlorine, 0.17% for bromine, and 0.25% for iodine.     

Curved Ferroelectric Liquid Crystal Matrix Displays Driven by Field-Sequential-Color and Active-Matrix Techniques

This paper describes a curved field-sequential-color matrix display using fast-response ferroelectric liquid crystal. Black matrix and transparent electrode patterns were formed on a thin plastic substrate by a transfer method from a glass substrate. While a composite film of liquid crystal and micro-polymers of walls and fibers was formed between the flexible substrates by printing, laminating and curing processes of a solution of monomers and liquid crystal, the mechanical stability was enhanced by use of multi-functional monomers to form large display panels. The image pixels of the matrix panel were driven by an active matrix scheme using an external switch transistor array at a frequency of 180 Hz for intermittent three-primary-color backlight illumination. The flexible A4-paper-sized color display with 24 × 16 pixels and 60 Hz field frequency was demonstrated by illuminating it with sequential three-primary-color lights from light-emitting diodes of the backlight. Our display system is useful in various information displays because of its freedom of setting and location.     

Determination in plasma of angiotensin-converting enzyme inhibitor by inhibitor-binding assay.

A method of determining a new angiotensin-converting enzyme inhibitor (CS-622) and its active metabolite (RS-5139) in plasma by inhibitor-binding assay has been developed using high-performance liquid chromatography. The assay is based on the principle that the amount of inhibitor bound to the enzyme is inversely related to the amount of hippuric acid liberated on hydrolysis from the artificial substrate (hippuryl-L-histidyl-L-leucine). Plasma was heated at 60 degrees C for 15 min, to inactivate endogenous enzyme, and preincubated with rabbit-lung angiotensin-converting enzyme at 37 degrees C for 3 min. The artificial substrate (5.75 mg/ml in pH 8.3 phosphate buffer containing sodium chloride) was added to the resulting solution, and the mixture was incubated for 30 min. The reaction was terminated by the addition of 2 M hydrochloric acid. The hippuric acid liberated on hydrolysis was extracted with ethyl acetate and determined by reversed-phase chromatography using methylparaben as an internal standard. The total concentration of the inhibitor and its metabolite were determined by this method after de-esterification by rat-plasma esterase. The standard curve was obtained by the regression analysis of log concentration against logit response. The within-day and day-to-day precision were satisfactory. The proposed method is simple, rapid and sensitive enough to determine angiotensin-converting enzyme inhibitor in plasma.     

Synthesis and evaluation of 3-methyl-4-oxo-6-phenyl-4,5,6,7-tetrahydrobenzofuran-2-carboxylic acid ethyl ester derivatives as potent antitumor agents

For the construction of new combinatorial libraries, a lead compound was created by replacing the core structure of a hit compound discovered by screening for cytotoxic agents against a tumorigenic cell line. The newly designed compound maintained biological activity and allowed alternative library construction for antitumor drugs.     

A new analysis of molecular orbital wave functions based on resonance theory

A new method to evaluate the weights of resonance structures from molecular orbital wave function is proposed, which is based on the second quantization of singlet-coupling. The present method is useful to analyze molecules of which the electronic structures are well localizable. The evaluation is carried out through localization of molecular orbitals followed by algebraic calculation of density matrices. This method is applied to H(2)O, H(3)O(+), and BH(3). The calculated weights of covalent and ionic structures are in excellent agreement with those of the previous works and our chemical intuition.     

Comparison of Bartlett-type adjusted tests in the multiparameter case

Considering some Bartlett-type adjusted tests for a simple hypothesis about a multidimensional parameter, this paper clarifies similarities and dissimilarities with the one-parameter case developed in the 1990s, where a major emphasis is put on the issue posed by Rao and Mukerjee [C.R. Rao, R. Mukerjee, Comparison of Bartlett-type adjustments for the efficient score statistic, J. Statist. Plann. Inference 46 (1995) 137-146] on the power under a sequence of local alternatives. Not surprisingly, there is an infinite number of adjustments which extend Chandra-Mukerjee and Taniguchi approaches to the multiparameter case. Revisiting their ideas, this paper presents four specific cases (type K, K=0,1,2,3) and gives a sufficient condition under which our generalized adjustment for each case is uniquely determined, where type 0 is a counterpart of Chandra and Mukerjee’s original proposal for Rao’s test statistic, whereas the latter three types are introduced as double adjustments related to the Cordeiro and Ferrari approach. If the adjustment of type 1 is made instead of type K, K=0,2,3, it is shown that Chandra and Mukerjee’s approach is equivalent to Taniguchi’s approach in terms of the third-order local power. The same is partially true for type 0, depending on the model under consideration. However, the adjustments of type K, K=2,3, reveal, in general, the non-equivalence of these two approaches in terms of the third-order local power.     

Effect of high pressure treatment on sarcoplasmic reticulum

Abstract

This paper describes the changes in biochemical activities of sarcoplasmic reticulum(SR) and Ca²⁺ release from SR in the rabbit skeletal muscle subjected to a high pressure treatment(100∽300 MPa) to investigate the mechanism for pressure-induced meat tenderization and acceleration of meat conditioning. Pressure-dependent changes were observed in the both extra and basal ATPase activities of SR prepared from the muscles exposed to high pressure. Ca²⁺ uptaking ability of SR vesicles measured by fluorescent chelating reagent, indo-1, decreased with increasing pressure applied to the muscle. Ultrastructural studies revealed that Ca²⁺ which was mainly localized in the SR region of the untreated fiber bundles was translocated into myofibrils in the pressurized muscle. Obtained results in this report may be one of the causes for meat tenderization and acceleration of meat conditioning induced by high pressure treatment.