Shell model description of interacting bosons

The interacting boson model, describing collective states of even-even nuclei, is introduced as a drastic truncation of large scale shell model calculations. The shell model hamiltonian can be diagonalized by using a correspondence, or mapping, of the nucleon states in the truncated space into states obtained by coupling proton and neutron s- and d-bosons. The equivalent boson hamiltonian in a simple case is obtained and diagonalized. Eigenstates with definite proton-neutron symmetry (good F-spin) emerge for certain values of proton and neutron numbers. In general the situation is more complex but the results obtained follow closely the experimental data.     

Nuclear moments. Concluding remarks

Studies of nuclear magnetic moments and nuclear weak interactions discussed in this Conference are reviewed. The importance of configuration mixing and meson exchange currents is examined, and it is emphasized that the second order configuration mixing (tensor correlation) is essential for the understanding of these phenomena. Recent results concerning nuclear quadrupole moments reported in this Conference are also discussed. Finally, the pairing effect in metal clusters is pointed out and the importance of measuring their spins and magnetic moments is mentioned.     

Cyclodextrin-based isolation of Ostwald's metastable polymorphs occurring during crystallization

We describe a novel approach for the selective isolation of Ostwald's intermediate metastable polymorphs occurring during an early stage of crystallization, by utilizing the inclusion complex formed with a cyclic oligosaccharide derivative, 2,6-di-O-methyl-beta-cyclodextrin.     

Temperature‐dependent Raman scattering study of multiferroic MnWO4

We have measured polarized Raman spectra of MnWO₄ single crystals at low temperatures, and studied the temperature dependence of the various phonon modes. From our Raman studies of the MnWO₄, a new transition temperature, ∼180 K, was found. We have completely assigned the symmetries of the 18 observed Raman modes of the MnWO₄, as expected from a group theoretical analysis. These Raman modes have been classified into three groups according to weak, intermediate and strong temperature dependence of the modes in each group. Six internal modes have been identified by their weak temperature dependence of the Raman wavenumbers. The temperature dependence of the wavenumbers of the B_g modes in Mg O bonds, modes of intermediate temperature dependence group, shows an anomalous behavior under 50 K. The phonon modes of strong temperature dependence show an anomalous change at ∼180 K in the linewidths. This is believed to be a new transition temperature which involves the changes in the inter‐WO₆ octahedra structure. Copyright © 2009 John Wiley & Sons, Ltd.     

Monatomic rarefied gas as a singular limit of polyatomic gas in extended thermodynamics

We show that, in the theory of extended thermodynamics, rarefied monatomic gases can be identified as a singular limit of rarefied polyatomic gases. Under naturally conditioned initial data we prove that the system of 14 field equations for polyatomic gases in the limit has the same solutions as those of the system of 13 field equations for monatomic gases where there exists no dynamic pressure. We study two illustrative examples in the process of the limit, that is, the linear waves and the shock waves in order to grasp the asymptotic behavior of the physical quantities, in particular, of the dynamic pressure.     

On the six-field model of fluids based on extended thermodynamics

We study the six-field model of fluids (ET6) derived from extended thermodynamics. The six fields are the mass density, the velocity, the temperature, and the dynamic pressure (nonequilibrium pressure). We present the basic system of field equations of ET6. And we elucidate its characteristic features through the studies of the singular limit from polyatomic to monatomic rarefied gases, of hydrodynamic fluctuation, and of a hard-sphere system. Open problems remained in ET6 at present are also pointed out.     

Simultaneous determination of beta-blockers in human plasma using liquid chromatography-tandem mass spectrometry

A detailed procedure for the analysis of four beta-blockers, acebutolol, labetalol, metoprolol and propranolol, in human plasma by high-performance liquid chromatography (LC)-tandem mass spectrometry (MS-MS) using an MSpak GF column, which enables direct injection of crude plasma samples, is presented. Protein and/or macromolecule matrix compounds were eluted first from the column, while the drugs were retained on the polymer stationary phase of the MSpak GF column. The analytes retained on the column were then eluted into an acetonitrile-rich mobile phase using a gradient separation technique. All drugs showed base peak ions due to [M + H]+ ions by LC-MS with positive ion electrospray ionization, and the product ions were produced from each [M + H]+ ion by LC-MS-MS. Quantification was performed by selected reaction monitoring. The recoveries of the four beta-blockers spiked into plasma were 73.5-89.9%. The regression equations for all compounds showed excellent linearity in the range 10-1000 ng/mL of plasma, with the exception of propranolol (10-800 ng/mL). The limits of detection and quantification for each drug were 1-3 and 10 ng/mL, respectively, of plasma. The intra- and inter-day coefficients of variation for all drugs in plasma were not greater than 10.9%.     

Improvement of solubility and oral bioavailability of 2-(N-cyanoimino)-5-[(E)-4-styrylbenzylidene]-4-oxothiazolidine (FPFS-410) with antidiabetic and lipid-lowering activities in dogs by 2-hydroxypropyl-beta-cyclodextrin

2-(N-Cyanoimino)-5-[(E)-4-styrylbenzylidene]-4-oxothiazolidine (FPFS-410) is a newly synthesized thiazolidine derivative having not only antidiabetic but also lipid-lowering activities. However, this compound has an extremely low aqueous solubility (2.8 (+/-0.33) x 10(-8) M (0.0094+/-0.0011 microg/ml) in 1.0 M phosphate buffer (pH 7.0) at 25 degrees C). In this study, we investigated the effect of various hydrophilic cyclodextrins (CyDs) on the solubility of FPFS-410 to select a CyD suitable for formulations of the compound. Among various CyDs, 2-hydroxypropyl-beta-CyD (HP-beta-CyD) had the highest solubilizing ability to FPFS-410, e.g., the solubility of the compound was increased 200000-fold by the addition of 40 mM HP-beta-CyD, which was attributable to the formation of the 1 : 2 (guest : host) inclusion complexes. The interaction of HP-beta-CyD with FPFS-410 was studied using 1H-nuclear magnetic resonance (NMR) spectroscopies including ROESY spectroscopy and a molecular modeling calculation. These results suggested that HP-beta-CyD forms a 1:2 (guest : host) inclusion complex with FPFS-410 by including both the stilbene and thiazolidine moieties. FPFS-410/HP-beta-CyD solid complexes with various stoichiometries were prepared by the spray drying and cogrinding methods, and confirmed by powder X-ray diffractometry that these complexes are in an amorphous state. The dissolution of FPFS-410 in water was significantly accelerated by the complexation with HP-beta-CyD. In vivo studies revealed that HP-beta-CyD markedly increases the bioavailability of FPFS-410 after oral administration in dogs. The present results suggest that HP-beta-CyD is useful for improvement of the extremely low bioavailability of FPFS-410.     

Critical analaysis of transfer reaction models from a microscopic point of view

Based on the resonating group method, transfer reaction form factors are derived in distorted wave Born approximation. As a direct consequence of antisymmetrization, renormalization operators of relative motion in entrance and exit channels are automatically included. These operators, when used in the passive core approximation, change the conventional reduced width amplitudes into those advocated by Fliessbach. In the present paper, however, his results are derived in a way which avoids the problematic use of non-orthogonal intermediate states in the cluster transfer approximation. It is proposed to use the conventional reduced width amplitudes, together with proper renormalization kernels, in order to separate structure effects from reaction dynamics (energy dependence, absorption etc.) which determines the actual importance of the renormalization operators in entrance and exit channels.