Determination of butanol distribution on salol-butanol crystals using Micro Raman Spectroscopy

We carried out several analytical studies in order to determine the butanol distribution on a salol-butanol crystal. This work is required for a research using microgravity condition focused upon the in-situ observation with an interferometer of the temperature and concentration field for the organic transparent crystal (salol-butanol). In order to evaluate the concentration field for the liquid phase with an interferometer in case of crystal growth from solution in space, it is significant to determine the distribution of solute (butanol) on starting crystal before sample launching using a non-destructive analytical method. The Micro Raman Spectroscopy (MRS) was choice as the most appropriate analytical method among several analytical methods. We prepared a salol-butanol crystal enclosed into the 1mm thick quartz glass ampoule in order to verify the propriety for MRS. Obtained Raman spectrums for salol, butanol and salolbutanol crystal show that the butanol 2D-distribution on salolbutanol crystal can be determined by MRS. These results also demonstrate that there are no influences of thick glass cell upon measurements and that 3D-measurement is possible. In conclusion, we argue that MRS is the most appropriate method for determination of the 2D- and/or 3D- distribution of solute on the crystal among several non-destructive analytical methods.     

Structural Development of Salicylanilide-Based SPAK Inhibitors as Candidate Antihypertensive Agents

Hypertension is an important target for drug discovery. We have focused on the with-no-lysine kinase (WNK)-oxidative stress-responsive 1 (OSR1) and STE20/SPS1-related proline-alanine-rich protein kinase (SPAK)-NaCl cotransporter (NCC) signal cascade as a potential target, and we previously developed a screening system for inhibitors of WNK-OSR1/SPAK-NCC signaling. Herein we used this system to examine the structure-activity relationship (SAR) of salicylanilide derivatives as SPAK kinase inhibitors. Structural design and development based on our previous hit compound, aryloxybenzanilide derivative 2 , and the veterinary anthelmintic closantel ( 3 ) led to the discovery of compound 10 a as a potent SPAK inhibitor with reduced toxicity. Compound 10 a decreased the phosphorylation level of NCC in mouse kidney in vivo, and appears to be a promising lead compound for a new class of antihypertensive drugs.     

Pharmacokinetics of etoposide in plasma and cerebrospinal fluid in the space left by tumor removal

PURPOSE: To report a case of Lyme disease that presented with a single nummular unilateral interstitial keratitis. METHODS: Case report and review of the literature. RESULTS: A 57-year-old black man who had contact with freshly killed deer had a chief complaint of foreign-body sensation in his right eye (OD) that had been diagnosed and treated for herpes simplex stromal keratitis. The patient underwent a systemic workup for interstitial keratitis. All results including RPR and MHA-TP were negative except for Lyme antibody titer (enzyme-linked immunosorbent assay [ELISA]) 178 U/ml (normal, <159 U/ml). CONCLUSION: Interstitial keratitis from Lyme disease has been regarded as a bilateral disease in the literature. We present this infrequent ocular manifestation of Lyme disease as a rare single nummular unilateral presentation.     

The Introduction of Economic Methods to Scientometrics: The Citing-Cited Table and the Autopoietic Systems of Citations

The paper is introducing an economic method (interindustry relations analysis) into studies of autopoietic systems and shows its application to scientometrics, which can also be regarded as the analysis of autopoietic systems. The merit of the application is discussed, and the outline of the proof of a related theorem is suggested in the appendix.     

Strain-induced crystallization of peroxide-crosslinked natural rubber

Effect of network-chain density (ν) on the strain-induced crystallization of peroxide-crosslinked natural rubber was studied by fast time-resolved synchrotron wide-angle X-ray diffraction. It was observed that the elongation ratio at the onset of strain-induced crystallization (α_c) became smaller with the increase of ν. The difference of the entropy between the undeformed and deformed states at each α_c was nearly equal in spite of the variation of ν. The calculated melting temperature at α_c of the samples was also almost the same regardless of their ν. These observations mean that the strain-induced crystallization occurred when the deformation brought about a definite entropic state for peroxide-crosslinked natural rubber. They agreed with the prediction by Flory and were consistent with the classical theory of rubber elasticity.     

Preparation and properties of fluoroalkyl end-capped oligomer/fluoresceins nanocomposites

Self-assembled fluorinated oligomeric aggregates formed by fluoroalkyl end-capped N-(1,1-dimethyl-3-oxobutyl)acrylamide oligomers, N,N-dimethylacrylamide oligomers, and acrylic acid oligomers in methanol could recognize selectively fluoresceins as guest molecules to form a new class of fluorinated aggregates/fluoresceins nanocomposites. These fluorinated fluoresceins nanocomposites were found to exhibit an extraordinarily enhanced light absorption (λ_max: ca. 440 nm) compared to that (λ_maxs: 452 and 480 nm) of the parent fluorescein in the absence of fluorinated aggregates. On the other hand, fluoroalkyl end-capped 2-carboxyethyl acrylate oligomers, which possess no aggregate characteristic in methanol solutions, could not afford such an enhanced light absorption peak under similar conditions. Not only fluorescein but also fluorescein derivatives such fluoresceinamine, carboxyfluorescein, and fluorescein isothiocyanate afforded similar enhanced narrow absorption peaks under similar conditions. Naphthofluorescein was also encapsulated into these fluorinated oligomeric aggregate cores to afford fluorinated aggregates/naphthofluorescein composites, and these fluorinated naphthofluorescein composites afforded an extremely enhanced narrow absorption peak around 520 nm.     

Synthesis of the Optically Active Polymer Consisting of Chiral Phosphorus Atoms and <Emphasis Type="Italic">p</Emphasis>-Phenylene-ethynylene Units

Summary We successfully synthesized optically active polymer 4 by using chiral bisphosphine, (S,S)-1,2-bis(boranato(t-butyl)methylphosphino)ethane (S,S)-1, as a key building block. The structure of the polymer was characterized by ¹H, ¹³C, and ³¹P NMR spectra. According to the CD spectra, the p-phenylene-ethynylene unit in the polymer main chain exhibited Cotton signals around the area of π-π^* transition band.     

Automated affinity capture-release of biotin-containing conjugates using a lab-on-valve apparatus coupled to UV/visible and electrospray ionization mass spectrometry

We report a new method for automated affinity capture and release of biotin-containing conjugates on immobilized streptavidin using a lab-on-valve (LOV) bead injection apparatus. The apparatus is also coupled to UV/visible and electrospray ionization mass spectrometry (ESI-MS) for monitoring the captured and released biotin-containing conjugates. Dissociation rate constants for release from streptavidin of two chromophore-tagged biotin conjugates were measured by UV/visible spectrometry and the dissociation was simultaneously monitored by ESI-MS. The LOV-ESI-MS instrument was also used for repetitive assays of lysosomal beta-galactosidase in human cell homogenates. Fast analysis in 4.5 min/full cycle and robust operation in 60 repetitive analyses are demonstrated that are promising for transfer of the LOV-ESI-MS technology into clinical practice.     

Transmission electron microscopy on thin film of high density magnetic composite prepared by FIB method

A thin specimen of a high density magnetic composite (HDMC), which is a type of powder magnetic cores was prepared for transmission electron microscopy (TEM) using a focused ion beam (FIB) method. A homogeneous thin film containing an insulator boundary between the constituent Fe powders was obtained successfully. Using this thin film, detailed flow of magnetic flux was visualized by electron holography, and the magnetic flux density was estimated to be 1.73 +/- 0.09 T being consistent with that of a bulk HDMC (1.70 T). Moreover, through Lorentz microscopy, the characteristic magnetization process of HDMC was observed by applying the magnetic field up to approximately 8 kA/m.