Temperature dependence of thermodynamic activity in volatile anesthetics: correlation between anesthetic potency and activity

Temperature dependence of the saturated concentration and the activity coefficient of anesthetics (1-propanol, diethyl ether, chloroform, and halothane) in water were evaluated using vapor pressure and H NMR measurement. We found that these physical values (quantities) correlate with anesthetic potencies estimated according to the thermodynamic equilibrium model. The anesthetic potency for hydrophilic anesthetic (diethyl ether) decreased with decreasing temperature because of the temperature specificity of this saturated concentration. In contrast, potencies of hydrophobic anesthetics (chloroform and halothane) increased with decreasing temperature because of the temperature specificity of those activity coefficients. By assuming that anesthetics interact with hydrated water of cell membranes, the temperature dependence of anesthetic potencies in vivo is qualitatively explicable.     

Une redécouverte de l'équation de Korteweg–de Vries et de Kadomtsev–Petviashvili

We show that the flux of long waves of water surface, propagating in each characteristic direction of the equations for a vibrating string, to a first approximation, are close to the solutions of the Korteweg–de Vries equation. In a three dimensional flow, the phenomenon is of the same order as the Kadomtsev–Petviashvili equation. To cite this article: T. Kano, T. Nishida, C. R. Acad. Sci. Paris, Ser. I 341 (2005).     

Photochemistry and photocuring properties of thiol‐substituted α‐aminoalkylphenone as radical photoinitiator

Thiol‐substituted α‐aminoalkylphenone was newly developed as a radical photoinitiator. Introduction of the thiol group drastically improved photosensitivity in an alkaline developable resist formulation composed of a prepolymer and a multifunctional acrylate monomer. The improvement in the photocuring speed was explained by a mechanism based on chain transfer reaction of the thiol group. Time‐resolved electron spin resonance (ESR) spectroscopy indicated that the thiol group attached to the chromophore does not influence the photochemical process to generate primary radicals. The photoinitiation of α‐aminoalkylphenone can be spectrally sensitized by 2,4‐diethylthioxanthone (DETX). However, thiol‐substituted α‐aminoalkylphenone showed smaller spectral sensitization than the corresponding compound without a thiol group. Time resolved laser flash photolysis indicated that the rate constant of the quenching of the triplet state of DETX by thiol‐substituted α‐aminoalkylphenone is twice as large as that by the corresponding one without a thiol group. This suggests that, besides energy transfer from DETX in the excited triplet state to the α‐aminoalkylphenone, the thiol group quenches the excited triplet state of DETX via charge transfer and/or hydrogen transfer, as supported by the ESR analysis using a spin trapping technique, and lowers the efficiency of the spectral sensitization effect. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 1684–1695, 2005     

Electrochemical luminescence of n-type ZnO semiconductor electrodes doped with rare earth metals under the anodic polarization

Electrochemical luminescence (ECL) at n-type ZnO semiconductor electrode was measured under anodic polarization. Scanning the potential imposed on the ZnO electrode, emission was suddenly observed around +20 V. Using the ZnO electrodes doped with rare earth metal ions as Sm³⁺, Eu³⁺, Dy³⁺, Ho³⁺ and Er³⁺, much brighter emission was obtained than the ECL of non-doped ZnO. These emission spectra are ascribed to the rare earth metal ions, respectively. This result would show that emission centers of doped ions were selectively excited by electrons that were injected from electrolyte to the electrode by avalanche breakdown under strong anodic bias on the ZnO.     

Dose equivalents inside the MIR Space Station measured by the combination of CR-39 plates and TLDs and their comparison with those on Space Shuttle STS-79, -84 and -91 missions

In 1997, four dosimeter packages, each of which contains two CR-39 plates and 18 TLDs (Mg2SiO4:Tb), were placed inside the MIR Space Station and flew on an orbit with an inclination angle of 51.6 degrees and an altitude of approximately 400 km for 40 days. We estimated the absorbed doses, dose equivalents and effective quality factors during the flight by combining CR-39 data and TLD data. We then compared these results to those obtained with the same analysis method from the dosimeter packages on board Space Shuttle missions STS-79, -84 and -91 that flew along the same orbit. Finally, the differences between our results and those obtained by another group using passive dosimeters on the MIR are discussed.     

Synthesis and biological activities of novel furo[2,3,4-jk][2]benzazepin-4(3H)-one derivatives

A novel seven-membered lactam formation method has been established by intramolecular ring closure reaction of 4-bromo-(E)-3-[(2-alkylvinyl)carbonylamino]benzo[b]furans under Heck coupling conditions. A number of furo[2,3,4-jk][2]benzazepin-4(3H)-ones, tricyclicbenzo[b]furans, have been prepared by this method and evaluated for their leukotriene B(4) (LTB(4)) receptor and poly(ADP-ribose)polymerase-1 (PARP-1) inhibitory activities.     

Action mechanism of water soluble ethanol on phospholipid monolayers using a quartz crystal oscillator

Interaction between phospholipid monolayers (dihexadecyl phosphate: DHP, dipalmitoyl phosphatidyl choline: DPPC) and water soluble ethanol has been studied using quartz crystal microbalance (QCM) method and quartz crystal impedance (QCI) method. The quartz crystal oscillator was attached horizontally on the DHP and DPPC monolayers that were formed on the water surface. At low concentration, increased ethanol concentration decreased the frequency for QCM and increased the resistance for QCI. Both frequency and resistance approached asymptotically to a saturation value. A further increase in ethanol concentration induced a sudden and discontinuous linear change (a decrease in frequency and an increase in resistance). Based on these results, we propose the following action mechanism of ethanol on phospholipid monolayers: at low concentration, the ethanol hydrates adsorb into the monolayer/water interface and saturate on the interface. The monolayer viscosity also increases with the adsorption of hydrates. A further increase in concentration causes multilayer formation of hydrates and/or penetration of hydrates into the monolayer core. The viscosity of the interfacial layer (monolayer and interfacial structured water) changes dramatically according to the action of ethanol hydrates.     

Local Resolvent Estimates for <Emphasis Type="Italic">N</Emphasis>-body Stark Hamiltonians

For an N-body Stark Hamiltonian , the resolvent estimate holds uniformly in with Re and Im , where , and is a compact interval. This estimate is well known as the limiting absorption principle. In this paper, we report that by introducing the localization in the configuration space, a refined resolvent estimate holds uniformly in with Re and Im . Dedicated to Professor Hideo Tamura on the occasion of his 60th birthday