Preparation of Micron‐Sized Monodisperse Poly(ionic liquid) Particles

Micron‐sized monodisperse poly(ionic liquid) (PIL) particles, poly([2‐(methacryloyloxy)ethyl]trimethylammonium bis(trifluoromethanesulfonyl)amide), were prepared by dispersion polymerization at 70 °C in methanol with poly(vinylpyrrolidone) as a stabilizer. The obtained particle size could be controlled by addition of ethanol to the methanol medium while maintaining narrow monodispersity. The PIL particles exhibit unique properties; they can be observed by scanning electron microscopy without platinum coating, which is generally used to avoid an electron charge. Moreover, the solubility of the PIL particles can be easily changed by changing the counter anion, similar to the process for ionic liquids.     

Red luminescence in MgO-GeO<Subscript>2</Subscript> gel glasses and glass ceramics doped with Mn ions prepared by sol-gel method

To obtain red luminants, MgO-GeO₂ gel glasses and glass ceramics doped with manganese ions were prepared by a sol-gel method and their properties were investigated by measuring X-ray diffraction (XRD), electron spin resonance (ESR), and luminescence and excitation spectra. Under UV irradiation at 254 nm, the gel glasses and glass ceramics showed red luminescence at 620–665 nm, the intensity of which became strong with increasing the heat-treatment temperature. A glass ceramic with the composition 1.0MnO-25MgO-75GeO₂ heat treated at 1000°C exhibited the strongest red luminescence at 661 nm. From the results of XRD and ESR, this luminescence is found to be due to the transition from the ⁴T_1g to the ⁶A_1g state of octahedrally coordinated Mn²⁺ ions located in MgGeO₃ polycrystals. The luminescence wavelength of the glass ceramics (∼665 nm) is long compared with Eu³⁺-containing phosphors (612 nm), therefore the glass ceramics can be expected for red luminants.     

Aggregation-induced photocatalytic activity and efficient photocatalytic hydrogen evolution of amphiphilic rhodamines in water

The development of photocatalysts is an essential task for clean energy generation and establishing a sustainable society. This paper describes the aggregation-induced photocatalytic activity (AI-PCA) of amphiphilic rhodamines and photocatalytic functions of the supramolecular assemblies. The supramolecular assemblies consisting of amphiphilic rhodamines with octadecyl alkyl chains exhibited significant photocatalytic activity under visible light irradiation in water, while the corresponding monomeric rhodamines did not exhibit photocatalytic activity. The studies on the photocatalytic mechanism by spectroscopic and microscopic analyses clearly demonstrated the AI-PCA of the rhodamines. Moreover, the supramolecular assemblies of the rhodamines exhibited excellent photocatalytic hydrogen evolution rates (up to 5.9 mmol g⁻¹ h⁻¹).

Simple amphiphilic rhodamines formed supramolecular assemblies and exhibited aggregation-induced photocatalytic activity and hydrogen evolution in water.     

Development characteristics of drag-reducing surfactant solution flow in a duct

Development characteristics of dilute cationic surfactant solution flow have been studied through the measurements of the time characteristics of surfactant solution by birefringence experiments and of the streamwise mean velocity profiles of surfactant solution duct flow by a laser Doppler velocimetry system. For both experiments, the concentration of cationic surfactant (oleylbishydroxymethylethylammonium chloride: Ethoquad O/12) was kept constant at 1000 ppm and the molar ratio of the counter ion of sodium salicylate to the surfactants was at 1.5. From the birefringence experiments, dilute surfactant solution shows very long retardation time corresponding to micellar shear induced structure formation. This causes very slow flow development of surfactant solution in a duct. Even at the end of the test section with the distance of 112 times of hydraulic diameter form the inlet, the flow is not fully developed but still has the developing boundary layer characteristics on the duct wall. From the time characteristics and the boundary layer development, it is concluded that the entry length of 1000 to 2000 times hydraulic diameter is required for fully developed surfactant solution flow.List of abbreviations and symbols A₁, A₂ Coefficients for time constant fitting [-] - B Breadth of the test duct [m] - C₁, C₂ Coefficients for time constant fitting [-] - D Pipe diameter [m] - D_H Hydraulic diameter [m] - g Impulse response function [Pa] - H Width of the test duct [m] - n Index of Bird-Carreau model [-] - Re Reynolds number (=U_mD_H/) - Re_D Pipe Reynolds number (=U_mD/) - Re_x Streamwise distance Reynolds number (=U₀x/) - T Absolute temperature [K] - t Time [s] - t_a Retardation time [s] - t_b Build-up time [s] - t_x Relaxation time [s] - t_x1, t_x2 Relaxation time for double time constant fitting [s] - t Time constant in Bird-Carreau model [s] - U Time mean velocity [m/s] - U_m Bulk mean velocity [m/s] - U_max Maximum velocity in a pipe [m/s] - U₀ Main flow velocity [m/s] - u Friction velocity [m/s] - x, y Coordinates [m] - Shear rate [s^–1] - Mean shear rate [s^–1] - n Birefringence [-] - 99% boundary layer thickness [m] - Solution viscosity [Pa·s] - _P, _S Surfactant and solvent viscosity [Pa·s] - ₀, Zero and infinite viscosity of Bird-Carreau model [Pa·s] - Characteristic time in Maxwell model [s] - Water kinematic viscosity [m²/s] - Density [kg/m³] - Solution shear stress [Pa] - _P, _S Surfactant and solvent shear stress [Pa] - Time in convolution [s]     

Increased levels of 8-hydroxy-2'-deoxyguanosine in Drosophila larval DNA after irradiation with 364-nm laser light but not with X-rays

Exposure to UVA light causes damage to cellular components such as DNA and membrane lipids. We showed previously that UVA irradiation can induce mutations in Drosophila larvae and that the major lesions responsible for mutations were not thymidine dimers when wavelengths tested became longer. The use of a longer wavelength with UVA laser apparatus (364 nm) has made it possible to test the effects of this powerful light in biological organisms. In the present study, we irradiated third instar larvae of the urate-null Drosophila mutant strain y v ma-l, which is sensitive to oxidative stress, and compared the effects of 364 nm light irradiation with the effects of X-rays. To assay viability, some of the larvae were kept at 25 degrees C until they eclosed in order to obtain a measure of viability. The remaining larvae were used to measure the amount of 8-hydroxydeoxyguanosine (8-OHdG), an indicator of oxidative DNA damage. The amount of 8-OHdG increased and viability decreased in response to increased UV dose in both the y v ma-l and wild-type strains. With irradiation of 600 kJ m(-2), 8-OHdG/10(6)dG was 7.2 +/- 3.2 and 6.2 +/- 2.0 in y v ma-l and wild-type strains, respectively, whereas the respective levels were 2.2 +/- 0.6 and 2.3 +/- 0.8 without irradiation. Our results indicated that irradiation with a 364-nm laser light caused significant oxidative damage in Drosophila larval DNA; however, induction of the damage was not prohibited by urate. To the best of our knowledge, this is the first report of a study in whole animals that shows increased levels of 8-OHdG in response to 364-nm UVA. X-ray ionizing radiation is also thought to generate reactive oxygen species in irradiated cells. We found that the amount of 8-OHdG in DNA following X-ray radiation remained unchanged in both strains, though survival rates were affected. X-ray-generated oxidative damage in Drosophila cells was followed by cell death but not DNA base oxidation, and the damage was suppressed by urate. The overall results suggest significant differences in the major in vivo oxidative damage caused by 364-nm light and X-rays.     

Medicinal Flowers. XXXV. Nor-oleanane-type and acylated oleanane-type triterpene saponins from the flower buds of Chinese Camellia japonica and their inhibitory effects on melanogenesis(1))

The methanolic extract and its 1-butanol-soluble fraction from the flower buds of Camellia japonica, cultivated in Yunnan Province, China, showed inhibitory effects on melanogenesis in theophylline-stimulated B16 melanoma 4A5 cells. From the 1-butanol-soluble fraction, a new 28-nor-oleanane-type and three new oleanane-type triterpene saponins, sanchakasaponins A-D, were isolated together with four known triterpene saponins. Their chemical structures were elucidated on the basis of chemical and physicochemical evidence. The inhibitory effects on melanogenesis in theophylline-stimulated B16 melanoma 4A5 cells and structure-activity relationships of the saponins were investigated.     

Alternative methods to evaluate the protective ability of sunscreen against photo-genotoxicity

Numerous epidemiological investigations show that sunlight is carcinogenic to humans and that the use of sunscreen may be effective in decreasing the risk of skin cancer. The biological activity of a sunscreen is evaluated by its ability to protect human skin from erythema as represented by a Sun Protection Factor (SPF). We propose that the sunscreen's protective effect against sunlight-induced genotoxicity, including mutation, should also be taken into account. In this study we examined the protective ability of sunscreens against natural sunlight and UV-induced genotoxicity in Drosophila somatic cells. We prepared three kinds of sunscreen samples, each with an SPF value of 20, 40 or 60 and compared their protective activities with commercial sunscreens. When a sunscreen of SPF 20, 40 or 60 was pasted on the plastic cover of a petri dish in which Drosophila larvae were exposed to the sun or UV lamps, genotoxicity decreased as the SPF of the sunscreen increased, relative to levels of genotoxicity observed in samples without sunscreen. However, the protective abilities of sunscreens were unexpectedly not so different from each other. To reveal the relationship between the protective activity of sunscreen and the wavelength of light with which larvae were irradiated through the sunscreen, we measured the transmittance of light through the petri dish cover on which the sunscreen was pasted. Effective protection was demonstrated by removing components of light whose wavelengths were below 315 nm. We suggest, that the measurement of anti-genotoxic activity and the determination of the wavelengths of light transmitted through the sunscreen should be an alternative method for evaluating the effectiveness of a sunscreen.     

Capillary electrophoresis as a nanoreactor of separation capability: on-capillary reaction catalyzed by transition metal ions

The catalytic oxidation of 1,2-dihydroxy-benzene-3,6-disulfonate (tiron) by metal ions has been studied for detection of the metal ions in capillary electrophoresis (CE). Although Co(2+) shows the strongest catalytic capability, some other metal ions also catalyze this reaction. If metal ions encounter a H(2)O(2 )zone after electrophoretic separation in the running buffer containing tiron, tiron is catalytically oxidized while the metal ion passes through the H(2)O(2) zone. Anionic tiron radicals produced by the reaction are finally measured by the detector; in this scheme, the capillary acts as a nano- or microreactor as well as a microseparator. The effective capillary length can be controlled by changing the interval between metal ion and H(2)O(2) injections. This scheme has been successfully applied to the detection of Co(2+), Cu(2+), Mn(2+), and VO(2+). The detectability is discussed from several viewpoints, such as the intrinsic catalyst ability of metal ions, the kinetics of the catalytic reaction, and reaction times determined by the mobility of the zone of the metal ion. Some strange behaviors, which cannot be predicted by batch experiments, are also reported.     

New tricyclic alkaloids, cassiarins G, H, J, and K from leaves of Cassia siamea

Four new alkaloids, cassiarins G, H, J, and K (1-4) which showed moderate antiplasmodial activity against Plasmodium falciparum 3D7, were isolated from the leaves of Cassia siamea (Leguminosae) and the structures of 1-4 were elucidated by 1D- and 2D-NMR analysis and X-ray crystallographic analysis.     

Luminescence and long-lasting afterglow in Mn<Superscript>2+</Superscript> and Eu<Superscript>3+</Superscript> co-doped ZnO–GeO<Subscript>2</Subscript> glasses and glass ceramics prepared by sol–gel method

To develop new fluorescent and afterglow materials, Mn²⁺ and Eu³⁺ co-doped ZnO–GeO₂ glasses and glass ceramics were prepared by a sol–gel method and their optical properties were investigated by measuring luminescence, excitation and afterglow spectra, and luminescence quantum yield (QY). Under UV irradiation at 254 nm, some glasses and all of the glass ceramics showed green luminescence peaking at 534 nm due to the ⁴T₁ → ⁶A₁ transition of tetrahedrally coordinated Mn²⁺ ions. The strongest luminescence was observed in a glass ceramic of 0.1MnO–0.3Eu₂O₃–25ZnO–75GeO₂ heat treated at 900 °C, with QY of 49.8%. All of the green-luminescent glasses and glass ceramics showed green afterglow, and the afterglow lasting for more than 60 min was obtained in a glass ceramic heat treated at 900 °C. It is considered that the Eu³⁺ ions may behave as electron trapping centers to be associated with the occurrence of the green afterglow due to the Mn²⁺ ions in the co-doped system.