[Application of photocatalysis to medicine].
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Air Pollution↗
Biomedical subjects
Akira Fujishima
Publications and source records attributed to Akira Fujishima.
Interference-based electrochemical biosensor for the measurement of the concentration and isomer ratio of urocanic acid.
Urocanic acid (UCA) is known to be synthesized as the trans isomer (trans-UCA) in the skin, and trans-UCA is transformed by UV light to the cis isomer (cis-UCA), which may be involved in photoimmunosuppression. An electrochemical method has been developed for the measurement of the concentration and isomer ratio of UCA. A heme peptide-modified electrode (HP electrode) reduces hydrogen peroxide at +150 mV vs Ag/AgCl, and the reduction current is inhibited by UCA. Since cis-UCA is a stronger inhibitor than trans-UCA, irradiation of a sample solution with UV light increases the percent inhibition. The concentration and isomer ratio of UCA in the sample solution can be estimated from the values of percent inhibition before and after the UV irradiation.
Biosensing Techniques↗
17 beta-estradiol degradation by TiO2 photocatalysis as a means of reducing estrogenic activity.
The degradation of 17 beta-estradiol (E2) in water by TiO2 photocatalysis was investigated; concurrently the estrogenic activity of the treated water was evaluated during the photocatalytic reactions by an estrogen screening assay. As a result, 10(-6) M of E2 was totally mineralized to CO2 in 1.0 g L-1 TiO2 suspension under UV irradiation for 3 h. 10 epsilon-17 beta-Dihydroxy-1,4-estradien-3-one and testosterone-like species were elucidated as intermediate products by GC/MS analysis. The mechanisms of E2 degradation by TiO2 photocatalysis were discussed not only experimentally but also theoretically by calculating the frontier electron densities of the E2 molecule. On the basis of the results obtained, it was concluded that the phenol moiety of the E2 molecule, one of the essential functional groups to interact with the estrogen receptor, should be the starting point of the photocatalytic oxidation of E2. This means that the estrogenic activity should be almost lost concurrently with the initiation of the photocatalytic degradation. Actually, the estrogenic activities of the intermediate products were negligible. TiO2 photocatalysis could be applied to water treatment to effectively remove natural and synthetic estrogens without producing biologically active intermediary products.
Carbon Dioxide↗
Control of the optical band structure of liquid crystal infiltrated inverse opal by a photoinduced nematic-isotropic phase transition.
Recently, photonic band gap (PBG) crystals with lattice parameters comparable to the wavelength of light have attracted much attention, because they offer unique ways in which to control the propagation of light. PBG crystals have applications in laser, quantum optical devices, and so on. For many of these applications, it is important to have the capability of tuning the photonic band structures. The fabrication of such tunable PBG crystals is still a challenge. In this paper, we proposed that switchable PBG crystals could be realized by taking advantage of the phase transition in liquid crystals induced by the photoisomerization of azo dyes. A dynamic change in the optical stop band was demonstrated. Such photoswitchable PBG crystals provide a method by which light can be routed using light.
Journal Article↗
Unusually long-lived light-induced metastable state in a thermochromic copper(II) complex.
We report the first observation of a color change from red to purple for a thermochromic complex, [Cu(dieten)2](BF4)2 (dieten = N,N-diethylethylenediamine), which is induced by illuminating with UV light.
Journal Article↗
Fabrication of a metal-coated three-dimensionally ordered macroporous film and its application as a refractive index sensor.
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Journal Article↗
Electrochemical generation of ferrate in acidic media at boron-doped diamond electrodes.
An extremely strong oxidant, ferrate (Fe(VI) or FeO4(2-), has been produced electrochemically in an acidic aqueous medium for the first time.
Journal Article↗
Syntheses of fused heterocyclic compounds and their inhibitory activities for squalene synthase.
A variety of fused heterocyclic compounds (2-11) were synthesized as a modification of the lead compound 1a and evaluated for their inhibition of squalene synthase. 4,1-Benzothiazepine derivative 2, 1,4-benzodiazepine derivative 6, 1,3-benzodiazepine derivative 7, 1-benzazepine derivative 9, and 4,1-benzoxazocine derivative 10 potently inhibited squalene synthase activity, whereas the 4,1-benzoxazepine derivatives 1 was the most potent inhibitor. 4,1-Benzothiazepine S-oxide derivative 4, 1,4-benzodiazepine derivative 5, 1,3,4-benzotriazepine derivative 8, and 1,2,3,4-tetrahydroquinoline derivative 11 were found to be weakly active. Comparison of the X-ray structures of these compounds (1a, 2, 4, 5, 7 and 10) suggests that orientation of the 5- (or 6)-phenyl group is important for activity.
Animals↗