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Biomedical subjects

Masakuni Yoshihara

Publications and source records attributed to Masakuni Yoshihara.

6 recordsLinked to original sources
PubMed2006

Dispersion stability of TiO2 nanoparticles covered with SiOx monolayers in water.

The repetition of a two-step route consisting of chemisorption of 1,3,5,7-tetramethylcyclotetrasiloxane (TMCTS) and its subsequent photooxidation has formed SiOx monolayers on the surfaces of TiO2 particles layer by layer (SiOx(n < or = 4)/TiO2, n = repeated number). The trace of these processes using diffuse reflectance FT-IR and solid-state 29Si NMR spectroscopy reveals that TMCTS is chemisorbed on TiO2 through Ti-O-Si bonds followed by growth of Si-O-Si networks via dehydration-condensation of the Si-OH groups generated by TiO2 photocatalytic oxidation of the Si-H and Si-CH3 groups. The point of zero charge of the TiO2 particles decreases from 6.5 to 5.4 at n = 1, reaching 4.9 at n2. As a result of coverage with the SiOx monolayers, the dispersion stability of TiO2 particles in neutral water is significantly improved without changing their optical properties. The dispersion stability further increases with accumulation of SiOx monolayers.

Journal Article↗
PubMed2005

Electron transfer behavior and water photodecomposition ability of calcined material from a cerium-S-phenylene-O-holmium-O-phenylene-S hybrid copolymer.

Calcination of a cerium-S-phenylene-O-holmium-O-phenylene-S hybrid copolymer under a vacuum gave cerium oxide-carbon cluster-holmium oxide composite material. The material calcined at 600 degrees C loaded with Pt particles could decompose water to H2 and O2 with a H2/O2 ratio of 2 under visible light irradiation. ESR spectral examinations of the calcined materials revealed the possibility of a two-step electron transfer in the process of CeO2 --> carbon cluster --> Ho2O3 --> Pt with an oxidation site at CeO2 particles and a reduction site at Pt particles.

Journal Article↗
PubMed2005

alpha-Helical polypeptide microcapsules formed by emulsion-templated self-assembly.

alpha-Helical peptide microcapsules were prepared by the emulsion-templated self-assembly of amphiphilic poly(gamma-benzyl L-glutamate)s (PBLG) 1. By mixing solutions of 1 in dichloromethane (in the form of a sodium salt) with water, oil-in-water emulsions were obtained. Spontaneous stripping of the dichloromethane phase caused a decrease in the diameter of the microdroplets and finally stable microcapsules formed. The microcapsules contain an inner aqueous phase as observed by confocal laser scanning microscopy (CLSM). Binding of hydrophobic pyrene molecules to the polypeptide shell was also demonstrated. The present polypeptide microcapsules are stable even after drying in air and they would serve as supramolecular vehicles for both hydrophobic and water-soluble molecules.

Capsules↗
PubMed2005

ATP as building blocks for the self-assembly of excitonic nanowires.

Supramolecular nanowires are specifically self-assembled from adenosine 5'-triphosphate (ATP) and dichloro-substituted thiacarbocyanine dyes. Spectral blue-shift and induced circular dichroism with exciton coupling are observed upon mixing the dye and ATP molecules in water. These observations indicate the formation of chiral 1/ATP supramolecular assemblies with excitation energy delocalized in the parallel-oriented (H-aggregated) chromophores. Interestingly, formation of H-aggregates is facilitated most in the presence of ATP and not by other nucleotides (ADP or AMP). In electron microscopy, aqueous 1/ATP mixture gives developed nanowires with a minimum width of ca. 10 nm and lengths of several micrometers. The ATP-directed nanowires exhibit reversible thermal self-assembly accompanied by supramolecular thermochromism. This is the first example of ATP-based supramolecular nanoassemblies, and the use of small biomolecules as building blocks for functional supermolecules provides a new perspective in the design of bio-nanomaterials.

Adenosine Triphosphate↗
PubMed2002

New colorimetric detection of glucose by means of electron-accepting indicators: ligand substitution of [Fe(acac)3-n(phen)n]n+ complexes triggered by electron transfer from glucose oxidase.

A new colorimetric detection technique for glucose, based on electron transfer from glucose oxidase (GODred) to iron(III) acetylacetonate(acac)/phenanthroline(phen) mixed complexes, is developed. When GOD is added to an aqueous mixture that contains tris(acetylacetonato)iron(III) complex (FeIII-(acac)3), 1,10-phenanthroline (phen), and glucose, the color immediately changes from pale yellow to red. The red color originates from formation of tris(1,10-phenanthroline)iron(II) complex ([FeII(phen)3]2+). Differential pulse voltammetry indicates that cationic, mixed-ligand complexes of [Fe(acac)3-n-(phen)n]n+ are formed upon mixing the labile FeIII(acac)3 complex and phenanthroline. The cationic mixed-ligand complexes electrostatically bind to GOD (pI 4.2), and are easily reduced by electron transfer from GODred. This electron transfer is not affected by the presence of oxygen. The reduced complex [FeII(acac)3-n(phen)n](n-1)+ then undergoes rapid ligand exchange to FeII (phen)3. Formation of the colored FeII complex is repressed when the salt concentration in the mixture is increased, or when anionic bathophenanthroline disulfonate (BPS) is employed in place of phenanthroline. The use of labile metal complexes as electron acceptors would be widely applicable to the design of new biochromic detection systems.

Electrochemistry↗