Photocatalytic partial oxidation of methylpyridine isomers on TiO2 particles under an anaerobic condition

Photocatalytic oxidation of methylpyridine isomers (2-methylpyridine, 3-methylpyridine, and 4-methylpyridine) was investigated in a mixed solution of acetonitrile and water or acetonitrile using various kinds of TiO2 powders as photocatalysts. The main products from methylpyridine isomers were pyridinecarboxaldehyde isomers (2-pyridinecarboxaldehyde, 3-pyridinecarboxaldehyde, and 4-pyridinecarboxaldehyde). Rutile large TiO2 particles showed the highest level of activity for oxidation of 2-methylpyridine probably because band bending was necessary for the oxidation of 2-methylpyridine. On the other hand, a fine particle having an anatase or rutile phase showed a higher level of activity than large TiO2 particles for oxidation of 3-methylpyridine. A rutile fine particle showed the highest level of activity for the reaction. It was found that pure rutile or pure anatase particles were inactive for oxidation of 4-mathylpyridine. If the particles are not extremely small, pure rutile and pure anatase powders show fairly high levels of activity, and those containing both anatase and rutile phases show the highest level of activity. The activity of pure rutile particles was also enhanced by physically mixing them with a small amount of small anatase particles, which were inactive for this reaction. These results can be explained by the synergism between rutile and anatase particles. All of these reactions effectively proceeded even under anaerobic conditions. Photocatalytic reduction of methylpyridine isomers concomitantly proceeded on TiO2 particles under the conditions used. These results suggest that the activities of TiO2 photocatalysts for oxidation of methylpyridine isomers are dominated by the oxidation potential of alkylpiridine and band bending of TiO2 particles

Photocatalytic Activity of a TiO2 Photocatalyst Doped with C4+ and S4+ Ions Having a Rutile Phase Under Visible Light

C4+ and S4+-codoped titanium dioxide (TiO2) having a rutile phase was prepared. By doping C4+ and S4+ ions into a TiO2 lattice, the absorption edge of rutile TiO2 powder was largely shifted from 400 to 700 nm. 2-Methylpyridine and methyleneblue were photocatalytically oxidized at high efficiency on C4+ and S4+-doped TiO2 under visible light at a wavelength longer than 5 nm

A Lipopeptide Facilitate Induction of Mycobacterium leprae Killing in Host Cells

Little is known of the direct microbicidal activity of T cells in leprosy, so a lipopeptide consisting of the N-terminal 13 amino acids lipopeptide (LipoK) of a 33-kD lipoprotein of Mycobacterium leprae, was synthesized. LipoK activated M. leprae infected human dendritic cells (DCs) to induce the production of IL-12. These activated DCs stimulated autologous CD4+ or CD8+ T cells towards type 1 immune response by inducing interferon-gamma secretion. T cell proliferation was also evident from the CFSE labeling of target CD4+ or CD8+ T cells. The direct microbicidal activity of T cells in the control of M. leprae multiplication is not well understood. The present study showed significant production of granulysin, granzyme B and perforin from these activated CD4+ and CD8+ T cells when stimulated with LipoK activated, M. leprae infected DCs. Assessment of the viability of M. leprae in DCs indicated LipoK mediated T cell-dependent killing of M. leprae. Remarkably, granulysin as well as granzyme B could directly kill M. leprae in vitro. Our results provide evidence that LipoK could facilitate M. leprae killing through the production of effector molecules granulysin and granzyme B in T cells

Influence of Pre-Etched Area and Functional Monomers on the Enamel Bond Strength of Orthodontic Adhesive Pastes

This study was performed to investigate the influence of pre-etching area and functional monomers in orthodontic adhesive pastes on enamel bond strength. Bovine enamel was partially pre-etched with phosphoric acid for 30 s over areas with a diameter of 1.0, 2.0 or 3.0 mm, and metal brackets were then bonded with or without functional monomers in the orthodontic adhesive paste. For the baseline groups, the whole adherent area was pre-etched. The shear bond strength (SBS) and adhesive remnant index (ARI) were determined. The adhesive paste/enamel interfaces were observed by scanning electron microscopy (SEM). Although the adhesive paste with functional monomers showed higher SBS than the functional monomer-free adhesive paste in all groups, there were no significant differences in SBS between them regardless of the pre-etched area. The SBS increased with increasing pre-etched area in both orthodontic adhesive pastes. In SEM images of adhesive paste/enamel interfaces, although adhesive with functional monomers showed excellent adaptation, the functional monomer-free adhesive paste showed gap formation at the interface. These findings suggested that the pre-etching area greatly influenced bond strength, regardless of the presence or absence of the functional monomer in the orthodontic adhesive paste