MiR-10a in Pancreatic Juice as a Biomarker for Invasive Intraductal Papillary Mucinous Neoplasm by miRNA Sequencing

New biomarkers are needed to further stratify the risk of malignancy in intraductal papillary mucinous neoplasm (IPMN). Although microRNAs (miRNAs) are expected to be stable biomarkers, they can vary owing to a lack of definite internal controls. To identify universal biomarkers for invasive IPMN, we performed miRNA sequencing using tumor-normal paired samples. A total of 19 resected tissues and 13 pancreatic juice samples from 32 IPMN patients were analyzed for miRNA expression by next-generation sequencing with a two-step normalization of miRNA sequence data. The miRNAs involved in IPMN associated with invasive carcinoma were identified from this tissue analysis and further verified with the pancreatic juice samples. From the tumor-normal paired tissue analysis of the expression levels of 2792 miRNAs, 20 upregulated and 17 downregulated miRNAs were identified. In IPMN associated with invasive carcinoma (INV), miR-10a-5p and miR-221-3p were upregulated and miR-148a-3p was downregulated when compared with noninvasive IPMN. When these findings were further validated with pancreatic juice samples, miR-10a-5p was found to be elevated in INV (p = 0.002). Therefore, three differentially expressed miRNAs were identified in tissues with INV, and the expression of miR-10a-5p was also elevated in pancreatic juice samples with INV. MiR-10a-5p is a promising additional biomarker for invasive IPMN.     

Continuous synthesis of Zn2SiO4:Mn fine particles in supercritical water at temperatures of 400-500 °C and pressures of 30-35 MPa

Sub-micron sized Zn₂SiO₄:Mn²⁺ phosphors particles were continuously synthesized in supercritical water with a flow reactor. Colloidal silica or sodium silicate was used as the Si source. Zn and Mn sources were chosen from their nitrates, sulfates, and acetates. The syntheses were carried out at temperatures from 400 to 500 °C, at pressures from 30 to 35 MPa, at NaOH concentrations from 0.014 to 0.025 M, and for residence times from 0.025 to 0.18 s. Sodium silicate formed α- and β-Zn₂SiO₄:Mn²⁺ phases regardless of the Zn and Mn sources, while colloidal silica formed phases dependent on the type of Zn and Mn sources used in addition to the use of alkali. As the reaction temperature increased, the crystallinity of α-Zn₂SiO₄:Mn²⁺ phase increased and the Mn substitution into the Zn sites of the α-Zn₂SiO₄ phase decreased. Of the conditions studied, the most highly crystalline α-Zn₂SiO₄:Mn²⁺ was produced at a temperature of 400 °C, a pressure of 30 MPa, a NaOH concentration of 0.14 M, and a residence time of 0.13 s with Zn and Mn sulfates and colloidal silica as starting materials. The α-Zn₂SiO₄:Mn²⁺ fine particles synthesized were round in shape, had an average diameter of 268 nm, and exhibited a green-emission with a peak wavelength of 524 nm.     

野外试验场黄土的理化分析

本实验为低,中水平放射性废物浅地层处置安全评价提供现场土壤的物理化学参数。采样深度在０．５－９．１ｍ范围内,每个样品进行１０项测定;矿物组成,粒度分布、密度、总孔隙度、有效孔隙度、给水度、持水度、渗透系数、阳离子交换容量、含水量。     

Anatase Sol Prepared from Peroxotitanium Complex Aqueous Solution Containing Niobium or Vanadium

Niobium- or vanadium-doped anatase sols were prepared by hydrothermal treatment of 0.1 mol/dm³ peroxotitanium complex aqueous solutions dissolving 0–10 mol% niobium or vanadium at 100°C for 8 h. Niobium-doping caused the increase of lattice constants of anatase and the shape change of anatase crystal from spindle-like to cubic-like structure, but no change of the optical absorbance. Vanadium-doping caused the decrease of lattice constant of c -axis, the miniaturization of anatase crystal and the increase of optical absorbance at the wavelength from 350–700 nm.     

Color registration error reduction method compensating the influence of belt thickness variation in electrophotographic process

This paper proposes a new belt drive control method for reducing a belt velocity-fluctuation that is caused by a belt thickness-variation in the circumferential direction. A belt driving system performs feedback control with a rotary encoder-output mounted on a driven roller. This proposed method correct the reference value of the feedback control for the purpose of the belt velocity regulation. The correction includes two steps. The first step acquires the encoder-output of the driven roller and calculates the rotational angular velocity-fluctuation with one cycle of the belt rotation. The second step converts from the velocity-fluctuation to the correction value of the feedback reference. The correction value cancels a detection error of the driven roller caused by the belt thickness-variation. After these steps, the belt driving system controls the belt velocity as compensating the belt velocity-fluctuation. Experimental result showed the significant fluctuation reduction on a typical tandem-engine printer.     

Reduction of Second-Order Temperature Dependence of Athermal AWG With Resin-Filled Groove by Pressure Control

In this letter, we have developed a novel technique for improving the temperature stability of an athermal silica-based arrayed-waveguide grating with a resin-filled groove. We compensated for the residual second-order temperature dependence of the passband wavelength using the pressure-induced refractive index change in a resin inserted into the optical paths. Pressure control under the temperature variation was achieved by using a structure composed of an optical fiber piston and bimetal actuators. We demonstrated that the passband wavelength variation was successfully reduced from 0.080 to 0.025 nm in a -40degC - 85degC temperature range, without any insertion loss increase or spectral change.     

POROSITY AND RESIDUAL EQUILIBRIUM SATURATION OF SINTERED SPHERES OF GLASS BEADS

Sintered spheres(made of glass beads) were simply produced with a definite diameter, with a precision of ±0·5 mm in diameter, for a wide range of sintered angles (0-27°). The experimental values of the porosity of the sintered spheres were consistent with the calculated results for the coordination number N ≠ 8. The residual equilibrium saturation, as one of the basic physical properties of sintered glass beads was investigated experimentally and theoretically, resulting in the presence of a distribution in the angle of pendular ring.     

Polymer coating method developed for carbon stripper foils

The problem of handling the fragile carbon foils (mounting on the frame, placing in the stripper changer) that easily break when self-supporting has been solved by coating carbon foils with poly-monochloro-para-xylylene. It was found that the polymer-coating method could also be used to produce carbon foils thicker than 100 μg/cm² by alternated deposition of carbon and poly-monochloro-para-xylylene layers. Carbon foil of 500 μg/cm² thick and 10 cm in diameter was produced by this method and mounted to a foil holder. Results of lifetime measurement for singly coated foils are also presented.     

Growth and structure of heteroepitaxial thin films of homologous compounds RAO3(MO)m by reactive solid-phase epitaxy: Applicability to a variety of materials and epitaxial template layers

A reactive solid-phase epitaxy (R-SPE) method combines deposition of a thick amorphous or polycrystalline layer with a desired chemical composition and post-deposition solid-phase epitaxial growth. The solid-phase epitaxial growth is invoked by thermal annealing with an assistance of a sacrificial layer working as an epitaxial template. Thereby it enables us to grow high-quality epitaxial films of complex oxides whose epitaxial films are not grown by conventional high-temperature growth techniques. It was reported that 2-nm-thick ZnO layers worked as template for growing InGaO₃(ZnO)_m (m = integer) epitaxial films. The present study extended the R-SPE technique to growth of various complex oxides with chemical compositions of RAO₃(MO)_m and to use of various epitaxial template layers. We found that mono oxide epitaxial layers such as In₂O₃ and Ga₂O₃ work as template layers as well. Alternatively, a ZnO epitaxial layer is also applicable to ZnO-free compounds. The films obtained were grown heteroepitaxially on YSZ(111) and single-crystalline when the fabrication conditions are optimized.