Nanocrystalline Composite Layer Realized by Simple Sintering Without Surface Treatment, Reducing Hydrophilicity and Increasing Thermal Conductivity.

The surface treatment for a polymer-ceramic composite is additionally performed in advanced material industries. To prepare the composite without a surface treatment, the simplest way to manufacture an advanced ceramic-particle is devised. The method is the formation of a nanocrystalline composite layer through the simple liquid-phase sintering. Using magnesia (MgO) which shows hydrophilicity, a nanocrystalline surface layer is realized by liquid-phase sintering. The amorphous matrix of nanocrystalline composite layer makes MgO hydrophobic and ensures miscibility with polymers, and the nanocrystalline MgO ensures high thermal conductivity. In addition, the liquid phase removes the open pores and makes the surface morphology smooth MgO with smooth surface (MgO-SM). Thermal interface materials (TIM) prepared with MgO-SM and epoxy show a high thermal conductivity of ≈7.5 W m-1 K-1 , which is significantly higher than 4.5 W m-1 K-1 of pure MgO TIM. Consequently, the formation process of a nanocrystalline surface layer utilizing simple liquid-phase sintering is proposed as a fabrication method for a next-generation ceramic-filler. In addition, it is fundamentally identified that the thermal conductivity of MgO depends on the Mg deficiency, and therefore a poly-crystal MgO-SM (produced at a low temperature) has a higher thermal conductivity than a single-crystal MgO (produced at a high temperature).

Proteome-wide identification of arginine methylation in colorectal cancer tissues from patients.

BACKGROUND: Protein arginine methylation reaction is catalyzed by protein arginine methyltransferase (PRMT) and the modification is implicated in various diseases including cancer. Currently, thousands of arginine methylation sites have been identified using high-resolution mass spectrometry-based proteomics technology. However, identification of arginine methylation using clinical samples at proteome level has not been reported yet. The objective of the present study was to identify, monomethyl-arginine (MMA) and asymmetric dimethyl-arginine (ADMA) sites in colorectal cancer (CRC) tissues at proteome level. METHODS: Pooled CRC tissue samples from 10 patients with stage II and III were digested by trypsin and these digests were further processed and lyophilized. Using monomethyl- or asymmetric dimethyl arginine (MMA or ADMA, respectively) motif kits, methylarginine-containing peptides were enriched and subsequently analyzed by high-resolution LC-MS/MS. DLD1 and HCT116 colon cancer cells were treated with type I PRMTs inhibitor (MS023) alone or combined with SN-38, and the effect of the drugs on CRC cell proliferation and apoptosis was measured by water-soluble tetrazolium salt (WST-1) assay and FACS analysis, respectively. RESULTS: In the present study, 455 MMA sites of 272 proteins and 314 ADMA sites of 155 proteins were identified from CRC tissues acquired from patients. In addition, 216 methylation sites and 75 substrates for PRMTs were newly identified. These results reveal the significant presence of MMA and ADMA sites on nucleic acid binding proteins and protein complexes involved in transcription. To investigate the effect of protein arginine methylation in CRC proliferation and apoptosis, MS023 was treated to two CRC cell lines. After 48 h treatment with various concentrations of MS023, CRC cell proliferation was significantly suppressed, with concomitant apoptosis induction. Furthermore, MS023 treatment significantly enhanced the inhibitory effect of SN-38 on CRC cell proliferation. CONCLUSION: This work reports the first comprehensive analysis of arginine methylation with clinical sample and suggests that type I PRMTs are potential therapeutic targets for drug discovery in CRC.

Me-too validation study for in vitro eye irritation test with 3D-reconstructed human cornea epithelium, MCTT HCETM.

The need for in vitro eye irritation test replacing in vivo is steadily increasing. The MCTT HCE™ eye irritation test (EIT) using 3D reconstructed human cornea-like epithelium, was developed to identify ocular irritants from non-irritants those that are not requiring classification and labelling for eye irritation. Here, we report the results of me-too validation study, which was conducted to evaluate the reliability and relevance of the MCTT HCETM EIT, according to performance standards (PS) of OECD TG 492. The optimal cutoff to determine irritation in the prediction model was preliminarily established at 45% with the receiver operation characteristics (ROC) curve for 141 reference substances. To demonstrate the reproducibility of within- and between-laboratory (WLR and BLR), a set of 30 PS reference chemicals were tested in three laboratories three times. The WLR and BLR concordance with the binary decision of whether non-irritant or irritant was estimated to be 90-100% and 90%, respectively, and both met the PS requirements. The predictive capacity of the respective laboratories for the 30 reference chemicals were evaluated based on three different estimation methods, and the results were comparable, with sensitivity ranging from 89.6 to 93.3%, the specificity ranging from 62.2 to 66.7%, and the accuracy ranging from 75.9 to 80.0%. Additional test with the new set of 30 PS substances in the revised OECD GD 216 yielded a performance of sensitivity ranging from 92.6-93.3%, the specificity 62.2-66.7% and the accuracy 77.4-80.0%. 95.0% sensitivity, 67.2% specificity, and 83.0% accuracy were obtained for 141 reference substances in total. Furthermore, separate cutoffs for liquids and solids, 35% and 60%, respectively, produced better predictivity, which was established as a final prediction model. Collectively, our study demonstrated that MCTT HCETM EIT meets the reproducibility and predictivity criteria stated in OECD TG 492 PS.

Monolithic Two-Dimensional Photonic Crystal Reflectors for the Fabrication of Highly Efficient and Highly Transparent Dye-Sensitized Solar Cells.

The transparent characteristic of dye-sensitized solar cells (DSCs) makes them suitable for building integrated photovoltaic (BIPV) devices. However, the diffusive scattering layer, which is usually used to increase the efficiency of these devices, greatly lowers the transparency of the DSC. This paper described a two-dimensional (2D) photonic crystal (PC) reflector with a sub-micrometer characteristic length that can improve the efficiency of these devices while maintaining transparency. This 2D PCs were fabricated directly onto TiO2 photoelectrodes using colloidal lithography and have the structure of a nanopillar array. A nanopillar with a height of 430 nm was observed to selectively reflect up to 40% of the light of 400-500 nm wavelength. The perceived transparency of the 2D PC electrode was 52%, which is much higher than 0.3% of the conventional scattering layer. The DSC fabricated using the 2D PC electrode demonstrated a maximum photon-to-electric conversion efficiency of 8.23%, which is 18% higher than the pristine electrode. The 2D PC is a highly efficient and wavelength-selective reflector that can be applied to various photoelectric conversion devices.

In Situ Gelation of Poly(vinylidene fluoride) Nanospheres for Dye-Sensitized Solar Cells: The Analysis on the Efficiency Enhancement upon Gelation.

The in situ gelation that utilizes the dissolution of polymers inside the cell is allowed high concentration polymer gel without concerns regarding high viscous electrolyte incorporation into the cell as in the conventional approach. We demonstrate the in situ gelation of polymer composite electrolytes using poly(vinylidene fluoride) nanospheres (PVdF NSs). The PVdF NSs were synthesized by high pressure emulsion polymerization using gaseous vinylidene fluoride monomers. Compared to the liquid electrolyte (LE) DSCs without PVdF gelation, the PVdF polymer gel electrolyte (PGE) DSCs displayed higher η than the LE DSCs; specifically, the 10 wt % PVdF PGE DSCs display 8.1% of the η, while the LE DSCs only display 6.5%. We characterized the effect of PVdF PGE on the photovoltaic parameters in detail. We also compared the long-term stability of DSCs containing LE and PVdF PGE. The DSCs with PVdF PGE exhibited high stability compared to the LE DSCs, similar to a conventional PGE system. We believe that this facile in situ gelation approach could be utilized for not only the practical application of polymer gel electrolytes DSCs but also for various energy-storage devices.

In-situ fabrication of macroporous films for dye-sensitised solar cells: formation of the scattering layer and the gelation of electrolytes.

Dye-sensitised solar cells (DSCs) are a promising substitute for conventional silicon solar cells. A scattering layer of submicrometer pores or particles has been widely introduced to achieve a high light-harvesting efficiency. However, many such fabrication processes require high temperatures and multiple steps to prepare the scattering layer. Here, we have developed an in-situ fabrication process for a macroporous (MP) scattering film. The macropores were formed inside the assembled cell via the dissolution of polystyrene (PS) spheres from a PS/TiO2 composite layer caused by exposure to an electrolyte solution. Specifically, the in-situ MP scattering layer decreased the transmittance of the electrode film from 58% to below 1%. The DSCs using these MP scattering layers exhibited an increase in the efficiency of 22%. Moreover, the dissolution of the PS improved the cell stability because of the gelation of the electrolyte solution; the efficiency of the DSCs was maintained at 80% of its initial value after ageing for 20 days, whereas the efficiency of the bare-electrode DSCs was found to have decreased by 50%. We believe that in-situ porous scattering layers show great promise for next-generation flexible DSCs. Moreover, this approach can be extended to various applications that utilize porous film/liquid systems.

1D nanorod-planted 3D inverse opal structures for use in dye-sensitized solar cells.

The effectiveness of the 1D nanorod (NR)-planted 3D inverse opal (IO) structure as an electrode for dye-sensitized solar cells (DSSCs) is demonstrated here. The NRs were grown on the surface of a macroporous IO structure and their longitudinal growth increased the surface area of the structure proportional to the growth duration. NR/IO electrodes with various NR growth times were compared. A remarkable JSC was obtained for the DSSCs utilizing a NR/IO electrode. The improvement of the JSC was analyzed in terms of its efficiency in light harvesting and electron transport. The growth of the NRs improved the dye adsorption density and scattering property of the electrode, resulting in an improvement in the light harvesting efficiency. Electrochemical impedance analysis revealed that the NRs also improved its electron transport properties. Further growth of the NRs tended to limit the increase of the JSC, which could be attributed to an overlap between them.

Bottom-up growth of hierarchical electrodes for highly efficient dye-sensitized solar cells.

The nonconventional bottom-up growth of TiO2 was first demonstrated in the preparation of hierarchical TiO2 electrodes for use in highly efficient dye-sensitized solar cells. The simple immersion of a substrate in a precursor solution enabled the growth of TiO2 particulate films. Here, we have implemented a hierarchical growth strategy in which two stages of controlled growth yielded first macroscale TiO2 particles, followed by mesoscale TiO2 particles. We successfully fabricated electrode films up to 20 µm thick via a growth rate of 0.3 µm/min. The specific area of the electrodes was controlled via the deposition of mesoscale TiO2 particles. The deposited particles displayed a rutile phase with an average size of several tens of nanometers in diameter, as confirmed by XRD and high-resolution TEM imaging. After depositing the second layer of mesoscale TiO2 particles, the photocurrent density increased by a factor of 3. A maximum efficiency of 6.84% was obtained for the hierarchically structured TiO2 electrodes under 1 sun illumination. The hierarchical TiO2 electrodes were compared with macroporous TiO2 electrodes, revealing that the higher photocurrent density could be attributed to a longer electron recombination lifetime and a high specific area. The longer recombination lifetime was supported by the presence of fewer defective TiO2 surfaces, as confirmed by the XPS spectrum.

[Development and testing of an instrument to measure family's emotional response toward physically restrained patients].

PURPOSE: This was a methodological research to develop an instrument to assess the emotional response of family members of physically restrained patients. METHODS: A primary instrument with 68 questions was developed based on literature review and semi-structured interviews with family members. A group of experts revised individual questions and removed 4 irrelevant questions. This secondary instrument, then, was tested with 199 family members of physically restrained patients in intensive care units of a university hospital. The validity and reliability of the instrument were tested by factor analysis. RESULTS: After item analysis, 3 questions with a correlation coefficient under .30 were discarded and the questions with a factor loading under .45 on Varimax Rotation were also removed. After factor analysis on the final 37 questions, 7 factors were identified; avoidance, shock, helplessness, grudge, depression, anxiousness, and acceptance. The total variance explained was 55.63%. The reliability of this instrument was 0.93 of Cronbach's alpha. CONCLUSION: This instrument was statistically reliable and valid to measure family's emotional response to physical restraints of the patients. This instrument can be useful in assessing the effects of nursing interventions for family members of restrained patients.