A novel mesoporous material (“nanopaper”) prepared from template‐synthesized, polyelectrolyte‐stabilized polymer nanotubes is reported. The stacked network of completely collapsed, flat nanotubes forms the porous structure, which has a water‐vapor permeability that can be tuned by the stabilizer. The transport mechanism is elucidated based on microscopy, thermal analysis, spectroscopy characterization, and mass‐transfer theory. The results suggest that the nanotube surface plays a key role in the through‐film transport process. This effect vanishes in the more open films formed from micro‐fibrillated cellulose having similar fibril diameters. Nanopaper mechanical properties are also reported. With a pore structure and functionality that can be varied, nanopaper is a promising functional membrane.
Unusual brown to yellow diamonds of mixed type Ib/IaAB were analyzed. The occurrence of nitrogen in a combination of A, B and C centers directly detectable by IR spectroscopy in natural diamonds is considered to be extremely rare. We propose to call such stones ABC diamonds for short. These diamonds are characterized by a color, luminescence, and anomalous double refraction distribution which results from mixed growth: a center core formed by cuboid growth, rich in nitrogen, covered by an outer rim of “normal” octahedral growth, with much less nitrogen. Nitrogen in the core is present in a more aggregated state than in the rim, which is practically pure type Ib.In the infrared spectra, besides A, B and C 1-phonon absorptions a large number of previously undescribed, tentatively H-related features were identified in some samples; these proposed H-related features were only present in the periphery of the core and the rim of the diamonds, in the core practically no hydrogen was detected. The low temperature Vis/NIR spectra were mainly characterized by two defect-induced centers: the H2 center, and the apparently new 905 nm vibronic absorption with phonon-side bands at 880, 867, 847 nm plus a feature at 806.5 nm. The 905 nm absorption can possibly be attributed to a hydrogen-related center. Although these diamonds present a combination of spectroscopic characteristics (A + B + C center absorptions, H2 absorptions) deemed characteristic of certain HPHT-treated type Ia diamonds, they cannot be confused for such treated diamonds on the basis of their color, color distribution and some spectral peculiarities. 相似文献
Our previous study demonstrated that the glutathione S-transferase Mu 5 (GSTM5) gene is highly CpG-methylated in bladder cancer cells and that demethylation by 5-aza-dC activates GSTM5 gene expression. The aim of the present study was to investigate the role of GSTM5 in bladder cancer. The levels of GSTM5 gene expression and DNA methylation were analyzed in patients with bladder cancer, and functional studies of GSTM5 were conducted using GSTM5 overexpression in cultured bladder cancer cells. Clinical analysis revealed that the GSTM5 mRNA expression was lower in bladder cancer tissues than in normal tissues and that the level of GSTM5 DNA methylation was higher in bladder cancer tissues than in normal urine pellets. Overexpression of GSTM5 decreased cell proliferation, migration and colony formation capacity. Glutathione (GSH) assay results indicated that cellular GSH concentration was decreased by GSTM5 expression and that GSH supplementation reversed the decrease in proliferation and migration of cells overexpressing GSTM5. By contrast, a GSH synthesis inhibitor significantly decreased 5637 cell GSH levels, survival and migration. Furthermore, GSTM5 overexpression inhibited the adhesion of cells to the extracellular matrix protein fibronectin. To elucidate the effect of GSTM5 on anticancer drugs used to treat bladder cancer, cellular viability was compared between cells with or without GSTM5 overexpression. GSTM5-overexpressed cells showed no significant change in the cytotoxicity of cisplatin or mitomycin C in 5637, RT4 and BFTC 905 cells. Though a degree of resistance to doxorubicin was noted in 5637 cells overexpressing GSTM5, no such resistance was observed in RT4 and BFTC 905 cells. In summary, GSTM5 plays a tumor suppressor role in bladder cancer cells without significantly affecting chemoresistance to cisplatin and mitomycin C, and the cellular GSH levels highlight a key mechanism underlying the cancer inhibition effect of GSTM5. These findings suggest that low gene expression and high DNA methylation levels of GSTM5 may act as tumor markers for bladder cancer. 相似文献