Increasing the filler content of POM/TD32.4 and POM/TD130 (130 nm) nanocomposites resulted in a decrease in tensile strength. The Young modulus, stress at break and impact strength of TiO2 nanocomposite did not improve with increasing filler contents, in opposition to the better agglomeration conditions of ZnO nanocomposite even at lower particle sizes. Because of agglomeration, STI571 mw the POM/TD32.4 nanocomposites had lower mechanical properties and lower degradation temperature than the POM/TD130 ones. The sizes of nanoparticles determined the agglomeration, but however, the agglomeration also depended on the type of nanoparticles,

even when using the same matrix (POM) and the same mixing method. TiO2 nanoparticles were more difficult PLX3397 price to mix and were more agglomerated in the POM matrix as compared to ZnO nanoparticles, regardless of the size of the nanoparticles. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci 123: 3217-3224, 2012″
“This manuscript presents the first observation of the space-charge-limited current (SCLC) conduction mechanism in individual heterostructure nanowires (NWs). This effect is exploited to extract size-dependent carrier densities and to demonstrate surface-dominated behavior for these technologically relevant nanostructures. Mobile carrier densities were shown to increase from 2.5 x 10(16) to 5.6 x 10(17) cm(-3), as

NW width decreased from 200 to 50 nm. This size-dependent behavior is a consequence of the increasing influence of near-surface confined carriers as widths decrease. Traps impact the SCLC response and were characterized as an exponential band edge tail with an average characteristic energy of 75 meV. In addition to the specific materials properties extracted, these results

further demonstrate the tendency for low-dimensional materials (1D NWs) to exhibit SCLC at much lower injection fluxes compared to their higher dimensional (2D heterostructure field-effect transistors) counterparts. (C) 2011 American Institute of Physics. [doi:10.1063/1.3622145]“
“Clusterin is a heterodimeric sulfated glycoprotein and plays a role in many different types of cancer as a cell survival factor and helps cancerous cells to evade stress-induced apoptosis. To investigate whether the regulation of compound inhibitor clusterin expression is involved in the mechanism of anticancer agent, we studied the effect of tamoxifen on clusterin expression in human prostate cancer PC-3 cells. Treatment of PC-3 cells with tamoxifen reduced cellular proliferation. Western blot analyses showed that treatment with tamoxifen suppressed clusterin expression in a concentration-dependent manner. Transfection with clusterin siRNA plasmid showed that clusterin is required for PC-3 cell survival. We found that tamoxifen resulted in a rapid decrease in the phosphorylation of Akt on Ser473 leading to prevent kinase activity.