Experimental observation of superscattering

Superscattering, induced by degenerate resonances, breaks the fundamental single-channel limit of scattering cross section of subwavelength structures; in principle, an arbitrarily large total cross section can be achieved via superscattering. It thus provides a unique way to strengthen the light-matter interaction at the subwavelength scale, and has many potential applications in sensing, energy harvesting, bio-imaging (such as magnetic resonance imaging), communication and optoelectronics. However, the experimental demonstration of superscattering remains an open challenge due to its vulnerability to structural imperfections and intrinsic material losses. Here we report the first experimental evidence for superscattering, by demonstrating the superscattering simultaneously in two different frequency regimes through both the far-field and near-field measurements. The underlying mechanism for the observed superscattering is the degenerate resonances of confined surface waves, by utilizing a subwavelength metasurface-based multilayer structure. Our work paves the way towards practical applications based on superscattering

Experimental Observation of Superscattering

Superscattering, induced by degenerate resonances, breaks the fundamental single-channel limit of the scattering cross section of subwavelength structures; in principle, an arbitrarily large total cross section can be achieved via superscattering. It thus provides a unique way to strengthen the light-matter interaction at the subwavelength scale, and has many potential applications in sensing, energy harvesting, bioimaging (such as magnetic resonance imaging), communication, and optoelectronics. However, the experimental demonstration of superscattering remains an open challenge due to its vulnerability to structural imperfections and intrinsic material losses. Here we report the first experimental evidence for superscattering by demonstrating the superscattering simultaneously in two different frequency regimes through both the far-field and near-field measurements. The underlying mechanism for the observed superscattering is the degenerate resonances of confined surface waves, by utilizing a subwavelength metasurface-based multilayer structure. Our work paves the way towards practical applications based on superscattering

Antidepressant Effects of Repetitive Transcranial Magnetic Stimulation Over Prefrontal Cortex of Parkinson's Disease Patients With Depression: A Meta-Analysis

Objective: The purpose of this meta-analysis was to investigate the antidepressant effects of repetitive transcranial magnetic stimulation (rTMS) over the prefrontal cortex (PFC) of patients with Parkinson's disease (PD) and to determine the optimal rTMS parameters, such as the intensity, frequency and the delivered pattern of rTMS stimulation.Methods: EMBASE, PubMed, Web of Science, MEDLINE, and Cochrane data bases were researched for papers published before March 12, 2018. Studies investigating the anti-depression effects of rTMS over PFC in patients with PD were considered. The main outcomes of pre- and post-rTMS treatment as well as score changes were all extracted. The mean effect size was estimated by calculating the standardized mean difference (SMD) with 95% confidence interval (CI) by using fixed or random effect models as appropriate.Results: Nine studies containing 137 PD patients with depression were included. The pooled results showed significant pre-post anti-depressive effects of rTMS over PFC in PD patients with depression (SMD = −0.80, P < 0.00001). The subgroup analyses of stimulation intensity, frequencies, and models also revealed significant effects (Intensities: 90% RMT: SMD = −1.16, P = 0.0006; >100% RMT: SMD = −0.82, P < 0.0001. Frequencies: < 1.0 Hz: SMD = −0.83, P = 0.03; 5.0 Hz: SMD = −1.10, P < 0.0001; ≥10.0 Hz: SMD = −0.55, P = 0.02. Models: Continuous: SMD = −0.79, P < 0.0001; Discontinuous: SMD = −0.84, P = 0.02). But the results of the studies with place-controlled designs were not significant (Overall: SMD = −0.27, P = 0.54. Intensities: 90% RMT: SMD = 0.27, P = 0.68; 100% RMT: SMD = −0.32, P = 0.33. Frequencies: 5.0 Hz: SMD = −0.87, P = 0.10; ≥10.0 Hz: SMD = 0.27, P = 0.66. Models: Continuous: SMD = −0.28, P = 0.68; Discontinuous: SMD = −0.32, P = 0.33). The greater effect sizes of rTMS with 90% RMT, 5.0 Hz in discontinuous days can be observed rather than the other parameters in both kinds of analyses across study design.Conclusions: rTMS may have a significant positive pre-post anti-depressive effect over PFC on patients with depression, especially by using 5.0 Hz frequency with 90% RMT intensity in discontinuous days, which may produce better effects than other parameters. The real effect, though, was not different from that of the placebo. Future studies with larger sample sizes and high-quality studies are needed to further corroborate our results and to identify the optimal rTMS protocols

Overexpression of sphingosine kinase 1 is associated with salivary gland carcinoma progression and might be a novel predictive marker for adjuvant therapy

<p>Abstract</p> <p>Background</p> <p>Overexpression of sphingosine kinase-1 (SPHK1) has been demonstrated to be associated with the development and progression in various types of human cancers. The current study was to characterize the expression of SPHK1 in salivary gland carcinomas (SGC) and to investigate the association between SPHK1 expression and progression of SGC.</p> <p>Methods</p> <p>The expression of SPHK1 was examined in 2 normal salivary gland tissues, 8 SGC tissues of various clinical stages, and 5 pairs of primary SGC and adjacent salivary gland tissues from the same patient, using real-time PCR and western blot analysis. Furthermore, the SPHK1 protein expression was analyzed in 159 clinicopathologically characterized SGC cases by immunohistochemistry. Statistical analyses were performed to determine the prognostic and diagnostic associations.</p> <p>Results</p> <p>SPHK1 expression was found to be markedly upregulated in SGC tissues than that in the normal salivary gland tissues and paired adjacent salivary gland tissues, at both mRNA and protein levels. Statistical analysis revealed a significant correlation of SPHK1 expression with the clinical stage (<it>P </it>= 0.005), T classification (<it>P </it>= 0.017), N classification (<it>P </it>= 0.009), M classification (<it>P </it>= 0.002), and pathological differentiation (<it>P </it>= 0.013). Patients with higher SPHK1 expression had shorter overall survival time, whereas patients with lower SPHK1 expression had better survival. Importantly, patients in the group without adjuvant therapy who exhibited high SPHK1 expression had significantly lower overall survival rates compared with those with low SPHK1 expression. Moreover, multivariate analysis suggested that SPHK1 expression might be an independent prognostic indicator for the survival of SGC patients.</p> <p>Conclusions</p> <p>Our results suggest that SPHK1 expression is associated with SGC progression, and might represent as a novel and valuable predictor for adjuvant therapy to SGC patients.</p

Unregulated miR-96 Induces Cell Proliferation in Human Breast Cancer by Downregulating Transcriptional Factor FOXO3a

FOXO transcription factors are key tumor suppressors in mammalian cells. Until now, suppression of FOXOs in cancer cells was thought to be mainly due to activation of multiple onco-kinases by a phosphorylation-ubiquitylation-mediated cascade. Therefore, it was speculated that inhibition of FOXO proteins would naturally occur through a multiple step post-translational process. However, whether cancer cells may downregulate FOXO protein via an alternative regulatory mechanism is unclear. In the current study, we report that expression of miR-96 was markedly upregulated in breast cancer cells and breast cancer tissues compared with normal breast epithelial cells (NBEC) and normal breast tissues. Ectopic expression of miR-96 induced the proliferation and anchorage-independent growth of breast cancer cells, while inhibition of miR-96 reduced this effect. Furthermore, upregulation of miR-96 in breast cancer cells resulted in modulation of their entry into the G1/S transitional phase, which was caused by downregulation of cyclin-dependent kinase (CDK) inhibitors, p27Kip1 and p21Cip1, and upregulation of the cell-cycle regulator cyclin D1. Moreover, we demonstrated that miR-96 downregulated FOXO3a expression by directly targeting the FOXO3a 3′-untranslated region. Taken together, our results suggest that miR-96 may play an important role in promoting proliferation of human breast cancer cells and present a novel mechanism of miRNA-mediated direct suppression of FOXO3a expression in cancer cells

Study on the Material Model and Hot Working Drawing of a New Type of High Temperature Titanium Alloy Ti-Al-Nb

This paper proposes an exploratory study on the preparation of titanium-based superalloys through the Ti+Al+Ti2AlNb three-component hybrid hot press sintering method. Through the hot press sintering experiment of the mixed powder under different heating and sintering processes, the plastic deformation behavior of the material is carried out on this basis Research, preliminarily discuss the constitutive relationship of the new high-temperature titanium alloy Ti-Al-Nb, establish the hot working map and recrystallization model

Study on the Influence of the New Type of Powder Metallurgy Ti-Al-Nb Alloy Hot Press Sintering Process on the Microstructure

Based on the hot-pressing sintering process, the kinetics of hot-pressing sintering crystal grain growth and the hot-pressing sintering densification kinetics, the mixing ratio of the raw material powder and the hot-pressing sintering system are designed. The pressure is maintained at 30 MPa from the temperature rise to the end of the sintering process, and wait until the temperature reaches the corresponding hot pressing sintering temperature (1200°C~1400°C), keep the corresponding time for 1.5h~4.5h, stop heating and depressurize, and the alloy billet is cooled to room temperature with the furnace. The main phases of Ti2AlNb powder and hot pressing sintering process are TiAl and Ti3Al