The Role of Matrix Metalloproteinase Polymorphisms in Ischemic Stroke

Stroke remains the fifth leading cause of mortality in the United States with an annual rate of over 128,000 deaths per year. Differences in incidence, pathogenesis, and clinical outcome have long been noted when comparing ischemic stroke among different ethnicities. The observation that racial disparities exist in clinical outcomes after stroke has resulted in genetic studies focusing on specific polymorphisms. Some studies have focused on matrix metalloproteinases (MMPs). MMPs are a ubiquitous group of proteins with extensive roles that include extracellular matrix remodeling and blood-brain barrier disruption. MMPs play an important role in ischemic stroke pathophysiology and clinical outcome. This review will evaluate the evidence for associations between polymorphisms in MMP-1, 2, 3, 9, and 12 with ischemic stroke incidence, pathophysiology, and clinical outcome. The role of polymorphisms in MMP genes may influence the presentation of ischemic stroke and be influenced by racial and ethnic background. However, contradictory evidence for the role of MMP polymorphisms does exist in the literature, and further studies will be necessary to consolidate our understanding of these multi-faceted proteins.     

Organic photovoltaics for low light applications

Here we report on organic photovoltaic's (OPV) suitable for low light applications. In this paper, we illustrate the impact of R_s and R_p for indoor and outdoor applications. In addition, we propose a simple physics approach to predict the behavior of organic solar cells under various illumination intensities through electrical modeling. The combination of simulation and modeling allows to define a set of design rules for OPVs under low light illumination. The performance of various organic solar cells under low light intensity is compared with our predictions and excellent correlation is found. OPV shows high performance under low light conditions.     

Characterization of High-k Gate Dielectric with Amorphous Nanostructure

In the present study, Zr _x La_1?x O _y amorphous nanostructures were prepared by the sol–gel method such that the Zr atomic fraction (x) ranged from 0% to 70%. An analytical model is described for the dielectric constant (k) of Zr _x La_1?x O _y nanostructures in a metal–oxide–semiconductor (MOS) device. The structure and morphology of Zr _x La_1?x O _y film was studied using x-ray diffraction, scanning electron microscopy, atomic force microscopy, and transmission electron microscopy. Elemental qualitative analysis was performed using energy-dispersive x-ray spectra and a map that confirmed the findings. Preliminary information on the influence of thermal annealing on the morphological control of Zr _x La_1?x O _y amorphous nanostructures is presented. The dielectric constant of the crystalline Zr_0.5La_0.5O _y thin film is about 36. Electrical property characterization was performed using a metal–dielectric–semiconductor structure via capacitance–voltage and current density–voltage measurements.     

Semitransparent polymer solar cells

Bulk heterojunction based polymer:fullerene solar cells have attracted intensive research interest both in academic and industrial communities in the last two decades, mainly related to their potential low‐cost production process. A power conversion efficiency of over 10% has been reported recently, making the commercialization of this clean and cheap solar energy convertor a realistic prospect for the near future. The intrinsic features of semitransparency and color tunability of the thin polymeric photoactive films are the greatest asset for polymer solar cells. Recently, aesthetic semitransparent polymer solar cells (ST‐PSCs) that can be integrated into transparent windows, roofs, glass and other semitransparent architectural elements have received much attention. In this perspective paper, we present the progress in achieving high performance ST‐PSCs, discuss the requirements for transparent electrodes, focusing on alternatives to tin‐doped indium oxide, and address the challenges ahead to make ST‐PSC viable for real applications. © 2013 Society of Chemical Industry     

A new dithienosilole-based oligothiophene with methyldicyanovinyl groups for high performance solution-processed organic solar cells

A new linear dithienosilole-based oligothiophene end-capped with methyl and electron-withdrawing dicyanovinyl groups, DTS(Oct)₂-(2T-DCV-Me)₂, was prepared in good yield. This oligomer exhibited broad absorption spectra in bulk down to the near-IR region with the optical edge at 900 nm, resulting in an initially high power conversion efficiency of 5.44% in solution-processed organic solar cells using PC₇₁BM as an acceptor.     

Hydrothermal synthesis of ZnO nanoflowes for rapid detection of sertraline and imipramine using the modified screen-printed electrode

ZnO nanoflowers-modified graphite screen-printed electrode had very good electrochemical catalytic activity toward sertraline and imipramine. Results showed significant decline in the oxidation overpotentials of sertraline and imipramine in comparison with the overpotential at the bare graphite screen-printed electrode. Moreover, differential pulse voltammetry has been utilized to simultaneously determine sertraline and imipramine in the ternary mixture. Based on the analyses, the peak separation between sertraline and imipramine was 200 mV. In addition, calibration curve for imipramine ranged from 0.1 to 550.0 μM. Furthermore, minimum limit of detection (S/N?=?3) equaled 0.035 μM imipramine. Finally, this new procedure exhibited acceptable sensitivity and selectivity so that it could be utilized for determining sertraline and imipramine in the pharmaceutical medicines and urine samples.

     

Calorimetric and rheokinetic analyses merged to capture crystallization kinetics in polyamide/clay nanocomposites: Revisiting predictability of models

Crystallization kinetics of polymer/clay systems was the subject of numerous investigations, but still there are some ambiguities in understanding thermal behavior of such systems under isothermal and nonisothermal circumstances. In this work, isothermal rheokinetic and nonisothermal calorimetric analyses are combined to demonstrate crystallization kinetics of polyamide6/nanoclay (PA6/NC) nanocomposites. As the main outcome of this work, we detected different regimes of crystallization and compared them by both isothermal dynamic rheometry and nonisothermal differential scanning calorimetry (DSC), which has not been simultaneously addressed yet. A novel analysis, somehow different from the common ones, is used to convert the storage modulus data to crystallinity values leading to more reasonable Avrami parameters in isothermal crystallization. It was found based on isothermal rheokinetic studies that increase of NC content and shear rate are responsible for erratic behavior of Avrami exponent and crystallization rates. Optimistically, however, isothermal crystallization by rheometer was confirmed by DSC. Nonisothermal calorimetric evaluations suggested an accelerated crystallization of PA6 upon increasing NC content and cooling rate. The crystallization behavior was quantified applying Ozawa (r² between 0.070 and 0.975), and combinatorial Avrami–Ozawa (r² between 0.984 and 0.998) models, where the latter appeared more appropriate for demonstration of nonisothermal crystallization of PA6/NC nanocomposites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46364.     

A New Two-Quadrant Squarer/Divider Circuit for true RMS-to-DC converters in MOS technology

In this paper, a new log-domain two-quadrant squarer/divider circuit for current mode RMS-to-DC converters is presented. The proposed circuit has been realized using MOSFET transistors that are operating in weak inverted saturation region. It features very low supply voltage (1 V), low power consumption (<3 μW), two-quadrant input current, wide input dynamic range, immune from body effect and low circuit complexity. Simulation results by HSPICE show high performance of the circuit and confirm the validity of the proposed design technique.     

The pozzolanic reactivity of monodispersed nanosilica hydrosols and their influence on the hydration characteristics of Portland cement

This study reveals that the nanosilica hydrosols with higher specific surface areas had faster pozzolanic reactivity, especially at early ages; moreover, the results are indicative of the accelerating influence of nanosilicas and silica fume on the hydration of cement. Faster initial and final setting times observed for cement pastes containing nanosilicas are consequence of these mechanisms. However, less hydration degree of cement compared to the plain paste was observed at age of 7 days and after. This can be attributed to the entrapment of some of mix water in the aggregates of nanosilicas formed in cement paste environment, making less water available for the progress of cement hydration. The same mechanism is believed to be responsible for the reduction of flowability of cement pastes.