General analysis on the use of tesla's resonators in domino forms for wireless power transfer

In this paper, we present a brief overview of historical developments of wireless power and an analysis on the use of Tesla's resonators in domino forms for wireless power transfer. Relay resonators are spaced between the transmitter and receiver coils with the objectives of maximizing energy efficiency and increasing the overall transmission distance between the power source and the load. Analytical expressions for the optimal load and maximum efficiency at resonance frequency are derived. These equations are verified with practical measurements obtained from both coaxial and noncoaxial domino resonator systems. To avoid the use of high operating frequency for wireless power transfer in previous related research, the technique presented here can be used at submegahertz operation so as to minimize the power loss in both the power supply and the output stage. We demonstrated both theoretically and practically that unequal spacing for the coaxial straight domino systems has better efficiency performance than the equal-spacing method. Also, the flexibility of using resonators in various domino forms is demonstrated. © 2012 IEEE.published_or_final_versio

Model peptides to study the effects of P2 and P3 substitutions in statine-containing HIV proteinase inhibitors

AbstractThrough a series of synthetic model peptides, we have examined the structural requirements of the P2 and P3 residues in statine-based HIV protease (PR) inhibitors. Results agree with the general observations that, the more bulky the P3 aromatic hydrophobic side chain, the more potent is the inhibitor. At P2, an isopropyl side chain is critical in maintaining potency. Three-dimensional modeling demonstrates that the steric bulk of a leucyl residue or the unfavorable energy transfer, from water to enzyme, for a basic amino acid residue at P2 markedly compromises activity. A naphthylalaninyl-valyl P3-P2 substituted analogue inhibits PR with an IC50 value of 6 nM, and was also effective as an antiviral agent

R-PEP-27, a Potent Renin Inhibitor, Decreases Plasma Angiotensin II and Blood Pressure in Normal Volunteers

The hemodynamic and humoral effects of the specific human renin inhibitor R-PEP-27 were studied in six normal human subjects on low and high sodium intake diets. An intravenous infusion of R-PEP-27 (0.5 to 16 μg/min/kg body wt) reduced blood pressure in a dose-dependent fashion; the mean arterial blood pressure at the end of the infusion fell from 128 ± 4/83 ± 4 to 119 ± 3/71 ± 3 mm Hg (mean ± SEM) (P < .01) during the low sodium intake diet. R-PEP-27 had no effect on blood pressure during the high sodium intake diet. R-PEP-27 significantly reduced plasma angiotensin II and aldosterone concentrations. The temporal response to R-PEP-27 suggests that it is a shortlived although highly potent competitive inhibitor of renin; this peptide is a valuable and specific physiologic probe of the renin-angiotensin system. Am J Hypertens 1994;7:295-30

Influences of dynamical disruptions on the evolution of pulsars in globular clusters

By comparing the physical properties of pulsars hosted by core-collapsed (CCed) and non-core-collapsed (Non-CCed) globular clusters (GCs), we find that pulsars in CCed GCs rotate significantly slower than their counterparts in Non-CCed GCs. Additionally, radio luminosities at 1.4 GHz in CCed GCs are higher. These findings are consistent with the scenario that dynamical interactions in GCs can interrupt angular momentum transfer processes and surface magnetic field decay during the recycling phase. Our results suggest that such effects in CCed GCs are stronger due to more frequent disruptions of compact binaries. This is further supported by the observation that both estimated disruption rates and the fraction of isolated pulsars are predominantly higher in CCed GCs.Comment: 9 pages, 8 figures, 3 tables, Accepted in MNRA

Comparative study of MCe0.75Zr0.25Oy (M = Cu, Mn, Fe) catalysts for selective reduction of NO by CO: Activity and reaction pathways

Basic oxygen furnace steelmaking leads to the production of CO-rich off-gas. When CO and NO are combined in off-gas, selective catalytic reduction by CO (CO-SCR) effectively achieves the synergistic removal of both pollutants. In this paper, CuCe 0.75Zr 0.25O y, MnCe 0.75Zr 0.25O y, and FeCe 0.75Zr 0.25O y catalysts are prepared and evaluated for their CO-SCR activity, and the results show that the reaction system needs to be anaerobic; thus, the CO-SCR reaction can be dominant. The T 90 values of CuCe 0.75Zr 0.25O y and FeCe 0.75Zr 0.25O y are 200 °C and 223 °C, respectively. The activities of these two catalysts are higher than that of MnCe 0.75Zr 0.25O y (T 90 = 375 °C). Linear nitrate and bridged bidentate nitrate are the main intermediate species involved in NO conversion on the catalyst surface, and bidentate CO 3 2− coordination is the main intermediate species involved in CO conversion on the catalyst surface. CuCe 0.75Zr 0.25O y has high lattice oxygen mobility and is more likely to react with NO and CO. In the presence of oxygen, most CO is oxidized by O 2, which increases continuously to 100%, 100%, and 98% for CuCe 0.75Zr 0.25O y, FeCe 0.75Zr 0.25O y, and MnCe 0.75Zr 0.25O y, respectively; additionally, CO is oxidized by O 2, and the CO-SCR reaction cannot be carried out

Enhanced electrochemical reduction of hydrogen peroxide by Co3O4 nanowire electrode

Crystalline Co3O4 nanowire arrays with different morphologies grown on Ni foam were investigated by varying the reaction temperature, the concentration of precursors, and reaction time. The Co3O4 nanowires synthesized under typical reaction condition had a diameter range of approximately 500–900 nm with a length of 17 µm. Electrochemical reduction of hydrogen peroxide (H2O2) of the optimized Co3O4 nanowire electrode was studied by cyclic voltammetry. A high current density of 101.8 mA cm−2 was obtained at −0.4 V in a solution of 0.4 M H2O2 and 3.0 M NaOH at room temperature compared to 85.8 mA cm−2 at −0.35 V of the Co3O4 nanoparticle electrode. Results clearly indicated that the Ni foam supported Co3O4 nanowire electrode exhibited superior catalytic activity and mass transport kinetics for H2O2 electrochemical reduction

Asiatic Acid Inhibits Liver Fibrosis by Blocking TGF-beta/Smad Signaling In Vivo and In Vitro

Liver fibrosis is a major cause of liver failure, but treatment remains ineffective. In the present study, we investigated the mechanisms and anti-hepatofibrotic activities of asiatic acid (AA) in a rat model of liver fibrosis induced by carbon tetrachloride (CCl4) and in vitro in TGF-beta1-stimulated rat hepatic stellate cell line (HSC-T6). Treatment with AA significantly attenuated CCl4-induced liver fibrosis and functional impairment in a dosage-dependent manner, including blockade of the activation of HSC as determined by inhibiting de novo alpha smooth muscle actin (a-SMA) and collagen matrix expression, and an increase in ALT and AST (all p<0.01). The hepatoprotective effects of AA on fibrosis were associated with upregulation of hepatic Smad7, an inhibitor of TGF-beta signaling, thereby blocking upregulation of TGF-beta1 and CTGF and the activation of TGF-beta/Smad signaling. The anti-fibrosis activity and mechanisms of AA were further detected in vitro in HSC-T6. Addition of AA significantly induced Smad7 expression by HSC-T6 cells, thereby inhibiting TGF-beta1-induced Smad2/3 activation, myofibroblast transformation, and collagen matrix expression in a dosage-dependent manner. In contrast, knockdown of Smad7 in HSC-T6 cells prevented AA-induced inhibition of HSC-T6 cell activation and fibrosis in response to TGF-beta1, revealing an essential role for Smad7 in AA-induced anti-fibrotic activities during liver fibrosis in vivo and in vitro. In conclusion, AA may be a novel therapeutic agent for liver fibrosis. Induction of Smad7-dependent inhibition of TGF-beta/Smad-mediated fibrogenesis may be a central mechanism by which AA protects liver from injury

Emodin Suppresses Migration and Invasion through the Modulation of CXCR4 Expression in an Orthotopic Model of Human Hepatocellular Carcinoma

10.1371/journal.pone.0057015PLoS ONE83