Upper bounds on the symbol-error probability of MPSK with phase error using pawula F-function IV

This letter presents an alternative derivation of the Case IV of Pawula F-function and an approximation for the corresponding probability density function (pdf) in the presence of the Tikhonov distributed phase error. The pdf of Case IV is used to obtain new upper bounds for the conditional and average symbol-error probabilities of M-ary phase shift keying with phase error over additive white Gaussian noise channels. Numerical results demonstrate the validity of the upper bounds.     

Expression characteristics of the maeA and maeB genes by extracellular malate and pyruvate in Escherichia coli

The malate-pyruvate conversion pathway is catalyzed by two malic enzyme isomers, MaeA and MaeB. qRT-PCR was carried out under malate and pyruvate supplemented conditions to understand the dynamics of maeA and maeB gene expression. maeA expression was elevated by malate, and maeB expression was inhibited by levels of both malate and pyruvate higher than 0.1 mM. Green fluorescent protein (GFP) reporter plasmids were also constructed by integration of the maeA/maeB promoter with the gfp gene. We showed that maeA driven GFP expression was positively and negatively correlated with extracellular malate and pyruvate induction. In contrast, no significant changes in maeB driven GFP expression were observed under both malate and pyruvate supplemented conditions.     

Enhanced transdermal deposition and characterization of quercetin-loaded ethosomes

We sought to evaluate the transdermal permeation potential of quercetin-loaded ethosomes. Quercetinloaded ethosomes were prepared and characterized with regard to particle size, loading efficiency, stability, and in vitro skin permeation. The optimized formulation of ethosomes was confirmed using 2% egg phosphatidylcholine and hydrated 20% ethanol. After quercetin was applied using this formulation, the stability of the ethosomes was determined when loaded with up to 0.04% quercetin. We observed that loading efficiency was improved with increasing concentrations of quercetin. Ethosomes loaded with 0.04% quercetin showed both the greatest loading efficiency (63.9%±6.0%) and an optimal size range (132±32 nm). Ethosomes loaded with quercetin were superior in skin permeation ability (29.5±7.0 μg/cm²) compared to either ethanolic solution or liposomes. Therefore, we concluded that quercetin-loaded ethosomes increased the skin delivery of quercetin. Our results suggest that quercetin-loaded ethosomes may enhance the effect of cosmetic materials.     

Anti-inflammatory effects of silkworm hemolymph on lipopolysaccharide-stimulated macrophages

Macrophages participate in several inflammatory pathologies such as sepsis and arthritis. We investigated the effect of silkworm hemolymph (SH) on the LPS-induced pro-inflammatory macrophages. SH inhibits LPS-induced nitric oxide (NO) production in RAW 264.7 cells and murine peritoneal macrophages. The decreased NO was reflected as a decreased amount of inducible nitric oxide synthase (iNOS) mRNA and protein. It was also found that SH inhibited pro-inflammatory cytokines, IL-1β, IL-6, and TNF-α production. To elucidate the mechanism by which SH inhibits NO production and iNOS expression, we investigated that SH suppressed IκB phosphorylation, which leads to the activation of NF-κB followed by degradation of IκB. This observation suggests that SH is a potential therapeutic modulator for inflammation-associated disorders.     

Selective hydrogenation of 4-isobutylacetophenone over a sodium-promoted Pd/C catalyst

The effect of sodium promotion on the selective hydrogenation of 4-isobutylacetophenone, 4-IBAP, was investigated over a Pd/C catalyst. A precipitation and deposition method was used to prepare the catalyst, and sodium was promoted on the Pd/C catalyst via post-impregnation while varying the sodium content. The sodium-promoted Pd/C catalyst resulted in a significantly improved yield greater than 96% of the desired product, 1-(4-isobutylphenyl) ethanol (4-IBPE), compared with the non-patented literature results under a mild hydrogenation condition. A detailed hydrogenation network over the Pd/C catalyst was suggested. The reaction mechanism for the yield and selectivity enhancement of 4-IBPE induced-by the promoted Pd/C was elucidated in relation to the geometric and electronic effects of reactant molecules in the microporous support depending on the reaction steps.     

Synthesis of polyethylene glycol-polystyrene core-shell structure particles in a plasma-fluidized bed reactor

Particles with core-shell structure with polystyrene (PS) core and polyethylene glycol (PEG) grafted on the surface were synthesized in a plasma-fluidized bed reactor. The virgin, plasma-treated, and grafted powders were characterized by the DPPH method, UV-vis spectrophotometer, NMR, FT-IR and SEM. The plasma-treated PS powders have well formed peroxide on the surface. By PEG grafting polymerization, PEG is well grafted and dispersed on the surface of the plasma-treated PS powders. The PEG-g-PS powder exhibits the core shell structure in the cross-sectional SEM image, and it can be claimed that well dispersed PEG grafting polymerization on PS surface can be achieved in the plasma fluidized bed reactor.     

The effect of rear surface polishing to the performance of thin crystalline silicon solar cells

As the thickness of crystalline silicon solar cells decreases, light loss cannot be avoided due to the absorption limit in long wavelength light. Internal rear side reflection can be enhanced by polishing the rear surface. The rear polishing processes are performed before the texturing and before and after doping the emitter layer to optimize the solar cell fabrication process sequences. All cells made by rear surface polishing showed improved light trapping in long wavelength region (900-1100 nm) compared to that in the conventional cells. However, silicon solar cells fabricated by rear polishing before and after doping have similar (35.5 mA/cm²) or lower (35.26 mA/cm²) short circuit current density compared to the cells produced by the conventional process (35.59 mA/cm²) due to pore damage to the anti-reflection layer and the surface of the emitter layer during rear polishing. This surface damage was effectively prevented adapting the rear surface polishing before the front surface texturing, which led to increasing the current density from 35.59 to 36.29 mA/cm².     

Regioselective Synthesis of 1,2‐ and 1,4‐Dihydroquinolines by Palladium‐Catalyzed Intramolecular N‐Arylation

A series of 1,2‐ and 1,4‐dihydroquinolines has been successfully prepared. The Pd‐catalyzed intramolecular N‐arylation of Z‐enamines, formally prepared by the Horner–Wadsworth–Emmons olefination, proceeded efficiently to furnish the cyclized products. Depending on the cyclization conditions, substituted 1,4‐dihydroquinolines and further isomerized 1,2‐dihydroquinolines were independently obtained in high yields with an excellent control of isomerization of the double bond.

     

Palladium‐Catalyzed Direct Arylations of 1,2‐Azolo[1,5‐a]pyridines using Copper(I) Chloride as a Lewis Acid Activator and the Synthesis of 2,6‐Disubstituted Pyridines

A direct method for the arylation of 1,2‐azolo[1,5‐a]pyridines has been developed. In the process, the fused pyridines react with aryl halides in the presence of the palladium complex Pd(OAc)₂(Phen) as a catalyst and copper(I) chloride (CuCl) as a Lewis acid to form arylated derivatives. While pyrazolo[1,5‐a]pyridines and [1,2,4]triazolo[1,5‐a]pyridines are arylated at ortho‐positions of their pyridine rings using this method, in situ ring‐opening of the formed C‐7 arylated [1,5‐a]pyridine takes place to generate the 2,6‐disubstituted pyridine. Also, upon treatment with lithium diisopropylamide (LDA), C‐7 arylated pyrazolo[1,5‐a]pyridine‐3‐carboxylates react to produce diversely substituted 2,6‐disubstituted pyridines. Finally, a sequential C‐3 arylation was accomplished through a two‐step sequence involving hydrolysis of pyrazolo[1,5‐a]pyridine‐3‐carboxylates followed by the bimetallic Pd/Cu‐catalyzed decarboxylative coupling reaction with aryl bromide.

     

Spin synthesis of monolayer of SiO2 thin films

The highly ordered monolayer of submicron size silica (SiO₂) particles (235 nm) is developed on p-silicon by using three-step spin-coating in colloidal suspension, which has significant potential in various applications. The influence of three-step spin speeds, spinning time, acceleration time between different steps, concentration of SiO₂ particles in the solution, solution quantity, and the ambient humidity (relative humidity) on the properties of monolayer SiO₂ are studied in order to achieve a large area monolayer film. A relatively high surface coverage and uniform monolayer film of SiO₂ particles in the range of 85%-90% are achieved by appropriate control of the preparative parameters. We conclude that this method can be useful in industrial applications, because of the fabrication speed, surface coverage and cost of the process.