High‐efficiency CMOS push‐pull power amplifier with multilayer center‐tapped transformer

This paper describes the design of a push‐pull power amplifier (PA) with a center‐tapped transformer for transmitter applications on the 5.2‐GHz band using 0.18μm CMOS technology. The type of the proposed PA is based on a double‐ended push–pull (DEPP) configuration. DEPP has a simple construction with only transistors and transformers. The PA has reverse‐phased cascode‐connected transistors. The proposed transformer has a multilayer structure and was designed using electromagnetic field simulation. To achieve high power added efficiency (PAE), we assumed the optimized output impedance technique with a tunable impedance antenna. The PA has 13.2 dB linearity gain, 14.9 dBm 1‐dB compression point (P1dB), and 27.4% maximum PAE. © 2016 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Novel Oleanane-Type Triterpene Glycosides from the Saponaria officinalis L. Seeds and Apoptosis-Inducing Activity via Mitochondria

Saponaria officinalis L., commonly known as “Soapwort”, is a rich source of triterpene glycosides; however, the chemical constituents of S. officinalis seeds have not been fully identified. In this study, we conducted a systematic phytochemical investigation of the seeds of S. officinalis and obtained 17 oleanane-type triterpene glycosides (1–17), including seven new glycosides (1–7). The structures of 1–7 were determined based on a detailed analysis of NMR spectroscopic data and chromatographic and spectroscopic analyses following specific chemical transformation. The cytotoxicities of the isolated compounds were evaluated against HL-60 human promyelocytic leukemia cells, A549 human adenocarcinoma lung cancer cells, and SBC-3 human small-cell lung cancer cells. The cytotoxicities of 1, 4, and 10 toward HL-60 cells and SBC-3 cells were nearly as potent as that of cisplatin. Compound 1, a bisdesmosidic triterpene glycoside obtained in good yield, arrested the cell cycle of SBC-3 cells at the G₂/M phase, and induced apoptosis through an intrinsic pathway, accompanied by ROS generation. As a result of the mitochondrial dysfunction induced by 1, mitochondria selective autophagy, termed mitophagy, occurred in SBC-3 cells.     

Osteoimmunology in Periodontitis: Local Proteins and Compounds to Alleviate Periodontitis

Periodontitis is one of the most common oral diseases resulting in gingival inflammation and tooth loss. Growing evidence indicates that it results from dysbiosis of the oral microbiome, which interferes with the host immune system, leading to bone destruction. Immune cells activate periodontal ligament cells to express the receptor activator of nuclear factor kappa-B (NF-κB) ligand (RANKL) and promote osteoclast activity. Osteocytes have active roles in periodontitis progression in the bone matrix. Local proteins are involved in bone regeneration through functional immunological plasticity. Here, we discuss the current knowledge of cellular and molecular mechanisms in periodontitis, the roles of local proteins, and promising synthetic compounds generating a periodontal regeneration effect. It is anticipated that this may lead to a better perception of periodontitis pathophysiology.     

Preparation and visible-light photocatalytic activity of Au-supported porous CeO2 spherical particles using templating

Porous spherical CeO₂ particles were prepared by impregnation of a cerium precursor solution into organic monolith sphere particles, with subsequent firing at 500 °C in air. The single-phase CeO₂ powder had specific surface area of greater than 140 m²/g. Photodeposition with UV illumination loaded Au onto the CeO₂ particle surface, which changed from yellowish to purple because of localized surface plasmon resonance (LSPR). The Au-loading increased photocatalytic decomposition activity of the CeO₂ powder for gaseous 2-propanol (IPA) under visible light. Thermal desorption of IPA, which was adsorbed to all porous spheres, provided flux to the photocatalytic reaction field of the sphere outer surface.     

Ultralong Room‐Temperature Phosphorescence from Amorphous Polymer Poly(Styrene Sulfonic Acid) in Air in the Dry Solid State

Polymer‐based room‐temperature‐phosphorescent (RTP) materials are attractive alternatives to low‐molecular‐weight organic RTP compounds because they can form self‐standing transparent films with high thermal stability. However, their RTP lifetimes in air are usually short (<≈0.4 s). Here, the simple organic amorphous polymer, poly(styrene sulfonic acid) (PSS), exhibits an ultralong RTP lifetime in air when desiccated. The maximum lifetime is 1.22 s, which is three times that of previously reported RTP amorphous organic polymers. The lifetime can be controlled by the PSS molecular weight and by the ratio of sulfonic acid groups introduced into the polymer. The dry polymers should enable unprecedented molecular engineering in organic molecule‐based optoelectronic devices because of the self‐standing and thermal stability attributes.     

A Diversity-Oriented Library of Fluorophore-Modified Receptors Constructed from a Chemical Library of Synthetic Fluorophores

The practical application of biosensors can be determined by evaluating the sensing ability of fluorophore-modified derivatives of a receptor with appropriate recognition characteristics for target molecules. One of the key determinants for successfully obtaining a useful biosensor is wide variation in the fluorophores attached to a given receptor. Thus, using a larger fluorophore-modified receptor library provides a higher probability of obtaining a practically useful biosensor. However, no effective method has yet been developed for constructing such a diverse library of fluorophore-modified receptors. Herein, we report a method for constructing fluorophore-modified receptors by using a chemical library of synthetic fluorophores with a thiol-reactive group. This library was converted into a library of fluorophore-modified adenosine-binding ribonucleopeptide (RNP) receptors by introducing the fluorophores to the Rev peptide of the RNP complex by alkylation of the thiol group. This method enabled the construction of 263 fluorophore-modified ATP-binding RNP receptors and allowed the selection of suitable receptor-based fluorescent sensors that target ATP.     

Phosphorylation of starch and dextrin by dry-heating in the presence of phosphate,and their calcium phosphate-solubilizing ability

Starch and dextrin were phosphorylated by dry-heating in the presence of phosphate, and their properties were examined. The phosphorylation of starch was accelerated with decreasing moisture, rising incubation temperature and prolongation of the incubation period. However, a rise in incubation temperature, and lengthened incubation period caused increased browning and degradation. A decrease in the pH from 5.5 to 3.0 resulted in a modest increase of phosphorylation, but also marked browning and degradation. When potato starch was phosphorylated at 140 degrees C and pH 5.5 for 24 h, its phosphorus content was increased up to 3.47%, with fewer side reactions. Phosphorlylated starch and dextrin had calcium phosphate-solubilizing abitity. Phosphorylated dextrin with 2.42% phosphorus had about half the calcium phosphate-solubilizing ability of casein phosphopeptide (CPP). The possibility of substituting of phosphorylated starch and dextrin for CPP as a calcium phosphate-absorption enhancing material is discussed herein.     

A new adsorption–desorption model for water adsorption in porous carbons

A new model is proposed to describe the adsorption and desorption branches of water adsorption in carefully synthesized mesoporous carbon materials. This model is an extension of a previous adsorption–desorption model proposed by Do et al. We prepared mesoporous resorcinol–formaldehyde carbon cryogels (RFCCs) by sol–gel polycondensation of resorcinol with formaldehyde in a slightly basic aqueous solution, followed by drying with freeze-drying and then carbonizing the RF cryogels at a high temperature under a nitrogen atmosphere. The resulting carbon materials have different surface and pore properties, which are valuable in the study of their effects on water vapor adsorption and desorption on RFCCs. The experimental data were used to test the model, and we have found that the model describes reasonably well all the data. We have also observed some interesting, but not unexpected, results in the analysis: the water cluster size in mesopore is larger than that in micropore, and the hysteresis loop of adsorption–desorption in mesopores is greater than that in micropores.