Near‐Infrared Fluorescent Silica/Porphyrin Hybrid Nanorings for In Vivo Cancer Imaging

Ring‐shaped silica nanoparticles are synthesized with a high tetrakis(4‐carboxyphenyl)porphyrin (TCPP) content or silica/TCPP hybrid nanorings (HNRs) using a one‐pot sol‐gel reaction with a TCPP‐binding silica precursor for fluorescence imaging of tumor. The shape of the HNRs is a reflection of abundant ring‐shaped TCPP aggregates in the silica matrix. The HNRs are of a size that makes them susceptible to the enhanced permeability and retention effect. For comparison, the TCPP‐doped silica nanoparticles are synthesized using a conventional method. The nanoparticles are spherical in shape because little TCPP is contained in the silica matrix and are designated as TCPP‐containing silica nanospheres (NSs). The absorption bands of the HNRs shift by about 20 nm toward longer wavelengths compared with the TCPP bands. This redshift leads the excitation wavelength of the HNRs into the near‐infrared (NIR) region. Therefore, the HNRs are excited by NIR light to emit strong fluorescence, although the NSs emit no fluorescence. The PEGylated HNRs (PEG‐HNRs) are uncharged and possess a significantly longer blood circulation time than PEG‐NSs. The PEG‐HNRs accumulate in tumor through multiple factors including their size, uncharged surface, unique shape, and long circulation time in blood, resulting in the acquisition of clear images of tumor.     

Doppler-free spectroscopy using a continuous-wave optical frequency synthesizer

A continuous-wave (cw) optical frequency synthesizer is demonstrated by using a monolithic-type cw optical parametric oscillator (cw-OPO) and an optical frequency comb. The cw-OPO is phase locked to an optical frequency comb that is phase locked to an atomic clock. The output frequency of the cw-OPO is frequency shifted with an electro-optic modulator, which makes it possible to tune the frequency continuously over 10 GHz. Furthermore, Doppler-free spectroscopy is performed using the optical frequency synthesizer for a cesium D1 line at 895 nm. The observed linewidth of 5 MHz is the natural linewidth of cesium. The center frequency of the line is consistent with a previous report.     

Electron Spin Dynamics in (DMe-DCNQI)2M (M = Li1-x Cu x (x < 0.14), Ag)

The quarter-filled π band systems, (DMe-DCNQI)_2M(M=Li_1-x Cu _x (x ≤ 0.14), Ag) were systematically studied with electron paramagnetic resonance (EPR). The intercolumn spin hopping rate in Li_1-x Cu _x -salt was obtained from the EPR linewidth. The temperature dependence of can be understood with the hole soliton model which also explains the DC conductivity. The π−d mixing of the Cu-salt enhances both and by 10³ times more than the Li-salt, which is consistent with the fact that the only Cu-salt has three-dimensional Fermi surface, but that Ag-salt is one-dimensional in spite of the mixing enhancement of by 10 times more than the Li-salt.     

Growth kinetics of Vibrio parahaemolyticus O3:K6 under varying conditions of pH, NaCl concentration and temperature

The growth responses of Vibrio parahamolyticus to pH, NaCl concentration and temperature changes were studied using serotype O3:K6 and other strains. Growth curves were obtained for 27 different sets of conditions, comprised of three levels of NaCl concentration, pH and temperature. The temperature, pH and NaCl concentrations most favorable for growth were in the order of 25 degrees C, 20 degrees C and 15 degrees C, pH 8, 7 and 5.8, and 1%, 3% and 7%, respectively. The bacteria grew most rapidly at 25 degrees C, at a pH of 7 or 8 in the presence of 1% or 3% NaCl, with the population (initial, ca. 2.5 log CFU/mL) reaching a level log 7 CFU/mL at 12 h. A growth predictive model using the Gompertz equation was generated from the experimental data for any combination of NaCl concentration, pH and temperature within the range used in this study.     

Anti‐HIV‐1 Peptide Derivatives Based on the HIV‐1 Co‐receptor CXCR4

The human immunodeficiency virus type 1 (HIV‐1) uses CD4 and the co‐receptor CCR5 or CXCR4 in the process of cell entry. The negatively charged extracellular domains of CXCR4 (CXCR4‐ED) interact with positive charges on the V3 loop of gp120, facilitating binding via electrostatic interactions. The presence of highly conserved positively charged residues in the V3 loop suggests that CXCR4‐ED‐derived inhibitors might be broadly effective inhibitors. Synthetic peptide derivatives were evaluated for anti‐HIV‐1 activity. The 39‐mer extracellular N‐terminal region (NT) was divided into three fragments with 10‐mer overlapping sites ( N1 – N3 ), and these linear peptides were synthesized. Peptide N1 contains Met 1–Asp 20 and shows significant anti‐HIV‐1 activity. Extracellular loops 1 and 2 (ECL1 and 2) were mimicked by cyclic peptides C1 and C2 , which were synthesized by chemoselective cyclization. Cyclic peptides C1 and C2 show higher anti‐HIV‐1 activity than their linear peptide counterparts, L1 and L2 . The cytotoxicities of C1 and C2 are lower than those of L1 and L2 . These results indicate that Met 1–Asp 20 segments of the NT and cyclic peptides of ECL1 and ECL2 are potent anti‐HIV‐1 drug candidates.     

Multi‐Enzymatic Synthesis of Optically Pure β‐Hydroxy α‐Amino Acids

A novel enzymatic production system of optically pure β‐hydroxy α‐amino acids was developed. Two enzymes were used for the system: an N‐succinyl L ‐amino acid β‐hydroxylase (SadA) belonging to the iron(II)/α‐ketoglutarate‐dependent dioxygenase superfamily and an N‐succinyl L ‐amino acid desuccinylase (LasA). The genes encoding the two enzymes are part of a gene set responsible for the biosynthesis of peptidyl compounds found in the Burkholderia ambifaria AMMD genome. SadA stereoselectively hydroxylated several N‐succinyl aliphatic L ‐amino acids and produced N‐succinyl β‐hydroxy L ‐amino acids, such as N‐succinyl‐L ‐β‐hydroxyvaline, N‐succinyl‐L ‐threonine, (2S,3R)‐N‐succinyl‐L ‐β‐hydroxyisoleucine, and N‐succinyl‐L ‐threo‐β‐hydroxyleucine. LasA catalyzed the desuccinylation of various N‐succinyl‐L ‐amino acids. Surprisingly, LasA is the first amide bond‐forming enzyme belonging to the amidohydrolase superfamily, and has succinylation activity towards the amino group of L ‐leucine. By combining SadA and LasA in a preparative scale production using N‐succinyl‐L ‐leucine as substrate, 2.3 mmol of L ‐threo‐β‐hydroxyleucine were successfully produced with 93% conversion and over 99% of diastereomeric excess. Consequently, the new production system described in this study has advantages in optical purity and reaction efficiency for application in the mass production of several β‐hydroxy α‐amino acids.

     

Au/Poly(3-methylthiophene)/10-(p-nitrobenzyl)-2(10H)-phenazinone/Al organic hetero-junction photovoltaic device

We proposed a novel concept of organic two-layer photovoltaic devices with D–σ–A molecule (Donor subunit–σ bond–Acceptor subunit)/conducting polymer heterojunction. Au/PMeT (poly(3-methylthiophene))/NBPN (10-(p-nitrobenzyl)-2(10H)-phenazinone)/Al was fabricated as a prototype of D–σ–A/polymer photovoltaic device. The power conversion efficiency of this photodiode was 5.1 × 10 ⁻²% under white illumination (8.46 mW/cm²). This value was larger than that of PMeT Schottky photodiode. This fact suggests that the concept of D–σ–A/polymer photovoltaic device is effective.     

Solubilization of Rhodium in Hydrochloric Acid Using an Alkali Metal Salt Method

Metallurgical and Materials Transactions B - Acids such as aqua regia, a 3:1 mixture of hydrochloric acid (HCl) and nitric acid, that contain strong oxidizing agents are used in the...