Silver ion beam irradiation effects on poly(lactide-co-glycolide) (PLGA)/clay nanocomposites

Swift heavy ions induced modification of thin films of blends of poly(lactide-co-glycolide) (PLGA) (50:50) with organically modified nanoclay (Cloisite^® 30B) has been studied, using optical, structural and surface morphological analysis. Presence of nanoclay is found to enhance the properties of this degradable copolymer by reducing the rate of degradation even at high irradiation fluence. Optical and structural analysis of the polymer nanocomposites suggests that both the cross-linking and chain scission phenomenon are caused by swift heavy ion irradiation. XRD measurements show intercalation of PLGA in the clay galleries. Surface morphology of a nanocomposite indicates significant changes after irradiation at various fluences.     

Label Free Fluorometric Characterization of DNA Interaction with Cholate Capped Gold Nanoparticles Using Ethidium Bromide as a Fluorescent Probe

We demonstrated label free ethidium bromide assisted characterization of DNA interaction with cholate capped AuNPs. Interactions between ss/ds DNA and AuNPs with two different lengths (0.5 and 0.85 kb) were analyzed through fluorescence spectrophotometer and agrose gel electrophoresis analysis. Further results were confirmed by UV–globally visible spectrophotometer, DLS and TEM. As 0.5 and 0.85 kb of ssDNA effectively interacted with AuNPs through the van der Waals interaction which consequently led to the prevention of salt induced aggregation, EtBr intercalations as well as fluorescence shift with less binding constant 0.098 and 0.108 μM, respectively. On the contrary, the same length of dsDNA (0.5 and 0.85 kb) not interacted with AuNPs which led to the NPs aggregation, EtBr intercalation as well as fluorescence shift with increased binding constant 0.166 and 0.599 μM, respectively. This approach helped to understand the mode of interactions of DNA with cholate capped AuNPs without any modifications in a simple method and the results could be readout through the naked eye under the UV transilluminator. Figure

Fluorometric characterization of interaction of different lengths of ss/dsDNA with cholate capped AuNPs using EtBr as fluorescence probe     

D-Cems on iron films on silicon and PTFE: Effects of ion bombardment in the electronic stopping region

Depth-selective Mössbauer measurements were performed on as evaporated and proton bombarded iron films grown on PTFE and silicon single crystals. The results contribute to the understanding of the phenomena induced at the film/substrate interface by ion bombardment in the electronic stopping region.     

Two dimension photonic crystal Y-branch beam splitter with variation of splitting ratio based on hybrid defect controlled

This article represents a new Y-branch hybrid design of 2D photonic crystal with defect control. The structure is made of hexagonal arrays of InP nano-rods surrounded by air. This system is comprised of a modified add/change to a polymethylmethacrylate (PMMA) rod, which can be applied to the beam splitter selection device. The optical properties and radial of PMMA defect rods have been transfigured. By selecting an appropriate temperature, a change of refractive index and expanded radius are occurred. The obtained results have shown that the selected optical amplitude in a hybrid semiconductor-polymer Y-branch can be separated to 50–50, 60–40 and 67–33 % at wavelength 1.557 µm. Both of the photonic band gap and transmission spectra are calculated by using 2D finite different time domain (FDTD) method via OptiFDTD software. Such a device can be useful for photonic crystal switching devices in the integrated optical circuit.     

Inelastic neutrino reaction on40Ar

The cross section for muon decay neutrino induced nuclear reaction is studied in the Statistical Model of Itoh-Kohyama-Fujii and the long wavelength limit of the Microscopic Model of Donnelly-Peccei. The energy and angle dependence of the emitted electron is estimated.     

Behavior of charges locally injected into nanothin high-k SmScO3 dielectric

The behavior of charges locally injected from the probe of an atomic force microscope into nanothin films of high-k SmScO₃ dielectric deposited on a silicon substrate is studied by the method of Kelvin probe force microscopy. Prior to examination, the films were annealed at different temperatures. At temperatures above 900°C, the amorphous as-prepared films exhibit polycrystalline inclusions. In the films annealed at 900°C, the injected charge persists for a long time that several tens of times exceeds the charge retention time observed when conventional dielectrics, such as SiO₂ and Si₃N₄, are used. In addition, the diffusion of carriers in the plane of the dielectric layers sharply slows down.     

The phase behavior of gamma and laser irradiated polytetrafluorine

By using thermomechanical spectroscopy, an amorphous and three crystalline (high melting, intermediate, and low melting forms) blocks of the topological structures of polytetrafluoroetylene (PTFE) were characterized and their behavior under γ-radiation up to 2420 kGy was explored. The influence of γ-radiation on the powder and sheet of PTFE is essentially the same leading to formation of amorphous character. The glass transition and melting point temperatures of PTFE continuously decreased with increasing dose of irradiation. On exposure to continuous CO₂ laser radiation, PTFE degrades at a high rate and its clusters have a fibrous form. Initial γ-irradiation of PTFE enhances the laser ablation process.     

Optimized AC conductivity correlated to structure,morphology and thermal properties of PVDF/PVA/Nafion composites

Polyvinylidene fluoride (PVDF) and polyvinyl alcohol (PVA) composites were prepared by controlled loading of Nafion (5 to 15 wt%) by solution casting using water and dimethylformamide (DMF) as a solvent. The surface morphology of composite analyzed by atomic force microscopy (AFM) reveals the presence of Nafion ionomers. The increase in interlayer spacing of modified PVDF/PVA polymer system as a function of Nafion was detected by X-ray diffraction (XRD). The major change in Fourier transform infrared (FTIR) spectroscopy confirms the chemical bond C=O stretching around 1,700 cm^?1 due to Nafion. Differential scanning calorimetry (DSC) demonstrates the thermal stability of polymer composites and the decrease in melting temperature (T _m). The optimized AC conductivity (σ) of the prepared composite was evaluated by using an impedance analyzer as a function of temperature (40 to 150 °C) at constant 30-MHz frequency. The highest conductivity of 1.3?×?10^?2 S m^?1 was observed at 80 °C for 10 wt% of Nafion and correlated with structure, morphology and thermal properties of modified PVDF/PVA/Nafion composites. The experimental results may be useful for sensors, fuel cells and battery application domains.     

Perpendicular magnetic anisotropy in FePt/AlN layered structure

FePt/AlN layered structures were deposited onto fused quartz substrate by magnetron sputtering method and found to show in-plane anisotropy. However, annealing of the films leads to a transition of magnetic anisotropy from in-plane to perpendicular direction, and the perpendicular anisotropy gets stronger as the annealing temperature increases. Structural analysis shows that the FePt and AlN layers are textured with (111) and (002) orientations, respectively, along the film normal, and no ordering transformation is found for FePt alloy. To study the origin of the developed anisotropy, stress condition was analyzed with an equal biaxial stress model using X-ray diffraction 2θ–ω scan method and interface quality was evaluated by X-ray reflectivity measurement and transmission electron microscopy observation. The results reveal that perpendicular magnetic anisotropy of the annealed FePt/AlN layered structure can be attributed to the enhanced interface anisotropy, which is due to flattening of the interfaces through annealing.     

Effect of SiO2–metal–SiO2 plasmonic structures on InGaAs/GaAs quantum well intermixing

Dielectric–metal–dielectric sandwich structures have been fabricated on top of an InGaAs/GaAs single quantum well (QW) structure to enhance atomic interdiffusion across the QW interfaces at elevated temperature during rapid thermal annealing using a halogen lamp as the heating source. The QW intermixing enhancement is realized during rapid thermal annealing. By placing a properly designed SiO₂–Ag–SiO₂ structure on top of the QW sample, a blueshift in photoluminescence emission from 920 to 882 nm was observed, larger than that obtained in a SiO₂-capped QW annealed at the same condition. Finite-difference time-domain simulation and optical reflectance measurements showed that the enhanced QW intermixing is due to the plasmonic resonance-enhanced light absorption and suppressed light reflection from the SiO₂–Ag–SiO₂ structure.     

Interaction of One Anthraquinone Derivative with ctDNA Analyzed by Spectroscopic and Modeling Methods

The interaction of one anthraquinone derivative (AOMan) with calf thymus deoxyribonucleic acid (ctDNA) was systematically investigated at physiological pH 7.4 by fluorescence spectroscopy and molecular modeling. Binding constants of ctDNA with AOMan were calculated at different temperatures. Thermodynamic parameters, enthalpy and entropy changes were calculated according to Van’t Hoff equation, which indicated that the reaction was spontaneous and predominantly enthalpically driven. The increasing viscosity of ctDNA indicated that AOMan could intercalate into the base pairs of ctDNA. This conclusion was also demonstrated by the results obtained from KI quenching, denatured DNA studies and fluorescence polarization experiment. Furthermore, the molecular modeling results showed that anthraquinone ring tended to slide into the G–C rich region of ctDNA through the hydrogen bond, which are consistent with the results from experimental methods. Studying the binding interaction of target anthraquinones with DNA is one of the key steps in their DNA-changing action and the design of new drugs.     

An in silico protocol for identifying mTOR inhibitors from natural products

The mammalian target of rapamycin (mTOR) is an anti-cancer target. In this study, we propose an in silico protocol for identifying mTOR inhibitors from the ZINC natural product database. First, a three-dimensional quantitative structure–activity relationship pharmacophore model was built based on known mTOR inhibitors. The model was validated with an external test set, Fischer’s randomization method, a decoy set and pharmacophore mapping conformation testing. The results showed that the model can predict the mTOR inhibition activity of the tested compounds. Virtual screening was performed based on the best pharmacophore model, and the results were then filtered using a molecular docking approach. In addition, molecular mechanics/generalized born surface area analysis was used to refine the selected candidates. The top 20 natural products were selected as potential mTOR inhibitors, and their structural scaffolds could serve as building blocks in designing drug-like molecules for mTOR inhibition.     

Development of a compact hardware/software package for noninvasive diagnostics of skin diseases in the THz frequency range

The key elements of a mobile hardware/software package for noninvasive diagnostics of skin diseases in the THz frequency range have been designed, produced, and approved in model experiments. These elements are a compact THz oscillator based on an all-fiber femtosecond laser system and a unit for recovering electrodynamic characteristics of layered objects from scattered THz radiation spectra. Generation of 250-fs optical pulses at a wavelength of 1.03 µm with energy of 0.3 µJ and a repetition frequency of 1MHz is demonstrated and the efficiency of optical-THz conversion is found to be 5×10^?6. The proposed algorithm is constructed based on an iterative procedure and can be used for dispersive and absorbing media. It has higher operating speed in comparison with the algorithms for solving inverse problems, which are based on functional minimization methods.     

Laser generated Ag and Ag–Au composite nanoparticles for refractive index sensor

Localized surface plasmon resonance (LSPR) wavelength of metal nanoparticles (NPs) is highly sensitive to size, shape and the surrounding medium. Metal targets were laser ablated in liquid for preparation of spherical Ag and Ag@Au core–shell NP colloidal solution for refractive index sensing. The LSPR peak wavelength and broadening of the NPs were monitored in different refractive index liquid. Quasi-static Mie theory simulation results show that refractive index sensitivity of Ag, Ag–Au alloy and Ag@Au core–shell NPs increases nearly linearly with size and shell thickness. However, the increased broadening of the LSPR peak with size, alloy concentration and Au shell thickness restricts the sensing resolution of these NPs. Figure-of-merit (FOM) was calculated to optimize the size of Ag NPs, concentration of Ag–Au alloy NPs and Au shell thickness of Ag@Au core–shell NPs. The refractive index sensitivity (RIS) and FOM were optimum in the size range 20–40 nm for Ag NPs. Laser generated Ag@Au NPs of Au shell thickness in the range of 1–2 nm showed optimum FOM, where thin layer of Au coating can improve the stability of Ag NPs.     

Carbon auger electron line shape after beam-foil excitation of molecular ions

Auger electrons of beam-foil excited C-projectiles and C-fragments of Coulomb exploding molecular CO-projectiles at 83 keV/u yield information on the excitation mechanisms and the interaction with the solid. A numerical procedure is developed to calculate the mean energy of the Coulomb explosion, the charge states of the fragment ions and their angular straggling behaviour inside the solid. The calculated results are compared with experimental data. From a detailed line shape calculation the magnitude of directional effects induced by the Wake-potential can be predicted.     

Observation of Conformational Exchange in Cyclosporin in Media of Varying Polarity by NMR Spectroscopy

The molecule of peptide cyclosporin A experiences chemical exchange in polar solvents. In apolar media, such as chloroform or benzene, this transformation is suppressed, but still leads to formation of a small fraction of a minor conformer. To elucidate the nature of this phenomenon, the peptide was dissolved in mixed solvents chloroform–DMSO and water–DMSO. Analysis of ¹H nuclear magnetic resonance and two-dimensional exchange spectroscopy spectra showed that the conformational exchange proceeds at a low rate of \(\sim\) 10^?1 s^?1 at the room temperature and involves passing over a high free energy barrier. Thus the situation resembles the exchange process in chloroform, associated with cis–trans isomerization of peptide bonds, but in the presence of DMSO transformation occurs at several sites independently, and the energy difference between arising conformers is small, 10²–10³ kJ/mol.     

Looking at hydrogen motions in confinement

Why in a barren and hot desert, clays can contain a significant fraction of water? Why does concrete crack? How can we demonstrate that complexation of a drug does not alter its conformation in a way that affects its functionality? In this paper we present results on various studies using Quasi-Elastic Neutron Scattering aimed at clarifying these questions. To allow for a better understanding of neutron scattering, a brief introduction to the basics of its theory is presented. Following the theoretical part, experimental results dealing with the effects of confinement on the water dynamics caused by the interfaces in clays and the nano- and micro-pores of concrete are reviewed in detail. At the end, recent Quasi-Elastic Neutron Scattering investigations on the complexation of the local anesthetics Bupivacaine (BVC.HCl, C₁₈H₂₈N₂₀.HCl.H₂O) and Ropivacaine (RVC.HCl, C₁₇H₂₆N₂₀.HCl.H₂O) into the cyclic β-cyclodextrin oligosaccharide are presented. To conclude, the perspectives that the European Spallation Source brings to this subject are discussed.     

Mössbauer effect studies of electrochemically hydrogenated austenitic steels

Electrochemically hydrogenated ASTM 310 and ASTM 316 austenitic steels were investigated by means of⁵⁷Fe Mössbauer spectroscopy. Starting with non-hydrogenated materials, freshly hydrogenated ones and one-day room temperature aged hydrogenated samples were studied. The resultant spectra were analysed with a modified Hesse-Rübartsch method [1] adopted to the case of isomer shift distribution.     

Enhanced effect of side-Ohmic contact processing on the 2DEG electron density and electron mobility of In0.17Al0.83N/AlN/GaN heterostructure field-effect transistors

From the capacitance–voltage curves and current–voltage characteristics of the In_0.17Al_0.83N/AlN/GaN heterostructure field-effect transistors (HFETs) with side-Ohmic contacts and normal-Ohmic contacts, two-dimensional electron gas (2DEG) electron mobility was calculated. It is found that the polarization Coulomb field scattering (PCF) is closely related to the normal-Ohmic contact processing, and the PCF was weakened by side-Ohmic contact processing in In_0.17Al_0.83N/AlN/GaN HFETs, similar to that in AlGaN/AlN/GaN HFET devices. Further, due to the stronger spontaneous polarization in the thinner In_0.17Al_0.83N barrier layer, the influence of the gate bias on the PCF in In_0.17Al_0.83N/AlN/GaN HFETs is greater than that in AlGaN/AlN/GaN HFETs. As a result, the PCF in In_0.17Al_0.83N/AlN/GaN HFETs with side-Ohmic contacts is stronger than that in AlGaN/AlN/GaN HFETs with side-Ohmic contacts. Moreover, the 2DEG electron density in the In_0.17Al_0.83N/AlN/GaN HFETs with side-Ohmic contacts is increased by more than twice compared with the 2DEG electron density in the In_0.17Al_0.83N/AlN/GaN HFETs with normal-Ohmic contacts.