The pH-induced thermosensitive poly (NIPAAm-<Emphasis Type="Italic">co</Emphasis>-AAc-<Emphasis Type="Italic">co</Emphasis>-HEMA)-<Emphasis Type="Italic">g</Emphasis>-PCL micelles used as a drug carrier

The macromonomer of 2-hydroxyethyl methyacrylate-caprolactone (HPCL) was synthesized by the ring-opening polymerization (ROP) of ε-caprolactone, which was initiated by 2-hydroxyethyl methyacrylate (HEMA). Then, the graft terpolymers of NIPAAm-co-AAc-co-HEMA-g-PCL (PHNA-CL) with varying mole ratios were subsequently synthesized by free radical polymerization of HEMA-PCL, N-isopropylacrylamide (NIPAAm) and acrylic acid (AAc). PHNA-CL was further self-assembled in different types of solvent. All the as-prepared copolymers were characterized by ¹H NMR, FT-IR and GPC. Micellization behaviors of micelles were studied by TEM and DLS. The micelles exhibited a phase transition temperature which can be readily adjusted by changing pH value of the micellization system. Micelle loaded with doxorubicin (DOX) was used to evaluate the drug release behavior. The release of DOX from micelles could be controlled by changing pH value and temperature in buffer solutions. The micelles are potentially to be used as a new anticancer drug carrier for intracellular delivery.     

Characterization of poly(ethylene-<Emphasis Type="Italic">co</Emphasis>-vinyl acetate-<Emphasis Type="Italic">co</Emphasis>-carbon monoxide)/layered silicate clay hybrids obtained by melt mixing

In recent times, polymer-layered silicate nanocomposites have drawn a great deal of attention because they often exhibit tremendous improvements in material properties compared with virgin polymers or conventional micro- or macro-composites. In the present study, nanocomposites were developed from organically modified clay and poly(ethylene-co-vinyl acetate-co-carbon monoxide) by melt mixing. FTIR spectroscopy reveals that the interaction between the organoclay and EVACO is thermodynamically favored. High resolution wide angle X-ray diffraction and transmission electron microscopy were used to study the morphology of the nanocomposites. Elemental mapping by scanning electron microscopy indicates good dispersion and distribution of the nanoclay in EVACO matrix. The mechanical properties of the nanocomposites are optimum at a clay loading of 3%.     

Body distribution of poly(<Emphasis Type="SmallCaps">d</Emphasis>,<Emphasis Type="SmallCaps">l</Emphasis>-lactide-<Emphasis Type="Italic">co</Emphasis>-glycolide) copolymer degradation products in rats

Poly (d,l-lactide-co-glycolide) (PLGA) copolymers are among the few synthetic polymers approved for human use, but the biocompatibility of PLGA-derived oligomers and particles remains questionable. Here, high molecular weight PLGA (Mw = 32,000) was radiolabeled with ¹²⁵I in chloroform solution, and the body distribution of PLGA copolymer degradation products was examined following subcutaneous implantation of round ¹²⁵I-PLGA films on the back of Sprague Dawley rats. Autoradiographic images of the PLGA implant taken at 2, 4, 6, 8, 10, and 12 weeks revealed that the central portion of the film degraded much more rapidly than the marginal portions. Examination of the body compartment distribution at these time points revealed that over one-half of the radioactivity was recovered from skin. The remaining radioactivity was concentrated in the blood, liver, and kidneys. Radioactivity steadily appeared in the blood and remained elevated up to 12 weeks after implantation, while the liver to kidney distribution began to decrease after 6 weeks. Cumulatively, these results indicate that the clearance of degraded particles and fragments from the implantation site is extremely delayed. Moreover, the degraded particles and fragments were selectively concentrated in the liver and kidneys, following release of degraded products into the bloodstream from the implantation site.     

Regenerated thermosetting styrene-<Emphasis Type="Italic">co</Emphasis>-acrylonitrile sandwich composite panels reinforced by jute fibre: structures and properties

Jute fibres-reinforced sandwich regenerated composite panels were fabricated using industrial waste thermosetting styrene-co-acrylonitrile (SAN) foam scraps via compression moulding for the purpose of recycling waste SAN foam and obtaining high physical performance. The jute fibres were, respectively, treated by heat, sodium hydroxide (NaOH) solution (5.0 wt%), and N,N-dimethylacetamide (DMAc) in order to improve the mechanical properties of the composites. The structures and mechanical properties of the composites were studied. The SAN matrix got compact and some crystalline region formed in SAN matrix via compression moulding. The composite reinforced by DMAc-treated jute fibres performed optimum mechanical properties among the regenerated panels whose impact strength, flexural strength, and compressive strength were 19.9 kJ m^?2, 41.7 MPa, and 61.0 MPa, respectively. Good interfacial bonding between DMAc-treated fibres and SAN matrix was verified by peel test and exhibited in SEM photographs. Besides, the water absorption of DMAc-treated fibres composite was lower than other SAN/jute fibre-reinforced sandwich composite panels.     

Electrospun poly(<Emphasis Type="SmallCaps">d</Emphasis>/<Emphasis Type="SmallCaps">l</Emphasis>-lactide-<Emphasis Type="Italic">co</Emphasis>-<Emphasis Type="SmallCaps">l</Emphasis>-lactide) hybrid matrix: a novel scaffold material for soft tissue engineering

Electrospinning is a long-known polymer processing technique that has received more interest and attention in recent years due to its versatility and potential use in the field of biomedical research. The fabrication of three-dimensional (3D) electrospun matrices for drug delivery and tissue engineering is of particular interest. In the present study, we identified optimal conditions to generate novel electrospun polymeric scaffolds composed of poly-d/l-lactide and poly-l-lactide in the ratio 50:50. Scanning electron microscopic analyses revealed that the generated poly(d/l-lactide-co-l-lactide) electrospun hybrid microfibers possessed a unique porous high surface area mimicking native extracellular matrix (ECM). To assess cytocompatibility, we isolated dermal fibroblasts from human skin biopsies. After 5 days of in vitro culture, the fibroblasts adhered, migrated and proliferated on the newly created 3D scaffolds. Our data demonstrate the applicability of electrospun poly(d/l-lactide-co-l-lactide) scaffolds to serve as substrates for regenerative medicine applications with special focus on skin tissue engineering.     

Elastomeric electrospun scaffolds of poly(<Emphasis Type="SmallCaps">l</Emphasis>-lactide-<Emphasis Type="Italic">co</Emphasis>-trimethylene carbonate) for myocardial tissue engineering

In myocardial tissue engineering the use of synthetically bioengineered flexible patches implanted in the infarcted area is considered one of the promising strategy for cardiac repair. In this work the potentialities of a biomimetic electrospun scaffold made of a commercial copolymer of (l)-lactic acid with trimethylene carbonate (P(l)LA-co-TMC) are investigated in comparison to electrospun poly(l)lactic acid. The P(l)LA-co-TMC scaffold used in this work is a glassy rigid material at room temperature while it is a rubbery soft material at 37°C. Mechanical characterization results (tensile stress–strain and creep-recovery measurements) show that at 37°C electrospun P(l)LA-co-TMC displays an elastic modulus of around 20 MPa and the ability to completely recover up to 10% of deformation. Cell culture experiments show that P(l)LA-co-TMC scaffold promotes cardiomyocyte proliferation and efficiently preserve cell morphology, without hampering expression of sarcomeric alpha actinin marker, thus demonstrating its potentialities as synthetic biomaterial for myocardial tissue engineering.     

The Activation Energy <Emphasis Type="Italic">U</Emphasis>(<Emphasis Type="Italic">T</Emphasis>,<Emphasis Type="Italic">H</Emphasis>) in Y-based Superconductors

Based on the Arrhenius equation, a method to calculate the activation energy from the resistance transition is proposed for high temperature superconductors. This method is applied to the Y-based superconductors. The activation energy is found to be U(T,H)∼(1−T/T _c )^4.8(H/H ₀)^−3.8 of YBCO crystal, and U(T,H)∼(1−T/T _c )^3.3(H/H ₀)^−2.2 of Er doped MTG YBCO crystal, respectively. With the obtained activation energy U(T,H), the lower part of the experimental curve ρ(T,H) and its derivative can be reproduced.      

Long-wavelength photodiodes based on <Emphasis Type="Italic">n</Emphasis>-GaSb/<Emphasis Type="Italic">n</Emphasis>-GaInAsSb/<Emphasis Type="Italic">p</Emphasis>-AlGaAsSb heterostructures

Photodiodes sensitive in the wavelength ranges 1–2.5 μm and 1–4.8 μm at room temperature have been created on the basis of n-GaSb/n-GaInAsSb/p-AlGaAsSb double-junction heterostructures of two types. The broadband photosensitivity of the diode structures of both types is indicative of the complete separation of photogenerated electron-hole pairs in the staggered n-p heterojunction (n-GaInAsSb/p-AlGaAsSb). The noise characteristics of photodetectors based on the proposed diode structures have been studied. Prospects of the use of these devices in thermophotovoltaic cells for low-temperature radiation sources are considered.     

Impact-ionization-stimulated electroluminescence in isotype <Emphasis Type="Italic">n</Emphasis>-GaSb/<Emphasis Type="Italic">n</Emphasis>-AlGaAsSb/<Emphasis Type="Italic">n</Emphasis>-GaInAsSb heterostructures

We have studied electroluminescence in n-GaSb/n-AlGaAsSb/n-GaInAsSb heterostructures with isotype heterojunctions, in which the quantum efficiency of emission is increased due to the additional production of electron-hole pairs as a result of the impact ionization that takes place near the heterointerface. The impact ionization in such heterostructures is possible due to the presence of deep wells in the energy band structure.     

Speed of sound in <Emphasis Type="Italic">n</Emphasis>-hexane, <Emphasis Type="Italic">n</Emphasis>-octane, <Emphasis Type="Italic">n</Emphasis>-decane,and <Emphasis Type="Italic">n</Emphasis>-hexadecane in the liquid state

This paper describes an improved experimental facility for measuring the speed of sound in liquids with an accuracy of up to 0.1%. Measurements of the speed of sound in liquid n-hexane, n-octane, n-decane, and n-hexadecane at temperatures of 298–433 K and pressures of 0.1–100 MPa have been made. It has been shown that in the possible comparison range the obtained values of the speed of sound are in good agreement with the literature data. Translated from Inzhenerno-Fizicheskii Zhurnal, Vol. 81, No. 4, pp. 732–736, July–August, 2008.     

<Emphasis Type="Italic">In situ</Emphasis> polymerization on biomacromolecules for nanomedicines

Biopharmaceuticals, including proteins, DNAs, and RNAs, hold vast promise for the treatment of many disorders, such as cancer, diabetes, autoimmune diseases, infectious diseases, and rare diseases. The application of biopharmaceuticals, however, is limited by their poor stability, immunogenicity, suboptimal pharmacokinetic performance, undesired tissue distribution, and low penetration through biological barriers. In situ polymerization provides an appealing and promising platform to improve the pharmacological characteristics of biopharmaceuticals. Instead of the traditional “grafting to” polymer–biomolecule conjugation, in situ polymerization grows polymers on the surfaces of the biomacromolecules, resulting in easier purification procedures, high conjugation yields, and unique structures. Herein, this review surveys recent advances in the polymerization methodologies. Additionally, we further review improved therapeutic performance of the resultant nanomedicines. Finally, the opportunities, as well as the challenges, of these nanocomposites in the biomedical fields are discussed.     

Inference with progressively censored <Emphasis Type="Italic">k</Emphasis>-out-of-<Emphasis Type="Italic">n</Emphasis> system lifetime data

A system with n independent components which works if and only if a least k of its n components work is called a k-out-of-n system. For exponentially distributed component lifetimes, we obtain point and interval estimators for the scale parameter of the component lifetime distribution of a k-out-of-n system when the system failure time is observed only. In particular, we prove that the maximum likelihood estimator (MLE) of the scale parameter based on progressively Type-II censored system lifetimes is unique. Further, we propose a fixed-point iteration procedure to compute the MLE for k-out-of-n systems data. In addition, we illustrate that the Newton–Raphson method does not converge for any initial value. Finally, exact confidence intervals for the scale parameter are constructed based on progressively Type-II censored system lifetimes.     

Synthesis,growth, optical,mechanical and electrical properties of <Emphasis Type="Italic">L</Emphasis>-lysine <Emphasis Type="Italic">L</Emphasis>-lysinium dichloride nitrate (<Emphasis Type="Italic">L</Emphasis>-LLDN) single crystal

Semi-organic nonlinear optical material, L-lysine L-lysinium dichloride nitrate (2C₆H₁₅N₂O₂⁺_{2}^{+} · H⁺ · NO₃^-_{3}^{-} · 2Cl⁻) was synthesized at room temperature. Single crystals of L-LLDN were grown by slow cooling solution growth technique. The grown crystal was confirmed by powder X-ray diffraction analysis. The crystalline perfection of the grown single crystal was characterized by high-resolution X-ray diffraction (HRXRD) studies. The cut-off wavelength was determined by UV-vis transmission spectral analysis. The frequency doubling of the grown crystal was confirmed by powder second harmonic generation (SHG) measurement. The refractive index and birefringence of the crystal were determined using He–Ne laser source. Mechanical property of the crystal was determined by Vickers hardness tester. The frequency and temperature dependence of dielectric constant (ε _r), dielectric loss (tan δ) and a.c. conductivity (σ _ac) were also measured.     

Synthesis and characterization of <Emphasis Type="Italic">n</Emphasis>-ZnO:Al/CoPc/<Emphasis Type="Italic">p</Emphasis>-Si structures

Photosensitive structures of the n-ZnO:Al/CoPc/p-Si type were synthesized for the first time using vacuum sublimation of cobalt phthalocyanine (CoPc) and magnetron sputtering of a ZnO:Al target. The maximum photoresponse is observed when the structure is illuminated from the side of the ZnO layer and amounts to ?400 V/W at T = 300 K. Mechanisms of current transfer and peculiarities of the photosensitivity spectrum are considered. It is suggested that the new photosensitive structures can be used in multiband photoconverters of natural radiation with a broad working spectral range.     

<Emphasis Type="Italic">p</Emphasis>-<Emphasis Type="Italic">n</Emphasis> junctions in ZnO implanted with group V ions

n-Type ZnO〈Ga〉 films were implanted with 150-keV N⁺ (As⁺) ions to a dose of 7 × 10¹⁵ cm⁻² and then annealed in atomic oxygen at different temperatures. p-Type conductivity was obtained at annealing temperatures in the range 770–870 K. The parameters of the p-type layers were determined by photoluminescence spectroscopy, secondary ion mass spectrometry, and Hall effect measurements. According to the Hall data, the p-type layers had a resistivity of ∼30 Ω cm, carrier mobility of ∼2 cm²/(V s), and carrier concentration of ∼10¹⁸ cm⁻³. The electroluminescence spectra of the p-n junctions produced by ion implantation showed a band at 440 nm, due to recombination via donor-acceptor pairs.     

Preparation,properties, and drug release of thermo- and pH-sensitive poly((2-dimethylamino)ethyl methacrylate)/poly(<Emphasis Type="Italic">N</Emphasis>,<Emphasis Type="Italic">N</Emphasis>-diethylacrylamide) semi-IPN hydrogels

In this paper, a series of semi-interpenetrating polymer network (semi-IPN) hydrogels based on poly((2-dimethylamino)ethyl methacrylate)/poly (N,N-diethylacrylamide) (PDMAEMA/PDEA) were synthesized by changing the initial PDMAEMA/DEA molar ratio at room temperature. The influence of this additive on the property of resulting PDEA hydrogels was investigated and characterized. The interior morphology by scanning electron microscopy (SEM) revealed that the semi-IPN hydrogels have interconnected porous network structures. The glass transition temperature (T _g) of the semi-IPN hydrogels was observed by differential scanning calorimetry (DSC). Equilibrium swelling ratio (ESR), swelling and deswelling dynamics of the hydrogels responding to temperature and pH were investigated in detail. Compared to PDEA, the semi-IPN hydrogels exhibited excellent mutative values in response to an alternation of the temperature and pH, and showed fast swelling and deswelling rates in response to temperature and pH change. The release behaviors of the model drug, aminophylline, were found dependent on hydrogel compositions and environmental temperature. These results suggest that the stimuli semi-IPN hydrogel have potential application as intelligent drug carriers.     

Mechanical properties and density of BC<Emphasis Type="Italic">x</Emphasis>N<Emphasis Type="Italic">y</Emphasis> films grown by low-pressure chemical vapor deposition from triethylamine borane

Boron carbonitride (BC _x N _y ) films of different compositions have been grown by low-pressure chemical vapor deposition using triethylamine borane as a single-source precursor and ammonia as an additional nitrogen source. Experiments were performed at various initial vapor compositions. The resultant films have been characterized by ellipsometry, IR spectroscopy, energy dispersive X-ray spectroscopy, scanning electron microscopy, nanoindentation, and surface acoustic wave spectroscopy. The mechanical properties of the films are shown to correlate with their density and chemical composition. With increasing initial ammonia partial pressure in the vapor phase, the elemental composition of the films moves away from boron carbide, approaching boron nitride, which is accompanied by a reduction in the Young’s modulus, hardness, and density of the films.     

The search for novel superhard and incompressible materials on the basis of higher borides of <Emphasis Type="Italic">s</Emphasis>, <Emphasis Type="Italic">p</Emphasis>, <Emphasis Type="Italic">d</Emphasis> metals

The state of the art in the search for novel superhard and (or) incompressible materials on the basis of higher borides of s, p, d metals has been briefly reviewed. The information has been considered about experimental and theoretical studies of the following groups of borides: diborides of 4d, 5d heavy metals (Tc, Ru, Rh, Re, Os, and Ir), hexagonal tetraborides with the WB₄-type structure, and AMB₁₄ borides (where A, M are s, p metals) as well as of a number of related systems.     

Nernst Signal in High-<Emphasis Type="Italic">T</Emphasis><Subscript><Emphasis Type="Italic">c</Emphasis></Subscript> Superconductors

The time-dependent Ginzburg–Landau equation with thermal noise is used to calculate the Nernst signal e _N , describing the Nernst effect, in type-II superconductor in the vortex-liquid regime. The Gaussian method used is an elaboration of the Hartree–Fock method. An additional assumption often made in analytical calculations that only the lowest Landau level significantly contributes to physical quantities of interest in the high-field limit is lifted by including all the Landau levels. The values of e _N are in good quantitative agreement with experimental data for temperature close to T _c on Bi₂Sr₂CaCu₂O_8+δ and Bi₂Sr₂Ca₂Cu₃O_10+δ .