Stabilizing RNA by the sonochemical formation of RNA nanospheres

Biological macromolecules, including DNA, RNA, and proteins, have intrinsic features that make them potential building blocks for the bottom-up fabrication of nanodevices. Unlike DNA, RNA is a more versatile molecule whose range in the cell is from 21 to thousands of nucleotides and is usually folded into stem and loop structures. RNA is unique in nanoscale fabrication due to its diversity in size, function, and structure. Because gene expression analysis is becoming a clinical reality and there is a need to collect RNA in minute amounts from clinical samples, keeping the RNA intact is a growing challenge. RNA samples are notoriously difficult to handle because of their highly labile nature and tendency to degrade even under controlled RNase-free conditions and maintenance in the cold. Silencing the RNA that induces the RNA interference is viewed as the next generation of therapeutics. The stabilization and delivery of RNA to cells are the major concerns in making siRNAs usable drugs. For the first time, ultrasonic waves are shown to convert native RNA molecules to RNA nanospheres. The creation of the nanobubbles is performed by a one-step reaction. The RNA nanospheres are stable at room temperature for at least one month. Additionally, the nanospheres can be inserted into mammalian cancer cells (U2OS). This research achieves: 1) a solution to RNA storage; and 2) a way to convert RNA molecules to RNA particles. RNA nanosphere formation is a reversible process, and by using denaturing conditions, the RNA can be refolded into intact molecules.     

Novel Synthesis of Ordered MCM-41 Titanosilicates with Very High Titanium Content via Ultrasound Radiation

A novel synthetic strategy has been developed for the fabrication of mesostructured titanosilicate with very high titanium content. By the combination of ultrasound radiation and a separate hydrolysis procedure, highly ordered MCM-41 titanosilicates can be synthesized within 3 h from gels with Ti/Si ratios up to 1. The physicochemical properties of the materials were characterized by means of XRD, TEM, FT-IR, UV-Vis DRS, ²⁹Si MAS NMR, and liquid nitrogen adsorption-desorption measurements. The results suggested that during crystallization, sonication re-dispersed and accelerated the condensation of inorganic species, and resulted in more condensed pore walls compared to those synthesized with the conventional methods. The presence of silica and ultrasound radiation remarkably suppressed the aggregation of titanium species, thus, at the medium titanium level, a relatively homogeneous dispersion of titanium within the MCM-41 framework was attained.     

Effects of command style and group cohesiveness on the performance effectiveness of self-selected tank crews.

94 3-men crews of Israeli male soldiers were studied throughout their performance on routine military activities. Level of cohesiveness was determined through a self-selection sociometric procedure. Command style of tank commanders was assessed with questionnaires. Performance was appraised by unit commanders. Results show only interaction effects of cohesiveness and command style on performance effectiveness. Specifically, performance effectiveness was high in the following combinations: low cohesiveness with command style that emphasizes people orientation and high cohesiveness with emphasis on both task and people orientation. (30 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

High yield one-step synthesis of carbon spheres produced by dissociating individual hydrocarbons at their autogenic pressure at low temperatures

Hydrocarbons containing 5–14 carbon atoms (pentane, cyclohexane, camphorquinone, xylene, mesitylene, camphene, decahydronaphthalene, diphenylmethane, and anthracene) are individually dissociated under their autogenic pressure developed at 700 °C to produce pure carbon moieties from the respective hydrocarbon precursor. From all of the hydrocarbons, more than 99% pure carbon is obtained in spherical, filament- or egg-like microstructures. One of the key peculiarities in the thermal dissociation of various hydrocarbons, followed by solidification under autogenic pressure, is the formation of products in micrometer dimensions. It is in contrast to previous work with organometallic precursors, which yield nanometric products via a similar method. These results are compared with those obtained for the thermal dissociation of the same hydrocarbons under flow conditions. Specific systematic morphological, structural, and compositional analysis is presented for the products obtained from the thermal dissociation of diphenylmethane. A possible formation mechanism for the obtained products is provided.     

Nanocrystalline γ-Alumina Synthesized by Sonohydrolysis of Alkoxide Precursor in the Presence of Organic Acids: Structure and Morphological Properties

γ-Al₂O₃ nanoparticles with an average size of 5 nm were synthesized by the hydrolysis of aluminum triisopropoxide under the influence of power ultrasound (100 W/cm²) and in the presence of formic or oxalic acids as peptizers, followed by calcination. The structural and morphological properties of the as-prepared precursor hydroxides and calcined nanocrystalline powders were characterized by XRD, SEM, TEM, TGA, IR, and BET. The ultrasound-driven cavitation process has been shown to affect the agglomeration of the precursor nanoparticles by condensation of interparticle hydroxyls. The oxalate anions were strongly adsorbed on the surface of the precursor nanoparticles and thus retarded the ultrasound-driven condensation of interparticle hydroxyls. Formic acid showed a lesser degree of adsorption on the surface of the precursor particles. The ultrasound-driven agglomeration of the primary particles as well as the role of organic modifiers on the microstructural properties of the precursor and the target alumina phases have been discussed.     

Self-assembled lamellar MoS2, SnS2 and SiO2 semiconducting polymer nanocomposites

Lamellar nanocomposites based on semiconducting polymers incorporated into layered inorganic matrices are prepared by the co-assembly of organic and inorganic precursors. Semiconducting polymer-incorporated silica is prepared by introducing the semiconducting polymers into a tetrahydrofuran (THF)/water homogeneous sol solution containing silica precursor species and a surface-active agent. Semiconducting polymer-incorporated MoS(2) and SnS(2) are prepared by Li intercalation into the inorganic compound, exfoliation and restack in the presence of the semiconducting polymer. All lamellar nanocomposite films are organized in domains aligned parallel to the substrate surface plane. The incorporated polymers maintain their semiconducting properties, as evident from their optical absorption and photoluminescence spectra. The optoelectronic properties of the nanocomposites depend on the properties of both the inorganic host and the incorporated guest polymer as demonstrated by integrating the nanocomposite films into light-emitting diodes. Devices based on polymer-incorporated silica and polymer-incorporated MoS(2) show no diode behaviour and no light emission due to the insulating and metallic properties of the silica and MoS(2) hosts. In contrast, diode performance and electroluminescence are obtained from devices based on semiconducting polymer-incorporated semiconducting SnS(2), demonstrating that judicious selection of the composite components in combination with the optimization of material synthesis conditions allows new hierarchical structures to be tailored for electronic and optoelectronic applications.     

Regulation of endogenous glucose production by glucose per se is impaired in type 2 diabetes mellitus

We examined the ability of an equivalent increase in circulating glucose concentrations to inhibit endogenous glucose production (EGP) and to stimulate glucose metabolism in patients with Type 2 diabetes mellitus (DM2). Somatostatin was infused in the presence of basal replacements of glucoregulatory hormones and plasma glucose was maintained either at 90 or 180 mg/dl. Overnight low-dose insulin was used to normalize the plasma glucose levels in DM2 before initiation of the study protocol. In the presence of identical and constant plasma insulin, glucagon, and growth hormone concentrations, a doubling of the plasma glucose levels inhibited EGP by 42% and stimulated peripheral glucose uptake by 69% in nondiabetic subjects. However, the same increment in the plasma glucose concentrations failed to lower EGP, and stimulated glucose uptake by only 49% in patients with DM2. The rate of glucose infusion required to maintain the same hyperglycemic plateau was 58% lower in DM2 than in nondiabetic individuals. Despite diminished rates of total glucose uptake during hyperglycemia, the ability of glucose per se (at basal insulin) to stimulate whole body glycogen synthesis (glucose uptake minus glycolysis) was comparable in DM2 and in nondiabetic subjects. To examine the mechanisms responsible for the lack of inhibition of EGP by hyperglycemia in DM2 we also assessed the rates of total glucose output (TGO), i.e., flux through glucose-6-phosphatase, and the rate of glucose cycling in a subgroup of the study subjects. In the nondiabetic group, hyperglycemia inhibited TGO by 35%, while glucose cycling did not change significantly. In DM2, neither TGO or glucose cycling was affected by hyperglycemia. The lack of increase in glucose cycling in the face of a doubling in circulating glucose concentrations suggested that hyperglycemia at basal insulin inhibits glucose-6-phosphatase activity in vivo. Conversely, the lack of increase in glucose cycling in the presence of hyperglycemia and unchanged TGO suggest that the increase in the plasma glucose concentration failed to enhance the flux through glucokinase in DM2. In summary, both lack of inhibition of EGP and diminished stimulation of glucose uptake contribute to impaired glucose effectiveness in DM2. The abilities of glucose at basal insulin to both increase the flux through glucokinase and to inhibit the flux through glucose-6-phosphatase are impaired in DM2. Conversely, glycogen synthesis is exquisitely sensitive to changes in plasma glucose in patients with DM2.     

The initiation of in situ polymerization of vinyl monomers in polyester by glow discharge

Glow discharge initiation of in situ polymerization of acrylic acid and other vinyl monomers incorporated in PET films was investigatigated. The influence of glow discharge conditions such as the gas used, plasma power, discharge current, and plasma treatment time on polymerization yield was determined. Though glow discharge effects are limited to the film surface, in situ polymerization of the vinyl monomers took place and the vinyl polymer could be found all through the film cross section. At short plasma treatment time only surface modification took place, while at longer treatment time bulk modification occurred, too. Good polymerization yields were obtained. Gel effect behavior was observed. Mechanical properties of the modified PET film were not changed, while the contact angle with water improved when polar vinyl monomers were used.     

One‐Step Solvent‐Free Synthesis and Characterization of Zn1−xMnxSe@C Nanorods and Nanowires

The carbon‐encapsulated, Mn‐doped ZnSe (Zn_1−xMn_xSe@C) nanowires, nanorods, and nanoparticles are synthesized by the solvent‐free, one‐step RAPET (reactions under autogenic pressure at elevated temperature) approach. The aspect ratio of the nanowires/nanorods is altered according to the Mn/Zn atomic ratio, with the maximum being observed for Mn/Zn = 1:20. A 10–20 nm amorphous carbon shell is evidenced from electron microscopy analysis. The replacement of Zn by Mn in the Zn_1−xMn_xSe lattice is confirmed by the hyperfine splitting values in the electron paramagnetic resonance (EPR) experiments. Raman experiments reveal that the Zn_1−xMn_xSe core is highly crystalline, while the shell consists of disordered graphitic carbon. Variable‐temperature cathodoluminescence measurements are performed for all samples and show distinct ZnSe near‐band‐edge and Mn‐related emissions. An intense and broad Mn‐related emission at the largest Mn alloy composition of 19.9% is further consistent with an efficient incorporation of Mn within the host ZnSe lattice. The formation of the core/shell nanowires and nanorods in the absence of any template or structure‐directing agent is controlled kinetically by the Zn_1−xMn_xSe nucleus formation and subsequent carbon encapsulation. Mn replaces Zn mainly in the (111) plane and catalyzes the nanowire growth in the [111] direction.