Filtration Performance Against Nanoparticles by Electrospun Nylon-6 Media Containing Ultrathin Nanofibers

We investigate the formation of ultrathin nanofibers (UNFs) with diameters below 20 nm by electrospinning Nylon-6 solution with various processing parameters. It is found that the UNF density and morphology are highly dependent on the solution concentration and age, collecting distance, and ambient humidity. The sequence that ribbon-like fibers are stretched by the electric force, followed by rapid phase separation of the splitting film is proposed as a formation mechanism of the UNFs. Based on the morphological study, a model of hexagonal nets is developed in order to estimate the filtration efficiency by the UNF structure. The estimated efficiency due to the UNFs is then combined with the contribution from the un-split nanofibers (NFs) to compute the total filtration efficiency and pressure drop for each of the electrospun media by applying a layered multiple zone model. The filtration performance of the electrospun media against nanoparticles is evaluated using the quality factor and specific filtration performance index, weighed against the pressure drop and basis weight of the media, respectively. Our results show UNFs are advantageous when high filtration efficiency is required and low weight is desired and/or little space is available for the filter media.

Copyright 2014 American Association for Aerosol Research     

Mitochondrial Aminoacyl-tRNA Synthetase and Disease: The Yeast Contribution for Functional Analysis of Novel Variants

In most eukaryotes, mitochondrial protein synthesis is essential for oxidative phosphorylation (OXPHOS) as some subunits of the respiratory chain complexes are encoded by the mitochondrial DNA (mtDNA). Mutations affecting the mitochondrial translation apparatus have been identified as a major cause of mitochondrial diseases. These mutations include either heteroplasmic mtDNA mutations in genes encoding for the mitochondrial rRNA (mtrRNA) and tRNAs (mttRNAs) or mutations in nuclear genes encoding ribosomal proteins, initiation, elongation and termination factors, tRNA-modifying enzymes, and aminoacyl-tRNA synthetases (mtARSs). Aminoacyl-tRNA synthetases (ARSs) catalyze the attachment of specific amino acids to their cognate tRNAs. Differently from most mttRNAs, which are encoded by mitochondrial genome, mtARSs are encoded by nuclear genes and then imported into the mitochondria after translation in the cytosol. Due to the extensive use of next-generation sequencing (NGS), an increasing number of mtARSs variants associated with large clinical heterogeneity have been identified in recent years. Being most of these variants private or sporadic, it is crucial to assess their causative role in the disease by functional analysis in model systems. This review will focus on the contributions of the yeast Saccharomyces cerevisiae in the functional validation of mutations found in mtARSs genes associated with human disorders.     

Mating Disruption of Plodia interpunctella in Small-Scale Plots: Effects of Pheromone Blend, Emission Rates, and Population Density

An indoor mating disruption experiment was performed on the stored-product pest Plodia interpunctella. The female of this species emits a four-component pheromone blend consisting of Z9,E12–14 : OAc, Z9,E12–14 : OH, Z9,E12–14 : Ald, and Z9–14 : OAc. Mating of Plodia interpunctella was disrupted up to 93% by using synthetic pheromone in small-scale plot experiments. The study was performed in 2.5 m × 2.5 m × 2.5 m polythene cubicles housed in a greenhouse, and pheromones were released by MSTRS spraying every 15~min. The disruption effect was tested at different doses 0.075, 0.75, and 3.75 mg/spray (corresponding to 5, 50, and 250 g/min), different pheromone formulas (one-component (Z9,E12–14 : OAc) and four-component), and at different population densities (10, 20, and 30 individuals, equivalent to 0.32, 0.64, and 0.96 individuals/m²). The moths were released into the cubicles and recaptured 24 hr later. The females were checked for spermatophore presence indicating successful mating. The mating was significantly suppressed in all treatments compared to the control. There was, however, no difference in mating activity between the one-component and four-component disruptants. In addition, EAG measurements were conducted with a portable device to keep track of aerial concentrations of pheromone. The results show that the one-component formula disrupts mating as efficiently as the more complete four-component blend at doses applied in this study. This fact improves the prospects for mating disruption of indoor pyralids, since many pyralid species share the major component in their pheromones, and, thus, can probably be controlled simultaneously by using this compound only.     

Characterisation and Antioxidant Activity of Crude Extract and Polyphenolic Rich Fractions from C. incanus Leaves

Cistus incanus (Cistaceae) is a Mediterranean evergreen shrub. Cistus incanus herbal teas have been used as a general remedy in traditional medicine since ancient times. Recent studies on the antioxidant properties of its aqueous extracts have indicated polyphenols to be the most active compounds. However, a whole chemical characterisation of polyphenolic compounds in leaves of Cistus incanus (C. incanus) is still lacking. Moreover, limited data is available on the contribution of different polyphenolic compounds towards the total antioxidant capacity of its extracts. The purpose of this study was to characterise the major polyphenolic compounds present in a crude ethanolic leaf extract (CEE) of C. incanus and develop a method for their fractionation. Superoxide anion, hydroxyl and DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging assays were also performed to evaluate the antioxidant properties of the obtained fractions. Three different polyphenolic enriched extracts, namely EAC (Ethyl Acetate Fraction), AF1 and AF2 (Aqueos Fractions), were obtained from CEE. Our results indicated that the EAC, enriched in flavonols, exhibited a higher antiradical activity compared to the tannin enriched fractions (AF1 and AF2). These findings provide new perspectives for the use of the EAC as a source of antioxidant compounds with potential uses in pharmaceutical preparations.     

Anomalous Resistance Hysteresis in Oxide ReRAM: Oxygen Evolution and Reincorporation Revealed by In Situ TEM

The control and rational design of redox‐based memristive devices, which are highly attractive candidates for next‐generation nonvolatile memory and logic applications, is complicated by competing and poorly understood switching mechanisms, which can result in two coexisting resistance hystereses that have opposite voltage polarity. These competing processes can be defined as regular and anomalous resistive switching. Despite significant characterization efforts, the complex nanoscale redox processes that drive anomalous resistive switching and their implications for current transport remain poorly understood. Here, lateral and vertical mapping of O vacancy concentrations is used during the operation of such devices in situ in an aberration corrected transmission electron microscope to explain the anomalous switching mechanism. It is found that an increase (decrease) in the overall O vacancy concentration within the device after positive (negative) biasing of the Schottky‐type electrode is associated with the electrocatalytic release and reincorporation of oxygen at the electrode/oxide interface and is responsible for the resistance change. This fundamental insight presents a novel perspective on resistive switching processes and opens up new technological opportunities for the implementation of memristive devices, as anomalous switching can now be suppressed selectively or used deliberately to achieve the desirable so‐called deep Reset.     

Biomimetic models of the actin cytoskeleton

The cytoskeleton is a complex polymer network that plays an essential role in the functionality of eukaryotic cells. It endows cells with mechanical stability, adaptability, and motility. To identify and understand the mechanisms underlying this large variety of capabilities and to possibly transfer them to engineered networks makes it necessary to have in vitro and in silico model systems of the cytoskeleton. These models must be realistic representatives of the cellular network and at the same time be controllable and reproducible. Here, an approach to design complementary experimental and numerical model systems of the actin cytoskeleton is presented and some of their properties discussed.     

Synthesis and characterization of polymer-coated quantum dots with integrated acceptor dyes as FRET-based nanoprobes

A fluorescence resonance energy transfer pair consisting of a colloidal quantum dot donor and multiple organic fluorophores as acceptors is reported and the photophysics of the system is characterized. Most nanoparticle-based biosensors reported so far use the detection of specific changes of the donor/acceptor distance under the influence of analyte binding. Our nanoparticle design on the other hand leads to sensors that detect spectral changes of the acceptor (under the influence of analyte binding) at fixed donor/acceptor distance by the introduction of the acceptor into the polymer coating. This approach allows for short acceptor-donor separation and thus for high-energy transfer efficiencies. Advantageously, the binding properties of the hydrophilic polymer coating further allows for addition of poly(ethylene glycol) shells for improved colloidal stability.     

Time correlated fluorescence characterization of an asymmetrically focused flow in a microfluidic device

In this study, we explore and model the behavior of a prototype microfluidic device which employs two non-mixing fluids (sheath and inlet fluids) displaying an asymmetric focused flow, in the presence of a fluorescent dye. Fluorescence correlation spectroscopy is employed, allowing the precise measure of flow speeds across the channels and of the concentration profile of the central focused flux along the flow direction. The system is modeled via a standard Navier–Stokes finite-element approach, coupled to convection–diffusion equations for the solute. Simulations reproduce accurately the shape, the position, and the width of the velocity and concentration profiles along the central channel and across the transversal and vertical sections of the microfluidic device. The observed asymmetric flow with respect to the center of the channel is reproduced numerically with an error in the position determination smaller than 1%.