Comparison of double-walled with single-walled carbon nanotube electrodes by electrochemistry

Double-walled carbon nanotubes (DWCNTs) were selectively functionalised by treatment with concentrated nitric and sulphuric acid, resulting in carboxylated outer and pristine inner tube constituents. The functionalised DWCNTs were then incorporated into two types of pre-existing carbon nanotube (CNT) electrode platforms, and the performance of each was compared to single-walled carbon nanotubes (SWCNTs). To make the CNT electrode platforms DWCNTs were covalently bound to fluorinated tin oxide glass (FTO) or electrografted aminophenyl tether layers on silicon. The performance of single- compared to double-walled CNTs on FTO or silicon supported electrodes was then determined through electrochemical methods, using the redox probes, ferrocene and ruthenium hexaamine, respectively. The DWCNTs showed an improved heterogeneous rate constant. This improvement was attributed to the protection of the electronic properties of the inner wall of the DWCNT during the chemical modification and suggests that DWCNTs may offer a useful alternative to SWCNTs in future electronic devices.     

Kindling-induced emotional behavior in male and female rats.

Modeling fear in animals is a critical approach for identifying the neural mechanisms involved in human disorders such as generalized anxiety and panic. Amygdala kindling has proven useful in this regard because it produces dramatic increases in fearful behavior. The purpose of this experiment was to compare the behavioral effects of kindling in male and female rats. Compared with the sham-stimulated rats, the kindled male and female rats showed similar increases in fearful behavior, with some sex differences in fear-related open-field activity. They also showed decreased immobility in the forced-swim test and increased sucrose consumption. These results suggest that kindling-induced fear is generally similar in male and female rats and that kindling does not appear to induce depression-like behavior. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Molecularly Targeted Agents as Radiosensitizers in Cancer Therapy—Focus on Prostate Cancer

As our understanding of the molecular pathways driving tumorigenesis improves and more druggable targets are identified, we have witnessed a concomitant increase in the development and production of novel molecularly targeted agents. Radiotherapy is commonly used in the treatment of various malignancies with a prominent role in the care of prostate cancer patients, and efforts to improve the therapeutic ratio of radiation by technologic and pharmacologic means have led to important advances in cancer care. One promising approach is to combine molecularly targeted systemic agents with radiotherapy to improve tumor response rates and likelihood of durable control. This review first explores the limitations of preclinical studies as well as barriers to successful implementation of clinical trials with radiosensitizers. Special considerations related to and recommendations for the design of preclinical studies and clinical trials involving molecularly targeted agents combined with radiotherapy are provided. We then apply these concepts by reviewing a representative set of targeted therapies that show promise as radiosensitizers in the treatment of prostate cancer.     

Enhancement of Surfactants in Nanoparticles Produced by an Electrospray Aerosol Generator

Electrospray aerosol generators (EAGs) disperse conducting solutions into air, promptly neutralize the particles to remove the excess charge, and evaporate the residual solvent with a dry air flow. For solutions containing multiple solutes, the particles may become enhanced in the more surface-active solutes. The extent of the enhancement was estimated for nanoparticles electrosprayed from a solution containing NaCl and surfactant sodium dodecyl sulfate (SDS) mixed in a 9:1 weight ratio. A tandem particle mobility analyzer was used to quantify the hygroscopic growth factor (GF). The relative fractions of NaCl and SDS in the particles were estimated from the measured GFs assuming that NaCl and SDS take up water independently of each other. The nanoparticles were considerably enhanced in SDS relative to the starting solution, with the NaCl:SDS weight ratio increasing with the distance from the EAG electrified capillary tip to the neutralizer, and reaching ～1:1 at the longest distances probed. The enhancement in SDS likely occurred during particle fission events as particles traveled from the capillary to the neutralizer. This study has practical ramifications for aerosol nanotechnology and aerosol-assisted drug delivery, which rely on EAG as an instrument of choice for nanoparticle generation.

Copyright 2012 American Association for Aerosol Research     

Properties and Stability of Solid Lipid Particle Dispersions Based on Canola Stearin and Poloxamer 188

Solid lipid particles (SLP) are one strategy for encapsulating lipophilic molecules, including for controlled release and enhanced bioavailability applications. SLP based on fully hydrogenated canola stearin (CaSt, 5, 10, 20, and 30 wt%) and the non-ionic surfactant Poloxamer 188 (P188, 0.0, 0.5, 1.0, 2.5, 5.0 and 10.0 wt%) were produced by high pressure melt homogenization using a microfluidizer. Spherical particles in the region of 140 nm were formed, depending on compostion and processing parameters. Surfactant concentration and pressure had a significant influence on particle diameter (P < 0.05), although number of homogenization cycles did not (P > 0.05). A maximum surfactant surface load of approximately 4 mg m⁻² was observed and, at or above 2.5% P188, excess surfactant was present in the continuous phase after production. P188 had the effect of decreasing particle size and facilitating transitions from the α to the β polymorph (P < 0.05) both through surface nucleation and size reduction effects. A stability study of the 10% CaSt SLP with 0.0, 1.0, or 5.0% P188 revealed particle growth for the 0.0 and 1.0% P188 SLP, especially at 20 versus 4 °C, but no changes in the 5.0% P188 SLP, which were exclusively in the β form, at both temperatures for up to 240 days.     

A microfluidic toolbox for cell fusion

Cellular fusion is a key process in many fields ranging from historical gene mapping studies and monoclonal antibody production, through to cell reprogramming. Traditional methodologies for cell fusion rely on the random pairing of different cell types and generally result in low and variable fusion efficiencies. These approaches become particularly limiting where substantial numbers of bespoke one‐to‐one fusions are required, for example, for in‐depth studies of nuclear reprogramming mechanisms. In recent years, microfluidic technologies have proven valuable in creating platforms where the manipulation of single cells is highly efficient, rapid and controllable. These technologies also allow the integration of different experimental steps and characterisation processes into a single platform. Although the application of microfluidic methodologies to cell fusion studies is promising, current technologies that rely on static trapping are limited both in terms of the overall number of fused cells produced and their experimental accessibility. Here we review some of the most exciting breakthroughs in core microfluidic technologies that will allow the creation of integrated platforms for controlled cell fusion at high throughput. © 2015 Society of Chemical Industry     

Kinetic,thermodynamic parameters and in vitro digestion of tannase from Aspergillus tamarii URM 7115

Tannase is an enzyme used in various industries and produced by a large number of microorganisms. The aim of this study was to evaluate tannase production to determine the biochemical, kinetic, and thermodynamic properties and to simulate tannase in vitro digestion. The tannase-producing fungal strain was isolated from “jamun” leaves and identified as Aspergillus tamarii. Temperature at 26°C for 67?h was the best combination for maximum tannase activity (6.35-fold; initial activity in Plackett–Burman design—15.53?U/mL and average final activity in Doehlert design—98.68?U/mL). The crude extract of tannase was optimally active at 40°C, pH 5.5 and 6.5. Moreover, tannase was stimulated by Na⁺, Ca²⁺, Mg²⁺, and Mn²⁺. The half-life at 40°C lasted 247.55?min. The free energy of Gibbs, enthalpy, and entropy, at 40°C, was 81.47, 16.85, and ?0.21?kJ/mol?·?K, respectively. After total digestion, 123.95% of the original activity was retained. Results suggested that tannase from A. tamarii URM 7115 is an enzyme of interest for industrial applications, such as gallic acid production, additive for feed industry, and for beverage manufacturing, due to its catalytic and thermodynamic properties.