Folate receptor targeted, carboxymethyl chitosan functionalized iron oxide nanoparticles: a novel ultradispersed nanoconjugates for bimodal imaging

This article delineates the design and synthesis of a novel, bio-functionalized, magneto-fluorescent multifunctional nanoparticles suitable for cancer-specific targeting, detection and imaging. Biocompatible, hydrophilic, magneto-fluorescent nanoparticles with surface-pendant amine, carboxyl and aldehyde groups were designed using o-carboxymethyl chitosan (OCMC). The free amine groups of OCMC stabilized magnetite nanoparticles on the surface allow for the covalent attachment of a fluorescent dye such as rhodamine isothiocyanate (RITC) with the aim to develop a magneto-fluorescent nanoprobe for optical imaging. In order to impart specific cancer cell targeting properties, folic acid and its aminated derivative was conjugated onto these magneto-fluorescent nanoparticles using different pendant groups (-NH(2), -COOH, -CHO). These newly synthesized iron-oxide folate nanoconjugates (FA-RITC-OCMC-SPIONs) showed excellent dispersibility, biocompatibility and good hydrodynamic sizes under physiological conditions which were extensively studied by a variety of complementary techniques. The cellular internalization efficacy of these folate-targeted and its non-targeted counterparts were studied using a folate-overexpressed (HeLa) and a normal (L929 fibroblast) cells by fluorescence microscopy and magnetically activated cell sorting (MACS). Cell-uptake behaviors of nanoparticles clearly demonstrate that cancer cells over-expressing the human folate receptor internalized a higher level of these nanoparticle-folate conjugates than normal cells. These folate targeted nanoparticles possess specific magnetic properties in the presence of an external magnetic field and the potential of these nanoconjugates as T(2)-weighted negative contrast MR imaging agent were evaluated in folate-overexpressed HeLa and normal L929 fibroblast cells.     

Effect of Constraint on Creep Behavior of 9Cr-1Mo Steel

The effect of constraint on creep rupture behavior of 9Cr-1Mo steel has been investigated. The constraint was introduced by incorporating a circumferential U-notch in a plain cylindrical creep specimen of 5 mm diameter. The degree of constraint was increased by decreasing the notch root radius from 5 to 0.25 mm. Creep tests were conducted on plain and notched specimens at stresses in the range of 110 to 210 MPa at 873 K (600 °C). The creep rupture life of the steel was found to increase under constrained conditions, which increased with the increase in degree of constraint and applied stress, and tended to saturate at a higher degree of constraint. The creep rupture ductility (pct reduction in area) of the steel was found to be lower under constrained conditions. The decrease in creep ductility was more pronounced at a higher degree of constraint and lower applied stresses. Scanning electron microscopic studies revealed a change in fracture behavior with stress and degree of constraint. The fracture surface appearance for relatively lower constrained specimens at higher stresses was predominantly transgranular dimple. Creep cavitation-induced intergranular brittle fracture near the notch root was observed for specimens having a higher degree of constraint at relatively lower stresses. The creep rupture life of the steel under constrained conditions has been predicted based on the estimation of damage evolution by continuum damage mechanics coupled with finite element analysis of the triaxial state of stress across the notch. It was found that the creep rupture life of the steel under constrained conditions was predominantly governed by the von-Mises stress and the principal stress became progressively important with increase in the degree of constraint and decrease in applied stress.     

An assessment of creep deformation and fracture behavior of 2.25Cr-1Mo similar and dissimilar weld joints

The evaluation of the creep deformation and fracture behavior of a 2.25Cr-1Mo steel base metal, a 2.25Cr-1Mo/2.25Cr-1Mo similar weld joint, and a 2.25Cr-1Mo/Alloy 800 dissimilar weld joint at 823 K over a stress range of 90 to 250 MPa has been carried out. The specimens for creep testing were taken from single-V weld pads fabricated by a shielded metal arc-welding process using 2.25Cr-1Mo steel (for similar-joint) and INCONEL 182 (for dissimilar-joint) electrodes. The weld pads were subsequently given a postweld heat treatment (PWHT) of 973 K for 1 hour. The microstructure and microhardness of the weld joints were evaluated in the as-welded, postweld heat-treated, and creep-tested conditions. The heat-affected zone (HAZ) of similar weld joint consisted of bainite in the coarse-prior-austenitic-grain (CPAG) region near the fusion line, followed by bainite in the fine-prior-austenitic-grain (FPAG) and intercritical regions merging with the unaffected base metal. In addition to the HAZ structures in the 2.25Cr-1Mo steel, the dissimilar weld joint displayed a definite INCONEL/2.25Cr-1Mo weld interface structure present either as a sharp line or as a diffuse region. A hardness trough was observed in the intercritical region of the HAZ in both weld joints, while a maxima in hardness was seen at the weld interface of the dissimilar weld joint. Both weld joints exhibited significantly lower rupture lives compared to the 2.25Cr-1Mo base metal. The dissimilar weld joint exhibited poor rupture life compared to the similar weld joint, at applied stresses lower than 130 MPa. In both weld joints, the strain distribution across the specimen gage length during creep testing varied significantly. During creep testing, localization of deformation occurred in the intercritical HAZ. In the similar weld joint, at all stress levels investigated, and in the dissimilar weld joint, at stresses ≥150 MPa, the creep failure occurred in the intercritical HAZ. The fracture occurred by transgranular mode with a large number of dimples. At stresses below 150 MPa, the failure in the dissimilar weld joint occurred in the CPAG HAZ near to the weld interface. The failure occurred by extensive intergranular creep cavity formation.     

Antimicrobial Ionic Liquid-Based Materials for Biomedical Applications

Excessive and unwarranted administration of antibiotics has invigorated the evolution of multidrug-resistant microbes. There is, therefore, an urgent need for advanced active compounds. Ionic liquids with short-lived ion-pair structures are highly tunable and have diverse applications. Apart from their unique physicochemical features, the newly discovered biological activities of ionic liquids have fascinated biochemists, microbiologists, and medical scientists. In particular, their antimicrobial properties have opened new vistas in overcoming the current challenges associated with combating antibiotic-resistant pathogens. Discussions regarding ionic liquid derivatives in monomeric and polymeric forms with antimicrobial activities are presented here. The antimicrobial mechanism of ionic liquids and parameters that affect their antimicrobial activities, such as chain length, cation/anion type, cation density, and polymerization, are considered. The potential applications of ionic liquids in the biomedical arena, including regenerative medicine, biosensing, and drug/biomolecule delivery, are presented to stimulate the scientific community to further improve the antimicrobial efficacy of ionic liquids.     

Non-isothermal decomposition kinetics of nano-scale CaCO3 as a function of particle size variation

We report the synthesis of nanocrystalline calcium carbonate with varying particle sizes by precipitation techniques from an aqueous solution of calcium nitrate and sodium carbonate at controlled pH. The particle size of the carbonate powder was precisely controlled by changing the precursor concentration. The synthesized carbonate powders were characterized by using scanning electron microscopy, X-ray diffraction technique, and transmission electron microscopy. The particle size, along with the crystallite size of as-synthesized carbonate powder, decreases with increasing precursor concentration. The non-isothermal decomposition kinetics of the carbonate powder was also evaluated by using near to the modified Arrhenius equation's exact solution. The experimental results were best fitted at n = 0.5, and the one-dimensional diffusion-controlled transport process mechanism (D₁) and one-dimensional phase boundary movement mechanism (R₁) was found to be very close fit of the corresponding evaluated g(α) value. The apparent activation energy of the nano calcium carbonate decomposition was found in the range of 120–175 kJ/mol, which is also inherently functioning with the average particle size. The apparent activation energy of decomposition of CaCO₃ found to be decreased with decreasing average particle size of nanocrystalline calcium carbonate.     

Characterisation of a Schottky ISFET as Hg-MOSFET and as cytochrome P450-ENFET

A cost-effective and simple method is proposed wherein a Schottky ion sensitive field effect transistor (Schottky ISFET)-based sensor is characterised as metal oxide semiconductor and enzyme field effect transistor (ENFET). This technique involves deposition of mercury (Hg) as gate material over the sensing layer mitigating the complexity of fabrication process, thereby eliminating the need of refabricating an identical device. A Schottky-based ISFET simplifies the fabrication process as the requisite for doping of source and drain regions becomes redundant. Steps involved in lithography process for fabricating metal oxide semiconductor field effect transistor (MOSFET) are reduced with the use of liquid metal Hg as gate over layer. Such a device can be transformed back to an ISFET without any additional etching process. Furthermore, the same ISFET device can be utilised as an ENFET when the former is used in conjunction with a biological element. In this work, a Schottky-based ISFET has been characterised as Hg-MOSFET and as cytochrome P450-ENFET. Multiple tests on the device exhibit that the same ISFET sensor can be used both as a MOSFET and an ENFET with good repeatability and versatility without losing its sensitivity.     

From Mountain Ranges to Sweeping Plains,in Droughts and Flooding Rains; River Murray Water Quality over the Last Four Decades

The aim of this paper was to analyse the spatial and temporal patterns and drivers of water quality in a large arid/semi-arid river system (River Murray, Australia) using a long term (1978???2015) dataset collected from 24 monitoring sites. The water quality is highly variable, but on average electrical conductivity (EC), pH, turbidity, dissolved and total nutrient, colour and chlorophyll a levels increase with distance downstream from the headwaters to the lower reaches. This is a function of the natural accumulation of dissolved and particulate components and intermittent, mostly diffuse source, pollutant inputs. The Darling tributary inflow increases turbidity, total phosphorus and pH in the main River Murray channel. Based on long-term trend analysis at four representative sites, EC, nutrients and colour showed declining trends on average at most sites except in the headwaters. Increased flow increases concentrations of most quality parameters, although at very high flows decreases in pH, EC, turbidity and oxidized nitrogen were apparent at many sites. The extreme “Millennium” drought (2002???2009) period resulted in lowered concentrations of many water quality parameters, indicating retention in the landscape. In the post-drought flooding (2010???2012) period a large amount of organic material was mobilised, resulting in much higher peak colour concentrations than when mid-range flooding was more frequent. It is critical that this monitoring program is continued as a Basin-wide water management plan is implemented.