Thermal product estimation method for aerodynamics experiments

This paper presents an experimental technique to estimate the appropriate thermal product values of rugged and fast response temperature probes (TPs) for hypersonic aerodynamic experiments. Two types of scratches were used, mainly abrasive papers with different grit sizes and scalpel blades with different thicknesses, to form the probe junction. The effect of the scratch technique on the probe’s thermal product is investigated. The probes are tested and calibrated in the test section and in the end wall of shock tube facility. It is observed that the thermal product of a particular TP depends on the Mach number, junction scratch technique, and junction location, as well as on the enthalpy conditions. It is noted that, depending on the scratch technique, some of the TPs do not require individual calibration; however, calibration for others is likely to be needed.     

Niosomal encapsulation of the antitubercular drug, pyrazinamide

It is estimated that more than one-third of the world population is infected with Mycobacterium tuberculosis. Pyrazinamide (PZA) plays a unique role in shortening therapy because it kills a population of semilatent tubercle bacilli residing in an acidic environment. Niosomes are vesicles made up of non-ionic surfactant and exhibit behavior similar to liposomes in vivo. Preparation of PZA niosomes took place using different molar ratios of Span 60 and Span 85, with cholesterol (CH) i.e. Span: CH (1:1) and (4:2). Dicetyl phosphate and stearyl amine were used in preparation of negative and positively charged niosomes, respectively. Free PZA was separated by cooling centrifugation and estimated spectrophotometrically at 268.4 nm. Niosomes were characterized by electron microscopy and differential scanning calorimetry. The highest percentage PZA entrapped was obtained using Span 60 and the molar ratio (4:2:1) negatively charged niosomes. This was followed by the neutral PZA neutral (4:2) Span 60 niosomes. Biological evaluation of selected PZA niosomal formulations took place on guinea pigs infected with M. tuberculosis. The present work is an attempt to target maximum concentration of PZA to the affected site (lungs) and to exclude undesirable side effects and decrease toxicity. Macrophage targeting and overcoming drug resistance is our final goal.     

Evaluation of the deuterium isotope effect in zwitterionic hydrophilic interaction liquid chromatography separations for implementation in a quantitative proteomic approach

Quantitative methodologies for the global in-depth comparison of proteomes are frequently based on chemical derivatization of peptides with isotopically distinguishable labeling agents. In the present work, we set out to study the feasibility of the dimethyl labeling method in combination with ZIC-cHILIC (zwitterionic hydrophilic interaction liquid chromatography) technology for quantitative proteomics. We first addressed the potential issue of isotope effects perturbing the essential coelution of differently labeled peptides under ZIC-cHILIC separation. The deuterium incorporation-induced effect can be largely eliminated by favoring the mixed-mode ZIC-cHILIC separation based on combined hydrophilic and ionic interactions. Then, we evaluated the performance and applicability of this strategy using a sample consisting of human cell lysate. We demonstrate that our approach is suitable to perform unbiased quantitative proteome analysis, still quantifying more than 2500 proteins when analyzing only a few micrograms of sample.     

Detection of lysozyme magnetic relaxation switches based on aptamer-functionalized superparamagnetic nanoparticles

Magnetic relaxation switch (MRSw) detection is based on aggregate formation or dissociation when magnetic nanoparticles (MNPs) bind to target molecules. In the aggregated state, the dephasing rate of nearby proton spins is higher than in the dispersed state, resulting in a decrease in the spin-spin relaxation time, T(2). In this work, an MRSw-based nanosensor for lysozyme (Lys) protein detection was achieved using iron oxide nanoparticles conjugated with either Lys aptamer or linker DNA, which can hybridize with the extended part of the aptamer to form clusters. Upon the addition of Lys, the aptamers bind with their targets, leading to disassembly of clusters and an increase in T(2). A detection limit in the nanomolar range was achieved for Lys detection in both buffer and human serum. The determination of Lys level in different types of cancer cell lysates was also performed to demonstrate detection in real clinical samples.     

Olive mills effluent (OME) wastewater post-treatment using activated clay

Olive mill effluent (OME) wastewater embodies a challenge for environmental scientists and engineers. It is characterized by high values of COD, BOD, and phenolic content. A series of treatment steps composed of settling, centrifugation, and filtration was consecutively used to condition OME wastewater. The filtrate was then subjected to a post-treatment process, namely adsorption on activated clay. The dynamic response of phenols concentration, pH, and COD, using different concentrations of activated clay, showed a peak at which maximum adsorption capacity was achieved. The maximum adsorption capacity for the tested concentrations of activated clay was reached in less than 4 h. It is thought that adsorption of phenols and organics is reversible and mainly due to hydrophobic interactions. The maximum removal of phenols was about 81%, while it reached about 71% for organic matter.