Cytochrome P450 inhibitory potential of selected Indian spices — possible food drug interaction

Spices constitute an important group of food which is virtually indispensable in the culinary art. In a view, these spices feared to pose a probability to affect the disposition of conventional pharmaceuticals through inhibition of human cytochrome P450 (CYPs) enzymes. In the present study an approach has been made to evaluate the possible CYP inhibition potential with some Indian spices (Capsicum annuum, Murraya koenigii, Zingiber officinale) and their major bioactive compounds, in combination with pooled microsome; as well as commercially available recombinant human CYP3A4, CYP2D6, CYP2C9 and CYP1A2. Quantification of the bioactive compound was determined through RP-HPLC, in order to standardize the plant material. CYP–carbon monoxide (CYP–CO) complex assay result indicated that all the plants and their bioactive compounds have an interaction potential with CYPs. Fluoregenic assay results indicated that the spice extracts have higher inhibition potential comparing to their single bioactive molecule. The higher enzyme inhibition potential by the extracts may be related to the synergistic effects due to the presence of other constituents in the extract. Capsaicin and C. annuum showed the lowest IC₅₀ value and 6-gingerol and Z. officinale extract showed the highest IC₅₀ value among the entire sample tested. The entire sample showed significantly less (P < 0.001, P < 0.01) interaction potential than known inhibitors. These findings indicate that selected spices are unlikely to cause clinically relevant drug interactions involving the inhibition of major CYP isozymes.     

Effect of Temperature on Hydraulic Parameters of Cable-In-Conduit-Conductor of SST-1

Stable operation of superconducting magnets depend critically on the balance of heat deposition rate versus heat extraction rate by the cryo-coolant. Thus, the mass flow rate of the coolant in case of force-flow cooled superconducting magnet with Cable-In-Co-nduit-Conductor (CICC) construction becomes an important factor for optimum stability of magnets. The Toroidal and Poloidal Field magnets of Steady-state Superconducting Tokamak-1 (SST-1) is made of superconducting CICC with a void fraction of 40 %±2 %. For adequate cooling of magnets, supercritical helium at 4 bar and 4.5 K is forced-flown through the voids. Effect of temperature on mass flow rate and pressure drop in SST-1 CICC is studied in a 7 m long piece wound helically. The experimental friction factor of the CICC is also measured at different temperatures and flow rates and is compared with the standard Katheder equation and Tada equation. Also, based on the new findings obtained from the experimental results, the dimensionless Reynolds number has been slightly modified. This new number is used to propose a modified Katheder correlation for the friction factor in CICCs similar to that of SST-1.     

Design and Characterization of a W-Band Folded-Waveguide Slow-Wave Structure

A single-section slow-wave structure for a W-band folded-waveguide traveling-wave tube with operating bandwidth of around 4% was designed for delivering the output power of 50 W at the operating voltage of 13.5 kV and operating beam current of 80 mA. The design was carried out using analytical formulations and 3D electromagnetic simulations. The beam-wave interaction analysis was carried out using large signal Lagrangian analysis and particle-in-cell simulation. The folded-waveguide slow-wave structure along with input-output couplers and RF windows were fabricated. Cold test measurements were carried out for dispersion characteristics of the slow-wave structure and voltage standing-wave ratio and insertion loss characteristics of the RF window. The measured cold circuit parameters show close agreement with the analysis.     

Physicochemical Characterization of Interaction of Ibuprofen by Solid-State Milling with Aluminum Hydroxide

This present study is a preliminary exploration of the affinity between a carboxylic model drug ibuprofen and aluminum hydroxide. Ibuprofen was comilled with aluminum hydroxide in different weight ratios in the solid state and was characterized by scanning electron microscopy (SEM), X-ray powder diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and in vitro dissolution studies. XRD and SEM studies indicated complete interaction of ibuprofen with aluminum hydroxide and complete amorphization of aluminum hydroxide–ibuprofen complexed salt as well, on comilling with aluminum hydroxide at 1:2 ratio. FTIR data showed the disappearance of acid carbonyl peak with the appearance and the corresponding increase in absorbance of new signal at 1,682 cm^?1 in the 1:1 and 1:2 ibuprofen–aluminum hydroxide-comilled powder. The accompanied increase in the absorbance of carboxylate peak in the ibuprofen–aluminum hydroxide physical mixture, and 1:0.1, 1:0.5, 1:1, and 1:2 (IBA_pm, and IB₁A_0.1, IB₁A_0.5, IB₁A₁, and IB₁A₂, respectively) comilled powder indicated an acid–base reaction between ibuprofen and aluminum hydroxide. On storage at 40°C and 75% relative humidity (RH) for 10 weeks, XRD study showed the absence of reversion to the crystalline state and FTIR data revealed continued increase of new signal at 1,682 cm^?1 relative to carboxylic acid peak and no reappearance of carboxylic acid peak. In vitro dissolution studies revealed that the percent release of ibuprofen from the aluminum hydroxide-comilled powder is in the following order: IB₁A₂ < IB₁A₁ < ibuprofen crystal < ibuprofen milled alone < IB₁A_0.1 < IB₁A_0.5. Aluminum metal cation might have interacted to form a complex through the carboxyl and carbonyl groups of ibuprofen. Improved dissolution of drug associated with IB₁A_0.1 and IB₁A_0.5 is because of the absence of a new signal at 1,682 cm^?1 and improved amorphization of the drug to some extent. Dissolution of drug affected in IB₁A₂ and IB₁A₁ may be because of the insoluble stable complex formation.     

Overlapping tracks processed by TIG melting TiC preplaced powder on low alloy steel surfaces

An overlapping composite track coating was produced on a steel surface by preplacing a 0·5 mm thick layer of TiC powder and then melting using a tungsten inert gas torch of constant energy input. The influence of the overlapping operation on preheating of the substrate, the dissolution of TiC particulates and the subsequent depth and hardness of the composite layer was analysed. The melt microstructure consisted of both undissolved and partially dissolved TiC particulates, together with a variety of morphologies and sizes of TiC particles precipitated during solidification. Preheating, resulting from the overlapping operation, occurred, producing additional melting of the TiC particulates and deeper melt depths but with a reduced volume fraction of TiC precipitates in the subsequent tracks. A maximum hardness of over 800 HV was developed in the composite layer. The high hardness was unevenly distributed in tracks melted at the initial and final stages, while it varied across the melt depths in other tracks.     

Effect of initial powder type on the hydrogen storage properties of high-pressure torsion consolidated Mg

While severe plastic deformation (SPD) on bulk samples has been widely applied for modifying the H-sorption properties, there has been little attention towards the use of SPD on powder materials. In this context, the aim of the present work was to compare the H-storage properties of high-pressure torsion (HPT) consolidated products obtained from two distinct Mg powder precursors: atomized micro-sized and condensed ultrafine powder particles. The results showed that the nature of the initial powder precursor had a pronounced effect on the H-sorption behavior. The HPT product obtained from the condensed ultrafine powder showed faster absorption kinetics than the consolidated product obtained from the atomized powder. However, the HPT product obtained from atomized powder could absorb more hydrogen and showed faster desorption kinetics corresponding to a lower activation energy. These results are discussed by taking into account the effectiveness of the HPT process to refine the grain sizes and differences in the dispersion of fine MgO oxide particles.     

Scope for improved properties of dissimilar joints of ferrous and non-ferrous metals

Dissimilar joints (DSJs) of ferrous and non-ferrous metals have huge technological importance in the frontiers of new designs in new machineries and improved design of conventional systems. This investigation was undertaken to improve mechanical properties of joints of two dissimilar metals: one is Ti-based and the other is Fe-based. DSJs were processed using bonding pressure from 1 to 9 MPa in step of 2 MPa at 750 °C for 60 min. Properties of the DSJs of these two metals using different mechanisms and methods were compared with the present research for verification. Experimental results from the diffusion bonding mechanism for joining the dissimilar metals validated the improvement in properties. Superior mechanical properties of dissimilar-metals joints were achieved mainly due to the third non-ferrous metallic foil, Ni of ~ 200-μm thickness, which avoided the formation of brittle Fe–Ti-based intermetallics in the diffusion zone. DSJs processed are able to achieve maximum strength of ~560 MPa along with substantial ductility of ~11.9%, which is the best ever reported in the literatures so far. Work hardening effect was detected in the DSJs when the bonding was processed at 5 MPa and above. Bulging ratio of the non-ferrous metal (Ti-based) was much higher than that of the ferrous metal (SS) of the DSJs processed. SEM analysis was carried out to know the details of reaction zone, while XRD was carried out to support the SEM results. Reasons for change in mechanical, physical, and fracture properties of the DSJs with the process parameter variations were clarified.     

Synthesis and characterization of niobium-doped potassium tetragonal tungsten bronzes, KxNbyW1?yO3

Needle-shaped crystals of sizes up to 5 μm × 5 μm × 40 μm of nominal composition K _x Nb _y W_1−y O₃ were synthesized by solid state method at 800 °C using appropriate amount of WO₃, WO₂, Nb₂O₅, and K₂WO₄. The samples were characterized with XRD, SEM, microprobe analysis, optical spectroscopy, and Raman spectroscopy. The XRD patterns of the samples show single phase of tetragonal tungsten bronze (TTB) type (P4/mbm, No. 127) up to y = 0.07. Structure refinements reveal an increase in cell parameter with increasing nominal niobium content within the TTB phase. The elemental compositions of the crystals determined by electron microprobe analysis also show an increase in Nb content with increasing y. With increasing Nb content the reflectivity minimum in the near infrared spectral range shifts towards lower wavenumber indicating the effect of decreasing carrier concentration. Pyrochlore type phase (KNbWO₆) is obtained as a second phase when nominal composition y > 0.07.     

The Structure And Properties of a Thermo‐mechanically Processed Low Carbon High Strength Steel

Research efforts were given towards development of low carbon high strength steels since recent past. The present study deals with the development of a low carbon high strength steel alloyed with Mn, Ni, Mo, Cu and microalloyed with Ti and Nb. The steel was subjected to three stage controlled rolling operation followed by accelerated cooling. The structure and properties of the steel at various processing conditions were evaluated. Microstructural observation reveals predominantly lath martensite along with twinned martensite structure at all processing conditions. High strength values at higher finish rolling temperatures have been obtained due to fine martensitic structure along with tiny precipitates of microalloying carbide and carbonitride. The strength value increases marginally at lower finishing temperature due to comparatively finer lath size of martensite and increased precipitation density of carbides, carbonitrides along with Cu particles. The variation in impact toughness properties at different finish rolling temperatures is found to be negligible at ambient and subambient temperatures. The formation of stable and large TiN/TiCN particles during casting have impaired the impact toughness values at ambient and at ‐40°C temperatures.     

Characterization and tribological behavior of cast In-Situ Al (Mg,Mo)-Al2O3 (MoO3) composite

Aluminum alloy—based cast in-situ composite has been synthesized by dispersion of externally added molybdenum trioxide particles (MoO₃) in molten aluminum at the processing temperature of 850 °C. During processing, the displacement reaction between molten aluminum and MoO₃ particles results in formation of alumina particles in situ and also releases molybdenum into molten aluminum. A part of this molybdenum forms solid solution with aluminum and the remaining part reacts with aluminum to form intermetallic phase Mo(Al_1−x Fe _x )₁₂ of different morphologies. Magnesium (Mg) is added to the melt in order to help wetting of alumina particles generated in situ, by oxidation of molten aluminum by molybdenum trioxide, and helps to retain these particles inside the melt. The mechanical properties of the cast in-situ composite, as indicated by ultimate tensile stress, yield stress, percentage elongation, and hardness, are relatively higher than those observed either in cast commercial aluminum or in cast Al-Mo alloy. The wear and friction of the resulting cast in-situ Al(Mg,Mo)-Al₂O₃(MoO₃) composites have been investigated using a pin-on-disc wear testing machine under dry sliding conditions at different normal loads of 9.8N, 14.7N, 19.6N, 24.5N, 29.4N, 34.3N, and 39.2 N and a constant sliding speed of 1.05 m/s. The results of the current investigation indicate that the cumulative volume loss and wear rate of cast in-situ composites are significantly lower than those observed either in cast commercial aluminum or in cast Al-Mo alloy, under similar load and sliding conditions. Beyond about 30 to 35 N loads, there appears to be a higher rate of increase in the wear rate in the cast in-situ composite as well as in cast commercial aluminum and cast Al-Mo alloy. For a given normal load, the coefficient of friction of cast in-situ composite is significantly lower than those observed either in cast commercial aluminum or in cast Al-Mo alloy. The coefficient of friction of cast in-situ composite increases gradually with increasing normal load while those observed in cast commercial aluminum or in cast Al-Mo alloy remain more or less the same. Beyond a critical normal load of about 30 to 35 N, the coefficient of friction decreases with increasing normal load in all the three materials.