Determination of tryptophan in raw materials, rat brain and human plasma by RP-HPLC technique

This paper describes tryptophan (TRP) estimation in raw human plasma and rat brain by reversed-phase high-performance liquid chromatography (RP-HPLC). Estimation was carried out on a Purospher STAR C18 column using water-acetonitrile (90:10 v/v, at pH 2.7) mixture at a rate of 1.5 mL/min as mobile phase. Eluents were monitored at 273 nm by an ultraviolet detector. The method was linear (R(2) > 0.999), precise (intra-day and inter-day precision <2%) in the range of 0.25-20 μg/mL. The detection and quantification limits were 0.0144 μg/mL and 0.0437 μg/mL, respectively. In human plasma, Day 1 and Day 2 precision were 0.054-2.29% and 1.66-3.7%; whereas precisions in rat brain were 1.23-2.3% and 0.677-4.2%, respectively. The method was applied to study TRP level in human smokers and in arthritic rat brain. An efficient RP-HPLC method was developed for TRP determination that worked for clinical and research purposes.     

Shape-directing role of cetyltrimethylammonium bromide in the preparation of silver nanoparticles

We report a simple chemical reduction method for the synthesis of different colored silver nanoparticles, AgNP, using tyrosine as a reducing agent. Effects of cetyltrimethylammonium bromide, CTAB, and tyrosine concentrations are analyzed by UV-visible measurements and scanning electron microscopy (SEM) to evaluate the mode of AgNP aggregation. The position and shape of the surface resonance plasmon absorption bands strongly depend on the reaction conditions, i.e., [CTAB], [tyrosine], and reaction time. Sub-, post-, and dilution-micellar effects are accountable for the fast and slow nucleation and growth processes. Spectrophotometric measurement also shows that the average size and the polydispersity of AgNP increase with [CTAB] in the solution. CTAB acted as a shape-directing agent.     

Synthesis and In Vitro Antibacterial Activity of Novel Steroidal (6R)‐Spiro‐1,3,4‐thiadiazoline Derivatives

Novel steroidal (6R)‐spiro‐1,3,4‐thiadiazoline derivatives were synthesized by the cyclization of steroidal thiosemicarbazones with acetic anhydride, screened in vitro against antibacterial activity using disc‐diffusion method and the minimum inhibitory concentration. The results showed that steroidal thiadiazoline derivatives exhibited better antibacterial activity than the steroidal thiosemicarbazone derivatives. Chloro and acetoxy substituents on the 3β‐position of the steroidal thiadiazoline ring increased the antibacterial activity. Among all the compounds, compound 7 and 8 were found better inhibitors of both types of bacteria (Gram‐positive and Gram‐negative) as compared to the respective drug amoxicillin. All the synthesized compounds were well characterized by spectroscopic methods such as IR, ¹H‐NMR, ¹³C‐NMR mass, and elemental analysis and their stereochemistry was also discussed.     

Energetics of anionic surfactant-additive systems at the cloud point

The energetics of clouding in anionic surfactant (SDBS) and tetrabutylammonium bromide system in the presence of additives, such as ureas, amino acids and sugars is reported. The change of standard Gibbs energy of solubilization (ΔG _s ^o) for all of the additives was found to be negative. The values of change of standard enthalpy (ΔH _s ^o) and that of standard entropy (TΔS _s ^o) values were found to depend on the type and chemistry of the additive. The results were explained on the basis including chemistry of additives, their effect on water structure, and solubilization of additives either in the micellar or in aqueous phases.     

Characterization through distributional properties of dual generalized order statistics

Distributional properties of two non-adjacent dual generalized order statistics have been used to characterize distributions. Further, one sided contraction and dilation for the dual generalized order statistics are discussed and then the results are deduced for generalized order statistics, order statistics, lower record statistics, upper record statistics and adjacent dual generalized order statistics.     

Mixed Convection of Water at 4°C Along a Wedge with Variable Surface Flux in a Porous Medium

In this study, the mixed convection of water at 4°C along a wedge in a porous medium is investigated numerically using finite difference method. In order to explore the effect of mixed convection, both forced and free convection-dominated regimes are considered. Non-similarity solutions are obtained for the variable wall flux boundary condition. Velocity and temperature profiles as well as local dimensionless skin friction and Nusselt number are obtained and compared with the available numerical results for various values of different parameters. The wedge angle geometry parameter m and mixed convection parameter ξ are ranged from 0 to 1 in both regimes whereas different values of λ are considered for the purpose of comparison of heat transfer results.     

Cyclic multiaxial and shear finite deformation responses of OFHC Cu. Part II: An extension to the KHL model and simulations

In this part, the Khan–Huang–Liang (KHL) constitutive model was extended to account for kinematic hardening characteristic behavior of materials. The extended model is then generalized and used to simulate experimental response of oxygen free high conductivity (OFHC) copper under cyclic shear straining and biaxial tension–torsion (multiaxial ratchetting) experiments presented in Part I (Khan et al., 2007). In addition, a new modification for the non-linear kinematic hardening rule of Karim–Ohno (Abdel-Karim and Ohno, 2000) is proposed to simulate multiaxial ratchetting behaviors. Although, the kinematic hardening contributes the most to the response, it is shown that, the loading rate effect, and a coupled isotropic and kinematic hardening effect should also be considered while simulating the multiaxial ratchetting behavior of OFHC copper. Furthermore, the newly modified kinematic hardening rules is able to fairly well simulate the multiaxial ratchetting experiments under different loading conditions, irrespective of the value of applied axial tensile stress, shear strain amplitude, pre-cyclic hardening and/or loading sequence.     

Heavy ion interactions of (14.0 MeV/u) Pb with U

The interactions of ²⁰⁸Pb projectiles with ^natU target have been studied at 14.0 MeV/u beam energy using two different threshold detectors; mica and lexan. The elastic scattering data have been separated from the binary events and used for the determination of quarter-point angle θ_1/4 (≡ grazing angle θ_gr). The values of maximum angular momentum , radius of interaction R_int and reaction cross-section σ_R^exp(el.) were then deduced by making use of the value of θ_1/4. The data of inelastic events of different multiplicities have been used to determine partial reaction cross-sections. The sum of the partial cross-sections, therefore, yielded another independent value of reaction cross-section σ_R^exp(inel.) that in turn was used to derive the alternative values of , θ_gr, and R_int independently. The average of these quantities provided the experimental values of the reaction parameters that are comparable to the theoretical predictions.     

Unexpected nitrosyl-group bending in six-coordinate [M(NO)](6) sigma-bonded aryl(iron) and -(ruthenium) porphyrins.

The six-coordinate nitrosyl sigma-bonded aryl(iron) and -(ruthenium) porphyrin complexes (OEP)Fe(NO)(p-C(6)H(4)F) and (OEP)Ru(NO)(p-C(6)H(4)F) (OEP = octaethylporphyrinato dianion) have been synthesized and characterized. Single-crystal X-ray structure determinations reveal an unprecedented bending and tilting of the MNO group for both [MNO](6) species as well as significant lengthening of trans axial bond distances. In (OEP)Fe(NO)(p-C(6)H(4)F) the Fe-N-O angle is 157.4(2) degrees, the nitrosyl nitrogen atom is tilted off of the normal to the heme plane by 9.2 degrees, Fe-N(NO) = 1.728(2) A, and Fe-C(aryl) = 2.040(3) A. In (OEP)Ru(NO)(p-C(6)H(4)F) the Ru-N-O angle is 154.9(3) degrees, the nitrosyl nitrogen atom is tilted off of the heme normal by 10.8 degrees, Ru-N(NO) = 1.807(3) A, and Ru-C(aryl) = 2.111(3) A. We show that these structural features are intrinsic to the molecules and are imposed by the strongly sigma-donating aryl ligand trans to the nitrosyl. Density functional-based calculations reproduce the structural distortions observed in the parent (OEP)Fe(NO)(p-C(6)H(4)F) and, combined with the results of extended Hückel calculations, show that the observed bending and tilting of the FeNO group indeed represent a low-energy conformation. We have identified specific orbital interactions that favor the unexpected bending and tilting of the FeNO group. The aryl ligand also affects the Fe-NO pi-bonding as measured by infrared and (57)Fe M?ssbauer spectroscopies. The solid-state nitrosyl stretching frequencies for the iron complex (1791 cm(-)(1)) and the ruthenium complex (1773 cm(-)(1)) are significantly reduced compared to their respective [MNO](6) counterparts. The M?ssbauer data for (OEP)Fe(NO)(p-C(6)H(4)F) yield the quadrupole splitting parameter +0.57 mm/s and the isomer shift 0.14 mm/s at 4.2 K. The results of our study show, for the first time, that bent Fe-N-O linkages are possible in formally ferric nitrosyl porphyrins.