Estimation of pioglitazone hydrochloride and metformin hydrochloride in tablets by derivative spectrophotometry and liquid chromatographic methods

Two simple and accurate methods of analysis to determine pioglitazone hydrochloride (PIO) and mefformin hydrochloride (MET) in combined dosage forms were developed using second-derivative spectrophotometry and reversed-phase liquid chromatography (LC). PIO and MET in combined preparations (tablets) were quantified using the second-derivative responses at 227.55 nm for PIO and 257.25 nm for MET in spectra of their solutions in a mixture of methanol and acetonitrile (30 + 70). The calibration curves were linear [correlation coefficient (r) = 0.9984 for PIO and 0.9986 for MET] in the concentration range of 8-40 microg/mL for PIO and 4-12 microg/mL for MET. In the LC method, analysis was performed on a Hypersil ODS-C18 column with 5 microm particle size using the mobile phase acetonitrile-water-acetic acid (75 + 25 + 0.3), adjusted to pH 5.5 with liquor ammonia, at a flow rate of 0.5 mL/min. Measurement was made at a wavelength of 230 nm. Both the drugs were well resolved on the stationary phase, and the retention times were 8.5 min for PIO and 16.0 min for MET. The calibration curves were linear (r = 0.9933 for PIO and 0.9958 for MET) in the concentration range of 4-20 microg/mL for PIO and MET. Both methods were validated, and the results were compared statistically. They were found to be accurate, precise, and specific. The methods were successfully applied to the estimation of PIO and MET in combined tablet formulations.     

Search for high-mass diphoton states and limits on Randall-Sundrum gravitons at CDF

We have performed a search for new particles which decay to two photons using 1.2 fb(-1) of integrated luminosity from pp[over] collisions at square root s = 1.96 TeV collected using the CDF II detector at the Fermilab Tevatron. We find the diphoton mass spectrum to be in agreement with the standard model expectation, and set limits on the cross section times branching ratio for the Randall-Sundrum graviton, as a function of diphoton mass. We subsequently derive lower limits for the graviton mass of 230 GeV/c(2) and 850 GeV/c(2), at the 95% confidence level, for coupling parameters (k/M[over](Pl)) of 0.01 and 0.1, respectively.     

Computational examination on monomeric,dimeric, trimeric structural and vibrational interactions,AIM, Hirshfeld,IGM and oxygenated solvent effect on optical properties for pyridine N-oxide

This work reports DFT (Density functional theory) and topological examination by means of AIM (Atom in molecule) theory, Laplacian electron density (ED), Electron –Localization function (ELF) and Hirshfeld surface were executed monomer, dimer and trimer structure of PNO molecule. These structures were optimized and Structural parameters like bond – length and Angles are compared by using B3LYP/6-311G++(d,p) basis set. Computed vibrational – frequencies and corresponding PED (Potential energy – Distribution) were also compared. Polarizability, Dipole moment and the electronic properties were calculated for all three cases of PNO molecule. Hirshfeld surface investigation has been executed to achieve the C–H?O/N–O?H type of hydrogen -bond intermolecular interactions. Moreover, Reactive site, inter/intra interactions are calculated, the optical behaviors for monomer structure of PNO were investigate by using UV–Vis spectroscopy in oxygenated solvents.     

Evidence of wormlike micellar behavior in chromonic liquid crystals: rheological, X-ray, and dielectric studies

We report rheological, X-ray, and dielectric investigations on a chromonic liquid-crystalline system formed by aqueous solutions of a food coloring agent, Sunset Yellow, in the absence and upon addition of salt. The salt-concentration dependence of the steady-state viscosity at low shear rates has a non-monotonic variation and is qualitatively similar to the behavior seen in wormlike micellar systems, a surprising result since chromonic systems are expected to be non-micellar in character. More interestingly, for a particular low concentration of the salt (20 mM), the viscosity increases by 3 orders of magnitude in comparison with that of the pure chromonic material. The dynamic (oscillatory) rheological data bring out features which can be described in terms of a microstructure formation. X-ray and dielectric studies show that certain characters of the aggregates formed by the Sunset Yellow molecules are not altered by the addition of salt.     

Polarizations of J/psi and psi(2S) mesons produced in pp collisions at square root s = 1.96 TeV

We have measured the polarizations of J/psi and psi(2S) mesons as functions of their transverse momentum p(T) when they are produced promptly in the rapidity range |y| < 0.6 with p(T) > or =5 GeV/c. The analysis is performed using a data sample with an integrated luminosity of about 800 pb(-1) collected by the CDF II detector. For both vector mesons, we find that the polarizations become increasingly longitudinal as p(T) increases from 5 to 30 GeV/c. These results are compared to the predictions of nonrelativistic quantum chromodynamics and other contemporary models. The effective polarizations of J/psi and psi(2S) mesons from B-hadron decays are also reported.     

Search for V+A current in top-quark decays in pp collisions at sqrts=1.96 TeV

We report an upper limit on the fraction of V+A current, fV+A, in top-quark decays, using approximately 700 pb-1 of pp[over ] collisions at sqrts=1.96 TeV acquired by the upgraded Collider Detector at Fermilab. For the decay t-->Wb-->lnub (where l=e or micro), the invariant mass of the charged lepton and the bottom quark jet is sensitive to the polarization of the W boson. We determine fV+A=-0.06+/-0.25 given a top-quark mass of 175 GeV/c2. We set an upper limit on fV+A of 0.29 at the 95% confidence level, an improvement by a factor of 2 on the previous best direct limit.     

Cryopreservation of in vitro grown shoots of ginger (Zingiber officinale Rosc.)

An efficient cryopreservation technique for in vitro grown shoots of ginger (Zingiber officinale Rosc) was developed based on encapsulation dehydration, encapsulation vitrification and vitrification procedures. Pregrowth and serial preculture were needed to obtain the best regrowth for all techniques. The vitrification procedure resulted in higher regrowth (80%) when compared to encapsulation vitrification (66%) and encapsulation dehydration (41%). In the vitrification procedure shoots were: precultured in liquid Murashige-Skoog medium containing 0.3 M sucrose for 3 days; cryoprotected with a mixture of 5% DMSO and 5% glycerol for 20 min at room temperature; osmoprotected with a mixture of 2 M glycerol and 0.4 m sucrose for 20 min at 25 degrees C; before being dehydrated with a highly concentrated vitrification solution (PVS2) for 40 min at 25 degrees C. The dehydrated shoots were transferred to 2 ml cryotubes, suspended in 1 ml PVS2 and plunged directly into liquid nitrogen. In all the three cryopreservation procedures tested, shoots grew from cryopreserved shoot tips without intermediary callus formation. The genetic stability of cryopreserved ginger shoot buds were confirmed using ISSR and RAPD profiling.     

Characterization of a slippage stopper for the 1,2-bis(pyridinium)ethane-[24]crown-8 ether [2]pseudorotaxane motif

Comparison of 1,2-bis(pyridinium)ethane axles containing iso-nicotinate esters (R=ethyl, iso-propyl, cyclohexyl, cycloheptyl) as the pyridinium unit shows that the cyclohexyl group provides a stopper size that allows slippage to be used as a method for pseudorotaxane/rotaxane formation employing dibenzo-24-crown-8 ether (DB24C8) as the wheel. Rates of complexation and decomplexation were measured in a number of solvent systems and the kinetic and thermodynamic parameters associated with the process reported.     

A rapid synthesis of quinoxalines starting from ketones

A fast and general synthesis of quinoxalines, performed in two stages or as a one-pot reaction, starting from ketones via their α-hydroxylimino ketone derivatives, and condensation of the latter with 1,2-diaminobenzene under microwave irradiation, is described.