Spectrophotometric determination of ceterizine hydrochloride with Alizarin Red S

A simple, rapid and sensitive spectrophotometric method has been developed for the assay of ceterizine hydrochloride (CTZH) in bulk drug and its pharmaceutical preparations. This method is based on the ion-pair complex reaction between CTZH and Alizarin Red S in Clarks-Lubs buffer. The chromogen being extractable with chloroform, could be measured quantitatively at 440 nm. All variables were studied to optimise the reaction conditions. Regression analysis of Beer's Law plot showed good correlation in the concentration range 2.5-22 microg ml(-1). The method has a detection limit of 0.1328 microg ml(-1). The proposed method has been successfully applied for the analysis of the bulk drug and its dosage forms such as tablets and syrups. No interference was observed from common pharmaceutical adjuvants.     

The onset of double diffusive convection in a viscoelastic fluid layer

The onset of double diffusive convection in a viscoelastic fluid layer is studied using a linear and a weak nonlinear stability analyses. The onset criterion for stationary, oscillatory and finite amplitude convection is derived analytically. There is a competition between the processes of thermal diffusion, solute diffusion and viscoelasticity that causes the convection to set in through oscillatory mode rather than stationary. The effect of Deborah number, retardation parameter, solutal Rayleigh number, Prandtl number, Lewis number on the stability of the system is investigated. It is shown that the critical frequency increases with Deborah number and solutal Rayleigh number while it decreases with retardation parameter and Lewis number. The nonlinear theory based on the truncated representation of Fourier series method is used to find the heat and mass transfers. The transient behaviour of the Nusselt number and Sherwood number is investigated by solving the finite amplitude equations using Runge-Kutta method. The effect of viscoelastic parameters on heat and mass transfer is brought out.     

Simultaneous determination of fluoxetine and its major active metabolite norfluoxetine in human plasma by LC‐MS/MS using supported liquid extraction

A rapid, sensitive and selective bioanalytical method was developed for the simultaneous determination of fluoxetine and its primary metabolite norfluoxetine in human plasma. Sample preparation was based on supported liquid extraction (SLE) using methyl tert‐butyl ether to extract the analytes from human plasma. Chromatography was performed on a Synergi 4 μ polar‐RP column using a fast gradient. The ionization was optimized using ESI (+) and selectivity was achieved by tandem mass spectrometric analysis using MRM functions, m/z 310 → 44 for fluoxetine, m/z 296 → 134 for norfluoxetine and m/z 315 → 44 for fluoxetine‐d₅ (internal standard). The method is linear over the range of 0.05–20 ng/mL (using a human plasma sample volume of 0.1 mL) with a coefficient determination of greater than 0.999. The method is accurate and precise with intra‐batch and inter‐batch accuracy (%bias) of <±15% and precision (%CV) of <15% for both analytes. A run time of 4 min means a high throughput of samples can be achieved. To our knowledge, this method appears to be the most sensitive one reported so far for the quantitation of fluoxetine and norfluoxetine and can be used for routine therapeutic drug monitoring or pharmacokinetic studies. Copyright © 2011 John Wiley & Sons, Ltd.     

Classical and quantum q-deformed physical systems

On the basis of non-commutative q-calculus, we investigate a q-deformation of the classical Poisson bracket in order to formulate a generalized q-deformed dynamics in the classical regime. The obtained q-deformed Poisson bracket appears invariant under the action of the q-symplectic group of transformations. Within this framework we introduce the q-deformed Hamilton equations and we derive the evolution equation for some simple q-deformed mechanical systems governed by a scalar potential dependent only on the coordinate variable. It appears that the q-deformed Hamiltonian, which is the generator of the equation of motion, is generally not conserved in time but, in correspondence, a new constant of motion is generated. Finally, by following the standard canonical quantization rule, we compare the well-known q-deformed Heisenberg algebra with the algebra generated by the q-deformed Poisson bracket. PACS 02.45.Gh, 45.20.-d, 03.65.-w, 02.20.Uw     

Zn(OTf)2 catalyzed addition-cyclization reaction of allenylphosphine oxides with propargyl alcohol-unexpected formation of 2,5-dimethylenetetrahydrofurans and 2-substituted furans

A novel synthesis of 2,5-dimethylenetetrahydrofurans, 2-substituted furans and a β,ω-diketophosphonate in good to excellent yields has been achieved by the reaction of allenylphosphine oxides/allenylphosphonate with propargyl alcohol using zinc triflate/triethylamine combination.     

Efficient passivation of SnO2 nano crystallites by Indoline D-149 via dual chelation

For the first time in SnO₂ based dye solar cells, here we report, efficiency exceeding 3% of the cells consisting with Indoline D-149 dye with unmodified SnO₂ nano-crystallites. The cells sensitized with metal free D-149 dye together with liquid electrolyte comprising with 0.5 M tetrapropyl ammonium iodide and 0.05 M iodine in a mixture of acetonitrile and ethylene carbonate (1:4 by volume) delivered a short circuit current density of 10.4 mA cm^?2 with an open circuit voltage of 530 mV under the illumination of 100 mW cm^?2 (AM1.5) having an efficiency of 3.1%. As evident from the FTIR measurement, strong surface passivation of recombination centers of SnO₂ crystallites due to the dual mode of attachment of dye molecules to the surface of SnO₂ via both COOH and S–O direct bond might be the possible reason for this enhancement in these SnO₂ based cells.     

Iminium ion cascade reaction in the total synthesis of (+)-vincadifformine

An iminium ion triggered cascade reaction is described in the total synthesis of (+)-vincadifformine by the coupling of 3,3-substituted tetrahydropyridine and indole derivative. The strategy allows simultaneous construction of two new rings, three new sigma bonds, and two new stereogenic centers in one pot with complete stereochemical control.     

To stay as allene or go further? Synthesis of novel phosphono-heterocycles and polycyclics via propargyl alcohols

The reaction of aryl-substituted propargyl alcohols possessing o-nitro and o-alkylidene groups with (RO)(2)PCl afford novel phosphono(tetrahydro)dibenzazepines, N-hydroxyindolinones or polycyclics (including one with three fused four-membered rings).