Stability indicating method for famotidine in pharmaceuticals using porous graphitic carbon column

A simple, sensitive and rapid HPLC method was developed and validated for the simultaneous determination of famotidine (FMT) and related impurities in pharmaceuticals. Chromatographic separation was accomplished within 10 min on a porous graphitic carbon (PGC) column using 50:50 v/v ACN-water containing 0.5% pentane sulphonic acid (PSA) as the mobile phase. Separation was achieved with a flow rate of 1 mL/min and a detection wavelength of 265 nm. The calibration curves were linear over a concentration range of 1.5-100 microg/mL. The intra- and interday RSDs (n = 5) for the retention times and peak area were all less than 2%. The method was sensitive with an LOD (S/N = 3) of 0.1 microg/mL for FMT, imp. C and 0.05 microg/mL for imp. 2, A and D. All recoveries were greater than 98%. The method was demonstrated to be precise, accurate and specific with no interference from the tablet ingredients and separation of the drug peak from the peaks of the degradation products (oxidative degradation and acid and base degradation). The results indicated that the proposed method could be used for the determination of FMT in commercial dosage forms and as a stability-indicating assay.     

Differential inequalities for Riesz means and Weyl-type bounds for eigenvalues

We derive differential inequalities and difference inequalities for Riesz means of eigenvalues of the Dirichlet Laplacian,

     

Alkynyl ruthenium colorimetric sensors: optimizing the selectivity toward fluoride anion

We report on the synthesis of alkynyl ruthenium colorimetric sensors whose receptors are constituted by thiazolidinedione, rhodanine, or barbituric heads as recognition centers for anions. As modifications in the charge density at these recognition centers affect the whole molecule, through the alkynyl ligand acting as a communicating wire, the effects of hydrogen-bonding interactions with the anions were observed with the naked eye and monitored by UV-vis absorption spectrometry. The selectivity of the sensors was improved through electronic modifications of the alkynyl ruthenium subunit: the higher the electron density at the receptor head, the higher the selectivity is. TD-DFT calculations rationalize the long-range electronic communication as a main characteristic of the alkynyl ruthenium species and as a key to improve the selectivity of alkynyl ruthenium-based sensors toward anions.     

Time-Domain Quantification of Multiple-Quantum-Filtered Na Signal Using Continuous Wavelet Transform Analysis

The application of continuous wavelet transform (CWT) analysis technique is presented to analyze multiple-quantum-filtered (MQF) ²³Na magnetic resonance spectroscopy (MRS) data. CWT acts on the free-induction-decay (FID) signal as a time-frequency variable filter. The signal-to-noise ratio (SNR) and frequency resolution of the output filter are locally increased. As a result, MQF equilibrium longitudinal magnetization and the apparent fast and slow transverse relaxation times are accurately estimated. A developed iterative algorithm based on frequency signal detection and components extraction, already proposed, was used to estimate the values of the signal parameters by analyzing simulated time-domain MQF signals and data from an agarose gel. The results obtained were compared to those obtained by measurement of signal height in frequency domain as a function of MQF preparation time and those obtained by a simple time-domain curve fitting. The comparison indicates that the CWT approach provides better results than the other tested methods that are generally used for MQF ²³Na MRS data analysis, especially when the SNR is low. The mean error on the estimated values of the amplitude signal and the apparent fast and slow transverse relaxation times for the simulated data were 2.19, 6.63, and 16.17% for CWT, signal height in frequency domain, and time-domain curve fitting methods, respectively. Another major advantage of the proposed technique is that it allows quantification of MQF ²³Na signal from a single FID and, thus, reduces the experiment time dramatically.     

Optimal Shape Design for Metal Forming Problems by the Finite Element Method

In this work, a method for calculation of the optimal shapes of axisymmetrical converging dies by the finite element method is presented. The shape optimization problem considered in this paper is to find the best shape of the die such that the flow rate will be uniform at the die exit.The optimization problem is to minimize an objective function by varying a part of boundary (ie: the shape of die) subject to constraints imposed by the metal forming problem. In this method, the B-spline functions allow us to determine the shape of the die, using its control points as design variables. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Effect of Host Medium on the Fluorescence Emission Intensity of Rhodamine B in Liquid and Solid Phase

In this work, we study the effect of concentration, host medium, PH and phase states on the fluorescence emission from the laser dye Rhodamine B pumped by UV laser as exited source. The polymethylmethacrylate PMMA is used as a host medium in case of solid phase samples while, ethanol and Tetrahydrofuran (THF) are used in case of a liquid one. Laser Induced Fluorescence (LIF) technique was used to study the fluorescence properties of both cases of liquid and thin film solid-state samples. In addition, the Dual Thermal Lens (DTL) technique was used to study the quantum yield of these samples. The concentrations of Rhodamine B in ethanol as solvent between 2 × 10⁻² M and 5 × 10⁻⁶ M were studied. The maximum fluorescence emission is observed at concentration of Rhodamine B C = 3 × 10⁻⁴ M. Comparison studies were investigated for different host medium such as ethanol, THF, PMMA in liquid phase state and PMMA in solid phase state. The measurements revealed that, the behavior of both phases state was analogous. Rhodamine B/PMMA thin film sample by ratio of 4:1 and thickness 0.12 mm was found to have the best photostability sample with a quantum yield about ≈0.82.     

Raman study of LiTaO3-related non-stoichiometric solid solutions isolated inside the ternary systems Li2O–Ta2O5–(M′O)2 with M′=Mn,Co

We have characterized by Raman spectroscopy the disorder and the local modifications of cation environment in the lithium tantalate structure resulting from the incorporation of bivalent cations Co²⁺ and Mn²⁺ as potential substitutes for Li and/or Ta ions. Frequency and damping of the E(TO1), E(TO6) and E(TO8) phonon modes of ceramic powders are studied along seven lines in the ternary phase diagrams Li₂O–Ta₂O₅–(M′O)₂ with M′=Mn and Co, and compared to those of the pure stoichiometric LiTaO₃. Raman spectroscopy is found to be very sensitive to the substitution ions and defects generated in the lattice vibration. Dopants occupy primarily the Li site in the region of lithium oxide excess. The site of Ta becomes progressively implicated in the substitution process when the concentration of dopant increases. In the Li-poor region of the ternary-phase diagram, corresponding to under-stoichiometric compositions, we retain the charge compensation mechanism involving both Li and Ta site according to: 3Li⁺+Ta⁵⁺→4M′²⁺ with M′²⁺=Mn²⁺ or Co²⁺.