Stress Degradation Behavior of Entacapone and Development of LC Stability-Indicating Related Substances and Assay Method

A new, sensitive, stability indicating gradient RP-LC related substances and assay method has been developed for the quantitative determination of entacapone in bulk drugs. Efficient chromatographic separation was achieved on a C18 stationary phase with simple mobile phase combination of buffer and acetonitrile. Buffer consisted of 0.1% orthophosphoric acid, delivered in a gradient mode and quantitation was carried out using ultraviolet detection at 220 nm with a flow rate of 1.5 mL min^?1. In the developed LC method the resolution (R _s ) between entacapone and its three potential process impurities were found to be >2.0. Regression analysis showed an r ² value (correlation coefficient) >0.99 for entacapone and its three potential impurities. This method was capable to detect all three process impurities of entacapone at a level of 0.003% with respect to test concentration of 0.5 mg mL^?1 for a 20 μL injection volume. The inter- and intra-day precision values for all three impurities and for entacapone was found to be within 2.0% RSD. The method has shown good and consistent recoveries for entacapone in bulk drugs (99.2–101.5%) and its three impurities (99.5–102.2%). The test solution was found to be stable in diluent for 48 h. The drug substances were subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. Considerable degradation was found to occur in acid stress, base stress and oxidative conditions. The stressed test solutions were assayed against the qualified working standard of entacapone and the mass balance in each case was close to 99.7% indicating that the developed method was stability-indicating. The developed RP-LC method was validated with respect to linearity, accuracy, precision and robustness.     

Energy transfer between Er3+:Sm3+codoped TeO2-Li2O glass

The energy transfer in Er3+: Sm3+ codoped binary TeO2-Li2O (TLO) glass has been studied using 532 nm laser radiation on the basis of fluorescence intensity and the lifetime measurements. It is observed that the trace of erbium ion can be utilized to sensitize the samarium. The mechanism involved in the present case is found to be dipole-dipole. The energy transfer efficiencies, probabilities of energy transfer and the average donor acceptor distance has been evaluated.     

o-hydroxylmethylphenylchalcogens: synthesis, intramolecular nonbonded chalcogen...OH interactions, and glutathione peroxidase-like activity

[Structure: see text]. The synthesis and characterization of a series of organochalcogen (Se, Te) compounds derived from benzyl alcohol 13 are described. The synthesis of the key precursor dichalcogenides 15, 22, and 29 was achieved by the ortho-lithiation route. Selenide 18 was obtained by the reaction of the dilithiated derivative 14 with Se(dtc)2. Oxidation of 15 and 22 with H2O2 afforded the corresponding cyclic ester derivatives 17 and 24, respectively. Oxidation of selenide 18 with H2O2 affords the spirocyclic compound 19. The presence of intramolecular interactions in dichalcogenides 15 and 22 has been proven by single-crystal X-ray studies. The cyclic compounds 17 and 19 have also been characterized by single-crystal X-ray studies. GP(X)-like antioxidant activity of selenium compounds has been evaluated by the coupled bioassay method. Density functional theory calculations at the mPW1PW91 level on ditelluride 22 have identified a fairly strong nonbonding interaction between the hydroxy oxygen and tellurium atom. The second-order perturbation energy obtained through NBO analysis conveys the involvement of n(O) --> sigma(Te-Te) orbital overlap in nonbonding interaction. Post wave function analysis with the Atoms in Molecules (AIM) method identified distinct bond critical point in 15 and 22 and also indicated that the nonbonding interaction is predominantly covalent. Comparison between diselenide 15 and ditelluride 22 using the extent of orbital interaction as well as the value of electron density at the bond critical points unequivocally established that a ditelluride could be a better acceptor in nonbonding interaction, when the hydroxy group acts as the donor.     

On experiments in harmonically excited cantilever plates with 1:2 internal resonance

Nonlinear Dynamics - This work presents some experimental results for resonant nonlinear response of hyperelastic plates for 1:2 internal resonance. Previously developed topology optimization...     

Intraspecific competition of predator for prey with variable rates in protected areas

Nonlinear Dynamics - In this present study, we systematically explore the periodicity (almost periodic nature) of a dynamical system in time-varying environment, which portrays a special case of...     

Using filament stretching rheometry to predict strand formation and “processability” in adhesives and other non-Newtonian fluids

The spinning of polymeric fibers, the processing of numerous foodstuffs and the peel and tack characteristics of adhesives are all associated with the formation, stability and, ultimately, the longevity of thin fluid `strands'. This tendency to form strands is usually described in terms of the tackiness of the fluid or by heuristic concepts such as `stringiness' (Lakrout et al. J Adhesion 1999). The dynamics of such processes are complicated due to spatially and temporally non-homogeneous growth of extensional stresses, the action of capillary forces and the evaporation of volatile solvents. We describe the development and application of a simple instrument referred to as a microfilament rheometer (MFR) that can be used to readily differentiate between the dynamical response of different pressure-sensitive adhesive fluid formulations. The device relies on a quantitative observation of the rate of extensional thinning or `necking' of a thin viscous or viscoelastic fluid filament in which the solvent is free to evaporate across the free surface. This high-resolution measurement of the radial profile provides a direct indication of the ultimate time to break up of the fluid filament. This critical time is a sensitive function of the rheological properties of the fluid and the mass transfer characteristics of the solvent, and can be conveniently reported in terms of a new dimensionless quantity we refer to as a processability parameter P. We demonstrate the usefulness of this technique by presenting our results in the form of a case study in which we measure the visco-elasto-capillary thinning of slender liquid filaments for a number of different commercial polymer/solvent formulations and relate this to the reported processing performance of the materials. We also compare the MFR observations with the prediction of a simple 1D theory derived from the governing equations that model the capillary thinning of an adhesive filament. Received: 22 December 1999/Accepted: 4 January 2000     

Velocity-dependent inertial induction and secular retardation of the earth’s rotation

According to the model of inertial induction proposed earlier, the inertia force consists of an acceleration-dependent term which comes out as identically equal to -ma. Besides, there is a velocity-dependent term which is exceedingly small to be easily detected. However, it has been shown that this results in a cosmological red shift of light coming from distant stars and galaxies; the magnitude of the red shift agrees very well with the observed values. Though this model yields correct results when applied to photons it needs modification before applying to other bodies. A modified form of the inertial induction model is now proposed where the proposed velocity-dependent inertia forces, when applied to the solar system, yields correct order of magnitude for the secular retardation of the earth’s rotation. Moreover, a combined model using the velocity term and the tidal friction also does not suggest any close proximity of the moon to the earth in the past. When the model is applied to the case of Phobos, a secular acceleration of the order of magnitude of 10⁻³ deg yr⁻² is obtained.     

The structure of some classes of <Emphasis Type="Italic">K</Emphasis>-contact manifolds

We study projective curvature tensor in K-contact and Sasakian manifolds. We prove that (1) if a K-contact manifold is quasi projectively flat then it is Einstein and (2) a K-contact manifold is ξ-projectively flat if and only if it is Einstein Sasakian. Necessary and sufficient conditions for a K-contact manifold to be quasi projectively flat and φ-projectively flat are obtained. We also prove that for a (2n + 1)-dimensional Sasakian manifold the conditions of being quasi projectively flat, φ-projectively flat and locally isometric to the unit sphere S ²ⁿ⁺¹ (1) are equivalent. Finally, we prove that a compact φ-projectively flat K-contact manifold with regular contact vector field is a principal S ¹-bundle over an almost Kaehler space of constant holomorphic sectional curvature 4.     

Upconversion in Er3+-doped Bi2O3-Li2O-BaO-PbO tertiary glass

Radiative properties of Er3+-doped tertiary bismuth glass has been analyzed by the Judd-Ofelt theory. NIR to visible upconversion in the Er3+-doped glass has been reported. The mechanism for the upconversion is explained on the basis of quadratic dependence on excitation power and on the energy-matching scheme. Energy transfer is noted as the dominant process including the long-lived 4I11/2 level as the intermediate state for the green and red upconversion emissions. The effect of temperature on the fluorescence intensity of the two bands due to 2H11/2-->4I15/2 and 4S3/2-->4I15/2 transitions as well as on the transitions due to Stark components of the 4S3/2 level have been monitored and it is concluded that their intensity ratio may serve as better temperature sensing device.