Simultaneous determination of N-butylscopolamine and oxazepam in pharmaceutical formulations by first-order digital derivative spectrophotometry

A simple method has been developed for the simultaneous determination of N-butylscopolamine bromide and oxazepam in pharmaceutical formulations using first-order digital derivative spectrophotometry. Acetonitrile was selected as the solvent in which both compounds showed well-defined bands. Both analytes showed good stability in this solvent when solutions of the analytes were exposed to light and temperatures between 20 degrees and 80 degrees C. The simultaneous determination of both drugs was performed by the zero-crossing method at 226.0 and 257.0 nm for N-butylscopolamine and oxazepam, respectively. The linear range of determination was found to be 2.5 x 10(-7) to 8.0 x 10(-5) mol/L for N-butylscopolamine and 7.1 x 10(-8) to 8.0 x 10(-5) mol/L for oxazepam. A very good level of repeatability (relative standard deviation) of 0.2% was observed for N-butylscopolamine and oxazepam. The ingredients commonly found in pharmaceutical formulations do not interfere. The proposed method was applied to the determination of these drugs in pharmaceutical formulations (capsules).     

Spectrophotometric and derivative spectrophotometric determination of iron by extraction of the iron(II)-TPYZ-picrate ion-association complex

A solvent extraction-spectrophotometric determination of microamounts of iron has been developed, based on the formation of an ion-association complex of iron(II) with 2,4,6-tris(2'-pyridyl)-1,3,5-triazine as primary ligand and picrate as counter-ion, which is extracted into 1,2-dichloroethane. The complex is formed at pH 4.0-7.0 and the iron concentration can be determined by measuring the absorbance directly in the organic phase. The apparent molar absorptivity is 2.2 x 10(5) l.mole(-1).cm(-1). As the method is practically free from interferences it was applied to the determination of iron in different biological and inorganic samples. Although the proposed method is very sensitive it can be further sensitized by employing the derivative spectrophotometric technique.     

Nonequilibrium phase transitions induced by multiplicative noise: effects of self-correlation

A recently introduced lattice model, describing an extended system which exhibits a reentrant (symmetry-breaking, second-order) noise-induced nonequilibrium phase transition, is studied under the assumption that the multiplicative noise leading to the transition is colored. Within an effective Markovian approximation and a mean-field scheme it is found that when the self-correlation time tau of the noise is different from zero, the transition is also reentrant with respect to the spatial coupling D. In other words, at variance with what one expects for equilibrium phase transitions, a large enough value of D favors disorder. Moreover, except for a small region in the parameter subspace determined by the noise intensity sigma and D, an increase in tau usually prevents the formation of an ordered state. These effects are supported by numerical simulations.     

The phase diagram of the Flory-Huggins-de Gennes model of a binary polymer blend

We undertake a numerical study of the Flory-Huggins-de Gennes functional ind=3 dimensions describing a polymer blend. By discretising the functional on a three-dimensional lattice and employing the hybrid Monte Carlo simulation algorithm, we investigate to what extent the inclusion of the term describing fluctuations in local polymer concentration alters the phase diagram of the model. We find that, despite the relatively small weight of the fluctuation term, the coexistence curve is shifted by an appreciable amount from that predicted by naive mean-field theory, which ignores such spatial fluctuations. The direction of the shift is consistent with that already observed in experiment and in simulations of microscopic models of polymer blends. A finite-size scaling analysis indicates that the critical behavior of the model seems to belong to the 3D Ising universality class rather than being mean-field in nature.It is a pleasure to dedicate this paper to Oliver Penrose on the occasion of his 65th birthday.