Formulation of sage essential oil (Salvia officinalis,L.) monoterpenes into chitosan hydrogels and permeation study with GC-MS analysis

This study deals with the formulation of natural drugs into hydrogels. For the first time, compounds from the sage essential oil were formulated into chitosan hydrogels. A sample preparation procedure for hydrophobic volatile analytes present in a hydrophilic water matrix along with an analytical method based on the gas chromatography coupled with the mass spectrometry (GC-MS) was developed and applied for the evaluation of the identity and quantity of essential oil components in the hydrogels and saline samples. The experimental results revealed that the chitosan hydrogels are suitable for the formulation of sage essential oil. The monoterpene release can be effectively controlled by both chitosan and caffeine concentration in the hydrogels. Permeation experiment, based on a hydrogel with the optimized composition [3.5% (w/w) sage essential oil, 2.0% (w/w) caffeine, 2.5% (w/w) chitosan and 0.1% (w/w) Tween-80] in donor compartment, saline solution in acceptor compartment, and semi-permeable cellophane membrane, demonstrated the useful permeation selectivity. Here, (according to lipophilicity) an enhanced permeation of the bicyclic monoterpenes with antiflogistic and antiseptic properties (eucalyptol, camphor and borneol) and, at the same time, suppressed permeation of toxic thujone (not exceeding its permitted applicable concentration) was observed. These properties highlight the pharmaceutical importance of the developed chitosan hydrogel formulating sage essential oil in the dermal applications.     

Characterization of Aluminum Foam Impact Response

Strength of Materials - The paper addresses the investigation of high-strain rate compressive behavior of Al foams subjected to impact at the intermediate striking velocity ranged from 40 to...     

Lignin from Annual Plants as Raw Material Source for Flavors and Basic Chemicals

The enzymatic conversion of lignins, possibly in combination with electrochemical oxidation, makes aromatics such as syringol, guaiacol, vanillin and catechol available in the qualities required by the fragrance industry. The lignins were obtained by soda digestion from wheat straw and Miscanthus, characterized and then converted with laccases. The overall yield amounted up to 9 wt % with a product spectrum confined to four substances. Catechol was the major product, with a fraction of ≈75 %. It can easily be isolated by extraction with acetone.     

Photoinduced recovery of gamma-irradiated fluoride glasses

Radiation-induced changes in the optical properties of fluoride glasses (FGs) were studied on samples of zirconium fluoride and aluminum fluoride based compositions gamma-irradiated to a total dose of 1.2 MGy. Upon exposure, the fundamental absorption edge smears and shifts toward longer wavelengths. The FGs studied exhibit self-recovery of the optical properties, whereby the radiation-induced absorption decreases in the course of storage without action of any external factors. Photostimulated recovery of the optical properties of the gamma-irradiated FGs was studied in the range of light wavelengths from 400 to 1200 nm at a light intensity of 1–3 mW/cm². The maximum rate of recovery for both zirconium and aluminum fluoride based glasses was observed for the photoannealing at 600 nm.     

Precision Spectrometric Determination of Th and Pu in Solutions with Arsenazo III Using Internal Standardization

A spectrophotometric procedure with internal standardization was suggested for precision determination of the concentrations of Th and Pu in the form of colored complexes with arsenazo III in nitric acid solutions. The sensitivity of the method was significantly improved owing to the use of colored complexes. The optical density optimum (0.3-0.5) of the solutions for spectrophotometric measurements can be achieved at concentrations in solution of the element analyzed as low as (2-3) ×10^-6 M, at the arsenazo and HNO₃ concentrations of 1 ×10^-4 and 6 M, respectively. With this composition of the solution, the relative rms deviation of the results for a single run is no greater than 0.15 and 0.3% for thorium and plutonium, respectively.     

Ozonation of Two Acidic Azo Dyes with Different Substituents

The ozonation of two differently substituted azo dyes (Schwarz GRS and Orange Acid 8) in water media is studied. The influence of pH on the effectiveness of the ozonation at various initial concentrations of each dye is explored. It was found out that the rates of decolorization for amino-group substituted dyes reflect the considerable influence by the widely varying initial pH from 4.5 to 10. Specifically, the highest effect of decolorization of this dye was obtained at the highest pH studied (pH 10) for all initial concentrations of the solutions. Considering the dye without an amino-group substitute, the rates of color disappearance in ozonation reflected to a lower degree the variations of the initial pH. Pseudo-first-order trends of decolorization were observed in all the experimental runs. Regarding the kinetic results obtained, an attempt to explain the different dyes reactivity was made based on the absolute electronegativity (E_lumo + E_homo) of both dyes. The COD/BOD analysis shows that the ozonation of both azo dyes can reduce the sample COD but it could not improve the biodegradability ratio (BOD₅/COD). BOD decrease with ozonation time indicates that the intermediates of the ozonation are of lower biodegradability. Oxalic acid was found as the final product of ozonation of both dyes.