Evaluation of the stability of polyamines in human serum at different storage temperatures using capillary electrophoresis with indirect ultraviolet detection.

Polyamines are low molecular weight compounds that are present in all living organisms. They are related to the pathological processes, and have been studied as biomarkers for tumor progression, being analyzed in patients' biological fluids. However, polyamines can undergo degradation in serum samples, depending on storage conditions, which impairs their quantification in these matrices. In this work, capillary electrophoresis using indirect ultraviolet detection has been developed and applied to evaluate the stability of polyamines [cadaverine (Cad), putrescine (Put), spermine (Spm), and spermidine (Spd)] in human serum at different storage temperatures. By using this method, Cad, Put, Spm, and Spd were separated in less than 4 min. The range of the correlation coefficients was 0.993-0.998. The corresponding limits of detection and quantification were as follows (in mg L-1 ): Spm: 0.209 and 0.697; Spd: 0.165 and 0.549; Put: 0.189 and 0.632; Cad: 0.125 and 0.417. Besides, the coefficient of variation was lower than 1% for all analytes and the recovery was 92%-110%. The method was successfully applied for polyamines spiked in human serum samples from healthy people. The results showed that the degradation of polyamines was lower in samples stored in a freezer (-20°C).

Experimental mixture design as a tool to evaluate coumarin (1,2-benzopyrone) extraction from Dipteryx odorata seeds.

Experimental mixture design was drawn to evaluated the effects of the interactions between water, methanol and ethyl acetate mixtures on the extraction efficiency of coumarin (1,2-benzopyrone) from Dipteryx odorata seeds. Solvents were defined considering those preferred as green solvents for natural products extraction. Ultrasonic-assisted extraction method developed was simple, fast, low cost and highly selective. Analyses were performed by reversed-phase liquid chromatography using acetonitrile/water (40:60 v/v) as mobile phase, a C18 column, and a diode-array detector at 274 nm. Results were evaluated in linear, quadratic, special cubic, and full cubic models. The Full cubic model showed the best extraction results with a total error of 3.67%. The optimal extraction point was obtained using 15% water, 20% methanol, and 65% ethyl acetate (v/v). Based on the Guide for the Expression of Uncertainty in Measurements and Monte Carlo simulations, the uncertainty expression presented deviations of 1.18 and 1.64, respectively, showing the reliability of the analytical method. D. odorata seeds are popularly used in the pharmaceutical, food, and cosmetic applications due to high content of coumarins. However, the yield of coumarins extraction depends on the proper choice of the extraction method and solvents. The ternary mixture was optimized and resulted in 3.82% coumarin (weight/seed), which, compared to literature, showed a good increase over that obtained using common solvents, without considering the mathematical modeling.

Photoelectrocatalytic degradation of 17α-ethinylestradiol and estrone under UV and visible light using nanotubular oxide arrays grown on Ti-0.5wt%W.

Environmental concern with emerging contaminants has increased in recent years, especially with regard to endocrine-disrupting compounds (EDCs), among them hormones. Conventional water treatment processes have been shown to be ineffective in removing these compounds from water and sewage, while heterogeneous photocatalysis has been demonstrated to be a promising technique. However, the catalytic efficiency is strongly related to the choice of the photocatalyst material. In order to obtain a fast and efficient degradation of these endocrine disruptors, nanotubes grown on Ti-0.5wt%W alloy (NT/Ti-0.5W) were used in photocatalytic (PC) and photoelectrocatalytic (PEC) processes for the degradation of estrone (E1) and 17α-ethinylestradiol (EE2) under irradiation with ultraviolet (UV) and visible light. The NT/Ti-0.5W catalysts were synthesized by an anodization process, followed by thermal treatment at 450 °C. Raman, X-ray diffraction and diffuse reflectance spectroscopic analyses indicated that the tungsten doping process had modified the nanotubular TiO2. The doped samples exhibited superior photoactivity compared to un-doped samples and other semiconductors under UV and visible irradiation due to a reduction in the rate of recombination of photogenerated charges and the displacement of the flat-band potential to more negative values. Higher values of the degradation rate constant were found for both hormones in the PEC process using NT/Ti-0.5W under UV radiation; the percentage removals of EE2 and E1 were 66% and 53.4%, respectively, after only 2 min of treatment. With visible light, 1.8 min and 4.6 h were required for the removal of 50% of E1 and EE2, respectively. The degradation of E1 could be fit with a zero-order kinetic model, while a first-order kinetic model was required for EE2 degradation. Degradation routes were suggested for E1 and EE2. The results demonstrate that the combined use of NT/Ti-0.5W and the PEC process provides excellent performance for the degradation of emerging contaminants in wastewater when compared to a NT/TiO2 electrode.

Optimization of chemometric approaches for the extraction of isorhamnetin-3-O-rutinoside from Calendula officinalis L.

The application of Design of Experiments (DoE) to the determination of optimum conditions for an extraction process relies on the correct selection of mathematical models. The linear model is the one typically used; however, in some cases it does not always have superior performance, ignoring the real nature of the data and its appropriate descriptive model. In order to evaluate the extraction efficiency of isorhamnetin-3-O-rutinoside from flowers of Calendula officinalis L. a multivariate factorial analysis was used. Simulations were conducted using linear, quadratic, full cubic and special cubic models. A Simplex-Centroid design was chosen as it delivered greater precision with only minor errors versus other models tested. Analyses were performed by capillary zone electrophoresis using sodium tetraborate buffer (40mmolL(-1), pH 9.4) containing 10% methanol. The detection was linear over a range of 8.0-50.0mgL(-1) (r(2)=0.996), and the limits of detection (LOD) and quantification (LOQ) for isorhamnetin-3-O-rutinoside were 3.44mgL(-1) and 11.47mgL(-1), respectively. The full cubic model showed the best extraction results, with an error of 3.40% compared to analysis of variance, and a determination coefficient of 0.974. The difference between the responses at the reference point, calculated by the model, and the experimental response, varies around 2.72% for full cubic model. Comparison of the four models showed the full cubic model was the most appropriate one, allowing greater efficiency in the extraction of isorhamnetin-3-O-rutinoside. Selection of the model made it possible to obtain a 60% increase in sensitivity compared to the linear model.