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The incidence of thrombotic complications in SARS-CoV-2 infections has become a global concern; thus, anticoagulants are an integral part of the treatment. Edoxaban (EDX) is an oral anticoagulant suitable for pharmacologic thromboprophylaxis. Herein, two novel analytical methods for EDX determination in tablets are developed and validated using capillary zone electrophoresis (CZE) and high-performance liquid chromatography (HPLC). Operating conditions such as the electrolyte's concentration and pH value, injection time, volume, and the capillary temperature, were optimized. The methods were successfully validated by establishing the linearity, intra- and inter-day precisions (relative standard deviation [%]), accuracy, and robustness. Adequate separation of excipients and degradation products of EDX generated by stress degradation conditions demonstrated the stability-indicating capability of the methods. The analytical procedures were linear in the range of 25-125 µg/ml (r 0.999), with the limits of detection and quantification of 3.26 and 10.87 µg/ml for CZE and 0.740 and 2.78 µg/ml for HPLC. Although both methodologies are suitable for determining EDX in tablets, CZE provides a greener alternative due to low-cost analysis using less organic solvents and minimizing waste generation.

A simple one-step electrodeposition without template allowed the synthesis of gold microstructures on a screen-printed carbon electrode. Chloroauric ions were reduced by applying a constant potential of − 0.6 V during 600 s. A preferential growth along the directions produced leaf-like structures as confirmed by scanning electron microscopy and X-ray diffraction. The as-prepared Au microstructures worked as a support for tyrosinase immobilization allowing the preparation of a highly selective and sensitive biosensor for bisphenol A (BPA) detection. The cyclic voltammograms exhibit a well-defined anodic peak at 0.24 V in phosphate buffer solution (0.1 mol L−1, pH 7.0). The enzyme creates favorable conditions for the adsorption of BPA, and after 10 min of accumulation time, the calibration curve was linear in the range of 0.5–50 μmol L−1 with a detection limit of 77 nmol L−1 (S/N = 3) and a relative standard deviation (RSD%) of 0.54% (n = 10). Furthermore, the proposed biosensor displayed long-term stability and was successfully applied to determine BPA in spiked water samples.

Euphorbia tirucalli (L.), commonly known as aveloz, has been indiscriminately used in popular medicine to treat various illnesses. However, some components can have devastating consequences. Injury to a cell's genetic material can cause mutations, cancer, and cell death. Our main goal in this work was to evaluate the genotoxic and cytotoxic effects of E. tirucalli extract on human leukocytes. For this purpose, we performed a phytochemical analysis to evaluate the plant's components. In the second step, we treated cultured human leukocytes with different concentrations of the dry extract of the plant and then evaluated the oxidative and genotoxic profiles of these leukocytes. We found that at 1% and 10% concentrations, the aveloz extract acted as a genotoxic agent that could damage DNA and increase oxidative damage. We conclude that despite its popular use, aveloz can act as a genotoxic agent, especially when it contains phorbol ester. Aveloz's indiscriminate use might actually promote tumors and therefore carry a considerable genetic risk for its users. RESUMO Euphorbia tirucalli (L.), comumente conhecida como aveloz, tem sido indiscriminadamente usada na medicina popular para o tratamento de várias doenças. Entretanto, alguns componentes podem ter consequências devastadoras. A lesão do material genético da célula pode causar mutações, câncer e morte celular. Nosso principal objetivo neste trabalho foi avaliar os efeitos genotóxicos e citotóxicos do extrato de E. tirucalli em leucócitos humanos. Para este propósito, realizamos uma análise fitoquímica dos componentes da planta. Em uma segunda etapa, culturas de leucócitos humanos foram tratados com diferentes concentrações do extrato seco da planta e então avaliamos os perfis oxidativos e genotóxicos nestes leucócitos. Nossos resultados mostraram que nas concentrações de 1% e 10%, o extrato de aveloz atua como agente genotóxico, o qual pode danificar o DNA e aumentar a dano oxidativo. Concluímos que, apesar do uso popular, a aveloz pode atuar como agente genotóxico, especialmente por conter o éster de forbol. O uso indiscriminado da aveloz pode na verdade promover tumores e, portanto, carrega um risco genético considerável para seus usuários.

Flaxseed (Linum usitatissimum L.) is composed mainly of bioactive components such as polyphenols, polyunsaturated fatty acids, fiber and lignans. Flaxseed can be found in different presentation forms (grain or flour) and varieties (brown or golden); however, questions have arisen as to whether the presentation form and/or variety may influence the health effects. The objective of this study was to evaluate the effects on blood pressure, anthropometric and oxidative parameters in healthy human volunteers. All subjects received 40 gram aliquots of flaxseed and were instructed to consume them in their entirety mixed with water in the morning for a period of 14 days. Oxidative parameters showed significant reductions (p < 0.05) in oxidative damage to lipids and proteins via dietary intervention with golden flaxseed grains. There were no significant differences in anthropometric parameters, blood pressure, DNA damage and micronuclei frequency after 14-day supplementation. This research indicates that golden flaxseed grains can be a valuable adjunct for disease prevention and protecting the organism against oxidative damage.