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Plant-based milk has gained considerable attention; however, its high nutritional variation highlights the need for improved formulation designs to enhance its quality. This study aimed to nutritionally compare cow milk with plant-based milk produced from hazelnuts (H), Brazil nuts (BN), cashew nuts (CN), soybeans (S), and sunflower seeds (SS), and to perform physicochemical and technological characterization. The plant-based milk produced with isolated grains showed a nutritional composition inferior to that of cow milk in almost all evaluated parameters, protein content (up to 1.1 g 100 g−1), lipids (up to 2.7 g 100 g−1), color parameters, minerals, and especially calcium (up to 62.4 mg L−1), which were originally high in cow milk (up to 1030 mg L−1). However, the plant-based milk designed using a blend composition was able to promote nutritional enhancement in terms of minerals, especially iron (Fe) and magnesium (Mg), high-quality lipids (up to 3.6 g 100 g−1), and carbohydrates (3.4 g 100 g−1 using CN, BN, and S). The protein content was 1.3% compared to 5.7 in cow milk, and the caloric value of plant-based milk remained 32.8 at 52.1 kcal, similar to cow milk. Satisfactory aspects were observed regarding the shelf life, especially related to microbiological stability during the 11 d of storage at 4 °C. For the designed plant-based milk to be equivalent to cow milk, further exploration for optimizing the blends used to achieve better combinations is required. Furthermore, analyzing possible fortification and preservation methods to increase shelf life and meet the nutritional and sensory needs of the public would be interesting. [ABSTRACT FROM AUTHOR]

A new screen-printed electrode (SPE) modified with carbon black and ternary oxide (SiO2/TiO2/Nb2O5), denominated SPE/CB/SiTiNb and was developed for the direct detection of triclosan in tap water and mouthwash samples. The morphological characterization and electrochemical behavior of the sensors were performed by scanning electron microscopy, energy dispersive spectroscopy, and cyclic voltammetry. Differential pulse voltammetry was used to evaluate the proposed sensor in Britton–Robinson buffer 0.1 mol L−1 and showed a limit detection of 1.23 nmol L−1 in a linear range from 0.025 to 57.01 µmol L−1. Studies with possible interferents were performed demonstrating a significant selectivity of the sensor to the triclosan oxidation reaction. The sensor was applied in tap water and mouthwash real sample analyses, whose recoveries ranged from 93.4 to 98.8%, demonstrating that the sensor shows promise in the detection of triclosan in different matrices allied to high sensitivity, selectivity, low-cost, portability, disposability, and low sample volume, without pre-treatment, per analysis. [ABSTRACT FROM AUTHOR]

Cobalt was included on the World Anti‐Doping Agency Prohibited List in 2015 due to its effect on stimulus of erythropoiesis via stabilization of hypoxia‐inducible factor. Although it has proven benefits for performance enhancement, the unavailability of inductively coupled plasma–mass spectrometry on routine of the accredited laboratories is a factor that reduces its applicability in anti‐doping analysis. Therefore, an analytical method for quantification of urinary cobalt as its diethyldithiocarbamate complex by liquid chromatography coupled with high‐resolution tandem mass spectrometry was developed and validated. Palladium was proposed as internal standard and rhodium as a complexation control. A microwave‐assisted acid digestion of the urine samples was essential, not only to eliminate the matrix effect but mainly to avoid the non‐specific bond of cobalt to endogenous molecules. A linear method was obtained over the studied range from a negative urine control to a spiked concentration of 25 ng/mL, with an estimated limit of quantification of 2.5 ng/mL, and an adequate combined standard uncertainty of 11.4%. Considering that all reagents are commercially available, the proposed strategy is feasible to be included on routine sample preparation. Monitoring urinary cobalt concentrations globally opens the perspective to support the anti‐doping system to define a suitable threshold value and to understand its potential misuse by athletes seeking for performance improvement. [ABSTRACT FROM AUTHOR]

Soybean meal (SBM) is a co-product of the soybean oil industry that is rich in bioactive compounds, such as isoflavones. We aimed to study the effects of processing SBM by fermentation (Saccharomyces cerevisiae) (FSBM) and enzymatic hydrolysis (CelluMax C, a commercial cellulase) (ESBM) on its chemical composition, with emphasis on isoflavones. Fermentation increased protein content by 9%, ash content by 7%, dietary fiber by 11% and minerals by up to 38%, except for iron, which decreased by 26%. Fermentation completely removed oligosaccharides from SBM, while enzymatic processing decreased oligosaccharides by 45% in SBM. Both processes converted glycosylated isoflavones into the corresponding aglycones, the content of which increased by up to 7.7-fold. Biscuits containing SBM, FSBM and ESBM could be labeled as dietary sources of dietary fibers, potassium, phosphorous, calcium and zinc, as well as high in proteins, copper, iron, manganese and magnesium. While FSBM biscuits had lower sensory scores compared to SBM biscuits, ESBM biscuits had equivalent scores. During storage for 180 days at room temperature, the isoflavone profile of all biscuits remained stable. Moreover, storage did not impair microbiological and sensory qualities of any biscuits. Altogether, ESBM biscuits show great marketing potential. [ABSTRACT FROM AUTHOR]

The study aimed to develop an electrochemical sensor based on glassy carbon, mixed oxide (SiO2/TiO2/Sb2O5), and carbon black. The material was synthesized, characterized, and used to determine thiamethoxam in raw honey and water. The morphologic structure and electrochemical performance of the sensor was characterized by scanning electron microscopy and cyclic voltammetry. Differential pulse voltammetry with a concentration of 0.1 mol L−1 of Britton-Robinson buffer at pH 7.0 allowed the generation of a method to determine thiamethoxam in a linear range of 0.25 to 100.5 μmol L−1 and with a limit of detection of 0.012 μmol L−1. The system efficiently quantified traces of thiamethoxam in raw honey and tap water samples. The modified sensor did not present interferences of K+, Na+, Ca2+, Mg2+, glyphosate, imidacloprid, and carbendazim. In addition, the device showed good recovery values for thiamethoxam when applied directly to honey and water samples without any treatment, presenting an electrochemical sensor to monitor real-time hazardous substances in environmental and food matrices. [ABSTRACT FROM AUTHOR]

Electrochemical sensors to quantify concentrations of emerging pollutants have attracted great attention from the industry and scientific community. Nanomaterials such as carbon black have been applied in sensors to identify substances that are toxic to the environment and human health due to their excellent electroanalytical properties. The aim of the study was to develop a novel electrochemical sensor for the endocrine disruptor hormone determination. To our knowledge, for the first time the synthesis of material based on carbon black containing immobilized palladium nanoparticles, with the application for the hormone ethinylestradiol, is reported in the literature. The material was synthesized, characterized, and applied to the determination in tap water and human urine of the synthetic hormone 17α‐ethinylestradiol (EE2), which is currently considered an emerging pollutant. The morphology, structure and electrochemical performance of the sensors were characterized by scanning electron microscopy (SEM) and cyclic voltammetry (CV). Differential pulse voltammetry (DPV) in sodium phosphate buffer solution at pH 5.0 allowed the generation of a method to quantify the concentration of 17α‐ethinylestradiol in a linear range of 0.5–119.0 μmol L−1, obtaining 81.0 nmol L−1 of calculated limit of detection (LOD). The system was efficient in detecting 17α‐ethinylestradiol in real urine samples and showed no interferences for ascorbic acid, uric acid, progesterone, and dopamine. It is noteworthy that the results obtained showed good recovery values, considering that the urine samples were not previously treated or pre‐concentrated, which suggests the development of an electrochemical sensor that works in situ and in real time to monitor relevant substances in the control clinical and environmental, with the possibility of point‐of‐care analyses. [ABSTRACT FROM AUTHOR]

The implementation of flow injection analysis (FIA) systems and correlated techniques in the laboratory routine provides an increase of analytical throughput and the reduction of risks of analyte losses and contamination. Naturally, it contributes to the reduction of reagent consumption and minimization of waste generation. This paper presents and discusses an overview of the main strategies adopted to make methods based on FIA systems more environmentally friendly, and offers a review of these methods that covers the period from January 2002 to December 2019. Strategies based on reagent management (adoption of procedures without reagents, replacement of toxic reagents, recycling and reuse of reagents and, use of immobilized reagents), the online waste treatment, and the improvements of FIA systems (flow system configurations that avoid reagent wastage, use of green detectors, automation, and miniaturization) are approached in this perspective. [ABSTRACT FROM AUTHOR]

Studies involving coastal sediment resuspension have shown that trace metals could be released to the water column due to changes in physical-chemical conditions. Therefore, if environmental agencies adopt screening protocols with insufficient evaluations of contaminant mobilization risks for a given area, the prediction of environmental impacts caused by dredging may be limited. This work evaluates the influence of spatial variation on the geochemical mobility of trace metals (Cd, Cu, Ni, Pb, Zn) after artificial sediment resuspension, using as study case the Iguaçu River estuary (Guanabara Bay, Brazil). The Iguaçu River drains the industrial complex of the metropolitan area of Rio de Janeiro State, besides the presence of agriculture and the input of untreated domestic wastes. Surface estuarine sediments were submitted to resuspension experiments in an open system, during 1h and 24h of agitation on local water. A clear tendency of metals' solubilization was observed after resuspension, especially considering the dissolved concentrations of Cu (average: 8.0 µg L-1) and Zn (average: 0.9 mg L-1), especially for the samples from the transects 2 and 3. However, evaluations of water quality changes due to sediment resuspension are not requested by the legislation regulating the dredging activities. In the sediments, the results suggested a higher geochemical mobility of Cu, indicated by the massive increase on the bioavailable fraction after resuspension, mainly on the transect number 3, on the river's mouth. The effects of resuspension were distinct between samples, suggesting that even in a small scale, important differences on metals' mobility are found. Thus, the combined assessment of changes in metal concentrations in water and in the metal partitioning linked to the solid-phase was demonstrated to be a promising tool for predicting the environmental risks of dredging due to changes in the bioavailability of metals. [ABSTRACT FROM AUTHOR]

This work aims to develop a method based on the tape-lift collection and Laser Ablation combined to Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS) measurements for Gunshot Residue (GSR) to be useful in forensic analysis. The most widely used method is the Scanning Electron Microscopy coupled to Energy Dispersive Spectroscopy (SEM-EDS); still, it has some disadvantages, such as long-time analysis. Thus, other analytical techniques have been used, such as LA-ICP-MS, since the GSR normally contain Pb, Ba, and Sb (together). The corresponding signals can be measured at the same ablation time, making it possible to obtain images of elemental distribution that can be overlaid to show the presence of GSR. It is well known that these elements have several commercial and industrial applications. Therefore, due to the similar composition and formation conditions, residues from other sources, such as fireworks, brake pads, airbags, and lighters can be confused with GSR, emphasizing the importance of its discrimination. To distinguish between real GSR and GSR-like residues, samples of five shooters and fifteen non-shooters were collected using a carbon adhesive tape (stub) by pressing it on the surface of the hands. Non-shooters samples were composed of brake pad mechanic's workers, people after using fireworks, and people who had never fired a gun (blanks). The images of elemental distribution were obtained using MATLAB™, resulting in a clear visual difference between the images from shooters and non-shooters samples. Ternary graphs were obtained using ORIGIN™ for each kind of sample, revealing a grouped distinctive distribution for the different GSR-like sources, demonstrating the ability of the developed method to discriminate GSR against a possible false positive. The developed method provided a discrimination between samples of shooters and non-shooters, by comparing their images of elemental distribution, without previous sample preparation and with an analysis time of 33 min. Unlabelled Image • Images of elemental distribution by LA-ICP-MS for GSR analysis. • Evidence of a notable visual difference between shooters and non-shooters samples. • Visual distinction of residues from other sources commonly confused with GSR. • Ability to discriminate GSR against a possible false positive using ternary graphs. [ABSTRACT FROM AUTHOR]

Background Understanding the chemical composition of fluorescent lamp residue, particularly potentially toxic elements, is crucial for reducing environmental impacts and human health risks after disposal. However, the challenge lies in effectively analyzing these heterogeneous solid samples. Techniques involving quantitative dissolution become imperative, playing a fundamental role in quantifying trace elements. Objective The aim of this work is to develop and present a new, faster, and more efficient and environmentally friendly method using ultrasound-assisted acid extraction to quantify potentially toxic elements (Cu, Mn, Ni, Sr, and Zn) present in fluorescent lamp waste using the inductively coupled plasma-optical emission spectrometry technique. Methods An ultrasound-assisted acid extraction method for the quantification of potentially toxic elements in fluorescent lamp waste was developed and applied as a greener alternative to conventional digestion methods. For variable optimization, a full factorial design with two levels and two variables (time and temperature) was used to determine which factors significantly affected the observed response. Results The results obtained for the developed extraction method were compared with a reference method employing a heating acid digestion (with a mixture of HCl, HClO4, and HF) using statistical tools. The best results were obtained using an extraction time of 10 min and a temperature of 25°C. Inductively coupled plasma optical emission spectrometry was applied for element quantification. Conclusion The proposed extraction method showed good results for Cu, Mn, Ni, Sr, and Zn. Furthermore, the proposed method based on ultrasound radiation presents additional criteria that align with the concepts of green analytical chemistry. Highlights A greener alternative method for the determination of Cu, Mn, Ni, Sr, and Zn in fluorescent lamp waste was developed. Optimal conditions for ultrasound extraction of potentially toxic elements were achieved in 10 min at a temperature of 25°C. Environmentally friendly aspects of ultrasound align with the requirements of green analytical chemistry. [ABSTRACT FROM AUTHOR]

• Fe, Cu, Zn and I analyzed in breast milk of pre-term and full-term births. • Colostrum, transitional and mature milk show differences in Fe, Cu and Zn. • Speciation of Fe, Cu and Zn show association to biomolecules (proteins). • Micronutrient speciation analysis provide a superior understanding of breastfeeding. The aim of this research was to quantify essential trace elements (iron, copper, zinc and iodine) and establish their speciation in human milk. Both the element and the species are important in new-born nutrition. Colostrum, and transitional and mature milks (25) were collected from 18 mothers of pre-term or full-term infants. Concentrations of the target elements were determined using ICP-MS. For speciation, HPLC coupled to ICP-MS was employed. Total contents of the micronutrients varied in mothers of pre-term (Fe = 0.997, Cu = 0.506, Zn = 4.15 and I = 0.458 mg L−1) and mothers of full-term (Fe = 0.733, Cu = 0.234, Zn = 2.91 and I = 0.255 mg L−1) infants. Fe, Cu and Zn were associated with biomolecules with high molecular mass compounds, such as immunoglobulins, albumin and lactoferrin whilst iodine was only found as iodide. [ABSTRACT FROM AUTHOR]

Since 1970 acyclovir (ACV) has been the reference drug in treating herpes simplex virus (HSV) infections. However, resistant herpes simplex virus type 1 (HSV-1) strains have emerged, narrowing the treatment efficacy. The antiviral activity of classical Na + , K + ATPase enzyme (NKA) inhibitors linked the viral replication to the NKA's activity. Herein, we evaluated the anti-HSV-1 activity of synthetic naphthoquinones, correlating their antiviral activity with NKA inhibition. We tested seven synthetic naphthoquinones initially at 50 μM on HSV-1-infected African green monkey kidney cells (VERO cells). Only one compound, 2-hydroxy-3-(2-thienyl)-1,4-naphthoquinone (AN-06), exhibited higher antiviral activity with a low cytotoxicity. AN-06 reduced the viral titer of 9 (log10) to 1.32 (log10) and decreased the steps of attachment and penetration. The addition of AN-06 up to 20 h postinfection (hpi) interfered with the viral cycle. The viral infection alone increases NKA activity 3 h postinfection (hpi), scaling up to 6 hpi. The addition of AN-06 in a culture infected with HSV-1 decreased NKA activity, suggesting that its antiviral action is linked to NKA inhibition. Also, docking results showed that this compound binds at the same site of NKA in which adenosine triphosphate (ATP) binds. AN-06 exhibited promising pharmacokinetic and toxicology properties. Thus, we postulate that AN-06 may be a good candidate for antiviral compounds with a mechanism of action targeting NKA activity., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

This study presents the development of an electrochemical sensor, denoted as GCE/CB/SiAlSn, based on the modification of a glassy carbon electrode surface with the ternary oxide SiO 2 /Al 2 O 3 /SnO 2 associated with carbon black, for direct determination of the neonicotinoid pesticide clothianidin in different matrices, such as environmental and food samples. Morphological characterization by the scanning electron microscopy technique, electroanalytical analyses using the cyclic voltammetry technique and differential pulse voltammetry are presented which demonstrated that the developed electrochemical platform presents high sensitivity in the electroanalytical clothianidin determination. The linear range studied was from 2.99 × 10 -7 to 6.04 × 10 -5 mol L -1 , with an LOD of 2.47 nmol L -1 . This high sensitivity was explained using the synergistic relationship between carbon black and ternary oxide that maximized the electroactive surface area of the GCE/CB/SiAlSn sensor. Interferent studies were performed that showed high selectivity of the sensor to the pesticide in the presence of Ca 2+ , K + , Na + , and Mg 2+ and carbendazim, glyphosate, imidacloprid and thiamethoxam pesticides. The sensor was applied to real samples of tap water and apple juice obtaining recoveries from 91.0% to 103.0%.