Adducts Research Articles

Using phenolic compounds from the Mediterranean Sea west of Egypt to categorize the sediment quality

Background and aimDespite having a low population, Egypt’s west coast is heavily industrialized resulting in large amounts of industrial wastewater that are dumped directly into the sea, severely polluting the area with various toxins. Numerous human activities release phenolic chemicals into the environment, which can be found in water and sediment. These materials are used to make compounds such as dyes, pesticides, explosives, and pharmaceuticals in a variety of industrial processes. Insufficient research has been done on the infiltration of phenolic compounds, which are organic serious pollutants, into the aquatic environment along the Mediterranean coast of Egypt, particularly the western shore. The research investigates the ecological dangers and concentration of eleven phenolic compounds found in bottom sediments on Egypt’s coastal area west of Alexandria.MethodsBefore analysis, stainless steel sieves were used in a mechanical sieving system to homogenize and size-fractionate samples of superficial sediment that were gathered from each of the 15 measurement locations along Egypt’s west coast. Total nitrogen and total organic carbon were also determined. Samples of dried bottom sediment were extracted with a solution of NaOH and methanol in order to determine the phenolic compounds, the final concentrated extract volume of each sample was reduced to 1.0 ml under a mild stream of purified nitrogen gas. A high performance liquid chromatograph (HPLC) (Series 1100, Agilent Technology Inc., Santa Clara, CA, USA) fitted with an autosampler, vacuum degasser, quaternary pump, and diode array detector was used to analyze eleven phenolic compounds.ResultsThe mean concentration of total eleven phenolic ranged between 1.02–5.62 µg g−1 with the mean value of 3.17 µg g−1 (SD, ±1.68), respectively. It was discovered that the concentration of additional phenolic compounds was not uniform, with their share of less than 10% in the total phenolic compounds.ConclusionPhenol was the most prevalent compound, with pentachlorophenol (PCP) coming in second with a normal centralization of 18.454 and 10.785 µg g−1, respectively. It was found that the remaining phenolic compounds had heterogeneous convergences, with less than 10% of them contributing to the total amount of phenolic compounds. Due to several activities, including force stations that utilize tar instead of gas, the oil pipe organization, and several tourist towns, the SidiKirir and Dabaa zones had the highest quantities of phenol and pentachlorophenol.

Valorization of Industrial Brine Sludge Waste for Augmented Spray Dry Scrubbing of SO₂ using Hygroscopic Additives

Detailed experiments were conducted using a laboratory-scale spray dryer under controlled conditions to investigate the effects of highly hygroscopic additives on the performance of hydrated lime (Ca(OH)2) in spray dry scrubbing (SDS) of sulfur dioxide (SO2). The experiment involved the preparation of hydrated lime sorbent from industrial brine sludge waste (IBSW) as the starting material. The evaluated additives included sodium hydroxide, ammonium nitrate, ammonium chloride, sodium chloride, and urea. The additives were chosen based on their hygroscopicity, as it is understood that the degree of desulfurization and sorbent conversion in an SDS is significantly enhanced in the prolonged liquid phase. Experiments were conducted at a constant inlet flue gas temperature of 140°C, sorbent particle size of -45μm, while the calcium to sulfur (Ca:S) ratio was varied in the range of 1.0 - 2.5. Slurry with 10 wt.% Ca(OH)2 was used while varying the additive concentration from 2 to 8 wt.%. The experimental findings revealed that all the investigated additives, except urea, promoted the removal efficiency of SO2 above baseline. Sodium hydroxide was the best-performing additive achieving 92.06% SO2 removal efficiency and a calcium conversion of 54.59%. Fourier-transform infrared spectroscopy (FTIR) analysis showed traces of additives present in the sulfation products. Similarly, X-Ray diffraction (XRD) analysis on the final product showed the presence of desulfurization products and the respective additive compounds. Scanning electron microscopy (SEM) depicted reaction products particles as course, irregular, and deformed.

Features of particle-phase PAHs from traffic emissions using tunnel measurement and urban roadside observation in China

Vehicle emissions are recognized as a primary source of particle-phase polycyclic aromatic hydrocarbons (PAHs), significant contributors to the hazardous properties of PM2.5. This study investigates the profiles of PAHs through measurements conducted in a tunnel and an urban roadside environment in 2020. We quantified real-world vehicle emission factors for mixed fleets in the Zhongshu tunnel in Guizhou, southwest China, and found that the total PAHs had an emission factor of 8.15 μg veh-1km-1, with higher factors observed for high-ring PAHs. Additionally, we analyzed concentrations of 15 PAHs at a roadside environment in Hefei, southern China, with an average concentration of 23.81 ng/m3. PAHs with 4, 5, and 6 rings comprised 80% of total PAHs at the roadside and 87% in the tunnel. Gasoline emissions were the predominant source in both the tunnel and roadside environments, supplemented by non-tailpipe emissions, catering, domestic cooking, and asphalt from road surfaces. Notably, while the total toxicity equivalent concentration of Benzo[a]pyrene (BaP) significantly exceeded the World Health Organization (WHO) guidelines of 1 ng/m3, the presence of additional compounds such as Dibenzo[a,h]anthracene (DahA) markedly increased the toxicological impact of PM2.5 from vehicle emissions. Therefore, it is essential to implement targeted pollution control strategies in central urban areas that address not only the overall concentration of PAHs but also their specific toxic contributions Continuous monitoring and assessment of PAHs in the urban environment are indispensable for effectively reducing their health impacts.

Pattern-Based Genome Mining Guides Discovery of the Antibiotic Indanopyrrole A from a Marine Streptomycete.

Terrestrial actinomycetes in the genus Streptomyces have long been recognized as prolific producers of small-molecule natural products, including many clinically important antibiotics and cytotoxic agents. Although Streptomyces can also be isolated from marine environments, their potential for natural product biosynthesis remains underexplored. The MAR4 clade of largely marine-derived Streptomyces has been a rich source of novel halogenated natural products of diverse structural classes. To further explore the biosynthetic potential of this group, we applied pattern-based genome mining, leading to the discovery of the first halogenated pyrroloketoindane natural products, indanopyrrole A (1) and B (2), and the bioinformatic linkage of these compounds to an orphan biosynthetic gene cluster (BCG) in 20 MAR4 genomes. Indanopyrrole A displays potent broad-spectrum antibiotic activity against clinically relevant pathogens. A comparison of the putative indanopyrrole BGC with that of the related compound indanomycin provides new insights into the terminal cyclization and offloading mechanisms in pyrroloketoindane biosynthesis. Broader searches of public databases reveal the rarity of this BGC while also highlighting opportunities for discovering additional compounds in this uncommon class.

Multi-omics analysis in mouse primary cortical neurons reveals complex positive and negative biological interactions between constituent compounds in Centella asiatica.

A water extract of the Ayurvedic plant Centella asiatica (CAW) improves cognitive function in mouse models of aging and Alzheimer's disease, and affects dendritic arborization, mitochondrial activity and oxidative stress in mouse primary neurons. Triterpenes (TT) and caffeoylquinic acids (CQA) are constituents associated with these bioactivities of CAW although little is known about how interactions between these compounds contribute to the plant's therapeutic benefit. Mouse primary cortical neurons were treated with CAW, or equivalent concentrations of four TT combined, eight CQA combined, or these twelve compounds combined (TTCQA). Treatment effects on the cell transcriptome (18,491 genes) and metabolome (192 metabolites) relative to vehicle control were evaluated using RNAseq and metabolomic analyses respectively. Extensive differentially expressed genes (DEGs) were seen with all treatments, as well as evidence of interactions between compounds. Notably many DEGs seen with TT treatment were not observed in the TTCQA condition, possibly suggesting CQA reduced the effects of TT. Moreover, additional gene activity seen with CAW as compared to TTCQA indicate the presence of additional compounds in CAW that further modulate TTCQA interactions. Weighted Gene Correlation Network Analysis (WGCNA) identified 4 gene co-expression modules altered by treatments that were associated with extracellular matrix organization, fatty acid metabolism, cellular response to stress and stimuli, and immune function. Compound interaction patterns were seen at the eigengene level in these modules. Interestingly, in metabolomics analysis, the TTCQA treatment saw the highest number of changes in individual metabolites (20), followed by CQA (15), then TT (8) and finally CAW (3). WGCNA analysis found two metabolomics modules with significant eigenmetabolite differences for TT and CQA, and possible compound interactions at this level. Four gene expression modules and two metabolite modules were altered by the four types of treatments applied. This methodology demonstrated the existence of both negative and positive interactions between TT, CQA and additional compounds found in CAW on the transcriptome and metabolome of mouse primary cortical neurons.

Pattern-based genome mining guides discovery of the antibiotic indanopyrrole A from a marine streptomycetef.

Terrestrial actinomycetes in the genus Streptomyces have long been recognized as prolific producers of small molecule natural products, including many clinically important antibiotics and cytotoxic agents. Although Streptomyces can also be isolated from marine environments, their potential for natural product biosynthesis remains underexplored. The MAR4 clade of largely marine-derived Streptomyces has been a rich source of novel halogenated natural products of diverse structural classes. To further explore the biosynthetic potential of this group, we applied pattern-based genome mining leading to the discovery of the first halogenated pyrroloketoindane natural products, indanopyrrole A (1) and B (2), and the bioinformatic linkage of these compounds to an orphan biosynthetic gene cluster (BCG) in 20 MAR4 genomes. Indanopyrrole A displays potent broad-spectrum antibiotic activity against clinically relevant pathogens. A comparison of the putative indanopyrrole BGC with that of the related compound indanomycin provides new insights into the terminal cyclization and offloading mechanisms in pyrroloketoindane biosynthesis. Broader searches of public databases reveal the rarity of this BGC while also highlighting opportunities for discovering additional compounds in this uncommon class.

Limosilactobacillus reuteri DSM 17938 Produce Bioactive Components during Formulation in Sucrose.

Improved efficacy of probiotics can be achieved by using different strategies, including the optimization of production parameters. The impact of fermentation parameters on bacterial physiology is a frequently investigated topic, but what happens during the formulation, i.e., the step where the lyoprotectants are added prior to freeze-drying, is less studied. In addition to this, the focus of process optimization has often been yield and stability, while effects on bioactivity have received less attention. In this work, we investigated different metabolic activities of the probiotic strain Limosilactobacillus reuteri DSM 17938 during formulation with the freeze-drying protectant sucrose. We discovered that the strain consumed large quantities of the added sucrose and produced an exopolysaccharide (EPS). Using NMR, we discovered that the produced EPS was a glucan with α-1,4 and α-1,6 glycosidic bonds, but also that other metabolites were produced. The conversion of the lyoprotectant is hereafter designated lyoconversion. By also analyzing the samples with GCMS, additional potential bioactive compounds could be detected. Among these were tryptamine, a ligand for the aryl hydrocarbon receptor, and glycerol, a precursor for the antimicrobial compound reuterin (3-hydroxypropionaldehyde). To exemplify the bioactivity potential of lyoconversion, lyoconverted samples as well as purified EPS were tested in a model for immunomodulation. Both lyoconverted samples and purified EPS induced higher expression levels of IL-10 (2 times) and IL-6 (4-6 times) in peripheral blood mononuclear cells than non-converted control samples. We further found that the initial cultivation of DSM 17938 with sucrose as a sugar substrate, instead of glucose, improved the ability to convert sucrose in the lyoprotectant into EPS and other metabolites. Lyoconversion did not affect the viability of the bacteria but was detrimental to freeze-drying survival, an issue that needs to be addressed in the future. In conclusion, we show that the metabolic activities of the bacteria during the formulation step can be used as a tool to alter the activity of the bacteria and thereby potentially improve probiotic efficacy.

Analysis of forensic polymer samples using double shot pyrolysis gas chromatography – Mass spectrometry

Polymers are present in many different products, such as paints, plastics, and rubbers, which are routinely encountered in forensic casework. Comparison of such samples involves an initial visual examination followed by comparison of the chemical compositions of the exhibits. Techniques such as Fourier transform infrared spectroscopy (FTIR) and pyrolysis gas chromatography – mass spectrometry (PyGC-MS) have been reported for determining the chemical compositions of polymers in forensic samples. Double-shot pyrolysis gas chromatography – mass spectrometry (DS-PyGC-MS) is an extension of single-shot pyrolysis gas chromatography – mass spectrometry (SS-PyGC-MS) which is the current PyGC-MS method used in most forensic laboratories. DS-PyGC-MS involves a preliminary thermal desorption GC-MS step, followed by the pyrolysis GC-MS step, with this second step being analogous to SS-PyGC-MS. The pyrolyser furnace operates at a lower temperature during the thermal desorption step, allowing low volatility compounds, such as additives, to be thermally desorbed and detected, minimising interference from the polymeric component of the sample. This pilot study analysed four different polymeric substrates, commonly encountered in forensic casework, by DS-PyGC-MS. The substrates chosen were tyre rubber, road cones, cling film, and shotgun wads. The aim was to investigate whether more chemical information was generated by DS-PyGC-MS compared to SS-PyGC-MS, potentially providing increased discrimination of such samples. Qualitative results showed that tyre rubber and road cones were ideal substrates for DS-PyGC-MS. A wide range of additives were detected in these samples in the thermal desorption step, which were not detected using SS-PyGC-MS. All of the rubber tyres (n=5) and road cones (n=6) were able to be uniquely distinguished using DS-PyGC-MS. Some additional compounds were detected in the thermal desorption analysis of shotgun wads (n=4), providing increased discrimination compared to SS-PyGC-MS. For the cling film samples analysed (n=7) the polyethylene-based cling films (n=6) could not be distinguished from each other, with no compounds detected in the thermal desorption step. The other cling film sample contained a mixture of polylactic acid (PLA) and polybutylene adipate terephthalate (PBAT) and could easily be distinguished from the polyethylene-based cling films using either SS- or DS-PyGC-MS, or other common analytical methods such as Fourier transform infrared spectroscopy (FTIR). This pilot study has demonstrated that DS-PyGC-MS has the potential to provide more comprehensive chemical composition information for some polymeric substrates and is a promising method for the forensic comparison of polymer evidence.

Diversity and Activity of Bacteria Cultured from a Cup-The Sponge Calyx nicaeensis.

Marine sponges are well-known for hosting rich microbial communities. Sponges are the most prolific source of marine bioactive compounds, which are frequently synthesized by their associated microbiota. Calyx nicaeensis is an endemic Mediterranean sponge with scarce information regarding its (bioactive) secondary metabolites. East Mediterranean specimens of mesophotic C. nicaeensis have never been studied. Moreover, no research has inspected its associated bacteria. Thus, we studied the sponge's bacterial diversity and examined bacterial interspecific interactions in search of a promising antibacterial candidate. Such novel antimicrobial agents are needed since extensive antibiotic use leads to bacterial drug resistance. Bacteria cultivation yielded 90 operational taxonomic units (OTUs). A competition assay enabled the testing of interspecific interactions between the cultured OTUs. The highest-ranked antagonistic bacterium, identified as Paenisporosarcina indica (previously never found in marine or cold habitats), was mass cultured, extracted, and separated using size exclusion and reversed-phase chromatographic methods, guided by antibacterial activity. A pure compound was isolated and identified as 3-oxy-anteiso-C15-fatty acid-lichenysin. Five additional active compounds await final cleaning; however, they are lichenysins and surfactins. These are the first antibacterial compounds identified from either the C. nicaeensis sponge or P. indica bacterium. It also revealed that the genus Bacillus is not an exclusive producer of lichenysin and surfactin.

Exploring strategies for valorizing wood processing waste: advancing sustainable, fully lignocellulosic biocomposites

This study presents the design and synthesis of bio-composites exhibiting high properties, wherein both the matrix and filler originate from wood biomass. Notably, no additional hardener compounds or treatments/modifications of the lignocellulosic filler were employed. Thermosetting materials were developed by homopolymerizing a bio-based aromatic epoxy monomer, the resorcinol diglycidyl ether (RDGE), with different percentages, from 1 wt% to 30 wt% of natural wood processing side-product, such as spruce bark powder (SB), which was used as such without additional treatments and modifications. The DSC analyses revealed enhanced reactivities with the bio-filler content, resulting in a reduced reaction temperature range and maximum reaction temperature. These findings provide evidence of the chemical interaction between the functional groups from spruce bark and the epoxides groups. The obtained fully based lignocellulosic materials show high E' values from 2.4 GPa to 2.5–3.5 GPa (glassy state) and from 64 MPa to 99–156 MPa in the rubbery region. The damping factor of the bio-composites with 1–10 wt% SB have shown an increase of the α transition temperature from 92 °C to 94–97 °C. The excellent filler/matrix interface and optimal adhesion between them were confirmed by SEM analysis.

ATH434, a promising iron-targeting compound for treating iron regulation disorders.

Cytotoxic accumulation of loosely bound mitochondrial Fe2+ is a hallmark of Friedreich's Ataxia (FA), a rare and fatal neuromuscular disorder with limited therapeutic options. There are no clinically approved medications targeting excess Fe2+ associated with FA or the neurological disorders Parkinson's disease and Multiple System Atrophy. Traditional iron-chelating drugs clinically approved for systemic iron overload that target ferritin-stored Fe3+ for urinary excretion demonstrated limited efficacy in FA and exacerbated ataxia. Poor treatment outcomes reflect inadequate binding to excess toxic Fe2+ or exceptionally high affinities (i.e. ≤10-31) for non-pathologic Fe3+ that disrupts intrinsic iron homeostasis. To understand previous treatment failures and identify beneficial factors for Fe2+-targeted therapeutics, we compared traditional Fe3+ chelators deferiprone (DFP) and deferasirox (DFX) with additional iron-binding compounds including ATH434, DMOG, and IOX3. ATH434 and DFX had moderate Fe2+ binding affinities (Kd's of 1-4 µM), similar to endogenous iron chaperones, while the remaining had weaker divalent metal interactions. These compounds had low/moderate affinities for Fe3+(0.46-9.59µM) relative to DFX and DFP. While all compounds coordinated iron using molecular oxygen and/or nitrogen ligands, thermodynamic analyses suggest ATH434 completes Fe2+ coordination using H2O. ATH434 significantly stabilized bound Fe2+ from ligand-induced autooxidation, reducing reactive oxygen species (ROS) production, whereas DFP and DFX promoted production. The comparable affinity of ATH434 for Fe2+ and Fe3+ position it to sequester excess Fe2+ and facilitate drug-to-protein iron metal exchange, mimicking natural endogenous iron binding proteins, at a reduced risk of autooxidation-induced ROS generation or perturbation of cellular iron stores.

Preparative separation of ten flavonoids from Scutellaria baicalensis Georgi roots using two-dimensional countercurrent chromatography with an online-storage, dilution, and mixing interface

The process of counter-current chromatography (CCC) separation for natural products typically necessitates the use of multiple solvent systems to accommodate constituents with a wide range of polarities. However, the incompatibility between these different solvent systems often results in unsuccessful online 2D successive separations. In this study, a 2D CCC system was developed, featuring an interface for online-storage, dilution, and mixing. It facilitated the implementation of online 2D CCC using different solvent systems. The method was subsequently applied for the preparative isolation of flavonoids from Scutellaria baicalensis Georgi roots. For 1D CCC, n-heptane-ethyl acetate–methanol-water (HepEMWat, 5:5:4:6, v/v) was utilized, while for 2D CCC, ethyl acetate-n-butanol-water (EBuWat, 0:5:5, v/v) was employed. The eluent with low resolution in 1D CCC was stored online, diluted three times using the lower phase of EBuWat (0:5:5, v/v), and subsequently transferred into 2D CCC for further isolation utilizing the same EBuWat (0:5:5, v/v) system. As results, six lipophilic compounds were isolated in 1D CCC in a normal mode, while two major hydrophilic constituents were isolated in a pH-peak-focusing mode in 2D CCC. Additionally, two additional compounds were purified through subsequent semi-preparative HPLC separation in order to resolve co-elution in 2D CCC. The developed 2D CCC system with a multifunctional interface demonstrated to be an exceptionally efficient and promising approach for the high-throughput purification of complex natural products.

Maple compounds prevent biofilm formation in Listeria monocytogenes via sortase inhibition.

The Pss exopolysaccharide (EPS) enhances the ability of the foodborne pathogen Listeria monocytogenes to colonize and persist on surfaces of fresh fruits and vegetables. Eradicating listeria within EPS-rich biofilms is challenging due to their increased tolerance to disinfectants, desiccation, and other stressors. Recently, we discovered that extracts of maple wood, including maple sap, are a potent source of antibiofilm agents. Maple lignans, such as nortrachelogenin-8'-O-β-D-glucopyranoside and lariciresinol, were found to inhibit the formation of, and promote the dispersion of pre-formed L. monocytogenes EPS biofilms. However, the mechanism remained unknown. Here, we report that these lignans do not affect Pss EPS synthesis or degradation. Instead, they promote EPS detachment, likely by interfering with an unidentified lectin that keeps EPS attached to the cell surfaces. Furthermore, the maple lignans inhibit the activity of L. monocytogenes sortase A (SrtA) in vitro. SrtA is a transpeptidase that covalently anchors surface proteins, including the Pss-specific lectin, to the cell wall peptidoglycan. Consistent with this, deletion of the srtA gene results in Pss EPS detachment from listerial cells. We also identified several additional maple compounds, including epicatechin gallate, isoscopoletin, scopoletin, and abscisic acid, which inhibit L. monocytogenes SrtA activity in vitro and prevent biofilm formation. Molecular modelling indicates that, despite their structural diversity, these compounds preferentially bind to the SrtA active site. Since maple products are abundant and safe for consumption, our finding that they prevent biofilm formation in L. monocytogenes offers a viable source for protecting fresh produce from this foodborne pathogen.

Rewireable Building Blocks for Enzyme-Powered DNA Computing Networks.

Neural networks enable the processing of large, complex data sets with applications in disease diagnosis, cell profiling, and drug discovery. Beyond electronic computers, neural networks have been implemented using programmable biomolecules such as DNA; this confers unique advantages, such as greater portability, electricity-free operation, and direct analysis of patterns of biomolecules in solution. Analogous to bottlenecks in electronic computers, the computing power of DNA-based neural networks is limited by the ability to add more computing units, i.e., neurons. This limitation exists because current architectures require many nucleic acids to model a single neuron. Each additional neuron compounds existing problems such as long assembly times, high background signal, and cross-talk between components. Here, we test three strategies to solve this limitation and improve the scalability of DNA-based neural networks: (i) enzymatic synthesis for high-purity neurons, (ii) spatial patterning of neuron clusters based on their network position, and (iii) encoding neuron connectivity on a universal single-stranded DNA backbone. We show that neurons implemented via these strategies activate quickly, with a high signal-to-background ratio and process-weighted inputs. We rewired our modular neurons to demonstrate basic neural network motifs such as cascading, fan-in, and fan-out circuits. Finally, we designed a prototype two-layer microfluidic device to automate the operation of our circuits. We envision that our proposed design will help scale DNA-based neural networks due to its modularity, simplicity of synthesis, and compatibility with various neural network architectures. This will enable portable computing power for applications in portable diagnostics, compact data storage, and autonomous decision making for lab-on-a-chips.

Detection of gasoline residues on household materials up to 60 days: Comparison of two extinguishing methods

Detection of ignitable liquid residues in a fire scene is essential for determining the origin. Although studies are focused on the detection of residues of accelerants depending on time or matrices, the time-dependent effect of the water extinguishing method in a fire has not yet been investigated. Experimental studies are needed to determine how long ignitable liquid residues can be detected in water-extinguished evidence compared to the smothering method. In this study, the effects of both extinguishing methods on gasoline residues were investigated after burning of carpet, sofa fabric, tablecloth, and towel by Solid Phase Micro Extraction- Gas Chromatography/Mass Spectrometry (SPME-GC/MS) technique. Four mandatory and 14 additional compounds were considered to prove the gasoline residue after the monitoring of possible interferences. Results showed that gasoline residues on the burned carpet and sofa fabric samples were successfully detected in both extinguishing methods up to 60 and 30 days after fire exposure, respectively due to multi-layered structures of related substrates. Additionally, the prolonged detection time of the water-extinguishing method made it particularly beneficial for single-layered products like tablecloths, where gasoline residues were found after an hour in this substrate. This is the first study investigating the effects of the extinguishing methods depending on time for textile products, which are the most used materials in houses. In addition, the fact that acrylamide-containing sofa fabric was investigated for the first time and that gasoline residues in carpet samples can be detected up to 60 days makes this study stand out.

ASSESSMENT OF USING WATER OBTAINED THROUGH EVODROP TECHNOLOGY EXPOSED TO ELECTROMAGNETIC WAVES ON CONCRETE PROPERTIES BASED ON FT-IR AND SEM ANALYSES

Various methods are applied to improve the quality of cement and concrete. Many efforts are made to enhance their quality by introducing additional compounds that can stabilize the chemical bonds between their components. Significant effects on hydrogen bonds under the influence of magnetic and electromagnetic waves have been observed. Results have been published with permanent magnetic fields for water treatment for concrete preparation with magnetic inductions B = 4000, 6000, 6000, 9000, and 9250 Gauss. Electromagnetic (e. m.) treated water has emerged as a promising approach for improving the properties of construction materials.Our investigation concerns the properties of concrete. Concrete is a composite building material mainly consisting of cement, aggregates, water, and various chemical additives. Water was activated with electromagnetic fields from solenoid, ranging from 20 to 40 kHz. The study employs Fourier Transform Infrared (FT-IR) spectroscopy analysis and the Scanning Electron Microscope (SEM) method. The experiments were performed on samples and control samples. The control samples were obtained with water before activation with EM fields. Treating the water in concrete preparation with electromagnetic fields leads to greater mixture homogeneity. SEM images substantiate this outcome. The FT-IR peaks are linked to heightened chemical reactivity from improved water parameters attributed to the treatment with the EVOdrop device.

Isolation and Characterization of Novel Pueroside B Isomers and Other Bioactive Compounds from Pueraria lobata Roots: Structure Elucidation, α-Glucosidase, and α-Amylase Inhibition Studies.

Pueraria lobata (Willd.) Ohwi is a traditional medicinal herb that has been extensively used in Chinese medicine for various therapeutic purposes. In this study, twelve chemical constituents were isolated from the roots of P. lobata, comprising three puerosides (compounds 1-3), six alkaloids (compounds 4-9), and three additional compounds (compounds 10-12). Notably, compound 1 (4R-pueroside B) was identified as a novel compound. The structures of all compounds were elucidated using a range of spectroscopic techniques, including CD spectroscopy for the first-time determination of the absolute configurations of pueroside B isomers (compounds 1 and 2). Enzyme inhibition assays revealed that, with the exception of compound 2, all isolated compounds exhibited varying degrees of α-glucosidase and α-amylase inhibitory activity. Remarkably, compound 12 demonstrated IC50 values of 23.25 μM for α-glucosidase inhibition and 27.05 μM for α-amylase inhibition, which are superior to those of the positive control, acarbose (27.05 μM and 36.68 μM, respectively). Additionally, compound 11 exhibited inhibitory activity against α-glucosidase and α-amylase comparable to the positive control, acarbose. Molecular docking studies indicated that compound 12 interacts with the active sites of the enzymes via hydrogen bonds, van der Waals forces, and hydrophobic interactions, which likely contribute to their inhibitory effects. These findings suggest that the chemical constituents of P. lobata could be potential natural sources of α-amylase and α-glucosidase inhibitors, with compound 12 being particularly promising for further investigation.

Optimizing nitrite content in powders from plasma-activated egg whites for meat preservation using response surface methodology

The study optimized the production of powders from two types of egg whites to be used as a nitrite source for meat curing, establishing a maximum utilization limit of 2%. The necessary quantity of nitrite was established through response surface methodology to guarantee its efficacy as a preservative agent and adherence to regulatory standards. High R2 values (0.9946 for hen, 0.9962 for ostrich) validated critical factors: plasma treatment time and distance, with minimal impact from drying temperature. Under specific experimental conditions (155.93 min, 16.84 cm, 41.10 °C), obtained nitrite concentration of 4000 mg kg⁻1 was confirmed through experiments. Stability tests showed that nitrite levels remained stable over four weeks under different conditions including vacuum and air-sealed packaging, as well as different temperatures (−18 °C, 4 °C, and 26 °C). Future research should investigate long-term stability, the formation of additional compounds, and the functional properties of powders to confirm their potential for food applications.

Comparison of 624-type Capillary Columns II

The present paper is the continuation of our "equivalent column" study. 624-type columns were investigated in a capillary gas chromatograph with a flame ionization detector (FID). In the preceding work, we used a homemade test mixture containing mainly acidic type compounds, which we complemented in the current study with additional basic test compounds to give a more precise description of the behaviour of the stationary phases. The columns had the same dimensions (30 m × 0.32 mm × 1.0 μm; length, internal diameter and film thickness, respectively) but were purchased from different manufacturers or the same manufacturer but from different batches. In addition, also their pre-life was different. These circumstances influence the condition of the stationary phase, and therefore their separation ability. These factors imply the necessity of testing the column from time to time. To distinguish between the separation ability of the columns, we compared the chromatograms, the retention times and retention order of the molecules, as well as peak asymmetry factors. Besides these parameters, quantitative determination is also performed based on the results of separation. We used the effective carbon number (ECN) and the limit of quantitation (LoQ) to demonstrate these differences which are caused by the different stationary phase conditions.

Enrichment of White Chocolate with Microencapsulated β-Carotene: Impact on Quality Characteristics and β-Carotene Stability during Storage.

This study developed functional white chocolate enriched with free (WC-F) and encapsulated β-carotene using whey protein isolate (WPI) and pullulan (PUL) blends through spray drying (WC-SP), freeze drying (WC-LP), and coaxial electrospinning (WC-EL). The thermal properties, rheological properties, hardness, and color of the chocolates were evaluated, and the stability of β-carotene was monitored over 4 months at 25 °C. No significant differences were found in melting profile temperatures among samples; however, WC-LP and WC-EL exhibited higher melting energies (30.88 J/g and 16.00 J/g) compared to the control (12.42 J/g). WC-F and WC-SP showed rheological behaviors similar to those of the control, while WC-LP and WC-EL displayed altered flow characteristics. Hardness was unaffected in WC-F and WC-SP (7.77 N/mm2 and 9.36 N/mm2), increased slightly in WC-LP (10.28 N/mm2), and decreased significantly in WC-EL (5.89 N/mm2). Over storage, melting point, rheological parameters, and hardness increased slightly, while color parameters decreased. β-carotene degradation followed a first-order reaction model, with degradation rate constants (k) of 0.0066 day-1 for WC-SP, 0.0094 day-1 for WC-LP, and 0.0080 day-1 for WC-EL, compared to 0.0164 day-1 for WC-F. WC-SP provided the best β-carotene retention, extending the half-life period by 2 times compared to WC-F (126.04 days vs. 61.95 days). Practical implications: The findings suggest that WC-SP, with its superior β-carotene stability, is particularly suitable for the development of functional confectionery products with extended shelf life, offering potential benefits in industrial applications where product stability is crucial. Future research directions: Further studies could explore the incorporation of additional bioactive compounds in white chocolate using similar encapsulation methods, as well as consumer acceptance and sensory evaluation of these enriched products.