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17 pages, 2168 KiB  
Article
Syntrichia laevipila Brid., a Bryophyta from Northwest Argentina as a Source of Antioxidants and Antimicrobials
by Luis Ignacio Jiménez, Florencia Maria Correa Uriburu, José Javier Martínez Chamás, Guillermo Martin Suárez, Iris Catiana Zampini, Mario J. Simirgiotis and María Inés Isla
Plants 2025, 14(2), 253; https://doi.org/10.3390/plants14020253 - 17 Jan 2025
Viewed by 269
Abstract
In recent years, numerous studies have emerged on the biological activities of bryophytes and their potential for therapeutic use. However, mosses appear to be a relatively overlooked group. The objective of this study was to conduct a phytochemical analysis of one hydroalcoholic extract [...] Read more.
In recent years, numerous studies have emerged on the biological activities of bryophytes and their potential for therapeutic use. However, mosses appear to be a relatively overlooked group. The objective of this study was to conduct a phytochemical analysis of one hydroalcoholic extract of Syntrichia laevipila and to evaluate its potential as an antioxidant and antimicrobial agent. The moss was collected in the Chaco Serrano region of Argentina, specifically on Jacaranda mimosifolia, and subsequently extracted by maceration in ethanol/water. UHPLC/ESI/MS/MS analysis identified 32 peaks, including phenolic compounds (phenolic acids, lignans, chalcones, and flavonoids) and non-hydrophilic compounds (terpenoids, fatty acids, and brassinosteroids). Maslinic and oleanolic acids, two triterpenoids present in S. laevipila, were also detected in J. mimosifolia, a substrate of this moss. The concentration of phenolic compounds was 19.05 ± 0.21 µg GAE/mL, while the total flavonoid concentration was 13.13 ± 0.33 µg QE/mL. The determination of reducing and total sugars yielded 0.22 ± 0.03 mg GE/mL and 1.26 ± 0.24 mg GE/mL, respectively, while the concentration of soluble proteins was 90.60 ± 4.50 µg BSAE/mL. The extract exhibited antioxidant properties by scavenging ABTS•+, H2O2, AAPH, and HO radicals. Additionally, it demonstrated antibacterial activity by inhibiting the growth of four strains of Staphylococcus aureus. The data obtained suggest that the hydroalcoholic extract of S. laevipila possesses significant potential as a natural antioxidant and antimicrobial agent, making it a promising candidate for the development of phytotherapeutic and cosmetic products. Full article
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<p><span class="html-italic">S. laevipila</span>, (<b>A</b>)—Habit of dry plant, (<b>B</b>)—Habit of wet plant, (<b>C</b>)—Specialized asexual propagule. The drawing was made by the authors.</p>
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<p>Flowchart of process of obtention of <span class="html-italic">S. laevipila</span> extracts and its characterization.</p>
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<p>UHPLC/ESI/MS/MS chromatogram of <span class="html-italic">S. laevipila</span> extract. The numbers above the peaks correspond to major components identified in the extract.</p>
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<p>Structures of some representative compounds detected in <span class="html-italic">S. laevipila</span>: peak 5, pinellic acid; peak 6, 2’,4’-Dihydroxychalcone; peak 12, hederagenin; peak 16, maslinic acid; peak 17, piperochromenoic acid; peak 21, mogroside I-A1; peak 22, recurvoside A; peak 23, oleanolic acid; and peak 27, cirsimaritin.</p>
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14 pages, 1594 KiB  
Article
Assessing Sugarcane Molasses’ Bioactive Compound Content upon Ultrasound-Assisted Hydroethanolic Extraction at Various pH Values
by Boukaga Farmani, Miljana Djordjević, Somayeh Mohammadkhani and Marijana Djordjević
Agriculture 2025, 15(2), 158; https://doi.org/10.3390/agriculture15020158 - 13 Jan 2025
Viewed by 369
Abstract
As widely generated by-products with significant bioactive compound content, sugarcane molasses exhibits high potential for valorization. For the purpose of bioactive compound extraction from sugarcane molasses, ultrasound-assisted extraction with various hydroethanolic solvents (0, 2.5, 5, 7.5, and 10% ethanol) at different pH values [...] Read more.
As widely generated by-products with significant bioactive compound content, sugarcane molasses exhibits high potential for valorization. For the purpose of bioactive compound extraction from sugarcane molasses, ultrasound-assisted extraction with various hydroethanolic solvents (0, 2.5, 5, 7.5, and 10% ethanol) at different pH values (4.11, 5.11, 6.11, and 7.11) was examined. In the obtained sugarcane molasses extracts, the content of total phenolics, monomeric anthocyanins, total flavonoids, total tannins, and antioxidant capacity (DPPH) was estimated alongside the determination of molasses’ major components through GC-MS analysis Based on the GC-MS analysis of molasses, sugars and nitrogenous compounds emerged as the most abundant compounds classes. Hydroethanolic solvent of 2.5% at pH 6.11 exhibited the most prominent extraction power regarding total phenolics (22074.98 µg GAE mL−1) and total flavonoids (245.42 µg QE mL−1). Furthermore, extraction with 2.5% hydroethanolic solvent at pH 5.11 displayed the highest total tannins (1177.85 µg CE mL−1). The behavior of monomeric anthocyanins in ultrasound-assisted extraction with hydroethanolic solvent was slightly different, where 2.5% hydroethanolic solvent extracted the highest amount at pH 4.11 (11.1 µg CGE mL−1) and 7.11 (10.68 µg CGE mL−1). The results of the DPPH assay indicated that extracts obtained using 2.5% hydroethanolic solvent at pH 4.11 (68.35%) and pH 5.11 (68.10%) evinced the highest neutralization power against DPPH free radicals. In conclusion, 2.5% ultrasound-assisted hydroethanolic solvent and pH 4.11-6.11 were the most suitable for extracting bioactive compounds from sugarcane molasses. Full article
(This article belongs to the Section Agricultural Product Quality and Safety)
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<p>Effect of ultrasound-assisted hydroethanolic (EtOH-ethanol share 0, 5, 7.5, and 10%) extraction and pH (4.11, 5.11, 6.11, 7.11) on sugarcane molasses: (<b>a</b>) total phenolic content; (<b>b</b>) total flavonoid content. Bars with different letters indicate a statistically significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of ultrasound-assisted hydroethanolic (EtOH–ethanol share 0, 5, 7.5, and 10%) extraction and pH (4.11, 5.11, 6.11, 7.11) on sugarcane molasses: (<b>a</b>) total tannin content; (<b>b</b>) monomeric anthocyanin content. Bars with different letters indicate a statistically significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Effect of ultrasonic-assisted hydroethanolic (EtOH–ethanol share 0, 5, 7.5, and 10%) extraction and pH (4.11, 5.11, 6.11, 7.11) on sugarcane molasses’ total antioxidant capacity. Bars with different letters indicate a statistically significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Principal Component Analysis (PCA) showing (<b>a</b>) the loading plot and (<b>b</b>) and score plot, describing the relationship between the determined bioactive compounds and different ultrasound-assisted hydroethanolic extraction conditions (ethanol share and pH). Eth, ethanol.</p>
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15 pages, 1161 KiB  
Article
Nutritional, Phytochemical, and Antimicrobial Properties of Carica papaya Leaves: Implications for Health Benefits and Food Applications
by Rajni Choudhary, Ravinder Kaushik, Ansab Akhtar, Suvendu Manna, Jyoti Sharma and Aarti Bains
Foods 2025, 14(2), 154; https://doi.org/10.3390/foods14020154 - 7 Jan 2025
Viewed by 792
Abstract
Background: Papaya leaves (PLs) are known for their therapeutic benefits and traditional use in treating inflammation, infections, and various health conditions. Rich in bioactive compounds, PLs are studied for their potential applications in functional foods. This study analyzed their nutritional, phytochemical, structural, thermal, [...] Read more.
Background: Papaya leaves (PLs) are known for their therapeutic benefits and traditional use in treating inflammation, infections, and various health conditions. Rich in bioactive compounds, PLs are studied for their potential applications in functional foods. This study analyzed their nutritional, phytochemical, structural, thermal, and antimicrobial properties to evaluate their role as a health-promoting ingredient. Methods: Phytochemicals were quantified spectrophotometrically and identified via GC-MS. Antioxidant activity was assessed using DPPH and FRAP assays. Mineral content was determined using ICP-OES. Structural and thermal properties were evaluated using FTIR, XRD, and calorimetry, and antimicrobial activity was tested via the agar well diffusion method. Results: PLs contained 25.75% crude protein, 41.49% carbohydrates, and high levels of flavonoids (21.00 mg QE/g), phenolics (8.85 mg GAE/g), and tannins (430 mg TAE/g). Antioxidant assays confirmed strong free radical scavenging potential. Mineral analysis showed abundant K, Ca, Mg, Na, and Fe (4071, 1079, 789.2, 361.2, and 228.2 mg/kg, respectively). Structural and thermal analysis revealed bioactive functional groups, 23.9% crystallinity, and thermal degradation characteristics. PLs exhibited antimicrobial activity, inhibiting E. coli, S. aureus, B. subtilis, and K. pneumoniae with zones of 22.05–25.15 mm. Conclusions: PLs demonstrate strong nutritional, antioxidant, and antimicrobial properties, supporting their inclusion in functional food. Full article
(This article belongs to the Section Nutraceuticals, Functional Foods, and Novel Foods)
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<p>GC−MS chromatogram of methanolic papaya leaf extract.</p>
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<p>FTIR spectra of papaya leaf powder.</p>
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<p>(<b>A</b>) X−ray diffraction pattern of papaya leaf powder. (<b>B</b>) DSC profile of papaya leaf powder in the temperature range of 25−300 °C, with a heating rate of 10 °C/min.</p>
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<p>Antibacterial activity of papaya leaf extract against Gram-positive and Gram-negative bacterial species. The letter (a, b, c) above the bars indicate statistically significant differences among the groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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22 pages, 2471 KiB  
Article
Bioactive Potential of Pogostemon benghalensis (Burm.f.) Kuntze: Antibacterial, Antioxidant, and Xanthine Oxidase Inhibitory Activities
by Nitesh Jaishwal, Mamta Jayswal, Deep Chand Gupta, Bishnu Dhakal, Santosh Koirala, Ram Bahadur Khadka, Hari Prasad Devkota and Jitendra Pandey
Bacteria 2025, 4(1), 3; https://doi.org/10.3390/bacteria4010003 - 6 Jan 2025
Viewed by 358
Abstract
This research is focused on assessing the antibacterial properties of Pogostemon benghalensis stem bark and inflorescence extracts, as well as their inhibitory effects on xanthine oxidase, antioxidant potential, overall phenolic content, and flavonoid concentration. The cold maceration technique was used to obtain extracts [...] Read more.
This research is focused on assessing the antibacterial properties of Pogostemon benghalensis stem bark and inflorescence extracts, as well as their inhibitory effects on xanthine oxidase, antioxidant potential, overall phenolic content, and flavonoid concentration. The cold maceration technique was used to obtain extracts using water, methanol, and ethyl acetate solvents. The disk diffusion method demonstrated the significant antibacterial efficacy of the methanol stem bark extract against Staphylococcus epidermidis, with a zone of inhibition (ZOI) of 13 mm, and the inflorescence methanol extract against Klebsiella pneumonia (ZOI: 12.9 mm). Moreover, the methanol stem bark extract exhibited the minimum bactericidal concentration (MBC) at 1.56 mg/mL and the minimum inhibitory concentration (MIC) at 0.78 mg/mL against S. epidermidis. The ethyl acetate inflorescence extract displayed noteworthy xanthine oxidase inhibition (IC50: 29.1 µg/mL) comparable to allopurinol (IC50: 12.7 µg/mL). Furthermore, the methanol stem bark extract exhibited a remarkable DPPH free radical inhibitory effect, showing an IC50 value of 42.5 µg/mL. The total polyphenol content ranged from 29.9 μg to 161.3 µg GAE per mg of dried extract weight in the methanol inflorescence extract, while the total flavonoid content ranged from 38.4 μg to 96.8 μg QE per mg of dried extract weight within the water-derived extract. Overall, these findings demonstrate the potent antibacterial properties, xanthine oxidase inhibition, and antioxidant activity of P. benghalensis extracts. Full article
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<p>(<b>a</b>) Fresh inflorescences of <span class="html-italic">P. benghalensis</span>; (<b>b</b>) shade-dried inflorescences of <span class="html-italic">P. benghalensis;</span> (<b>c</b>) dried stem barks of <span class="html-italic">P. benghalensis</span> peeled off from stems.</p>
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<p>Photographs depicting ZOIs produced by different extracts of <span class="html-italic">P. benghalensis</span> stem bark and inflorescence against different bacterial strains ((<b>A</b>) methanol stem bark extract against <span class="html-italic">S. epidemidis</span>; (<b>B</b>) ethyl acetate stem bark extract against <span class="html-italic">S. pneumonia</span>; (<b>C</b>) ethyl acetate stem bark extract against <span class="html-italic">S. epidermidis</span>, and (<b>D</b>) ethyl acetate inflorescence extract against <span class="html-italic">S. pneumonia</span>).</p>
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<p>Bar chart representing the IC<sub>50</sub> values of four distinct extracts obtained from <span class="html-italic">P. benghalensis</span> inflorescence and stem bark in terms of DPPH free radical inhibition. The chart also includes the IC<sub>50</sub> value of ascorbic acid for comparison. Abbreviations: (PBBEA: <span class="html-italic">P. benghalensis</span> bark ethyl acetate extract; PBBM: <span class="html-italic">P. benghalensis</span> bark methanol extract; PBFEA: <span class="html-italic">P. benghalensis</span> inflorescence ethyl acetate extract; PBFM: <span class="html-italic">P. benghalensis</span> inflorescence methanol extract; AA: ascorbic acid).</p>
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<p>Graphical representation illustrating the inhibitory effect of ethyl acetate, methanol, and aqueous extracts of <span class="html-italic">P. benghalensis</span> inflorescence and stem bark on XO activity at different concentrations, in comparison to the standard drug allopurinol. Abbreviations: (PBFEA: <span class="html-italic">P. benghalensis</span> inflorescence ethyl acetate extract; PBBEA: <span class="html-italic">P. benghalensis</span> bark ethyl acetate extract; PBFM: <span class="html-italic">P. benghalensis</span> inflorescence methanol extract; PBBA: <span class="html-italic">P. benghalensis</span> bark aqueous extract; PBBM: <span class="html-italic">P. benghalensis</span> bark methanol extract; PBFA: <span class="html-italic">P. benghalensis</span> inflorescence aqueous extract).</p>
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<p>Bar graph illustrating the IC<sub>50</sub> values of six different extracts derived from <span class="html-italic">P. benghalensis</span> inflorescence and stem bark for inhibiting xanthine oxidase enzyme activity alongside the reference drug allopurinol. Abbreviations: (PBBEA: <span class="html-italic">P. benghalensis</span> bark ethyl acetate extract; PBBM: <span class="html-italic">P. benghalensis</span> bark methanol extract; PBBA: <span class="html-italic">P. benghalensis</span> bark aqueous extract; PBFEA: <span class="html-italic">P. benghalensis</span> inflorescence ethyl acetate extract; PBFM: <span class="html-italic">P. benghalensis</span> inflorescence methanol extract; PBFA: <span class="html-italic">P. benghalensis</span> inflorescence aqueous extract).</p>
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<p>Pictures depicting MBC shown by ethyl acetate extract of <span class="html-italic">P. benghalensis</span> inflorescence against two different bacteria ((<b>A</b>) against <span class="html-italic">K. pneumonia</span>; (<b>B</b>) against <span class="html-italic">S. pneumonia</span>).</p>
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24 pages, 9580 KiB  
Article
Preliminary Data on Silybum marianum Metabolites: Comprehensive Characterization, Antioxidant, Antidiabetic, Antimicrobial Activities, LC-MS/MS Profiling, and Predicted ADMET Analysis
by Sabrina Lekmine, Ouided Benslama, Mohammad Shamsul Ola, Nabil Touzout, Hamza Moussa, Hichem Tahraoui, Haroun Hafsa, Jie Zhang and Abdeltif Amrane
Metabolites 2025, 15(1), 13; https://doi.org/10.3390/metabo15010013 - 3 Jan 2025
Viewed by 528
Abstract
Background/Objectives: Silybum marianum extract, obtained via microwave-enhanced extraction, was evaluated for its antioxidant, antidiabetic, and antimicrobial activities to explore its therapeutic potential. Methods: The extraction was performed using microwave-enhanced techniques, and LC-MS/MS was employed to profile the metabolites in the extract. Total phenolic [...] Read more.
Background/Objectives: Silybum marianum extract, obtained via microwave-enhanced extraction, was evaluated for its antioxidant, antidiabetic, and antimicrobial activities to explore its therapeutic potential. Methods: The extraction was performed using microwave-enhanced techniques, and LC-MS/MS was employed to profile the metabolites in the extract. Total phenolic and flavonoid contents were quantified using spectrophotometric methods. Antioxidant activity was assessed using DPPH, ABTS, CUPRAC, Phenanthroline, and FRAP assays. Enzyme inhibition assays were conducted to evaluate antidiabetic activity against α-glucosidase and α-amylase. Antimicrobial activity was determined using the disc diffusion method, and in silico ADMET and drug-likeness analyses were performed for key metabolites. Results: The extract contained 251.2 ± 1.2 mg GAE/g of total phenolics and 125.1 ± 1.6 mg QE/g of total flavonoids, with 33 metabolites identified, including phenolic acids, tannins, flavonoids, and flavolignans. Strong antioxidant activity was observed, with IC50 values of 19.2 ± 2.3 μg/mL (DPPH), 7.2 ± 1.7 μg/mL (ABTS), 22.2 ± 1.2 μg/mL (CUPRAC), 35.2 ± 1.8 μg/mL (Phenanthroline), and 24.1 ± 1.2 μg/mL (FRAP). Antidiabetic effects were significant, with IC50 values of 18.1 ± 1.7 μg/mL (α-glucosidase) and 26.5 ± 1.3 μg/mL (α-amylase). Antimicrobial activity demonstrated inhibition zones of 8.9 ± 1.1 mm (Bacillus subtilis), 12.6 ± 1.6 mm (Escherichia coli), 8.2 ± 1.2 mm (Fusarium oxysporum), and 9.2 ± 1.1 mm (Aspergillus niger). In silico analyses showed high absorption, favorable metabolism and excretion, and minimal toxicity, with no hERG channel inhibition or hepatotoxicity. Conclusions: The comprehensive results highlight the significant antioxidant, antidiabetic, and antimicrobial activities of S. marianum extract, suggesting its potential for therapeutic and preventive applications. Full article
(This article belongs to the Special Issue Metabolism of Bioactives and Natural Products)
16 pages, 3144 KiB  
Article
Photoconductive Dynamics of Photorefractive Poly((4-Diphenylamino)benzyl Acrylate)-Based Composites Sensitized by Perylene Bisimide
by Naoto Tsutsumi, Takafumi Sassa, Tam Van Nguyen, Ha Ngoc Giang, Sho Tsujimura, Boaz Jessie Jackin, Kenji Kinashi and Wataru Sakai
Polymers 2025, 17(1), 96; https://doi.org/10.3390/polym17010096 - 1 Jan 2025
Viewed by 473
Abstract
The transient dynamics of photocurrents for poly((4-diphenylamino)benzyl acrylate) (PDAA)-based photorefractive (PR) polymers sensitized with perylene bisimide derivative N,N′-diisopropylphenyl-1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxyl bisimide (PBI) at various composition ratios were studied. The PR polymer included (4-(diphenylamino)phenyl)methanol (TPAOH) photoconductive plasticizer and (4-(azepan-1-yl)-benzylidene) malononitrile nonlinear optical dye as well, which [...] Read more.
The transient dynamics of photocurrents for poly((4-diphenylamino)benzyl acrylate) (PDAA)-based photorefractive (PR) polymers sensitized with perylene bisimide derivative N,N′-diisopropylphenyl-1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxyl bisimide (PBI) at various composition ratios were studied. The PR polymer included (4-(diphenylamino)phenyl)methanol (TPAOH) photoconductive plasticizer and (4-(azepan-1-yl)-benzylidene) malononitrile nonlinear optical dye as well, which are needed for inducing PR effects. All the photocurrents measured at 640 nm were well simulated by a two-trapping site model considering photocarrier generation and recombination processes of the charge transfer (CT) complex between PBI and PDAA. The process of photocurrent simulation allowed for analyses of the dependences of hole mobility, quantum efficiency (QE) of photocarrier generation, trapping parameters, and recombination coefficient on the PDAA/TPAOH content. Finally, the PDAA content dependences of the trapping and recombination properties were compared with those of the PR parameters of the optical diffraction efficiency, optical gain, and response time. Full article
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<p>Transient photocurrents for PDAA45, PDAA40, PDAA35, PDAA30, and PDAA30/0.1. Key features, such as plateau regions or steep initial slopes, are confirmed for PDAA35 and PDAA30.</p>
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<p>PYS spectra and ionization potential (<span class="html-italic">I</span><sub>p</sub>) for (<b>a</b>) PDAA45, (<b>b</b>) PDAA40, (<b>c</b>) PDAA35, and (<b>d</b>) PDAA30. Dot is the PYS spectra. The intersection of slope and baseline is the ionization potential.</p>
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<p>Gaussian peaks at the lowest photon energy extracted from the DOS spectra for PDAA45, PDAA40, PDAA35, and PDAA30. Dotted curve: Gaussian peaks fitted with the proper width of the DOS, <span class="html-italic">σ</span>.</p>
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<p>Transient photocurrent plots in the initial time region for PDAA45, PDAA40, PDAA35, PDAA30, and PDAA30/0.1. The solid lines are the curves fitted by Equation (9).</p>
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<p>Absorption spectra and separated spectrum by Gaussian peak separation. (<b>a</b>) Absorption spectra of all composite films. The insert shows enlarged spectra in the wavelength range from 600 to 700 nm. (<b>b</b>–<b>f</b>) Separated Gaussian peaks. Blue spectrum: absorption due to 0–0 band, A<sub>0–0</sub>, of PBI alone. Red spectrum: absorption due to 0–1 band of PBI alone. Green spectrum: absorption due to PBI-PDAA CT complex and mixture of absorption due to PBI-PDAA CT complex and that due to PBI aggregates. Dashed orange spectrum: reproduced spectrum by summation of these spectra. (<b>b</b>) PDAA30/0.1, (<b>c</b>) PDAA45, (<b>d</b>) PDAA40, (<b>e</b>) PDAA35, and (<b>f</b>) PDAA30.</p>
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<p>Comparison of measured and simulated photocurrents for (<b>a</b>) PDAA45, (<b>b</b>) PDAA40, (<b>c</b>) PDAA35, and (<b>d</b>) PDAA30. Black and pale curves: measured and simulated transient photocurrents, respectively; red curve: transient density of CT complex anions <span class="html-italic">N</span><sub>A</sub><sup>−</sup>; blue curve: that of the filled shallow traps <span class="html-italic">T</span><sup>+</sup>; green curves: that of filled deep traps <span class="html-italic">M</span><sup>+</sup>.</p>
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<p>(<b>a</b>) PDAA (or TPAOH) content dependences of <span class="html-italic">γ</span><sub>T</sub> and <span class="html-italic">β</span><sub>T</sub>, (<b>b</b>) those of <span class="html-italic">γ</span><sub>M</sub> and <span class="html-italic">β</span><sub>M</sub>, (<b>c</b>) those of <span class="html-italic">αϕ</span> and <span class="html-italic">γ</span><sub>R</sub>, and (<b>d</b>) those of the PR <span class="html-italic">η</span><sub>ext</sub> and <span class="html-italic">Γ</span> taken from our previous paper [<a href="#B37-polymers-17-00096" class="html-bibr">37</a>]. The solid lines are guides for the eye.</p>
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21 pages, 1246 KiB  
Article
Real Exchange Rate Channel of QE Monetary Transmission Mechanism in Selected EU Members: The Pooled Mean Group Panel Approach
by Stefan Stojkov, Emilija Beker Pucar and Aleksandar Sekulić
J. Risk Financial Manag. 2025, 18(1), 12; https://doi.org/10.3390/jrfm18010012 - 30 Dec 2024
Viewed by 473
Abstract
Since the Great 2008 Recession, central banks around the world have been coping with monetary consequences that highlight structural costs of the economic system and the rise of unconventional monetary measures. This research aims to capture the heterogeneous effects of expansionary balance sheet [...] Read more.
Since the Great 2008 Recession, central banks around the world have been coping with monetary consequences that highlight structural costs of the economic system and the rise of unconventional monetary measures. This research aims to capture the heterogeneous effects of expansionary balance sheet (Quantitative easing) policy on the real effective exchange rate and current account balance under the different exchange rate regimes in crisis circumstances. The sample is structured of two groups of EU countries differentiated by level of monetary autonomy: EZ members (Austria, Belgium, France, Germany, Netherlands, Italy, and Spain) are represented by countries with the highest level of asset purchases by ECB and emerging monetary autonomous EU economies (Czech, Hungary, Poland, and Romania). Empirical findings are based on the framework of cross-sectional dependent, non-stationary, heterogeneous, dynamic panels using the (Pooled) Mean Group estimator during the 2014Q1–2023Q1 time horizon. Results indicate a positive long-run relationship between the central bank balance sheet assets, the real interest rate, and the real effective exchange rate. A negative long-term relationship with the current account balance is confirmed, suggesting a diminishing external position. While error-correction parameters are significant and heterogeneous, research confirms higher real effective exchange rate reaction for the EZ members with higher adjustment toward worsening competitiveness along with external balance. Full article
(This article belongs to the Special Issue Open Economy Macroeconomics)
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<p>APP structure and ECB balance sheet. (<b>a</b>) Largest asset purchases by ECB per country in the period 2014–2023; (<b>b</b>) ECB balance sheet assets. Source: author’s research according to FRED (2024) data.</p>
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<p>Fluctuation of REER and ECB balance sheet dynamics in the EZ member states (Austria, France, Germany, Netherlands, Italy, Spain, and Belgium) in the period 2014Q1–2023Q1. Source: author’s research according to quarterly IMF and FRED (2024) data.</p>
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<p>Fluctuation of REER and ECB balance sheet dynamics in the EZ member states (Austria, France, Germany, Netherlands, Italy, Spain, and Belgium) in the period 2014Q1–2023Q1. Source: author’s research according to quarterly IMF and FRED (2024) data.</p>
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<p>Fluctuation of REER and central bank’s balance sheet dynamics in the monetary autonomous EU countries (Czech, Poland, Hungary, and Romania) in the period 2014Q1–2023Q1. Source: author’s research according to quarterly IMF and FRED (2024) data.</p>
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<p>Average current account position (% of GDP) for EZ members in the period 2014Q1–2023Q1. Source: author’s research according to quarterly OECD data.</p>
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13 pages, 4389 KiB  
Article
Light Absorption-Enhanced Ultra-Thin Perovskite Solar Cell Based on Cylindrical MAPbI3 Microstructure
by Wenfeng Fu, Chong Pan, Aixuan Zhou, Pengcheng Shi, Zao Yi and Qingdong Zeng
Materials 2024, 17(24), 6284; https://doi.org/10.3390/ma17246284 - 23 Dec 2024
Viewed by 557
Abstract
In order to promote power conversion efficiency and reduce energy loss, we propose a perovskite solar cell based on cylindrical MAPbI3 microstructure composed of a MAPbI3 perovskite layer and a hole transport layer (HTL) composed of PEDOT:PSS. According to the charge transport [...] Read more.
In order to promote power conversion efficiency and reduce energy loss, we propose a perovskite solar cell based on cylindrical MAPbI3 microstructure composed of a MAPbI3 perovskite layer and a hole transport layer (HTL) composed of PEDOT:PSS. According to the charge transport theory, which effectually increases the contact area of the HTL, promoting the electronic transmission capability, the local field enhancement and scattering effects of the surface plasmon polaritons help to couple the incident light to the solar cell, which can increase the absorption of light in the active layer of the solar cell and improve its light absorption efficiency (LAE). based on simulation results, a cylindrical microstructure of the perovskite layer increases the contact area of the hole transport layer, which could improve light absorption, quantum efficiency (QE), short-circuit current density (JSC), and electric power compared with the perovskite layer of other structures. In the AM 1.5 solar spectrum, the average light absorption efficiency is 93.86%, the QE is 80.7%, the JSC is 24.50 mA/cm2, and the power conversion efficiency (PCE) is 20.19%. By enhancing the efficiency and reducing material usage, this innovative design approach for perovskite solar cells is expected to play a significant role in advancing solar technology and positively impacting the development of renewable energy solutions. Full article
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<p>(<b>a</b>) The structure of the cylindrical MAPBI3 microstructure PSCs; (<b>b</b>) the side view of the designed structure; (<b>c</b>) the top view of the structure (period D = 240 nm).</p>
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<p>PEDOT:PSS/MAPBI<sub>3</sub> organic–inorganic hybrid perovskite solar cell band map and schematic diagram of carrier transport under sunlight.</p>
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<p>(<b>a</b>,<b>b</b>) Light absorption and average absorption with different heights of the cylindrical MAPBI3 structure (r = 120 nm; h = 166 nm,174 nm,182 nm,190 nm, and 198 nm); (<b>c</b>,<b>d</b>) light absorption and average absorption with different radiuses of the cylindrical MAPBI3 structure (r = 60 nm, 80 nm, 100 nm, 120 nm, and 140 nm).</p>
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<p>(<b>a</b>,<b>b</b>) QE and AQE with different heights of cylindrical MAPbI3 structure; (<b>c</b>,<b>d</b>) QE and AQE with different radiuses of cylindrical MAPbI3 structure.</p>
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<p>(<b>a</b>,<b>b</b>) The J<sub>SC</sub> and electric power curves of the designed cells with different cylindrical MAPbI3 structure heights; (<b>c</b>,<b>d</b>) the short-circuit current density and electric power curves of the designed batteries with different cylindrical MAPbI3 structure radiuses.</p>
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<p>(<b>a</b>) The light absorption spectrum of PSCs with and without a cylindrical MAPbI3 structure and the planar MAPbI<sub>3</sub> cells with the same volume; (<b>b</b>) the light absorption spectrum of a cylindrical MAPbI3 PSC in different polarization states of TE and TM.</p>
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<p>(<b>a</b>) The light absorption spectrum of the cell in the AM 1.5 solar spectrum with and without a MAPbI<sub>3</sub> cylinder structure and with the cylinder replaced by a plane layer of the same volume; (<b>b</b>) the QE and integral current of the cell with and without a MAPbI<sub>3</sub> cylinder structure and with the cylinder replaced by a plane layer of the same volume.</p>
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<p>(<b>a</b>) The I-V curve of the solar cell with and without the cylindrical MAPbI<sub>3</sub> structure and the cylinder under the optimal parameters of the cylindrical MAPbI<sub>3</sub> structure; (<b>b</b>) The P-V curve of the solar cell with and without the cylindrical MAPbI<sub>3</sub> structure and the cylinder with a plane layer of the same volume.</p>
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14 pages, 1356 KiB  
Article
Innovative Nafion- and Lignin-Based Cation Exchange Materials Against Standard Resins for the Removal of Heavy Metals During Water Treatment
by Sara Bergamasco, Luis Alexander Hein, Laura Silvestri, Robert Hartmann, Giampiero Menegatti, Alfonso Pozio and Antonio Rinaldi
Separations 2024, 11(12), 357; https://doi.org/10.3390/separations11120357 - 21 Dec 2024
Viewed by 575
Abstract
The contamination of water by heavy metals poses an escalating risk to human health and the environment, underscoring the critical need for efficient removal methods to secure safe water resources. This study evaluated the performance of four cationic exchange materials (labeled “PS—DVB”, “PA—DVB”, [...] Read more.
The contamination of water by heavy metals poses an escalating risk to human health and the environment, underscoring the critical need for efficient removal methods to secure safe water resources. This study evaluated the performance of four cationic exchange materials (labeled “PS—DVB”, “PA—DVB”, “TFSA”, and “OGL”) in removing or harvesting metals such as copper, silver, lead, cobalt, and nickel from aqueous solutions, several of which are precious and/or classified as Critical Raw Materials (CRMs) due to their economic importance and supply risk. The objective was to screen and benchmark the four ion exchange materials for water treatment applications by investigating their metal sequestration capacities. Experiments were conducted using synthetic solutions with controlled metal concentrations, analyzed through ICP-OES, and supported by kinetic modeling. The adsorption capacities (qe) obtained experimentally were compared with those predicted by pseudo-first-order and pseudo-second-order models. This methodology enables high precision and reproducibility, validating its applicability for assessing ion exchange performance. The results indicated that PS—DVB and PA—DVB resins proved to be of “wide range”, exhibiting high efficacy for most of the metals tested, including CRM-designated ones, and suggesting their suitability for water purification. Additionally, the second-life Nafion-based “TFSA” material demonstrated commendable performance, highlighting its potential as a viable and technologically advanced alternative in water treatment. Lastly, the lignin-based material, “OGL”, representing the most innovative and sustainability apt option, offered relevant performance only in selected cases. The significant differences in performance among the resins underscore the impact of structural and compositional factors on adsorption efficiency. This study offers valuable insights for investigating and selecting new sustainable materials for treating contaminated water, opening new pathways for targeted and optimized solutions in environmental remediation. Full article
(This article belongs to the Special Issue Separation Technology for Metal Extraction and Removal)
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<p>Photographic images of the ion exchange materials utilized: (<b>A</b>) polystyrene–divinylbenzfene resin (PS–DVB), (<b>B</b>) polyacrylic–divinylbenzene resin (PA–DVB), (<b>D</b>) regenerated Nafion granules (TFSA), and (<b>D</b>) lignin-based powder material (OGL).</p>
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<p>Time-dependent concentration of the available metal ions (Cu<sup>2+</sup>, Pb<sup>2+</sup>, Co<sup>2+</sup> and Ni<sup>2+</sup>) in bulk solution (ppm) examined by ICP-EOS. Each panel shows the remaining concentration of a specific metal ion over time (0, 5, 10, 20, and 40 min): (<b>A</b>) Cu<sup>2+</sup> concentration in bulk, (<b>B</b>) Pb<sup>2+</sup> concentration in bulk, (<b>C</b>) Co<sup>2+</sup> concentration in bulk, and (<b>D</b>) Ni<sup>2+</sup> concentration in bulk.</p>
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22 pages, 2940 KiB  
Article
Adsorptive Elimination of Cu(II) Ions from Aqueous Solution onto Chitosan Modified with Uracil
by Muneera Alrasheedi, Ard elshifa M. E. Mohammed, Nouf F. Al-harby, Ghada E. Khedr and Nadia A. Mohamed
Water 2024, 16(24), 3695; https://doi.org/10.3390/w16243695 - 21 Dec 2024
Viewed by 494
Abstract
The remediation of industrial wastewater to eliminate heavy metal ions represents a pressing environmental requirement. A previously prepared adsorbent, based on chitosan modified with uracil (UCs), was investigated for the first time in this work to eliminate Cu(II) ions. The best conditions for [...] Read more.
The remediation of industrial wastewater to eliminate heavy metal ions represents a pressing environmental requirement. A previously prepared adsorbent, based on chitosan modified with uracil (UCs), was investigated for the first time in this work to eliminate Cu(II) ions. The best conditions for elimination were as follows: adsorbent dose = 0.01 g, Cu(II) ions solution concentration = 0.2 g L−1, pH = 6, and temperature = 25 °C. The adsorption kinetics were favorable for the pseudo second order due to the correlation coefficient’s value being the highest (R2 = 1.0). The experimental value of qe (99.65 mg g−1) was comparable to that of the theoretical one (100 mg g−1). The removal efficiency reached 99.65%, and the adsorption isotherm coincided with the Freundlich model, denoting that the nature of its adsorption was multi-layered. Cu(II) ions removal mainly relies on the physisorption phenomenon. The desorption percentages reached 92.65, 75.29, 49.29, and 19.92% after four successive cycles. So, the insertion of nitrogen-rich uracil along the chitosan chains, as binding sites for Cu(II), is deemed to be an outstanding opportunity to produce an appropriate, efficacious adsorbent that is a good choice to apply in the metal removal domains. Full article
(This article belongs to the Section Wastewater Treatment and Reuse)
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<p>EDS spectra with the percentage of elements of: (<b>a</b>) chitosan and (<b>b</b>) UCs.</p>
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<p>pHzpc plot for UCs.</p>
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<p>Optimization of the Cu(II) ions’ adsorption by UCs adsorbent: (<b>A</b>) the influence of the initial Cu(II) ion solution concentrations, (<b>B</b>) the impact of the temperature, (<b>C</b>) the effect of the UCs dose, and (<b>D</b>) the influence of pH of the medium.</p>
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<p>Linear representations of various kinetic models for Cu(II) ions adsorption by UCs adsorbent.</p>
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<p>Plots of different isotherm models for adsorption of Cu(II) ions by UCs adsorbent.</p>
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<p>Plots of different isotherm models for adsorption of Cu(II) ions by UCs adsorbent.</p>
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<p>Desorption percent of Cu(II) ions from UCs adsorbent at different cycles.</p>
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<p>The optimized configuration of (<b>a</b>) UCs, (<b>b</b>) UCs–Cu<sup>2+</sup>(I), (<b>c</b>) UCs–Cu<sup>2+</sup>(II), density of state of (<b>d</b>) UCs, (<b>e</b>) UCs–Cu<sup>2+</sup>(I), and (<b>f</b>) UCs–Cu<sup>2+</sup>(II).</p>
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<p>The four-step procedure for preparation of UC adsorbents.</p>
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18 pages, 1054 KiB  
Article
Bioactive Compounds, Antioxidant Properties, and Antimicrobial Profiling of a Range of West Algerian Honeys: In Vitro Comparative Screening Prior to Therapeutic Purpose
by Dalila Bereksi-Reguig, Hocine Allali, Nadjat Taib, Nadia Aissaoui, Marzena Wlodarczyk-Stasiak and Radoslaw Kowalski
Foods 2024, 13(24), 4120; https://doi.org/10.3390/foods13244120 - 20 Dec 2024
Viewed by 438
Abstract
Honey is a complex natural nutrient with well-established therapeutic properties recognized in traditional medicine. The purpose of the current work was to compare, in vitro, the bioactive compounds, antioxidants, and antimicrobial properties of 37 honey samples collected from the western region of Algeria [...] Read more.
Honey is a complex natural nutrient with well-established therapeutic properties recognized in traditional medicine. The purpose of the current work was to compare, in vitro, the bioactive compounds, antioxidants, and antimicrobial properties of 37 honey samples collected from the western region of Algeria and to identify the best sample for potential therapeutic purposes. Estimation of bioactive compounds was carried out by determining the total phenolic and flavonoid contents. Large variability among the samples was observed regarding the total phenolic content (from 24.17 ± 1.38 to 122.15 ± 3.55 mg GAE/100 g honey) and total flavonoid content (from 0.07 ± 0.01 to 33.49 ± 4.90 mg QE/100 g honey). Additionally, antioxidant activity, evaluated by four spectrophotometric assays, displayed fluctuating results among the samples. High positive correlations were observed between β-carotene and DPPH (0.766) and between β-carotene and ABTS (0.600), while inverse correlations were observed between bioactive compounds and antioxidant activity, except for the FRAP method. The antimicrobial activity, determined by well-diffusion assays, exhibited a dose-dependent antibacterial effect, with significant inhibition toward methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa reference strains. However, no activity was observed against Candida albicans strains. The MIC and MBC values were identical in most samples (range: 60 to 80% w/v) and predominantly exhibited bactericidal effects. The content of bioactive compounds played a significant role in the antibacterial properties. To summarize, the best honey sample for potential therapeutic purposes corresponded to mild white mustard (S6) and might be used as an alternative in therapeutic applications. Full article
(This article belongs to the Section Nutraceuticals, Functional Foods, and Novel Foods)
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<p>Map of the western region of Algeria showing the distribution of honey samples studied.</p>
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<p>Dendrogram of the cluster analysis using the average Euclidean distance for 37 honey samples collected from the western region of Algeria, in relation to the studied parameters.</p>
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<p>Dendrogram of the effect of honey samples on bacterial strains using the Euclidean distance.</p>
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19 pages, 4582 KiB  
Article
Anti-Allergic Effects of Lonicera caerulea L. Extract and Cyanidin-3-Glucoside on Degranulation and FcεRI Signaling Pathway of RBL-2H3 Cells
by Ye-Eun Choi, Jung-Mo Yang, Chae-Won Jeong, Sung-Hwan Park, Hee-Won Yoo, Hyun-Duck Jo and Ju-Hyun Cho
Appl. Sci. 2024, 14(24), 11722; https://doi.org/10.3390/app142411722 - 16 Dec 2024
Viewed by 542
Abstract
(i) Background: The increasing prevalence of allergic diseases highlights the need for effective treatments. Lonicera caerulea fruit has been recognized for its anti-inflammatory, anti-cancer, and neuroprotective effects, but the mechanisms underlying its anti-allergic properties remain unclear. (ii) Objective: This study aims to evaluate [...] Read more.
(i) Background: The increasing prevalence of allergic diseases highlights the need for effective treatments. Lonicera caerulea fruit has been recognized for its anti-inflammatory, anti-cancer, and neuroprotective effects, but the mechanisms underlying its anti-allergic properties remain unclear. (ii) Objective: This study aims to evaluate the total phenolic, total flavonoid, and cyanidin-3-glucoside (C3G) contents of Lonicera caerulea extract (HR2302-30E) and to investigate its antioxidant and anti-allergic activities. (iii) Methods: Using an IgE-stimulated RBL-2H3 cell model, we assessed the effects of HR2302-30E and C3G on mast cell degranulation, β-hexosaminidase and histamine release. Western blot analysis was performed to evaluate the expression of high-affinity IgE receptor (FcεRI)β/γ and the phosphorylation of Src family kinases (Syk, Fyn). We also examined the phosphorylation of downstream factors phospholipase Cγ, protein kinase Cδ, and mitogen-activated protein kinase. (iv) Results: Total phenolic, flavonoid, and C3G contents of HR2302-30E were 18.73 mg GAE/g, 11.83 mg QE/g, and 7.02 mg/g, respectively. In IgE-activated mast cells, HR2302-30E and C3G inhibited β-hexosaminidase and histamine release. Western blot analysis revealed reduced expression of FcεRIβ/γ and decreased phosphorylation of key downstream signaling molecules. Conclusions: These findings suggest that HR2302-30E and C3G modulate FcεRI signaling, indicating their potential as natural anti-allergic agents. Full article
(This article belongs to the Special Issue Advances in Biological Activities and Application of Plant Extracts)
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<p>Antioxidant activity of HR2302-30E. (<b>a</b>) 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging activity. (<b>b</b>) 2,2′-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging activity. (<b>c</b>) Ferric reducing antioxidant power (FRAP). (<b>d</b>) Oxygen radical absorbance capacity (ORAC) plot. ORAC values are expressed as the net area under the curve. Data are represented as the mean ± standard error of the mean (SEM) of three independent experiments. Different letters on the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) in the Duncan multiple range test. a~g, significant differences among various samples. AsA, Ascorbic acid.</p>
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<p>High-performance liquid chromatography (HPLC) chromatograms and photodiode array (PDA) spectra of cyanidin-3-glucoside (C3G) (<b>a</b>,<b>c</b>) and HR2302-30E (<b>b</b>,<b>d</b>).</p>
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<p>Effects of HR2302-30E and C3G on the viability of RBL-2H3 mast cells. Cell viability was measured using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Negative control: untreated cells. Data are represented as the mean ± SEM of three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. −, No treatment.</p>
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<p>Effects of HR2302-30E and C3G on (<b>a</b>) β-hexosaminidase and (<b>b</b>) histamine release in RBL-2H3 mast cells. IgE-primed RBL-2H3 cells were incubated with 250 ng/mL of DNP-HSA and HR2302-30E (500, 1000, and 2000 μg/mL) and C3G (5 and 10 μg/mL). Negative control: non-IgE-primed RBL-2H3 cells without DNP-HSA; positive control: IgE-primed RBL-2H3 cells with DNP-HSA and PP2. Data are represented as the mean ± SEM of the three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01 and *** <span class="html-italic">p</span> &lt; 0.001 vs. anti-DNP IgE plus DNP-HSA (IgE/Ag); ### <span class="html-italic">p</span> &lt; 0.001 vs. control. −, No treatment, +, Treatment.</p>
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<p>Effects of HR2302-30E and C3G on the high-affinity IgE receptor (FcεRI) signaling cascade in RBL-2H3 cells. IgE-primed RBL-2H3 cells were incubated with 250 ng/mL of DNP-HSA and HR2302-30E (1000 and 2000 μg/mL) and C3G (5 and 10 μg/mL). The protein expression of (<b>a</b>,<b>b</b>) FcεRI β and FcεRI γ, (<b>c</b>,<b>d</b>) Syk, Fyn, and Src were determined using immunoblotting. Data are represented as the mean ± SEM of the three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 vs. anti-DNP IgE plus DNP-HSA (IgE/Ag); ### <span class="html-italic">p</span> &lt; 0.001 vs. control. −, No treatment, +, Treatment.</p>
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<p>Effects of HR2302-30E and C3G on the high-affinity IgE receptor (FcεRI) signaling cascade in RBL-2H3 cells. IgE-primed RBL-2H3 cells were incubated with 250 ng/mL of DNP-HSA and HR2302-30E (1000 and 2000 μg/mL) and C3G (5 and 10 μg/mL). The protein expression of (<b>a</b>,<b>b</b>) FcεRI β and FcεRI γ, (<b>c</b>,<b>d</b>) Syk, Fyn, and Src were determined using immunoblotting. Data are represented as the mean ± SEM of the three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 vs. anti-DNP IgE plus DNP-HSA (IgE/Ag); ### <span class="html-italic">p</span> &lt; 0.001 vs. control. −, No treatment, +, Treatment.</p>
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<p>Effects of HR2302-30E and C3G on mitogen-activated protein kinase (MAPK), phospholipase C (PLC)-γ, and protein kinase C (PKC)-δ levels in RBL-2H3 cells. IgE-primed RBL-2H3 cells were incubated with 250 ng/mL of DNP-HSA and HR2302-30E (1000 and 2000 μg/mL) and C3G (5 and 10 μg/mL). The protein expression of (<b>a</b>,<b>b</b>) p38, ERK, and JNK, (<b>c</b>,<b>d</b>) PLCγ and PKCδ were determined using immunoblotting. Data are represented as the mean ± SEM of the three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 vs. anti-DNP IgE plus DNP-HSA (IgE/Ag); ### <span class="html-italic">p</span> &lt; 0.001 vs. control. −, No treatment, +, Treatment.</p>
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<p>Effects of HR2302-30E and C3G on mitogen-activated protein kinase (MAPK), phospholipase C (PLC)-γ, and protein kinase C (PKC)-δ levels in RBL-2H3 cells. IgE-primed RBL-2H3 cells were incubated with 250 ng/mL of DNP-HSA and HR2302-30E (1000 and 2000 μg/mL) and C3G (5 and 10 μg/mL). The protein expression of (<b>a</b>,<b>b</b>) p38, ERK, and JNK, (<b>c</b>,<b>d</b>) PLCγ and PKCδ were determined using immunoblotting. Data are represented as the mean ± SEM of the three independent experiments. The statistical analyses were performed using the Dunnett <span class="html-italic">t</span>-test. PP2 is a general Src family kinase inhibitor. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001 vs. anti-DNP IgE plus DNP-HSA (IgE/Ag); ### <span class="html-italic">p</span> &lt; 0.001 vs. control. −, No treatment, +, Treatment.</p>
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<p>HR2302-30E and C3G suppress mast cell degranulation by inhibiting FcεRI signaling pathway. HR2302-30E and C3G inhibit FcεRI signaling by suppressing Src family kinases (Syk, Fyn) and downstream pathways (PLCγ, PKCδ, MAPK), thereby reducing the release of allergic mediators.</p>
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21 pages, 7763 KiB  
Article
The Antioxidant and Anti-Inflammatory Activities of the Methanolic Extract, Fractions, and Isolated Compounds from Eriosema montanum Baker f. (Fabaceae)
by Gaétan Tchangou Tabakam, Emmanuel Mfotie Njoya, Chika Ifeanyi Chukwuma, Samson Sitheni Mashele, Yves Martial Mba Nguekeu, Mathieu Tene, Maurice Ducret Awouafack and Tshepiso Jan Makhafola
Molecules 2024, 29(24), 5885; https://doi.org/10.3390/molecules29245885 - 13 Dec 2024
Viewed by 1028
Abstract
Background: Inflammation is a natural body’s defense mechanism against harmful stimuli such as pathogens, chemicals, or irradiation. But when the inflammatory response becomes permanent, it can lead to serious health problems. In the present study, the antioxidant and anti-inflammatory potentials of the Eriosema [...] Read more.
Background: Inflammation is a natural body’s defense mechanism against harmful stimuli such as pathogens, chemicals, or irradiation. But when the inflammatory response becomes permanent, it can lead to serious health problems. In the present study, the antioxidant and anti-inflammatory potentials of the Eriosema montanum methanolic extract (EMME), as well as its isolated fractions (FA-FJ) and compounds (17), were evaluated by using in vitro and cellular models. Methods: The total phenolic and flavonoid contents were determined using, respectively, Folin–Ciocalteu and aluminum chloride colorimetric methods, while 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid (ABTS), 2,2′-diphenyl-1-picrylhy-drazyl (DPPH), and ferric ion reducing antioxidant power (FRAP) were used to determine the antioxidant activity. Thin Layer Chromatography (TLC) and column chromatography (CC) were used to isolate and purify the compounds and their elucidation using their NMR spectroscopic data. Results: EMME had moderate antioxidant and anti-inflammatory activities, while fraction FF showed much higher efficacy with IC50 values of 34.64, 30.60, 16.43, and 77.29 μg/mL against DPPH, ABTS, NO, and 15-LOX inhibitory activities, respectively. The EMME fraction was found to be very rich in flavonoids and phenolic compounds, with 82.11 mgQE/g and 86.77 mgGAE/g of dry extract, respectively. Its LC-MS profiling allowed us to identify genistin (5) as the most concentrated constituent in this plant species, which was further isolated together with six other known compounds, namely, n-hexadecane (1), heptacosanoic acid (2), tricosan-1-ol (3), lupinalbin A (4), d-pinitol (6), and stigmasterol glucoside (7). Given these compounds, genistin (5) showed moderate activity against reactive oxygen species (ROS) and NO production in LPS-stimulated RAW264.7 cells compared to EMME, which suggested a synergy of (5) with other compounds. To the best of our knowledge, compounds (1), (2), and (3) were isolated for the first time from this plant species. Full article
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<p>Extraction protocol, fractionation, and isolation of compounds from <span class="html-italic">E. montanum</span>.</p>
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<p>Chemical structures of compounds identified in <span class="html-italic">E. montanum</span>.</p>
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<p>Liquid chromatography–mass spectrometric (LC-MS) profile of <span class="html-italic">E. montanum</span> methanolic extract (<span class="html-italic">EMME</span>). Major compounds detected: Anopyranosylapigenin (t<sub>R</sub>: 7.585 min), genistin (t<sub>R</sub>: 7.902 min), and genistein (t<sub>R</sub>: 11.055 min).</p>
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<p>Nitric oxide (NO) production and cell viability in LPS-stimulated RAW 264.7 cells pre-treated with extract, fractions, and purified compounds. (<b>A</b>) The cytotoxic effect of tested samples was evaluated using MTT assay; (<b>B</b>) RAW 264.7 cells were pre-treated with tested samples at 100 µg/mL for 2 h, followed by exposure to 500 ng/mL of LPS for 24 h to quantify NO in cell supernatants. Each bar depicts the mean ± SD of three replicates (n = 3). One-way ANOVA combined Dunnett or Student–Newman–Keuls’s tests were used for data analysis. * <span class="html-italic">p</span> &lt; 0.05 vs. Ctrl. # <span class="html-italic">p</span> &lt; 0.05 vs. LPS, ns: non-significant.</p>
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<p>Bioactive samples’ concentration-dependent NO inhibitory action. The means ± SD of duplicate (n = 2) studies are shown for each bar. One-way ANOVA and either Dunnett’s or Student–Newman–Keuls tests were used to evaluate the data. # <span class="html-italic">p</span> &lt; 0.01 versus Ctrl. * <span class="html-italic">p</span> &lt; 0.01 about LPS.</p>
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<p>Reactive oxygen species (ROS) production in LPS-stimulated RAW 264.7 cells. RAW 264.7 cells were pre-treated with different concentrations (25, 50, and 100 µg/mL) of <span class="html-italic">E. montanum</span> methanolic extract (<span class="html-italic">EMME</span>), genistin, and ascorbic acid (AA) for two hours, then exposed to 200 ng/mL of LPS for twenty-four hours. Cell fluorescence was monitored at 485 nm (excitation) and 535 nm (emission) (<b>A</b>), and intracellular ROS levels were assessed using the DCFH-DA probe (10 µM). Percentages of negative control cells (<b>B</b>) are used to represent intracellular ROS levels. The means ± SD of three studies in triplicate are shown by each bar. One-way ANOVA and either Dunnett’s or Student–Newman–Keuls tests were used to evaluate the data. * <span class="html-italic">p</span> &lt; 0.05 vs. LPS, # <span class="html-italic">p</span> &lt; 0.05 vs. Ctrl.</p>
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19 pages, 1609 KiB  
Article
Formulation of Biological Sunscreen from Calendula arvensis Capitula Extracts: Antioxidant, Anti-Aging, Surface Tension, and UVB Protection Properties Assessed
by Najlae El-Otmani, Ikrame Zeouk and Ahmed Zahidi
Cosmetics 2024, 11(6), 216; https://doi.org/10.3390/cosmetics11060216 - 9 Dec 2024
Viewed by 1502
Abstract
Skin protection against ultraviolet (UV) radiation has long been crucial due to its role in photoaging, sunburn, and wrinkles. This study focuses on developing a bio-based sunscreen from Calendula arvensis capitula extract. Various extraction methods (maceration, sonication, and infusion) and solvents (EtOH, EtOH-H [...] Read more.
Skin protection against ultraviolet (UV) radiation has long been crucial due to its role in photoaging, sunburn, and wrinkles. This study focuses on developing a bio-based sunscreen from Calendula arvensis capitula extract. Various extraction methods (maceration, sonication, and infusion) and solvents (EtOH, EtOH-H2O, and H2O) were explored in order to identify the most effective extract for use in a sunscreen formulation. Each extract was analyzed for its phenolic content, as well as antioxidant activities (assessed through DPPH, CAT, and FRAP assays). Enzyme inhibition assays for tyrosinase, elastase, and collagenase highlighted the low IC50 values of the hydroethanolic extract. Furthermore, the in vitro sun protection factor (SPF) against UVB radiation was measured using ultraviolet spectrophotometry. A phytochemical analysis showed phenolic levels between 8 and 27 mg GAE/g, flavonoid concentrations of 7–13 mg QE/g, and tannin levels of 1.15–1.68 mg/mL, alongside moderate antioxidant activity. The ethanol maceration extract reduced the interfacial tension to 2.15 mN/m in 600 s, outperforming the conventional emulsifier polysorbate 20. The sonicated hydroethanolic extract demonstrated remarkable SPF efficacy (SPF = 193.65 ± 0.02), far exceeding that of the standard zinc oxide (SPF = 11.88 ± 0.03). The proposed formulations meet the COSMOS standards, suggesting their potential for certification as biological products. Further clinical and in vivo studies are necessary to confirm their safety and commercial viability. Full article
(This article belongs to the Special Issue Skin Anti-Aging Strategies)
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<p>Surface tension (ST) and interfacial tension (IFT) profiles of <span class="html-italic">C. arvensis</span> extracts as a function of time and solvent conditions.</p>
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<p>Sun Protection Factor (SPF) screening of sunscreens based on <span class="html-italic">C. arvensis</span> extracts, with similar letters in the same concentration (%) indicate that there is no significant difference, <span class="html-italic">p</span> &lt; 0.05 (n = 3) (<b>a</b>), and analysis of the UVB absorbance spectra of the various <span class="html-italic">C. arvensis</span> extracts (<b>b</b>).</p>
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<p>A guideline illustration, inspired by the COSMOS technical reference, for calculating the biological percentage of plant extracts through an extraction process.</p>
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<p>Characterization of sunscreen formulation parameters at different time intervals (day 1, day 30, day 60, and day 90) for assessment of stability over time (n = 3): (<b>a</b>) pH values, (<b>b</b>) peroxide value, (<b>c</b>) conductivity, and (<b>d</b>) viscosity analysis.</p>
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21 pages, 2189 KiB  
Article
In Vitro and In Silico Biological Activities Investigation of Ethyl Acetate Extract of Rubus ulmifolius Schott Leaves Collected in Algeria
by Amina Bramki, Djamila Benouchenne, Maria Michela Salvatore, Ouided Benslama, Anna Andolfi, Noureddine Rahim, Mohamed Moussaoui, Sourore Ramoul, Sirine Nessah, Ghozlane Barboucha, Chawki Bensouici, Alessio Cimmino, Jesùs Garcìa Zorrilla and Marco Masi
Plants 2024, 13(23), 3425; https://doi.org/10.3390/plants13233425 - 6 Dec 2024
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Abstract
This investigation aimed to assess the in vitro and in silico biological properties of the ethyl acetate (EtOAc) extract obtained from leaves of Rubus ulmifolius Schott collected in Algeria. The phytochemical screening data disclosed that flavonoids, tannins, coumarins, saponins, and anthocyanins were abundant. [...] Read more.
This investigation aimed to assess the in vitro and in silico biological properties of the ethyl acetate (EtOAc) extract obtained from leaves of Rubus ulmifolius Schott collected in Algeria. The phytochemical screening data disclosed that flavonoids, tannins, coumarins, saponins, and anthocyanins were abundant. High levels of total phenolics, total flavonoids and flavonols (523.25 ± 3.53 µg GAE/mg, 20.41 ± 1.80, and 9.62 ± 0.51 µg QE/mg respectively) were detected. Furthermore, GC-MS analysis was performed to identify low molecular weight compounds. d-(-)-Fructofuranose, gallic acid, caffeic acid, and catechin were detected as main metabolites of the EtOAc extract. The outcomes revealed that the extract exerted a potent antioxidant apt, and ensured significant bacterial growth inhibitory capacity, where the inhibition zone diameters ranged from 20.0 ± 0.5 to 24.5 ± 0.3 mm. These outcomes were confirmed through molecular docking against key bacterial enzymes that revealed significant interactions and binding affinities. d-(-)-Fructofuranose was identified as the most polar and flexible compound. Gallic acid and caffeic acid demonstrated higher unsaturation. Caffeic acid was well absorbed in the blood–brain barrier (BBB) and human intestine. Catechin was well absorbed in CaCO3, and can act as an inhibitor of CYP1A2. These results highlight how crucial it is to keep looking into natural substances in the quest for more potent and targeted pathology therapies. Full article
(This article belongs to the Section Phytochemistry)
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<p>Chemical structures of compounds identified in the crude EtOAc extract by GC-MS.</p>
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<p>2D and 3D visualizations of the best-docked compound interaction within the active site for each studied enzyme.</p>
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<p>2D and 3D visualizations of the best-docked compound interaction within the active site for each studied enzyme.</p>
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