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18 pages, 976 KiB  
Review
Resveratrol in Grapevine Components, Products and By-Products—A Review
by Ramona Căpruciu
Horticulturae 2025, 11(2), 111; https://doi.org/10.3390/horticulturae11020111 - 21 Jan 2025
Abstract
Resveratrol, a valuable compound found in grapevines, is found in significant amounts in grapes and wine, but also in other parts of the plant (leaves, roots, shoots) and derived products (juice, raisins, powders, grape pomace). Synthesis factors considerably influence the resveratrol content, and [...] Read more.
Resveratrol, a valuable compound found in grapevines, is found in significant amounts in grapes and wine, but also in other parts of the plant (leaves, roots, shoots) and derived products (juice, raisins, powders, grape pomace). Synthesis factors considerably influence the resveratrol content, and research aims to optimise these factors to maximise yield, with applications in agriculture, food, cosmetics, and medicine. This literature survey aims to review and synthesise existing knowledge on aspects of resveratrol’s chemical structure and isomers, biological properties, and the factors influencing resveratrol synthesis and content in grapevine and sources of resveratrol in grapevine components, products, and by-products. Current research is focusing on methods to stabilise resveratrol to increase the functionality of food products and the bioavailability of the compound in the colon, thereby contributing to human health, which reflects the interdisciplinary interest in the use of resveratrol as an ingredient with nutraceutical properties. Full article
(This article belongs to the Section Viticulture)
24 pages, 3290 KiB  
Article
The Impact of Organic Micropollutants on the Biochemical Composition and Stress Markers in Wolffia arrhiza
by Urszula Kotowska, Alicja Piotrowska-Niczyporuk, Justyna Kapelewska and Lilla Lane Jasinska
Molecules 2025, 30(3), 445; https://doi.org/10.3390/molecules30030445 - 21 Jan 2025
Viewed by 33
Abstract
For many years, there has been a growing pollution of the aquatic environment with personal care products and industrial chemicals, the main source of which is municipal and industrial wastewater. This raises the need to assess the impact of these pollutants on ecosystems, [...] Read more.
For many years, there has been a growing pollution of the aquatic environment with personal care products and industrial chemicals, the main source of which is municipal and industrial wastewater. This raises the need to assess the impact of these pollutants on ecosystems, including plants living in the aquatic environment. It is important to develop methods for their removal from wastewater, among which using plants for phytoremediation is a promising solution. This study aimed to evaluate the response of the aquatic plant Wolffia arrhiza (Lemnaceae) to low concentrations of bisphenol A (BPA), N,N-diethyl-m-toluamide (DEET), triclosan (TRC), benzophenone (BPH), endosulfan alpha (α-END), and endosulfan beta (β-END). The plant growth, the content of cellular components, and oxidative stress markers were assessed in response to plant contact with single compounds at concentrations of 0.1 mg/L and 1 mg/L, and their mixture at a total concentration of 1 mg/L. All of the pollutants used in the study inhibited the W. arrhiza growth and stimulated the degradation of proteins but enhanced the level of saccharides. TRC, BPH, α-END, and β-END had a negative impact on the content of photosynthetic pigments. Increased concentrations of the oxidative stress markers MDA and H2O2 were registered in the plants exposed to BPA, TRC, and β-END. The mixture of pollutants had higher toxic effects than individual substances. Full article
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Figure 1
<p>Dry mass (<b>A</b>), protein (<b>B</b>), and monosaccharide (<b>C</b>) contents in <span class="html-italic">Wolffia arrhiza</span> cultures under the influence of the following micropollutants: BPA (0.1 and 1 mg/L), DEET (0.1 and 1 mg/L), TRC (0.1 and 1 mg/L), BPH (0.1 and 1 mg/L), α-END (0.1 and 1 mg/L), and β-END (0.1 and 1 mg/L), as well as their mixture, in relation to control on the 7th day of culture. Data are the means of three independent experiments ± SD. Treatments with at least one letter being the same indicate a non-significant difference according to Tukey’s post hoc test.</p>
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<p>The content of chlorophyll <span class="html-italic">a</span> (<b>A</b>) and <span class="html-italic">b</span> (<b>B</b>) in <span class="html-italic">Wolffia arrhiza</span> cultures under the influence of the following micropollutants: BPA (0.1 and 1 mg/L), DEET (0.1 and 1 mg/L), TRC (0.1 and 1 mg/L), BPH (0.1 and 1 mg/L), α-END (0.1 and 1 mg/L), and β-END (0.1 and 1 mg/L), as well as their mixture, in relation to the control on the 7th day of culture. Data are the means of three independent experiments ± SD. Treatments with at least one letter being the same indicate a non-significant difference according to Tukey’s post hoc test.</p>
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<p>The content of α-carotene (<b>A</b>) and β-carotene (<b>B</b>) in <span class="html-italic">Wolffia arrhiza</span> cultures under the influence of the following micropollutants: BPA (0.1 and 1 mg/L), DEET (0.1 and 1 mg/L), TRC (0.1 and 1 mg/L), BPH (0.1 and 1 mg/L), α-END (0.1 and 1 mg/L), and β-END (0.1 and 1 mg/L), as well as their mixture, in relation to the control on the 7th day of culture. Data are the means of three independent experiments ± SD. Treatments with at least one letter being the same indicate a non-significant difference according to Tukey’s post hoc test.</p>
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<p>Malondialdehyde (MDA) (<b>A</b>) and hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) (<b>B</b>) contents in <span class="html-italic">Wolffia arrhiza</span> cultures under the influence of the following micropollutants: BPA (0.1 and 1 mg/L), DEET (0.1 and 1 mg/L), TRC (0.1 and 1 mg/L), BPH (0.1 and 1 mg/L), α-END (0.1 and 1 mg/L), and β-END (0.1 and 1 mg/L), as well as their mixture, in relation to the control on the 7th day of culture. Data are the means of three independent experiments ± SD. Treatments with at least one letter being the same indicate a non-significant difference according to Tukey’s post hoc test.</p>
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19 pages, 3444 KiB  
Article
Maya Vanilla (Vanilla cribbiana Soto Arenas): A New Species in Commerce
by Araceli Pérez-Silva, Eduardo Peña-Mojica, Abimael Ortega-Galeana, Jocelyn I. López-Cruz, Carlos A. Ledesma-Escobar, Mónica Rivera-Rivera and Ernestina Paz-Gamboa
Plants 2025, 14(3), 300; https://doi.org/10.3390/plants14030300 - 21 Jan 2025
Viewed by 152
Abstract
Vanilla-producing regions in Mexico and around the world are experiencing declining yields due to global climate change. However, Mexico, Guatemala, and other parts of Central America possess underutilized genetic resources within the Vanilla genus, which can be used to increase their production. One [...] Read more.
Vanilla-producing regions in Mexico and around the world are experiencing declining yields due to global climate change. However, Mexico, Guatemala, and other parts of Central America possess underutilized genetic resources within the Vanilla genus, which can be used to increase their production. One such resource is Vanilla cribbiana Soto Arenas, known as Maya vanilla, which is native to Guatemala and Mexico. This study evaluated some of the physical and chemical characteristics as well as the aromatic and fatty acid profiles of cured vanilla pods of Maya vanilla. A 5 kg batch of cured vanilla pods from Cobán, Guatemala, was analyzed for length, weight, humidity content, and proximate chemical composition and aromatic profile using HPLC-DAD and GC-MS. The pod lengths ranged from 6 to 16 cm, and weights ranged from 2.2 to 8.2 g. The humidity content varied between 22% and 38.63%. The main component in the cured vanilla pods was insoluble crude fiber (51.18%). The vanillin, vanillic acid, p-hydroxybenzoic acid, and p-hydroxybenzaldehyde concentrations in the cured vanilla beans were 2.13 ± 0.68, 0.105 ± 0.035, 0.38 ± 0.05, and 0.345 ± 0.115 g/100 g dry matter, respectively. A total of 70 volatile compounds were identified with GC-MS—16 acids, 12 alcohols, 8 aldehydes, 15 esters, 12 hydrocarbons, 5 ketones, and 2 furans—among which were compounds characteristic of other commercial vanilla species. Oleic acid and linoleic acid represented over 82% of the total fatty acids. This study provides fundamental insights into the physicochemical and aromatic characteristics of Maya vanilla, highlighting the differences between this species and vanilla species traditionally used in commerce. Vanilla cribbiana Soto Arenas represents an excellent alternative for the vanilla market as a flavoring agent for the food and perfume industries. Full article
(This article belongs to the Special Issue Genetic Resources and Ethnobotany in Aromatic and Medicinal Plants)
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Figure 1
<p><span class="html-italic">Vanilla cribbiana</span> Soto Arenas (Maya vanilla). (<b>A</b>) Flower. (<b>B</b>) Fruits from “Rápidos Che’ sib’ ik” Farm, Coban, Alta Verapaz, Guatemala. Photographs by Araceli Pérez-Silva (2022).</p>
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<p>Cured vanilla beans of <span class="html-italic">V. cribbiana</span> Soto Arenas (Maya vanilla). Photographs by Araceli Pérez-Silva (2022).</p>
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<p>HPLC-DAD chromatogram at 230 nm (<b>A</b>), 254 nm (<b>B</b>), and 280 nm (<b>C</b>) of standard compounds: <span class="html-italic">p</span>-hydroxybenzyl alcohol (1), glucovanillin (2), vanillyl alcohol (3), <span class="html-italic">p</span>-hydroxybenzoic acid (4), <span class="html-italic">p</span>-hydroxybenzaldehyde (5), vanillic acid (6), vanillin (7), anisyl alcohol (8), anisaldehyde (9), and anisic acid (10).</p>
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<p>HPLC-DAD chromatogram at 230 nm (<b>A</b>), 254 nm (<b>B</b>), and 280 nm (<b>C</b>) of cured <span class="html-italic">Vanilla cribbiana</span> Soto Arenas beans: <span class="html-italic">p</span>-hydroxybenzyl alcohol (1), vanillyl alcohol (3), <span class="html-italic">p</span>-hydroxybenzoic acid (4), <span class="html-italic">p</span>-hydroxybenzaldehyde (5), vanillic acid (6), vanillin (7), anisyl alcohol (8), and anisic acid (10). NI: Not identified.</p>
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<p>Harvest of fruits (<b>A</b>) and curing of <span class="html-italic">V. cribbiana</span> Soto Arenas beans (Maya vanilla) (<b>B</b>) from “Rápidos Che’ sib’ ik” Farm, Coban, Alta Verapaz, Guatemala. Photographs by Darío Ramírez-Fontana (2022).</p>
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21 pages, 6277 KiB  
Article
Characterization and Adsorption Behavior of Newly Synthesized Aminated Cellulose with Jeffamine EDR148 Towards Ni(II), Cu(II), and Pb(II) Heavy Metal Ions
by Jawaher Y. Al Nawah and Amany S. El-Khouly
Polymers 2025, 17(2), 255; https://doi.org/10.3390/polym17020255 - 20 Jan 2025
Viewed by 277
Abstract
Industrial wastewater containing heavy metal ions presents serious economic risk to the environment. In this study, a novel compound of aminated cellulose with jeffamine EDR148 was prepared to improve cellulose’s adsorptive behavior towards metal ions. This study undertook a straightforward and efficient cellulose [...] Read more.
Industrial wastewater containing heavy metal ions presents serious economic risk to the environment. In this study, a novel compound of aminated cellulose with jeffamine EDR148 was prepared to improve cellulose’s adsorptive behavior towards metal ions. This study undertook a straightforward and efficient cellulose modification through homogeneous chlorination in N,N′-butylmethylimidazolium chloride to produce 6-deoxychlorocellulose (Cell-Cl), followed by a reaction with jeffamine EDR148 and ultimately resulting in the formation of aminated cellulose (Cell-Jef148). Structural and chemical characteristics of Cell-Cl and Cell-Jef148 were determined using different techniques. Various adsorption conditions were applied to evaluate the optimal adsorption conditions for the removal of Cu(II), Ni(II), and Pb(II) ions. Cell-Jef48 revealed a greater affinity and higher adsorption efficiency of 480.3, 420.5, and 463.2 mg/g for Cu(II), Ni(II), and Pb(II) ions, respectively. Different kinetics and adsorption isothermal models were studied to investigate the adsorption mechanism and interactions between Cell-Jef148 and metal ions. The results fitted the Langmuir and pseudo-second-order models. Corresponding to the Langmuir model, Cell-Jef148’s maximum adsorption capacities were 952.38, 609.76, and 769.23 mg/g for Cu(II), Ni(II), and Pb(II) ions, respectively, with a high correlation coefficient, R2, in the range of 0.99575–0.99855. The research results of this study support Cell-Jef148’s adsorption of heavy metal ions, and the regeneration of adsorbent highlights the potential applications of cellulose-based materials in wastewater treatment. Full article
(This article belongs to the Section Polymer Applications)
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<p>SEM images of (<b>a</b>) Pure-Cell, (<b>b</b>) Cell-Cl, and (<b>c</b>) Cell-Jef148.</p>
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<p>(<b>A</b>) FT-IR spectra of (a) Pure-Cell, (b) Cell-Cl, and (c) Cell-Jef148. (<b>B</b>). FT-IR spectra of Cell-Jef48 after adsorption of the metal ions, (a) Cu(II), (b) Ni(II), and (c) Pb(II).</p>
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<p><sup>13</sup>C CP MAS NMR spectra of Pure-Cell, Cell-CL, and Cell-Jef148.</p>
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<p>(<b>A</b>) X-ray diffraction of (a) Pure-Cell, (b) Cell-Cl, and (c) Cell-Jef148. (<b>B</b>) X-ray diffraction of Cell-Jef148 after the adsorption of metal ions (a) Cu(II), (b) Ni(II), and (c) Pb(II).</p>
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<p>TG graphs of Pure-Cell, Cell-Cl, and Cell-Jef148.</p>
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<p>Influence of pH on the adsorption of heavy metal ions.</p>
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<p>(<b>a</b>) Influence of temperature and (<b>b</b>) on the adsorption of heavy metal ions.</p>
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<p>(<b>a</b>) Influence of temperature and (<b>b</b>) on the adsorption of heavy metal ions.</p>
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<p>Influence of adsorbent dose on the adsorption of heavy metal ions.</p>
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<p>Influence of metal ion concentration on the adsorption of the heavy metal ions.</p>
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<p>Langmuir (<b>a</b>), Freundlich (<b>b</b>), and Temkin (<b>c</b>) isothermal models for the adsorption of Cu(II), Ni(II), and Pb(II).</p>
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<p>Linear plots of (<b>a</b>) pseudo-first-order and (<b>b</b>) pseudo-second-order models for adsorption of Cu(II), Ni(II), and Pb(II) metal ions onto Cell-Jef148.</p>
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<p>The proposal mechanism of adsorption of heavy metal ions onto Cell-Jef148.</p>
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<p>The percent uptake of Cell-Jef148 after several regeneration cycles.</p>
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<p>Preparation reactions of Cell-Cl and Cell-Jef148.</p>
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18 pages, 3492 KiB  
Article
Physical Foam Injection Molding of Cellulose Fiber Reinforced Polypropylene by Using CO2: Parameter Variation and Comparison to Chemical Foam Injection Molding
by Claudia Pretschuh, Matthias Mihalic, Christian Sponner, Thomas Lummerstorfer, Andreas Steurer and Christoph Unterweger
J. Compos. Sci. 2025, 9(1), 50; https://doi.org/10.3390/jcs9010050 - 20 Jan 2025
Viewed by 363
Abstract
The use of cellulose fiber-filled polypropylene (PP) composites in combination with foam injection molding has enabled the lightweight design of injection-molded parts. The study provides achievements for the physical foam injection molding (MuCell®) process of PP–cellulose fiber compounds by using CO [...] Read more.
The use of cellulose fiber-filled polypropylene (PP) composites in combination with foam injection molding has enabled the lightweight design of injection-molded parts. The study provides achievements for the physical foam injection molding (MuCell®) process of PP–cellulose fiber compounds by using CO2 as the direct foaming agent, including a comparison of MuCell® foaming with N2 and a comparison to a chemical foaming process. Weight and density reductions, foam structure and specific mechanical properties are highly dependent on the applied processing parameters. The maximum weight reduction reached values of up to 16%, and density reduction even reached 33% in relation to the compact plates. The extent of weight and density reduction could be adjusted, among other factors, by a reduction in the shot volume. Setting the density reduction to 22% allowed for simultaneously decreasing weight while sustaining the specific flexural properties and limiting the loss of specific impact strength. By using optimized FIM parameters, the mechanical performance could be improved, with specific modulus values even outperforming the compact reference sample. This presents a significant benefit for the preparation of lightweight products and sets the basis for further optimization and modeling studies. Full article
(This article belongs to the Special Issue Feature Papers in Journal of Composites Science in 2024)
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<p>Research design and aim of the present study.</p>
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<p>Reduction in weight of several PP–cellulose plates prepared with MuCell<sup>®</sup> FIM with CO<sub>2</sub> and N<sub>2</sub>, and with chemical FIM for the complete plates (y-axis) and for the middle part of the plate (x-axis). The line represents equal values for weight reduction in the middle and complete plates.</p>
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<p>Flexural modulus (<b>a</b>) and flexural strength (<b>b</b>) of the PP–cellulose plates prepared using FIM.</p>
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<p>Specific flexural modulus (<b>a</b>) and specific flexural strength (<b>b</b>) of the PP–cellulose plates, prepared using FIM in relation to a compact reference. Error bars represent the 95% confidence interval.</p>
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<p>Charpy impact strength, notched (<b>a</b>) and unnotched (<b>b</b>) of PP–cellulose plates, prepared using FIM.</p>
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<p>Charpy impact strength, specific, notched (<b>a</b>) and unnotched (<b>b</b>), of PP–cellulose plates, prepared using FIM in relation to a compact reference. Error bars represent a 95% confidence interval.</p>
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<p>Microscopy images of foamed PP–cellulose. MuCell<sup>®</sup> with CO<sub>2</sub>: Sample 1 (<b>a</b>), Sample 5 (<b>b</b>), Sample 6 (<b>c</b>) and Sample 7 (<b>d</b>); MuCell<sup>®</sup> with N<sub>2</sub>: Sample 10 (<b>e</b>) and Sample 16, derived using chemical FIM (<b>f</b>).</p>
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30 pages, 1673 KiB  
Article
The Role of Extracts of Edible Parts and Production Wastes of Globe Artichoke (Cynara cardunculus L. var. scolymus (L.)) in Counteracting Oxidative Stress
by Valentina Laghezza Masci, Irene Mezzani, Enrica Alicandri, William Tomassi, Anna Rita Paolacci, Stefano Covino, Vittorio Vinciguerra, Elisabetta Catalani, Davide Cervia, Mario Ciaffi, Stefania Garzoli and Elisa Ovidi
Antioxidants 2025, 14(1), 116; https://doi.org/10.3390/antiox14010116 - 20 Jan 2025
Viewed by 211
Abstract
In addition to the immature edible flower heads, the cultivation of globe artichoke (Cynara cardunculus L. var. scolymus (L.) Fiori) generates substantial quantities of by-products, including leaves, stems, and roots, which constitute potential sources of bioactive compounds and prebiotic dietary fiber. Preserving [...] Read more.
In addition to the immature edible flower heads, the cultivation of globe artichoke (Cynara cardunculus L. var. scolymus (L.) Fiori) generates substantial quantities of by-products, including leaves, stems, and roots, which constitute potential sources of bioactive compounds and prebiotic dietary fiber. Preserving agricultural biodiversity and promoting socioeconomic development are essential for enhancing domestic production and fostering innovation. In the search for new biomolecules with antioxidant properties, this research focused on a globe artichoke landrace at risk of genetic erosion, still cultivated in the northern part of the Lazio region, known as the “Carciofo Ortano”. To investigate the antioxidant properties of various globe artichoke tissues from the “Carciofo Ortano” landrace, methanolic extracts were prepared from the immature main and secondary flower heads, stems, and leaves of representative genotypes of this landrace. Additionally, extracts were obtained from the same tissues of four landraces/clones included in the varietal platform of the PGI “Carciofo Romanesco del Lazio”, which served as reference genotypes: Campagnano, Castellammare, C3, and Grato 1. The antioxidant properties of these extracts were assessed using FRAP, ABTS, DPPH assays, and total phenolic content (TPC). The stem and secondary flower head extracts of two representative “Carciofo Ortano” genotypes and the Grato 1 clone, which have higher phenolic content, demonstrated the highest antioxidant activity. These extracts were therefore studied for their chemical profile using HPLC-DAD and SPME-GC/MS analysis. Additionally, the same extracts were investigated in vitro for their antioxidant capacity in differentiated SH-SY5Y cells, assessing their effects on ROS levels and the restoration of GSH levels. Furthermore, the in vivo beneficial effects of counteracting oxidative stress were evaluated in high sucrose-fed Drosophila melanogaster, as oxidative stress is a typical hallmark of hyperglycemic status. Overall, the results indicated that the edible immature inflorescences of the “Carciofo Ortano” landrace, along with the byproducts of its cultivation, are sources of raw materials containing biomolecules whose properties can be exploited for further applications in the pharmaceutical and medical sectors. Full article
(This article belongs to the Special Issue Antioxidant Activities of Phytochemicals in Fruits and Vegetables)
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Figure 1
<p>PCA biplot on antioxidant activities (FRAP, ABTS, DPPH) and total phenolic content (TPC) across the different genotypes and tissues. In the biplot, leaf tissues are represented in green, primary flower heads (PFH) in purple, secondary flower heads (SFH) in orange, and stem tissues in blue.</p>
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<p>Reduction of H<sub>2</sub>O<sub>2</sub> induced in intracellular free radical ROS following treatment with stem and SFH extracts of Orte 1 F4 P10, Orte 2 F7 P2 and Grato 1 P3 genotypes. * <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Increased GSH levels following treatment with stem and SFH extracts of Orte 1 F4 P10, Orte 2 F7 P2 and Grato 1 genotypes. * <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Mitochondrial activity assessment by MTT absorbance in adult flies‘ heads reared on standard diet (STD), high sucrose diet (HSD), or HSD supplemented with 0.03, 0.1, 0.3 mg/mL SFH (<b>A</b>) or stem (<b>B</b>) extracts. Results are expressed as arbitrary units (a.u.). Data have been obtained from three independent experiments using at least 300 heads for each experimental group. **** <span class="html-italic">p</span> &lt; 0.0001 HSD vs. CTRL; §§ <span class="html-italic">p</span> &lt; 0.01, §§§ <span class="html-italic">p</span> &lt; 0.001, §§§§ <span class="html-italic">p</span> &lt; 0.0001 HSD vs. HSD + SFH or HSD + STEM (<b>B</b>).</p>
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61 pages, 5717 KiB  
Review
Ellagic Acid: A Green Multi-Target Weapon That Reduces Oxidative Stress and Inflammation to Prevent and Improve the Condition of Alzheimer’s Disease
by Silvana Alfei and Guendalina Zuccari
Int. J. Mol. Sci. 2025, 26(2), 844; https://doi.org/10.3390/ijms26020844 - 20 Jan 2025
Viewed by 283
Abstract
Oxidative stress (OS), generated by the overrun of reactive species of oxygen and nitrogen (RONS), is the key cause of several human diseases. With inflammation, OS is responsible for the onset and development of clinical signs and the pathological hallmarks of Alzheimer’s disease [...] Read more.
Oxidative stress (OS), generated by the overrun of reactive species of oxygen and nitrogen (RONS), is the key cause of several human diseases. With inflammation, OS is responsible for the onset and development of clinical signs and the pathological hallmarks of Alzheimer’s disease (AD). AD is a multifactorial chronic neurodegenerative syndrome indicated by a form of progressive dementia associated with aging. While one-target drugs only soften its symptoms while generating drug resistance, multi-target polyphenols from fruits and vegetables, such as ellagitannins (ETs), ellagic acid (EA), and urolithins (UROs), having potent antioxidant and radical scavenging effects capable of counteracting OS, could be new green options to treat human degenerative diseases, thus representing hopeful alternatives and/or adjuvants to one-target drugs to ameliorate AD. Unfortunately, in vivo ETs are not absorbed, while providing mainly ellagic acid (EA), which, due to its trivial water-solubility and first-pass effect, metabolizes in the intestine to yield UROs, or irreversible binding to cellular DNA and proteins, which have very low bioavailability, thus failing as a therapeutic in vivo. Currently, only UROs have confirmed the beneficial effect demonstrated in vitro by reaching tissues to the extent necessary for therapeutic outcomes. Unfortunately, upon the administration of food rich in ETs or ETs and EA, URO formation is affected by extreme interindividual variability that renders them unreliable as novel clinically usable drugs. Significant attention has therefore been paid specifically to multitarget EA, which is incessantly investigated as such or nanotechnologically manipulated to be a potential “lead compound” with protective action toward AD. An overview of the multi-factorial and multi-target aspects that characterize AD and polyphenol activity, respectively, as well as the traditional and/or innovative clinical treatments available to treat AD, constitutes the opening of this work. Upon focus on the pathophysiology of OS and on EA’s chemical features and mechanisms leading to its antioxidant activity, an all-around updated analysis of the current EA-rich foods and EA involvement in the field of AD is provided. The possible clinical usage of EA to treat AD is discussed, reporting results of its applications in vitro, in vivo, and during clinical trials. A critical view of the need for more extensive use of the most rapid diagnostic methods to detect AD from its early symptoms is also included in this work. Full article
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Graphical abstract
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<p>Some of the endogenous factors and possible biological targets involved in AD pathology. Readapted with PERMISSION/LICENSE GRANTED AT NO CHARGE by ACS Chemical Neuroscience (American Chemical Society) from [<a href="#B8-ijms-26-00844" class="html-bibr">8</a>].</p>
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<p>Chemical structure of ellagitannins (ETs), ellagic acid (EA), and gallic acid (GA).</p>
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<p>Multifactorial pathogenic cascade leading to the onset and development of AD.</p>
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<p>Schematic routes of the multifactorial events leading to neuronal death. General mechanisms, such as protein non-correct folding and aggregation, OS, metal (M) dyshomeostasis, mitochondrial impairments, and distorted protein phosphorylation, have been found in several neuronal disorders. Readapted with PERMISSION/LICENSE GRANTED AT NO CHARGE by ACS Chemical Neuroscience (American Chemical Society) from [<a href="#B7-ijms-26-00844" class="html-bibr">7</a>].</p>
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<p>Schematic pathways of ROS production and their main effects on biological systems. Nrf2 = erythroid nuclear transcription factor-2; NF-kB = transcription factor involved in cellular responses to stimuli such as stress, cytokines, free radicals, heavy metals, ultraviolet irradiation, oxidized low-density lipoproteins (LDL), etc. Reproduced from our previous articles [<a href="#B17-ijms-26-00844" class="html-bibr">17</a>,<a href="#B30-ijms-26-00844" class="html-bibr">30</a>].</p>
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<p>Possible molecular causes of neuronal death and protective cyclic mechanisms in AD. The central event in AD pathogenesis is an imbalance between Aβ production and clearance. The enhanced activity of β- and γ-secretases leads to increased release of amyloidogenic Aβ42, which forms oligomers and then extracellular deposits (senile plaques). In this regard, one way to confront AD pathogenesis may be to combat the oligomerization processes by means of small molecules. The role of metal ions and ROS in Aβ oligomerization has also been advanced. Therefore, metal chelation and antioxidants are two general mechanisms to be considered in the search for disease-modifying anti-AD drug candidates. Also, β- and γ-secretase inhibitors may be promising lead compounds because they tackle an early event in AD pathogenesis. Mitochondrial dysfunction plays a fundamental role in the neuronal death associated with AD, as it is likely that intracellular Aβ could compromise the function of this organelle. τ hyperphosphorylation leading to tangle formation is regarded as a downstream event but could contribute to reinforcing neuronal dysfunction and cognitive impairment. Readapted with PERMISSION/LICENSE GRANTED AT NO CHARGE by ACS Chemical Neuroscience (American Chemical Society) from [<a href="#B7-ijms-26-00844" class="html-bibr">7</a>].</p>
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<p>Ideal and efficient MTSMs (equal to, say, MTDLs) for AD therapy, showing their corresponding pharmacophoric groups (PG). Readapted with PERMISSION/LICENSE GRANTED AT NO CHARGE by ACS Chemical Neuroscience (American Chemical Society) from [<a href="#B8-ijms-26-00844" class="html-bibr">8</a>].</p>
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<p>Structure of traditional AChEIs.</p>
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<p>Chemical structures of casuarictin, EA, and the most commonly known UROs. The scheme is a reproduction of the original one produced by authors [<a href="#B17-ijms-26-00844" class="html-bibr">17</a>].</p>
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<p>Alternative approaches to the one-molecule/one-target drug. MMT = multimodal therapy; MCM = multiple-compound medication (single compounds hitting multiple targets can also be abbreviated as MTDLs).</p>
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<p>The main possible forms of AD.</p>
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<p>Developmental root to the clinical implementation of new active principles (PA) for MDTs. FDA = Food and Drug Administration; EMA = European Medical Agency; MHPRA = Medicine and Healthcare Products Regulatory Agency; * refers to donanemab.</p>
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<p>Antioxidant mechanism of EA.</p>
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<p>Percentages of in vitro, in vivo, and clinical reports on the pharmacological activity of EA-containing plants among 56 studies considered.</p>
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17 pages, 3010 KiB  
Article
Inhibiting Autophagy by Chemicals During SCAPs Osteodifferentiation Elicits Disorganized Mineralization, While the Knock-Out of Atg5/7 Genes Leads to Cell Adaptation
by Damien Le Nihouannen, Claudine Boiziau, Sylvie Rey, Nicole Agadzhanian, Nathalie Dusserre, Fabrice Cordelières, Muriel Priault and Helene Boeuf
Cells 2025, 14(2), 146; https://doi.org/10.3390/cells14020146 - 20 Jan 2025
Viewed by 356
Abstract
SCAPs (Stem Cells from Apical Papilla), derived from the apex of forming wisdom teeth, extracted from teenagers for orthodontic reasons, belong to the MSCs (Mesenchymal Stromal Cells) family. They have multipotent differentiation capabilities and are a potentially powerful model for investigating strategies of [...] Read more.
SCAPs (Stem Cells from Apical Papilla), derived from the apex of forming wisdom teeth, extracted from teenagers for orthodontic reasons, belong to the MSCs (Mesenchymal Stromal Cells) family. They have multipotent differentiation capabilities and are a potentially powerful model for investigating strategies of clinical cell therapies. Since autophagy—a regulated self-eating process—was proposed to be essential in osteogenesis, we investigated its involvement in the SCAP model. By using a combination of chemical and genetic approaches to inhibit autophagy, we studied early and late events of osteoblastic differentiation. We showed that blocking the formation of autophagosomes with verteporfin did not induce a dramatic alteration in early osteoblastic differentiation monitored by ALP (alkaline phosphatase) activity. However, blocking the autophagy flux with bafilomycin A1 led to ALP repression. Strikingly, the mineralization process was observed with both compounds, with calcium phosphate (CaP) nodules that remained inside cells under bafilomycin A1 treatment and numerous but smaller CaP nodules after verteporfin treatment. In contrast, deletion of Atg5 or Atg7, two genes involved in the formation of autophagosomes and essential to trigger canonical autophagy, indicated that both genes could be involved differently in the mineralization process with a modification of the ALP activity while final mineralization was not altered. Full article
(This article belongs to the Section Autophagy)
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<p>Active autophagy flux in SCAPs, based on LC3 staining. Representative pictures of SCAPs (donors N1 and N3), grown for 4 days in regular cell medium, treated for 5 h before PFA fixation (<b>A</b>) with bafilomycin A1 or (<b>B</b>,<b>C</b>) with bafilomycin A1 (Bafilo) or verteporfin (Verte) or both and immunolabeled with the indicated antibodies. The scale bars are 25 µm.</p>
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<p>Chemical blockade of autophagy flux alters ALP activity. (<b>A</b>,<b>B</b>) Representative pictures of ALP activity (pink staining) after ImageJ treatment (the original pictures are shown in <a href="#app1-cells-14-00146" class="html-app">Figure S2</a>). SCAP banks were either not treated (Osteo) or treated with bafilomycin A1 (Osteo+Bafilo) or verteporfin (Osteo+Verte) at different time points during the osteodifferentiation process, as indicated. The scale bars are 100 µm. (<b>C</b>) Graph of ALP staining quantification (in percentage of stained surface, <a href="#app1-cells-14-00146" class="html-app">Figure S1</a>), showing the mean of donors with all independent donors. For each donor, the stained surface was analyzed on one to three fields. Statistics: Kruskal–Wallis test (<span class="html-italic">p</span> = 0.013%) and Mann–Whitney (*: <span class="html-italic">p</span> = 0.016; **: <span class="html-italic">p</span> = 0.009, two-tailed).</p>
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<p>Chemical blockade of autophagy has a donor-dependent effect on mineralization. Representative pictures of calcein staining of SCAP banks from donors as indicated, either non-treated (Osteo) or treated either with bafilomycin A1 (Osteo+Bafilo) (<b>A</b>), with magnified images of the white squares shown in insets, or with verteporfin (Osteo+Verte) (<b>B</b>). Treatments were applied at different time points during the osteodifferentiation process, as indicated. The scale bars are 100 µm.</p>
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<p>Efficient knock-out (KO) of ATG5 or ATG7 leading to the absence of LC3-II: SCAPs (donor N1) were transduced with different CRISPR/Cas9 lentivirus. (<b>A</b>) Western blot analysis of SCAPs treated or not for 2 h with 0.1 µM bafilomycin A1 before cell lysates preparation. Cells non-transduced (Mock), transduced with the control lentivirus (Lenti-Ctr), or with the lentivirus expressing the RNA guide for <span class="html-italic">Atg5</span> (KO ATG5) or <span class="html-italic">Atg7</span> (KO ATG7) were analyzed with the indicated antibodies. (<b>B</b>) Representative pictures of SCAPs treated for 2 h with 0.1 µM bafilomycin A1 before fixation in 4% PFA and immunolabeling with the anti-LC3 antibody. Nuclei were stained with DAPI. The scale bar is 25 µm.</p>
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<p>Effects of KO of ATG5 or ATG7 on ALP activity and mineralization. (<b>A</b>): Representative pictures of the different SCAP cell lines incubated in an osteogenic medium and processed at different time points for ALP activity (D14 and D18), alizarin red (AR, at D21), or calcein staining (Cal, at D21). The scale bar is 100 µm. Graph of ALP (<b>B</b>) and AR signals (<b>C</b>) quantification (in percentage of stained surface); mean of five to six fields (<b>B</b>) and two to three fields (<b>C</b>). Statistics: non-parametric statistical analysis was performed (Kruskal–Wallis and Mann–Whitney tests) to assess the effect of <span class="html-italic">Atg5</span> or <span class="html-italic">Atg7</span> deletion on ALP activity (KW: <span class="html-italic">p</span> = 0.05, MW: **: <span class="html-italic">p</span> = 0.006, two-tailed, at D14, non-significant at D18) and on AR staining (non-significant difference at D21). NS: Non Statistical difference.</p>
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19 pages, 1629 KiB  
Article
The Effect of the Glucosinolate Sinigrin on Alterations in Molecular Biomarkers of the Myocardium in Swiss Mice
by Nikola Ferara, Vedran Balta, Domagoj Đikić, Dyana Odeh, Ana Mojsović-Ćuić, Lana Feher Turković, Dario Dilber, Anđelo Beletić, Irena Landeka Jurčević and Ivana Šola
Foods 2025, 14(2), 327; https://doi.org/10.3390/foods14020327 - 20 Jan 2025
Viewed by 396
Abstract
Glucosinolates are chemically stable compounds that exhibit biological activity in the body following hydrolysis catalyzed by the enzyme myrosinase. While existing in vitro and in vivo studies suggest that the hydrolysis products of glucosinolates predominantly exert beneficial effects in both human and animal [...] Read more.
Glucosinolates are chemically stable compounds that exhibit biological activity in the body following hydrolysis catalyzed by the enzyme myrosinase. While existing in vitro and in vivo studies suggest that the hydrolysis products of glucosinolates predominantly exert beneficial effects in both human and animal organisms, some studies have found that the excessive consumption of glucosinolates may lead to toxic and anti-nutritional effects. Given that glucosinolates are primarily ingested in the human diet through dietary supplements and commercially available cruciferous vegetables, we investigated the in vivo effects of the glucosinolate sinigrin on molecular markers in the myocardia of healthy Swiss mice. This study aims to elucidate whether sinigrin induces positive or negative physiological effects in mammals following consumption. The alterations in myocardial parameters were assessed by measuring metabolic, inflammatory, structural, and antioxidant markers. Our findings revealed that subchronic exposure to sinigrin in the myocardia of female mice resulted in a significant increase (p ≤ 0.05) in the levels of the myokine irisin, matrix metalloproteinases (MMP-2, MMP-9), catalase (CAT), and total glutathione (tGSH), alongside a marked decrease (p ≤ 0.05) in the levels of atrial natriuretic peptide (ANP), compared to the control group consisting of both female and male mice. These results suggest that the hydrolysis products of sinigrin may exert a potentially toxic effect on the myocardial tissue of female mice and possess the capability to modulate transcription factors in vivo in a sex-dependent manner. This observation calls for further investigation into the mechanisms regulating the actions of glucosinolate hydrolysis products, their interactions with sex hormones, and the determination of permissible intake levels associated with both beneficial and adverse outcomes. Full article
(This article belongs to the Section Plant Foods)
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<p>The effect of sinigrin on the concentrations of (<b>a</b>) adropin, (<b>b</b>) irisin, (<b>c</b>) atrial natriuretic peptide (ANP), and (<b>d</b>) peroxisomal acyl-CoA oxidase I (ACOX1) in cardiac tissue homogenates. Mice (N = 6) in both female and male control groups were treated intragastrically (<span class="html-italic">ig</span>) with 0.3 mL of physiological saline, while in the experimental groups, females and males were treated <span class="html-italic">ig</span> with 0.3 mL of an aqueous solution of sinigrin at a dose of 10 mg/kg once daily for 28 days. #: statistically significantly different from the Cont.F group (<span class="html-italic">p</span> ≤ 0.05); *: statistically significantly different from the Sinig.<sub>M</sub> group (<span class="html-italic">p</span> ≤ 0.05); **: statistically significantly different from the Cont.<sub>M</sub> group (<span class="html-italic">p</span> ≤ 0.05). The results are presented as the mean ± standard error. Abbreviations: Cont.<sub>M</sub>—male control group; Cont.<sub>F</sub>—female control group; Sinig.<sub>M</sub>—group of males treated with an aqueous solution of sinigrin; Sinig.<sub>F</sub>—group of females treated with an aqueous solution of sinigrin.</p>
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<p>The effect of sinigrin on the concentration of high-sensitivity cardiac troponin I (hs-cTnI) in cardiac tissue homogenates. Mice (N = 6) in both the female and male control groups were treated intragastrically (<span class="html-italic">ig</span>) with 0.3 mL of physiological saline, while in the experimental groups, females and males were treated <span class="html-italic">ig</span> with 0.3 mL of an aqueous solution of sinigrin at a dose of 10 mg/kg once daily for 28 days. The results are presented as the mean ± standard error. Abbreviations: Cont.<sub>M</sub>—male control group; Cont.<sub>F</sub>—female control group; Sinig.<sub>M</sub>—experimental group of males treated with an aqueous solution of sinigrin; Sinig.<sub>F</sub>—experimental group of females treated with an aqueous solution of sinigrin.</p>
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<p>The effect of sinigrin on the concentrations of (<b>a</b>) matrix metalloproteinase 2 (MMP-2), (<b>b</b>) matrix metalloproteinase 9 (MMP-9), (<b>c</b>) pentraxin 3 (PTX3), and (<b>d</b>) nitric oxide (NO) in cardiac tissue homogenates. Mice (N = 6) in both the female and male control groups were treated intragastrically (<span class="html-italic">ig</span>) with 0.3 mL of physiological saline, while in the experimental groups, females and males were treated <span class="html-italic">ig</span> with 0.3 mL of an aqueous solution of sinigrin at a dose of 10 mg/kg once daily for 28 days. #: statistically significantly different from the Cont.<sub>F</sub> group (<span class="html-italic">p</span> ≤ 0.05). The results are presented as the mean ± standard error. Abbreviations: Cont.<sub>M</sub>—male control group; Cont.<sub>F</sub>—female control group; Sinig.<sub>M</sub>—experimental group of males treated with an aqueous solution of sinigrin; Sinig.<sub>F</sub>—experimental group of females treated with an aqueous solution of sinigrin.</p>
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<p>The effect of sinigrin on (<b>a</b>) superoxide dismutase (SOD) activity, (<b>b</b>) catalase (CAT) activity, (<b>c</b>) malondialdehyde (MDA) concentration, and (<b>d</b>) total glutathione (tGSH) concentration in cardiac tissue homogenates. Mice (N = 6) in both the female and male control groups were treated intragastrically (<span class="html-italic">ig</span>) with 0.3 mL of physiological saline, while in the experimental groups, females and males were treated <span class="html-italic">ig</span> with 0.3 mL of an aqueous solution of sinigrin at a dose of 10 mg/kg once daily for 28 days. #: statistically significantly different from the Cont.F group (<span class="html-italic">p</span> ≤ 0.05); *: statistically significantly different from the Sinig.<sub>M</sub> group (<span class="html-italic">p</span> ≤ 0.05). The results are presented as the mean ± standard error. Abbreviations: Cont.<sub>M</sub>—male control group; Cont.<sub>F</sub>—female control group; Sinig.<sub>M</sub>—experimental group of males treated with an aqueous solution of sinigrin; Sinig.<sub>F</sub>—experimental group of females treated with an aqueous solution of sinigrin.</p>
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23 pages, 757 KiB  
Review
Fungal Biocontrol Agents in the Management of Postharvest Losses of Fresh Produce—A Comprehensive Review
by Phathutshedzo Ramudingana, Ndivhuho Makhado, Casper Nyaradzai Kamutando, Mapitsi Silvester Thantsha and Tshifhiwa Paris Mamphogoro
J. Fungi 2025, 11(1), 82; https://doi.org/10.3390/jof11010082 - 20 Jan 2025
Viewed by 396
Abstract
Postharvest decay of vegetables and fruits presents a significant threat confronting sustainable food production worldwide, and in the recent times, applying synthetic fungicides has become the most popular technique of managing postharvest losses. However, there are concerns and reported proofs of hazardous impacts [...] Read more.
Postharvest decay of vegetables and fruits presents a significant threat confronting sustainable food production worldwide, and in the recent times, applying synthetic fungicides has become the most popular technique of managing postharvest losses. However, there are concerns and reported proofs of hazardous impacts on consumers’ health and the environment, traceable to the application of chemical treatments as preservatives on fresh produce. Physical methods, on the other hand, cause damage to fresh produce, exposing it to even more infections. Therefore, healthier and more environmentally friendly alternatives to existing methods for managing postharvest decays of fresh produce should be advocated. There is increasing consensus that utilization of biological control agents (BCAs), mainly fungi, represents a more sustainable and effective strategy for controlling postharvest losses compared to physical and chemical treatments. Secretion of antifungal compounds, parasitism, as well as competition for nutrients and space are the most common antagonistic mechanisms employed by these BCAs. This article provides an overview of (i) the methods currently used for management of postharvest diseases of fresh produce, highlighting their limitations, and (ii) the use of biocontrol agents as an alternative strategy for control of such diseases, with emphasis on fungal antagonists, their mode of action, and, more importantly, their advantages when compared to other methods commonly used. We therefore hypothesize that the use of fungal antagonists for prevention of postharvest loss of fresh produce is more effective compared to physical and chemical methods. Finally, particular attention is given to the gaps observed in establishing beneficial microbes as BCAs and factors that hamper their development, particularly in terms of shelf life, efficacy, commercialization, and legislation procedures. Full article
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<p>The relationship between biocontrol, pathogen, and host (mechanism of biocontrol action) is an intricate process consisting of multiple developments. The biocontrol agents impact fungal pathogens by instigating oxidative stress that triggers ROS, releases volatile organic acid and diffusible antifungal metabolites, and mycoparasitism via the production of lytic enzymes. In fruits, induction of phytoalexins R-protein and PR-protein and an upsurge in ROS generation lead to an increase in fruit defense resistance by antioxidant enzymes.</p>
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27 pages, 9904 KiB  
Article
Phenolic Compounds and Pharmacological Potential of Lavandula angustifolia Extracts for the Treatment of Neurodegenerative Diseases
by Olha Mykhailenko, Viktoriia Hurina, Nataliia Herbina, Yuliia Maslii, Liudas Ivanauskas, Inna Vladymyrova, Dmytro Lytkin, Zigmantas Gudžinskas, Hanna Severina, Olena Ruban and Victoriya Georgiyants
Plants 2025, 14(2), 289; https://doi.org/10.3390/plants14020289 - 20 Jan 2025
Viewed by 280
Abstract
The search for neuroprotective compounds in lavender is driven by its traditional use for brain health, with antioxidant activity serving as a key mechanism in reducing oxidative stress and supporting cognitive function. Lavender’s potential to protect neurons is based on its calming, anti-stress [...] Read more.
The search for neuroprotective compounds in lavender is driven by its traditional use for brain health, with antioxidant activity serving as a key mechanism in reducing oxidative stress and supporting cognitive function. Lavender’s potential to protect neurons is based on its calming, anti-stress properties, which increase the brain’s resistance to neurodegeneration. Although lavender is not a traditional medicinal plant in Ukraine, it is increasingly recognised for its medicinal properties and is widely cultivated in the country. Lavender use in Ukraine is influenced by both global herbal practices and local medical traditions. The aim of this study was to optimise the preparation of lavender herb extracts, perform chemical profiling and evaluate their antioxidant and neuroprotective activities. The study focused on Lavandula angustifolia cultivated in Lviv, Ukraine. Modern analytical methods were used, including HPLC, spectrophotometry, molecular docking, lyophilisation and pharmacological testing. The selection of the optimal conditions for obtaining lavender herb extracts was determined on the basis of the results of the total yield of phenolic compounds in each extract, where it was found that the raw material–solvent ratio (1:10) in water and 50% ethanol gave the highest yield of substances; the preferred extraction time was 20 min, and the temperature was 60–70 °C, especially for water extraction. Further HPLC analysis identified marker compounds including rosmarinic acid (28.31 mg/g), chlorogenic acid (1.64 mg/g) and luteolin (0.23 mg/g) in the lyophilised ethanol extract, which were previously recognised as neuroprotective markers by molecular docking. The water extract showed higher antioxidant (total 50.85 mg/g) and neuroprotective activity, probably due to synergistic interactions among the components. Behavioural tests further demonstrated the neuroprotective potential of lavender herb. These results demonstrate the potential neuroprotective activity of lavender herb and open new possibilities for its use in the treatment of various neurodegenerative diseases. Full article
(This article belongs to the Section Phytochemistry)
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<p>The design of the experiment.</p>
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<p><span class="html-italic">Lavandula angustifolia</span> and its raw material: (<b>a</b>) general view of plants cultivated in the Lviv Botanical Garden of National University named after Ivan Franko (Lviv, Ukraine, 2022), photo by O. Mykhailenko; (<b>b</b>) general appearance of dry lavender herb; (<b>c</b>) separated flowers, leaves and stems of lavender.</p>
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<p>Quantity of phenolic compounds extracted from herb, flowers and stems of lavender. Whiskers represent the standard deviation. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between variants.</p>
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<p>Effect of extraction time, type of extractant and ratio of HRM to extractant on total content of phenolic compounds from lavender herb. Whiskers represent standard deviation.</p>
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<p>Effect of temperature on quantity of phenolic compounds extracted from lavender herb. Different letters above bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between variants. Whiskers represent standard deviation.</p>
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<p>Combined conformational arrangement of the reference inhibitor donepezil (grey) and (<b>a</b>) apigenin (green) and 6,7-dihydroxyisoflavone (blue), and (<b>b</b>) chlorogenic (purple), neochlorogenic (blue) and rosmarinic acids (yellow) in the active site of AChE.</p>
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<p>Interaction of luteolin (<b>a</b>) and rosmarinic acid (<b>b</b>) with amino acid residues of the NMDAR inhibitor site.</p>
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<p>Typical HPLC chromatogram of lavender herb detected at 325 nm: 1—chlorogenic acid (RT 11.64 min); 2—rosmarinic acid (RT 37.18 min); 3—luteolin (RT 43.37 min).</p>
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<p>Typical HPLC-ABTS chromatogram of lavender herb extract (LLEE, 50% ethanol) detected at 325 nm (HPLC, green) and 650 nm (ABTS, red): 1—unknown compound; 2—chlorogenic acid; 3—rosmarinic acid; 4—luteolin.</p>
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27 pages, 3101 KiB  
Article
Development of a Sustainable Flexible Humidity Sensor Based on Tenebrio molitor Larvae Biomass-Derived Chitosan
by Ezekiel Edward Nettey-Oppong, Riaz Muhammad, Emmanuel Ackah, Hojun Yang, Ahmed Ali, Hyun-Woo Jeong, Seong-Wan Kim, Young-Seek Seok and Seung Ho Choi
Sensors 2025, 25(2), 575; https://doi.org/10.3390/s25020575 - 20 Jan 2025
Viewed by 298
Abstract
This study presents the fabrication of a sustainable flexible humidity sensor utilizing chitosan derived from mealworm biomass as the primary sensing material. The chitosan-based humidity sensor was fabricated by casting chitosan and polyvinyl alcohol (PVA) films with interdigitated copper electrodes, forming a laminate [...] Read more.
This study presents the fabrication of a sustainable flexible humidity sensor utilizing chitosan derived from mealworm biomass as the primary sensing material. The chitosan-based humidity sensor was fabricated by casting chitosan and polyvinyl alcohol (PVA) films with interdigitated copper electrodes, forming a laminate composite suitable for real-time, resistive-type humidity detection. Comprehensive characterization of the chitosan film was performed using Fourier-transform infrared (FTIR) spectroscopy, contact angle measurements, and tensile testing, which confirmed its chemical structure, wettability, and mechanical stability. The developed sensor exhibited a broad range of measurements from 6% to 97% relative humidity (RH), a high sensitivity of 2.43 kΩ/%RH, and a rapid response time of 18.22 s with a corresponding recovery time of 22.39 s. Moreover, the chitosan-based humidity sensor also demonstrated high selectivity for water vapor when tested against various volatile organic compounds (VOCs). The superior performance of the sensor is attributed to the structural properties of chitosan, particularly its ability to form reversible hydrogen bonds with water molecules. This mechanism was further elucidated through molecular dynamics simulations, revealing that the conductivity in the sensor is modulated by proton mobility, which operates via the Grotthuss mechanism under high-humidity and the packed-acid mechanism under low-humidity conditions. Additionally, the chitosan-based humidity sensor was further seamlessly integrated into an Internet of Things (IoT) framework, enabling wireless humidity monitoring and real-time data visualization on a mobile device. Comparative analysis with existing polymer-based resistive-type sensors further highlighted the superior sensing range, rapid dynamic response, and environmental sustainability of the developed sensor. This eco-friendly, biomass-derived, eco-friendly sensor shows potential for applications in environmental monitoring, smart agriculture, and industrial process control. Full article
(This article belongs to the Special Issue Humidity Sensors Based on Spectroscopy)
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<p>The sequential steps involved in extracting chitosan from mealworm shells. (<b>A</b>) Mealworms cartoon depiction. (<b>B</b>) Mealworm shells are obtained. (<b>C</b>) These flakes are finely pulverized into a powder form during pretreatment. (<b>D</b>) The purification process begins with demineralization, wherein the powder is dissolved in acetic acid solution to remove minerals present in the biomass. (<b>E</b>) Deproteinization is carried out using an alkali digestion method, wherein a sodium hydroxide solution is employed to remove protein content from the material. The proteins are associated with the chitin structure through glycosidic bonds. (<b>F</b>) This step isolates chitin as the primary product. (<b>G</b>) Chitosan is then derived from chitin via a deacetylation process, which involves treating chitin with a concentrated sodium hydroxide solution. During this reaction, the N-acetyl groups within the chitin are transformed into amino groups, yielding chitosan. (<b>H</b>) The resulting chitosan is subsequently cast onto a petri dish for further use. Digital photos of the resulting chitosan film are shown above along with the obtained mealworm shells (biomass), the extracted chitin, and the synthesized chitosan (far right).</p>
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<p>Step-by-step procedure for fabricating the biomass-derived chitosan-based humidity sensor. (<b>A</b>) The biomass-derived chitosan film serves as the primary sensing material. (<b>B</b>) Copper tape is affixed to the chitosan film, and an interdigitated electrode (IDE) pattern is precisely cut. (<b>C</b>) Polyvinyl alcohol (PVA) solution is drop-cast onto the chitosan film with the IDE pattern, (<b>D</b>) resulting in the formation of the laminate composite chitosan-based humidity sensor. (<b>E</b>) Dimensions of the developed sensor are shown, along with (<b>F</b>) a digital photograph displaying the front and back views of the final humidity sensor assembly.</p>
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<p>Schematic representation of the experimental setup for evaluating humidity-sensing performance. (<b>A</b>) Controlled relative humidity (RH) levels are established using saturated salt solutions placed in sealed containers to create stable testing environments. (<b>B</b>) A Keithley source meter is utilized to apply voltage and measure the resistance of the chitosan-based humidity sensor in real-time. (<b>C</b>) Data acquisition and analysis are conducted via a connected PC, enabling continuous monitoring of sensor responses. (<b>D</b>) Sample data showing resistance change over time as humidity varies.</p>
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<p>Molecular dynamics simulation illustrating the structural evolution of solvated chitosan. (<b>A</b>) The modeled chitin structure with a composition of four units of β-1,4-linked N-acetylglucosamine along with a methyl ester saturation. The carbon (C) atoms are denoted in green, oxygen (O) atoms in red, hydrogen (H) atoms in white, and nitrogen (N) atoms in blue. (<b>B</b>) The transformation of chitin to chitosan during the deacetylation process, depicted by the removal of N-acetyl groups, reveals the emergence of amino groups critical for humidity-sensing applications. (<b>C</b>) A snapshot of the simulation cell. Notably, the resulting chitosan structure is entirely solvated by water molecules within a cubic box, with a designated offset of 10 Å to ensure comprehensive solvation. This solvation process incorporates a total of 2626 water molecules to fully immerse the chitosan structure, as depicted in the simulation snapshot.</p>
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<p>Comprehensive characterization of the fabricated chitosan film. (<b>A</b>) Fourier-transform infrared (FTIR) spectroscopy analysis elucidates the chemical structure and composition of the biomass-derived chitosan. (<b>B</b>) Contact angle measurement shows a contact angle of 84 ± 1.58°, indicating moderate wettability. (<b>C</b>) Stress–strain analysis demonstrates the mechanical robustness of the film, with an ultimate tensile strength (UTS) of 39.92 MPa and an elongation at break (EAB) of 17.49%, reflecting a balance of strength and flexibility. (<b>D</b>) Flexibility assessment of the film through deformation tests, demonstrating its ability to bend and fold without structural failure.</p>
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<p>Performance evaluation of the chitosan-based humidity sensor. (<b>A</b>) Dynamic response of the chitosan-based humidity sensor to varying relative humidity levels. The graph depicts the resistance of the sensor as a function of time, showcasing its real-time adaptability as the humidity transitions from 6% to 97%. This temporal profile highlights the sensor’s ability to dynamically adjust its resistance based on moisture adsorption and desorption processes, a key attribute for applications requiring continuous monitoring of environmental humidity. (<b>B</b>) Response and recovery characteristics, with an average response time of 18.22 s and an average recovery time of 22.39 s, showcasing fast adsorption and desorption rates. (<b>C</b>) Hysteresis analysis of the sensor, quantified at 9.04% at 53% RH, confirmed the sensor’s reliability in responding to RH changes. (<b>D</b>) A linear decrease in resistance with increasing RH shows a strong correlation with a high R<sup>2</sup> value. (<b>E</b>) Sensor response (Ro/Rx) as a function of RH, with a high correlation coefficient (R<sup>2</sup> = 0.98), indicating reliable linear performance. (<b>F</b>) Reproducibility and reversibility assessment, illustrating the sensor’s consistent response across multiple cycles and RH levels, demonstrates its stability for long-term application.</p>
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<p>Statistical analysis, selectivity, and IoT demonstration of the biomass-derived chitosan-based humidity sensor. (<b>A</b>) Statistical analysis displaying standard deviation (SD) and standard error of the mean (SEM) for resistance measurements across varying relative humidity levels (6% to 97% RH). The low SD and SEM values indicate consistent performance with minimal variability, underscoring the reliability and stability of the developed sensor. (<b>B</b>) Response of the chitosan-based humidity sensor to various volatile organic compounds (VOCs)—acetone, ethanol, isopropanol, and methanol—highlighting the sensor’s high selectivity towards water vapor with minimal interference from VOCs.</p>
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<p>Humidity-sensing mechanism and molecular interaction in the chitosan-based humidity sensor. (<b>A</b>) Schematic representation of the humidity-sensing mechanism, detailing the interaction between chitosan and water molecules. The illustration highlights the primary and secondary layers of water molecule adsorption, the formation of hydrogen bonds, proton hopping, and unreacted molecules of water. (<b>B</b>) The impact of humidity levels on the developed chitosan-based humidity sensor. In high-humidity conditions, the sensing material interacts with a significant number of water molecules, whereas in low-humidity conditions, the interaction is minimal. (<b>C</b>) Presents a plot of the energy evolution during the simulated chitosan solvation process, demonstrating successful equilibration and a constant energy state throughout the simulated timesteps. (<b>D</b>) The plot of the quantity of hydrogen bonds formed between the structure of chitosan and the water molecules over the simulated timesteps, with an average of 17 hydrogen bonds observed. (<b>E</b>) The solvent-accessible surface area, with an indicated average of 99 nm<sup>2</sup>.</p>
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<p>IoT-enabled system setup and real-time monitoring interface for the chitosan-based humidity sensor. (<b>A</b>) Schematic of the IoT configuration including the input voltage, resistor, ADC, microcontroller, and Wi-Fi module, enabling the sensor’s integration within an IoT framework. (<b>B</b>) Digital photograph of the hardware interface including the chitosan-based humidity sensor, ESP32 microcontroller, and humidifier (left) (model G15 USB Humidifier, Dongguan Leang Electronics Co., Ltd., Dongguan, China). Remote monitoring dashboard on Adafruit IO, displaying RH readings as a percentage gauge and visual indicator, showcasing the sensor’s responsiveness to environmental humidity levels and suitability for real-time IoT applications (right).</p>
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24 pages, 2364 KiB  
Article
Characterization of Cantal and Salers Protected Designation of Origin Cheeses Based on Sensory Analysis, Physicochemical Characteristics and Volatile Compounds
by Cécile Bord, Louis Lenoir, Julie Benoit, Delphine Guérinon, Gilles Dechambre, Christophe Chassard and Christian Coelho
Appl. Sci. 2025, 15(2), 961; https://doi.org/10.3390/app15020961 - 19 Jan 2025
Viewed by 413
Abstract
In this work, the aim was to characterize and differentiate two Protected Designation of Origin (PDO) semi-hard French cheese categories (Salers and Cantal cheeses) by focusing on their sensory, biochemical and volatile characteristics. A total of twelve cheeses, including six Cantal and six [...] Read more.
In this work, the aim was to characterize and differentiate two Protected Designation of Origin (PDO) semi-hard French cheese categories (Salers and Cantal cheeses) by focusing on their sensory, biochemical and volatile characteristics. A total of twelve cheeses, including six Cantal and six Salers cheeses, were analyzed. The provenance of milk from two dairy cow breeds (Salers and non-Salers) was discussed sensorially and chemically for each cheese sample and for each cheese category. Despite very few significant differences in biochemical parameters, differences were observed concerning the volatile composition and sensory profiles between each cheese category. Salers cheeses were clearly differentiated by their appearance and their more intense aromatic characteristics compared to Cantal cheeses. A large number of volatile compounds (VOCs) belonging to acids, alcohols, aldehydes, ketones and esters were detected in each cheese category (n = 78). The relative quantity of each compound varied depending on the cheese category but was lowly impacted by the origin of the breed’s milk. The results suggest that the provenance of milk (Salers vs. non-Salers) have a low impact on the chemical and sensory differentiation of cheeses regardless of the PDO cheese category. However, the PDO cheese categories (Salers vs. Cantal) were clearly differentiated by their volatile and sensory characteristics. The PDO Salers cheeses presented the highest flavor variability compared to the PDO Cantal cheeses due to compounds belonging to alcohols, acids, aldehydes and ester conferring ammonia, vegetal and animal flavors compared to the PDO Cantal cheeses that were perceived as more pungent and bitter. Full article
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<p>Average percentages of classes of volatile compounds identified for each condition of cheese category: (<b>A</b>) Cantal cheeses vs. (<b>B</b>) Salers cheeses and cow breeds’ milk: (<b>C</b>) OB_M vs. (<b>D</b>) Salers_M (OB_M = other breeds’ milk; Salers_M = <span class="html-italic">Salers</span> milk).</p>
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<p>A principal component analysis performed on the volatile compounds and on the cheese samples (<span class="html-italic">n</span> = 24). A correlation circle from the PCA (F1-F2) realized on volatile compounds was used as the loading for the PCA (<b>A</b>). Score plots or cheese sample variables were represented with the 95% confidence ellipse for each milk’s origin (<b>B</b>) and cheese category (<b>C</b>) (OB_M = other breeds’ milk; Salers_M = <span class="html-italic">Salers</span> milk).</p>
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<p>Principal component analysis performed on sensory data and on cheese samples (<span class="html-italic">n</span> = 36). Correlation circle from PCA (F1–F2) performed on significant sensory attributes used as loadings of PCA (<b>A</b>). Score plots or cheese sample variables were represented with 95% confidence ellipse for each milk’s origin (<b>B</b>) and cheese category (<b>C</b>) (OB_M = other breeds’ milk; Salers_M = <span class="html-italic">Salers</span> milk).</p>
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<p>Principal component analysis performed on sensory data and on cheese samples (<span class="html-italic">n</span> = 36). Correlation circle from PCA (F1–F2) performed on significant sensory attributes used as loadings of PCA (<b>A</b>). Score plots or cheese sample variables were represented with 95% confidence ellipse for each milk’s origin (<b>B</b>) and cheese category (<b>C</b>) (OB_M = other breeds’ milk; Salers_M = <span class="html-italic">Salers</span> milk).</p>
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<p>Partial least squares regression loading for t1 and t2 performed on significant volatile compounds (X; <span class="html-italic">n</span> = 45; red point) and sensory flavor attributes (Y; <span class="html-italic">n</span> = 11; blue point) and cheese samples (green capital letters, <span class="html-italic">n</span> = 12). Blue circle includes samples from Salers category and orange circle includes samples from Cantal category. Number for variables (VOCs) refers to opposite table.</p>
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24 pages, 5932 KiB  
Article
Evaluation of Cinnamon Essential Oil and Its Emulsion on Biofilm-Associated Components of Acinetobacter baumannii Clinical Strains
by Tea Ganić, Ilinka Pećinar, Biljana Nikolić, Dušan Kekić, Nina Tomić, Stefana Cvetković, Stefana Vuletić and Dragana Mitić-Ćulafić
Antibiotics 2025, 14(1), 106; https://doi.org/10.3390/antibiotics14010106 - 19 Jan 2025
Viewed by 527
Abstract
Background/Objectives: Acinetobacter baumannii, one of the most dangerous pathogens, is able to form biofilm structures and aggravate its treatment. For that reason, new antibiofilm agents are in need, and new sources of antibiofilm compounds are being sought from plants and their products. [...] Read more.
Background/Objectives: Acinetobacter baumannii, one of the most dangerous pathogens, is able to form biofilm structures and aggravate its treatment. For that reason, new antibiofilm agents are in need, and new sources of antibiofilm compounds are being sought from plants and their products. Cinnamon essential oil is associated with a wide spectrum of biological activities, but with a further improvement of its physicochemical properties it could provide even better bioavailability. The aim of this work was the evaluation of the antibiofilm properties of cinnamon essential oil and its emulsion. Methods: In order to evaluate the antibiofilm activity, crystal violet assay was performed to determine biofilm biomass. The main components of the biofilm matrix were measured as well as the motile capacity of the tested strains. Gene expression was monitored with RT-qPCR, while treated biofilms were observed with Raman spectroscopy. Results: A particularly strong potential against pre-formed biofilm with a decreased biomass of up to 66% was found. The effect was monitored not only with regard to the whole biofilm biomass, but also on the individual components of the biofilm matrix such as exopolysaccharides, proteins, and eDNA molecules. Protein share drops in treated biofilms demonstrated the most consistency among strains and rose to 75%. The changes in strain motility and gene expressions were investigated after the treatments were carried out. Raman spectroscopy revealed the influence of the studied compounds on chemical bond types and the components present in the biofilm matrix of the tested strains. Conclusions: The results obtained from this research are promising regarding cinnamon essential oil and its emulsion as potential antibiofilm agents, so further investigation of their activity is encouraged for their potential use in biomedical applications. Full article
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<p>Antibiofilm activity of CEO and EM against <span class="html-italic">A. baumannii</span> clinical isolates GN 189 (<b>A</b>,<b>B</b>), GN 242 (<b>C</b>,<b>D</b>), and GN 1105 (<b>E</b>,<b>F</b>). Bolded values represent MIC concentrations. Statistical significance was estimated according to the negative control for EM or DMSO for CEO using one-way ANOVA, Dunnet’s post hoc test. The threshold was estimated to be * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of CEO and EM on the already-formed biofilm of <span class="html-italic">A. baumannii</span> clinical isolates GN 189 (<b>A</b>,<b>B</b>), GN 242 (<b>C</b>,<b>D</b>), and GN 1105 (<b>E</b>,<b>F</b>). Bolded values represent MIC concentrations. Statistical significance was estimated according to the negative control for EM or DMSO for CEO using one-way ANOVA, Dunnet’s post hoc test. The threshold was estimated to be * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Total share of exopolysaccharides isolated from the biofilm matrix of <span class="html-italic">A. baumannii</span> clinical isolates GN 189 (<b>A</b>), GN 242 (<b>B</b>), and GN 1105 (<b>C</b>). The tested concentrations of CEO and EM are the MIC values of GN 189 (0.5 mg/mL for CEO and 0.125 mg/mL for EM), GN 242 (0.25 mg/mL for CEO and 0.125 mg/mL for EM), and GN 1105 (1 mg/mL for CEO and 0.125 mg/mL for EM).The statistical significance was estimated according to the negative control for EM or DMSO for CEO, and by using one-way ANOVA, Dunnet’s post hoc test. The statistically significant threshold was * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Total share of proteins extracted from biofilm matrix <span class="html-italic">A. baumannii</span> clinical isolates GN 189 (<b>A</b>), GN 242 (<b>B</b>), and GN 1105 (<b>C</b>). The tested concentrations of CEO and EM are the MIC values of GN 189 (0.5 mg/mL for CEO and 0.125 mg/mL for EM), GN 242 (0.25 for CEO and 0.125 mg/mL), and GN 1105 (1 mg/mL for CEO and 0.125 mg/mL). Statistical significance was defined by comparing treatments with the negative control for EM or DMSO for CEO, using one-way ANOVA, Dunnet’s post hoc test. The threshold was estimated to be * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effects of CEO and EM on the motility of strains GN 189 (<b>A</b>), GN 242 (<b>B</b>), and GN 1105 (<b>C</b>). The tested concentrations of CEO and EM are the MIC of GN 189 (0.25 mg/mL for CEO and 0.062 mg/mL for EM), GN 242 (0.125 for CEO and 0.062 mg/mL), and GN 1105 (0.5 mg/mL for CEO and 0.062 mg/mL). Statistical significance was determined according to the negative control for EM or DMSO for CEO, performed using one-way Anova, Dunnet’s post hoc test, while the threshold was * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Gene expression analysis of the <span class="html-italic">A. baumannii</span> biofilm of clinical isolates GN 189 (<b>A</b>), GN 242 (<b>B</b>), and GN 1105 (<b>C</b>), treated with CEO and EM. The tested concentrations of CEO and EM are the MIC values of GN 189 (0.5 mg/mL for CEO and 0.125 mg/mL for EM), GN 242 (0.25 for CEO and 0.125 mg/mL), and GN 1105 (1 mg/mL for CEO and 0.125 mg/mL). The results are presented as the normalized gene expression. Statistical significance regarding the negative control (C in graphs) for EM and DMSO for CEO was determined using one-way ANOVA with Dunnet’s post hoc test and the threshold was * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Averages of normalized Raman spectra of the <span class="html-italic">A. baumannii</span> biofilm matrix: GN 189 (<b>A</b>), GN 242 (<b>B</b>), GN 1105 (<b>C</b>); (C—control, CEO–cinnamon essential oil, EM—cinnamon emulsion). Spectral range is from 350 to 1800 cm<sup>−1</sup>.</p>
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<p>PC analysis of score plots (<b>A</b>) and loading plots (<b>B</b>,<b>C</b>) obtained from the Raman spectra of the <span class="html-italic">A.baumannii</span> GN 189 biofilm.</p>
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<p>PC analysis score plots (<b>A</b>) and loading plots (<b>B</b>,<b>C</b>) obtained from the Raman spectra of the <span class="html-italic">A.baumannii</span> GN 242 biofilm.</p>
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<p>PC analysis score plots (<b>A</b>) and loading plots (<b>B</b>,<b>C</b>) obtained from the Raman spectra of the <span class="html-italic">A.baumannii</span> GN 1105 biofilm.</p>
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35 pages, 3573 KiB  
Review
Analytical Methods for Atmospheric Carbonyl Compounds: A Review
by Xiaoshuai Gao, Xin Zhang, Yan Nie, Jiemeng Bao, Junling Li, Rui Gao, Yunfeng Li, Wei Wei, Xiaoyu Yan, Yongxin Yan and Hong Li
Atmosphere 2025, 16(1), 107; https://doi.org/10.3390/atmos16010107 - 19 Jan 2025
Viewed by 268
Abstract
Atmospheric carbonyl compounds have significant impacts on the atmospheric environment and human health, making the selection of appropriate analytical techniques crucial for accurately detecting these compounds in specific environments. Based on extensive literature research, this study summarized the development history, relevant features, and [...] Read more.
Atmospheric carbonyl compounds have significant impacts on the atmospheric environment and human health, making the selection of appropriate analytical techniques crucial for accurately detecting these compounds in specific environments. Based on extensive literature research, this study summarized the development history, relevant features, and applicable scenarios of the main analytical techniques for atmospheric carbonyl compounds; pointed out the main problems and challenges in this field; and discussed the needs and prospects of future research and application. It was found that the direct sampling methods of atmospheric carbonyl compounds were applicable to low-molecular-weight carbonyl species with low reactivity, low boiling points, high polarity, and high volatility, while indirect sampling methods were suitable for a wider range and various types and phases of species. For formaldehyde, offline detection was primarily influenced by chemical reagents and reaction conditions, whereas online monitoring relied on sufficiently stable operating environments. For multiple carbonyl compounds, offline detection results were greatly influenced by detectors coupled with chromatography, whereas online monitoring techniques were applicable to all types of volatile organic compounds (VOCs), including some carbonyl compounds, providing higher temporal resolution and improved isomer identification with the development of online mass spectrometry. The combined use of proton transfer reaction-mass spectrometry (PTR-MS) and liquid chromatography-mass spectrometry (GC-MS) was suitable for the detection of carbonyl compounds in atmospheric photochemical smog chamber simulation studies. Currently, offline analytical techniques for carbonyl compounds require significant time and advanced experimental skills for multiple optimization experiments to detect a broader range of species. Online monitoring techniques face challenges such as poor stability and limited species coverage. In smog chamber simulation studies, the detection of carbonyl compounds is heavily influenced by both the sampling system and the chamber itself. Future efforts should focus on improving the environmental adaptability and automation of carbonyl compound analytical techniques, the synergistic use of various techniques, developing new sampling systems, and reducing the impact of the chamber itself on carbonyl compound detection, in order to enhance detection sensitivity, selectivity, time resolution, accuracy, and operability. Full article
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<p>PRISMA flow diagram.</p>
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<p>Distribution of 151 materials on analytical methods for atmospheric carbonyl compounds from the perspectives of countries and content.</p>
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<p>Development of main sampling methods for atmospheric carbonyl compounds.</p>
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<p>Development of simultaneous analytical methods for multiple atmospheric carbonyl compounds.</p>
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