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14 pages, 291 KiB  
Article
Nutritional Potential and Low Heavy Metals Content of Oryctes monoceros (Olivier, 1789) and Rhynchophorus phoenicis (Fabricius, 1801) Adults, Two Coleopteran Species Consumed in Togo
by Fègbawè Badanaro, Narcis Barsan, Mamatchi Mélila, Kamilou Ouro-Sama, Koami Améyran, Florin-Marian Nedeff, Oana Irimia and Valentin Nedeff
Appl. Sci. 2025, 15(3), 1317; https://doi.org/10.3390/app15031317 - 27 Jan 2025
Abstract
Oryctes monoceros (Olivier, 1789) (Scarabaeidae) and Rhynchophorus phoenicis (Fabricius, 1801) (Curculionidae) are two insects generally known as formidable pests of oil palms and coconuts trees. Although little known, different developmental stages of these insects are consumed. The aim of this study is to [...] Read more.
Oryctes monoceros (Olivier, 1789) (Scarabaeidae) and Rhynchophorus phoenicis (Fabricius, 1801) (Curculionidae) are two insects generally known as formidable pests of oil palms and coconuts trees. Although little known, different developmental stages of these insects are consumed. The aim of this study is to determine the composition of these adult Coleopteran species in order to promote their consumption as a strategy for enhancing food security. Chemical analyses were carried out on adults of both species. Samples of O. monoceros and R. phoenicis were collected in three localities in Togo. The ash, protein, vitamin, and lipid contents were determined according to the AOAC reference methods. The fiber contents were obtained by the method of Weende. The minerals and heavy metals were analyzed by atomic absorption spectrophotometry and colorimetry. Fatty acid composition was determined by gas chromatography. The results showed the average protein content ranges from 44.32 ± 0.83 to 45.89 ± 0.83%. The lipid level is between 15.06 ± 0.28% and 14.64 ± 0.54. Their lipids contain unsaturated fatty acids, notably oleic (40.84 ± 0.112 vs. 40.84 ± 0.11%), linoleic (4.49 ± 0.00 vs. 5.07 ± 0.02%), and α-linolenic (5.07 ± 0.02 vs. 6.35 ± 0.01%) acid. They are excellent sources of minerals and vitamins. They are also free of heavy metals. These species could, therefore, contribute to the nutritional balance of consumers. They deserve to be better promoted for human consumption, as they could make a significant contribution to the fight against malnutrition and constitute a novel food source. Full article
18 pages, 3629 KiB  
Article
Isolation, In Vitro Antioxidant Capacity, Hypoglycemic Activity and Immunoactivity Evaluation of Polysaccharides from Coriandrum sativum L.
by Weiwei Jin, Huan Zhou, Haijun Zhao, Yue Pei, Fengxian Su, Yan Li and Tao Luo
Antioxidants 2025, 14(2), 149; https://doi.org/10.3390/antiox14020149 - 27 Jan 2025
Abstract
Coriander (Coriandrum sativum) is a classical medicinal and edible herb as well as a spice, but the physicochemical and biological properties of its polysaccharides have not been fully studied. In this study, the polysaccharides were extracted using an ultrasonic-assisted method and [...] Read more.
Coriander (Coriandrum sativum) is a classical medicinal and edible herb as well as a spice, but the physicochemical and biological properties of its polysaccharides have not been fully studied. In this study, the polysaccharides were extracted using an ultrasonic-assisted method and purified from fresh coriander, and then the coriander polysaccharide (CSP) fraction was separated using an agarose gel Q-Sepharose Fast Flow column. The total sugar content, protein content and monosaccharides composition of CSPs were determined using a phenol–sulfuric acid method, Coomassie Brilliant Blue method and HPLC. The structural characterization was detected using ultraviolet spectrophotometry and FT-IR spectroscopy. DPPH and ABTS free radicals were used to explore their antioxidant activities, while the inhibitory abilities of α-amylase and α-glucosidase were used to evaluate their hypoglycemic activity. After that, the immunomodulatory and antitumor activities were investigated using macrophage RAW264.7 and HepG2 cells as the targets. The results showed that the total sugar and protein contents of CSPs were 66.90 ± 1.44% and 1.06 ± 0.32%, respectively. CSPs were mainly composed of fucose, rhamnose, arabinose, galactose, glucose, galacturonic acid and glucuronic acid, with a molar ratio of 1.13:15.11:9.60:25.98:1.55:44.33:2.29, and may be an acidic heteropolysaccharide containing pyran rings, α- and β-glycosidic bonds and glucuronic acid. Results from in vitro experiments of biological activities showed that the IC50 of CSPs for scavenging DPPH and ABTS free radicals were 0.759 mg/mL and 1.758 mg/mL, respectively; the IC50 values for inhibiting the activities of α-amylase and α-glucosidase were 0.634 mg/mL and 2.178 mg/mL, respectively; the CSPs with a concentration of 25~200 μg/mL showed no obvious toxicity to macrophage RAW264.7, and when treated with 100 μg/mL of CSPs, the relative cell phagocytosis capacity and secreted nitric oxide amount of RAW264.7 were 153.75 ± 12.01% and 133.56 ± 5.37%, respectively; CSPs showed a concentration-dependent ability to inhibit the growth of HepG2 cells within the test concentration of 0.25–2.0 mg/mL. Summarizing the results, due to their excellent antioxidant, immunomodulatory and anti-tumor activities, the coriander acid polysaccharides were expected to show good potential in comprehensive development of food and medicine. Full article
(This article belongs to the Special Issue Plant Materials and Their Antioxidant Potential, 2nd Edition)
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Figure 1

Figure 1
<p>Q Sepharose <sup>TM</sup> Fast Flow elution curve of coriander polysaccharides.</p>
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<p>UV–visible spectrum of CSPs.</p>
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<p>FT-IR spectroscopy of CSPs.</p>
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<p>Ion chromatograms of standard monosaccharides (<b>A</b>) and CSPs (<b>B</b>).</p>
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<p>In vitro DPPH and ABTS antioxidant activity of CSPs. Vc was used as a positive control. Different lowercase letters represent significant difference at 0.05 level.</p>
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<p>In vitro hypoglycemic activity of CSPs. Acarbose was used as a reference. Different lowercase letters represent significant difference at 0.05 level.</p>
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<p>Effects of CSPs on RAW264.7 cytotoxicity. Compared with the control group, *** represents <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effects of CSPs on phagocytosis of RAW264.7 cells. Compared with the negative control group, * represents <span class="html-italic">p</span> &lt; 0.05 and *** represents <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effects of CSPs on NO secretion in RAW264.7 cells. Compared with the blank control group, * represents <span class="html-italic">p</span> &lt; 0.05, ** represents <span class="html-italic">p</span> &lt; 0.01, and *** represents <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effects of CSPs on proliferation of HepG2 cells. Compared with the control group, * represents <span class="html-italic">p</span> &lt; 0.05 and *** represents <span class="html-italic">p</span> &lt; 0.001.</p>
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13 pages, 1053 KiB  
Article
Investigation on the Interaction of Dendritic Core Multi-Shell Nanoparticles with Human Red Blood Cells
by Jakob Krauß, Radostina Georgieva, Miroslav Karabaliev, Moritz Hackmann, Pichayut Rerkshanandana, Saranya Chaiwaree, Ulrich Kalus, Axel Pruß, Yu Xiong and Hans Bäumler
Nanomaterials 2025, 15(3), 187; https://doi.org/10.3390/nano15030187 - 24 Jan 2025
Viewed by 253
Abstract
The use of nanoparticles is becoming increasingly apparent in a growing number of medical fields. To exploit the full potential of these particles, it is essential to examine their behavior in the blood and their possible interactions with blood cells. Dendritic core multi-shell [...] Read more.
The use of nanoparticles is becoming increasingly apparent in a growing number of medical fields. To exploit the full potential of these particles, it is essential to examine their behavior in the blood and their possible interactions with blood cells. Dendritic core multi-shell DendroSol™ nanoparticles (DS-NPs) are able to penetrate into viable layers of human skin, but nothing is known about their interaction with blood cells. In the present study, we analyze the effect of DS-NPs on red blood cells (RBCs) using confocal laser scanning microscopy (CLSM), flow cytometry, sedimentation rate analysis, spectrophotometry, and hemolysis assays. DS-NPs labeled with Nile red (NR) were added to RBC suspensions and their accumulation in the area of the RBC membranes was demonstrated by CLSM as well as by flow cytometry. In the presence of DS-NPs, the RBCs show an increased sedimentation rate, which also confirms the binding of the NPs to the cells. Interestingly, in the presence of DS-NPs, the RBCs are stabilized against hypotonic hemolysis as well as against the hemolytic action of Triton X-100. This proven anti-hemolytic effect could be utilized to enhance the circulation time of RBCs loaded with drugs for prolonged sustained release and drug delivery with enhanced bioavailability. Full article
(This article belongs to the Section Biology and Medicines)
19 pages, 1450 KiB  
Article
Infrared Laser-Assisted Extraction of Bioactive Compounds from Rosa canina L.
by Andreia Alecu, Camelia Albu, Georgiana-Ileana Badea, Aurelia Alionte, Alin-Alexandru Enache, Gabriel-Lucian Radu and Simona-Carmen Litescu
Int. J. Mol. Sci. 2025, 26(3), 992; https://doi.org/10.3390/ijms26030992 - 24 Jan 2025
Viewed by 251
Abstract
The extraction of bio-compounds from medicinal plants provides opportunities for using the plant extract for health benefits. Rosa canina L. is considered a “natural superfood”, and the valorization of its active compounds requires an extraction technique that ensures a suitable extraction yield while [...] Read more.
The extraction of bio-compounds from medicinal plants provides opportunities for using the plant extract for health benefits. Rosa canina L. is considered a “natural superfood”, and the valorization of its active compounds requires an extraction technique that ensures a suitable extraction yield while preserving the compounds’ activity. In our study, infrared laser irradiation (IRLIR) technology was used for the first time in the bioactive compound’s extraction from Rosa canina L. Different solvents (water–ethanol, hexane–ethanol) and different extraction times were tested to obtain a high extraction yield. Chromatographic and spectrophotometry methods were used to monitor the profile of bioactive compounds and the antioxidant activity of the extracts. The results obtained for IRLIR were compared with those obtained by accelerated solvent extraction (ASE), an advanced extraction method. The IRLIR technology proved to be a more reliable analytical tool for the extraction of (+)-catechin, gallic acid, and lutein. In addition, a richer extract formula was obtained by IRLIR extraction with respect to ASE, with the IRLIR process ensuring a short extraction time, low volume of the extraction solvent, low energy consumption, and a less expensive device. Full article
(This article belongs to the Section Bioactives and Nutraceuticals)
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Graphical abstract

Graphical abstract
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<p>Chromatograms obtained for <span class="html-italic">Rosa canina</span> L. extract after IRLIRE in 80% ethanol (1—gallic acid, [M − H]<sup>−</sup> 169; 2—chlorogenic acid, [M − H]- 353; 3—(+)-catechin, [M − H]- 289; 4—rutin, [M − H]- 609; 5—ellagic acid, [M-H]- 301; 6—quercetin 3-β-D-glucoside, [M − H]- 463; 7—quercitrin, [M − H]- 447; 8—quercetin, [M − H]- 301) by HPLC-MS.</p>
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<p>Chromatograms obtained for <span class="html-italic">Rosa canina</span> L. lipophilic extract after IRLIRE in ethanol–hexane mixture (1—lycopene; 2—lutein; 3—β-carotene; 4—α tocopherol) by HPLC-DAD.</p>
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<p>The antioxidant capacity of standard polyphenolic compounds in 20% ethanol.</p>
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14 pages, 2926 KiB  
Article
Portable Cell Tracking Velocimetry for Quantification of Intracellular Fe Concentration of Blood Cells
by Linh Nguyen T. Tran, Karla Mercedes Paz Gonzalez, Hyeon Choe, Xian Wu, Jacob Strayer, Poornima Ramesh Iyer, Maciej Zborowski, Jeffrey Chalmers and Jenifer Gomez-Pastora
Micromachines 2025, 16(2), 126; https://doi.org/10.3390/mi16020126 - 23 Jan 2025
Viewed by 312
Abstract
Hematological analysis is crucial for diagnosing and monitoring blood-related disorders. Nevertheless, conventional hematology analyzers remain confined to laboratory settings due to their high cost, substantial space requirements, and maintenance needs. Herein, we present a portable cell tracking velocimetry (CTV) device for the precise [...] Read more.
Hematological analysis is crucial for diagnosing and monitoring blood-related disorders. Nevertheless, conventional hematology analyzers remain confined to laboratory settings due to their high cost, substantial space requirements, and maintenance needs. Herein, we present a portable cell tracking velocimetry (CTV) device for the precise measurement of the magnetic susceptibility of biological entities at the single-cell level, focusing on red blood cells (RBCs) in this work. The system integrates a microfluidic channel positioned between permanent magnets that generate a well-defined magnetic field gradient (191.82 TA/mm2). When the cells are injected into the chamber, their particular response to the magnetic field is recorded and used to estimate their properties and quantify their intracellular hemoglobin (Hb) concentration. We successfully track over 400 RBCs per condition using imaging and trajectory analysis, enabling detailed characterizations of their physical and magnetic properties. A comparison of the mean corpuscular hemoglobin measurements revealed a strong correlation between our CTV system and standard ultraviolet–visible (UV-Vis) spectrophotometry (23.1 ± 5.8 pg vs. 22.4 ± 3.9 pg, p > 0.05), validating the accuracy of our measurements. The system’s single-cell resolution reveals population distributions unobtainable through conventional bulk analysis methods. Thus, this portable CTV technology provides a rapid, label-free approach for magnetic cell characterization, offering new possibilities for point-of-care hematological analysis and field-based research applications. Full article
(This article belongs to the Special Issue Research Progress of Microfluidic Bioseparation and Bioassay)
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Figure 1

Figure 1
<p>Schematic diagram of the CTV system showing the optical setup, measurement chamber dimensions, and sample trajectory analysis. Magnets are located inside the measurement chamber and an onset is provided along with the magnetic field intensity in the measurement area.</p>
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<p>Representative particle trajectories of polystyrene beads in MnCl<sub>2</sub> solutions at different concentrations: (<b>A</b>) 0.025 M, (<b>B</b>) 0.05 M, and (<b>C</b>) 0.075 M.</p>
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<p>COMSOL-simulated magnetic energy gradient. The red rectangle in the channel presents the ROI used for tracing the particles in our experiments.</p>
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<p>Representative cell trajectories of (<b>A</b>) oxyhemoglobin-containing RBCs and (<b>B</b>) methemoglobin-containing RBCs inside the CTV device. Note the different trajectories of both cell types, with the non-magnetic (diamagnetic) oxyhemoglobin cells moving only downwards due to gravity and with the paramagnetic metHb-RBCs moving in both directions (horizontally and vertically) due to the effect of the magnetic and gravitational fields.</p>
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<p>Distribution plots showing the relationship between MCH content (pg of Hb per cell), magnetically induced velocity (mm/s), and settling velocity (mm/s) measured from a representative RBC sample. Top panel: MCH distribution with cumulative frequency. Bottom panels: scatter plot of settling velocity versus magnetically induced velocity (<b>left</b>) and corresponding settling velocity distribution (<b>right</b>).</p>
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<p>MCH content analysis by CTV and UV–Vis spectrophotometry. (<b>A</b>) Individual MCH values across donors HD1–HD4. (<b>B</b>) Statistical comparison of mean MCH values (pg) between methods. Error bars represent standard deviation; ns: not significant (paired <span class="html-italic">t</span>-test, <span class="html-italic">p</span> &gt; 0.05).</p>
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11 pages, 3311 KiB  
Article
Simple and Robust Approach for Determination of Total Protein Content in Plant Samples
by Yulia S. Vershinina, Ilya V. Mitin, Andrey V. Garmay, Gleb K. Sugakov and Irina A. Veselova
Foods 2025, 14(3), 358; https://doi.org/10.3390/foods14030358 - 22 Jan 2025
Viewed by 461
Abstract
The determination of total protein in plant samples is a difficult task, as classical nitrogen-based methods are not selective for the nature of nitrogen, and the results of biochemical methods are influenced by both associated compounds and the complex composition of the protein [...] Read more.
The determination of total protein in plant samples is a difficult task, as classical nitrogen-based methods are not selective for the nature of nitrogen, and the results of biochemical methods are influenced by both associated compounds and the complex composition of the protein matrix. Using electrophoretic separation of three commercial sunflower protein samples, it was determined that the studied proteins are a mixture of salt-soluble globulins and water-soluble albumins of different molecular weights. The total protein content of the studied samples was determined using five spectrophotometric methods: direct spectrophotometry, bicinchoninic acid assay, and Benedict’s, Bradford’s, and Lowry’s methods. After comparing the results obtained, it was concluded that, for the determination of protein in these plant materials, the use of the Dumas nitrogen-based method in tandem with Lowry’s spectrophotometric method is the most suitable. Full article
(This article belongs to the Section Plant Foods)
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Figure 1

Figure 1
<p>SDS-PAGE electrophoresis of soluble (SF) and insoluble (IF) fractions of three commercial SMP samples.</p>
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<p>UV spectra of (<b>a</b>) standard solution of BSA (200 μg/mL) and (<b>b</b>) tested solutions of three commercial SMP samples.</p>
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<p>(<b>a</b>) UV spectra of the free and bound forms of the dye; (<b>b</b>) calibration curve for the Bradford’s method.</p>
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<p>Calibration curve for the (<b>a</b>) Benedict’s method, (<b>b</b>) BCA method, and (<b>c</b>) Lowry’s method.</p>
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23 pages, 8886 KiB  
Article
Multicore, SDS-Based Polyelectrolyte Nanocapsules as Novel Nanocarriers for Paclitaxel to Reduce Cardiotoxicity by Protecting the Mitochondria
by Marzena Szwed, Anastazja Poczta-Krawczyk, Katarzyna D. Kania, Kacper Wiktorowski, Kamila Podsiadło, Agnieszka Marczak and Krzysztof Szczepanowicz
Int. J. Mol. Sci. 2025, 26(3), 901; https://doi.org/10.3390/ijms26030901 - 22 Jan 2025
Viewed by 406
Abstract
The clinical application of paclitaxel (PTX), a widely used anticancer drug, is constrained by cardiac arrhythmias and disruptions in vascular homeostasis. To mitigate the non-specific, high toxicity of PTX towards cardiomyocytes, we propose the application of newly synthesized SDS-based polyelectrolyte multicore nanocapsules. This [...] Read more.
The clinical application of paclitaxel (PTX), a widely used anticancer drug, is constrained by cardiac arrhythmias and disruptions in vascular homeostasis. To mitigate the non-specific, high toxicity of PTX towards cardiomyocytes, we propose the application of newly synthesized SDS-based polyelectrolyte multicore nanocapsules. This study aims to verify the hypothesis that SDS-based NCs can mitigate the cytotoxic effects of PTX on cardiac cells and serve as effective nanocarriers for this drug. We investigated two types of multicore NCs with differing polyelectrolyte coatings: poly-L-lysine (PLL) and a combination of PLL with poly-L-glutamic acid (PGA). The cytotoxicity of the formulated nanosystems was evaluated using HL-1 cardiomyocytes. Oxygraphy, flow cytometry, spectrophotometry, spectrofluorimetry, fluorescence microscopy, and RT-PCR were employed to assess disruptions in cardiac cellular homeostasis. Our data revealed that, among the tested NCs, SDS/PLL/PGA/PTX exhibited reduced cardiotoxicity and were better tolerated by HL−1 cardiomyocytes compared to SDS/PLL/PTX or PTX alone. In addition, SDS/PLL/PGA/PTX showed a marginal disruption of mitochondria’s homeostasis, and no changes in APT level and intracellular calcium concentrations were observed. These findings underscore the potential of SDS-based multicore nanocarriers in anticancer therapy, particularly due to diminished cardiotoxicity and long-term stability in the biological fluids. Full article
(This article belongs to the Special Issue Mitochondrial Respiration and Energy Metabolism in Cancer Cells)
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Figure 1
<p>Schematic illustration of SDS-based nanocarriers and their physicochemical properties. (<b>A</b>) Structural representation of empty and PTX-loaded SDS-based NCs along with the key components of the nanocarriers. (<b>B</b>) Representative data for diameter, polydispersity index (PDI), and zeta potential of the NCs together with the exemplary diameter size distribution histograms.</p>
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<p>Cytotoxic effects of SDS/PLL and SDS/PLL/PGA nanocapsules (with and without PTX) on HL-1 cardiac cells. (<b>A</b>) Cell viability of HL-1 cardiomyocytes after exposure to empty SDS-based NCs for up to 72 h, assessed using the Alamar Blue assay (<b>left</b> panel) and the MTT test (<b>right</b> panel). (<b>B</b>) Dose-dependent cytotoxicity of SDS/PLL/PTX, SDS/PLL/PGA/PTX, and free PTX following 72 h of treatment, evaluated using the Alamar Blue assay (<b>left</b> panel) and the MTT test (<b>right</b> panel). Results are expressed as percentages relative to untreated control cells and are presented as mean values ± SD from four independent experiments. (<b>C</b>) IC<sub>50</sub> values for free PTX, SDS/PLL/PTX, and SDS/PLL/PGA/PTX in HL-1 cells, calculated from cell viability curves.</p>
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<p>Morphological changes in HL-1 cells induced by PTX and SDS-based NCs. Inverted phase-contrast microscopy images of HL-1 cells treated for 48 h with IC<sub>50</sub> concentrations of SDS/PLL, SDS/PLL/PGA, free PTX, SDS/PLL/PTX, or SDS/PLL/PGA/PTX. The scale bar represents 50 µm. Black arrows indicate clumped and shrunken cells. Magnification: 100×. The photos were acquired using inverted microscope equipped with digital camera (Olympus IX70, Tokyo, Japan).</p>
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<p>DNA and ATP synthesis alterations in HL-1 cells treated with free PTX or PTX encapsulated in SDS-based NCs. Data are presented as a mean ± SD from four independent experiments. All values are normalized to untreated control cells (set at 100%). +++ <span class="html-italic">p</span> &lt; 0.001 indicates statistically significant differences between treatments PTX or SDS/PLL/PTX, SDS/PLL/PGA/PTX-treated cells, and ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 denotes significant differences between SDS/PLL/PTX and SDS/PLL/PGA/PTX treatments (<b>A</b>) Cellular ATP levels in HL-1 cardiomyocytes treated with IC<sub>50</sub> concentrations of PTX alone, SDS/PLL/PTX, or SDS/PLL/PGA/PTX for 24, 48, and 72 h. (<b>B</b>) DNA content in HL-1 cell cultures after treatment with SDS/PLL/PTX, SDS/PLL/PGA/PTX, or free PTX (IC<sub>50</sub> concentrations) for 24, 48, and 72 h. DNA levels were quantified via Hoechst 33258 staining of permeabilized cells, with fluorescence measured at excitation 355 nm and emission 460 nm. Fluorescence from untreated control cells was set at 100%.</p>
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<p>Effects of PTX and the drug trapped in SDS-based NCs on intracellular Ca<sup>2+</sup> levels in HL-1 cells. (<b>A</b>) Intensity of Fluo-4 Direct™ fluorescence was measured to evaluate cytosolic Ca<sup>2+</sup> levels. Fluorescence intensity in control cells was set at 100%. Data represent the mean ± SD of four independent experiments. *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01 indicates significant differences compared to control cells; ++ <span class="html-italic">p</span> &lt; 0.01 denotes differences between treatments PTX or SDS/PLL/PTX, SDS/PLL/PGA/PTX-treated cells; ## <span class="html-italic">p</span> &lt; 0.01 highlights differences between the SDS/PLL/PTX and SDS/PLL/PGA/PTX treatments. (<b>B</b>) Fluorescence microscopy images of HL-1 cells stained with Fluo-4 Direct™ probe after 24 h of treatment with PTX, SDS/PLL/PTX, or SDS/PLL/PGA/PTX. Images were captured using an Olympus IX70 inverted fluorescence microscope (Olympus, Tokyo, Japan) at 400× magnification. The scale bar represents 50 µm.</p>
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<p>The impact of free PTX and PTX encapsulated in SDS-based nanocarriers on mitochondrial membrane potential in HL-1 Cells. (<b>A</b>) Mitochondrial membrane potential in HL-1 cells was assessed at 24, 48, and 72 h of treatment with the investigated anticancer compounds, using the JC-1 assay. The fluorescence ratio of JC-1 dimers to JC-1 monomers in control cells was set at 100%. Data are expressed as a mean ± SD from four independent experiments, normalized to control fluorescence. Statistical significance relative to control cells is indicated as * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001, while ++ <span class="html-italic">p</span> &lt; 0.01, +++ <span class="html-italic">p</span> &lt; 0.001 denote significant differences between free PTX and encapsulated PTX formulations. Additionally, ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 indicate significant differences between SDS/PLL/PTX and SDS/PLL/PGA/PTX-treated samples. (<b>B</b>) Representative fluorescence microscopy images of control cells treated with PBS and cells exposed to PTX-loaded nanocarriers at IC<sub>50</sub> concentrations. Red fluorescence of JC-1 dimers indicates areas of high mitochondrial membrane potential, whereas green fluorescence of JC-1 monomers reflects areas of low mitochondrial membrane potential. Images were acquired using an Olympus IX70 inverted fluorescence microscope (Olympus, Tokyo, Japan) at 400× magnification.</p>
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<p>mRNA expression alterations of genes associated with apoptosis and cardiomyocytes function in HL-1 cells treated with SDS-based PTX nanocarriers and free PTX. The expression of Bax, Bcl-2, Bcl-xl, Myl2, and Actc1 was analyzed in HL-1 cardiomyocytes treated with SDS/PLL/PTX, SDS/PLL/PGA/PTX, or free PTX (at IC<sub>50</sub> concentrations) for 48 h. Gene expression was quantified using average Ct values normalized to the housekeeping genes <span class="html-italic">β-actin</span> and <span class="html-italic">Gapdh</span>. Data were standardized to mRNA levels in untreated control cells, which were set to 1. Results are presented as a mean ± SD (<span class="html-italic">n</span> = 4). Statistically significant differences in gene expression between drug-treated and control cells are indicated as *** <span class="html-italic">p</span> &lt; 0.001, while ++ <span class="html-italic">p</span> &lt; 0.01, +++ <span class="html-italic">p</span> &lt; 0.001 highlight significant differences between SDS/PLL/PTX, SDS/PLL/PGA/PTX, and free PTX-treated cells. Differences between SDS/PLL/PTX and SDS/PLL/PGA/PTX-treated samples are shown as # <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Differential effects of PTX and PTX encapsulated in SDS-based nanocarriers on mitochondrial function in HL-1 cells. (<b>A</b>) Mitochondrial respiration in HL-1 cardiomyocytes was evaluated following 72 h of treatment with IC<sub>50</sub> concentrations of PTX, SDS/PLL/PTX, or SDS/PLL/PGA/PTX. Data are presented as the median oxygen consumption rate (pmol O<sub>2</sub>/s/1 × 10⁶ cells) measured in permeabilized cells. Parameters assessed include routine respiration, state 3 respiration, state D respiration, and electron transfer system (ETS) capacity. Significant differences relative to control of untreated cells are marked as * <span class="html-italic">p</span> &lt; 0.05, while + <span class="html-italic">p</span> &lt; 0.05 denotes differences between free PTX and SDS-based NCs. Comparisons between SDS/PLL/PTX and SDS/PLL/PGA/PTX-treated samples are marked as # <span class="html-italic">p</span> &lt; 0.05. (<b>B</b>) Mitochondrial respiratory efficiency parameters, including L/E, L/P, and 1−L/E ratios, were determined in permeabilized HL-1 cells after 72 h of treatment with IC<sub>50</sub> concentrations of free PTX or PTX encapsulated in SDS/PLL and SDS/PLL/PGA NCs. Statistical significance relative to untreated control cells is indicated as * <span class="html-italic">p</span> &lt; 0.05. Significant differences between free PTX or encapsulated formulations of PTX are denoted as + <span class="html-italic">p</span> &lt; 0.05, and differences between SDS/PLL/PTX and SDS/PLL/PGA/PTX-treated samples are marked as # <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Simplified model illustrating the differential effects of free PTX or SDS/PLL/PTX versus SDS/PLL/PGA/PTX on HL-1 cardiomyocytes. Our findings show that free PTX or trapped in SDS/PLL NCs markedly depleted DNA synthesis (red arrow) and ATP levels (blue arrow), accompanied by a significant reduction in mitochondrial membrane potential and decrease in an oxygen consumption rate (brown arrows) and altered mRNA expression of genes associated with apoptosis and cardiomyocytes’ function. By contrast, the cytotoxic effects were less pronounced when PTX was encapsulated in SDS/PLL/PGA nanocarriers. In addition, this form of PTX demonstrated the lowest cytotoxicity towards cardiac cell cultures, with slim modification of cardiac cells’ homeostasis. Our finding indicates SDS/PLL/PGA/PTX potential as a safer formulation for reduction of the adverse effects of PTX on cardiomyocytes.</p>
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<p>Analytical setup for high-resolution spirometry of HL-1 cells and assessment of cellular oxygen consumption. (<b>A</b>) Schematic representation of the sequential addition of substrates during oxygen consumption rate (OCR) measurements. (<b>B</b>) Overview of the rationale for using specific chemical compounds in mitochondrial bioenergetics analysis.</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 531
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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14 pages, 2070 KiB  
Article
Physicochemical and Sensory Evaluation of Gummy Candies Fortified with Microcapsules of Guinea Pig (Cavia porcellus) Blood Erythrocytes and Tumbo (Passiflora tarminiana) Juice
by Carlos A. Ligarda-Samanez, Eliana Villano-Limache, Williams Pichihua-Oscco, David Choque-Quispe, Reynaldo Sucari-León, Dante Fermín Calderón Huamaní, Germán De la Cruz, Rober Luciano-Alipio, Wilber Cesar Calsina Ponce, Yolanda Aroquipa-Durán and María José Victoria Campos-Huamaní
Appl. Sci. 2025, 15(2), 917; https://doi.org/10.3390/app15020917 - 17 Jan 2025
Viewed by 575
Abstract
Recently, interest in developing functional foods that promote health has grown significantly. This study aimed to evaluate the feasibility of microencapsulating guinea pig blood erythrocytes by vacuum drying and incorporating them into gummies fortified with tumbo juice. Physicochemical analysis (proximate analysis, iron content, [...] Read more.
Recently, interest in developing functional foods that promote health has grown significantly. This study aimed to evaluate the feasibility of microencapsulating guinea pig blood erythrocytes by vacuum drying and incorporating them into gummies fortified with tumbo juice. Physicochemical analysis (proximate analysis, iron content, color, pH, soluble solids, and particle size) and functional group analysis by Fourier transform infrared spectrophotometry were performed on three formulations of gummy candy with added encapsulated erythrocytes from guinea pig blood (EEGPB): F1 (4% EEGPB), F2 (5% EEGPB), and F3 (6% EEGPB). The results showed a significant decrease in the moisture content (52.02% in F1 to 43.27% in F3) and increases in protein (11.44% in F3) and iron (2.63 mg Fe/g in F3) contents when higher EEGPB levels were used. Sensory evaluation revealed that F3 was the most acceptable formulation in terms of taste, aroma, and texture, with no significant differences in color. FTIR analysis confirmed physical incorporation with no chemical interactions between ingredients. These results demonstrate that the encapsulation of erythrocytes by vacuum drying not only preserves the bioactive compounds but also improves the organoleptic properties of the gummies, making them an attractive product for consumers. In conclusion, this technique is effective for fortifying functional foods and has potential application in other food products. This approach represents a significant advance in the development of innovative functional foods. Full article
(This article belongs to the Special Issue Extraction of Functional Ingredients and Their Application)
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<p>Characterization of the microcapsules: (<b>a</b>) morphology of powders obtained via SEM; (<b>b</b>) elemental analysis by SEM-EDS in terms of iron content and particle size.</p>
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<p>Gummy candies with added encapsulated erythrocytes from guinea pig blood (F1, F2, and F3 are the formulations).</p>
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<p>FTIR spectra of gummy candies with added encapsulated erythrocytes from guinea pig blood (F1, F2, and F3 are the formulations).</p>
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<p>(<b>a</b>) Acceptability scores for color, aroma, taste, and texture; (<b>b</b>) preference test results (% of participants favoring each formulation); (<b>c</b>) gender distribution of the sensory panel.</p>
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<p>PCA (F1, F2, and F3 are the formulations).</p>
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14 pages, 1503 KiB  
Article
Synergistic Antifungal Activity of Terbinafine in Combination with Light-Activated Gelatin–Silver Nanoparticles Against Candida albicans Strains
by Atif Ullah, Fawad Ali, Farman Ullah, Sajid Khan Sadozai, Saeed Ahmed Khan, Sajid Hussain, Abdulwahed Fahad Alrefaei and Sajid Ali
Pharmaceutics 2025, 17(1), 125; https://doi.org/10.3390/pharmaceutics17010125 - 17 Jan 2025
Viewed by 410
Abstract
The development of resistance to traditional antifungal therapies has necessitated the exploration of alternative treatment strategies to effectively manage fungal infections, particularly those induced by Candida albicans (C. albicans). This research investigates the possibility of integrating silver nanoparticles (AgNPs) with Terbinafine [...] Read more.
The development of resistance to traditional antifungal therapies has necessitated the exploration of alternative treatment strategies to effectively manage fungal infections, particularly those induced by Candida albicans (C. albicans). This research investigates the possibility of integrating silver nanoparticles (AgNPs) with Terbinafine to improve antifungal effectiveness. Terbinafine, while potent, faces challenges with specific fungal strains, highlighting the need for strategies to enhance its treatment efficacy. Silver nanoparticles were produced through a light-activated, gelatin-based method, resulting in particle sizes ranging from 56.8 nm to 66.2 nm, confirmed by dynamic light scattering and scanning electron microscopy. Stability studies indicated that AgNPs produced with 30 mg of silver nitrate (AgNO₃) exhibited the greatest stability over 60 days across different temperature conditions. The analysis through UV-visible spectrophotometry revealed a notable shift in the absorption spectra as AgNO₃ concentrations increased, which was associated with a strengthening of plasmon resonance. The effectiveness of the AgNPs and Terbinafine combination was assessed against three strains of C. albicans (ATCC 10231, ATCC 90028, and ATCC 18804). Terbinafine demonstrated strong antifungal properties with minimum inhibitory concentrations (MIC) values ranging from 2–4 µg/mL, whereas AgNPs on their own displayed moderate effectiveness. The integrated formulation notably enhanced effectiveness, especially against strain ATCC 90028, revealing a synergistic effect (FIFi = 0.369). These results were complemented by the findings of the time-to-kill assay, where the same strain showed a 3.2 log₁₀ CFU/mL decrease in viable cell count. The process by which AgNPs boost activity entails the disruption of the fungal cell membrane and its internal components, probably as a result of silver ion release and the generation of free radicals. The results indicate that the combination of Terbinafine and AgNPs may act as a powerful alternative for addressing resistant fungal infections, presenting an encouraging direction for future antifungal treatments. Full article
(This article belongs to the Section Nanomedicine and Nanotechnology)
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<p>(<b>a</b>) DLS studies showing particle size and PDI value at 28 °C. (<b>b</b>) SEM image of 1% gelatin AgNPs.</p>
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<p>UV-Visible absorption spectra of AgNPs and gelatin-stabilized AgNPs at different AgNO₃ levels. Sample 1 (blue): commercial AgNPs, Sample 2 (green): gelatin-stabilized AgNPs (1% gelatin, 10 mg AgNO₃),Sample 3 (orange): gelatin-stabilized AgNPs (1% gelatin, 20 mg AgNO₃), Sample 4 (red): gelatin-stabilized AgNPs (1% gelatin, 30 mg AgNO₃). The shaded region reveals AgNPs’ 300–400 nm plasmon resonance. Due to particle size or aggregation, higher silver nitrate concentrations redshift the plasmon peak.</p>
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<p>Stability studies of 1% gelatin AgNPs of various formulations.</p>
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<p>The time to kill assay graph compares Terbinafine (green squares), DMSO (green triangles), AgNPs (blue circles), and Terbinafine with AgNPs for <span class="html-italic">Candida albicans</span> ATCC 18804 (yellow squares with lines). Microbial viability decreased considerably over 70 h with the combined treatment, showing synergy.</p>
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12 pages, 1111 KiB  
Article
Changes in the Microcirculation and Physiologic Perfusion Dynamics of Free DIEP Flaps in the First 72 h After Breast Reconstruction
by Denis Ehrl, Verena Alt, Sara Taha, Konstantin Frank, Nikolaus Wachtel, Karl J. Bodenschatz, Wolfram Demmer, Benedikt Fuchs, Riccardo E. Giunta and Nicholas Moellhoff
J. Clin. Med. 2025, 14(2), 520; https://doi.org/10.3390/jcm14020520 - 15 Jan 2025
Viewed by 384
Abstract
Background/Objectives: The autologous reconstruction of the female breast using a microsurgical DIEP flap is a reliable and safe method. To detect impairments early and preserve the microvascular flap through timely revision, a better understanding of physiologic perfusion dynamics is necessary. This exploratory study [...] Read more.
Background/Objectives: The autologous reconstruction of the female breast using a microsurgical DIEP flap is a reliable and safe method. To detect impairments early and preserve the microvascular flap through timely revision, a better understanding of physiologic perfusion dynamics is necessary. This exploratory study examines changes in microcirculation in free DIEP flaps within the first 72 h after vascular anastomosis using laser Doppler flowmetry and white-light spectrophotometry. Methods: This single-center study analyzed retro- and prospectively collected data from female patients who underwent uneventful breast reconstruction using a DIEP flap and were monitored using the O2C device (LEA Medizintechnik, Giessen, Germany). Microcirculation was monitored continuously postoperatively for a period of 72 h. Results: A total of 36 patients with a mean age of 48.86 (9.36) years and a mean BMI of 26.78 (4.12) kg/m2 received 40 DIEP flaps (four bilateral reconstructions). Microcirculatory blood flow showed a continuous increase, reaching up to 15% above its initial value within the first 72 h following anastomosis. The average tissue oxygen saturation (sO2) and relative hemoglobin (rHB) levels remained fairly stable throughout the study period, with overall reductions of 5.46% and 5.30%, respectively. Conclusions: Autologous breast reconstruction using a microvascular DIEP flap is a safe and reliable technique. This study showed an increase in blood flow over the 72 h study period. At the same time, sO2 and rHb showed stable levels. Deviations in these values could be interpreted as indicators of a perfusion disorder of the microvascular flap. Full article
(This article belongs to the Special Issue Clinical Advances in Plastic Surgery)
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<p>Preoperative marking (<b>left</b>) and 6-month postoperative result (<b>right</b>) of a 53-year-old patient receiving immediate breast reconstruction with a free DIEP flap after nipple-sparing mastectomy and sentinel node biopsy. Images obtained using VECTRA XT 3D imaging system (Canfield Scientific, Parsippany, NJ, USA).</p>
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<p>Exemplary image of the placement of the LFx37 probe of the O2C measuring device (both LEA Medizintechnik, Gießen, Germany) on the skin island of the DIEP flap in the inframammary fold (<b>left</b>) or at the position of the previous nipple–areolar complex (<b>right</b>).</p>
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<p>Overview of the course of microcirculation during the investigated time period.</p>
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23 pages, 8764 KiB  
Article
Towards the Sustainable Removal of Heavy Metals from Wastewater Using Arthrospira platensis: A Laboratory-Scale Approach in the Context of a Green Circular Economy
by Lamprini Malletzidou, Eleni Kyratzopoulou, Nikoletta Kyzaki, Evangelos Nerantzis and Nikolaos A. Kazakis
Appl. Sci. 2025, 15(2), 791; https://doi.org/10.3390/app15020791 - 15 Jan 2025
Viewed by 534
Abstract
The use of living Arthrospira platensis (A. platensis) cultures emerges as a promising green solution for the bioremediation of water contaminated by toxic metal waste. The scope of the present study is to evaluate the microalga’s potential in heavy metal remediation, [...] Read more.
The use of living Arthrospira platensis (A. platensis) cultures emerges as a promising green solution for the bioremediation of water contaminated by toxic metal waste. The scope of the present study is to evaluate the microalga’s potential in heavy metal remediation, in the case of multi-metal-treated (multi-MT) systems. For this reason, A. platensis cultures were exposed to mono- and multi-metal solutions of Cu, Cd, Ni, Pb, and Zn, and their metal adsorption ability was investigated. The heavy metal removal efficiency of A. platensis cultures was evaluated using atomic absorption spectroscopy (AAS). Additionally, the cultures were examined using Fourier transform infrared (FTIR) spectroscopy, Near-Infrared (NIR) Spectroscopy, UV-Vis spectrophotometry, and optical microscopy, together with pH and electrical conductivity (EC) measurements to evaluate the quality of the cultures and the changes induced by heavy metal stress. The results showed that metal removal is still efficient in multi-MT cultures. In particular, Cu, Cd, Pb, and Zn removal of multi-MT cultures is elevated or relative to the respective removal of the mono-metal-treated (mono-MT) cultures, showing a synergistic or cooperative interaction between the metals, while the removal of Ni of multi-MT cultures decreased compared to Ni of mono-MT cultures, showing an antagonistic interaction to the other metals. The study shows that A. platensis is considered an effective microalga toward the bioremediation of multi-metal polluted cultures. Full article
(This article belongs to the Special Issue Advances in Environmental Applied Physics—2nd Edition)
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<p>Optical microscopy images from all cultures as collected with ×10 objective lens on Day 7 of cultivation.</p>
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<p>Representative optical microscopy images collected with ×60 objective lens on Day 7 of cultivation: (<b>a</b>) Control, (<b>b</b>) Mix 5 ppm, (<b>c</b>) Cu 10 ppm, and (<b>d</b>) Ni 5 ppm.</p>
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<p>NIR reflectance response of cultures at 1062.6 nm: (<b>a</b>) Cd-MT; (<b>b</b>) Zn-MT; (<b>c</b>) Pb-MT; (<b>d</b>) Cu-MT; (<b>e</b>) Ni-MT; (<b>f</b>) Multi-MT. Values were normalized to Day 0 of cultivation to account for slight variations in initial biomass. Each value is average of two measurements, with uncertainties less than 3% over each value.</p>
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<p>pH measurements of cultures during all cultivation days: (<b>a</b>) Cu-MT; (<b>b</b>) Cd-MT; (<b>c</b>) Ni-MT; (<b>d</b>) Pb-MT; (<b>e</b>) Zn-MT; (<b>f</b>) Multi-MT. Each value is average of two measurements, with uncertainties less than 4% over each value.</p>
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<p>Chlorophyll-a content on Days 0 and 7 of cultivation of all cultures (Control and MT). Each value is average of two measurements, with uncertainties less than 5% over each one.</p>
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<p>ATR-FTIR spectra of <span class="html-italic">A. platensis</span> biomass collected from Control culture on initial (Day 0) and final days (Day 7) of cultivation.</p>
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<p>ATR-FTIR spectra of <span class="html-italic">A. platensis</span> biomass collected from all cultures on Day 7 of cultivation: (<b>a</b>) Cu-MT; (<b>b</b>) Cd-MT; (<b>c</b>) Ni-MT; (<b>d</b>) Pb-MT; (<b>e</b>) Zn-MT; (<b>f</b>) Multi-MT. Control culture spectrum is also shown for comparative reasons.</p>
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<p>FPA/FTIR imaging analysis in micro-ATR mode of <span class="html-italic">A. platensis</span> filament (Control culture, Day 7 of cultivation). (<b>a</b>) Optical image (350 μm × 350 μm). Micro-ATR measured area is indicated with red rectangle (70 μm × 70 μm). FPA chemical images showing distribution of FTIR bands at (<b>b</b>) 1643, (<b>c</b>) 1728, and (<b>d</b>) 837 cm<sup>−1</sup>, that correspond to amide I, lipids, and saccharides, respectively.</p>
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<p>Removal (%) of heavy metals from culture media by <span class="html-italic">A. platensis</span> after mono- (<b>a</b>) and multi-metal (<b>b</b>) treatment of cultures. Each value is average of two measurements, with uncertainties less than 5%.</p>
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18 pages, 4325 KiB  
Article
Experimental Study on the Photothermal Properties of Thermochromic Glass
by Mingyi Gao, Dewei Qian, Lihua Zhao and Rong Jin
Buildings 2025, 15(2), 233; https://doi.org/10.3390/buildings15020233 - 15 Jan 2025
Viewed by 342
Abstract
Reducing energy consumption in buildings is critical to reducing CO2 emissions and mitigating global warming. Studies have shown that heating and cooling loads account for more than 40% of building energy consumption, and thermochromic glass (TCG) with dynamically adjustable solar transmittance is [...] Read more.
Reducing energy consumption in buildings is critical to reducing CO2 emissions and mitigating global warming. Studies have shown that heating and cooling loads account for more than 40% of building energy consumption, and thermochromic glass (TCG) with dynamically adjustable solar transmittance is an excellent way to reduce this load. Although a large number of studies have tested the spectral parameters of TCG in totally transparent and totally turbid states, the impact of dynamic changes in optical properties on the simulation accuracy of building energy consumption has been neglected. In this study, a method is proposed for a hydrogel-type TCG to dynamically test its spectral parameters based on spectrophotometry. The method uses a spectrophotometer and a PID heater to achieve the dynamic optical parameter testing of TCGs at different temperatures. In this paper, the transmission and reflection spectra of the two TCGs at 20~25 °C, 30~35 °C, 40 °C, 45 °C, 50 °C, and 55 °C were obtained, and the regression segmentation functions of visible transmittance and solar transmittance were established. The R2 of the function model is 0.99. In addition, the test results show that the thermochromic glass selected in this paper can selectively transmit different wavelengths of light, and its transmission mainly occurs in the visible and near-infrared wavelengths from 320 to 1420 nm, while the transmission rate of other wavelengths is very low. As the temperature increases, the visible, solar, and ultraviolet transmittances decrease at a similar rate. In addition, the higher the temperature acting on the thermochromic (TC) layer, the greater its haze. Full article
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<p>Schematic diagram of the internal structure changes of TC glass in two states.</p>
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<p>Process of thermochromic glass atomization.</p>
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<p>Cross-sectional views of a thermochromic window, air cavity, and rear glass cover. Possible light paths through the window are marked.</p>
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<p>TC glass optical parameter test system.</p>
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<p>Experimental set-up for measuring transmittance and reflectance: (<b>a</b>) schematic diagram of the double-beam optical path; (<b>b</b>) use of the integrating sphere/spectrometer to qualify transmitted and reflected components.</p>
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<p>Causes of errors in optical experiments.</p>
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<p>Spectral transmittance of TCG 1 at 25 °C.</p>
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<p>Spectral transmittance of TCG 1 at different temperatures.</p>
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<p>Spectral transmittance of TCG 2 at 25 °C.</p>
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<p>Spectral transmittance of TCG 2 at different temperatures.</p>
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<p>Regression function between visible light transmittance and temperature for TCG 1.</p>
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<p>Regression function between solar transmittance and temperature for TCG 1.</p>
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<p>Regression function between visible light transmittance and temperature for TCG 2.</p>
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<p>Regression function between solar transmittance and temperature for TCG 2.</p>
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25 pages, 2950 KiB  
Article
Ajuga reptans L. Herb Extracts: Phytochemical Composition and Pharmacological Activity Screening
by Svitlana Maliuvanchuk, Andriy Grytsyk, Oksana Popadynets, Taras Kotyk, Ain Raal and Oleh Koshovyi
Plants 2025, 14(2), 219; https://doi.org/10.3390/plants14020219 - 14 Jan 2025
Viewed by 452
Abstract
The genus Ajuga (Lamiaceae family) comprises approximately 300 species, which are widely used in traditional medicine for their diaphoretic, antiseptic, hemostatic, and anti-inflammatory properties, but scarcely in official ones. Therefore, the study of Ajuga reptans holds promise for developing new medicinal products. In [...] Read more.
The genus Ajuga (Lamiaceae family) comprises approximately 300 species, which are widely used in traditional medicine for their diaphoretic, antiseptic, hemostatic, and anti-inflammatory properties, but scarcely in official ones. Therefore, the study of Ajuga reptans holds promise for developing new medicinal products. In aqueous and aqueous-alcoholic soft extracts of the A. reptans herb, 16 amino acids, 20 phenolics, and 10 volatile substances were identified by HPLC and GC/MS. The assays of the main substances’ groups were also determined by spectrophotometry (vitamin K1, polyphenols, tannins, flavonoids, and hydroxycinnamic acids) and titrometry (ascorbic and organic acids). A. reptans herb extracts are practically non-toxic, exhibit hepatoprotective activity (dose 25 mg/kg) in experimental carbon tetrachloride-induced hepatitis, moderate anti-inflammatory activity (dose 100 mg/kg) in carrageenan-induced edema models, and possess significant local hemostatic (reducing bleeding time by 40.6%) and wound-healing properties (complete wound healing after 9 days). The aqueous-ethanolic soft A. reptans extract (extractant 50% ethanol) demonstrated the most pronounced hepatoprotective and anti-inflammatory effects. A. reptans extracts are capable of inhibiting the growth of microorganisms and showing higher activity against Gram-positive bacteria. A. reptans herb extracts are promising agents for implementation in official medicine as wound healing and hepatoprotective remedies after further preclinical and clinical studies. Full article
(This article belongs to the Special Issue Medicinal Plants: Phytochemistry and Pharmacology Studies)
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<p><span class="html-italic">Ajuga reptans</span> L.</p>
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<p>TLC chromatogram of phenolic compounds in <span class="html-italic">Ajuga reptans</span> L. herb extracts: 1–3—extracts of <span class="html-italic">A. reptans</span>; 4—<span class="html-italic">A. reptans</span> extract (extraction agent: 50% ethanol); 5—<span class="html-italic">A. reptans</span> extract (extraction agent: 70% ethanol); 6—comparison solution (rutin (R<sub>f</sub> = 0.05), apigenin-7-glucoside (R<sub>f</sub> = 0.07), chlorogenic acid (R<sub>f</sub> = 0.22), isoquercitrin (R<sub>f</sub> = 0.24), hyperoside (R<sub>f</sub> = 0.26), apigenin (R<sub>f</sub> = 0.35), luteolin (R<sub>f</sub> = 0.42), caffeic acid (R<sub>f</sub> = 0.45), ferulic acid (R<sub>f</sub> = 0.77), quercetin (R<sub>f</sub> = 0.79)).</p>
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<p>Structural features of liver lobules under the influence of the toxicant. 1—destructured hepatocytes, 2—lymphocytes. Staining: hematoxylin and eosin. Magnification: ×200.</p>
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<p>Structural features of liver lobules in animals administered AR2: 1—hepatic plates, 2—sinusoids, 3—blood vessels. Staining: hematoxylin and eosin. Magnification: ×200.</p>
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<p>Structural features of liver lobules in animals that received the “Silibor” preparation. 1—hepatic plates, 2—sinusoid, 3—central vein. Staining: hematoxylin and eosin. Magnification: ×200.</p>
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<p>Antimicrobial activity of <span class="html-italic">Ajuga reptans</span> L. herb extracts prepared using AR1 (extraction agent: purified water) (1), AR2 (extraction agent: 50% ethanol) (2), AR3 (extraction agent: 70% ethanol) (3), and gentamicin (4) against cultures of <span class="html-italic">Enterococcus faecalis</span> (<b>A</b>) and β-hemolytic <span class="html-italic">Streptococcus</span> group G (<b>B</b>).</p>
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18 pages, 3443 KiB  
Article
Annealing Temperature Effects of Seeded ZnO Thin Films on Efficiency of Photocatalytic and Photoelectrocatalytic Degradation of Tetracycline Hydrochloride in Water
by Ghaida M. Wazzan, Jwaher M. AlGhamdi, Nuhu Dalhat Mu’azu, Tarek Said Kayed, Emre Cevik and Khaled A. Elsayed
Catalysts 2025, 15(1), 71; https://doi.org/10.3390/catal15010071 - 14 Jan 2025
Viewed by 450
Abstract
In this study, seeded zinc oxide (Z-ZnO) thin films were fabricated by a two-step electrochemical deposition process. Different annealing temperatures (300, 400, 500, and 600 °C) were investigated to determine the most effective temperature for the photocatalytic activity. Comprehensive analyses were conducted using [...] Read more.
In this study, seeded zinc oxide (Z-ZnO) thin films were fabricated by a two-step electrochemical deposition process. Different annealing temperatures (300, 400, 500, and 600 °C) were investigated to determine the most effective temperature for the photocatalytic activity. Comprehensive analyses were conducted using X-Ray Diffraction (XRD), scanning electron microscopy (SEM), and UV–visible spectrophotometry. The XRD results confirmed the formation of a wurtzite hexagonal structure, with the highest crystallinity observed at 400 °C. The lowest band gap value, 3.29 eV, was also recorded for Z-ZnO thin film annealed at 400 °C. SEM images revealed that the thin film treated at 400 °C exhibited a well-defined and uniform structure, contributing to its enhanced properties. The photocatalytic efficiency of ZnO (without seeding layer) and Z-ZnO thin films annealed at 400 °C was evaluated through the degradation of tetracycline hydrochloride (TCH) to prove the effect of the presence of a primary seeding layer on ZnO 400 °C thin film efficiency. The degradation efficiency of ZnO thin film without seeding layer was 69.8%. By applying a seeding layer in Z-ZnO 400 °C thin film, the degradation efficiency has been increased to 75.8%. On the other hand, Z-ZnO 400 °C thin film achieved a high degradation efficiency of 82.6% over 300 min in the photoelectrocatalytic system. The obtained Z-ZnO thin films annealed at 400 °C are highly effective photocatalysts and photoelectrocatalysts, offering a significant potential for the degradation of pharmaceuticals and other pollutants in water. Full article
(This article belongs to the Section Photocatalysis)
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Graphical abstract
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<p>XRD spectrum for Z-ZnO 300 °C, Z-ZnO 400 °C, Z-ZnO 500 °C, and Z-ZnO 600 °C thin film samples.</p>
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<p>UV-Vis absorption spectra for the optical properties. (<b>a</b>) UV-VIS absorption spectra for Z-ZnO 300 °C, Z-ZnO 400 °C, Z-ZnO 500 °C, Z-ZnO 600 °C thin films and (<b>b</b>) TAUC plot between (ahv)<sup>2</sup> and hv to calculate the band gap for Z-ZnO 300 °C, Z-ZnO 400 °C, Z-ZnO 500 °C, Z-ZnO 600 °C thin films.</p>
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<p>SEM characterization for Z-ZnO thin film comparing different annealing temperatures (300, 400, 500, 600 °C).</p>
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<p>(<b>a</b>) Effect of different annealing temperatures (300, 400, 500, 600 °C) of Z-ZnO on the photocatalytic degradation of 30 ppm TCH under UV light for 300 min. (<b>b</b>) Effect of seeding layer on ZnO thin film for the photocatalytic degradation of 30 ppm TCH under UV light for 300 min.</p>
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<p>The degradation of 30 ppm TCH under UV light for 300 min using Z-ZnO 400 °C thin film (in the dark), photolysis, photocatalysis, and photoelectrocatalysis methods.</p>
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<p>Scheme diagram for FTO glass pretreatment.</p>
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<p>Scheme diagram for ZnO thin film preparation method. (<b>a</b>) Seeding layer (Z); (<b>b</b>) electrodeposition of ZnO layer.</p>
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<p>The photoelectrochemical reactor setups.</p>
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