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Search Results (303)

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21 pages, 6646 KiB  
Article
Extraction, Purification, Sulfated Modification, and Biological Activities of Dandelion Root Polysaccharides
by Xiao Wu, Na Li, Zeng Dong, Qin Yin, Tong Zhou, Lixiang Zhu, Hanxi Yan, Ziping Chen and Kefeng Zhai
Foods 2024, 13(15), 2393; https://doi.org/10.3390/foods13152393 - 29 Jul 2024
Viewed by 389
Abstract
In this study, polysaccharides were extracted at a rate of 87.5% ± 1.5% from native dandelion roots, and the dandelion root polysaccharides (DRPs) were then chemically modified to obtain sulfated polysaccharides (SDRPs) with a degree of substitution of 1.49 ± 0.07. The effects [...] Read more.
In this study, polysaccharides were extracted at a rate of 87.5% ± 1.5% from native dandelion roots, and the dandelion root polysaccharides (DRPs) were then chemically modified to obtain sulfated polysaccharides (SDRPs) with a degree of substitution of 1.49 ± 0.07. The effects of modification conditions, physicochemical characterizations, structural characteristics, antioxidant properties, hypoglycemic activity, and proliferative effects on probiotics of DRP derivatives were further investigated. Results showed that the optimum conditions for sulfation of DRPs included esterification reagents (concentrated sulfuric acid: n-butanol) ratio of 3:1, a reaction temperature of 0 °C, a reaction time of 1.5 h, and the involvement of 0.154 g of ammonium sulfate. The DRPs and SDRPs were composed of six monosaccharides, including mannose, glucosamine, rhamnose, glucose, galactose, and arabinose. Based on infrared spectra, the peaks of the characteristic absorption bands of S=O and C-O-S appeared at 1263 cm−1 and 836 cm−1. Compared with DRPs, SDRPs had a significantly lower relative molecular mass and a three-stranded helical structure. NMR analysis showed that sulfated modification mainly occurred on the hydroxyl group at C6. SDRPs underwent a chemical shift to higher field strength, with their characteristic signal peaking in the region of 1.00–1.62 ppm. Scanning electron microscopy (SEM) analysis indicated that the surface morphology of SDRPs was significantly changed. The structure of SDRPs was finer and more fragmented than DRPs. Compared with DRPs, SDRPs showed better free radical scavenging ability, higher Fe2+chelating ability, and stronger inhibition of α-glucosidase and α-amylase. In addition, SDRPs had an excellent promotional effect on the growth of Lactobacillus plantarum 10665 and Lactobacillus acidophilus. Therefore, this study could provide a theoretical basis for the development and utilization of DRPs. Full article
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<p>Separation (<b>A</b>) and purification (<b>B</b>,<b>C</b>) of dandelion polysaccharides.</p>
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<p>Effect of reaction time (<b>A</b>), esterifier dosage (<b>B</b>), ammonium sulfate addition (<b>C</b>), and reaction temperature (<b>D</b>) on the degree of substitution of dandelion polysaccharides.</p>
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<p>Contour plots (<b>A</b>,<b>C</b>,<b>E</b>) and three-dimensional response surface plots (<b>B</b>,<b>D</b>,<b>F</b>) about the effects of reaction time, esterifier dosage, the additional amount of ammonium sulfate, and interaction on the DS of sulfate of DRP.</p>
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<p>Contour plots (<b>A</b>,<b>C</b>,<b>E</b>) and three-dimensional response surface plots (<b>B</b>,<b>D</b>,<b>F</b>) about the effects of reaction time, esterifier dosage, the additional amount of ammonium sulfate, and interaction on the DS of sulfate of DRP.</p>
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<p>FT-IR spectra of DRP, SDRP (<b>A</b>), and Congo red test (<b>B</b>).</p>
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<p>Chromatograms of monosaccharide compositions of standard substance mixture (<b>A</b>), DRP (<b>B</b>), and SDRP (<b>C</b>).</p>
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<p>The NMR spectra of DRP and SDRP.((<b>A</b>,<b>B</b>) were the <sup>13</sup>C NMR spectrum of DRPs and SDRPs respectively; (<b>C</b>,<b>D</b>) were the <sup>1</sup>H NMR spectrum of DRPs and SDRPs respectively).</p>
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<p>Scanning electron microscopy images of DRP (<b>A1</b>–<b>A3</b>) and SDRP (<b>B1</b>–<b>B3</b>).</p>
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<p>(<b>A</b>) DPPH radical scavenging assay; (<b>B</b>) superoxide anion scavenging activity assay; (<b>C</b>) hydroxyl radical scavenging ability assay; and (<b>D</b>) measurement of ferrous ion chelating capacity.</p>
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<p>Studies on the hypoglycemic activity of sulfated dandelion polysaccharides in vitro ((<b>A</b>) Inhibition of α-amylase by polysaccharides and (<b>B</b>) inhibition of α-glucosidase by polysaccharides).</p>
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<p>Probiotic proliferative effects (<b>A</b>,<b>B</b>) and probiotic growth curves (<b>C</b>,<b>D</b>). (<b>a</b>) SDRP medium OD<sub>600nm</sub>; (<b>b</b>) FOS mediumOD<sub>600nm</sub>; (<b>c</b>) SDRP medium pH; and (<b>d</b>) FOS medium pH. *: When the mass concentration of polysaccharides is the same, there is a significant difference (<span class="html-italic">p</span> &lt; 0.05) between S-DRP, DRP, and FOS.</p>
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13 pages, 3660 KiB  
Article
Degradation of Diclofenac by Bisulfite Coupled with Iron and Manganous Ions: Dual Mechanism, DFT-Assisted Pathway Studies, and Toxicity Assessment
by Hongbin Wang, Shijie Kuang, Youlun Su, Xu Ren, Bowen Yang and Yongliang Sun
Water 2024, 16(14), 1994; https://doi.org/10.3390/w16141994 - 14 Jul 2024
Viewed by 476
Abstract
Diclofenac (DCF) is often detected in diverse aquatic bodies, and ineffective management can lead to detrimental effects on human health and ecosystems. In this study, degradation of DCF by Fe(III) and Mn(II) activating bisulfite (BS) was investigated. In the Fe(III)/Mn(II)/BS system, 93.4% DCF [...] Read more.
Diclofenac (DCF) is often detected in diverse aquatic bodies, and ineffective management can lead to detrimental effects on human health and ecosystems. In this study, degradation of DCF by Fe(III) and Mn(II) activating bisulfite (BS) was investigated. In the Fe(III)/Mn(II)/BS system, 93.4% DCF was degraded at 200 μM BS within 120 s, and additional research on 1000 μM BS achieved 88.4% degradation efficacy. Moreover, kinetics fitting of DCF degradation with the different BS concentrations was studied to find the two highest reaction rates (200 and 1000 μM, kobs = 0.0297 and 0.0317 s−1, respectively). Whereafter, SO4•− and Mn(III) were identified as the main active species at these two concentrations, respectively. Density functional theory (DFT) calculations, molecular frontier orbital theory, and surface electrostatic potential (ESP) forecast electrophilic attack sites. DCF degradation pathways by radical and non-radical ways were proposed by attack site prediction and thirteen intermediates identified by UPLC-QTOF-MS. ECOSAR software 2.2 was used for toxicity assessment. This work studied DCF degradation by the Fe(III)/Mn(II)/BS process in the presence of different concentrations of BS, providing a new insight into water purification. Full article
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<p>DCF degradation (<b>a</b>) by different systems; reaction conditions: [DCF]<sub>0</sub> = [Fe(II)]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [BS]<sub>0</sub> = 200 μM, [pH]<sub>0</sub> = 4.0, T = 25 °C; (<b>b</b>) kinetic analysis; reaction conditions: [DCF]<sub>0</sub> = [Fe(II)]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [BS]<sub>0</sub> = 200 μM, [pH]<sub>0</sub> = 4.0, T = 25 °C; (<b>c</b>) under different pH in Fe(III)/Mn(II)/BS system; reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [BS]<sub>0</sub> = 200 μM, T = 25 °C; (<b>d</b>) compared with Fe(III)/BS systems; reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [BS]<sub>0</sub> = 200 μM, T = 25 °C; (<b>e</b>) via different Mn(II)/Fe(III) ratios in Fe(III)/Mn(II)/BS system; reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [BS]<sub>0</sub> = 200 μM, [pH]<sub>0</sub> = 4.0, T = 25 °C; (<b>f</b>) via different BS concentrations in Fe(III)/Mn(II)/BS system; reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [pH]<sub>0</sub> = 4.0, T = 25 °C.</p>
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<p>(<b>a</b>) Kinetic fitting of different BS concentrations; (<b>b</b>) <span class="html-italic">k</span><sub>obs</sub> of different BS concentrations.</p>
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<p>Alcohol inhibitory tests. Reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = 10 μM, [Mn(II)]<sub>0</sub> = 5 μM, [BS]<sub>0</sub> = 200 μM, [pH]<sub>0</sub> = 4.0, T = 25 °C.</p>
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<p>(<b>a</b>) Scavenging experiments with alcohols; (<b>b</b>) different cations and PP complex full-wavelength scanning curve; (<b>c</b>) DCF and SMX competition in Fe(III)/Mn(II)/BS system. Reaction conditions: [DCF]<sub>0</sub> = [Fe(III)]<sub>0</sub> = [Mn(II)]<sub>0</sub> = 10 μM, [BS]<sub>0</sub> = 1 mM, [pH]<sub>0</sub> = 4.0, T = 25 °C.</p>
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<p>(<b>a</b>) Optimized DCF molecule; (<b>b</b>) Condensed Fukui Function; (<b>c</b>) DCF HOMO; (<b>d</b>) ESP of DCF.</p>
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<p>DCF degradation pathways by SO<sub>4</sub><sup>•−</sup> and Mn(III).</p>
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<p>(<b>a</b>) Toxicity assessment for SO<sub>4</sub><sup>•−</sup> pathways; (<b>b</b>) toxicity assessment for Mn(III) pathways.</p>
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14 pages, 2659 KiB  
Article
Can Hyaluronic Acid Combined with Chondroitin Sulfate in Viscosupplementation of Knee Osteoarthritis Improve Pain Symptoms and Mobility?
by Augustin Dima, Magda Dragosloveanu, Andreea Ramona Romila, Alexandru Cristea, Georgiana Marinică, Alexandru-Tiberiu Dănilă, Alexandru Mandici, Daniel Cojocariu, Robert-Alexandru Vlad, Adriana Ciurba and Magdalena Bîrsan
Biomolecules 2024, 14(7), 832; https://doi.org/10.3390/biom14070832 - 11 Jul 2024
Viewed by 631
Abstract
The objective of the present study was to assess the effect of intra-articular Hyaluronic acid (HA) and Chondroitin sulfate (CS) supplementation (Hialurom® Hondro (HH)) on pain symptoms and joint mobility. In total, 60 mg/mL sodium hyaluronate and 90 mg/mL CS were administered [...] Read more.
The objective of the present study was to assess the effect of intra-articular Hyaluronic acid (HA) and Chondroitin sulfate (CS) supplementation (Hialurom® Hondro (HH)) on pain symptoms and joint mobility. In total, 60 mg/mL sodium hyaluronate and 90 mg/mL CS were administered to 21 patients (17 females and 4 males) respecting the in-force requirements, excluding patients with some specific comorbidities. In addition to the clinical study (where the pain intensity (severity) and joint mobility were assessed), rheological characterization was conducted evaluating the following parameters: elastic modulus (G′), loss modulus (G″) oscillatory frequency (fc) at 0.5 Hz and 2.5 Hz, crossover frequency (fc), relaxation time (λ) where it was noticed that the addition of chondroitin sulfate (CS) to sodium hyaluronate (SH) significantly enhances and improves the viscoelastic properties, particularly at higher shear frequencies. A significant decrease in pain intensity felt by the subjects was found, from 7.48 (according to Wong–Baker scale)—pain close to 8 (the patient is unable to perform most activities), to more reduced values of 5.86—at 6 weeks after injection, 4.81—at 3 months after injection, and 5.24—at 6 months after injection, improvements in symptoms was fast and durable. Data related to the evolution of joint mobility show that at 6 weeks after injection, the mobility of joints increased by 17.8% and at 6 months by 35.61%. No serious adverse events were reported with undesired effects so that they would impose additional measures. Better resistance to enzymatic degradation and free radicals could be expected from the synergic combination of sodium hyaluronate and chondroitin sodium sulfate, this having a special importance for the patients, granting them the ability to perform more ample movements and reducing dependency on attendants, thus increasing quality of life. Full article
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<p>The knee injection of HH by a specialist physician to patients with stage II or stage III KOA: the best approach is the path of least obstruction and maximal access to the synovial cavity, which could be superolateral, superomedial, or anteromedial/anterolateral.</p>
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<p>Significant reduction in pain intensity (<b>a</b>) (* <span class="html-italic">p</span> &lt; 0.001) and pain severity (<b>b</b>) (* <span class="html-italic">p</span> &lt; 0.001) at weeks 6, 12 and 24 vs. baseline.</p>
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<p>Joint mobility as measured in degrees (<b>a</b>) (mean ± SD) and percent (%) increase in joint mobility (<b>b</b>) (mean ± SD) at weeks 6, 12, and 24 compared to baseline.</p>
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<p>The average rate of joint mobility variation (average ± SD).</p>
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<p>Visco-elasticity profile of HH in a commercial batch at 25 ± 0.01 °C (<b>a</b>) and 37 ± 0.01 °C (<b>b</b>).</p>
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<p>Visco-elasticity profile of positive control commercial batch of HA-hydrogel polymer solution at 25 °C.</p>
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<p>Dynamic viscosity profile for HH commercial batch.</p>
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16 pages, 7646 KiB  
Article
Impact of Composition and Autoclave Sterilization on the Mechanical and Biological Properties of ECM-Mimicking Cryogels
by Laura Di Muzio, Susi Zara, Amelia Cataldi, Claudia Sergi, Vito Cosimo Carriero, Barbara Bigi, Simone Carradori, Jacopo Tirillò, Stefania Petralito, Maria Antonietta Casadei and Patrizia Paolicelli
Polymers 2024, 16(13), 1939; https://doi.org/10.3390/polym16131939 - 7 Jul 2024
Viewed by 663
Abstract
Cryogels represent a valid strategy as scaffolds for tissue engineering. In order to adequately support adhesion and proliferation of anchorage-dependent cells, different polymers need to be combined within the same scaffold trying to mimic the complex features of a natural extracellular matrix (ECM). [...] Read more.
Cryogels represent a valid strategy as scaffolds for tissue engineering. In order to adequately support adhesion and proliferation of anchorage-dependent cells, different polymers need to be combined within the same scaffold trying to mimic the complex features of a natural extracellular matrix (ECM). For this reason, in this work, gelatin (Gel) and chondroitin sulfate (CS), both functionalized with methacrylic groups to produce CSMA and GelMA derivatives, were selected to prepare cryogel networks. Both homopolymer and heteropolymer cryogels were produced, via radical crosslinking reactions carried out at −12 °C for 2 h. All the scaffolds were characterized for their mechanical, swelling and morphological properties, before and after autoclave sterilization. Moreover, they were evaluated for their biocompatibility and ability to support the adhesion of human gingival fibroblasts and tenocytes. GelMA-based homopolymer networks better withstood the autoclave sterilization process, compared to CSMA cryogels. Indeed, GelMA cryogels showed a decrease in stiffness of approximately 30%, whereas CSMA cryogels of approximately 80%. When GelMA and CSMA were blended in the same network, an intermediate outcome was observed. However, the hybrid scaffolds showed a general worsening of the biological performance. Indeed, despite their ability to withstand autoclave sterilization with limited modification of the mechanical and morphological properties, the hybrid cryogels exhibited poor cell adhesion and high LDH leakage. Therefore, not only do network components need to be properly selected, but also their combination and ability to withstand effective sterilization process should be carefully evaluated for the development of efficient scaffolds designed for tissue engineering purposes. Full article
(This article belongs to the Special Issue Biopolymer-Based Biomimetic Scaffolds II)
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<p>Swelling behavior of homopolymer (GelMA and CSMA) and heteropolymer (GelMA/CSMA) cryogels, in comparison with commercial Spongostan, used as a control. Swelling studies were performed in PBS (pH = 7.4) at 37.0 ± 0.5 °C.</p>
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<p>Compressive properties, i.e., modulus, plateau stress and densification stress, of Spongostan benchmark and GelMA, CSMA and GelMA/CSMA cryogels neat, refined and sterilized and the related compressive curves.</p>
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<p>SEM micrograph of Spongostan benchmark.</p>
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<p>SEM micrographs of GelMA, CSMA and GelMA/CSMA cryogels neat, refined and sterilized. Red circles and red arrows evidence areas of microstructural changes within cryogel samples.</p>
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<p>(<b>A</b>) MTS assay in tenocytes cultured on GelMA, CSMA, GelMA/CSMA and Spongostan for 48 and 72 h. The histogram represents the O.D. spectrophotometrically detected. ** vs. Spongostan <span class="html-italic">p</span> &lt; 0.005, * vs. Gel-MA <span class="html-italic">p</span> &lt; 0.05. (<b>B</b>) LDH assay of tenocytes cultured on GelMA, CSMA, GelMA/CSMA and Spongostan for 48 and 72 h. LDH released is reported as % LDH leakage. 48 h: **** vs. GelMA, Spongostan, <span class="html-italic">p</span> &lt; 0.0001, ** vs. CSMA <span class="html-italic">p</span> &lt; 0.005, * vs. Spongostan <span class="html-italic">p</span> &lt; 0.05; 72 h: **** vs. Spongostan <span class="html-italic">p</span> &lt; 0.0001, °°°° vs. GelMA <span class="html-italic">p</span> &lt; 0.0001, <sup>§§§§</sup> vs. CSMA <span class="html-italic">p</span> &lt; 0.0001, ** vs. GelMA <span class="html-italic">p</span> &lt; 0.005. For both data values, the most representative of five different experiments is shown.</p>
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<p>Collagen type I secretion in tenocytes cultured on GelMA, CSMA and GelMA/CSMA cryogels for 48 and 72 h. Secretion levels are reported as µg/mL per MTS O.D. values. The results are the mean ± SD of three samples; the most representative of three different experiments is shown.</p>
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<p>SEM morphological analysis of tenocytes cultured on GelMA ((<b>A</b>,<b>B</b>), magnification 1750× and 3800, respectively), CSMA ((<b>C</b>,<b>D</b>), magnification 1550× and 2850, respectively), GelMA/CSMA ((<b>E</b>,<b>F</b>), magnification 1650× and 4100, respectively) cryogels and Spongostan ((<b>G</b>,<b>H</b>), magnification 2200× and 3000, respectively) after 72 h of culture. Red arrows indicate adhered cells, while red circles indicate dead grouped cells.</p>
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19 pages, 697 KiB  
Article
Antioxidant Activity, Antiproliferative Activity, Antiviral Activity, NO Production Inhibition, and Chemical Composition of Essential Oils and Crude Extracts of Leaves, Flower Buds, and Stems of Tetradenia riparia
by Jéssica da Silva Sena, Selma Alves Rodrigues, Karina Sakumoto, Rodrigo Sadao Inumaro, Pamela González-Maldonado, Emilio Mendez-Scolari, Ranulfo Piau, Daniela Dib Gonçalves, Filipa Mandim, Josiana Vaz, José Eduardo Gonçalves, Pablo Hernan Sotelo, Juliana Silveira do Valle and Zilda Cristiani Gazim
Pharmaceuticals 2024, 17(7), 888; https://doi.org/10.3390/ph17070888 - 4 Jul 2024
Viewed by 711
Abstract
The chemical composition of extracts (CEs) and essential oils (EOs) from Tetradenia riparia leaves, flower buds, and stems was analyzed. Antiproliferative activity against tumor cell lines, NO production inhibition, and antioxidant and antiviral activities were assessed. The CEs contained flavonoids, phenolic acids, coumarins, [...] Read more.
The chemical composition of extracts (CEs) and essential oils (EOs) from Tetradenia riparia leaves, flower buds, and stems was analyzed. Antiproliferative activity against tumor cell lines, NO production inhibition, and antioxidant and antiviral activities were assessed. The CEs contained flavonoids, phenolic acids, coumarins, and saturated fatty acids. The EOs included monoterpenes, oxygenated sesquiterpenes, and diterpenes. NO production inhibition ranged from 76 to 247 µg mL−1, and antiproliferative activity exhibited GI50 between 20 and >204 µg mL−1, with low cytotoxicity (SI: 1.08 to 4.75). Reactive oxygen species inhibition ranged from 45 to 82%. Antioxidant activity varied when determined by the 2,2-diphenyl-1-picrylhydrazyl radical scavenging assay (IC50: 0.51 to 8.47 mg mL−1) and ferric reducing antioxidant power (0.35 to 0.81 µM ferrous sulfate per mg). The reduction in β-carotene–linoleic acid co-oxidation varied between 76.13 and 102.25%. The total phenolic content of CEs and EOs was 10.70 to 111.68 µg gallic acid mg−1. Antiviral activity against herpes simplex virus type 1 (HSV-1) showed an EC50 between 9.64 and 24.55 µg mL−1 and an SI between 8.67 and 15.04. Leaf EOs exhibited an EC50 of 9.64 µg mL−1 and an SI of 15.04. Our study unveils the diverse chemical composition and multifaceted pharmacological properties of T. riparia, demonstrating its potential as a valuable source of bioactive compounds for therapeutic applications. Full article
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<p>Antiviral activity of extract and essential oils of <span class="html-italic">T. riparia</span>. Vero cells were infected at MOI 1.5, followed by the addition of the corresponding extract or essential oil. The virus genome production in the supernatant was quantitated by using qPCR after 48 h. The percentage of inhibition was determined as the ratio between treated and untreated infected cells. (<b>A</b>) leaves extract, (<b>B</b>) stem extract, (<b>C</b>) flower extract, (<b>D</b>) leaves essential oil, (<b>E</b>) stem essential oil, and (<b>F</b>) flower essential oil. The results represent the means ± standard deviation of three separate assays.</p>
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18 pages, 3128 KiB  
Article
Activation of Peroxymonosulfate by P-Doped Cow Manure Biochar for Enhancing Degradation of 17β-Estradiol
by Wu You, Gongduan Fan, Junhou Zhou, Ruiyu Lin, Xingfeng Cao, Yiqing Song, Jing Luo, Jianyong Zou, Zhanglin Hong, Kai-Qin Xu and Quanda Luo
Water 2024, 16(12), 1754; https://doi.org/10.3390/w16121754 - 20 Jun 2024
Cited by 1 | Viewed by 512
Abstract
Sulfate radical-based advanced oxidation processes exhibit great potential for the degradation of organic pollutants. In this study, P-doped biochar (PBC500) was successfully synthesized by the pyrolysis of H3PO4-impregnated cow manure waste and was employed to activate peroxymonosulfate (PMS) for [...] Read more.
Sulfate radical-based advanced oxidation processes exhibit great potential for the degradation of organic pollutants. In this study, P-doped biochar (PBC500) was successfully synthesized by the pyrolysis of H3PO4-impregnated cow manure waste and was employed to activate peroxymonosulfate (PMS) for the elimination of 17β-estradiol (E2). The characterization results showed that the surface area, defective structure, and functional groups (C=O and phosphorus-containing groups) of biochar increased after H3PO4 modification. PBC500 exhibited high PMS activation activity and excellent E2 degradation capacity; 97.91% of 3 mg/L E2 can be removed within 90 min using 0.2 g/L PBC500 and 1 mM PMS. Based on the quenching experiments and X-ray photoelectron spectroscopy (XPS) analysis, defective structures, C=O, and P-C groups on biochar act as active sites to promote the catalytic oxidation of E2 by generating O2 and 1O2. In addition, PBC500 displayed excellent reusability, achieving 65.15% E2 degradation after three reuse cycles. Overall, this study presented a new technique that supports a high efficiency, environmentally friendly, and low cost treatment method for E2 wastewater and simultaneously provided a new option for the resource utilization of livestock waste. Full article
(This article belongs to the Special Issue Application of Biochar and Activated Carbon in Water Treatment)
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<p>SEM images of the following: (<b>a</b>) CBC500; (<b>b</b>) PBC500.</p>
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<p>(<b>a</b>) N<sub>2</sub> adsorption/desorption isotherms (Inset: Pore size distribution) of CBC500 and PBC500. (<b>b</b>) XRD patterns of CBC500 and PBC500. (<b>c</b>) FTIR spectra of CBC500 and PBC500. (<b>d</b>) TG and DTG curves of untreated and H<sub>3</sub>PO<sub>4</sub>-treated cow manure.</p>
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<p>C 1s spectra of (<b>a</b>) CBC500 and (<b>b</b>) PBC500; O 1s spectra of (<b>c</b>) CBC500 and (<b>d</b>) PBC500; (<b>e</b>) P 2p spectra of PBC500 and (<b>f</b>) XPS survey spectra of PBC500 and CBC500.</p>
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<p>(<b>a</b>) Removal of E2 in different systems; (<b>b</b>) Kinetic fitting curves (experiment conditions: [E2] = 3 mg/L, [PMS] = 2.0 mM, and [biochar] = 0.1 g/L).</p>
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<p>Effects of (<b>a</b>) PBC500 dosage ([E2] = 3 mg/L, [PMS] = 2 mM); (<b>b</b>) PMS concentration ([E2] = 3 mg/L, [PBC500] = 0.2 g/L); (<b>c</b>) E2 concentration ([PMS] = 1 mM, [PBC500] = 0.2 g/L); (<b>d</b>) pH, (<b>e</b>) Cl<sup>−</sup>; (<b>f</b>) HA ([E2] = 3 mg/L, [PMS] = 1 mM, [PBC500] = 0.2 g/L) on the degradation of E2 in PBC500/PMS system.</p>
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<p>(<b>a</b>) The effect of quenchers on E2 degradation. (<b>b</b>) Kinetic fitting curves (experiment conditions: [E2] = 3 mg/L, [PMS] = 1.0 mM, and [PBC500] = 0.2 g/L).</p>
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<p>Mechanism of PMS activated by PBC500 for E2 degradation.</p>
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<p>(<b>a</b>) The reusability of the PBC500/PMS system in three consecutive cycles and (<b>b</b>) the adsorption and catalytic performance of ash modified biochar (experiment conditions: [E2] = 3 mg/L, [PMS] = 1.0 mM, and [biochar] = 0.2 g/L).</p>
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17 pages, 2480 KiB  
Article
Impact of Inorganic Anions on the Photodegradation of Herbicide Residues in Water by UV/Persulfate-Based Advanced Oxidation
by Gabriel Pérez-Lucas, Aitor Campillo and Simón Navarro
Catalysts 2024, 14(6), 376; https://doi.org/10.3390/catal14060376 - 13 Jun 2024
Viewed by 817
Abstract
The removal of pesticides and other organic pollutants from water through advanced oxidation processes (AOPs) holds great promise. The main advantage of these technologies is that they remove, or at least reduce, pesticide levels by mineralization rather than transfer, as in conventional processes. [...] Read more.
The removal of pesticides and other organic pollutants from water through advanced oxidation processes (AOPs) holds great promise. The main advantage of these technologies is that they remove, or at least reduce, pesticide levels by mineralization rather than transfer, as in conventional processes. This study first evaluated the effectiveness of UV/S2O8= compared to heterogeneous photocatalysis using UV/TiO2 processes on the degradation of two commonly used herbicides (terbuthylazine and isoproturon) in aqueous solutions using a laboratory photoreactor. In addition, the effect of the UV wavelength on the degradation efficiency of both herbicides was investigated. Although the degradation rate was greater under UV(254)/S2O8= nm than under UV(365)/S2O8= nm, complete degradation of the herbicides (0.2 mg L−1) was achieved within 30 min under UV-366 nm using a Na2S2O8 dose of 250 mg L−1 in the absence of inorganic anions. To assess the impact of the water matrix, the individual and combined effects of sulfate (SO4=), bicarbonate (HCO3), and chloride (Cl) were evaluated. These can react with hydroxyl (HO) and sulfate (SO4•−) radicals generated during AOPs to form new radicals with a lower redox potential. The results showed negligible effects of SO4=, while the combination of HCO3 and Cl seemed to be the key to the decrease in herbicide removal efficiency found when working with complex matrices. Finally, the main intermediates detected during the photodegradation process are identified, and the likely pathways involving dealkylation, dechlorination, and hydroxylation are proposed and discussed. Full article
(This article belongs to the Special Issue Recent Advances in Photocatalytic Treatment of Pollutants in Water)
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<p>Evolution of herbicide residues over time in photolytic, PS, and UV/PS tests.</p>
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<p>Degradation kinetics of herbicides in UV/PS and UV/TiO<sub>2</sub> systems.</p>
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<p>Anion-influenced UV/PS herbicide degradation.</p>
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<p>Speciation of carbonate species in water as a function of pH. Adapted from Manaham [<a href="#B51-catalysts-14-00376" class="html-bibr">51</a>].</p>
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<p>Evolution of DOC in the UV/PS system as a function of the anionic content.</p>
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<p>Proposed degradation pathways for ISP, including <span class="html-italic">N</span>-dealquilations (A1 and A2) and hydrolysis to aniline derivatives (B), and TBZ, involving dealkylations (A1 and A2), dechlorination, and subsequent hydroxylation (B).</p>
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26 pages, 10621 KiB  
Article
Comparative Effect of Antioxidant and Antibacterial Potential of Zinc Oxide Nanoparticles from Aqueous Extract of Nepeta nepetella through Different Precursor Concentrations
by Nouzha Fodil, Djaaboub Serra, Johar Amin Ahmed Abdullah, Juan Domínguez-Robles, Alberto Romero and Amrouche Abdelilah
Materials 2024, 17(12), 2853; https://doi.org/10.3390/ma17122853 - 11 Jun 2024
Viewed by 560
Abstract
Antibiotic resistance is a global health crisis caused by the overuse and misuse of antibiotics. Accordingly, bacteria have developed mechanisms to resist antibiotics. This crisis endangers public health systems and medical procedures, underscoring the urgent need for novel antimicrobial agents. This study focuses [...] Read more.
Antibiotic resistance is a global health crisis caused by the overuse and misuse of antibiotics. Accordingly, bacteria have developed mechanisms to resist antibiotics. This crisis endangers public health systems and medical procedures, underscoring the urgent need for novel antimicrobial agents. This study focuses on the green synthesis of ZnO nanoparticles (NPs) using aqueous extracts from Nepeta nepetella subps. amethystine leaves and stems, employing different zinc sulfate concentrations (0.5, 1, and 2 M). NP characterization included transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray diffraction (XRD), along with Fourier transform infrared spectroscopy (FTIR) analysis. This study aimed to assess the efficacy of ZnO NPs, prepared at varying concentrations of zinc sulfate, for their capacity to inhibit both Gram-positive and Gram-negative bacteria, as well as their antioxidant potential using the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. SEM and TEM results showed predominantly spherical NPs. The smallest size (18.5 ± 1.3 nm for leaves and 18.1 ± 1.3 nm for stems) occurred with the 0.5 M precursor concentration. These NPs also exhibited remarkable antibacterial activity against both Gram-positive and Gram-negative bacteria at 10 µg/mL, as well as the highest antioxidant activity, with an IC50 (the concentration of NPs that scavenge 50% of the initial DPPH radicals) of 62 ± 0.8 (µg/mL) for the leaves and 35 ± 0.6 (µg/mL) for the stems. NPs and precursor concentrations were modeled to assess their impact on bacteria using a 2D polynomial equation. Response surface plots identified optimal concentration conditions for antibacterial effectiveness against each species, promising in combating antibiotic resistance. Full article
(This article belongs to the Section Advanced Nanomaterials and Nanotechnology)
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<p>Original photo of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> taken at Djebel Aissa at an altitude of 1600 m (photo taken by Dr. Gordo Belkacem).</p>
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<p>XRD spectrum of the synthesized ZnO NPs using the extract of different parts of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> and different precursor concentrations.</p>
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<p>Zeta potential values of the ZnO NPs using the extracts of different parts of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> and different precursor concentrations (0.5 M, 1 M, and 2 M).</p>
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<p>FTIR spectrum of the synthesized ZnO NPs using the extract of different parts of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> and different precursor concentrations.</p>
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<p>Scanning electron microscopy (SEM) of the synthesized ZnO NPs using the extracts of leaves and stems of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> and different precursor concentrations (0.5 M, 1 M, and 2 M).</p>
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<p>Transmission electron microscopy (TEM) of the synthesized ZnO NPs using the extracts of leaves and stems of <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> and different precursor concentrations (0.5 M, 1 M, and 2 M).</p>
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<p>DPPH IC<sub>50</sub> values (µg/mL) for the ZnO NPs from the different parts of the plant (leaves and stems) and the different precursor concentrations (0.5 M, 1 M, and 2 M).</p>
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<p>Response surface plots (3D) showing the interactive effect of variables (CC = nanoparticle concentration and CP = precursor concentration) on the inhibition (ZI = inhibition zone) of each bacterial species and for each part of the plant <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> (<b>a</b>–<b>j</b>).</p>
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<p>Response surface plots (3D) showing the interactive effect of variables (CC = nanoparticle concentration and CP = precursor concentration) on the inhibition (ZI = inhibition zone) of each bacterial species and for each part of the plant <span class="html-italic">Nepeta nepetella</span> subps. <span class="html-italic">amethystine</span> (<b>a</b>–<b>j</b>).</p>
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23 pages, 3458 KiB  
Article
New Insight into the Degradation of Sunscreen Agents in Water Treatment Using UV-Driven Advanced Oxidation Processes
by Tajana Simetić, Jasmina Nikić, Marija Kuč, Dragana Tamindžija, Aleksandra Tubić, Jasmina Agbaba and Jelena Molnar Jazić
Processes 2024, 12(6), 1156; https://doi.org/10.3390/pr12061156 - 3 Jun 2024
Viewed by 683
Abstract
This study evaluates, for the first time, the effects of UV/PMS and UV/H2O2/PMS processes on the degradation of sunscreen agents in synthetic and natural water matrices and compares their effectiveness with the more conventional UV/H2O2. [...] Read more.
This study evaluates, for the first time, the effects of UV/PMS and UV/H2O2/PMS processes on the degradation of sunscreen agents in synthetic and natural water matrices and compares their effectiveness with the more conventional UV/H2O2. Investigations were conducted using a mixture of organic UV filters containing 4-methylbenzylidene camphor (4-MBC) and 2-ethylhexyl-4-methoxycinnamate. Among the investigated UV-driven AOPs, UV/PMS/H2O2 was the most effective in synthetic water, while in natural water, the highest degradation rate was observed during the degradation of EHMC by UV/PMS. The degradation of UV filters in the UV/PMS system was promoted by sulfate radical (68% of the degradation), with hydroxyl radical contributing approximately 32%, while both radical species contributed approximately equally to the degradation in the UV/H2O2/PMS system. The Vibrio fischeri assay showed an increase in inhibition (up to 70%) at specific stages of UV/H2O2 treatment when applied to natural water, which further decreased to 30%, along with an increase in UV fluence and progressive degradation. The Pseudomonas putida test recorded minor toxicity (<15%) after treatments. Magnetic biochar utilized in conjunction with UV-driven AOPs exhibited superior performance in eliminating residual contaminants, providing an efficient and sustainable approach to mitigate sunscreen agents in water treatment. Full article
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<p>(<b>a</b>,<b>b</b>) Degradation of sunscreen agents in ultrapure water using different processes: H<sub>2</sub>O<sub>2</sub>, PMS, PMS/H<sub>2</sub>O<sub>2</sub>, UV-C alone (control processes), and UV-driven AOPs. Experimental conditions: [4-MBC]<sub>0</sub> = [EHMC]<sub>0</sub> = 100 µg/L; [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 mM (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); pH = 7.0 ± 0.3.</p>
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<p>4-MBC and EHMC degradation rate constants in ultrapure water obtained during the UV-C photolysis, UV/H<sub>2</sub>O<sub>2</sub>, UV/PMS, and UV/PMS/H<sub>2</sub>O<sub>2</sub> processes.</p>
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<p>The quenching effect of MeOH and TBA on the degradation of 4-MBC in ultrapure water using the (<b>a</b>) UV/H<sub>2</sub>O<sub>2</sub>, (<b>b</b>) UV/PMS, and (<b>c</b>) UV/PMS/H<sub>2</sub>O<sub>2</sub> processes. Experimental conditions: [4-MBC]<sub>0</sub> = [EHMC]<sub>0</sub> = 100 µg/L, [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 mM, [MeOH]<sub>0</sub> = [TBA]<sub>0</sub> = 50 mM (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM, [MeOH]<sub>0</sub> = [TBA]<sub>0</sub> = 50 mM and 200 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); pH = 7.0 ± 0.3.</p>
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<p>The quenching effect of MeOH and TBA on the degradation of EHMC in ultrapure water using the (<b>a</b>) UV/H<sub>2</sub>O<sub>2</sub>, (<b>b</b>) UV/PMS, and (<b>c</b>) UV/PMS/H<sub>2</sub>O<sub>2</sub> processes. Experimental conditions: [4-MBC]<sub>0</sub> = [EHMC]<sub>0</sub> = 100 µg/L, [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 mM, [MeOH]<sub>0</sub> = [TBA]<sub>0</sub> = 50 mM (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM, [MeOH]<sub>0</sub> = [TBA]<sub>0</sub> = 50 mM and 200 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); pH = 7.0 ± 0.3.</p>
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<p>Degradation of sunscreen agents in natural water using different processes: UV and UV-driven AOPs (<b>a</b>,<b>b</b>). Experimental conditions: [4-MBC]<sub>0</sub> = [EHMC]<sub>0</sub> = 100 µg/L; [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 and 0.3 mM (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); pH = 7.81 ± 0.23.</p>
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<p>4-MBC and EHMC degradation rate constants in natural water obtained during the UV-C photolysis and UV-driven AOPs (<b>a</b>,<b>b</b>). Experimental conditions: [4-MBC]<sub>0</sub> = [EHMC]<sub>0</sub> = 100 µg/L; [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 and 0.3 mM (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); pH = 7.81 ± 0.23.</p>
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<p>Toxicity evaluation by (<b>a</b>) <span class="html-italic">Vibrio fischeri</span> and (<b>b</b>) <span class="html-italic">Pseudomonas putida</span> during 4-MBC and EHMC degradation in ultrapure water.</p>
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<p>Toxicity evaluation by (<b>a</b>) <span class="html-italic">Vibrio fischeri</span> and (<b>b</b>) <span class="html-italic">Pseudomonas putida</span> during 4-MBC and EHMC degradation in natural water.</p>
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<p>(<b>a</b>) XRD pattern and (<b>b</b>) FTIR spectra of pristine biochar (BC) and magnetic biochar (MBC).</p>
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<p>Adsorption of 4-MBC and EHMC on magnetic biochar after the application of (<b>a</b>) UV/H<sub>2</sub>O<sub>2</sub>, (<b>b</b>) UV/PMS, and (<b>c</b>) UV/PMS/H<sub>2</sub>O<sub>2</sub> in natural water. Experimental conditions: [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.03 (UV/H<sub>2</sub>O<sub>2</sub> and UV/PMS); [H<sub>2</sub>O<sub>2</sub>]<sub>0</sub> = [PMS]<sub>0</sub> = 0.015 mM (UV/PMS/H<sub>2</sub>O<sub>2</sub>); [adsorbent]<sub>0</sub> = 0.3 g/L; reaction time 30–240 min; pH = 7.81 ± 0.23.</p>
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32 pages, 8198 KiB  
Article
Anti-Vasculogenic, Antioxidant, and Anti-Inflammatory Activities of Sulfated Polysaccharide Derived from Codium tomentosum: Pharmacokinetic Assay
by Marwa Lakhrem, Malek Eleroui, Zakaria Boujhoud, Amal Feki, Amel Dghim, Sanah Essayagh, Said Hilali, Marwa Bouhamed, Choumous Kallel, Nathalie Deschamps, Bertrand de Toffol, Jean Marc Pujo, Riadh Badraoui, Hatem Kallel and Ibtissem Ben Amara
Pharmaceuticals 2024, 17(6), 672; https://doi.org/10.3390/ph17060672 - 23 May 2024
Viewed by 591
Abstract
The purpose of this paper was to investigate the anti-inflammatory and anti-angiogenic activities of sulfated polysaccharide from C. tomentosum (PCT) using carrageenan (CARR)-induced paw edema in a rat model and anti-vasculogenic activity on a chorioallantoic membrane assay (CAM) model. Based on in vitro [...] Read more.
The purpose of this paper was to investigate the anti-inflammatory and anti-angiogenic activities of sulfated polysaccharide from C. tomentosum (PCT) using carrageenan (CARR)-induced paw edema in a rat model and anti-vasculogenic activity on a chorioallantoic membrane assay (CAM) model. Based on in vitro tests of anti-radical, total antioxidant, and reducing power activities, PCT presents a real interest via its antioxidant activity and ability to scavenge radical species. The in vivo pharmacological tests suggest that PCT possesses anti-inflammatory action by reducing paw edema and leukocyte migration, maintaining the redox equilibrium, and stabilizing the cellular level of several pro-/antioxidant system markers. It could significantly decrease the malondialdehyde levels and increase superoxide dismutase, glutathione peroxidase, and glutathione activities in local paw edema and erythrocytes during the acute inflammatory reaction of CARR. PCT pretreatment was effective against DNA alterations in the blood lymphocytes of inflamed rats and reduced the hematological alteration by restoring blood parameters to normal levels. The anti-angiogenic activity results revealed that CAM neovascularization, defined as the formation of new vessel numbers and branching patterns, was decreased by PCT in a dose-dependent manner, which supported the in silico bioavailability and pharmacokinetic findings. These results indicated the therapeutic effects of polysaccharides from C. tomentosum and their possible use as anti-proliferative molecules based on their antioxidant, anti-inflammatory, and anti-angiogenic activities. Full article
(This article belongs to the Topic Research in Pharmacological Therapies)
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<p>Structural analysis of polysaccharide extracted from <span class="html-italic">C. tomentosum</span>. (<b>A</b>) UV–visible absorption spectrum. (<b>B</b>) Monosaccharide composition analysis using HPLC-FID.</p>
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<p>Structural analysis of polysaccharide extracted from <span class="html-italic">C. tomentosum</span>. (<b>A</b>) UV–visible absorption spectrum. (<b>B</b>) Monosaccharide composition analysis using HPLC-FID.</p>
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<p>XRD spectrum of PCT.</p>
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<p>Morphological structure of PCT using scanning electron microscopy: (<b>A</b>) magnification ×10; (<b>B</b>) magnification ×50; (<b>C</b>) magnification ×100.</p>
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<p>(<b>A</b>) Illustration of the oral bioavailability of PCT building blocks based on their physicochemical properties: lipophilicity (LIPO), molecular size (SIZE), polarity (POLAR), insolubility (INSOLU), insaturation (INSATU), and flexibility (FLEX). Regarding less lipophilicity, most of the studied monosaccharides and paroxetine possessed good oral bioavailability. (<b>B</b>) Illustration of the boiled egg model for the PCT monosaccharides. None of the studied PCT monosaccharides are blood–brain barrier (BBB)-permeant. Rhamnose is a P-glycoprotein substrate (PGP+) that has positive human intestinal absorption (HIA). Fucose and glucuronic acid possess the highest gastrointestinal (GI) absorption. (1) Arabinose; (2) fructose; (3) galacturonic acid; (4) glucuronic acid; (5) rhamnose; (6) xylose.</p>
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<p>Antioxidant potentials of PCT. (<b>A</b>) DPPH radical scavenging activity. (<b>B</b>) Total antioxidant activity. (<b>C</b>) Reducing power. Gallic acid used as standard in DPPH test, and BHT used as standard in reducing power assay and total antioxidant activity.</p>
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<p>(<b>A</b>) Effect of PCT on paw edema in rats induced by carrageenan during 5 h: (<b>a</b>) control group, (<b>b</b>) CARR group, (<b>c</b>) CARR + PCT group, and (<b>d</b>) CARR + DICL group. Red arrows in the photos indicate edema on the paws of the rats. (<b>B</b>) Paw edema thickness (mm). (<b>C</b>) Percentage of edema inhibition. (<b>D</b>) Percentage of edema inflammation. Control: normal rats injected with NaCl 0.9%; CARR: rats injected with carrageenan 1%; CARR + PCT: inflamed rats treated with 20 mg/kg; CARR + DICL: inflamed rats treated with diclofenac 25 mg/kg. Values represent means ± SEM (n = 6) in each group; ns, no difference; ** <span class="html-italic">p</span> &lt; 0.01; and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>(<b>A</b>) Blood smears stained with May–Grünwald–Giemsa examined with a light microscope at ×400 magnification (scale bar = 50 μm): (<b>a</b>) control group, (<b>b</b>) CARR group, (<b>c</b>) CARR + PCT group, and (<b>d</b>) CARR + DICL group. The arrows indicate <span class="html-fig-inline" id="pharmaceuticals-17-00672-i001"><img alt="Pharmaceuticals 17 00672 i001" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i001.png"/></span> lymphocytes and <span class="html-fig-inline" id="pharmaceuticals-17-00672-i002"><img alt="Pharmaceuticals 17 00672 i002" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i002.png"/></span> platelet aggregates. (<b>B</b>,<b>C</b>) Semi-quantitative scores of necrosis and platelet aggregates in the blood smears of adult rats, respectively. (<b>D</b>,<b>E</b>) Effect of PCT on lymphocytes and neutrophil cell infiltration in carrageenan-induced paw edema, respectively. Values are expressed as means ± SD; ns, no difference; * <span class="html-italic">p</span> &lt; 0.05 and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>(<b>A</b>) Effect of inflammation induced by CARR and treatment with PCT or DICL on genetic materials of white blood cells after 5 h based on MN test assay (scale bar = 20 μm): (<b>a</b>) control group, (<b>b</b>) CARR group, (<b>c</b>) CARR + PCT group, and (<b>d</b>) CARR + DICL group. Green spot indicates intact DNA, and the red spots reflect damaged DNA. (<b>B</b>) Semi-quantitative scores of apoptosis of adult rats. Values are expressed as means ± SD. ns, no difference *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>(<b>A</b>) Effect of inflammation induced by CARR and treatment with PCT or DICL on genetic materials of white blood cells after 5 h based on MN test assay (scale bar = 20 μm): (<b>a</b>) control group, (<b>b</b>) CARR group, (<b>c</b>) CARR + PCT group, and (<b>d</b>) CARR + DICL group. Green spot indicates intact DNA, and the red spots reflect damaged DNA. (<b>B</b>) Semi-quantitative scores of apoptosis of adult rats. Values are expressed as means ± SD. ns, no difference *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effect of PCT and DICL on CARR-induced histological modification in rat skin. H&amp;E-stained skin sections were examined with a light microscope at ×50 (scale bar = 100 μm) and ×200 magnifications (scale bar = 50 μm). (<b>A</b>) Tissue sections of skin rats from the control group; (<b>B</b>) tissue sections of rats from the CARR group; (<b>C</b>) tissue sections of skin rats from the PCT group; and (<b>D</b>) tissue sections of rats from the diclofenac group. Arrows indicate the following: D: dermis, E: epidermis, <span class="html-fig-inline" id="pharmaceuticals-17-00672-i003"><img alt="Pharmaceuticals 17 00672 i003" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i003.png"/></span> lymphocyte infiltration, <span class="html-fig-inline" id="pharmaceuticals-17-00672-i004"><img alt="Pharmaceuticals 17 00672 i004" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i004.png"/></span> edema. (<b>E1</b>–<b>E3</b>) Score of inflammatory infiltrate, apoptosis, and edema. Significance: ns: no difference; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effect of PCT and DICL on CARR-induced histological modification in rat skin. H&amp;E-stained skin sections were examined with a light microscope at ×50 (scale bar = 100 μm) and ×200 magnifications (scale bar = 50 μm). (<b>A</b>) Tissue sections of skin rats from the control group; (<b>B</b>) tissue sections of rats from the CARR group; (<b>C</b>) tissue sections of skin rats from the PCT group; and (<b>D</b>) tissue sections of rats from the diclofenac group. Arrows indicate the following: D: dermis, E: epidermis, <span class="html-fig-inline" id="pharmaceuticals-17-00672-i003"><img alt="Pharmaceuticals 17 00672 i003" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i003.png"/></span> lymphocyte infiltration, <span class="html-fig-inline" id="pharmaceuticals-17-00672-i004"><img alt="Pharmaceuticals 17 00672 i004" src="/pharmaceuticals/pharmaceuticals-17-00672/article_deploy/html/images/pharmaceuticals-17-00672-i004.png"/></span> edema. (<b>E1</b>–<b>E3</b>) Score of inflammatory infiltrate, apoptosis, and edema. Significance: ns: no difference; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effect of PCT on CAM angiogenesis (<b>A</b>) Morphological micrographs: (a) negative controls; (b) positive control (CAM treated with choriogonadotropin (0.5 μg/g eggs)); (c) negative control (CAM treated with diclofenac (5 μg/g eggs)); (d,e) CAM treated with 25 μg and 50 μg/g eggs of PCT (scale bar = 50 mm); 1: photographs of blood vessels; 2: photomicrographs treated with ImageJ software 3: photomicrographs treated with angiotools software. (<b>B</b>) Number of vessels. (<b>C</b>) Length of blood vessels. (<b>D</b>) Lacunarity. (<b>E</b>) Number of junctions. Values are expressed as means ± SD for 6 eggs in each group. ns: no difference; ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Location of the algae collection site (Chebba, Mahdia, Tunisia).</p>
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19 pages, 5235 KiB  
Article
Inherited Structure Properties of Larch Arabinogalactan Affected via the TEMPO/NaBr/NaOCl Oxidative System
by Vladislav A. Ionin, Yuriy N. Malyar, Valentina S. Borovkova, Dmitriy V. Zimonin, Roksana M. Gulieva and Olga Yu. Fetisova
Polymers 2024, 16(11), 1458; https://doi.org/10.3390/polym16111458 - 22 May 2024
Viewed by 621
Abstract
Arabinogalactan (AG), extracted from larch wood, is a β-1,3-galactan backbone and β-1,6-galactan side chains with attached α-1-arabinofuranosyl and β-1-arabinopyranosyl residues. Although the structural characteristics of arabinogalactan II type have already been studied, its functionalization using 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) oxidation remains a promising avenue. In [...] Read more.
Arabinogalactan (AG), extracted from larch wood, is a β-1,3-galactan backbone and β-1,6-galactan side chains with attached α-1-arabinofuranosyl and β-1-arabinopyranosyl residues. Although the structural characteristics of arabinogalactan II type have already been studied, its functionalization using 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) oxidation remains a promising avenue. In this study, the oxidation of AG, a neutral polysaccharide, was carried out using the TEMPO/NaBr/NaOCl system, resulting in polyuronides with improved functional properties. The oxidation of AG was controlled by analyzing portions of the reaction mixture using spectrophotometric and titration methods. To determine the effect of the TEMPO/NaBr/NaOCl system, air-dried samples of native and oxidized AG were studied by Fourier-transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopy, as well as by gel permeation chromatography. Compounds that model free (1,1-diphenyl-2-picrylhydrazyl (DPPH)) and hydroxyl radicals (iron(II) sulfate, hydrogen peroxide, and salicylic acid) were used to study the antioxidant properties. It was found that, in oxidized forms of AG, the content of carboxyl groups increases by 0.61 mmol compared to native AG. The transformation of oxidized AG into the H+ form using a strong acid cation exchanger leads to an increase in the number of active carboxyl groups to 0.76 mmol. Using FTIR spectroscopy, characteristic absorption bands (1742, 1639, and 1403 cm−1) were established, indicating the occurrence of oxidative processes with a subsequent reduction in the carboxyl group. The functionality of AG was also confirmed by gel permeation chromatography (GPC), which is reflected in an increase in molecular weights (up to 15,700 g/mol). A study of the antioxidant properties of the oxidized and protonated forms of AG show that the obtained antioxidant activity (AOA) values are generally characteristic of polyuronic acids. Therefore, the TEMPO oxidation of AG and other neutral polysaccharides can be considered a promising approach for obtaining compounds with the necessary controlled characteristics. Full article
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<p>Structure of arabinogalactan units.</p>
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<p>Scheme of TEMPO/NaBr/NaOCl-mediated oxidation of larch wood arabinogalactan.</p>
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<p>Gel permeation chromatograms of native and purified AG-T after dialysis.</p>
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<p>Calibration curve of D-galacturonic acid solutions.</p>
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<p>Dynamics of 0.1 M NaOH consumption and uronic acid content.</p>
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<p>Potentiometric titration curves of arabinogalactan samples: (<b>1</b>) native AG; (<b>2</b>) AG-T; (<b>3</b>) AG-TH.</p>
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<p>Dissolving the native arabinogalactan (<b>a</b>) 100 mg/mL; (<b>b</b>) 50 mg/mL; (<b>c</b>) 33 mg/mL.</p>
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<p>Dissolving the arabinogalactan samples up to a 100 mg/mL concentration (<b>a</b>) AG-T; (<b>b</b>) AG-TH.</p>
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<p>Dissolving the arabinogalactan samples up to a 33 mg/mL concentration: (<b>a</b>) native AG; (<b>b</b>) AG-T; (<b>c</b>) AG-TH.</p>
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<p>IR spectra of arabinogalactan samples’ absorbance units: (<b>1</b>) native AG; (<b>2</b>) AG-T; (<b>3</b>) AG-TH.</p>
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<p><sup>1</sup>H (<b>a</b>) and <sup>13</sup>C (<b>b</b>) NMR spectra of native and oxidized AG recorded in D<sub>2</sub>O.</p>
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<p>Molecular weight distribution of arabinogalactan samples.</p>
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<p>TGA/DTG thermal degradation profiles of native and oxidized AG samples.</p>
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<p>Activity of arabinogalactan samples scavenging (<b>a</b>) DPPH and (<b>b</b>) hydroxyl radicals.</p>
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<p>Impact of AG-TH volume on flocculation rate and flocculation activity in the presence of CaCl<sub>2</sub> and FeCl<sub>3</sub>.</p>
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15 pages, 1301 KiB  
Article
Perspectives for Photochemical Leaching Processes of Chalcopyrite: A Solar Radical-Leaching Process
by Orlando Yepsen, Lorena Cornejo-Ponce and Rodrigo Yepsen
Mining 2024, 4(2), 352-366; https://doi.org/10.3390/mining4020020 - 11 May 2024
Viewed by 573
Abstract
This paper review presents a comparison between conventional leaching and advanced photochemical leaching processes and their potential for use in chalcopyrite leaching. Likewise, it presents an analysis of the differences between the advanced leaching processes, photoleaching and radical-leaching, indicating that the photochemical mechanisms [...] Read more.
This paper review presents a comparison between conventional leaching and advanced photochemical leaching processes and their potential for use in chalcopyrite leaching. Likewise, it presents an analysis of the differences between the advanced leaching processes, photoleaching and radical-leaching, indicating that the photochemical mechanisms (photooxidation/photoreduction and generation of radical oxygen species (ROS) and radical sulfur species (RSS)) would improve the oxidative dissolution of chalcopyrite, taking advantage of the high oxidizing power of free radicals. Initial experimental results of solar-assisted radical-leaching on chalcopyrite are presented, demonstrating that sulfate radicals (SO4) allow copper to be leached at a rate 4.7 times higher than in the absence of radicals and sunlight. With these results, a radical-leaching process is presented for the first time, with a perspective toward the future development of a new hydrometallurgical route: solar-assisted radical-leaching. Full article
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<p>Diagram of the smelting and conversion processes for obtaining copper from sulfide ores (Chalcopyrite CuFeS<sub>2</sub>).</p>
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<p>Projected copper production for 2030 according to product [<a href="#B6-mining-04-00020" class="html-bibr">6</a>].</p>
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<p>Scheme of photoleaching process for chalcopyrite leaching.</p>
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<p>Leaching copper extraction from CuFeS<sub>2</sub> via solar-assisted radical-leaching in comparison with oxidant reagent (H<sub>2</sub>O<sub>2</sub>) and control reaction. Chalcopyrite 0.5 g L<sup>−1</sup>, pH 6 (radical-leaching), pH 3 (oxidant and control reactions), [H<sub>2</sub>O<sub>2</sub>] 145 µL/200 mL solution, PS 0.12 g/200 mL, magnetic stirrer (1500 r.p.m.), 1 atm pressure, solar radiation: UVA = 5.22 Wm<sup>−2</sup>, Vis = 361.4 Wm<sup>−2</sup>. Copper released is presented as total Cu concentration released (ppm) in the pregnant leaching solution (PLS).</p>
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16 pages, 4845 KiB  
Article
Degradation of Levofloxacin by Electroactivated Sodium Persulfate on Carbon Cloth Cathode Modified with Cerium-Based Metal Organic Frameworks (Ce-MOF) Derivatives
by Xinbiao Mao, Mingyu Ou, Wenjun Zhao, Shuangting Yu and Hao Xu
Separations 2024, 11(5), 144; https://doi.org/10.3390/separations11050144 - 7 May 2024
Viewed by 818
Abstract
Levofloxacin (LFX), which is difficult to degrade effectively due to its molecular stability, has become an problem that needs to be solved urgently. The advanced oxidation technology of persulfate has received increasing attention from researchers. In this study, a Ce-MOF derivative (Ce-MOF-T) was [...] Read more.
Levofloxacin (LFX), which is difficult to degrade effectively due to its molecular stability, has become an problem that needs to be solved urgently. The advanced oxidation technology of persulfate has received increasing attention from researchers. In this study, a Ce-MOF derivative (Ce-MOF-T) was prepared by hydrothermal synthesis and calcination, which synergistically responded to electroactivation to generate sulfate radicals for the efficient degradation of LFX. It has been proven that electrical activation and the Ce-MOF derivatives work together to generate sulfate radicals and effectively degrade LFX. Ce-MOF-550-modified carbon cloth was used as the cathode and a platinum electrode as the anode, the concentration of LFX was 20 mg·L−1, the loading of Ce-MOF-550 was 15 mg, pH = 5, the concentration of sodium persulfate (PMS) was 0.3 g·L−1, the current density was 100 A·m−2, and the degradation rate was 82.05% after 1 h of reaction and 95% after 3 h of reaction. After five cycle tests, the degradation rate was still higher than 75.00%, indicating that the material had good stability. In addition, the degradation of LFX was consistent with a quasi-primary kinetic reaction with apparent rate constants of 2.26 × 10−2 min−1. Full article
(This article belongs to the Special Issue Applications of Electrochemistry in Water and Wastewater Treatment)
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<p>XRD patterns of Ce-MOF, Ce-MOF-450, Ce-MOF-550, Ce-MOF-650, and Ce-MOF-750.</p>
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<p>SEM spectra of Ce-MOF (<b>a</b>), Ce-MOF-450 (<b>b</b>), Ce-MOF-550 (<b>c</b>), Ce-MOF-650 (<b>d</b>), and Ce-MOF-750 (<b>e</b>) and EDS analysis of Ce-MOF-550 (<b>f</b>).</p>
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<p>Nitrogen adsorption–desorption isotherms of Ce-MOF, Ce-MOF-450, Ce-MOF-550, and Ce-MOF-650.</p>
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<p>Degradation rate of LFX by different systems (namely, pure electrolysis, pure catalyst, catalyst-combined electrolysis) (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; (A) M<sub>cat.</sub>: 0 mg, i: 50 A·m<sup>−2</sup>; (B) M<sub>cat.</sub>: 15 mg, i: 0 A·m<sup>−2</sup>; (C) M<sub>cat.</sub>: 15 mg, i: 50 A·m<sup>−2</sup>).</p>
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<p>Effect of Ce-MOF derivatives on degradation rate after calcination at different temperatures. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; i: 50 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>Effect of loading on degradation rate. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; i: 50 A·m<sup>−2</sup>; M<sub>cat.</sub>: 7.5, 10, 12.5, 15, 17.5, 20 mg).</p>
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<p>Effect of PMS concentration on degradation rate. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.1, 0.2, 0.3, 0.4, 0.5 g·L<sup>−1</sup>; pH: 5; i: 50 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>Effect of pH on degradation rate. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; i: 50 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>Effects of different current densities on degradation rate. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; M<sub>cat.</sub>: 15 mg).</p>
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<p>Effect of LFX concentration on degradation rate. (C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; i: 100 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>XRD patterns of pure carbon cloth, unused Ce-MOF-550, and used Ce-MOF-550.</p>
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<p>Effect of C recycling on degradation rate. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; i: 100 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>Degradation rate constants of LFX. (C<sub>LFX</sub>: 20 mg·L<sup>−1</sup>; C<sub>PMS</sub>: 0.3 g·L<sup>−1</sup>; pH: 5; i: 100 A·m<sup>−2</sup>; M<sub>cat.</sub>: 15 mg).</p>
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<p>(<b>a</b>,<b>b</b>) The intermediate products of the reaction.</p>
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<p>The degradation process of LFX.</p>
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24 pages, 4645 KiB  
Article
Extraction of Protein and Bioactive Compounds from Mediterranean Red Algae (Sphaerococcus coronopifolius and Gelidium spinosum) Using Various Innovative Pretreatment Strategies
by Jihen Dhaouafi, Naima Nedjar, Mourad Jridi, Montassar Romdhani and Rafik Balti
Foods 2024, 13(9), 1362; https://doi.org/10.3390/foods13091362 - 28 Apr 2024
Cited by 1 | Viewed by 3315
Abstract
In this study, the release of proteins and other biomolecules into an aqueous media from two red macroalgae (Sphaerococcus coronopifolius and Gelidium spinosum) was studied using eight different cell disruption techniques. The contents of carbohydrates, pigments, and phenolic compounds coextracted with [...] Read more.
In this study, the release of proteins and other biomolecules into an aqueous media from two red macroalgae (Sphaerococcus coronopifolius and Gelidium spinosum) was studied using eight different cell disruption techniques. The contents of carbohydrates, pigments, and phenolic compounds coextracted with proteins were quantified. In addition, morphological changes at the cellular level in response to the different pretreatment methods were observed by an optical microscope. Finally, the antioxidant capacity of obtained protein extracts was evaluated using three in vitro tests. For both S. coronopifolius and G. spinosum, ultrasonication for 60 min proved to be the most effective technique for protein extraction, yielding values of 3.46 ± 0.06 mg/g DW and 9.73 ± 0.41 mg/g DW, respectively. Furthermore, the highest total contents of phenolic compounds, flavonoids, and carbohydrates were also recorded with the same method. However, the highest pigment contents were found with ultrasonication for 15 min. Interestingly, relatively high antioxidant activities like radical scavenging activity (31.57–65.16%), reducing power (0.51–1.70, OD at 700 nm), and ferrous iron-chelating activity (28.76–61.37%) were exerted by the different protein extracts whatever the pretreatment method applied. This antioxidant potency could be attributed to the presence of polyphenolic compounds, pigments, and/or other bioactive substances in these extracts. Among all the used techniques, ultrasonication pretreatment for 60 min appears to be the most efficient method in terms of destroying the macroalgae cell wall and extracting the molecules of interest, especially proteins. The protein fractions derived from the two red macroalgae under these conditions were precipitated with ammonium sulfate, lyophilized, and their molecular weight distribution was determined using SDS-PAGE. Our results showed that the major protein bands were observed between 25 kDa and 60 kDa for S. coronopifolius and ranged from 20 kDa to 150 kDa for G. spinosum. These findings indicated that ultrasonication for 60 min could be sufficient to disrupt the algae cells for obtaining protein-rich extracts with promising biological properties, especially antioxidant activity. Full article
(This article belongs to the Section Food Nutrition)
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<p>A schematic of different cell disruption and protein extraction methods applied to two red macroalgae (<span class="html-italic">S. coronopifolius</span> and <span class="html-italic">G. spinosum</span>).</p>
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<p>Cell morphology observation of <span class="html-italic">S. coronopifolius</span> (<b>1</b>) and <span class="html-italic">G. spinosum</span> (<b>2</b>) under 40× magnification: untreated cells (<b>A</b>), US for 15 min (<b>B</b>), US for 30 min (<b>C</b>), US for 60 min (<b>D</b>), MG (<b>E</b>), MG-US30 (<b>F</b>), TPP (<b>G</b>), UATPP (<b>H</b>), FD-US30 (<b>I</b>), BB (<b>J</b>), and FP (<b>K</b>). Scale bar, 10 mm.</p>
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<p>Mass extraction yields of <span class="html-italic">S. coronopifolius</span> (<b>A</b>) and <span class="html-italic">G. spinosum</span> (<b>B</b>) pretreated with different cell disruption techniques. a, b, c, d, e, f, g, h and k: different letters mean significant differences between extracts (<span class="html-italic">p</span> &lt; 0.05). Results are expressed as average ± standard deviation (SD) (<span class="html-italic">n</span> = 3). US, ultrasonication; MG, manual grinding; TPP, three-phase partitioning; UATPP, ultrasonication-assisted three-phase partitioning; MG-US30, manual grinding + ultrasonication for 30 min; FD-US30, freeze drying + ultrasonication for 30 min; FP, French press; and BB, bead-beating.</p>
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<p>Protein contents of <span class="html-italic">S. coronopifolius</span> (<b>A</b>) and <span class="html-italic">G. spinosum</span> (<b>B</b>) extracts using different techniques of cell disruption. a, b, c, d, e, and f: different letters mean significant differences between extracts (<span class="html-italic">p</span> &lt; 0.05). Results are expressed as average ± standard deviation (SD) (<span class="html-italic">n</span> = 3). US, ultrasonication; MG, manual grinding; TPP, three-phase partitioning; UATPP, ultrasonication-assisted three-phase partitioning; MG-US30, manual grinding + ultrasonication for 30 min; FD-US30, freeze drying + ultrasonication for 30 min; FP, French press; and BB, bead-beating.</p>
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<p>Sodium dodecyl sulphate polyacrylamide gel electrophoresis profiles of red macroalgae soluble protein extracts. Lane 1: molecular weight standards. Lane 2: water soluble protein from <span class="html-italic">S. coronopifolius</span>. Lane 3: water soluble protein from <span class="html-italic">G. spinosum</span>.</p>
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<p>Carbohydrate contents of <span class="html-italic">S. coronopifolius</span> (<b>A</b>) and <span class="html-italic">G. spinosum</span> (<b>B</b>) extracts using different techniques of cell disruption. a, b, c, d, e, f, g, and h: different letters mean significant differences between extracts (<span class="html-italic">p</span> &lt; 0.05). Results are expressed as average ± standard deviation (SD) (<span class="html-italic">n</span> = 3). US, ultrasonication; MG, manual grinding; TPP, three-phase partitioning; UATPP, ultrasonication-assisted three-phase partitioning; MG-US30, manual grinding + ultrasonication for 30 min; FD-US30, freeze drying + ultrasonication for 30 min; FP, French press; and BB, bead-beating.</p>
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<p>Pigment contents of <span class="html-italic">S. coronopifolius</span> (<b>A</b>) and <span class="html-italic">G. spinosum</span> (<b>B</b>) extracts using different techniques of cell disruption. a, b, c, d, e, f, g, h, i, j, and k: different letters mean significant differences between extracts of the same pigment (<span class="html-italic">p</span> &lt; 0.05). Results are expressed as average ± standard deviation (SD) (<span class="html-italic">n</span> = 3). US, ultrasonication; MG, manual grinding; TPP, three-phase partitioning; UATPP, ultrasonication-assisted three-phase partitioning; MG-US30, manual grinding + ultrasonication for 30 min; FD-US30, freeze drying + ultrasonication for 30 min; FP, French press and BB, bead-beating.</p>
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<p>Antioxidant activity of <span class="html-italic">S. coronopifolius</span> and <span class="html-italic">G. spinosum</span> extracts using different techniques of cell disruption. DPPH free radical scavenging activity of <span class="html-italic">S. coronopifolius</span> (<b>A</b>) and <span class="html-italic">G. spinosum</span> (<b>B</b>); reducing power of <span class="html-italic">S. coronopifolius</span> (<b>C</b>) and <span class="html-italic">G. spinosum</span> (<b>D</b>); and ferrous ion-chelating ability of <span class="html-italic">S. coronopifolius</span> (<b>E</b>) and <span class="html-italic">G. spinosum</span> (<b>F</b>). a, b, c, d, e, f, g, h, and i: different letters mean significant differences between extracts of the same antioxidant test (<span class="html-italic">p</span> &lt; 0.05). Results are expressed as average ± standard deviation (SD) (<span class="html-italic">n</span> = 3). US, ultrasonication; MG, manual grinding; TPP, three-phase partitioning; UATPP, ultrasonication-assisted three-phase partitioning; MG-US30, manual grinding + ultrasonication for 30 min; FD-US30, freeze drying + ultrasonication for 30 min; FP, French press and BB, bead-beating.</p>
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32 pages, 1105 KiB  
Review
Selected Micropollutant Removal from Municipal Wastewater
by Ján Derco, Andreja Žgajnar Gotvajn, Patrícia Guľašová, Nikola Šoltýsová and Angelika Kassai
Processes 2024, 12(5), 888; https://doi.org/10.3390/pr12050888 - 27 Apr 2024
Viewed by 863
Abstract
Micropollutants belong to various groups of chemicals. One of the most diverse and large group of them are pharmaceuticals. The presence of pharmaceutical residues in wastewater poses a significant challenge to water quality and environmental health. This paper provides an overview of recent [...] Read more.
Micropollutants belong to various groups of chemicals. One of the most diverse and large group of them are pharmaceuticals. The presence of pharmaceutical residues in wastewater poses a significant challenge to water quality and environmental health. This paper provides an overview of recent advancements in the removal of pharmaceuticals from water, focusing on various treatment processes and their effectiveness in eliminating micropollutants. Through a review of the literature, including studies on ozonation, UV irradiation, sulfate radical-based technologies, and photocatalytic processes, insights into degradation mechanisms and optimal conditions for their removal are synthesized. Additionally, with new legislation mandating the monitoring of selected micropollutants and the implementation of quaternary treatment in wastewater treatment plants, the paper discusses prospects for future research and recommendations for effective pharmaceutical removal. Key actions include conducting comprehensive laboratory and pilot trials, implementing quaternary treatment of wastewater, continuously monitoring water quality, investing in research and development, and promoting collaboration and knowledge sharing among stakeholders. By embracing these strategies, we can work towards safeguarding water resources and protecting public health from the adverse effects of pharmaceutical contamination. Full article
(This article belongs to the Section Environmental and Green Processes)
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<p>Pathways of the distribution of selected micropollutants (MPs) in the environment.</p>
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<p>5-methyl-benzotriazole—5MeBZT [<a href="#B13-processes-12-00888" class="html-bibr">13</a>].</p>
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<p>Advanced oxidation processes for the removal of MPs.</p>
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