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21 pages, 5068 KiB  
Article
Enhancing Functional Compounds in Sesame Oil through Acid-Soaking and Microwave-Heating of Sesame Seeds
by Jitkunya Yuenyong, Suchintana Limkoey, Chonlathit Phuksuk, Thitima Winan, Chonlada Bennett, Sudarat Jiamyangyuen, Sugunya Mahatheeranont and Phumon Sookwong
Foods 2024, 13(18), 2891; https://doi.org/10.3390/foods13182891 - 12 Sep 2024
Viewed by 257
Abstract
This study investigated whether pre-treating sesame (Sesamum indicum L.) seeds with a combination of acid-soaking and microwave-heating could significantly enhance the quality of the resulting sesame oil, particularly by increasing its content of functional compounds such as lignans, tocopherol, phytosterol, and squalene. [...] Read more.
This study investigated whether pre-treating sesame (Sesamum indicum L.) seeds with a combination of acid-soaking and microwave-heating could significantly enhance the quality of the resulting sesame oil, particularly by increasing its content of functional compounds such as lignans, tocopherol, phytosterol, and squalene. The study revealed that soaking the sesame seeds in a solution of HCl and citric acid, along with microwave-heating, significantly increased the content of these compounds. The detected ranges were sesamin (1365–6927 µg g−1), sesamolin (605–3493 µg g−1), tocopherol (69.31–282.76 µg g−1), asarinin (ND–383.52 µg g−1), sesamol (ND–49.59 µg g−1), phytosterol (3690–6201 µg g−1), and squalene (532−1628 µg g−1). Additionally, the study found that the pre-treatment of sesame seeds had a minimal effect on the fatty acid composition, antioxidant activity (92.94–95.08% DPPH scavenging activity), and oxidative stability (2.13–2.90 mg MDA kg−1 oil). This is the first study to demonstrate that using acid-soaking and microwave-heating to prepare sesame seeds can produce sesame oil enriched with functional compounds, potentially benefiting cosmetic, pharmaceutical, and health applications. Full article
(This article belongs to the Special Issue Plant Oil: Processing, Chemical Contents and Nutritional Effects)
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Graphical abstract

Graphical abstract
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<p>Diagram for experimentation including acid-soaking, microwave treatment, and sesame oil extraction.</p>
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<p>The effect of acid-soaking on (<b>A</b>) yield, and content of (<b>B</b>) lignans, (<b>C</b>) tocopherol, (<b>D</b>) phytosterol, and (<b>E</b>) squalene of the extracted sesame oil. Means denoted by different letters indicate significant differences between treatments (<span class="html-italic">p</span> &lt; 0.05). Means with the same letters indicate no significant difference between the values.</p>
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<p>The effect of microwave-heating on (<b>A</b>) yield, and content of (<b>B</b>) lignans, (<b>C</b>) tocopherol, (<b>D</b>) phytosterol, and (<b>E</b>) squalene of the extracted sesame oil. Means denoted by different letters indicate significant differences between treatments (<span class="html-italic">p</span> &lt; 0.05). Means with the same letters indicate no significant difference between the values.</p>
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<p>The influence of type of acid solution on (<b>A</b>) yield, and content of (<b>B</b>) lignans, and (<b>C</b>) tocopherol of the extracted sesame oil. Means denoted by different letters indicate significant differences between treatments (<span class="html-italic">p</span> &lt; 0.05). Means with the same letters indicate no significant difference between the values.</p>
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<p>Three-dimensional response surfaces, contour plots, and Pareto charts illustrating lignans content under different pre-treatment conditions of HCl (<b>A</b>,<b>C</b>,<b>E</b>) and citric acid (<b>B</b>,<b>D</b>,<b>F</b>) systems. The red dot indicates the location of the optimum condition.</p>
Full article ">Figure 6
<p>Comparison of the different pre-treatment methods of sesame seeds prior to oil extraction, including explosion-puffing (EP) [<a href="#B24-foods-13-02891" class="html-bibr">24</a>], general microwave-heating (MW) [<a href="#B25-foods-13-02891" class="html-bibr">25</a>,<a href="#B32-foods-13-02891" class="html-bibr">32</a>], vacuum microwave-heating (VM) [<a href="#B26-foods-13-02891" class="html-bibr">26</a>], and roasting (RT) [<a href="#B26-foods-13-02891" class="html-bibr">26</a>]. Means denoted by different letters indicate significant differences between treatments (<span class="html-italic">p</span> &lt; 0.05). Means with the same letters indicate no significant difference between the values.</p>
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<p>Fatty acid composition of sesame oil samples (%).</p>
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16 pages, 2509 KiB  
Article
Comparative Transcriptomic Analysis on the Effect of Sesamol on the Two-Stages Fermentation of Aurantiochytrium sp. for Enhancing DHA Accumulation
by Xuewei Yang, Liyang Wei, Shitong Liang, Zongkang Wang and Shuangfei Li
Mar. Drugs 2024, 22(8), 371; https://doi.org/10.3390/md22080371 - 16 Aug 2024
Viewed by 660
Abstract
Aurantiochytrium is a well-known long-chain polyunsaturated fatty acids (PUFAs) producer, especially docosahexaenoic acid (DHA). In order to reduce the cost or improve the productivity of DHA, many researchers are focusing on exploring the high-yield strain, reducing production costs, changing culture conditions, and other [...] Read more.
Aurantiochytrium is a well-known long-chain polyunsaturated fatty acids (PUFAs) producer, especially docosahexaenoic acid (DHA). In order to reduce the cost or improve the productivity of DHA, many researchers are focusing on exploring the high-yield strain, reducing production costs, changing culture conditions, and other measures. In this study, DHA production was improved by a two-stage fermentation. In the first stage, efficient and cheap soybean powder was used instead of conventional peptone, and the optimization of fermentation conditions (optimal fermentation conditions: temperature 28.7 °C, salinity 10.7‰, nitrogen source concentration 1.01 g/L, and two-nitrogen ratio of yeast extract to soybean powder 2:1) based on response surface methodology resulted in a 1.68-fold increase in biomass concentration. In the second stage, the addition of 2.5 mM sesamol increased the production of fatty acid and DHA by 93.49% and 98.22%, respectively, as compared to the optimal culture condition with unadded sesamol. Transcriptome analyses revealed that the addition of sesamol resulted in the upregulation of some genes related to fatty acid synthesis and antioxidant enzymes in Aurantiochytrium. This research provides a low-cost and effective culture method for the commercial production of DHA by Aurantiochytrium sp. Full article
(This article belongs to the Special Issue Algal Cultivation for Obtaining High-Value Products)
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Graphical abstract
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<p>Effects of various nitrogen sources on the biomass concentration of <span class="html-italic">Aurantiochytrium</span> sp. DECR-KO. Cell dry weight (DCW) was obtained by culture for 65 h with 2.5 g/L different nitrogen source.</p>
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<p>(<b>A</b>) The effects of six different temperature levels; (<b>B</b>) the effects of six different salinity levels; (<b>C</b>) the effects of six different nitrogen sources; (<b>D</b>) the effect of the ratio of two nitrogen sources (yeast extract: soybean powder). Contour plots showing the effect of (<b>E</b>) temperature and salt (<b>F</b>), temperature and nitrogen ratio (<b>G</b>), temperature and nitrogen source concentration to dry cell weight (DCW). Response surface plots show the effect of (<b>H</b>) temperature and salt, (<b>I</b>) temperature and N ratio, (<b>J</b>) temperature and nitrogen source concentration to DCW.</p>
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<p>(<b>A</b>) Schematic diagram of enhancing lipid production in <span class="html-italic">Aurantiochytrium</span> sp. DECR-KO. (<b>B</b>) The difference of biomass concentration in YS and M4 culture after exponential phase. (<b>C</b>) Effects of DMSO and ethanol on cell concentration and neutral lipid content of <span class="html-italic">Aurantiochytrium</span> sp. DECR-KO at different volume concentrations. Solvent addition amount is expressed as volume concentration (<span class="html-italic">v</span>/<span class="html-italic">v</span>), and YS culture without adding any solvent was used as the control group. Cell concentration was shown as the number of cells per milliliter of culture medium, and neutral lipid content was represented by the relative fluorescence intensity of Nile red in each cell. (<b>D</b>,<b>E</b>): Effects of varying sesamol concentrations on DECR-KO strains’ fatty acid yield and DHA synthesis. M4: experimental group before fermentation optimization; YS: experimental group cultured with yeast extract and soybean powder after fermentation optimization; YS-S: experimental group YS treated with 2.5 mM sesamol. DHA: docosahexaenoic acid; UFAs: unsaturated fatty acids; SFAs: saturated fatty acids. ns: not significant, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Difference of (<b>A</b>) biomass concentration, (<b>B</b>) fatty acids and (<b>C</b>) DHA yield in fermentation optimization experiments. ** <span class="html-italic">p</span> &lt; 0.01 and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>The relative expression levels of related enzyme genes by qRT-PCR. *** <span class="html-italic">p</span> &lt; 0.001, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Schematic map of transcriptional analysis of the pathways associated with lipid and carbon metabolism in <span class="html-italic">Aurantiochytrium</span> sp. DECR-KO. HADH: 3-hydroxyacyl-CoA dehydrogenase; ECH: enoyl-CoA hydratase; ACD: acyl-CoA dehydrogenase; KAT: 3-ketoacyl-CoA thiolase; SOD: superoxide dismutase; GST: glutathione S-transferase; ACC: acetyl-CoA carboxylase; MCAT: malonyl-CoA:ACP transacylase; ME: malic enzyme; FAS: fatty acid synthase; KS: 3-ketoacyl-synthase; KR: ketoreductase; PFK: 6-phosphofructokinase; TPI: triosephosphate isomerase; GAPDH: glyceraldehyde 3-phosphate dehydrogenase.</p>
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18 pages, 1340 KiB  
Article
Assessment of the Sunscreen Properties of Sesame Oil Using the Hemispherical Directional Reflectance Method
by Małgorzata Bożek, Julia Trybała, Agata Lebiedowska, Anna Stolecka-Warzecha, Paula Babczyńska and Sławomir Wilczyński
Appl. Sci. 2024, 14(15), 6545; https://doi.org/10.3390/app14156545 - 26 Jul 2024
Viewed by 483
Abstract
Sesame oil has been widely used for centuries. It is not only used as a kitchen ingredient, but it is also used to apply to the skin. Sesame oil contains natural compounds such as sesamol, sesamolin and sesamide, which have the ability to [...] Read more.
Sesame oil has been widely used for centuries. It is not only used as a kitchen ingredient, but it is also used to apply to the skin. Sesame oil contains natural compounds such as sesamol, sesamolin and sesamide, which have the ability to reflect or absorb certain UV rays. These substances can act as UV filters, helping to minimize the effects of harmful UV radiation on the skin. The aim of the study was to investigate the radioprotective/sun protection properties of sesame oil. The influence of sesame oils from different manufacturers on the directional reflectance of the skin was analyzed at various time intervals. To assess the sunscreen properties of the oil, a new technique was used: the 410-Solar hemispherical directional reflectometer. Sesame oil can be used in sunscreen preparations, but only when combined with other, more powerful ingredients. The oil itself is not sufficient protection against solar radiation. The study revealed no significant disparities in performance between the tested sesame oils from diverse manufacturers. Full article
15 pages, 17198 KiB  
Article
Antifungal Activity of Sesamol on Pestalotiopsis neglecta: Interfering with Cell Membrane and Energy Metabolism
by Weihu Ma, Jingyu Ji, Bowen Zhang, Wenzhuo Sun, Jinyan Zhao, Jie Zhang and Guocai Zhang
J. Fungi 2024, 10(7), 488; https://doi.org/10.3390/jof10070488 - 15 Jul 2024
Viewed by 658
Abstract
This paper investigated the inhibitory effect of Sesamol (Ses) on Pestalotiopsis neglecta. The potential inhibitory mechanisms were explored by observing changes in cell morphology, measuring alterations in cell membrane-related indices, as well as energy metabolism-related indices and changes in enzyme activities related [...] Read more.
This paper investigated the inhibitory effect of Sesamol (Ses) on Pestalotiopsis neglecta. The potential inhibitory mechanisms were explored by observing changes in cell morphology, measuring alterations in cell membrane-related indices, as well as energy metabolism-related indices and changes in enzyme activities related to virulence. The results show that Ses completely inhibited the growth of P. neglecta at 600 μg/mL (minimum inhibitory concentration and minimum fungicidal concentration), with an EC50 of 142 ± 13.22 μg/mL. As observed with scanning electron microscopy (SEM) and transmission electron microscopy (TEM), Ses treatment resulted in the breakage and crumpling of P. neglecta cell membrane and organelle lysis. Ergosterol content and the total lipid in P. neglecta treated with 300 μg/mL Ses was 91.52% and 54% of that in the control groups, respectively. In addition, spores were stained, increased leakage of intracellular constituents at 260 nm, and decreased extracellular pH. This suggests damage to the cell membrane integrity and permeability. Furthermore, Ses decreased the ATP levels and key enzymes in the tricarboxylic acid (TCA) cycle, indicating interference with the fungal energy metabolism. Moreover, the activities of polygalacturonase (PG) and endoglucanase (EG) of P. neglecta treated with 300 μg/mL of Ses were only 28.20% and 29.13% of that in the control groups, respectively, indicating that Ses can reduce the virulence of P. neglecta. In conclusion, our results show that Ses should be considered as a potential plant-derived fungicide due to its ability to disrupt the morphology of P. neglecta, damage cell membrane integrity and permeability in P. neglecta, interfere with energy metabolism, and reduce its virulence, ultimately affecting the fungal growth. Full article
(This article belongs to the Section Fungal Pathogenesis and Disease Control)
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Figure 1

Figure 1
<p>(<b>A</b>) The inhibition of mycelial growth of <span class="html-italic">P. neglecta</span> at 25 °C 7 days after Ses treatment; the positive drug is bromothalonil (600 µg/mL). (<b>B</b>) Inhibition of mycelial growth of <span class="html-italic">P. neglecta</span> at 25 °C 7 days after Ses treatment. The bars represent the standard error of the mean (<span class="html-italic">n</span> = 3). The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The cell membrane integrity in <span class="html-italic">P. neglecta</span> spores after Ses treatment. PI-stained spores of <span class="html-italic">P. neglecta</span> after treatment with 600, 300, 150, 75, and 37.5 µg/mL Ses for 8 h was observed at 100× (<b>A</b>). Staining percentage of spores stained after PI treatment (<b>B</b>). The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The cell membrane integrity in <span class="html-italic">P. neglecta</span> spores after Ses treatment. PI-stained spores of <span class="html-italic">P. neglecta</span> after treatment with 600, 300, 150, 75, and 37.5 µg/mL Ses for 8 h was observed at 100× (<b>A</b>). Staining percentage of spores stained after PI treatment (<b>B</b>). The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Impact of Ses on <span class="html-italic">P. neglecta</span> surface morphology. Red arrows represent untreated <span class="html-italic">P. neglecta</span> mycelium, while green arrows represent <span class="html-italic">P. neglecta</span> mycelium treated with EC<sub>50</sub>.</p>
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<p>Impact of Ses on <span class="html-italic">P. neglecta</span> ultra-microstructure. Red arrows represent untreated <span class="html-italic">P. neglecta</span> cells, while green arrows represent <span class="html-italic">P. neglecta</span> mycelium treated with EC<sub>50</sub>.</p>
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<p>The impact of various concentrations of Ses on the total lipid content (<b>A</b>) and ergosterol content (<b>B</b>) in <span class="html-italic">P. neglecta</span>. The bars represent the standard error of the mean (<span class="html-italic">n</span> = 3). The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The impact of various concentrations of Ses on leakage of intracellular constituents at 260 nm (<b>A</b>), relative conductivity (<b>B</b>) and extracellular pH (<b>C</b>) of <span class="html-italic">P. neglecta</span>. Values were calculated as means (<span class="html-italic">n</span> = 3), and vertical bars represent standard errors. ** (<span class="html-italic">p</span> &lt; 0. 01) *** (<span class="html-italic">p</span> &lt; 0.001) vs. control group; the significant difference between DMSO and CK was ns.</p>
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<p>The impact of different concentrations of Ses on ATP content (<b>A</b>), CS activity (<b>B</b>), MDH activity (<b>C</b>), NAD-ICDH activity (<b>D</b>), SDH activity (<b>E</b>), α-KGDH activity (<b>F</b>) of <span class="html-italic">P. neglecta</span>. Values were calculated as means (<span class="html-italic">n</span> = 3), and vertical bars represent standard errors. The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The impact of different concentrations of Ses on PG (<b>A</b>) and EG (<b>B</b>) activities of <span class="html-italic">P. neglecta</span>. The different letters represent statistically significant differences between the effects of different concentrations, according to the Tukey test (<span class="html-italic">p</span> &lt; 0.05).</p>
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20 pages, 5522 KiB  
Article
Optimization of Solid Lipid Nanoparticle Formulation for Cosmetic Application Using Design of Experiments, PART II: Physical Characterization and In Vitro Skin Permeation for Sesamol Skin Delivery
by Margot Cassayre, Auriane Oline, Caroline Orneto, Emmanuel Wafo, Lydia Abou, Alexandre Altié, Magalie Claeys-Bruno, Christophe Sauzet and Philippe Piccerelle
Cosmetics 2024, 11(4), 120; https://doi.org/10.3390/cosmetics11040120 - 15 Jul 2024
Viewed by 1125
Abstract
Our research focuses on evaluating the preliminary stability of solid lipid nanoparticles (SLNs) in order to identify an optimal formulation for studying the skin penetration of SLNs loaded with sesamol, with a view to developing potential cosmetic applications. For this study, SLNs were [...] Read more.
Our research focuses on evaluating the preliminary stability of solid lipid nanoparticles (SLNs) in order to identify an optimal formulation for studying the skin penetration of SLNs loaded with sesamol, with a view to developing potential cosmetic applications. For this study, SLNs were prepared with varying lipid and surfactant compositions and produced through homogenization and ultrasonication. The particle size (PS), polydispersity index (PDI), zeta potential (ZP), and encapsulation efficiency (EE) were analyzed for the different formulations. We identified OP2Se as the optimal formulation for skin penetration assessment due to its stable PS, PDI, ZP, and EE over time, with a Turbiscan Stability Index (TSI) below 1 after a month, indicating favorable stability conditions. The in vitro skin permeation study compared sesamol-loaded SLNs with a control sesamol hydrogel, revealing controlled release characteristics ideal for localized skin effects without significant bloodstream penetration, attributed to the SLNs’ 200 nm particle size. Further exploration could enhance skin retention and targeting, potentially extending penetration studies and reducing particle size to improve accumulation in hair follicles. Exploring SLN applications beyond sesamol, such as incorporating mineral filters for suncare, offers promising avenues, underscoring SLNs’ versatility in cosmetic formulations and skincare applications. Full article
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<p>Responses for the desirability function approach. (<b>A</b>) Desirability for particle size (nm); (<b>B</b>) Desirability for PDI; (<b>C</b>) Desirability for zeta potential (mV).</p>
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<p>(<b>A</b>) Mean values ± SD of the encapsulation efficiency (EE) of the produced nanoparticles at D-0 and (<b>B</b>) Student’s <span class="html-italic">t</span>-test results of the percentage of encapsulation efficiency (%EE).</p>
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<p>Mean PS distribution of blank (b) and sesamol (Se)-loaded optimized SLNs at different times (D-0, D-15, and D-30). * Significant difference in PS during storage (<span class="html-italic">p</span> &lt; 0.05) (<span class="html-italic">n</span> = 3).</p>
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<p>Mean PDI distribution of blank (b) and sesamol (Se)-loaded optimized SLNs at different times (D-0, D-15, and D-30). * Significant difference in PDI during storage (<span class="html-italic">p</span> &lt; 0.05) (<span class="html-italic">n</span> = 3).</p>
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<p>Mean zeta potential values of blank and loaded optimized SLNs at different times. * Significant difference in zeta potential during storage (<span class="html-italic">p</span> &lt; 0.05) (<span class="html-italic">n</span> = 3).</p>
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<p>Mean encapsulation efficiency percentage values of loaded optimized SLNs at different times. * Significant difference in encapsulation efficiency percentage during storage (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Representation of the Turbiscan Stability Index (TSI) of the optimized SLNs with and without sesamol.</p>
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<p>Representation of the delta retrodiffusion of OP1Se during storage (example of an unstable formulation).</p>
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<p>Representation of the delta retrodiffusion of OP2Se during storage (example of a stable formulation).</p>
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<p>Size distribution of OP2b SLNs by DLS measurement (<b>A</b>) and scanning electron microscopy (SEM): ×7500 (<b>B</b>); ×10,000 (<b>C</b>).</p>
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<p>Size distribution of OP2Se SLNs by DLS measurement (<b>A</b>) and scanning electron microscopy (SEM): ×2000 (<b>B</b>); ×15,000 (<b>C</b>).</p>
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<p>DSC thermographs of pure carnauba wax (CW) (blue), glyceryl behenate (GB) (green), glyceryl distearate (GDS) (red), and sesamol (Se) (brown).</p>
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<p>DSC thermographs of unloaded (OP2b) and loaded (OP2Se) solid lipid nanoparticles (loaded with 0.2% sesamol and obtained after 10 min of sonication).</p>
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<p>Permeation profile of sesamol throughout human skin explant (hydrogel vs. OP2Se SLNs).</p>
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<p>Skin distribution of sesamol after 8 h of penetration on human skin explant (hydrogel vs. OP2Se SLNs). * Significant difference (<span class="html-italic">p</span> &lt; 0.05) (<span class="html-italic">n</span> = 3).</p>
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26 pages, 20027 KiB  
Article
Design and Optimization of Sesamol Nanosuspensions to Potentiate the Anti-Tumor Activity of Epirubicin against Ehrlich Solid Carcinoma-Bearing Mice
by Kholoud A. Elzanaty, Gamal A. Omran, Ehab Kotb Elmahallawy, Ashraf Albrakati, Ayman A. Saleh, Naief Dahran, Alaa S. Alhegaili, Ahmad Salahuddin, Heba Abd-El-Azim, Ahmed Noreldin and Tarek M. Okda
Pharmaceutics 2024, 16(7), 937; https://doi.org/10.3390/pharmaceutics16070937 - 13 Jul 2024
Viewed by 934
Abstract
There is a growing interest in discovering natural sources of anti-cancer drugs. Sesamol (SES) is a phenolic compound with antitumor effects. The present study aimed to investigate the anticancer properties of SES and its nano-suspensions (SES-NS) combined with Epirubicin (EPI) in breast cancer [...] Read more.
There is a growing interest in discovering natural sources of anti-cancer drugs. Sesamol (SES) is a phenolic compound with antitumor effects. The present study aimed to investigate the anticancer properties of SES and its nano-suspensions (SES-NS) combined with Epirubicin (EPI) in breast cancer (BC) using mice bearing a solid Ehrlich tumor. The study involved 35 female albino mice and investigated the effects of SES and EPI on tumor growth, proliferation, apoptosis, autophagy, angiogenesis, and oxidative stress. Methods including ELISA, qRT-PCR, and immunohistochemistry were utilized. The findings revealed reductions in tumor growth and proliferation using SES either alone or combined and evidenced by decreased AKT (AKT Serine/Threonine kinase1) levels, angiogenesis indicated by lower levels of VEGFR (vascular endothelial growth factor), and apoptosis demonstrated by elevated caspase3 and BAX levels. Furthermore, autophagy increased and was indicated by increased levels of beclin1 and lc3, along with decreased oxidative stress as evidenced by elevated TAC (total antioxidant capacity) and reduced MDA (malondialdehyde) levels. Interestingly, SES-NS demonstrated more significant effects at lower doses. In summary, this study underscores the potential of SES as a promising agent for BC treatment. Moreover, SES-NS potentiated the beneficial effects of EPI while mitigating its adverse effects. Full article
(This article belongs to the Special Issue Natural Nanoparticle for Cancer Diagnosis and Treatment, 2nd Edition)
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Figure 1

Figure 1
<p>Tumor weight in all experimental groups. The abbreviations used are as follows: EST (Ehrlich solid tumor), SES (sesamol), SES-NS (nanosuspension of sesamol), EPI (Epirubicin), SES + EPI (sesamol + Epirubicin), and SES-NS + EPI (nanosuspension of sesamol + Epirubicin).</p>
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<p>(<b>a</b>) Particle size distribution of SES-NS formulations. (<b>b</b>) PDI of SES-NS formulations. Means ± SD, <span class="html-italic">n</span> = 3, ** Significant, ns non-significant difference using one-way ANOVA and Tukey post hoc test.</p>
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<p>The particle size distribution and polydispersity index (PDI) values of SES-NS formulations during a two-month storage period at 4 °C. The data are presented as mean ± standard deviation (SD), with three samples analyzed at each time point.</p>
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<p>(<b>a</b>) mRNA expression of AKT in all studied groups, (<b>b</b>) mRNA expression of Beclin1 in all studied groups, and (<b>c</b>) mRNA expression of LC3 in all studied groups using qRt-PCR with specific primers. Data expressed as mean ± SD. *, #, &amp;, <span>$</span>, ^, and @ indicate significant change from control, EST, SES, SES-NS, EPI, and SES + EPI respectively.</p>
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<p>(<b>a</b>) Expression of AKT in all studied groups and (<b>b</b>) expression of LC3 in all studied groups using ELISA technique. Data expressed as mean ± SD. *, #, &amp;, <span>$</span>, ^, and @ indicate significant change from control, EST, SES, SES-NS, EPI, and SES + EPI respectively.</p>
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<p>(<b>a</b>) Serum levels of caspase3 in all studied groups, (<b>b</b>) serum levels of BAX in all studied groups, (<b>c</b>) serum levels of MDA in all studied groups, and (<b>d</b>) serum levels of TAC in all studied groups. Data expressed as mean ± SD (<span class="html-italic">n</span> = 5). *, #, &amp;, <span>$</span>, ^, and @ indicate significant change from control, EST, SES, SES-NS, EPI, and SES + EPI respectively.</p>
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<p>(<b>a</b>) Levels of VEGFR2 in all studied groups, (<b>b</b>) levels of TnI in all studied groups, and (<b>c</b>) levels of CK-MB in all studied groups. Data expressed as mean ± SD (<span class="html-italic">n</span> = 5). *, #, &amp;, <span>$</span>, ^, and @ indicate significant change from control, EST, SES, SES-NS, EPI, and SES + EPI respectively.</p>
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<p>A representative photomicrograph illustrates VEGFR2 immunohistochemical expression in a mouse tumor from (<b>A</b>) EST, (<b>B</b>) SES, (<b>C</b>) SES-NS, (<b>D</b>) EPI, (<b>E</b>) SES + EPI, and (<b>F</b>) SES-NS + EPI. Arrowheads indicate positive immune expression. Scale bar = 100 µm. (<b>G</b>) One-way ANOVA was performed at <span class="html-italic">p</span> ≤ 0.05 and the data are presented as mean ± SE.</p>
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<p>Histopathological analysis was conducted on solid mammary tumors excised from mice treated with various therapies. (<b>A</b>) EST. (<b>B</b>) SES. (<b>C</b>) SES-NS. (<b>D</b>) EPI. (<b>E</b>) SES + EPI. (<b>F</b>) SES-NS + EPI. Arrows indicate the neoplastic tumors and arrowheads indicate the necrotic areas with different stages. Scale bar = 100 µm. (<b>G</b>) H and E semi-quantitative scoring of tumor necrosis. One-way ANOVA was performed at <span class="html-italic">p</span> ≤ 0.05 and the data are presented as mean ± SE.</p>
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<p>Representative photomicrographs for H&amp;E-stained liver in mouse from (<b>A</b>) negative control, (<b>B</b>) EST, (<b>C</b>) SES, (<b>D</b>) SES-NS, (<b>E</b>) EPI, (<b>F</b>) SES + EPI and (<b>G</b>) SES-NS + EPI. Thick arrow: pleomorphic, hyperchromatic, metastatic tumor foci; arrowheads: invasion of sinusoids with tumor and Kupffer cells. Scale bar = 50 µm. (<b>H</b>) Semi-quantitative scoring of histopathological lesion score. One-way ANOVA was performed at <span class="html-italic">p</span> ≤ 0.05 and the data are presented as mean ± SE.</p>
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<p>Representative photomicrographs for H&amp;E-stained kidney in mouse from (<b>A</b>) negative control, (<b>B</b>) EST, (<b>C</b>) SES, (<b>D</b>) SES-NS, (<b>E</b>) EPI, (<b>F</b>) SES + EPI and (<b>G</b>) SES-NS + EPI. Thick arrow: periglomerular and perivascular inflammatory infiltration; thin arrow: degenerated tubules; arrowhead: intervascular congestion. Scale bar = 50 µm. (<b>H</b>) Semi-quantitative scoring of histopathological lesion score. One-way ANOVA was performed at <span class="html-italic">p</span> ≤ 0.05 and the data are presented as mean ± SE.</p>
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<p>Representative photomicrographs for H&amp;E-stained heart in mouse from (<b>A</b>) negative control, (<b>B</b>) EST, (<b>C</b>) SES, (<b>D</b>) SES-NS, (<b>E</b>) EPI, (<b>F</b>) SES + EPI and (<b>G</b>) SES-NS + EPI. Thick arrow: degeneration and lysis of cardiac myocytes; thin arrow: infiltration of mononuclear chronic inflammatory cells; arrowhead: degeneration in tunica media and adventitia of arterial wall. Scale bar = 50 µm. (<b>H</b>,<b>I</b>) Semi-quantitative scoring of histopathological lesion score. One-way ANOVA was performed at <span class="html-italic">p</span> ≤ 0.05 and the data are presented as mean ± SE.</p>
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Article
Screening and Characterization of Antioxidant Film Applicable to Walnut Kernels from Juglans sigillata
by Ping Li, Yujia Zhang, Changwei Cao, Yaxi Luo, Huan Kan and Yun Liu
Foods 2024, 13(9), 1313; https://doi.org/10.3390/foods13091313 - 25 Apr 2024
Viewed by 1060
Abstract
Walnuts play a positive role in human health due to their large amounts of unsaturated fatty acids, whereas lipid oxidation can easily occur during storage. Herein, three natural antioxidants (epicatechin, sesamol, and myricetin) were added to the composite film cross-linked with chitosan and [...] Read more.
Walnuts play a positive role in human health due to their large amounts of unsaturated fatty acids, whereas lipid oxidation can easily occur during storage. Herein, three natural antioxidants (epicatechin, sesamol, and myricetin) were added to the composite film cross-linked with chitosan and soy protein peptide, and the antioxidant film appropriate for the preservation of walnut kernels from Juglans sigillata was screened to improve the storage quality of walnuts. The results showed that three antioxidant films could all enhance the storage performance of walnut kernels, with sesamol being the best. The characterization of antioxidant film cross-linked with chitosan and soy protein peptide containing sesamol (C/S-ses film) revealed that the composite film improved the slow release and stability of sesamol; in addition, the presence of sesamol could effectively reduce the light transmittance and water vapor permeability of the composite film, together with significantly enhancing the antioxidant and antimicrobial activities, resulting in an effective prolongation of the storage period of walnut kernels. These findings indicated that C/S-ses possess excellent potential for retarding the oxidative rancidity of unsaturated fatty acids and will provide an effective strategy for the preservation of walnut kernels. Full article
(This article belongs to the Section Food Packaging and Preservation)
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Figure 1

Figure 1
<p>The effect of the accelerated oxidation process on PV (<b>A</b>), AV (<b>B</b>), CV (<b>C</b>), and MDA (<b>D</b>) evaluated for the walnut kernels, as control, C, C/S, C/S-epi, C/S-ses, and C/S-myr. Different letters indicate significant differences between groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The effect of the accelerated oxidation process on K<sub>232</sub> (<b>A</b>), K<sub>268</sub> (<b>B</b>), browning degree (<b>C</b>), and MC (<b>D</b>) evaluated for the walnut kernels, as control, C, C/S, C/S-epi, C/S-ses, and C/S-myr. Different letters indicate significant differences between groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Mechanical properties (<b>A</b>), thickness (<b>B</b>), moisture content and water solubility (<b>C</b>), and WVP and OP (<b>D</b>) of C, C/S, and C/S-ses films. * indicates <span class="html-italic">p</span> &lt; 0.05, ** indicates <span class="html-italic">p</span> &lt; 0.01, and ns denotes non-significance.</p>
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<p>SEM micrographs acquired using 5000× magnification for the surface of the chitosan-based films for C (<b>A</b>), C/S (<b>B</b>), and C/S-ses (<b>C</b>).</p>
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<p>FTIR (<b>A</b>) spectra and DSC curves (<b>B</b>) recorded for C, C/S, and C/S-ses films.</p>
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<p>Inhibition zone diameters (<b>A</b>,<b>B</b>) and DPPH radical scavenging rates (<b>C</b>) of C, C/S, and C/S-ses films. * indicates <span class="html-italic">p</span> &lt; 0.05, ** indicates <span class="html-italic">p</span> &lt; 0.01, *** indicates <span class="html-italic">p</span> &lt; 0.001, and ns denotes non-significance.</p>
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<p>Stability of sesamol in C/S-ses (<b>A</b>) and slow release of sesamol in C/S-ses (<b>B</b>). *** indicates <span class="html-italic">p</span> &lt; 0.001, and ns denotes non-significance.</p>
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30 pages, 11132 KiB  
Review
Solvent Replacement Strategies for Processing Pharmaceuticals and Bio-Related Compounds—A Review
by Jia Lin Lee, Gun Hean Chong, Masaki Ota, Haixin Guo and Richard Lee Smith
Liquids 2024, 4(2), 352-381; https://doi.org/10.3390/liquids4020018 - 9 Apr 2024
Cited by 1 | Viewed by 1820
Abstract
An overview of solvent replacement strategies shows that there is great progress in green chemistry for replacing hazardous di-polar aprotic solvents, such as N,N-dimethylformamide (DMF), 1-methyl-2-pyrrolidinone (NMP), and 1,4-dioxane (DI), used in processing active industrial ingredients (APIs). In synthetic chemistry, alcohols, carbonates, ethers, [...] Read more.
An overview of solvent replacement strategies shows that there is great progress in green chemistry for replacing hazardous di-polar aprotic solvents, such as N,N-dimethylformamide (DMF), 1-methyl-2-pyrrolidinone (NMP), and 1,4-dioxane (DI), used in processing active industrial ingredients (APIs). In synthetic chemistry, alcohols, carbonates, ethers, eucalyptol, glycols, furans, ketones, cycloalkanones, lactones, pyrrolidinone or solvent mixtures, 2-methyl tetrahydrofuran in methanol, HCl in cyclopentyl methyl ether, or trifluoroacetic acid in propylene carbonate or surfactant water (no organic solvents) are suggested replacement solvents. For the replacement of dichloromethane (DCM) used in chromatography, ethyl acetate ethanol or 2-propanol in heptanes, with or without acetic acid or ammonium hydroxide additives, are suggested, along with methanol acetic acid in ethyl acetate or methyl tert-butyl ether, ethyl acetate in ethanol in cyclohexane, CO2-ethyl acetate, CO2-methanol, CO2-acetone, and CO2-isopropanol. Supercritical CO2 (scCO2) can be used to replace many organic solvents used in processing materials from natural sources. Vegetable, drupe, legume, and seed oils used as co-extractants (mixed with substrate before extraction) can be used to replace the typical organic co-solvents (ethanol, acetone) used in scCO2 extraction. Mixed solvents consisting of a hydrogen bond donor (HBD) solvent and a hydrogen bond acceptor (HBA) are not addressed in GSK or CHEM21 solvent replacement guides. Published data for 100 water-soluble and water-insoluble APIs in mono-solvents show polarity ranges appropriate for the processing of APIs with mixed solvents. When water is used, possible HBA candidate solvents are acetone, acetic acid, acetonitrile, ethanol, methanol, 2-methyl tetrahydrofuran, 2,2,5,5-tetramethyloxolane, dimethylisosorbide, Cyrene, Cygnet 0.0, or diformylxylose. When alcohol is used, possible HBA candidates are cyclopentanone, esters, lactone, eucalytol, MeSesamol, or diformylxylose. HBA—HBA mixed solvents, such as Cyrene—Cygnet 0.0, could provide interesting new combinations. Solubility parameters, Reichardt polarity, Kamlet—Taft parameters, and linear solvation energy relationships provide practical ways for identifying mixed solvents applicable to API systems. Full article
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Figure 1
<p>ACS Green Chemistry Institute and Pharmaceutical Roundtable (GCIPR) solvent selection tool <a href="https://www.acsgcipr.org/tools-for-innovation-in-chemistry/solvent-tool/" target="_blank">https://www.acsgcipr.org/tools-for-innovation-in-chemistry/solvent-tool/</a> (accessed on 1 April 2024) described by Diorazio et al. [<a href="#B20-liquids-04-00018" class="html-bibr">20</a>]. Copyright ACS, 2023.</p>
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<p>Reichardt E<sub>T</sub><sup>N</sup> parameters plotted against Kamlet—Taft dipolarity/polarizability parameters for selected molecular solvents.</p>
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<p>Kamlet—Taft basicity parameter plotted against acidity parameter for selected molecular solvents.</p>
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<p>Kamlet—Taft acidity (<span class="html-italic">α</span>) and basicity (<span class="html-italic">β</span>) versus dipolar/polarizability (<span class="html-italic">π</span>*) for aqueous and non-aqueous mixed solvents and pure solvents. Dashed lines show approximate behavior of mixed solvent KT parameters with composition.</p>
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<p>Dynamic viscosity (<span class="html-italic">η</span>) of water (HBD) –hydrogen bond acceptor (HBA) mixed solvent systems as a function of mole fraction of HBA solvent (<span class="html-italic">x</span><sub>2</sub>) at 25 °C. HBA solvents are ordered in terms of Hunter basicity (<math display="inline"><semantics> <mrow> <msubsup> <mrow> <mi>β</mi> </mrow> <mrow> <mn>2</mn> </mrow> <mrow> <mi mathvariant="normal">H</mi> </mrow> </msubsup> </mrow> </semantics></math>) values (low to high): acetonitrile (<span class="html-fig-inline" id="liquids-04-00018-i001"><img alt="Liquids 04 00018 i001" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i001.png"/></span> ACN), <span class="html-italic">γ</span>-valerolactone (<span class="html-fig-inline" id="liquids-04-00018-i002"><img alt="Liquids 04 00018 i002" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i002.png"/></span> GVL), <span class="html-italic">γ</span>-butyrolactone (<span class="html-fig-inline" id="liquids-04-00018-i003"><img alt="Liquids 04 00018 i003" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i003.png"/></span> GBL), tetrahydrofuran (<span class="html-fig-inline" id="liquids-04-00018-i004"><img alt="Liquids 04 00018 i004" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i004.png"/></span> THF), 1,4-dioxane (<span class="html-fig-inline" id="liquids-04-00018-i005"><img alt="Liquids 04 00018 i005" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i005.png"/></span> DI), acetone (<span class="html-fig-inline" id="liquids-04-00018-i006"><img alt="Liquids 04 00018 i006" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i006.png"/></span> Ace), pyridine (<span class="html-fig-inline" id="liquids-04-00018-i007"><img alt="Liquids 04 00018 i007" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i007.png"/></span> PYR), <span class="html-italic">N</span>-methyl-2-pyrrolidone (<span class="html-fig-inline" id="liquids-04-00018-i008"><img alt="Liquids 04 00018 i008" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i008.png"/></span> NMP), <span class="html-italic">N</span>,<span class="html-italic">N-</span>dimethylformamide (<span class="html-fig-inline" id="liquids-04-00018-i009"><img alt="Liquids 04 00018 i009" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i009.png"/></span> DMF), <span class="html-italic">N</span>,<span class="html-italic">N-</span>dimethylacetamide (<span class="html-fig-inline" id="liquids-04-00018-i010"><img alt="Liquids 04 00018 i010" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i010.png"/></span> DMA), and dimethyl sulfoxide (<span class="html-fig-inline" id="liquids-04-00018-i011"><img alt="Liquids 04 00018 i011" src="/liquids/liquids-04-00018/article_deploy/html/images/liquids-04-00018-i011.png"/></span> DMSO). Reprinted with permission from [<a href="#B42-liquids-04-00018" class="html-bibr">42</a>]. Copyright American Chemical Society, 2017.</p>
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<p>Concept of solubility parameter and Kamlet—Taft windows for identifying replacement solvents of an API (paracetamol): (<b>a</b>) window for solubility parameter, (<b>b</b>) window for API acidity, (<b>c</b>) window for API basicity, (<b>d</b>) window for API dipolarity/polarizability. (<b>left</b>): Range of solubility and Kamlet—Taft parameters for dissolution of API in known solvents, including hazardous ones. (<b>right</b>): Range of solubility and Kamlet—Taft parameters superimposed onto theoretical calculations and available literature data to determine working composition ranges for a given mixed solvent pair (acetone—water). Reprinted with permission from ref. [<a href="#B86-liquids-04-00018" class="html-bibr">86</a>]. Copyright American Chemical Society, 2016.</p>
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<p>Reichardt E<sub>T</sub><sup>N</sup> and Kamlet—Taft parameters of mono-solvents that solvate <span class="underline">water-soluble APIs</span> at ca. 25 °C. Data from refs. [<a href="#B1-liquids-04-00018" class="html-bibr">1</a>,<a href="#B92-liquids-04-00018" class="html-bibr">92</a>,<a href="#B93-liquids-04-00018" class="html-bibr">93</a>,<a href="#B94-liquids-04-00018" class="html-bibr">94</a>,<a href="#B95-liquids-04-00018" class="html-bibr">95</a>,<a href="#B96-liquids-04-00018" class="html-bibr">96</a>,<a href="#B97-liquids-04-00018" class="html-bibr">97</a>,<a href="#B98-liquids-04-00018" class="html-bibr">98</a>,<a href="#B99-liquids-04-00018" class="html-bibr">99</a>,<a href="#B100-liquids-04-00018" class="html-bibr">100</a>,<a href="#B101-liquids-04-00018" class="html-bibr">101</a>,<a href="#B102-liquids-04-00018" class="html-bibr">102</a>,<a href="#B103-liquids-04-00018" class="html-bibr">103</a>,<a href="#B104-liquids-04-00018" class="html-bibr">104</a>,<a href="#B105-liquids-04-00018" class="html-bibr">105</a>,<a href="#B106-liquids-04-00018" class="html-bibr">106</a>,<a href="#B107-liquids-04-00018" class="html-bibr">107</a>,<a 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class="html-bibr">190</a>,<a href="#B191-liquids-04-00018" class="html-bibr">191</a>,<a href="#B192-liquids-04-00018" class="html-bibr">192</a>,<a href="#B193-liquids-04-00018" class="html-bibr">193</a>,<a href="#B194-liquids-04-00018" class="html-bibr">194</a>,<a href="#B195-liquids-04-00018" class="html-bibr">195</a>,<a href="#B196-liquids-04-00018" class="html-bibr">196</a>,<a href="#B197-liquids-04-00018" class="html-bibr">197</a>,<a href="#B198-liquids-04-00018" class="html-bibr">198</a>,<a href="#B199-liquids-04-00018" class="html-bibr">199</a>,<a href="#B200-liquids-04-00018" class="html-bibr">200</a>,<a href="#B201-liquids-04-00018" class="html-bibr">201</a>,<a href="#B202-liquids-04-00018" class="html-bibr">202</a>,<a href="#B203-liquids-04-00018" class="html-bibr">203</a>,<a href="#B204-liquids-04-00018" class="html-bibr">204</a>,<a href="#B205-liquids-04-00018" class="html-bibr">205</a>,<a href="#B206-liquids-04-00018" class="html-bibr">206</a>,<a 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class="html-bibr">223</a>,<a href="#B224-liquids-04-00018" class="html-bibr">224</a>,<a href="#B225-liquids-04-00018" class="html-bibr">225</a>,<a href="#B226-liquids-04-00018" class="html-bibr">226</a>,<a href="#B227-liquids-04-00018" class="html-bibr">227</a>,<a href="#B228-liquids-04-00018" class="html-bibr">228</a>,<a href="#B229-liquids-04-00018" class="html-bibr">229</a>,<a href="#B230-liquids-04-00018" class="html-bibr">230</a>,<a href="#B231-liquids-04-00018" class="html-bibr">231</a>,<a href="#B232-liquids-04-00018" class="html-bibr">232</a>,<a href="#B233-liquids-04-00018" class="html-bibr">233</a>,<a href="#B234-liquids-04-00018" class="html-bibr">234</a>,<a href="#B235-liquids-04-00018" class="html-bibr">235</a>,<a href="#B236-liquids-04-00018" class="html-bibr">236</a>,<a href="#B237-liquids-04-00018" class="html-bibr">237</a>,<a href="#B238-liquids-04-00018" class="html-bibr">238</a>,<a href="#B239-liquids-04-00018" class="html-bibr">239</a>,<a href="#B240-liquids-04-00018" class="html-bibr">240</a>,<a href="#B241-liquids-04-00018" class="html-bibr">241</a>,<a href="#B242-liquids-04-00018" class="html-bibr">242</a>,<a href="#B243-liquids-04-00018" class="html-bibr">243</a>,<a href="#B244-liquids-04-00018" class="html-bibr">244</a>,<a href="#B245-liquids-04-00018" class="html-bibr">245</a>,<a href="#B246-liquids-04-00018" class="html-bibr">246</a>,<a href="#B247-liquids-04-00018" class="html-bibr">247</a>,<a href="#B248-liquids-04-00018" class="html-bibr">248</a>,<a href="#B249-liquids-04-00018" class="html-bibr">249</a>,<a href="#B250-liquids-04-00018" class="html-bibr">250</a>,<a href="#B251-liquids-04-00018" class="html-bibr">251</a>,<a href="#B252-liquids-04-00018" class="html-bibr">252</a>,<a href="#B253-liquids-04-00018" class="html-bibr">253</a>,<a href="#B254-liquids-04-00018" class="html-bibr">254</a>,<a href="#B255-liquids-04-00018" class="html-bibr">255</a>,<a href="#B256-liquids-04-00018" class="html-bibr">256</a>,<a href="#B257-liquids-04-00018" class="html-bibr">257</a>,<a href="#B258-liquids-04-00018" class="html-bibr">258</a>,<a href="#B259-liquids-04-00018" class="html-bibr">259</a>,<a href="#B260-liquids-04-00018" class="html-bibr">260</a>,<a href="#B261-liquids-04-00018" class="html-bibr">261</a>,<a href="#B262-liquids-04-00018" class="html-bibr">262</a>,<a href="#B263-liquids-04-00018" class="html-bibr">263</a>,<a href="#B264-liquids-04-00018" class="html-bibr">264</a>,<a href="#B265-liquids-04-00018" class="html-bibr">265</a>,<a href="#B266-liquids-04-00018" class="html-bibr">266</a>,<a href="#B267-liquids-04-00018" class="html-bibr">267</a>,<a href="#B268-liquids-04-00018" class="html-bibr">268</a>,<a href="#B269-liquids-04-00018" class="html-bibr">269</a>,<a href="#B270-liquids-04-00018" class="html-bibr">270</a>,<a href="#B271-liquids-04-00018" class="html-bibr">271</a>,<a href="#B272-liquids-04-00018" class="html-bibr">272</a>,<a href="#B273-liquids-04-00018" class="html-bibr">273</a>,<a href="#B274-liquids-04-00018" class="html-bibr">274</a>,<a href="#B275-liquids-04-00018" class="html-bibr">275</a>,<a href="#B276-liquids-04-00018" class="html-bibr">276</a>,<a href="#B277-liquids-04-00018" class="html-bibr">277</a>,<a href="#B278-liquids-04-00018" class="html-bibr">278</a>,<a href="#B279-liquids-04-00018" class="html-bibr">279</a>,<a href="#B280-liquids-04-00018" class="html-bibr">280</a>,<a href="#B281-liquids-04-00018" class="html-bibr">281</a>,<a href="#B282-liquids-04-00018" class="html-bibr">282</a>,<a href="#B283-liquids-04-00018" class="html-bibr">283</a>,<a href="#B284-liquids-04-00018" class="html-bibr">284</a>,<a href="#B285-liquids-04-00018" class="html-bibr">285</a>,<a href="#B286-liquids-04-00018" class="html-bibr">286</a>,<a href="#B287-liquids-04-00018" class="html-bibr">287</a>,<a href="#B288-liquids-04-00018" class="html-bibr">288</a>,<a href="#B289-liquids-04-00018" class="html-bibr">289</a>,<a href="#B290-liquids-04-00018" class="html-bibr">290</a>,<a href="#B291-liquids-04-00018" class="html-bibr">291</a>,<a href="#B292-liquids-04-00018" class="html-bibr">292</a>,<a href="#B293-liquids-04-00018" class="html-bibr">293</a>,<a href="#B294-liquids-04-00018" class="html-bibr">294</a>,<a href="#B295-liquids-04-00018" class="html-bibr">295</a>,<a href="#B296-liquids-04-00018" class="html-bibr">296</a>,<a href="#B297-liquids-04-00018" class="html-bibr">297</a>,<a href="#B298-liquids-04-00018" class="html-bibr">298</a>,<a href="#B299-liquids-04-00018" class="html-bibr">299</a>,<a href="#B300-liquids-04-00018" class="html-bibr">300</a>,<a href="#B301-liquids-04-00018" class="html-bibr">301</a>,<a href="#B302-liquids-04-00018" class="html-bibr">302</a>]. Water (<span style="color:blue">Blue</span>). Less-hazardous solvents (<span style="color:#009900">Green</span>). Hazardous solvents (<span style="color:red">Red</span>). Detailed information in <a href="#app1-liquids-04-00018" class="html-app">Supplementary Materials</a>.</p>
Full article ">Figure 8
<p>Reichardt E<sub>T</sub><sup>N</sup> and Kamlet—Taft parameters of mono-solvents that solvate <span class="underline">water-insoluble</span> APIs at ca. 25 °C. Data from refs. [<a href="#B1-liquids-04-00018" class="html-bibr">1</a>,<a href="#B92-liquids-04-00018" class="html-bibr">92</a>,<a href="#B93-liquids-04-00018" class="html-bibr">93</a>,<a href="#B94-liquids-04-00018" class="html-bibr">94</a>,<a href="#B95-liquids-04-00018" class="html-bibr">95</a>,<a href="#B96-liquids-04-00018" class="html-bibr">96</a>,<a href="#B97-liquids-04-00018" class="html-bibr">97</a>,<a href="#B98-liquids-04-00018" class="html-bibr">98</a>,<a href="#B99-liquids-04-00018" class="html-bibr">99</a>,<a href="#B100-liquids-04-00018" class="html-bibr">100</a>,<a href="#B101-liquids-04-00018" class="html-bibr">101</a>,<a href="#B102-liquids-04-00018" class="html-bibr">102</a>,<a href="#B103-liquids-04-00018" class="html-bibr">103</a>,<a href="#B104-liquids-04-00018" class="html-bibr">104</a>,<a href="#B105-liquids-04-00018" class="html-bibr">105</a>,<a href="#B106-liquids-04-00018" class="html-bibr">106</a>,<a href="#B107-liquids-04-00018" class="html-bibr">107</a>,<a 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class="html-bibr">256</a>,<a href="#B257-liquids-04-00018" class="html-bibr">257</a>,<a href="#B258-liquids-04-00018" class="html-bibr">258</a>,<a href="#B259-liquids-04-00018" class="html-bibr">259</a>,<a href="#B260-liquids-04-00018" class="html-bibr">260</a>,<a href="#B261-liquids-04-00018" class="html-bibr">261</a>,<a href="#B262-liquids-04-00018" class="html-bibr">262</a>,<a href="#B263-liquids-04-00018" class="html-bibr">263</a>,<a href="#B264-liquids-04-00018" class="html-bibr">264</a>,<a href="#B265-liquids-04-00018" class="html-bibr">265</a>,<a href="#B266-liquids-04-00018" class="html-bibr">266</a>,<a href="#B267-liquids-04-00018" class="html-bibr">267</a>,<a href="#B268-liquids-04-00018" class="html-bibr">268</a>,<a href="#B269-liquids-04-00018" class="html-bibr">269</a>,<a href="#B270-liquids-04-00018" class="html-bibr">270</a>,<a href="#B271-liquids-04-00018" class="html-bibr">271</a>,<a href="#B272-liquids-04-00018" class="html-bibr">272</a>,<a href="#B273-liquids-04-00018" class="html-bibr">273</a>,<a href="#B274-liquids-04-00018" class="html-bibr">274</a>,<a href="#B275-liquids-04-00018" class="html-bibr">275</a>,<a href="#B276-liquids-04-00018" class="html-bibr">276</a>,<a href="#B277-liquids-04-00018" class="html-bibr">277</a>,<a href="#B278-liquids-04-00018" class="html-bibr">278</a>,<a href="#B279-liquids-04-00018" class="html-bibr">279</a>,<a href="#B280-liquids-04-00018" class="html-bibr">280</a>,<a href="#B281-liquids-04-00018" class="html-bibr">281</a>,<a href="#B282-liquids-04-00018" class="html-bibr">282</a>,<a href="#B283-liquids-04-00018" class="html-bibr">283</a>,<a href="#B284-liquids-04-00018" class="html-bibr">284</a>,<a href="#B285-liquids-04-00018" class="html-bibr">285</a>,<a href="#B286-liquids-04-00018" class="html-bibr">286</a>,<a href="#B287-liquids-04-00018" class="html-bibr">287</a>,<a href="#B288-liquids-04-00018" class="html-bibr">288</a>,<a href="#B289-liquids-04-00018" class="html-bibr">289</a>,<a href="#B290-liquids-04-00018" class="html-bibr">290</a>,<a href="#B291-liquids-04-00018" class="html-bibr">291</a>,<a href="#B292-liquids-04-00018" class="html-bibr">292</a>,<a href="#B293-liquids-04-00018" class="html-bibr">293</a>,<a href="#B294-liquids-04-00018" class="html-bibr">294</a>,<a href="#B295-liquids-04-00018" class="html-bibr">295</a>,<a href="#B296-liquids-04-00018" class="html-bibr">296</a>,<a href="#B297-liquids-04-00018" class="html-bibr">297</a>,<a href="#B298-liquids-04-00018" class="html-bibr">298</a>,<a href="#B299-liquids-04-00018" class="html-bibr">299</a>,<a href="#B300-liquids-04-00018" class="html-bibr">300</a>,<a href="#B301-liquids-04-00018" class="html-bibr">301</a>,<a href="#B302-liquids-04-00018" class="html-bibr">302</a>]. Less-hazardous solvents (<span style="color:#009900">Green</span>). Hazardous solvents (<span style="color:red">Red</span>). Detailed information in <a href="#app1-liquids-04-00018" class="html-app">Supplementary Materials</a>.</p>
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<p>Kamlet—Taft acidity, basicity, and polarity for selected mixed solvents versus HBA solvent mole fraction: (<b>a</b>,<b>d</b>,<b>g</b>) water—HBA; (<b>b</b>,<b>e</b>,<b>h</b>) methanol—HBA; (<b>c</b>,<b>f</b>,<b>i</b>) ethanol—HBA. Trends shown are based on estimations (dashed lines) and actual data (solid lines) [<a href="#B51-liquids-04-00018" class="html-bibr">51</a>,<a href="#B86-liquids-04-00018" class="html-bibr">86</a>,<a href="#B90-liquids-04-00018" class="html-bibr">90</a>,<a href="#B91-liquids-04-00018" class="html-bibr">91</a>].</p>
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16 pages, 3249 KiB  
Article
Antibacterial Effect and Possible Mechanism of Sesamol against Foodborne Pathogens
by Zhuosi Li, Mengjie Wu, Hui Yan, Zheyan Meng, Binru Gao and Qingli Dong
Foods 2024, 13(3), 435; https://doi.org/10.3390/foods13030435 - 29 Jan 2024
Cited by 1 | Viewed by 1812
Abstract
Food safety problems caused by foodborne pathogens have become a major public issue, and the search for efficient and safe bacteriostatic agents has gained attention. Sesamol (SE), a phenolic compound abundant in sesame oil, offers numerous health benefits and exhibits certain antibacterial properties. [...] Read more.
Food safety problems caused by foodborne pathogens have become a major public issue, and the search for efficient and safe bacteriostatic agents has gained attention. Sesamol (SE), a phenolic compound abundant in sesame oil, offers numerous health benefits and exhibits certain antibacterial properties. The purpose of this study was to evaluate the antibacterial effect and potential mechanisms of SE against representative foodborne pathogens, including Listeria monocytogenes, Staphylococcus aureus, Bacillus cereus, Escherichia coli, and Salmonella serovar Enteritidis. The results showed that SE significantly inhibited the growth of the five pathogenic bacteria in sterile saline and pasteurized milk by 2.16–4.16 log10 CFU/g within 48 h. The results of the minimum bactericidal concentration and time–kill assay showed that SE had a greater inhibitory effect on L. monocytogenes compared with other bacteria. Additionally, SE was found to alter the cell membranes’ permeability in these bacteria, resulting in the release of intercellular proteins and DNA. A scanning electron microscopy analysis showed that exposure to SE resulted in significant changes in bacterial morphology, producing cell shrinkage and deformation. These findings suggest that SE could inhibit both Gram-negative and Gram-positive bacteria by interfering with the function and morphology of bacterial cells. Full article
(This article belongs to the Section Food Microbiology)
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Figure 1
<p>Time–kill curves for SE against <span class="html-italic">L. monocytogenes</span> (<b>A</b>,<b>B</b>), <span class="html-italic">S. aureus</span> (<b>C</b>,<b>D</b>), <span class="html-italic">B. cereus</span> (<b>E</b>,<b>F</b>), <span class="html-italic">S.</span> Enteritidis (<b>G</b>,<b>H</b>), and <span class="html-italic">E. coli</span> (<b>I</b>,<b>J</b>) in SSS and pasteurized milk. Bacteria at a starting inoculum of 10<sup>6</sup> CFU/mL were treated with or without SE (1/2× MIC and 1× MIC) for 0, 6, 12, 24, and 48 h at 37 °C. (●) C: Control, (<span style="color:#ED7D31">■</span>) SE (1/2× MIC), and (<span style="color:#70AD47">▲</span>) SE (1× MIC). Different lowercase letters (a, b, and c) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) among different groups at the same time point.</p>
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<p>Effect of SE on bacterial membrane conductivity. <span class="html-italic">L. monocytogenes</span> (<b>A</b>), <span class="html-italic">S. aureus</span> (<b>B</b>), <span class="html-italic">B. cereus</span> (<b>C</b>), <span class="html-italic">S.</span> Enteritidis (<b>D</b>), and <span class="html-italic">E. coli</span> (<b>E</b>) were used in experiments. The bacteria at a starting inoculum of 10<sup>8</sup>–10<sup>9</sup> CFU/mL were treated with or without SE (1× MIC and 2× MIC) for 0, 12, 24, and 48 h at 37 °C. Different lowercase letters (a, b, and c) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between treatments at each time point.</p>
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<p>Changes in bacterial OD<sub>260nm</sub>. <span class="html-italic">L. monocytogenes</span> (<b>A</b>), <span class="html-italic">S. aureus</span> (<b>B</b>), <span class="html-italic">B. cereus</span> (<b>C</b>), <span class="html-italic">S.</span> Enteritidis (<b>D</b>), and <span class="html-italic">E. coli</span> (<b>E</b>) were used in experiments. The bacteria at a starting inoculum of 10<sup>8</sup>–10<sup>9</sup> CFU/mL were treated with or without SE (1× MIC and 2× MIC) for 0, 12, 24, and 48 h at 37 °C. Different lowercase letters (a, b, and c) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between treatments at each time point.</p>
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<p>The effect of SE on the concentration of leaked proteins from <span class="html-italic">L. monocytogenes</span> (<b>A</b>), <span class="html-italic">S. aureus</span> (<b>B</b>), <span class="html-italic">B. cereus</span> (<b>C</b>), <span class="html-italic">S.</span> Enteritidis (<b>D</b>), and <span class="html-italic">E. coli</span> (<b>E</b>). The bacteria at a starting inoculum of 10<sup>8</sup>–10<sup>9</sup> CFU/mL were treated with or without SE (1× MIC and 2× MIC) for 0, 12, 24, and 48 h at 37 °C. Different lowercase letters (a, b, and c) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between treatments at each time point.</p>
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<p>The effect of SE on the ATP content in <span class="html-italic">L. monocytogenes</span> (<b>A</b>), <span class="html-italic">S. aureus</span> (<b>B</b>), <span class="html-italic">B. cereus</span> (<b>C</b>), <span class="html-italic">S.</span> Enteritidis (<b>D</b>), and <span class="html-italic">E. coli</span> (<b>E</b>). The bacteria at a starting inoculum of 10<sup>8</sup>–10<sup>9</sup> CFU/mL were treated with or without SE (1× MIC and 2× MIC) for 0, 12, 24, and 48 h at 37 °C. Different lowercase letters (a, b, and c) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05) between treatments at each time point.</p>
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<p>SEM observation of <span class="html-italic">L. monocytogenes</span>, <span class="html-italic">S. aureus</span>, <span class="html-italic">B. cereus</span>, <span class="html-italic">S.</span> Enteritidis, and <span class="html-italic">E. coli</span> exposed to SE. The bacteria at a starting inoculum of 10<sup>6</sup> CFU/mL were treated with or without SE (1× MIC and 2× MIC) for 24 h at 37 °C.</p>
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13 pages, 3588 KiB  
Article
Ternary Heterojunction Graphitic Carbon Nitride/Cupric Sulfide/Titanium Dioxide Photoelectrochemical Sensor for Sesamol Quantification and Antioxidant Synergism
by Likun Huang, Jingshi Yang, Zhishan Liang, Ruilian Liang, Hui Luo, Zhonghui Sun, Dongxue Han and Li Niu
Biosensors 2023, 13(9), 859; https://doi.org/10.3390/bios13090859 - 30 Aug 2023
Cited by 2 | Viewed by 1317
Abstract
Sesamol (SM) is a potent natural antioxidant that can quench free radicals and modulate the cholinergic system in the brain, thereby ameliorating memory and cognitive impairment in Alzheimer’s disease patients. Moreover, the total antioxidant capacity can be amplified by synergistic interactions between different [...] Read more.
Sesamol (SM) is a potent natural antioxidant that can quench free radicals and modulate the cholinergic system in the brain, thereby ameliorating memory and cognitive impairment in Alzheimer’s disease patients. Moreover, the total antioxidant capacity can be amplified by synergistic interactions between different antioxidants. Here, we constructed a ternary heterojunction graphitic carbon nitride/cupric sulfide/titanium dioxide (g-C3N4/CuS/TiO2) photoelectrochemical (PEC) sensor for the quantification of SM and its synergistic interactions with other antioxidants. Crucially, the Schottky barrier in ternary semiconductors considerably enhances electron transfer. The PEC sensor showed a wide linear range for SM detection, ranging from 2 to 1277 μmol L−1, and had a limit of detection of 1.8 μmol L−1. Remarkably, this sensing platform could evaluate the synergism between SM and five typical lipid-soluble antioxidants: tert-butyl hydroquinone, vitamin E, butyl hydroxyanisole, propyl gallate, and butylated hydroxytoluene. Owing to its low redox potential, SM could reduce antioxidant radicals and promote their regeneration, which increased the overall antioxidant performance. The g-C3N4/CuS/TiO2 PEC sensor exhibited high sensitivity, satisfactory selectivity, and stability, and was successfully applied for SM determination in both soybean and peanut oils. The findings of this study provide guidance for the development of nutritional foods, nutrition analysis, and the treatment of diseases caused by free radicals. Full article
(This article belongs to the Special Issue Photonics for Bioapplications: Sensors and Technology)
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Graphical abstract

Graphical abstract
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<p>(<b>A</b>) Schematic showing the preparation of g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>. (<b>B</b>,<b>C</b>) Scanning electron microscopy (SEM) images, (<b>D</b>,<b>E</b>) transmission electron microscopy (TEM) images (inset: corresponding magnified picture of CuS nanoparticles), (<b>F</b>) high-resolution transmission electron microscopy (HR-TEM) images (inset: corresponding magnified HR-TEM image of CuS nanoparticles) and (<b>G</b>) energy-dispersive X-ray spectroscopy (EDX) of g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>.</p>
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<p>(<b>A</b>) X-ray powder diffractometry (XRD) and (<b>B</b>) Electrochemical impedance spectroscopy (EIS) plots of TiO<sub>2</sub>, CuS/TiO<sub>2</sub>, and g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>. (<b>C</b>) Photocurrent responses of TiO<sub>2</sub>, CuS, g-C<sub>3</sub>N<sub>4</sub>, CuS/TiO<sub>2</sub>, and g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>-modified FTO electrodes in the (a<sub>0</sub>–e<sub>0</sub>) absence and (a<sub>1</sub>–e<sub>1</sub>) presence of 123.46 μmol L<sup>−1</sup> SM. (<b>D</b>) UV-Vis absorbance spectra and (<b>E</b>) Kubelka–Munk plots of TiO<sub>2</sub>, CuS/TiO<sub>2</sub>, and g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>. (<b>F</b>) Mott–Schottky plots of g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub> at frequencies of 1000 and 2000 Hz.</p>
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<p>Photocurrent response curves of SM (<b>A<sub>1</sub></b>), PG (<b>B<sub>1</sub></b>), and SM+PG in equal proportions (<b>C<sub>1</sub></b>) generated for the g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>-based PEC sensing platform at different analyte concentrations. Calibration plot of photocurrent versus different concentrations of SM (<b>A<sub>2</sub></b>), PG (<b>B<sub>2</sub></b>), and SM+PG (<b>C<sub>2</sub></b>).</p>
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<p>Photocurrents of the g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub> PEC sensor in the presence of 484.812 μmol L<sup>−1</sup> SM, VE, TBHQ, BHA, BHT, PG, and a mixture of SM and other antioxidants in equal molar ratios.</p>
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<p>(<b>A</b>) Samples and interferences test in the presence of fructose, glucose, sucrose, <span class="html-small-caps">l</span>-malic acid, <span class="html-small-caps">l</span>-citric acid, ethanol, <span class="html-small-caps">l</span>-threonine, <span class="html-small-caps">l</span>-proline, <span class="html-small-caps">l</span>-lysine, and <span class="html-small-caps">l</span>-histidine, as well as Na<sup>+</sup>, K<sup>+</sup>, Mg<sup>2+</sup>, and Ca<sup>2+</sup>, on the photocurrent response of the g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>-based PEC sensor. (<b>B</b>) Detection stability and reusability (after 15 days) of the g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub>-modified FTO electrode in the presence of 1270.574 μmol L<sup>−1</sup> SM. The PEC sensor was operated at 0 V under 630 nm light excitation in 0.1 mol L<sup>−1</sup> PBS (pH = 7.4).</p>
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<p>Schematic of antioxidant capacity analysis based on the g-C<sub>3</sub>N<sub>4</sub>/CuS/TiO<sub>2</sub> PEC sensing platform. AO, antioxidant; FTO, fluorine-doped tin oxide; SM, sesamol; VE, vitamin E; TBHQ, <span class="html-italic">tert</span>-butyl hydroquinone; BHA, butyl hydroxyanisole; BHT, butylated hydroxytoluene; PG, propyl gallate.</p>
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18 pages, 1749 KiB  
Review
Byproducts of Sesame Oil Extraction: Composition, Function, and Comprehensive Utilization
by Yuan Wan, Qiaoyun Zhou, Mengge Zhao and Tao Hou
Foods 2023, 12(12), 2383; https://doi.org/10.3390/foods12122383 - 15 Jun 2023
Cited by 10 | Viewed by 5761
Abstract
Sesame is principally used to generate oil, which is produced by chemical refining or pressing. Sesame meal, as a main byproduct of sesame oil extraction, is usually discarded, causing resource waste and economic loss. Sesame meal is rich in sesame protein and three [...] Read more.
Sesame is principally used to generate oil, which is produced by chemical refining or pressing. Sesame meal, as a main byproduct of sesame oil extraction, is usually discarded, causing resource waste and economic loss. Sesame meal is rich in sesame protein and three types of sesame lignans (sesamin, sesamolin, and sesamol). Sesame protein extracted via a physical method and an enzymic method has balanced amino acid composition and is an important protein source, and thus it is often added to animal feed and used as a human dietary supplement. Extracted sesame lignan exhibits multiple biological activities such as antihypertensive, anticancer, and cholesterol-lowering activities, and therefore it is used to improve the oxidative stability of oils. This review summarizes the extraction methods, functional activities, and comprehensive utilization of four active substances (sesame protein, sesamin, sesamolin, and sesamol) in sesame meal with the aim to provide theoretical guidance for the maximum utilization of sesame meal. Full article
(This article belongs to the Section Food Nutrition)
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<p>Framework schematic. Byproducts of sesame oil extraction: composition, function, and comprehensive utilization.</p>
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<p>Schematic of interconversion process and conditions of lignans and compounds isolated from sesame. The major aglycon lignans are sesamin and sesamolin. The minor aglycon lignans of sesame oil include sesamol, sesaminol, sesamolinol, pinoresinol, and episesamin.</p>
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<p>Schematic diagram of extraction, separation, and detection of sesame lignans.</p>
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<p>Schematic diagram of anti-inflammation by sesamin. HAC, human articular chondrocytes; GAGs, glycosaminoglycans; CSPGs, chondroitin sulfate proteoglycans; ACAN, XT-1, XT-2, chondroitin sulfate proteoglycan (CSPGs) synthesis genes; MMP, matrix metalloproteinase; IL-8, IL-6, prostaglandin E 2 and nitric oxide (NO); TNF-α, tumor necrosis factor-alpha; IL-1, interleukin-1.</p>
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<p>Schematic diagram of anticancer activity of sesamolin. Sesamolin regulates the anticancer mechanism of NK cells and Raji cells. HCT116, colorectal cancer cells; STAT3, transcription 3; DC, dendritic cells; NK cell, natural killer cells. Raji is a stable human cell line derived from the B-lymphocytes of a male Burkitt’s lymphoma patient.</p>
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13 pages, 975 KiB  
Article
Alpha-Tocopherol Significantly Improved Squalene Production Yield of Aurantiochytrium sp. TWZ-97 through Lowering ROS levels and Up-Regulating Key Genes of Central Carbon Metabolism Pathways
by Memon Kashif Ali, Xiuping Liu, Jiaqian Li, Xingyu Zhu, Biswarup Sen and Guangyi Wang
Antioxidants 2023, 12(5), 1034; https://doi.org/10.3390/antiox12051034 - 30 Apr 2023
Cited by 3 | Viewed by 2030
Abstract
Media supplementation has proven to be an effective technique for improving byproduct yield during microbial fermentation. This study explored the impact of different concentrations of bioactive compounds, namely alpha-tocopherol, mannitol, melatonin, sesamol, ascorbic acid, and biotin, on the Aurantiochytrium sp. TWZ-97 culture. Our [...] Read more.
Media supplementation has proven to be an effective technique for improving byproduct yield during microbial fermentation. This study explored the impact of different concentrations of bioactive compounds, namely alpha-tocopherol, mannitol, melatonin, sesamol, ascorbic acid, and biotin, on the Aurantiochytrium sp. TWZ-97 culture. Our investigation revealed that alpha-tocopherol was the most effective compound in reducing the reactive oxygen species (ROS) burden, both directly and indirectly. Adding 0.7 g/L of alpha-tocopherol led to an 18% improvement in biomass, from 6.29 g/L to 7.42 g/L. Moreover, the squalene concentration increased from 129.8 mg/L to 240.2 mg/L, indicating an 85% improvement, while the squalene yield increased by 63.2%, from 19.82 mg/g to 32.4 mg/g. Additionally, our comparative transcriptomics analysis suggested that several genes involved in glycolysis, pentose phosphate pathway, TCA cycle, and MVA pathway were overexpressed following alpha-tocopherol supplementation. The alpha-tocopherol supplementation also lowered ROS levels by binding directly to ROS generated in the fermentation medium and indirectly by stimulating genes that encode antioxidative enzymes, thereby decreasing the ROS burden. Our findings suggest that alpha-tocopherol supplementation can be an effective method for improving squalene production in Aurantiochytrium sp. TWZ-97 culture. Full article
(This article belongs to the Section ROS, RNS and RSS)
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<p>Comparison of glucose consumption patterns between with and without alpha-tocopherol-supplemented groups during fermentation by TWZ-97 strain. The significance code '**' indicated a significant difference at (<span class="html-italic">p</span>-value &lt; 0.01) between the supplemented and non-supplemented ROS data.</p>
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<p>Time course profile of intracellular reactive oxygen species (ROS) levels in non-supplemented and supplemented cultures of TWZ-97 strain. The significance code '**' indicated a significant difference at (<span class="html-italic">p</span>-value &lt; 0.01) between the supplemented and non-supplemented ROS data.</p>
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<p>Time course profile of total antioxidant capacity (T-AOC) levels in non-supplemented and supplemented cultures of TWZ-97 strain.</p>
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18 pages, 517 KiB  
Review
Hypolipidemic and Anti-Atherogenic Effects of Sesamol and Possible Mechanisms of Action: A Comprehensive Review
by Amin F. Majdalawieh, Aaram E. Eltayeb, Imad A. Abu-Yousef and Sarah M. Yousef
Molecules 2023, 28(8), 3567; https://doi.org/10.3390/molecules28083567 - 19 Apr 2023
Cited by 3 | Viewed by 2045
Abstract
Sesamol is a phenolic lignan isolated from Sesamum indicum seeds and sesame oil. Numerous studies have reported that sesamol exhibits lipid-lowering and anti-atherogenic properties. The lipid-lowering effects of sesamol are evidenced by its effects on serum lipid levels, which have been attributed to [...] Read more.
Sesamol is a phenolic lignan isolated from Sesamum indicum seeds and sesame oil. Numerous studies have reported that sesamol exhibits lipid-lowering and anti-atherogenic properties. The lipid-lowering effects of sesamol are evidenced by its effects on serum lipid levels, which have been attributed to its potential for significantly influencing molecular processes involved in fatty acid synthesis and oxidation as well as cholesterol metabolism. In this review, we present a comprehensive summary of the reported hypolipidemic effects of sesamol, observed in several in vivo and in vitro studies. The effects of sesamol on serum lipid profiles are thoroughly addressed and evaluated. Studies highlighting the ability of sesamol to inhibit fatty acid synthesis, stimulate fatty acid oxidation, enhance cholesterol metabolism, and modulate macrophage cholesterol efflux are outlined. Additionally, the possible molecular pathways underlying the cholesterol-lowering effects of sesamol are presented. Findings reveal that the anti-hyperlipidemic effects of sesamol are achieved, at least in part, by targeting liver X receptor α (LXRα), sterol regulatory element binding protein-1 (SREBP-1), and fatty acid synthase (FAS) expression, as well as peroxisome proliferator-activated receptor α (PPARα) and AMP activated protein kinase (AMPK) signaling pathways. A detailed understanding of the molecular mechanisms underlying the anti-hyperlipidemic potential of sesamol is necessary to assess the possibility of utilizing sesamol as an alternative natural therapeutic agent with potent hypolipidemic and anti-atherogenic properties. Research into the optimal sesamol dosage that may bring about such favorable hypolipidemic effects should be further investigated, most importantly in humans, to ensure maximal therapeutic benefit. Full article
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<p>A summary of the regulatory effects of sesamol on serum lipid profile and signaling factors and proteins involved in fatty acid synthesis, fatty acid oxidation, cholesterol metabolism, and macrophage cholesterol homeostasis. The major signaling pathways targeted by sesamol are denoted as well. (* with the addition of sesame oil). TC: total cholesterol; TG: triglyceride; LDL-C: low-density lipoprotein cholesterol; HDL: high-density lipoprotein cholesterol; VLDL: very low-density lipoprotein; PPARα: peroxisome proliferator-activated receptor α; SREBP-1: sterol regulatory element binding protein-1; NADPH: nicotinamide adenine dinucleotide phosphate; DGLA: dihomo-γ-linolenic acid; AA: arachidonic acid; PUFA: polyunsaturated fatty acid; TFA: total fatty acids; CPT1A: carnitine palmitoyltransferase-1A; PGC1A: peroxisome proliferator-activated receptor-gamma coactivator-1A; β-HB: β-hydroxybutyric acid; HSL: hormone-sensitive lipase; pHSL: phosphorylated hormone-sensitive lipase; LPL: lipoprotein lipase; HMGCR: 3-hydroxy-3-methylglutaryl-CoA reductase; ACAT2: acetyl-CoA acetyltransferase 2; LXRα: liver X receptor α; LXRβ: liver X receptor α; ABCG5: ATP-binding cassette sub-family G member 5; ABCG8: ATP-binding cassette sub-family G member 8; ABCA1: ATP-binding cassette sub-family A member 1; CYP7A1: cytochrome P450 family 7 subfamily A member 1; PPARγ1: peroxisome proliferator-activated receptor γ 1; ApoAI: apolipoprotein AI; FAS: fatty acid synthase; AMPK: AMP-activated protein kinase; MAPK: mitogen-activated protein kinase.</p>
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16 pages, 3255 KiB  
Article
Improvement of Oxidative Stability of Fish Oil-in-Water Emulsions through Partitioning of Sesamol at the Interface
by Zhihui Gao, Zhongyan Ji, Leixi Wang, Qianchun Deng, Siew Young Quek, Liang Liu and Xuyan Dong
Foods 2023, 12(6), 1287; https://doi.org/10.3390/foods12061287 - 17 Mar 2023
Cited by 4 | Viewed by 1679
Abstract
The susceptibility of polyunsaturated fatty acids to oxidation severely limits their application in functional emulsified foods. In this study, the effect of sesamol concentration on the physicochemical properties of WPI-stabilized fish oil emulsions was investigated, focusing on the relationship between sesamol–WPI interactions and [...] Read more.
The susceptibility of polyunsaturated fatty acids to oxidation severely limits their application in functional emulsified foods. In this study, the effect of sesamol concentration on the physicochemical properties of WPI-stabilized fish oil emulsions was investigated, focusing on the relationship between sesamol–WPI interactions and interfacial behavior. The results relating to particle size, zeta-potential, microstructure, and appearance showed that 0.09% (w/v) sesamol promoted the formation of small oil droplets and inhibited oil droplet aggregation. Furthermore, the addition of sesamol significantly reduced the formation of hydrogen peroxide, generation of secondary reaction products during storage, and degree of protein oxidation in the emulsions. Molecular docking and isothermal titration calorimetry showed that the interaction between sesamol and β-LG was mainly mediated by hydrogen bonds and hydrophobic interactions. Our results show that sesamol binds to interfacial proteins mainly through hydrogen bonding, and increasing the interfacial sesamol content reduces the interfacial tension and improves the physical and oxidative stability of the emulsion. Full article
(This article belongs to the Special Issue Lipid Delivery System and Functional Food)
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Graphical abstract

Graphical abstract
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<p>Changes in the mean droplet size D<sub>4,3</sub> (<b>A</b>) and ζ-potential (<b>B</b>) of emulsions containing different levels of sesamol during storage (30mL of emulsion in a 50mL glass bottle with screw cap stored at room temperature and protected from light).</p>
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<p>The effects of sesamol on the visual appearance (<b>A</b>) (from left to right: 0% sesamol, 0.01% sesamol, 0.03% sesamol and 0.09% sesamol) and emulsions’ confocal micrographs (<b>B</b>) (30 mL of emulsion in a 50 mL glass bottle with screw cap stored at room temperature and protected from light).</p>
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<p>Effect of sesamol on lipid hydrogen peroxide (<b>A</b>) and TBARS (<b>B</b>) concentrations in WPI-stabilized fish oil emulsions during storage (30 mL of emulsion in a 50 mL glass bottle with screw cap stored at room temperature and protected from light).</p>
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<p>Effect of different sesamol concentrations on protein sulfhydryl (<b>A</b>) and carbonyl (<b>B</b>) groups in emulsions during storage (30 mL of emulsion in a 50 mL glass bottle with screw cap stored at room temperature and protected from light).</p>
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<p>Correction heat rate versus time and enthalpy change corresponding to 20 mM sesamol titration of 0.3 mM WPI.</p>
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<p>Schematic diagram of the 3D docking model and 2D interaction between β-lactoglobulin (β-LG) and sesamol.</p>
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<p>Effect of sesamol on the interfacial tension between the oil phase and WPI solution with time.</p>
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<p>Interfacial partitioning of sesamol in emulsions. Content of sesamol in the aqueous phase, oil phase, and interfacial layer per ml of emulsion ((<b>A</b>): 0.01% sesamol, (<b>B</b>): 0.03% sesamol, (<b>C</b>): 0.09% sesamol). Percentage partitioning of sesamol in the aqueous phase, oil phase and interfacial layer ((<b>D</b>): 0.01% sesamol, (<b>E</b>): 0.03% sesamol, (<b>F</b>): 0.09% sesamol).</p>
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25 pages, 1655 KiB  
Review
Formulation Strategies for Enhancing Pharmaceutical and Nutraceutical Potential of Sesamol: A Natural Phenolic Bioactive
by Anroop B. Nair, Pooja Dalal, Varsha Kadian, Sunil Kumar, Minakshi Garg, Rekha Rao, Rashed M. Almuqbil, Ahmed S. Alnaim, Bandar Aldhubiab and Fatemah Alqattan
Plants 2023, 12(5), 1168; https://doi.org/10.3390/plants12051168 - 3 Mar 2023
Cited by 5 | Viewed by 2424
Abstract
Natural plants and their products continue to be the major source of phytoconstituents in food and therapeutics. Scientific studies have evidenced the benefits of sesame oil and its bioactives in various health conditions. Various bioactives present in it include sesamin, sasamolin, sesaminol, and [...] Read more.
Natural plants and their products continue to be the major source of phytoconstituents in food and therapeutics. Scientific studies have evidenced the benefits of sesame oil and its bioactives in various health conditions. Various bioactives present in it include sesamin, sasamolin, sesaminol, and sesamol; among these, sesamol represents a major constituent. This bioactive is responsible for preventing various diseases including cancer, hepatic disorders, cardiac ailments, and neurological diseases. In the last decade, the application of sesamol in the management of various disorders has attracted the increasing interest of the research community. Owing to its prominent pharmacological activities, such as antioxidant, antiinflammatory, antineoplastic, and antimicrobial, sesamol has been explored for the above-mentioned disorders. However, despite the above-mentioned therapeutic potential, its clinical utility is mainly hindered owing to low solubility, stability, bioavailability, and rapid clearance issues. In this regard, numerous strategies have been explored to surpass these restrictions with the formulation of novel carrier platforms. This review aims to describe the various reports and summarize the different pharmacological activities of sesamol. Furthermore, one part of this review is devoted to formulating strategies to improve sesamol’s challenges. To resolve the issues such as the stability, low bioavailability, and high systemic clearance of sesamol, novel carrier systems have been developed to open a new avenue to utilize this bioactive as an efficient first-line treatment for various diseases. Full article
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<p>Chemical structure of (<b>a</b>) sesamol, (<b>b</b>) sesamolin, (<b>c</b>) sesamin, and (<b>d</b>) sesaminols.</p>
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<p>The basic mechanism of action of sesamol includes an increase in free radical scavenging, upregulation of various antioxidant enzymes, suppression of IL-1β, TNFα, LOX-1, and 5-LOX expressions, inhibition of NF-κB signaling, induction of cell apoptosis, cell cycle arrest and modulation of p53, caspase, Bcl2, and Bax expressions.</p>
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<p>Therapeutic potential of sesame.</p>
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<p>Nanoformulations of Sesamol.</p>
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