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Keywords = eriocitrin

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18 pages, 958 KiB  
Article
Mint-Scented Species in Lamiaceae: An Abundant and Varied Reservoir of Phenolic and Volatile Compounds
by Tilen Zamljen, Mariana Cecilia Grohar and Aljaz Medic
Foods 2024, 13(12), 1857; https://doi.org/10.3390/foods13121857 - 13 Jun 2024
Viewed by 764
Abstract
This investigation aimed to identify the most favorable cultivar based on plant metabolites for potential targeted cultivation in the pharmaceutical industry. The analysis revealed the presence of 19 individual phenolics and 80 individual volatiles across the cultivars, a breadth of data not previously [...] Read more.
This investigation aimed to identify the most favorable cultivar based on plant metabolites for potential targeted cultivation in the pharmaceutical industry. The analysis revealed the presence of 19 individual phenolics and 80 individual volatiles across the cultivars, a breadth of data not previously explored to such an extent. Flavones emerged as the predominant phenolic group in all mint-scented cultivars, except for peppermint, where hydroxycinnamic acids dominated. Peppermint exhibited high concentrations of phenolic acids, particularly caffeic acid derivatives and rosmarinic acid, which are known for their anti-inflammatory and antioxidant properties. Luteolin-rich concentrations were found in several mint varieties, known for their antioxidative, antitumor, and cardio-protective properties. Swiss mint and spearmint stood out with elevated levels of flavanones, particularly eriocitrin, akin to citrus fruits. Monoterpene volatiles, including menthol, camphor, limonene, and carvone, were identified across all cultivars, with Swiss mint and spearmint exhibiting the highest amounts. The study underscores the potential for targeted cultivation to enhance volatile yields and reduce agricultural land use. Notably, chocolate mint demonstrated promise for volatile content, while apple mint excelled in phenolics, suggesting their potential for broader agricultural, pharmaceutical, and food industry production. Full article
(This article belongs to the Special Issue Bioactive Phenolic Compounds from Agri-Food and Its Wastes)
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Figure 1
<p>Individual phenolic groups and total analyzed phenolic contents in eleven mint cultivars (<b>A</b>) and their relative contents (<b>B</b>). a–d: statistical significant differences among different mint scented cultivars.</p>
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<p>Individual phenolic groups and total analyzed phenolic contents in eleven mint cultivars (<b>A</b>) and their relative contents (<b>B</b>). a–d: statistical significant differences among different mint scented cultivars.</p>
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<p>Individual volatile groups and total analyzed volatile contents in eleven mint cultivars (<b>A</b>) and their relative contents (<b>B</b>). a–e: statistical significant differences among different mint scented cultivars.</p>
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17 pages, 5261 KiB  
Article
Eriocitrin Inhibits Angiogenesis by Targeting VEGFR2-Mediated PI3K/AKT/mTOR Signaling Pathways
by Ji-Yoon Baek, Jeong-Eun Kwak and Mok-Ryeon Ahn
Nutrients 2024, 16(7), 1091; https://doi.org/10.3390/nu16071091 - 8 Apr 2024
Viewed by 1275
Abstract
Eriocitrin, a flavanone found in peppermint and citrus fruits, is known to possess many physiological activities. However, the anti-angiogenic effects of eriocitrin are yet to be fully elucidated. Therefore, the objective of this research was to explore the anti-angiogenic effects of eriocitrin both [...] Read more.
Eriocitrin, a flavanone found in peppermint and citrus fruits, is known to possess many physiological activities. However, the anti-angiogenic effects of eriocitrin are yet to be fully elucidated. Therefore, the objective of this research was to explore the anti-angiogenic effects of eriocitrin both in vitro and in vivo as well as its underlying mechanism. Anti-angiogenic effects of eriocitrin were evaluated utilizing in vitro models of angiogenesis, including inhibition of tube formation, and induction of apoptosis in human umbilical vein endothelial cells (HUVECs). A chorioallantoic membrane (CAM) assay in chick embryos was also performed to evaluate the in vivo effects of eriocitrin on angiogenesis. Results showed significant eriocitrin effects on proliferation, tube formation, migration, and apoptosis in HUVECs. Furthermore, in vivo analysis revealed that eriocitrin significantly suppressed the formation of new blood vessels. In particular, it regulated MAPK/ERK signaling pathway and VEGFR2, inhibited the downstream PI3K/AKT/mTOR signaling pathway, and activated apoptosis signals such as caspase cascades. In HUVECs, the expression of matrix metalloproteinases (MMP-2 and MMP-9) exhibited an inhibitory effect on angiogenesis through the suppression of the signaling pathway. Therefore, eriocitrin presents potential for development into an antiangiogenic therapeutic agent. Full article
(This article belongs to the Special Issue Functional Foods and Health Promotion)
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Figure 1

Figure 1
<p>Chemical structure of eriocitrin and its effects on proliferation of HUVECs. (<b>A</b>) Chemical structure of eriocitrin. After cells were cultured with eriocitrin at different concentrations (25–100 µM), (<b>B</b>) cell viability and (<b>C</b>) cytotoxicity were assessed. Data are shown as mean ± SE, n = 3.</p>
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<p>Eriocitrin attributes the formation of tubular structures in HUVECs. (<b>A</b>) HUVECs were cultured within a sandwich configuration of collagen gels, exposed to various concentrations of eriocitrin (25–100 µM). The bar indicates 100 μm. (<b>B</b>) The extent of tubular structure formation was quantitatively assessed. Data are shown as mean ± SE, n = 3. * <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; NS, non-significant vs. among groups.</p>
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<p>Eriocitrin suppresses the migration of HUVECs in vitro. (<b>A</b>) A monolayer of HUVECs was mechanically disrupted to create a linear wound, followed by exposure to differing concentrations (25–100 µM) of eriocitrin for a duration of 24 h. The bar indicates 200 μm. (<b>B</b>) The extent of HUVEC migration into the wounded area at the 24 h mark was quantified. Data are shown as mean ± SE, n = 3. ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; NS, non-significant vs. among groups.</p>
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<p>Eriocitrin triggers apoptotic cell death in HUVECs. (<b>A</b>) The induction of apoptosis in HUVECs by eriocitrin over a 24 h period was assessed using flow cytometry subsequent to staining with annexin V-fluorescein isothiocyanate (FITC) and PI. (<b>B</b>) The percentage of apoptotic cells relative to the total cell population is quantified. Data are shown as mean ± SE, n = 3. * <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; NS, non-significant vs. among groups.</p>
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<p>Analysis of apoptotic morphological changes through AO/EB staining. (<b>A</b>) Comparing fluorescently dyed HUVECs with varied concentrations of eriocitrin (25–100 μM) to untreated and positive (H<sub>2</sub>O<sub>2</sub>) controls are shown in representative photographs. Apoptosis in HUVECs exposed to eriocitrin for 24 h was assessed using AO/EB staining. The bar indicates 200 μm. (<b>B</b>) The percentage of apoptotic cells relative to the total cell population is quantified. Data are shown as mean ± SE, n = 3. * <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; NS, non-significant vs. among groups.</p>
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<p>Effect of eriocitrin on apoptosis as evidenced by TUNEL staining. (<b>A</b>) Compared to untreated and positive (H<sub>2</sub>O<sub>2</sub>) controls, fluorescent microscopy images depict human umbilical vein endothelial cells (HUVECs) subjected to various concentrations of eriocitrin (25–100 μM). TUNEL labeling is used to measure apoptosis in HUVECs exposed to eriocitrin for 48 h. Rhodamine (red) and DAPI (blue) as markers for TUNEL-positive cells are used to identify their nuclei. The bar indicates 200 μm. (<b>B</b>) The percentage of apoptotic cells relative to the total cell population is quantified. Data are shown as mean ± SE, n = 3. ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001 vs. among groups.</p>
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<p>Eriocitrin attenuates embryonic angiogenesis as observed in the CAM assay. (<b>A</b>) Eriocitrin exhibits an inhibitory influence on tumor-induced angiogenesis within an in vivo experimental setup dedicated to studying angiogenesis. The bar indicates 2 mm. (<b>B</b>) Administration of retinoic acid (5 nmol/egg retinoic acid) or eriocitrin (ranging from 5 to 50 nmol/egg) resulted in a diminished rate of neovascular formation. The experiment was repeated at least five times and representative data are shown. *** <span class="html-italic">p</span> &lt; 0.001; NS: non-significant vs. among groups.</p>
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<p>Eriocitrin deactivates the phosphorylation of c-Raf, MEK1/2, and ERK 1/2. (<b>A</b>) Proteins were harvested from tube-forming HUVECs subjected to treatment with various concentrations of eriocitrin (25–100 μM) for 12 h. Alterations in the expression levels of of c-Raf, MEK 1/2, and ERK 1/2 were examined via Western blot analysis. (<b>B</b>) The experiment was repeated at least three times and representative data are shown. ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; NS, non-significant vs. among groups.</p>
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<p>Eriocitrin impedes the phosphorylation of VEGFR2 and attenuates the activation of downstream signaling cascades mediated by VEGFR2. (<b>A</b>) Expression profiles of total and phosphorylated forms of proteins associated with the VEGFR2 and PI3K/AKT/mTOR signaling pathways in HUVECs, following exposure to various concentrations of eriocitrin (25–100 μM) for 24 h, were evaluated via Western blot analysis. (<b>B</b>) The experiment was repeated at least three times and representative data are shown. * <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; NS, non-significant vs. among groups.</p>
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<p>Eriocitrin promotes apoptosis in tube-forming HUVECs by activating pro-apoptotic signals such as caspases. (<b>A</b>) Proteins were harvested from tube-forming HUVECs subjected to treatment with various concentrations of eriocitrin (25–100 μM) for 24 h. Alterations in the expression levels of caspase-9, caspase-3, and PARP were examined via Western blot analysis. (<b>B</b>) The experiment was repeated at least three times and representative data are shown. ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; NS, non-significant vs. among groups.</p>
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<p>Eriocitrin reduces the expression of MMPs protein. (<b>A</b>) The expression levels of MMP-2 and MMP-9 proteins were quantified using Western blot analysis and normalized to β-actin level. (<b>B</b>) The experiment was repeated at least three times and representative data are shown. * <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; NS, non-significant vs. among groups.</p>
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15 pages, 3101 KiB  
Article
Exploring the Antioxidant Properties of Citrus limon (Lemon) Peel Ultrasound Extract after the Cloud Point Extraction Method
by Vassilis Athanasiadis, Theodoros Chatzimitakos, Martha Mantiniotou, Eleni Bozinou and Stavros I. Lalas
Biomass 2024, 4(1), 202-216; https://doi.org/10.3390/biomass4010010 - 1 Mar 2024
Cited by 2 | Viewed by 2505
Abstract
Each year, a substantial amount of food is discarded around the globe. A significant portion of this waste consists of by-products derived from Citrus fruits such as lemons. The purpose of this research is to examine the polyphenol extraction and the antioxidant ability [...] Read more.
Each year, a substantial amount of food is discarded around the globe. A significant portion of this waste consists of by-products derived from Citrus fruits such as lemons. The purpose of this research is to examine the polyphenol extraction and the antioxidant ability of lemon peel using cloud point extraction (CPE), a sustainable approach. CPE was conducted using three steps with a 20% w/v concentration of Span 20 as the surfactant, which has a critical micellar concentration of 6.13 × 10−5 mol/L. The pH was set at 7 and a salt concentration of 20% was maintained at 45 °C for 20 min. The subsequent outcomes of the analysis were obtained: total polyphenol content (TPC): 526.32 mg gallic acid equivalents per liter; total flavonoid content (TFC): 90.22 mg rutin equivalents per liter; FRAP, DPPH, and hydrogen peroxide assays: 2.40, 2.68 and 1.03 mmol ascorbic acid equivalents per liter, respectively, and 168.63 mg/L ascorbic acid content. The quantification of the polyphenolic compounds through High-Performance Liquid Chromatography showed that the most abundant compounds in the lemon peels are eriocitrin (159.43 mg/L) and hesperidin (135.21 mg/L). The results indicate that the proposed CPE technique is successful in extracting antioxidant compounds from lemon peels. The generated extracts have the potential to be exploited as dietary additives to enhance human health and can also be utilized for nutraceuticals or pharmaceutical purposes. Full article
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<p>Effect of various surfactants on the recovery of polyphenols from lemon peels. Error bars are used to denote standard deviations, whereas lowercase letters (e.g., (a–d)) are used to indicate means that have statistically significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The impact of pH on the extraction efficiency of polyphenols from lemon peels. Error bars are used to denote standard deviations, whereas lowercase letters (e.g., (a, b)) denote means that have statistically significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The impact of salt concentration on the recovery of polyphenols from lemon peels. Error bars are used to denote standard deviations, whereas lowercase letters (e.g., (a–e)) denote statistically significant differences in means (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The impact of varying concentrations of Span 20 on the extraction efficiency of polyphenols from lemon peels. Error bars are used to denote standard deviations, whereas lowercase letters (e.g., (a, b)) denote means that have differences of statistical significance (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total polyphenol content (TPC) from lemon peel extract with 20% <span class="html-italic">w/v</span> Span 20. Standard deviations are presented with error bars.</p>
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<p>Representative HPLC chromatogram at 280 and 320 nm of lemon peel extract, demonstrating polyphenolic compounds that were identified. 1: neochlorogenic acid; 2: catechin; 3: chlorogenic acid; 4: caffeic acid; 5: syringic acid; 6: epicatechin; 7: eriocitrin; 8: rutin; 9: luteolin 7-glucoside; 10: kaempferol 3-glucoside; 11: hesperidin.</p>
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<p>Bivariate analysis of initial lemon peel extract by optimal total SP phase sample. Line of fit and confidence limits (curves) for the expected values are also presented. Asterisks and colored values denote statistically significant values, while inset tables include statistics relevant to the evaluation of the resulting bivariate platform model.</p>
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11 pages, 2469 KiB  
Article
The Effect and Potential Mechanism of Fulvic Acid on Flavonoids in Lemon Leaves
by Youdi Ren, Fan Yang, Weifeng Dai, Cheng Yuan, Yi Qin, Jinxue Li and Mi Zhang
Horticulturae 2024, 10(2), 144; https://doi.org/10.3390/horticulturae10020144 - 1 Feb 2024
Cited by 1 | Viewed by 1155
Abstract
Citrus limon (L.) Burm. f. is a horticultural crop known for its abundance of valuable secondary metabolites, including flavonoids, which are found in its fruits and leaves. Our previous research has shown that treating C. limon with fulvic acid (FA) can enhance the [...] Read more.
Citrus limon (L.) Burm. f. is a horticultural crop known for its abundance of valuable secondary metabolites, including flavonoids, which are found in its fruits and leaves. Our previous research has shown that treating C. limon with fulvic acid (FA) can enhance the levels of vitamin C, total acid, total sugar, total flavonoids, and phenols in its fruits as well as the volatiles and total flavonoids in its leaves. In this current study, we established a method to analyze eight specific flavonoids in lemon leaves and evaluated the impact of irrigation with FA on the content of these flavonoids over a six-month period using HPLC-DAD/MS analysis. Moreover, we investigated the potential mechanisms of FA through ELISA and q-PCR methods. The results indicated that FA increased the contents of four flavonoids, namely, isoorientin, eriocitrin, vitexin, and rutin, and promoted the activity and gene expression of phenylalanineammonialyase (PAL), 4-coumaric acid coenzyme A ligase (4CL), chalcone synthase (CHS), flavonoid 3′-hydroxylase (F3′H), and flavonol synthase (FLS). Furthermore, the relationship between flavonoid content and the activities of biosynthetic enzymes was analyzed using orthogonal partial least squares discriminant analysis (OPLS-DA), which revealed a positive correlation between seven flavonoid levels and the activity of five biosynthetic enzymes under FA treatment. Full article
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Figure 1
<p>HPLC-DAD/MS chromatograms of a standard prepared with standard compounds and a sample prepared from lemon leaves: (<b>a</b>) HPLC-DAD chromatogram of the standard; UV detection (λ = 283 nm); (<b>b</b>) HPLC–MS analysis of the standard, performed on an Agilent 1260 Series coupled with an Agilent 6530 Accurate-Mass Q-TOF mass spectrometer (Agilent Ltd.) in negative electrospray modes. (<b>c</b>) HPLC-DAD chromatogram of the sample; UV detection (λ = 283 nm); (<b>d</b>) HPLC–MS analysis of the sample, performed on an Agilent 1260 Series coupled with an Agilent 6530 Accurate-Mass Q-TOF mass spectrometer (Agilent Ltd.) in negative electrospray modes. 1: vicenin 2; 2: isoorientin; 3: eriocitrin; 4: vitexin; 5: rutin; 6: narcissoside; 7: hesperidin; 8: diosmin.</p>
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<p>The contents of flavonoids in samples extracted from lemon leaves treated with FA over a six-month period as determined by HPLC-DAD: (<b>a</b>) vicenin 2; (<b>b</b>) isoorientin; (<b>c</b>) eriocitrin; (<b>d</b>) vitexin; (<b>e</b>) rutin; (<b>f</b>) narcissoside; (<b>g</b>) hesperidin; (<b>h</b>) diosmin. Data are presented as means ± standard deviation (<span class="html-italic">n</span> = 6). ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, vs. the control group.</p>
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<p>The activities of five enzymes involved in flavonoid biosynthesis in samples extracted from <span class="html-italic">C. limon</span> leaves treated with FA and untreated over a six-month period as determined by ELISA: (<b>a</b>) phenylalanineammonialyase (PAL); (<b>b</b>) coenzyme A ligase 4-coumaric acid (4CL); (<b>c</b>) flavonoid 3′-hydroxylase (F3′H); (<b>d</b>) chalcone synthase (CHS); (<b>e</b>) flavonol synthase (FLS). Data are presented as means ± standard deviation (<span class="html-italic">n</span> = 3).</p>
Full article ">Figure 4
<p>The gene expression levels of five enzymes involved in flavonoid biosynthesis in samples extracted from <span class="html-italic">C. limon</span> leaves treated with FA and untreated over a six-month period as determined by q-PCR: (<b>a</b>) phenylalanineammonialyase (PAL); (<b>b</b>) coenzyme A ligase 4-coumaric acid (4CL); (<b>c</b>) chalcone synthase (CHS); (<b>d</b>) flavonoid 3′-hydroxylase (F3′H); (<b>e</b>) flavonol synthase (FLS). Data are presented as means ± standard deviation (<span class="html-italic">n</span> = 3). *** <span class="html-italic">p</span> &lt; 0.001, ** <span class="html-italic">p</span> &lt; 0.01, * <span class="html-italic">p</span> &lt; 0.05, vs. the control group.</p>
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<p>Correlation between the content of eight flavonoids and the activities of five enzymes involved in flavonoid biosynthesis as analyzed by the orthogonal partial least squares discriminant analysis (OPLS-DA) method.</p>
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14 pages, 3217 KiB  
Article
Eriocitrin Disrupts Erythrocyte Membrane Asymmetry through Oxidative Stress and Calcium Signaling and the Activation of Casein Kinase 1α and Rac1 GTPase
by Sumiah A. Alghareeb, Jawaher Alsughayyir and Mohammad A. Alfhili
Pharmaceuticals 2023, 16(12), 1681; https://doi.org/10.3390/ph16121681 - 2 Dec 2023
Cited by 1 | Viewed by 1468
Abstract
Background: Hemolysis and eryptosis result in the premature elimination of circulating erythrocytes and thus contribute to chemotherapy-related anemia, which is extremely prevalent in cancer patients. Eriocitrin (ERN), a flavanone glycoside in citrus fruits, has shown great promise as an anticancer agent, but the [...] Read more.
Background: Hemolysis and eryptosis result in the premature elimination of circulating erythrocytes and thus contribute to chemotherapy-related anemia, which is extremely prevalent in cancer patients. Eriocitrin (ERN), a flavanone glycoside in citrus fruits, has shown great promise as an anticancer agent, but the potential toxicity of ERN to human erythrocytes remains unstudied. Methods: Erythrocytes were exposed to anticancer concentrations of ERN (10–100 μM) for 24 h at 37 °C, and hemolysis and associated markers were quantified using colorimetric assays. Eryptosis was assessed by flow cytometric analysis to detect phosphatidylserine (PS) exposure by annexin-V-FITC, intracellular Ca2+ using Fluo4/AM, and oxidative stress with 2-,7-dichlorodihydrofluorescin diacetate (H2DCFDA). ERN was also tested against specific signaling inhibitors and anti-hemolytic agents. Results: ERN caused significant, concentration-dependent hemolysis at 20–100 μM. ERN also significantly increased the percentage of eryptotic cells characterized by Ca2+ elevation and oxidative stress. Furthermore, the hemolytic activity of ERN was significantly ameliorated in the presence of D4476, NSC23766, isosmotic urea and sucrose, and polyethylene glycol 8000 (PEG). In whole blood, ERN significantly elevated MCV and ESR, with no appreciable effects on other peripheral blood cells. Conclusions: ERN promotes premature erythrocyte death through hemolysis and eryptosis characterized by PS externalization, Ca2+ accumulation, membrane blebbing, loss of cellular volume, and oxidative stress. These toxic effects, mediated through casein kinase 1α and Rac1 GTPase, can be ameliorated by urea, sucrose, and PEG. Altogether, these novel findings are relevant to the further development of ERN as an anticancer therapeutic. Full article
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Graphical abstract

Graphical abstract
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<p>ERN induces hemolysis. (<b>A</b>) Molecular structure of ERN. (<b>B</b>) Concentration-responsive hemolytic activity of ERN (10–100 μM) in PBS. (<b>C</b>) Concentration-responsive hemolytic activity of ERN (10–100 μM) in Ringer solution. ERN-induced (40–100 μM) leakage of hemolytic markers (<b>D</b>) K<sup>+</sup>, (<b>E</b>) LDH, (<b>F</b>) AST, and (<b>G</b>) CK. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance, while * (<span class="html-italic">p &lt;</span> 0.05), ** (<span class="html-italic">p &lt;</span> 0.01), *** (<span class="html-italic">p &lt;</span> 0.001), and **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>Effect of ERN on extracellular pH and AChE. (<b>A</b>) pH and (<b>B</b>) AChE activity in control and ERN-treated (40–100 μM) cells. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance. *** (<span class="html-italic">p &lt;</span> 0.001); **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>ERN induces eryptosis. (<b>A</b>) Representative histograms of annexin-V-FITC fluorescence of control (black line) and treated cells (100 μM; brown line). (<b>B</b>) Geomean annexin-V-FITC fluorescence (a.u.) of control and treated (40–100 μM) cells. (<b>C</b>) Percentage of eryptotic cells (40–100 μM). (<b>D</b>) ESR of control and treated (100 μM) cells. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). * (<span class="html-italic">p &lt;</span> 0.05) and **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>ERN raises cytosolic Ca<sup>2+</sup> levels. (<b>A</b>) Representative histograms of Fluo4 fluorescence of control (black line) and treated cells (100 μM; brown line). (<b>B</b>) Geomean Fluo4 fluorescence (fold change) of control and treated (40–100 μM) cells. (<b>C</b>) Percentage of cells with excess Ca<sup>2+</sup> accumulation (40–100 μM). Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance, while * (<span class="html-italic">p &lt;</span> 0.05) and ** (<span class="html-italic">p &lt;</span> 0.01).</p>
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<p>ERN elicits oxidative damage. (<b>A</b>) Representative histograms of DCF fluorescence of control (black line) and treated cells (100 μM; brown line). (<b>B</b>) Geomean DCF fluorescence (fold change) of control and treated (40–100 μM) cells. (<b>C</b>) Percentage of oxidized cells (40–100 μM). Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance, while **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>Effect of ERN on RBC morphology. (<b>A</b>) Representative histograms of FSC of control (black line) and treated cells (100 μM; brown line). (<b>B</b>) Geomean FSC (a.u.) of control and treated (40–100 μM) cells. (<b>C</b>) Percentage of shrinkage in control and treated (40–100 μM) cells. (<b>D</b>) Distribution of control and treated (100 μM) cells relative to FSC-H and annexin-V-FITC. (<b>E</b>) Percentage of swelling in control and treated cells (40–100 μM). (<b>F</b>) Geomean SSC (a.u.) of control and treated (40–100 μM) cells (<b>G</b>) SEM micrographs (×10,000; scale bar: 1 μM) of control and treated (100 μM) cells. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance, while * (<span class="html-italic">p &lt;</span> 0.05), ** (<span class="html-italic">p &lt;</span> 0.01), and **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>Inhibitors of ERN-induced RBC death. Effect of (<b>A</b>) D4476 (20 uM), (<b>B</b>) ATP (500 μM), (<b>C</b>) NSC23766 (100 uM), (<b>D</b>) urea (300 mM), (<b>E</b>) sucrose (250 mM), (<b>F</b>) KCl (125 mM), (<b>G</b>) extracellular Ca<sup>2+</sup> (1 mM) removal, and (<b>H</b>) PEG 8000 (10%) on ERN-induced hemolysis (80 μM). Results are shown as means ± SEM (<span class="html-italic">n</span> = 9). ns indicates no statistical significance, while * (<span class="html-italic">p &lt;</span> 0.05), ** (<span class="html-italic">p &lt;</span> 0.01), and **** (<span class="html-italic">p &lt;</span> 0.0001).</p>
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<p>ERN exhausts corpuscular Hb in whole blood. (<b>A</b>) Representative histograms of RBC volume. (<b>B</b>) RBC count. (<b>C</b>) Hb. (<b>D</b>) MCH. (<b>E</b>) MCHC. (<b>F</b>) MCV. (<b>G</b>) RDW-CV. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9) for control and treated (100 μM) whole blood. ns indicates no statistical significance. ** (<span class="html-italic">p &lt;</span> 0.01); *** (<span class="html-italic">p &lt;</span> 0.001).</p>
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<p>Effect of ERN on white blood cells. (<b>A</b>) Leukocyte count. (<b>B</b>) Representative scattergrams of fluorescence and side scatter intensity of leukocytes. Viability of (<b>C</b>) neutrophils, (<b>D</b>) lymphocytes, (<b>E</b>) monocytes, (<b>F</b>) eosinophils, and (<b>G</b>) basophils. Results are shown as means ± SEM (<span class="html-italic">n</span> = 9) for control and treated (100 μM) whole blood. ns indicates no statistical significance, while * (<span class="html-italic">p &lt;</span> 0.05).</p>
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27 pages, 773 KiB  
Review
Mentha piperita: Essential Oil and Extracts, Their Biological Activities, and Perspectives on the Development of New Medicinal and Cosmetic Products
by Nataliia Hudz, Lesya Kobylinska, Katarzyna Pokajewicz, Vladimira Horčinová Sedláčková, Roman Fedin, Mariia Voloshyn, Iryna Myskiv, Ján Brindza, Piotr Paweł Wieczorek and Jacek Lipok
Molecules 2023, 28(21), 7444; https://doi.org/10.3390/molecules28217444 - 6 Nov 2023
Cited by 12 | Viewed by 5942
Abstract
This review aims to analyze Mentha piperita L. as a potential raw material for the development of new health-promoting products (nutraceuticals, cosmetics, and pharmaceutical products). A lot of scientific publications were retrieved from the Scopus, PubMed, and Google Scholar databases which enable the [...] Read more.
This review aims to analyze Mentha piperita L. as a potential raw material for the development of new health-promoting products (nutraceuticals, cosmetics, and pharmaceutical products). A lot of scientific publications were retrieved from the Scopus, PubMed, and Google Scholar databases which enable the study and generalization of the extraction procedures, key biologically active compounds of essential oil and extracts, biological properties, and therapeutic potential of M. piperita, along with perspectives on the development of its dosage forms, including combinations of synthetic active substances and herbal preparations of M. piperita. The results of this review indicate that M. piperita is a source rich in phytoconstituents of different chemical nature and can be regarded as a source of active substances to enhance health and to develop medicinal products for complementary therapy of various conditions, especially those related with oxidant stress, inflammation, and moderate infections. Essential oil has a broad spectrum of activities. Depending on the test and concentration, this essential oil has both anti- and prooxidant properties. Gram-positive bacteria are more sensitive to the essential oil of M. piperita than Gram-negative ones. This review also considered some facets of the standardization of essential oil and extracts of M. piperita. Among the identified phenolics of extracts were caffeic acid, rosmarinic acid, eriocitrin, luteolin derivates (luteolin-7-O-rutinoside, luteolin-7-O-glucoronide), and hesperidin. The concentration of these phenolics depends on the solvent used. This review also considered the relationships between the chemical component and biological activity. The results showed that the essential oil and extracts reduced inflammation in vitro by inhibiting the production of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6), and in vivo by reducing the paw edema induced using carrageenan injection in rats. Therefore, herbal preparations of M. piperita are promising medicinal and cosmetic preparations for their usage in skincare and oral cavity care products with antimicrobial, anti-inflammatory, and wound-healing properties. This plant can also be regarded as a platform for the development of antibacterial preparations and combined anti-inflammatory and cardioprotective medicinal products (synthetic active substances plus herbal preparations). This review could be considered for the justification of the composition of some medicinal products during their pharmaceutical development for writing a registration dossier in the format of Common Technical Document. Full article
(This article belongs to the Special Issue Essential Oils: From Extraction to Application)
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<p>The chemical structure of main flavonoids of <span class="html-italic">M. piperira</span>.</p>
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13 pages, 2760 KiB  
Article
Virtual Insights into Natural Compounds as Potential 5α-Reductase Type II Inhibitors: A Structure-Based Screening and Molecular Dynamics Simulation Study
by Sibhghatulla Shaikh, Shahid Ali, Jeong Ho Lim, Khurshid Ahmad, Ki Soo Han, Eun Ju Lee and Inho Choi
Life 2023, 13(11), 2152; https://doi.org/10.3390/life13112152 - 1 Nov 2023
Viewed by 1738
Abstract
Androgenic alopecia (AGA) is a dermatological disease with psychosocial consequences for those who experience hair loss. AGA is linked to an increase in androgen levels caused by an excess of dihydrotestosterone in blood capillaries produced from testosterone by 5α-reductase type II (5αR2), which [...] Read more.
Androgenic alopecia (AGA) is a dermatological disease with psychosocial consequences for those who experience hair loss. AGA is linked to an increase in androgen levels caused by an excess of dihydrotestosterone in blood capillaries produced from testosterone by 5α-reductase type II (5αR2), which is expressed in scalp hair follicles; 5αR2 activity and dihydrotestosterone levels are elevated in balding scalps. The diverse health benefits of flavonoids have been widely reported in epidemiological studies, and research interest continues to increase. In this study, a virtual screening approach was used to identify compounds that interact with active site residues of 5αR2 by screening a library containing 241 flavonoid compounds. Here, we report two potent flavonoid compounds, eriocitrin and silymarin, that interacted strongly with 5αR2, with binding energies of −12.1 and −11.7 kcal/mol, respectively, which were more significant than those of the control, finasteride (−11.2 kcal/mol). Molecular dynamic simulations (200 ns) were used to optimize the interactions between compounds and 5αR2 and revealed that the interaction of eriocitrin and silymarin with 5αR2 was stable. The study shows that eriocitrin and silymarin provide developmental bases for novel 5αR2 inhibitors for the management of AGA. Full article
(This article belongs to the Special Issue Therapeutic Effects of Natural Products on Human Diseases)
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<p>Visualization of finasteride (black), eriocitrin (red), and silymarin (cyan) in the 5αR2 binding pocket (<b>A</b>). 2D views of 5αR2 residues interacting with eriocitrin (<b>B</b>), silymarin (<b>C</b>), and finasteride (<b>D</b>).</p>
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<p>MD simulation studies of docked complexes. RMSD plot (<b>A</b>), average RMSD plot (<b>B</b>), RMSD plots of ligands in the 5αR2 catalytic pocket (<b>C</b>), and corresponding RMSF plots (<b>D</b>). Black, red, and cyan indicate finasteride, eriocitrin, and silymarin, respectively.</p>
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<p>Rg plot of complexes (<b>A</b>), SASA plot (<b>B</b>), number of H-bonds formed with ligands (<b>C</b>), and MSD plot (<b>D</b>). Black, red, and cyan indicate finasteride, eriocitrin, and silymarin, respectively.</p>
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<p>2D projections of complexes (<b>A</b>) and Gibbs energy landscape plots (<b>B</b>–<b>D</b>).</p>
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16 pages, 1160 KiB  
Article
Enriching the Bioactive Components and Antioxidant Capacity of Concentrated Lime Juices Prepared by Cryogenic and Vacuum Processes
by Dat Tien Huynh, Mai Thi Nguyet Vo and Tuyen Chan Kha
Processes 2023, 11(7), 1883; https://doi.org/10.3390/pr11071883 - 23 Jun 2023
Viewed by 1721
Abstract
Lime juice is rich in bioactive components and exerts a wide range of therapeutic effects, especially antioxidant activity. Freeze concentration is considered an essential method to maintain the nutritional values and bioactives of fruit juices. This study aimed to compare the ability in [...] Read more.
Lime juice is rich in bioactive components and exerts a wide range of therapeutic effects, especially antioxidant activity. Freeze concentration is considered an essential method to maintain the nutritional values and bioactives of fruit juices. This study aimed to compare the ability in enriching ascorbic acid, total phenolic compounds, and major flavonoids and the antioxidant activity (DPPH) of concentrated lime juices prepared by vacuum and freeze-concentrations. The ascorbic acid in the juices was analyzed using the HPLC-PDA method. The total phenolic content and DPPH inhibition ability were measured by the colorimetric method. The polyphenol profiles of two lime varieties (C. latifolia and C. limonia) were qualitatively analyzed using LC-TOF MS/MS; then, the major juices’ flavonoids were analyzed by HPLC-PDA against/based on commercial standards. The results showed that C. latifolia was superior to C. limonia in ascorbic acid, TPC, major flavonoids, and antioxidants. C. latifolia was also more diverse than C. limonia in its polyphenol profile through the identified compounds (18 vs. 15). Freeze-concentrated lime juices were significantly higher than the vacuum-concentrated counterparts in ascorbic acid (mean difference from 9.41 to 22.01 mg, p < 0.01), and TPC (from 60.76 to 149.88 mgGAE). The quantification of major flavonoids showed that the freeze-concentrated lime juices retained high levels of hesperidin, eriocitrin, and rutin (p < 0.01) whereas the vacuum concentration preserved higher ones in diosmin and naringin (p < 0.01). The freeze-concentrated lime juice was significantly higher than vacuum-concentrated lime juices in the DPPH scavenging activity by at least 15% (p < 0.01). Overall, freeze concentration enriched bioactive compounds in lime juices almost threefold and improved antioxidants at least twofold. Thus, freeze concentration is promising for the industry in producing high-quality lime juice to preserve its thermal liable bioactive component. Full article
(This article belongs to the Special Issue Bio-Active Compounds in Food Production)
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<p>Changes in ascorbic acid, TPC contents, and retention (<b>A</b>,<b>C</b>,<b>E</b>,<b>G</b> in <span class="html-italic">C. latifolia</span>; <b>B</b>,<b>D</b>,<b>F</b>,<b>H</b> in <span class="html-italic">C. limonia</span>) during freeze and vacuum concentrations. The values are expressed as mean ± SD of triplicates. Different uppercase letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) between freeze-concentrated juices. Different lowercase letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) between vacuum-concentrated juices. OJ: original juice, JC: juice concentrate.</p>
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<p>Changes in DPPH scavenging activity of (<b>A</b>) <span class="html-italic">C. latifolia</span> and (<b>B</b>) <span class="html-italic">C. limonia</span> lime juices during freeze and vacuum concentrations. The values are expressed as mean ± SD of triplicates. Different uppercase letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) between freeze-concentrated juices. Different lowercase letters indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05) between vacuum-concentrated juices. OJ: original juice, JC: juice concentrate.</p>
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18 pages, 3977 KiB  
Article
LDPE and PLA Active Food Packaging Incorporated with Lemon by-Products Extract: Preparation, Characterization and Effectiveness to Delay Lipid Oxidation in Almonds and Beef Meat
by Mariana A. Andrade, Cássia H. Barbosa, Sandra Mariño-Cortegoso, Letricia Barbosa-Pereira, Raquel Sendón, Giovanna G. Buonocore, Mariamelia Stanzione, Anabela Coelho, Cristina Belo Correia, Margarida Saraiva, Ana Rodríguez-Bernaldo de Quirós, Fernanda Vilarinho, Khaoula Khwaldia, Ana Sanches Silva and Fernando Ramos
Foods 2023, 12(13), 2450; https://doi.org/10.3390/foods12132450 - 22 Jun 2023
Cited by 6 | Viewed by 2249
Abstract
Low-density polyethylene-based packaging with 4% lemon extract (LDPE/4LE) and two polylactic-based (PLA) packaging materials with 4% and 6% lemon extract (PLA/PEG/4LE and PLA/6LE) were produced. O2 and water permeability tests were performed, the total and individual phenolic compounds content were measured, and [...] Read more.
Low-density polyethylene-based packaging with 4% lemon extract (LDPE/4LE) and two polylactic-based (PLA) packaging materials with 4% and 6% lemon extract (PLA/PEG/4LE and PLA/6LE) were produced. O2 and water permeability tests were performed, the total and individual phenolic compounds content were measured, and the films’ antioxidant activities were determined. The films’ ability to delay lipid oxidation was tested in two model foods: almonds, packaged with LDPE/4LE, PLA/4LE and PLA/6LE for a maximum period of 60 days at 40 °C (accelerated assay); and beef meat, packaged with the PLA/6LE for a maximum period of 11 days at 4 °C. The LE improved the WVP in all of the active films by 33%, 20% and 60% for the LDPE/4LE, PLA/4LE and PLA/6LE films, respectively. At the end of 10 days, the migration of phenolic compounds through the PLA films was measured to be 142.27 and 114.9 μg/dm2 for the PLA/4LE and PLA/6LE films, respectively, and was significantly higher than phenolic compounds migration measured for the LDPE/4LE (15.97 μg/dm2). Naringenin, apigenin, ferulic acid, eriocitrin, hesperidin and 4-hydroxybenzoic acid were the main identified compounds in the PLA, but only 4-hydroxybenzoic acid, naringenin and p-coumaric acid were identified in the LDPE films. Regarding the films’ ability to delay lipid oxidation, LDPE/4LE presented the best results, showing a capacity to delay lipid oxidation in almonds for 30 days. When applied to raw beef meat, the PLA/6LE packaging was able to significantly inhibit lipid oxidation for 6 days, and successfully inhibited total microorganisms’ growth until the 8th day of storage. Full article
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<p>Active (LDPE/4LE and PLA/4LE) films over the Portuguese National Institute of Health logo (Instituto Nacional de Saúde Doutor Ricardo Jorge).</p>
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<p>Water vapor (<b>a</b>) and O<sub>2</sub> permeability (<b>b</b>) of the control (LDPE and PLA) and active (LDPE/4LE, PLA/4LE, PLA/6LE) films. Legend: LDPE—low density polyethylene; LE—lemon extract; PLA—polylactic acid; PEG—polyethylene glycol.</p>
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<p>Results from the TBARS assay, evaluating the model foods beef, almonds and pistachios. Different letters represent results with significant differences. The lowercase letters compare the same sample over time.</p>
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<p>Results of the thiobarbituric reactive substances assay from almonds packed with the control (LDPE, PLA/PEG and PLA) and active (LDPE/4LE, PLA/PEG/4, PLA/6LE) films. The uppercase letters compare samples within the same storage day. The lowercase letters compare samples with the same packaging over time (for instance, LDPE at 0 and 7 days presented no significant differences, as noted by the lowercase “a”. On the other hand, on the 7th day of storage, the LDPE and LDPE/4LE presented no significant differences, as identified by the uppercase “A”). Different letters for either lowercase/uppercase comparisons represent results with significant differences.</p>
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<p>Results of the <span class="html-italic">p</span>-anisidine assay from almonds packed with the control (LDPE, PLA/PEG and PLA) and active (LDPE/4LE, PLA/PEG/4, PLA/6LE) films. The uppercase letters compare samples within the same storage day. The lowercase letters compare samples with the same packaging over time. Different letters for either lowercase/uppercase comparisons represent results with significant differences.</p>
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<p>Results of the peroxide determination assay from almonds packaged with the control (PLA) and active (PLA/6LE) films. The uppercase letters compare samples within the same storage day. The lowercase letters compare samples with the same packaging over time. Different letters for either lowercase/uppercase comparisons represent results with significant differences.</p>
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<p>Results of the TBARS assay from meat packed with the control (PLA) and active (PLA/6LE) films. The uppercase letters compare samples within the same storage day. The lowercase letters compare samples with the same packaging over time. Different letters for either lowercase/uppercase comparisons represent results with significant differences.</p>
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<p>Results of the microbiological assay for meat packed with the control (PLA) and active (PLA/6LE) films. The uppercase letters compare samples within the same storage day. The lowercase letters compare samples with the same packaging over time. Different letters for either lowercase/uppercase comparisons represent results with significant differences.</p>
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11 pages, 1352 KiB  
Article
Exploring the Association between Citrus Nutraceutical Eriocitrin and Metformin for Improving Pre-Diabetes in a Dynamic Microbiome Model
by Thais Cesar, Mateus Kawata Salgaço, Victoria Mesa, Adilson Sartoratto and Katia Sivieri
Pharmaceuticals 2023, 16(5), 650; https://doi.org/10.3390/ph16050650 - 26 Apr 2023
Cited by 4 | Viewed by 2009
Abstract
Pre-diabetes is recognized as an altered metabolic state, which precedes type 2 diabetes, and it is associated with great dysfunction of the intestinal microbiota, known as dysbiosis. Natural compounds, capable of reducing blood glucose without side effects and with a beneficial effect on [...] Read more.
Pre-diabetes is recognized as an altered metabolic state, which precedes type 2 diabetes, and it is associated with great dysfunction of the intestinal microbiota, known as dysbiosis. Natural compounds, capable of reducing blood glucose without side effects and with a beneficial effect on the microbiota, have been studied as substitutes or adjuvants to conventional hypoglycemic agents, such as metformin. In this work, the effect of the nutraceutical Eriomin®, a mixture of citrus flavonoids (eriocitrin, hesperidin, naringin, and didymin), which reduces glycemia and increases glucagon-like peptide-1 (GLP-1) in pre-diabetic patients, was tested in the Simulator of Human Intestinal Microbial Ecosystem (SHIME®), inoculated with pre-diabetic microbiota. After treatment with Eriomin® plus metformin, a significant increase in acetate and butyrate production was observed. Furthermore, sequencing of the 16S rRNA gene of the microorganisms showed that Eriomin® plus metformin stimulated the growth of Bacteroides and Subdoligranulum genera. Bacteroides are the largest fraction of the intestinal microbiota and are potential colonizers of the colon, with some species producing acetic and propionic fatty acids. In addition, Subdoligranulum species are associated with better host glycemic metabolism. In conclusion, Eriomin® associated with metformin improved the composition and metabolism of the intestinal microbiota, suggesting a potential use in pre-diabetes therapy. Full article
(This article belongs to the Section Natural Products)
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<p>Eriomin<sup>®</sup> associated with metformin-induced changes in the metabolic activity of the intestinal microbiome in vitro. The production of SCFAs was monitored for 7 days of fermentation with the following treatments: Control (microbiota without treatment); 200 mg/d Eriomin<sup>®</sup> (ERM200); 500 mg/d of Eriomin<sup>®</sup> (ERM500); 500 mg/d of metformin (MTF), 500 mg/d of metformin + 200 mg/d of Eriomin<sup>®</sup> (MTF + ERM200); 500 mg/d of metformin + 500 mg/d of Eriomin<sup>®</sup> (MTF + ERM500). Data are expressed as the average of each SCFA produced. The symbols * and # mean statistical increase or decrease, respectively, between treatments for each SCFA (<span class="html-italic">p</span> ≤ 0.05).</p>
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<p>Variations in the alpha diversity of Eriomin<sup>®</sup> combined with metformin. Legend: Control, microbiota without treatment; ERM200, 200 mg/d of Eriomin<sup>®</sup>; ERM500, 500 mg/d of Eriomin<sup>®</sup>; MTF, 500 mg/d of metformin; MTF + ERM200, 500 mg/d of metformin + 200 mg/d of Eriomin<sup>®</sup>; MTF + ERM500, 500 mg/d of metformin + 500 mg/d of Eriomin<sup>®</sup>. The symbol ** mean statistical increase or decrease, respectively, between treatments for alpha diversity index (<span class="html-italic">p</span> ≤ 0.05).</p>
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<p>Principal coordinate analysis (PCoA) of the weighted and unweighted UniFrac distances variations in beta diversity of Eriomin<sup>®</sup> combined with metformin. Legend: Control, microbiota without treatment; ERM200, 200 mg/d of Eriomin<sup>®</sup>; ERM500, 500 mg/d of Eriomin<sup>®</sup>; MTF, 500 mg/d of metformin; MTF + ERM200, 500 mg/d of metformin + 200 mg/d of Eriomin<sup>®</sup>; MTF + ERM500, 500 mg/d of metformin + 500 mg/d of Eriomin<sup>®</sup>.</p>
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<p>Histogram of the community composition of gut microbiota at the phylum level. Control, microbiota without treatment; ERM200, 200 mg/d of Eriomin<sup>®</sup>; ERM500, 500 mg/d of Eriomin<sup>®</sup>; MTF, 500 mg/d of metformin; MTF + ERM200, 500 mg/d of metformin + 200 mg/d of Eriomin<sup>®</sup>; MTF + ERM500, 500 mg/d of metformin + 500 mg/d of Eriomin<sup>®</sup>.</p>
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<p>Histogram of the community composition of gut microbiota at the genus level. Legend: Control, microbiota without treatment; ERM200, 200 mg/d of Eriomin<sup>®</sup>; ERM500, 500 mg/d of Eriomin<sup>®</sup>; MTF, 500 mg/d of metformin; MTF + ERM200, 500 mg/d of metformin +200 mg/d of Eriomin<sup>®</sup>; MTF + ERM500, 500 mg/d of metformin +500 mg/d of Eriomin<sup>®</sup>.</p>
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21 pages, 3626 KiB  
Article
In Vitro Antiglycation and Methylglyoxal Trapping Effect of Peppermint Leaf (Mentha × piperita L.) and Its Polyphenols
by Izabela Fecka, Katarzyna Bednarska and Adam Kowalczyk
Molecules 2023, 28(6), 2865; https://doi.org/10.3390/molecules28062865 - 22 Mar 2023
Cited by 3 | Viewed by 2471
Abstract
The most significant reactive α-dicarbonyl RCS involved in the pathomechanism of glycation and related diseases is methylglyoxal (MGO). Hyperglycemia promotes the generation of MGO and leads to the formation of advanced glycation end products (AGEs). Therefore, MGO trapping and glycation inhibition appear to [...] Read more.
The most significant reactive α-dicarbonyl RCS involved in the pathomechanism of glycation and related diseases is methylglyoxal (MGO). Hyperglycemia promotes the generation of MGO and leads to the formation of advanced glycation end products (AGEs). Therefore, MGO trapping and glycation inhibition appear to be important therapeutic targets in prediabetes, diabetes, and in the early prevention of hyperglycemic complications. Peppermint leaf is commonly used as herbal tea, rich in polyphenols. Eriocitrin, its predominant component, in a double-blind, randomized controlled study reversed the prediabetic condition in patients. However, the antiglycation activity of this plant material and its polyphenols has not been characterized to date. Therefore, the aim of this study was to evaluate the ability of a peppermint leaf dry extract and its polyphenols to inhibit non-enzymatic protein glycation in a model with bovine serum albumin (BSA) and MGO as a glycation agent. Peppermint polyphenols were also evaluated for their potential to trap MGO in vitro, and the resulting adducts were analyzed by UHPLC-ESI-MS. To relate chemical composition to glycation inhibitory activity, the obtained peppermint extract was subjected to qualitative and quantitative analysis. The capability of peppermint leaf polyphenols to inhibit glycation (27.3–77.2%) and form adducts with MGO was confirmed. In the case of flavone aglycones, mono- and di-adducts with MGO were observed, while eriodictyol and eriocitrin effectively produced only mono-adducts. Rosmarinic acid and luteolin-7-O-glycosides did not reveal this action. IC50 of the peppermint leaf dry extract was calculated at 2 mg/mL, equivalent to a concentration of 1.8 μM/mL of polyphenols, including ~1.4 μM/mL of flavonoids and ~0.4 μM/mL of phenolic acids. The contribution of the four major components to the anti-AGE activity of the extract was estimated at 86%, including eriocitrin 35.4%, rosmarinic acid 25.6%, luteolin-7-O-rutinoside 16.9%, luteolin-7-O-β-glucuronoside 8.1%, and others 14%. The effect of peppermint dry extract and polyphenols in inhibiting MGO-induced glycation in vitro was comparable to that of metformin used as a positive control. Full article
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<p>Structures of peppermint polyphenols.</p>
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<p>HPLC chromatograms of peppermint leaf dry extract (1.5 mg/mL, 50% aq. methanol); red at 280 nm, blue 320 nm, and black 360 nm. Peak labeling: 1, eriocitrin; 2, luteolin-7-<span class="html-italic">O</span>-rutinoside; 3, luteolin-7-<span class="html-italic">O</span>-β-glucuronoside; 4, narirutin; 5, isorhoifolin; 6, diosmin; 7, hesperidin; 8, lithospermic acid; 9, rosmarinic acid; 10, caffeic acid; 11, eriodictyol.</p>
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<p>Antiglycation activity after seven-day incubation of bovine serum albumin with methylglyoxal (0.5 mM) and the test compound (1.5 mM) or peppermint leaf dry extract (3 mg/mL) expressed as % inhibition of MGO-induced AGE formation. Results are representative of three experiments performed as mean ± SD. Data were analyzed by one-way ANOVA (<span class="html-italic">p</span> &lt; 0.0001) followed by Tukey’s multiple comparisons test; values not sharing a common letter are significantly different. Abbreviations: AP, apigenin; LU, luteolin; LU-7GR, luteolin-7-<span class="html-italic">O</span>-β-glucuronoside; LU-7R, luteolin-7-<span class="html-italic">O</span>-rutinoside; LU-7G, luteolin-7-<span class="html-italic">O</span>-β-glucoside; HT, hesperetin; ED, eriodictyol; ED-7R, eriocitrin; RA, rosmarinic acid; DPE, peppermint leaf dry extract; MET, metformin.</p>
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<p>Proposed hemiacetal structures of mono-MGO and di-MGO adducts of luteolin (R1, -OH), apigenin (R1, -H), eriodictyol (R2, -OH) and eriocitrin (R2, -O-rutinoside).</p>
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<p>Scheme of the hemiacetal and hemiketal adducts of MGO with flavones and flavanones (2,3-dihydrofuran ring).</p>
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<p>MS spectra of luteolin and luteolin-MGO; (<b>a</b>) authentic standard, (<b>b</b>) mono-adduct 1, (<b>c</b>) mono-adduct 2, (<b>d</b>) di-adduct with MGO.</p>
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<p>MS spectra of apigenin and apigenin-MGO; (<b>a</b>) authentic standard, (<b>b</b>) mono-adduct 1, (<b>c</b>) mono-adduct 2, (<b>d</b>) di-adduct with MGO.</p>
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<p>MS spectra of eriocitrin and eriocitrin-MGO; (<b>a</b>) authentic standard, (<b>b</b>) mono-adduct 1, (<b>c</b>) mono-adduct 2, (<b>d</b>) mono-adduct 3, (<b>e</b>) mono-adduct 4.</p>
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15 pages, 1138 KiB  
Article
Evaluation of the Efficacy of Antioxidant Extract from Lemon By-Products on Preservation of Quality Attributes of Minimally Processed Radish (Raphanus sativus L.)
by Angela Zappia, Angelica Spanti, Rossella Princi, Valeria Imeneo and Amalia Piscopo
Antioxidants 2023, 12(2), 235; https://doi.org/10.3390/antiox12020235 - 20 Jan 2023
Cited by 5 | Viewed by 2505
Abstract
The aim of this work was to enhance the use of a food-grade antioxidant extract obtained from lemon processing byproducts (peel, pulp and seeds) to extend the shelf life of minimally processed radishes. The extract (LPE) was previously characterized in terms [...] Read more.
The aim of this work was to enhance the use of a food-grade antioxidant extract obtained from lemon processing byproducts (peel, pulp and seeds) to extend the shelf life of minimally processed radishes. The extract (LPE) was previously characterized in terms of total phenolic (6.75 ± 0.34 mg GAE g−1 d.w.) and flavonoid content (2.04 ± 0.09 mg CE g−1 d.w.) and antioxidant activity, and eriocitrin and hesperidin were identified as the most prevalent phenolic compounds by a UHPLC system. The effects of different dipping aqueous solutions (UCR, DRa, DRb) and alginate-based edible coating formulations (CRc, CRd) with and without the antioxidant extract were studied on the quality parameters of minimally processed radishes, characterized regarding their microbiological and physicochemical characteristics for up to 14 days at 3 °C. The coating formulated with LPE delayed the radish respiration process, as well as resulting in less color variation (ΔE < 3) and reduced mesophilic aerobic count values (4.49 ± 1.43 log CFU g−1), proving the effectiveness of LPE as a value-added ingredient in developing post-harvest strategies to prolong the shelf life of minimally processed vegetables. Indeed, coated samples without the extract showed a clear development of rotting, which led to the end of their shelf life on their 7th day of storage. Full article
(This article belongs to the Special Issue Impact of Processing on Antioxidant Rich Foods - 2nd Edition)
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<p>Minimal processing steps for cut radish treatments: (<b>a</b>) dipping, (<b>b</b>) coating and (<b>c</b>) packaging. Abbreviations: UCR, uncoated minimally processed radishes; DRa, minimally processed radishes dipped in 0.3% citric acid solution, <span class="html-italic">w</span>/<span class="html-italic">v</span>; DRb, minimally processed radishes dipped in 1% LP<sub>E</sub> solution, <span class="html-italic">v</span>/<span class="html-italic">v</span>; CRc, minimally processed radishes coated with an alginate-based coating (2%, <span class="html-italic">w</span>/<span class="html-italic">v</span>); CRd, minimally processed radishes coated with an alginate-based coating (2%, <span class="html-italic">w</span>/<span class="html-italic">v</span>) with LP<sub>E</sub> (1%, <span class="html-italic">v</span>/<span class="html-italic">v</span>).</p>
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<p>(<b>a</b>) Headspace gas composition values (O<sub>2</sub>%) of uncoated and coated minimally processed radishes throughout 7 days of storage at 3 °C. (<b>b</b>) Headspace gas composition values (CO<sub>2</sub>%) of uncoated and coated minimally processed radishes throughout 7 days of storage at 3 °C. Abbreviations: UCR, uncoated minimally processed radishes; DRa, minimally processed radishes dipped in 0.3% citric acid solution, <span class="html-italic">w</span>/<span class="html-italic">v</span>; DRb, minimally processed radishes dipped in 1% LP<sub>E</sub> solution, <span class="html-italic">v/v</span>; CRc, minimally processed radishes coated with an alginate-based coating (2%, <span class="html-italic">w</span>/<span class="html-italic">v</span>); CRd, minimally processed radishes coated with an alginate-based coating (2%, <span class="html-italic">w</span>/<span class="html-italic">v</span>) with LP<sub>E</sub> (1%, <span class="html-italic">v</span>/<span class="html-italic">v</span>).</p>
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<p>Color variation values (ΔE) of uncoated and coated minimally processed radishes between the last day (14th day) and the 1st day of storage at 3 °C. Lowercase letters indicate differences among treatments for the outer side. Uppercase letters indicate differences among treatments for the inner side. Abbreviations: UCR; DRa; DRb; CRc; CRd (see <a href="#antioxidants-12-00235-f002" class="html-fig">Figure 2</a>).</p>
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16 pages, 2199 KiB  
Article
Anti-Allergic and Antioxidant Potential of Polyphenol-Enriched Fractions from Cyclopia subternata (Honeybush) Produced by a Scalable Process
by Carla Dippenaar, Hitoshi Shimbo, Kazunobu Okon, Neil Miller, Elizabeth Joubert, Tadashi Yoshida and Dalene de Beer
Separations 2022, 9(10), 278; https://doi.org/10.3390/separations9100278 - 1 Oct 2022
Cited by 5 | Viewed by 2046
Abstract
Anti-allergic activity was previously demonstrated for extracts of Cyclopia subternata Vogel plant material, containing substantial amounts of xanthones, benzophenones, dihydrochalcones, flavanones and flavones. Fractionation of a hot water extract on macroporous resin was performed aiming to increase its potency. Operating conditions for scaled-up [...] Read more.
Anti-allergic activity was previously demonstrated for extracts of Cyclopia subternata Vogel plant material, containing substantial amounts of xanthones, benzophenones, dihydrochalcones, flavanones and flavones. Fractionation of a hot water extract on macroporous resin was performed aiming to increase its potency. Operating conditions for scaled-up fractionation of the extract were determined, using small-scale static and dynamic sorption/desorption experiments. The anti-allergic potential of the fractions was assessed based on inhibition of β-hexosaminidase release from IgE-sensitized RBL-2H3 cells. Given the role of oxidative stress in allergic reactions, the extract and fractions were also tested for their ability to scavenge the superoxide anion radical and inhibit xanthine oxidase (XO), an enzyme involved in its generation. The routine DPPH and ORAC assays were used for determination of the antioxidant capacity of the fractions. 3-β-D-Glucopyranosyl-4-O-β-D-glucopyranosyliriflophenone (IDG) had the lowest affinity for the resin, dictating selection of the optimal separation conditions. The extract was separated into four fractions on XAD1180N, using step-wise gradient elution with EtOH-water solutions. The major phenolic compounds present in the fractions were IDG and 3-β-D-glucopyranosyliriflophenone (fraction 1), mangiferin, isomangiferin, 3′,5′-di-β-D-glucopyranosyl-3-hydroxyphloretin and vicenin-2 (fraction 2), 3′,5′-di-β-D-glucopyranosylphloretin, eriocitrin and scolymoside (fraction 3) and hesperidin and p-coumaric acid (fraction 4). Fractionation was only partially effective in increasing activity compared to the extract, i.e., fractions 2, 3 and 4 in the DPPH and XO assays, fractions 1 and 2 in the ORAC assay and fraction 1 in the β-hexosaminidase release assay. In vivo testing will be required to determine whether the increased activity of fractions is worth the effort and expense of fractionation. Full article
(This article belongs to the Special Issue Isolation, Elucidation and Synthesis of Bioactive Natural Products)
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<p>Desorption ratios of <italic>Cyclopia subternata</italic> benzophenones, dihydrochalcones and xanthones (<bold>a</bold>) and flavanones, flavones and a phenolic acid (<bold>b</bold>) on XAD 1180N macroporous resin as a function of ethanol concentration (% <italic>v</italic>/<italic>v</italic>), using static desorption. Data are given as mean ± standard deviation (n = 3). Abbreviations: IDG, 3-β-D-glucopyranosyl-4-<italic>O</italic>-β-D-glucopyranosyliriflophenone; IMG, 3-β-d-glucopyranosyliriflophenone; HPDG, 3′,5′-di-β-D-glucopyranosyl-3-hydroxyphloretin; PDG, 3′,5′-di-β-D-glucopyranosylphloretin.</p>
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<p>Dynamic breakthrough curves of <italic>Cyclopia subternata</italic> phenolic compounds on XAD 1180N macroporous resin at 2 BV/h in the small-scale column. Abbreviations: IDG, 3-β-D-glucopyranosyl-4-<italic>O</italic>-β-D-glucopyranosyliriflophenone; IMG, 3-β-D-glucopyranosyliriflophenone.</p>
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<p>Dynamic desorption curves of <italic>Cyclopia subternata</italic> benzophenones, dihydrochalcones and xanthones (<bold>a</bold>) and flavanones, flavones and a phenolic acid (<bold>b</bold>) using different concentrations of ethanol solutions in the small-scale column. Abbreviations: IDG, 3-β-D-glucopyranosyl-4-<italic>O</italic>-β-D-glucopyranosyliriflophenone; IMG, 3-β-D-glucopyranosyliriflophenone; HPDG, 3′,5′-di-β-D-glucopyranosyl-3-hydroxyphloretin; PDG, 3′,5′-di-β-D-glucopyranosylphloretin.</p>
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<p>Xanthine oxidase (XO) inhibitory activity of a green <italic>Cyclopia subternata</italic> hot water extract and four fractions from large-scale fractionation on XAD 1180N as a function of sample concentration. Data are given as mean ± standard deviation (n = 3). Different letters above bars indicate significant differences (<italic>p</italic> &lt; 0.05) at 400 μg/mL. * Value not available due to background absorbance of the fraction at this concentration.</p>
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<p>β-Hexosaminidase release inhibitory activity of (<bold>a</bold>) a green <italic>Cyclopia subternata</italic> hot water extract and four fractions from large-scale fractionation on XAD 1180N at 250 μg/mL and (<bold>b</bold>) the extract and (<bold>c</bold>) fraction 1 at three concentrations (62.5, 125 and 250 μg/mL). * and ** indicate significant differences versus the control at <italic>p</italic> &lt; 0.05 and <italic>p</italic> &lt; 0.01, respectively.</p>
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8 pages, 1053 KiB  
Article
Analysis of Citrus Bioflavonoid Content and Dipeptidyl Peptidase-4 Inhibitory Potential of Commercially Available Supplements
by Ankit Gupta, Hayder A. Al-Aubaidy, Christian K. Narkowicz, Herbert F. Jelinek, David S. Nichols, John R. Burgess and Glenn A. Jacobson
Molecules 2022, 27(15), 4741; https://doi.org/10.3390/molecules27154741 - 25 Jul 2022
Cited by 3 | Viewed by 2048
Abstract
Citrus bioflavonoids are polyphenolic plant-derived pigments found in high levels in oranges, lemons, grapefruits and other citrus fruits. The three most abundant types of citrus bioflavonoids are hesperidin, naringenin and eriocitrin. Citrus bioflavonoids have long been known to possess powerful free radical-scavenging properties [...] Read more.
Citrus bioflavonoids are polyphenolic plant-derived pigments found in high levels in oranges, lemons, grapefruits and other citrus fruits. The three most abundant types of citrus bioflavonoids are hesperidin, naringenin and eriocitrin. Citrus bioflavonoids have long been known to possess powerful free radical-scavenging properties and cardioprotective effects. The study involved the analysis of 10 commercially available citrus bioflavonoid supplements from three different countries: Australia, the United States and Canada. The supplements were tested for their citrus bioflavonoid content which varied from 0.8 to 33.3% w/w. The daily bioflavonoid dose varied from 19 mg to 560 mg. Hesperidin was the major citrus bioflavonoid in nine out of ten supplements. One supplement was found to contain less than 10% of the quantity of rutin claimed to have been added. The DPP-4 inhibitory potential, compared through an estimation of rutin equivalence, ranged from 1.9 mg to 400 mg per day. This data highlights the variability between the supplements in their potential to inhibit DPP-4 for subsequent health benefits. Full article
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<p>Chromatograms of the citrus bioflavonoids’ standard peaks. ER, eriocitrin; ED, eriodictyol; NR, naringin; NG, naringenin; HD, hesperidin; HT, hesperetin.</p>
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<p>Example chromatograms of supplements CBF-1 and CBF-6, showing bioflavonoid peaks.</p>
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11 pages, 467 KiB  
Article
Red Orange and Bitter Orange IntegroPectin: Structure and Main Functional Compounds
by Antonino Scurria, Marzia Sciortino, Ana Rosa Garcia, Mario Pagliaro, Giuseppe Avellone, Alexandra Fidalgo, Lorenzo Albanese, Francesco Meneguzzo, Rosaria Ciriminna and Laura M. Ilharco
Molecules 2022, 27(10), 3243; https://doi.org/10.3390/molecules27103243 - 19 May 2022
Cited by 4 | Viewed by 2176
Abstract
DRIFT, HPLC-MS, and SPME-GC/MS analyses were used to unveil the structure and the main functional compounds of red (blood) orange (Citrus sinensis) and bitter orange (Citrus aurantium). The IntegroPectin samples show evidence that these new citrus pectins are comprised [...] Read more.
DRIFT, HPLC-MS, and SPME-GC/MS analyses were used to unveil the structure and the main functional compounds of red (blood) orange (Citrus sinensis) and bitter orange (Citrus aurantium). The IntegroPectin samples show evidence that these new citrus pectins are comprised of pectin rich in RG-I hairy regions functionalized with citrus biophenols, chiefly flavonoids and volatile molecules, mostly terpenes. Remarkably, IntegroPectin from the peel of fresh bitter oranges is the first high methoxyl citrus pectin extracted via hydrodynamic cavitation, whereas the red orange IntegroPectin is a low methoxyl pectin. C. aurantium IntegroPectin has a uniquely high concentration of adsorbed flavonoids, especially the flavanone glycosides hesperidin, naringin, and eriocitrin. Full article
(This article belongs to the Section Applied Chemistry)
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<p>DRIFT spectra of the pectin samples in the 500–2000 cm<sup>−1</sup> region, normalized to the ν<sub>as</sub>COO<sup>−</sup> band carboxylate groups, at ~1610 cm<sup>−1</sup>.</p>
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