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Search Results (2,615)

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10 pages, 1847 KiB  
Communication
The Effect of Temperature and Humidity on Yellow Tea Volatile Compounds during Yellowing Process
by Weiwei Wang, Zhihui Feng, Rui Min, Junfeng Yin and Heyuan Jiang
Foods 2024, 13(20), 3283; https://doi.org/10.3390/foods13203283 - 16 Oct 2024
Abstract
Yellowing is the key processing technology of yellow tea, and environmental conditions have a significant impact on the yellowing process. In this study, volatile compounds of the yellowing process under different environmental conditions were analyzed by GC–MS. Results showed that a total of [...] Read more.
Yellowing is the key processing technology of yellow tea, and environmental conditions have a significant impact on the yellowing process. In this study, volatile compounds of the yellowing process under different environmental conditions were analyzed by GC–MS. Results showed that a total of 75 volatile compounds were identified. A partial least squares discriminant analysis (PLS-DA) determined that 42 of them were differential compounds, including 12 hydrocarbons, 8 ketones, 8 aldehydes, 6 alcohols, and 8 other compounds, and compared the contents of differential compounds under the conditions of 40 °C with 90% humidity, 50 °C with 50% humidity, and 30 °C with 70% humidity, then analyzed the variation patterns of hydrocarbons under different yellowing environmental conditions. A 40 °C with 90% humidity treatment reduced the content of more hydrocarbons and increased the aldehydes. The content of 3-hexen-1-ol was higher when treated at 50 °C with 50% humidity and was consistent with the results of sensory evaluation. This study could provide a theoretical basis for future research on the aroma of yellow tea. Full article
(This article belongs to the Section Food Engineering and Technology)
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Figure 1
<p>Flowchart of yellow tea process.</p>
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<p>(<b>a</b>) Tea and tea infusion. (<b>b</b>) Radar map of the sensory of yellow tea.</p>
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<p>Metabolomics analysis of volatile compounds in different yellow teas: PLS-DA score plot (<b>a</b>), cross-validation plot (<b>b</b>), VIP plot (<b>c</b>).</p>
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<p>Heat map of differential volatile compounds in yellow teas.</p>
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<p>Trend chart of changes in alkanes during the yellowing process.</p>
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16 pages, 3212 KiB  
Article
Synthesis, Characterization and Structural Study of the Two Ionic Hydrogen-Bonded Organic Frameworks Based on Sterically Crowded Bifunctional Moieties
by Kira E. Vostrikova, Vladimir P. Kirin and Denis G. Samsonenko
Chemistry 2024, 6(5), 1271-1286; https://doi.org/10.3390/chemistry6050073 (registering DOI) - 16 Oct 2024
Abstract
Small bifunctional molecules are attractive for use as models in different areas of knowledge. How can their functional groups interact in solids? This is important to know for the prediction of the physical and chemical properties of the materials based on them. In [...] Read more.
Small bifunctional molecules are attractive for use as models in different areas of knowledge. How can their functional groups interact in solids? This is important to know for the prediction of the physical and chemical properties of the materials based on them. In this study, two new hydrogen-bonded organic frameworks (HOFs) based on sterically demanding molecular compounds, bis(1-hydroxy-2-methylpropane-2-aminium) sulfate (1) and 2-methyl-4-oxopentan-2-aminium hydrogen ethanedioate hydrate (2), were synthesized and fully characterized by means of FTIR and NMR spectroscopies, as well as by X-ray powder diffraction and thermogravimetric analyses. Their molecular and crystal structures were established through single-crystal X-ray diffraction analysis. It was shown that both compounds have a layered structure due to the formation of a 2D hydrogen-bonding network, the layers being linked by systematically arranged Van der Waals contacts between the methyl groups of organic cations. To unveil some dependencies between the chemical nature of bifunctional molecules and their solid structure, Hirschfeld surface (HS) analysis was carried out for HOFs 1, 2, and their known congeners 1-hydroxy-2-methylpropan-2-aminium hemicarbonate (3) and 1-hydroxy-2-methylpropan-2-aminium (1-hydroxy-2-methylpropan-2-yl) carbamate (4). HS was performed to quantify and visualize the close intermolecular atomic contacts in the crystal structures. It is clearly seen that H–H contacts make the highest contributions to the amino alcohol based compounds 1, 3 and 4, with a maximal value of 65.2% for compound 3 having CO32− as a counterion. A slightly lower contribution of H–H contacts (64.4%) was found for compound 4, in which the anionic part is represented by 1-hydroxy-2-methylpropan-2-yl carbamate. The significant contribution of the H–H contacts in the bifunctional moieties is due to the presence of a quaternary carbon atom with a short three-carbon chain. Full article
(This article belongs to the Section Supramolecular Chemistry)
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Figure 1
<p>Asymmetric unit of the compounds: (<b>a</b>) bis(1-hydroxy-2-methylpropane-2-ammonium) sulfate (<b>1</b>); (<b>b</b>) 2-methyl-4-oxopentan-2-aminium hydrogen ethanedioate hydrate (<b>2</b>).</p>
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<p>Formation of a layer in the crystal of compound <b>1</b> due to hydrogen bonding (view along <span class="html-italic">b</span> axis).</p>
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<p>Eight types of hydrogen bonds in compound <b>1</b>. The distances of the hydrogen bonds are given between the atoms O and N or O and O in Å.</p>
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<p>The 2D network organization and the interlayer Van der Waals interactions, which are realized through contacts between the methyl groups of 2-methyl-4-oxopentan-2-aminium moieties in the crystal of compound <b>2</b> (view along <span class="html-italic">b</span> axis).</p>
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<p>Hirschfeld surface for the compounds (view along <span class="html-italic">a</span>-axis): (<b>a</b>) <b>1</b>; (<b>b</b>) <b>2</b>; (<b>c</b>) <b>3</b> [<a href="#B11-chemistry-06-00073" class="html-bibr">11</a>]; (<b>d</b>) <b>4</b> [<a href="#B12-chemistry-06-00073" class="html-bibr">12</a>].</p>
Full article ">Scheme 1
<p>Bifunctional molecules amino alcohol and amino ketone, as well as their derivatives.</p>
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<p>Reaction of addition of ammonia to mesityl oxide (<b>top</b>); titration of the reaction mixture with an ethanol solution of oxalic acid (<b>bottom</b>).</p>
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15 pages, 2286 KiB  
Article
The Degradation of Polyethylene by Trichoderma and Its Impact on Soil Organic Carbon
by Lixia Zhu, Yaqin Chen, Wenke Ni, Jiaxuan Zeng, Xin Li, Chunhong Hu and Lili Li
Agriculture 2024, 14(10), 1821; https://doi.org/10.3390/agriculture14101821 (registering DOI) - 16 Oct 2024
Abstract
Polyethylene mulching film, which is widely utilized in arid and semi-arid agriculture, leaves residual pollution. A novel approach to addressing this issue is microbial degradation. To screen the strains that degrade polyethylene efficiently and clarify the effect of degrading strains on the turnover [...] Read more.
Polyethylene mulching film, which is widely utilized in arid and semi-arid agriculture, leaves residual pollution. A novel approach to addressing this issue is microbial degradation. To screen the strains that degrade polyethylene efficiently and clarify the effect of degrading strains on the turnover of soil organic carbon, a polyethylene-degrading fungus PF2, identified as Trichoderma asperellum, was isolated from long-time polyethylene-covered soil. Strain PF2 induced surface damage and ether bonds, ketone groups and other active functional groups in polyethylene, with 4.15% weight loss after 30 days, where laccase plays a key role in the degradation of polyethylene. When applied to soil, the Trichoderma-to-soil weight ratios were the following: B1: 1:100; B2: 1:200; B3: 1:300 and B4: 1:400. Trichoderma asperellum significantly increased the cumulative CO2 mineralization and soil organic carbon mineralization in the B1 and B2 treatments compared with the control (B0). The treatments B1, B3 and B4 increased the stable organic carbon content in soil. An increase in the soil organic carbon content was observed with the application of Trichoderma asperellum, ranging from 27.87% to 58.38%. A positive correlation between CO2 emissions and soil organic carbon was observed, with the soil carbon pool management index (CPMI) being most correlated with active organic carbon. Trichoderma treatments improved the CPMI, with B3 showing the most favorable carbon retention value. Thus, Trichoderma asperellum not only degrades polyethylene but also contributes to carbon sequestration and soil fertility when applied appropriately. Full article
(This article belongs to the Special Issue Risk Assessment and Remediation of Agricultural Soil Pollution)
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<p>The phylogenetic tree concluding strain PF2.</p>
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<p>The degradation effect and laccase activity of strain PF2 on the polyethylene film after a 30-day incubation period. (<b>a</b>) The surface morphology of the degraded polyethylene with (right) or without (left) strain PF2; (<b>b</b>) the Fourier transform infrared spectrum of the degraded polyethene after biodegradation with strain PF2; (<b>c</b>) the laccase activity in the culture supernatant. Different letters on the error bars represent significant changes (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The soil organic carbon and mineralization dynamic in different treatments. (<b>a</b>) Cumulative CO<sub>2</sub> emissions, (<b>b</b>) CO<sub>2</sub> emissions rate, (<b>c</b>) soil organic carbon content and (<b>d</b>) mineralization intensity. B0: control, soil without <span class="html-italic">Trichoderma asperellum</span>; B1, B2, B3 and B4: <span class="html-italic">Trichoderma asperellum</span> applied at ratios of 1:100, 1:200, 1:300 and 1:400, respectively. The values in the figures are means ± standard deviations of the three replicates. The lowercase letters above the bars in (<b>c</b>,<b>d</b>) indicate significant difference at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Soil carbon management pool indexes in different treatments. (<b>a</b>) Different lowercase letters indicate significant differences in the CPA, and different uppercase letters indicate significance in the CPAI; (<b>b</b>) different lowercase letters indicate significant differences in the CPI, and uppercase letters indicate significant differences in the CPMI. B0: control, soil without Trichoderma asperellum; B1, B2, B3 and B4: Trichoderma asperellum applied at ratios of 1:100, 1:200, 1:300 and 1:400, respectively. Values in the figures are means ± standard deviations of three replicates.</p>
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<p>The correlation analysis between CO<sub>2</sub> emission and soil organic carbon.</p>
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22 pages, 1236 KiB  
Review
Research Progress on the Mechanism of the Impact of Myofibrillar Protein Oxidation on the Flavor of Meat Products
by Lingping Zhang, Dongsong Yang, Ruiming Luo, Yulong Luo and Yanru Hou
Foods 2024, 13(20), 3268; https://doi.org/10.3390/foods13203268 (registering DOI) - 15 Oct 2024
Viewed by 413
Abstract
Myofibrillar proteins primarily consist of myosin, actin, myogenin, and actomyosin. These proteins form complex networks within muscle fibers and are crucial to the physical and chemical properties of meat. Additionally, myofibrillar proteins serve as significant substrates for the adsorption of volatile flavor compounds, [...] Read more.
Myofibrillar proteins primarily consist of myosin, actin, myogenin, and actomyosin. These proteins form complex networks within muscle fibers and are crucial to the physical and chemical properties of meat. Additionally, myofibrillar proteins serve as significant substrates for the adsorption of volatile flavor compounds, including aldehydes, alcohols, ketones, and sulfur and nitrogen compounds, which contribute to the overall flavor profile of meat products. A series of chemical reactions occur during the processing, storage, and transportation of meat products. Oxidation is one of the most significant reactions. Oxidative modification can alter the physical and chemical properties of proteins, ultimately impacting the sensory quality of meat products, including flavor, taste, and color. In recent years, considerable attention has been focused on the effects of protein oxidation on meat quality and its regulation. This study investigates the impact of myofibrillar protein oxidation on the sensory attributes of meat products by analyzing the oxidation processes and the factors that initiate myofibrillar protein oxidation. Additionally, it explores the control of myofibrillar protein oxidation and its implications on the sensory properties of meat products, providing theoretical insights relevant to meat processing methods and quality control procedures. Full article
(This article belongs to the Section Meat)
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Graphical abstract

Graphical abstract
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<p>Schematic representation of forces in protein structure.</p>
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<p>Schematic diagram of myofibrillar protein oxidation mechanism.</p>
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<p>Flavor formation diagram of meat products.</p>
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18 pages, 1552 KiB  
Article
The Anisotropic Mechanical and Tribological Behaviors of Additively Manufactured (Material Extrusion) Implant-Grade Polyether Ether Ketone (PEEK)
by Mohammad Reza Maydanshahi, Mohammad Reza Najari, Tom Slatter and Mahdi Mohammadpour
Lubricants 2024, 12(10), 347; https://doi.org/10.3390/lubricants12100347 - 12 Oct 2024
Viewed by 368
Abstract
In this study, we investigated the mechanical and tribological properties of the layer-by-layer structure of additively manufactured implant-grade Polyether Ether Ketone (PEEK) through the Material Extrusion (ME) process as a potential substitute for artificial joints. The effective elasticity modulus of the anisotropic 3D-printed [...] Read more.
In this study, we investigated the mechanical and tribological properties of the layer-by-layer structure of additively manufactured implant-grade Polyether Ether Ketone (PEEK) through the Material Extrusion (ME) process as a potential substitute for artificial joints. The effective elasticity modulus of the anisotropic 3D-printed PEEK was determined to be 2.505 GPa along the vertical and horizontal build orientations. The lubricated friction and wear performance were assessed using a pin-on-disk test under various loads, including 14, 30, 50, and 70 N, with a sliding speed of 50 mm/s over a total distance of 1 km at 37 °C. The contact parameters between the hemispherical steel pin and 3D-printed PEEK disks, involving contact pressures over the circle of contact, were observed to increase as the load increased. The results indicated that the wear coefficient exhibited a rise from 1.418 × 105 to 2.089 × 101  as the applied loads increased, signaling a shift from mild to severe wear regimes. Fetal Bovine Serum (FBS) as a lubricant exhibited a mixed mechanism, ascertained through the Stribeck curve, as well as a minimum fluid film thickness of 1.346 nm under an isoviscous–elastic regime, as calculated by the maximum load. Moreover, the mechanism governing wear during sliding, influenced by both normal axial and shear loads, primarily involved adhesion. Full article
(This article belongs to the Special Issue Wear in Additive Manufacturing)
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<p>(<b>a</b>) Schematic of additive manufacturing of PEEK filament in the horizontal build orientation (<b>left</b>), and the vertical build orientation. (<b>b</b>) The uniaxial compressive test machine for assessing compression behavior of the horizontal build orientation (<b>left</b> and <b>middle-up</b>), and the vertical build orientation (<b>right</b> and <b>middle-down</b>). (<b>c</b>) Stress–strain graph of the 3D-printed PEEK subjected to the compressive load parallel to the deposited layer direction (<b>left</b>), and perpendicular to the deposited layer direction (<b>right</b>).</p>
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<p>(<b>a</b>) Schematic diagram of the pin-on-disk tribometer, (<b>b</b>) contact pressure distribution over circle of contact by load was varied from 14 N to 70 N, the inner circle correspond to the former, and the outer circle correspond to the latter, and (<b>c</b>) indentation mean contact pressure as a function of load for the surface of a 3D-printed specimen with yield stress of 58 MPa pressed by a hard stainless steel ball of diameter of 6 mm.</p>
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<p>(<b>a</b>) Friction coefficient behavior of anti-friction 52,100 bearing steel and 3D-printed PEEK with respect to sliding distance in varying loads of 14, 30, 50, and 70 N. (<b>b</b>) Graph of wear rates as a function of the load identifying the dimensionless wear coefficient (K) for the different wear regimes. (<b>c</b>) Stribeck diagram illustrating the average coefficient of friction as a function of the Sommerfeld number characterized different regimes of lubrication.</p>
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<p>FE-SEM images of worn surfaces of the 3D-printed PEEK disks penetrated with different loads (<b>a</b>) 14 N, (<b>b</b>) 30 N, (<b>c</b>) 50 N, and (<b>d</b>) 70 N.</p>
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12 pages, 1596 KiB  
Perspective
Lactobacillus Eats Amyloid Plaque and Post-Biotically Attenuates Senescence Due to Repeat Expansion Disorder and Alzheimer’s Disease
by Suresh C. Tyagi
Antioxidants 2024, 13(10), 1225; https://doi.org/10.3390/antiox13101225 - 12 Oct 2024
Viewed by 498
Abstract
Patients with Alzheimer’s disease and related dementia (ADRD) are faced with a formidable challenge of focal amyloid deposits and cerebral amyloid angiopathy (CAA). The treatment of amyloid deposits in ADRD by targeting only oxidative stress, inflammation and hyperlipidemia has not yielded significant positive [...] Read more.
Patients with Alzheimer’s disease and related dementia (ADRD) are faced with a formidable challenge of focal amyloid deposits and cerebral amyloid angiopathy (CAA). The treatment of amyloid deposits in ADRD by targeting only oxidative stress, inflammation and hyperlipidemia has not yielded significant positive clinical outcomes. The chronic high-fat diet (HFD), or gut dysbiosis, is one of the major contributors of ADRD in part by disrupted transport, epigenetic DNMT1 and the folate 1-carbon metabolism (FOCM) cycle, i.e., rhythmic methylation/de-methylation on DNA, an active part of epigenetic memory during genes turning off and on by the gene writer (DNMT1) and eraser (TET2/FTO) and the transsulfuration pathway by mitochondrial 3-mercaptopyruvate sulfur transferase (3MST)-producing H2S. The repeat CAG expansion and m6A disorder causes senescence and AD. We aim to target the paradigm-shift pathway of the gut–brain microbiome axis that selectively inhibits amyloid deposits and increases mitochondrial transsulfuration and H2S. We have observed an increase in DNMT1 and decreased FTO levels in the cortex of the brain of AD mice. Interestingly, we also observed that probiotic lactobacillus-producing post-biotic folate and lactone/ketone effectively prevented FOCM-associated gut dysbiosis and amyloid deposits. The s-adenosine-methionine (SAM) transporter (SLC25A) was increased by hyperhomocysteinemia (HHcy). Thus, we hypothesize that chronic gut dysbiosis induces SLC25A, the gene writer, and HHcy, and decreases the gene eraser, leading to a decrease in SLC7A and mitochondrial transsulfuration H2S production and bioenergetics. Lactobacillus engulfs lipids/cholesterol and a tri-directional post-biotic, folic acid (an antioxidant and inhibitor of beta amyloid deposits; reduces Hcy levels), and the lactate ketone body (fuel for mitochondria) producer increases SLC7A and H2S (an antioxidant, potent vasodilator and neurotransmitter gas) production and inhibits amyloid deposits. Therefore, it is important to discuss whether lactobacillus downregulates SLC25A and DNMT1 and upregulates TET2/FTO, inhibiting β-amyloid deposits by lowering homocysteine. It is also important to discuss whether lactobacillus upregulates SLC7A and inhibits β-amyloid deposits by increasing the mitochondrial transsulfuration of H2S production. Full article
(This article belongs to the Special Issue Oxidative Stress as a Therapeutic Target of Alzheimer’s Disease)
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<p>Chronic high fat dysbiosis diet leads to increase methionine and long-chain fatty acids (LCFA). This causes hyperhomocysteinemia (HHcy), lowers short chain fatty acids (SCFA), folate, ketone/lactone, hydrogen sulfide (H<sub>2</sub>S). The probiotic lactobacillus reveres.</p>
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<p>Schematics of how gut dysbiosis leads to epigenetic methylation alterations and causes Alzheimer’s disease (AD). ADAR, adenosine deaminase acting on RNA; CAG, cytidine-adenosine-guanidine), m<sup>1</sup>A, methyl-1-adinosine; SAM, s-adenosine methionine; SAH, s-adenosine homocysteine; SAHH, s-adenosine homocysteine hydrolase; DNMT, DNA methyltransferase; TET, ten eleven translocators; HDAC, histone de-acetylase; SIRT, Histone-protein de-acetylase; H3K4, histone-3 lysine 4 [<a href="#B21-antioxidants-13-01225" class="html-bibr">21</a>,<a href="#B60-antioxidants-13-01225" class="html-bibr">60</a>,<a href="#B61-antioxidants-13-01225" class="html-bibr">61</a>].</p>
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<p>Repeat nucleotide sequences (CAG) cause random mutations, leading to ALS and AD. The tannic acid inhibits transporter SLC25A and mitigates ALS and AD.</p>
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<p>During ischemic conditions such as COPD, sleep apnea and decrease pulmonary function, initially mitochondrial synthesizes H<sub>2</sub>S and coups with dys-bioenergetics. COPD, chronic obstructive pulmonary diseases; TCA, tri-carboxylic acid; CAT, cysteine transferase; 3MST, 3mercaprtopyruvate sulfotransferase; CBS, cystathionine beta transferase; Piezo, mechano-thermal Na/Ca/Mg and transient receptor potential receptor/channels.</p>
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<p>The probiotics lactobacillus mitigates folate deficiency and improves mitochondrial pyruvates and H<sub>2</sub>S levels, post-biotically. PCP, phosphatidylcartinine phosphatase; BHMT, betaine homocysteine methyl transferase.</p>
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<p>The hypothesis is that the chronic gut-dysbiosis induces SLC25A, <b>gene writer (DNMT1)</b>, HHcy and decreases gene eraser (TET2/FTO), leading to decrease SLC7A and mitochondrial transsulfuration H<sub>2</sub>S production and bioenergetics. Lactobacillus, a tri-directional, <b>folic acid (an inhibitor of beta amyloid deposits</b>, reduces Hcy levels), and lactate ketone-body (fuel for mitochondria) producer <b>increases SLC7A and</b> H<sub>2</sub>S production and inhibits amyloid deposits.</p>
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16 pages, 2668 KiB  
Article
Enhanced Yield of Methyl Ethyl Ketone through Levulinic Acid Decarboxylation in the AgNO3/K2S2O8 System: Mechanistic Insights and Characterization of Metallic Species
by Nydia I. Guzmán Barrera, Jérôme Peydecastaing, Jérôme Esvan, Joël Albet, Carlos Vaca-Garcia, Philippe Behra, Emeline Vedrenne and Sophie Thiébaud-Roux
Molecules 2024, 29(20), 4822; https://doi.org/10.3390/molecules29204822 - 11 Oct 2024
Viewed by 334
Abstract
Methyl ethyl ketone (MEK) is among the most extensively utilized solvents in various industrial applications. In this study, we present a highly efficient synthesis route for MEK via the decarboxylation of biomass-derived levulinic acid, using potassium persulfate (K2S2O8 [...] Read more.
Methyl ethyl ketone (MEK) is among the most extensively utilized solvents in various industrial applications. In this study, we present a highly efficient synthesis route for MEK via the decarboxylation of biomass-derived levulinic acid, using potassium persulfate (K2S2O8) and silver nitrate (AgNO3) as key reagents. The specific roles of AgNO3 and K2S2O8 were thoroughly investigated. Additional silver species, such as Ag2O and AgO, were also detected during the reaction. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analyses provided evidence of the evolution of solid phases throughout the reaction. Based on these findings, we propose a radical decarboxylation mechanism initiated by the generation of sulfate radicals (SO4•⁻) through the catalytic breakdown of K2S2O8 by AgNO3. This mechanistic understanding, combined with a parametric study, enabled us to achieve an unprecedented level of levulinic acid conversion (97.9%) and MEK yield (86.6%) with this system, surpassing all previously reported results in the literature. Full article
(This article belongs to the Special Issue Applied Chemistry in Europe 2024)
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<p>Decarboxylation of LA with 1 eq. of K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> in the absence of AgNO<sub>3</sub>. Experimental conditions: K<sub>2</sub>HPO<sub>4</sub>/KH<sub>2</sub>PO<sub>4</sub> (0.1/0.1 M), 100 °C.</p>
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<p>LA decarboxylation at different temperatures and reaction times (<b>a</b>) 100, (<b>b</b>) 60, and (<b>c</b>) 25 °C. Experimental conditions: AgNO<sub>3</sub>/K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> (1/1), KH<sub>2</sub>PO<sub>4</sub>/K<sub>2</sub>HPO<sub>4</sub> (0.1/0.1 M).</p>
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<p>XRD patterns for the solid phase (<b>a</b>) before and (<b>b</b>) after the reaction. Experimental conditions: AgNO<sub>3</sub>/K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> (1/1), KH<sub>2</sub>PO<sub>4</sub>/K<sub>2</sub>HPO<sub>4</sub> (0.2 M), 100 °C, 30 min.</p>
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<p>AgMNN Auger signals of the solid phase (<b>a</b>) before and (<b>b</b>) after levulinic acid decarboxylation.</p>
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<p>XRD patterns for the solid phase: (<b>a</b>) after M1 neutralization, (<b>b</b>) after the second cycle of the reaction, with the addition of K<sub>2</sub>S<sub>2</sub>O<sub>8</sub>. Experimental conditions: AgNO<sub>3</sub>/K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> (1/1), KH<sub>2</sub>PO<sub>4</sub>/K<sub>2</sub>HPO<sub>4</sub> (0.1/0.1 M), 100 °C.</p>
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<p>AgMNN Auger signals for the solid phase: (<b>a</b>) after M1 neutralization, (<b>b</b>) after the second cycle of reaction. Experimental conditions: AgNO<sub>3</sub>/K<sub>2</sub>S<sub>2</sub>O<sub>8</sub> (1/1), KH<sub>2</sub>PO<sub>4</sub>/K<sub>2</sub>HPO<sub>4</sub> (0.1/0.1 M), 100 °C, 30 min.</p>
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<p>Proposed mechanisms.</p>
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<p>AcOH production via MEK oxidation.</p>
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14 pages, 2693 KiB  
Article
Thermal Properties of Seed Cake Biomasses and Their Valorisation by Torrefaction
by Elena Butnaru, Elena Stoleru, Daniela Ioniță and Mihai Brebu
Polymers 2024, 16(20), 2872; https://doi.org/10.3390/polym16202872 - 11 Oct 2024
Viewed by 300
Abstract
Seed cakes, by-products from the cold press extraction of vegetable oils, are valuable animal feed supplements due to their high content of proteins, carbohydrates, and minerals. However, the presence of anti-nutrients, as well as the rancidification and development of aflatoxins, can impede their [...] Read more.
Seed cakes, by-products from the cold press extraction of vegetable oils, are valuable animal feed supplements due to their high content of proteins, carbohydrates, and minerals. However, the presence of anti-nutrients, as well as the rancidification and development of aflatoxins, can impede their intended use, requiring alternative treatment and valorisation methods. Thermal treatment as a procedure for the conversion of seed cakes from walnuts, hemp, pumpkin, flax, and sunflower into valuable products or energy has been investigated in this paper. Thermogravimetry shows the particular behaviour of seed cakes, with several degradation stages at around 230–280 and 340–390 °C, before and after the typical degradation of cellulose. These are related to the volatilisation of fatty acids, which are either free or bonded as triglycerides, and with the thermal degradation of proteins. Torrefaction at 250 °C produced ~75–82 wt% solids, with high calorific values of 24–26 kJ/g and an energy yield above 90%. The liquid products have a complex composition, with most parts of the compounds partitioning between the aqueous phase (strongly dominant) and the oily one (present in traces). The structural components of seed cakes (hemicelluloses, cellulose, and lignin) produce acetic acid, hydroxy ketones, furans, and phenols. In addition to these, most compounds are nitrogen-containing aromatic compounds from the degradation of protein components, which are highly present in seed cakes. Full article
(This article belongs to the Special Issue Thermal Properties Analysis of Polymers)
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<p>Visual aspects of seed cakes from walnuts, hemp, pumpkin, flax, and sunflower.</p>
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<p>TG/DTG curves of seed cakes from walnuts, hemp, pumpkin, flax, and sunflower.</p>
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<p>The product yield form the torrefaction of various seed cakes.</p>
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<p>The energetic values (the high heating rate, energy density, and energy yield) from the torrefaction of seed cakes.</p>
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<p>The position of seed cake samples in the Van Krevelen diagram before and after torrefaction at 250 °C.</p>
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<p>The NP-grams of the liquid products from the torrefaction of seed cakes.</p>
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<p>The GC-MS chromatograms of the liquid products from the torrefaction of seed cakes.</p>
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<p>The MS spectrum of the GC peak (upper side, in red) and of the corresponding database compound (lower side, in blue) for hydantoin derivatives at 13.030 min (<b>a</b>) and 14.224 min (<b>b</b>).</p>
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<p>A schematic representation of the torrefaction set-up.</p>
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16 pages, 861 KiB  
Review
Multifaceted Impact of SGLT2 Inhibitors in Heart Failure Patients: Exploring Diverse Mechanisms of Action
by Christos Piperis, Anastasios Marathonitis, Artemis Anastasiou, Panagiotis Theofilis, Konstantinos Mourouzis, Alexios Giannakodimos, Elsi Tryfou, Evangelos Oikonomou, Gerasimos Siasos and Dimitris Tousoulis
Biomedicines 2024, 12(10), 2314; https://doi.org/10.3390/biomedicines12102314 - 11 Oct 2024
Viewed by 638
Abstract
Heart failure (HF) is a growing concern due to the aging population and increasing prevalence of comorbidities. Despite advances in treatment, HF remains a significant burden, necessitating novel therapeutic approaches. Sodium–glucose cotransporter 2 inhibitors (SGLT2is) have emerged as a promising treatment option, demonstrating [...] Read more.
Heart failure (HF) is a growing concern due to the aging population and increasing prevalence of comorbidities. Despite advances in treatment, HF remains a significant burden, necessitating novel therapeutic approaches. Sodium–glucose cotransporter 2 inhibitors (SGLT2is) have emerged as a promising treatment option, demonstrating benefits across the entire spectrum of HF, regardless of left ventricular ejection fraction (LVEF). This review explores the multifaceted mechanisms through which SGLT2is exert cardioprotective effects, including modulation of energy metabolism, reduction of oxidative stress, attenuation of inflammation, and promotion of autophagy. SGLT2is shift myocardial energy substrate utilization from carbohydrates to more efficient fatty acids and ketone bodies, enhancing mitochondrial function and reducing insulin resistance. These inhibitors also mitigate oxidative stress by improving mitochondrial biogenesis, reducing reactive oxygen species (ROS) production, and regulating calcium-signaling pathways. Inflammation, a key driver of HF progression, is alleviated through the suppression of proinflammatory cytokines and modulation of immune cell activity. Additionally, SGLT2is promote autophagy, facilitating the clearance of damaged cellular components and preserving myocardial structure and function. Beyond their glucose-lowering effects, SGLT2is provide significant benefits in patients with chronic kidney disease (CKD) and HF, reducing the progression of CKD and improving overall survival. The pleiotropic actions of SGLT2is highlight their potential as a cornerstone in HF management. Further research is needed to fully elucidate their mechanisms and optimize their use in clinical practice. Full article
(This article belongs to the Special Issue Cardiomyopathies and Heart Failure: Charting the Future)
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<p><b>Mechanisms of Actions of SGLT2is:</b> SGLT2 inhibitors reduce glucose and sodium reabsorption and promote increased diuresis and glycosuria, plasma volume reduction, and blood pressure reduction. Increased glycosuria leads to reduction in glucose plasma levels and improvement in insulin resistance. SGLT2is also reduce cardiac pre- and after-load, myocardial fibrosis, intracellular calcium in cardiomyocytes, and cardiac fat accumulation. Increased production of erythropoietin leads to the improvement of hematocrit levels. Furthermore, SGLT2is promote reduction in proinflammatory cytokines, TNF-a, and CRP levels. On the other hand, increased mitochondrial numbers and decreased cellular ROS production lead to decreased oxidative damage and enhanced autophagic mechanisms in cardiomyocytes.</p>
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19 pages, 3995 KiB  
Article
Identification of Volatile Organic Compounds and Analysis of Aroma Characteristics in Ten Pear Syrups
by Yang Wang, Wei Tong, Wenhui Wang, Yanmin Du, Xiaohui Jia, Zhihua Wang, Jianyi Zhang and Hailong Sun
Foods 2024, 13(20), 3223; https://doi.org/10.3390/foods13203223 - 10 Oct 2024
Viewed by 480
Abstract
Aroma in food plays an important role in food perception and acceptance, which depends on various mixtures of volatile organic compounds (VOCs). Moreover, VOCs are of great significance for aroma identification. In this study, headspace solid-phase microextraction (HS-SPME) combined with gas chromatography–mass spectrometry [...] Read more.
Aroma in food plays an important role in food perception and acceptance, which depends on various mixtures of volatile organic compounds (VOCs). Moreover, VOCs are of great significance for aroma identification. In this study, headspace solid-phase microextraction (HS-SPME) combined with gas chromatography–mass spectrometry (GC-MS) technology was used to determine the VOCs in 10 pear syrups. A total of 127 VOCs were quantitatively determined, including 9 common VOCs and 46 characteristic VOCs of 10 pear syrups. The pear syrups were divided into three categories by cluster analysis, and thirty-eight differential VOCs were obtained using orthogonal partial least squares discrimination analysis (OPLS-DA) and fourteen key VOCs were selected by odor activity value (OAV). It was revealed that the key and common aroma components of pear syrups were butanoic acid, methyl ester, 2-methyl-, methyl ester and Hexanoic acid, and ethyl ester. The characteristic and differential VOCs were 10-Undecen-1-ol, Hexadecanal, n-Propylacetate, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1S,2R,5S)-, Methional, Disulfide, dimethyl, 8-Nonenoic acid, ethyl ester, Naphthalene, 1,2-dihydro-1,1,6-trimethyl-, 3H-Purin-6-amine, N,N,3-trimethyl-, 2-Octanol,2,6-dimethyl-, Furyl hydroxymethyl ketone, Heptane, 2,2,4,6,6-pentamethyl-, and Butanoic acid,2-methyl-,methyl ester. The above results showed that different pear syrups had rich diversity in aroma compounds, with some components being shared among them while others are exclusive to specific syrups. Full article
(This article belongs to the Section Food Analytical Methods)
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<p>General classification diagram (<b>a</b>) and comparison diagram of various component content (<b>b</b>) in 10 pear syrups.</p>
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<p>Upset map of VOCs in 10 pear syrups.</p>
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<p>Clustering heat map of VOCs in 10 pear syrups.</p>
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<p>VOCs of 10 pear syrups and an OPLS-DA score chart (<b>a</b>), OPLS-DA model validation (<b>b</b>), and differential VOC clustering heat map (<b>c</b>).</p>
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13 pages, 2542 KiB  
Article
Controllable Synthesis of Thioacetals/Thioketals and β-Sulfanyl Ketones Mediated by Methanesulfonic Anhydride and Sulfuric Acid Sulfuric Acid from Aldehyde/Acetone and Thiols
by Hexia Ye, Xinyao Zhao, Yajie Fu, Haibo Liu, Junchen Li and Xiaojing Bi
Molecules 2024, 29(20), 4785; https://doi.org/10.3390/molecules29204785 - 10 Oct 2024
Viewed by 375
Abstract
A novel and controllable synthesis of thioacetals/thioketals and β-sulfanyl ketones mediated by the reaction of aldehyde/acetone with thiols has been developed. In this protocol, β-sulfanyl ketones can be generated without the prior preparation of α, β-unsaturated carbonyl compounds. A variety of thiols reacted [...] Read more.
A novel and controllable synthesis of thioacetals/thioketals and β-sulfanyl ketones mediated by the reaction of aldehyde/acetone with thiols has been developed. In this protocol, β-sulfanyl ketones can be generated without the prior preparation of α, β-unsaturated carbonyl compounds. A variety of thiols reacted with aldehyde/acetone and provided the corresponding thioacetals/thioketals and β-sulfanyl ketones in good to excellent yields, respectively. This protocol is operationally simple, mild, and atom-economical, providing controllable access to thioacetals/thioketals and thia-Michael addition products under mild conditions. Full article
(This article belongs to the Special Issue Organosulfur and Organoselenium Chemistry)
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<p>Examples of applications of thioacetals/thioketals.</p>
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<p>Overview of synthetic strategies to access thioacetals/thioketals and β-sulfanyl ketones. (<b>a</b>) The synthesis strategies of thioacetals and thioketals; (<b>b</b>) The synthesis strategies of β-sulfanyl ketones; (<b>c</b>) Our work.</p>
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<p>Control experiments. (<b>a</b>) Acetone converted into α, β-unsaturated ketone in the absence of 4-methylbenzenethiol under optimal reaction conditions; (<b>b</b>) 4-Methylbenzenethiol reacted with <b>A</b> to form <b>4a</b>; (<b>c</b>) Thioketal <b>3a</b> reacted with 3 eq acetone under optimal reaction conditions to produce <b>4a</b> in a yield of 71%; (<b>d</b>) Thioketal <b>3a</b> reacted with <b>A</b> to produce the target compound <b>4a</b> with a yield of 35%.</p>
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<p>Gram-scale experiment.</p>
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<p>Plausible mechanism.</p>
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20 pages, 3265 KiB  
Article
Oxidative Catalytic Depolymerization of Lignin into Value-Added Monophenols by Carbon Nanotube-Supported Cu-Based Catalysts
by Chen Tang, Yang Cao, Jie Gao, Gang Luo, Jiajun Fan, James H. Clark and Shicheng Zhang
Molecules 2024, 29(19), 4762; https://doi.org/10.3390/molecules29194762 - 8 Oct 2024
Viewed by 441
Abstract
Lignin valorisation into chemicals and fuels is of great importance in addressing energy challenges and advancing biorefining in a sustainable manner. In this study, on the basis of the high microwave absorption performance of carbon nanotubes (CNTs), a series of copper-oxide-loaded CNT catalysts [...] Read more.
Lignin valorisation into chemicals and fuels is of great importance in addressing energy challenges and advancing biorefining in a sustainable manner. In this study, on the basis of the high microwave absorption performance of carbon nanotubes (CNTs), a series of copper-oxide-loaded CNT catalysts (CuO/CNT) were developed to facilitate the oxidative depolymerization of lignin under microwave heating. This catalyst can promote the activation of hydrogen peroxide and air, effectively generating a range of reactive oxygen species (ROS). Through the application of electron paramagnetic resonance techniques, these ROS generated under different oxidation conditions were detected to elucidate the oxidation mechanism. The results demonstrate that the OH and O2•− play a crucial role in the formation of aldehyde and ketone products through the cleavage of lignin Cβ-O and Cα-Cβ bonds. We further evaluated the catalytic performance of the CuO/CNT catalysts with three typical lignin feedstocks to determine their applicability for lignin biorefinery. The bio-enzymatic lignin produced a 13.9% monophenol yield at 200 °C for 20 min under microwave heating, which was higher than the 7% yield via hydrothermal heating conversion. The selectivity of G-/H-/S-type products was slightly affected, while lignin substrate had a noticeable effect on the selective production. Overall, this study explored the structural characteristics of CuO/CNT catalysts and their implications for lignin conversion and offered an efficient oxidation approach that holds promise for sustainable biorefining practices. Full article
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<p>(<b>a</b>,<b>b</b>) SEM images of CuO/CNT 600 catalyst and (<b>c</b>) the element mapping of Cu, O, and C; (<b>d</b>) FTIR spectra of Cu/CNT 600; (<b>e</b>) XRD patterns of various catalysts.</p>
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<p>Chemical state of Cu catalysts. (<b>a</b>) The full spectrum scan of XPS spectra; (<b>b</b>) Cu 2p XPS spectra; (<b>c</b>) C 1s XPS spectra; (<b>d</b>) O 1s spectra for Cu/CNT 600.</p>
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<p>Effect of (<b>a</b>) catalyst calcination temperature and (<b>b</b>) H<sub>2</sub>O<sub>2</sub> dosage on monophenol yield in the oxidative catalytic depolymerization of BL; (<b>c</b>) monophenol yield and (<b>d</b>) selectivity from BL depolymerization with various catalysts (200 °C, 20 min); effect of reaction temperature on (<b>e</b>) monophenol yield and (<b>f</b>) selectivity; (<b>g</b>) chemical structures of various monophenols.</p>
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<p>Effect of reaction temperature on (<b>a</b>) monophenol yield and (<b>b</b>) selectivity from BL depolymerization; selectivity of (<b>c</b>) H-/G-/S-type products and (<b>d</b>) P3 and P4 products at different reaction times. (Reaction conditions: 0.1 g BL, 0.15 g catalyst, 1 mL H<sub>2</sub>O<sub>2</sub>, 1 M NaOH, 200 °C).</p>
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<p>The effect of NaOH concentration on the (<b>a</b>) yield and (<b>b</b>) selectivity of monophenols; (<b>c</b>) selectivity of S-/G-/H-type products from BL depolymerization. Recyclability test on the (<b>d</b>) yield and (<b>e</b>) selectivity of monophenol yield from BL depolymerization with the CuO/BCN catalyst (microwave and hydrothermal); (<b>f</b>) selectivity of S/G/H-type products from BL depolymerization. (Reaction conditions: 0.2 g BL, 0.15 g catalyst, 1 mL H<sub>2</sub>O<sub>2</sub>, 1 M NaOH, 200 °C, 20 min).</p>
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<p>Pearson correlation map for reaction factors and monomer yields.</p>
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<p>SEM images of the spent CuO/CNT catalysts after the reaction.</p>
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<p>(<b>a</b>) FTIR spectra of lignin samples; (<b>b</b>) TG profiles of lignin samples; monophenol (<b>c</b>) yields and (<b>d</b>) selectivity with three types of lignin feedstocks. (Reaction conditions: 0.1 g lignin, 0.15 g catalyst, 1 mL H<sub>2</sub>O<sub>2</sub>, 1 M NaOH, 200 °C, 20 min).</p>
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<p>EPR detection of (<b>a</b>) hydroxyl radicals and (<b>b</b>) superoxide radicals; (<b>c</b>) monophenol yield with different radicals involved reactions; (<b>d</b>) selectivity of the products with different radicals involved reactions. (Reaction conditions: 0.1 g BL, 0.15 g catalyst, 1 M NaOH, 200 °C, 20 min).</p>
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<p>Proposed oxidative pathway for lignin depolymerization by ROS.</p>
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45 pages, 18357 KiB  
Review
Advances in the Application of Sulfonated Poly(Ether Ether Ketone) (SPEEK) and Its Organic Composite Membranes for Proton Exchange Membrane Fuel Cells (PEMFCs)
by Xiang Li, Tengling Ye, Xuan Meng, Dongqing He, Lu Li, Kai Song, Jinhai Jiang and Chuanyu Sun
Polymers 2024, 16(19), 2840; https://doi.org/10.3390/polym16192840 - 8 Oct 2024
Viewed by 990
Abstract
This review discusses the progress of research on sulfonated poly(ether ether ketone) (SPEEK) and its composite membranes in proton exchange membrane fuel cells (PEMFCs). SPEEK is a promising material for replacing traditional perfluorosulfonic acid membranes due to its excellent thermal stability, mechanical property, [...] Read more.
This review discusses the progress of research on sulfonated poly(ether ether ketone) (SPEEK) and its composite membranes in proton exchange membrane fuel cells (PEMFCs). SPEEK is a promising material for replacing traditional perfluorosulfonic acid membranes due to its excellent thermal stability, mechanical property, and tunable proton conductivity. By adjusting the degree of sulfonation (DS) of SPEEK, the hydrophilicity and proton conductivity of the membrane can be controlled, while also balancing its mechanical, thermal, and chemical stability. Researchers have developed various composite membranes by combining SPEEK with a range of organic and inorganic materials, such as polybenzimidazole (PBI), fluoropolymers, and silica, to enhance the mechanical, chemical, and thermal stability of the membranes, while reducing fuel permeability and improving the overall performance of the fuel cell. Despite the significant potential of SPEEK and its composite membranes in PEMFCs, there are still challenges and room for improvement, including proton conductivity, chemical stability, cost-effectiveness, and environmental impact assessments. Full article
(This article belongs to the Special Issue Polymer Electrolyte Membrane Fuel Cells: Technology and Applications)
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<p>Fuel cell mechanism diagram [<a href="#B13-polymers-16-02840" class="html-bibr">13</a>]. Reproduced under terms of the CC−BY license [<a href="#B13-polymers-16-02840" class="html-bibr">13</a>]. Copyright 2022, <span class="html-italic">MDPI</span>.</p>
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<p>Overview of progressive improvements in PEMFCs to meet future high-power density requirements and a schematic explanation of the working principle [<a href="#B16-polymers-16-02840" class="html-bibr">16</a>]. Reproduced with permission from [<a href="#B16-polymers-16-02840" class="html-bibr">16</a>]. Copyright 2021, <span class="html-italic">Nature</span>.</p>
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<p>Perfluorinated PEM Structure [<a href="#B17-polymers-16-02840" class="html-bibr">17</a>]. Reproduced with permission from [<a href="#B17-polymers-16-02840" class="html-bibr">17</a>]. Copyright 2000, Elsevier Ltd.</p>
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<p>Chemical structure of Nafion.</p>
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<p>SEM image of (<b>A</b>) a damaged membrane, (<b>B</b>) SPEEK, (<b>C</b>) SP100, (<b>D</b>) SP30, (<b>E</b>) SP20, (<b>F</b>) SP10, and (<b>G</b>) SP0 after healing at 45 °C for 2 days [<a href="#B67-polymers-16-02840" class="html-bibr">67</a>]. Reproduced with permission from [<a href="#B67-polymers-16-02840" class="html-bibr">67</a>]. Copyright 2019, <span class="html-italic">Chemical Engineering Journal</span>.</p>
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<p>Sulfonation of PEEK [<a href="#B80-polymers-16-02840" class="html-bibr">80</a>]. Reproduced with permission from [<a href="#B70-polymers-16-02840" class="html-bibr">70</a>] Copyright 2021, <span class="html-italic">Physicochemical and Engineering Aspects</span>.</p>
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<p>Variations of the proton conductivities of the SPEEK and SPEEK/PSf−BIm blend (3:1 weight ratio) membranes with temperature under anhydrous condition [<a href="#B90-polymers-16-02840" class="html-bibr">90</a>]. Reproduced with permission from [<a href="#B90-polymers-16-02840" class="html-bibr">90</a>]. Copyright 2006, <span class="html-italic">Electrochemistry Communications</span>.</p>
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<p>Synthesis scheme of polysulfone bearing 5-amino-benzotriazole side groups [<a href="#B92-polymers-16-02840" class="html-bibr">92</a>]. Reproduced with permission from [<a href="#B92-polymers-16-02840" class="html-bibr">92</a>]. Copyright 2010, <span class="html-italic">Journal of Membrane Science</span>.</p>
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<p>Comparison of the proton conductivities of the Nafion 115, pristine SPEEK, and SPEEK/PSf-BTraz (with various PSf−BTraz-158 contents) blend membranes under anhydrous conditions at various temperatures [<a href="#B92-polymers-16-02840" class="html-bibr">92</a>]. Reproduced with permission from [<a href="#B92-polymers-16-02840" class="html-bibr">92</a>]. Copyright 2010, Elsevier.</p>
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<p>(<b>a</b>) Water uptake of the thermally-crosslinked SPEEK/SPAES membranes (<b>b</b>) swelling ratio of the thermally-crosslinked SPEEK/SPAES membranes [<a href="#B84-polymers-16-02840" class="html-bibr">84</a>]. Reproduced with permission from [<a href="#B84-polymers-16-02840" class="html-bibr">84</a>]. Copyright 2021, Elsevier.</p>
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<p>Proton conductivity of thermally cross−linked SPEEK/SPAES membranes and Nafion112 [<a href="#B84-polymers-16-02840" class="html-bibr">84</a>]. Reproduced with permission from [<a href="#B84-polymers-16-02840" class="html-bibr">84</a>]. Copyright 2021, Elsevier.</p>
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<p>Mechanical strain–stress curves of SPEEK, SPFAES, and CMB membranes: a. SPEEK; b. SPFAES; c. CMB1; d. CMB2; e. CMB3; f. CMB4 [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Reproduced with permission from [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Copyright 2021, Higher Education Press.</p>
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<p>Proton conductivity of pristine SPEEK and CMB composite membranes at different temperatures [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Reproduced with permission from [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Copyright 2021, Higher Education Press.</p>
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<p>Polarization curves and power density profiles of single-cell test assembled with CMB4 and Nafion 112 membranes at 80 °C and 100% RH [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Reproduced with permission from [<a href="#B95-polymers-16-02840" class="html-bibr">95</a>]. Copyright 2021, <span class="html-italic">Chem. J. Chinese Universities</span>.</p>
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<p>(<b>A</b>) Contact angle and wetting energy of pristine SPEEK and blending membranes at ambient temperature; (<b>B</b>) Water sorption/desorption properties with respect to humidity and (<b>C</b>) Water sorption/desorption properties with respect to time of pristine SPEEK and blending membranes at ambient temperature; (<b>D</b>) Water uptake and degree of swelling for pristine SPEEK and hybrids at 60 C and their IEC for pristine SPEEK and blending membranes at ambient temperature; (<b>E</b>) At different temperatures under 100% RH and (<b>F</b>) at different temperatures under 20% RH; proton conductivity plots of pristine SPEEK and blended membranes [<a href="#B96-polymers-16-02840" class="html-bibr">96</a>]. Reproduced with permission from [<a href="#B96-polymers-16-02840" class="html-bibr">96</a>]. Copyright 2023, Composites Part B: Engineering.</p>
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<p>The structure of SPEEK/PBI composite membranes [<a href="#B112-polymers-16-02840" class="html-bibr">112</a>]. Reproduced with permission from [<a href="#B112-polymers-16-02840" class="html-bibr">112</a>]. Copyright 2016, Elsevier Ltd.</p>
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<p>Water uptake of SPEEK/PBI composite membranes containing BPO<sub>4</sub> [<a href="#B116-polymers-16-02840" class="html-bibr">116</a>]. Reproduced with permission from [<a href="#B116-polymers-16-02840" class="html-bibr">116</a>] Copyright 2005, Elsevier Ltd.</p>
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<p>Proton conductivity of composite SPEEK/PBI blend membranes containing BPO<sub>4</sub> [<a href="#B116-polymers-16-02840" class="html-bibr">116</a>]. Reproduced with permission from [<a href="#B117-polymers-16-02840" class="html-bibr">117</a>] Copyright 2005, Elsevier Ltd.</p>
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<p>The proton conductivity of blended membranes and Nafion117 [<a href="#B117-polymers-16-02840" class="html-bibr">117</a>]. Reproduced with permission from [<a href="#B117-polymers-16-02840" class="html-bibr">117</a>] Copyright 2012, Elsevier.</p>
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<p>Synthesis of phenylated polybenzimidazole [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>]. Reproduced with permission from [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>] Copyright 2013, SAGE Publications Ltd.</p>
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<p>Synthesis of phenylated-sulfonated poly(ether ether ketone) [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>]. Reproduced with permission from [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>] Copyright 2013, SAGE Publications Ltd.</p>
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<p>Proton conductivity of phenylated sulfonated poly(ether ether ketone), Nafion, and blend membranes [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>]. Reproduced with permission from [<a href="#B118-polymers-16-02840" class="html-bibr">118</a>] Copyright 2013, SAGE Publications Ltd.</p>
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<p>The proton conductivity of SPEEK/SPBI/S-GO composite membranes [<a href="#B120-polymers-16-02840" class="html-bibr">120</a>]. Reproduced with permission from [<a href="#B120-polymers-16-02840" class="html-bibr">120</a>] Copyright 2018, Wiley.</p>
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<p>Single-cell performances of the membranes with H<sub>2</sub>/air operated under 25 °C. The flux rates of H<sub>2</sub> and air are 100 and 150 mL/min, respectively [<a href="#B120-polymers-16-02840" class="html-bibr">120</a>]. Reproduced with permission from [<a href="#B120-polymers-16-02840" class="html-bibr">120</a>] Copyright 2018, Wiley.</p>
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<p>Preparation of cross-linked polymer composite membranes using SPEEK and SPBI as polymer matrix and PrSGO as filler [<a href="#B121-polymers-16-02840" class="html-bibr">121</a>]. Reproduced with permission from [<a href="#B121-polymers-16-02840" class="html-bibr">121</a>] Copyright 2023, Wiley.</p>
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<p>(<b>a</b>) Proton conductivity of XSPEEK/SPBI/PrSGO composite membranes, (<b>b</b>) performance of single cell with XSPEEK/SPBI/PrSGO nanocomposite membranes at 80 °C and 100% RH [<a href="#B121-polymers-16-02840" class="html-bibr">121</a>]. Reproduced with permission from [<a href="#B121-polymers-16-02840" class="html-bibr">121</a>] Copyright 2023, Elsevier Ltd.</p>
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<p>Schematic representation of the SPEEK/o-PBI/TMBP composite membranes [<a href="#B122-polymers-16-02840" class="html-bibr">122</a>]. Reproduced with permission from [<a href="#B122-polymers-16-02840" class="html-bibr">122</a>] Copyright 2011, Elsevier.</p>
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<p>Preparation process of OPBI−SPEEK membranes [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>]. Reproduced with permission from [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>] Copyright 2021, Elsevier.</p>
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<p>Proton conductivity for OPBI and OPBI−SPEEK membranes at high temperature from 80 to 160 °C under anhydrous: (<b>a</b>), at low temperature from 40 to 80 °C under 98% RH (<b>b</b>); proton conductivity Arrhenius plots of for OPBI and OPBI−SPEEK membranes at high temperature from 80 to 160 °C under anhydrous (<b>c</b>), at low temperature from 40 to 80 °C under 98% RH (<b>d</b>). [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>]. Reproduced with permission from [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>] Copyright 2021, Elsevier.</p>
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<p>Stability test of proton conductivity for the OPBI−30% SPEEK at 160 °C under 0% RH and at 60 °C under 98% RH [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>]. Reproduced with permission from [<a href="#B123-polymers-16-02840" class="html-bibr">123</a>] Copyright 2021, Elsevier.</p>
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<p>The stress–strain plots of SPEEK/PVDF blended membranes [<a href="#B125-polymers-16-02840" class="html-bibr">125</a>]. Reproduced with permission from [<a href="#B125-polymers-16-02840" class="html-bibr">125</a>] Copyright 2010, Elsevier.</p>
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<p>Optical micrographs of (<b>a</b>) SPEEK44/PVDF, (<b>b</b>) SPEEK56/PVDF, (<b>c</b>) SPEEK67/PVDF, and (<b>d</b>) SPEEK73/PVDF blended membranes with different PVDF contents, (<b>e</b>) SPEEK67/PVDF-50, (<b>f</b>) SPEEK73/PVDF-10, (<b>g</b>) SPEEK73/PVDF-50 blended membranes, and (<b>h</b>) PVDF [<a href="#B127-polymers-16-02840" class="html-bibr">127</a>]. Reproduced under terms of the CC-BY license [<a href="#B127-polymers-16-02840" class="html-bibr">127</a>]. Copyright 2019, <span class="html-italic">MDPI</span>.</p>
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<p>Current density−potential (I–V) and power density curves of the DMFC assembled with different membranes at 30 °C [<a href="#B132-polymers-16-02840" class="html-bibr">132</a>]. Reproduced with permission from [<a href="#B132-polymers-16-02840" class="html-bibr">132</a>] Copyright 2016, Royal Society of Chemistry.</p>
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<p>Schematic illustration of the synthesis process and microstructure of SPEEK/PDA@PVDF composite membrane [<a href="#B134-polymers-16-02840" class="html-bibr">134</a>]. Reproduced with permission from [<a href="#B134-polymers-16-02840" class="html-bibr">134</a>] Copyright 2019, Elsevier.</p>
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<p>(<b>A</b>) Area swelling, (<b>B</b>) thickness swelling, (<b>C</b>) water uptake, and (<b>D</b>) proton conductivity of SPEEK and composite membranes at different temperatures [<a href="#B134-polymers-16-02840" class="html-bibr">134</a>]. Reproduced with permission from [<a href="#B134-polymers-16-02840" class="html-bibr">134</a>] Copyright 2019, Elsevier.</p>
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<p>Preparation process of SPEEK-PDA/PEI@PVDF composite membranes [<a href="#B135-polymers-16-02840" class="html-bibr">135</a>]. Reproduced with permission from [<a href="#B135-polymers-16-02840" class="html-bibr">135</a>] Copyright 2024, Elsevier.</p>
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<p>OCV curves: (<b>A</b>) and power density curves (<b>B</b>) of membranes with 2 M methanol at 80 °C [<a href="#B135-polymers-16-02840" class="html-bibr">135</a>]. Reproduced with permission from [<a href="#B135-polymers-16-02840" class="html-bibr">135</a>] Copyright 2024, Elsevier.</p>
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18 pages, 1875 KiB  
Article
Wheat Peptides as Catalysts for Athletic Performance Improvement in Cross-Country Skiers: A Randomized Controlled Trial
by Mai Xiang, Qi Han, Yue Chen, Shenglin Duan, Xiaofeng Han, Xuemei Sui, Chaoxue Ren and Qirong Wang
Metabolites 2024, 14(10), 538; https://doi.org/10.3390/metabo14100538 - 7 Oct 2024
Viewed by 353
Abstract
Objectives: This study investigated the efficacy of wheat peptide supplementation compared to regular proteins in elite cross-country skiers, providing insights into the metabolic and performance effects of these supplements in order to guide athletes in selecting optimal energy sources for training and competition. [...] Read more.
Objectives: This study investigated the efficacy of wheat peptide supplementation compared to regular proteins in elite cross-country skiers, providing insights into the metabolic and performance effects of these supplements in order to guide athletes in selecting optimal energy sources for training and competition. Methods: Nineteen healthy male cross-country skiers were enrolled and assigned to either the peptide group (PEP, n = 9) or the protein group (PRO, n = 10). A four-week intervention study involving supplementation with wheat peptides/regular proteins was conducted, and pre- and post-intervention assessments were performed to evaluate exercise capacity and metabolic profiles. Results: The study found that the PEP group and the PRO group showed distinct within-group effects on exercise performance. The PEP group demonstrated improved aerobic capacity, including better performance in 10 km roller skating, an increased lactate threshold, and reduced resting blood lactate levels. The PRO group enhanced anaerobic capacity, such as improved sprint time, hexagon test performance, and lactate clearance. Metabolomic analysis revealed specific metabolic pathways affected in each group, with the PEP group showing impacts on the α-linolenic acid pathway and the PRO group on ketone body synthesis and degradation as well as vitamin B6 metabolism. Conclusions: Our findings indicate that wheat oligopeptides and regular proteins have comparable effects on exercise performance. However, the wheat peptides may offer greater advantages in enhancing aerobic capacity. No significant variations were observed in blood metabolite profiles between the two groups, but distinct metabolic pathways exhibited different responses. Full article
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<p>General experimental design.</p>
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<p>Comparative analysis of (<b>A</b>) blood lactate concentration levels, (<b>B</b>) heart rate during tests of aerobic capacity, and (<b>C</b>) blood lactate levels during tests of anaerobic capacity at baseline and following intervention for cross-country skiers supplemented with either wheat peptide bars or regular protein bars. Data are presented as mean ±SD. Significant differences between groups post-intervention (<sup>b</sup> <span class="html-italic">p</span> &lt; 0.05), within the PRO group (<sup>c</sup> <span class="html-italic">p</span> &lt; 0.05), and within the PEP group (<sup>d</sup> <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The PCA and OPLS-DA score plots. (<b>A</b>) PCA score plots compare the PEP and PRO groups at baseline (<b>left</b>) and post-intervention (<b>right</b>); (<b>B</b>) PCA score plots compare the different timepoints of baseline and post-intervention within the PEP group (<b>left</b>) and PRO group (<b>right</b>); (<b>C</b>) OPLS-DA score plots compare the different timepoints of baseline and post-intervention within the PEP group (<b>left</b>) and PRO group (<b>right</b>). The plots show the distribution of samples from the two groups based on principal component analysis (PCA) and/or Orthogonal Partial Least Squares Discriminant Analysis (OPLS-DA). Each point represents an individual sample, and the positioning of the points reflects their similarity or dissimilarity in terms of metabolite profiles.</p>
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<p>Volcano plots and differential metabolite classes in (<b>A</b>) PEP group; (<b>B</b>) PRO group. The x-axis represents log2(fold change), while the y-axis represents false discovery rate on a -log10 scale.</p>
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<p>Pathway analysis overview of metabolic pathways in the PEP and PRO groups. The circles represent the involved pathways, and significantly changed pathways are labeled with names.</p>
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<p>Illustration summarizing the described factors contributing to the improved aerobic and anaerobic capacities of cross-country skiers following supplementation with wheat peptide or regular protein bars.</p>
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16 pages, 2225 KiB  
Article
Resistant Potato Starch Supplementation Reduces Serum Free Fatty Acid Levels and Influences Bile Acid Metabolism
by Jason R. Bush, Izuchukwu Iwuamadi, Jun Han, David J. Schibli, David R. Goodlett and Edward C. Deehan
Metabolites 2024, 14(10), 536; https://doi.org/10.3390/metabo14100536 - 5 Oct 2024
Viewed by 763
Abstract
Background: Resistant starches, such as high-amylose maize starch and resistant potato starch (RPS), have prebiotic effects that are linked to improved metabolism at >15 g/day, but the effects at lower doses have not been reported. Methods: We performed an exploratory post [...] Read more.
Background: Resistant starches, such as high-amylose maize starch and resistant potato starch (RPS), have prebiotic effects that are linked to improved metabolism at >15 g/day, but the effects at lower doses have not been reported. Methods: We performed an exploratory post hoc analysis of free fatty acids (FFAs), bile acids (BAs), and ketone bodies in serum previously collected from a randomized, double-blind, placebo-controlled clinical trial evaluating the effects of one- and four-week consumption of 3.5 g/day RPS versus a placebo using two-way ANOVA adjusted by pFDR. Associations between week 4 changes in FFAs, BAs, and ketone bodies were assessed by Pearson’s correlations. Results: RPS consumption reduced total FFAs relative to the placebo, including multiple unsaturated FFAs and octanedioic acid, with reductions in taurine- and glycine-conjugated secondary BAs also detected (q < 0.05). No changes in ketone bodies were observed (q > 0.05). Changes in 7-ketodeoxycholic acid (r = −0.595) and glycolithocholic acid (r = −0.471) were inversely correlated with treatment-induced reductions in FFAs for RPS but not the placebo, suggesting the effects were from the prebiotic. Shifts in β-hydroxybutyrate were further correlated with FFA changes in both treatments (q < 0.05). Conclusions: These findings demonstrate that low doses of RPS positively influence fatty acid metabolism in humans, reducing circulating levels of FFA and conjugated BAs. Full article
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Graphical abstract
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<p>Effects of RPS and placebo on FFA levels. Total FFA levels were not different between placebo and RPS groups across baseline, week 1, and week 4 (<b>A</b>). RPS significantly reduced total FFA levels compared to placebo (<b>B</b>). Individual FFAs were similarly distributed in both placebo and RPS groups across baseline, week 1, and week 4 (<b>C</b>). Pooled unsaturated fats, including FA(8:1), FA(10:1), FA(12:1), FA(14:1), FA(16:1), FA(18:1), FA(18:2), FA(18:3), FA(18:4), FA(20:1), FA(20:2), FA(20:3), FA(20:4), FA(20:5), FA(22:1), FA(22:4), FA(22:5), FA(22:6), and FA(24:1), were reduced by RPS when compared to placebo (<b>D</b>). Saturated fats, including FA(7:0), FA(8:0), FA(9:0), FA(10:0), FA(11:0), FA(12:0), FA(13:0), FA(14:0), FA(15:0), FA(16:0), FA(17:0), FA(18:0), FA(19:0), FA(20:0), FA(21:0), FA(22:0), FA(23:0), FA(24:0), FA(25:0), and FA(26:0), were not significantly reduced in the RPS group compared to the placebo (<b>E</b>). See <a href="#app1-metabolites-14-00536" class="html-app">Table S1</a> for full analysis. (ANOVA; mean ± SEM).</p>
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<p>Effects of RPS and placebo on bile acid levels. Total bile acid levels were not significantly different between placebo and RPS groups across baseline, week 1 and week 4 (<b>A</b>). Changes in total bile acid levels tended to decrease in the RPS group compared to the placebo group, but this effect was not significant (<b>B</b>). Conjugated (<b>C</b>) and unconjugated (<b>D</b>) bile acid levels were similar in both treatment groups across baseline, week 1, and week 4. Total conjugated (<b>E</b>) and glycine-conjugated (<b>F</b>) bile acids tended to be reduced in the RPS group. RPS consumption significantly reduced taurine-conjugated bile acids (<b>G</b>) but had no effect on unconjugated bile acids (<b>H</b>). (ANOVA; mean ± SEM).</p>
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<p>Effects of RPS and placebo on 7-ketodeoxycholic acid levels. Week 4 changes in 7-ketodeoxycholic acid are correlated with changes in FFA levels in the RPS but not placebo group (<b>A</b>). Levels of 7-ketodeoxycholic acid were not different between groups across baseline, week 1, or week 4 (<b>B</b>), nor were changes in 7-ketodeoxycholic acid between groups (<b>C</b>). (ANOVA; mean ± SEM).</p>
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<p>Effects of RPS and placebo on ketone bodies. Week 4 changes in β-hydroxybutyrate were significantly correlated with changes in FFA levels in both placebo and RPS (<b>A</b>) groups. Week 4 changes in acetoacetate were significantly correlated with changes in acetate levels in both placebo and RPS (<b>B</b>) groups. Week 4 changes in β-hydroxybutyrate were significantly correlated with changes in acetate levels in both placebo and RPS (<b>C</b>) groups. Week 4 changes in β-hydroxybutyrate were significantly correlated with changes in acetoacetate levels in both placebo and RPS (<b>D</b>) groups. β-hydroxybutyrate levels were not significantly different between placebo and RPS groups across baseline, week 1, or week 4 (<b>E</b>), nor were changes in β-hydroxybutyrate between treatment groups (<b>F</b>). (ANOVA; mean ± SEM).</p>
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<p>Interactions between FFAs, bile acids, and ketone bodies. Heatmap shows associations between week 4 changes in select FFAs, bile acids, and ketone bodies in the placebo (<b>A</b>) and RPS (<b>B</b>) groups. Color gradient indicates Pearson correlation coefficients; * <span class="html-italic">q</span> values &lt; 0.05.</p>
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<p>Effects of RPS and placebo on glycolithocholic acid levels. Week 4 changes in glycolithocholic acid are correlated with changes in FFA levels in the RPS group but not the placebo group (<b>A</b>). Levels of glycolithocholic acid were not significantly different between treatment group across baseline, week 1, and week 4 (<b>B</b>), but changes in glycolithocholic acid between treatment groups were significantly different (<b>C</b>). (ANOVA; mean ± SEM).</p>
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