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Search Results (341)

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14 pages, 1160 KiB  
Article
Smoking and Risk of Fatty Liver Disease: A Meta-Analysis of Cohort Studies
by Moonhyung Lee, Seung-Kwon Myung, Sang Hee Lee and Yoosoo Chang
Gastroenterol. Insights 2025, 16(1), 1; https://doi.org/10.3390/gastroent16010001 - 2 Jan 2025
Viewed by 424
Abstract
Background/Objectives: It remains inconclusive whether or not smoking is associated with an increased risk of fatty liver disease (FLD). We investigated the association between smoking and the risk of FLD by using a meta-analysis of cohort studies. Methods: PubMed and EMBASE [...] Read more.
Background/Objectives: It remains inconclusive whether or not smoking is associated with an increased risk of fatty liver disease (FLD). We investigated the association between smoking and the risk of FLD by using a meta-analysis of cohort studies. Methods: PubMed and EMBASE were searched using keywords from their inception to September 2023 to identify relevant studies. Results: Out of 806 articles searched from the databases, a total of 20 cohort studies were included in the final analysis. In the meta-analysis, smoking was significantly associated with an increased risk of FLD (odds ratio/relative risk/hazard ratio, 1.14; 95% confidence interval, 1.05–1.24; n = 20). Subgroup analyses showed a significant positive association between them in prospective cohort studies (odds ratio/relative risk/hazard ratio, 1.15; 95% confidence interval, 1.05–1.18; n = 5) but not in retrospective cohort studies and cross-sectional studies based on cohort studies. In the subgroup meta-analysis by gender in Asians, smoking significantly increased the risk of FLD in men, while there was no significant association between FLD and smoking in women. Conclusions: This meta-analysis showed that smoking increases the risk of FLD. In addition to well-known risk factors of FLD, clinicians should recommend smoking cessation for the management of FLD. Full article
(This article belongs to the Section Liver)
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Figure 1
<p>Flow diagram of identifying relevant Studies.</p>
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<p>Smoking and risk of fatty liver disease in the meta-analysis (n = 20). OR, odds ratio; RR, relative risk; HR, hazard ratio; CI, confidence interval.</p>
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<p>Begg’s funnel plot and Egger’s test to test publication bias (n = 20). OR, odds ratio; RR, relative risk; HR, hazard ratio; S.E., standard error.</p>
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27 pages, 6354 KiB  
Article
Potential Clinical Application of Analysis of Bisphenols in Pericardial Fluid from Patients with Coronary Artery Disease with the Use of Liquid Chromatography Combined with Fluorescence Detection and Triple Quadrupole Mass Spectrometry
by Tomasz Tuzimski, Szymon Szubartowski, Janusz Stążka, Kamil Baczewski, Daria Janiszewska, Viorica Railean, Bogusław Buszewski and Małgorzata Szultka-Młyńska
Molecules 2025, 30(1), 140; https://doi.org/10.3390/molecules30010140 - 1 Jan 2025
Viewed by 365
Abstract
Bisphenols may negatively impact human health. In this study, we propose the use of HPLC–FLD for the simultaneous determination of bisphenols in pericardial fluid samples collected from patients with coronary artery disease undergoing coronary artery bypass surgery. For sample preparation, a fast, simple, [...] Read more.
Bisphenols may negatively impact human health. In this study, we propose the use of HPLC–FLD for the simultaneous determination of bisphenols in pericardial fluid samples collected from patients with coronary artery disease undergoing coronary artery bypass surgery. For sample preparation, a fast, simple, and ”green” DLLME method was used, achieving mean recovery values in the range of 62%–98% with relative standard deviations between 2% and 6% for all analytes. Quantitative analysis of bisphenols in the samples was then performed by LC–MS/MS on a triple quadrupole (QqQ) mass spectrometer and electrospray ionization (ESI-/ESI+) was applied in the negative and positive ion modes, respectively. The LODs and LOQs ranged from 0.04 ng/mL to 0.37 ng/mL and 0.12 ng/mL to 1.11 ng/mL, respectively. Pericardial fluid was collected from patients with coronary artery disease during coronary artery bypass surgery. Bisphenol residues were identified and quantified in samples from 19 patients. The procedure was successfully applied to the biomonitoring of free forms of 14 bisphenols in pericardial fluid. After statistical examination of the relationships between the selected variables, a strongly positive correlation was found between creatinine kinase and troponin I, as well as the number of venous anastomoses, circulation time, and clamp cap time. Full article
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Figure 1
<p>The diagram shows the recovery values for the analyzed bisphenols with relative standard deviations between 2% and 6% for all analytes.</p>
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<p>Example chromatograms obtained during the HPLC–FLD analysis: mixture of bisphenol standards (25 ng/mL) and three spiked samples at 10 ng/mL, 20 ng/mL, and 30 ng/mL. 1—BADGE∙2H<sub>2</sub>O, 2—BPF, 3—BPE, 4—BPA, 5—BADGE∙2HCl, 6—BADGE, 7—BPP.</p>
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<p>QqQ–ESI–MS and MS/MS spectra of following bisphenols residues detected in pericardial fluid samples: (<b>a</b>) BPS (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 249), (<b>b</b>) BPF (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 199), (<b>c</b>) BPE (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 213), (<b>d</b>) BPA (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 227), (<b>e</b>) BPB (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 241), (<b>f</b>) BPP (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 345), (<b>g</b>) BPZ (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 267), (<b>h</b>) BPAF (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 335), (<b>i</b>) BPAP (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 335), (<b>j</b>) BADGE•2H<sub>2</sub>O (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 394), (<b>k</b>) BADGE•H<sub>2</sub>O (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 376), (<b>l</b>) BADGE•H<sub>2</sub>O•HCl (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 412), (<b>m</b>) BADGE•2HCl (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 430), and (<b>n</b>) BADGE (<span class="html-italic">m</span>/<span class="html-italic">z</span> = 358).</p>
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<p>Selected clinical data of 19 patients with coronary artery diseases and undergoing coronary artery bypass surgery.</p>
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<p>Heatmap showing the distribution and concentration (ng/mL) of quantified bisphenols in pericardial fluids collected from 19 patients with coronary artery diseases and undergoing coronary artery bypass surgery. The samples numbers (1–19) indicate the name of samples analyzed by LC–ESI–QqQ. Hierarchical cluster analysis shows the correlations between the analyzed bisphenols. #a, #b, #c—indicates the main formed clusters.</p>
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<p>PCA score plots for bisphenols concentration (<b>A</b>) in pericardial fluids determined by LC–ESI–QqQ and patients (<b>B</b>) with coronary artery diseases.</p>
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<p>Heat map showing pairwise correlation matrix of the input variables (clinical data of 19 patients with coronary artery diseases) and quantified bisphenols. CCS/central cord syndrome; CCTime/circulation time (min); CLCTime/clamp cap time (min); NTAA/no of thoracic artery anastomoses; NVA/no of venous anastomoses; NRAA/no of radial artery anastomoses; CK24h/creatinine kinase (U/L), 24 h after the surgency; CK48h/creatinine kinase (U/L), 48 h after the surgency; Tr/I_24h/Troponin I (ng/L), 24 h after the surgency; Tr/I_48h/Troponin I (ng/L), 48 h after the surgency; Tr/I_HD/Troponin I (ng/L), Hospital discharge data.</p>
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<p>PCA score plots for clinical data and quantified bisphenols referred to 19 patients (<b>A</b>) and the scatter plot for patients (<b>B</b>) with coronary artery diseases. The numbers plotted in (<b>A</b>) represent the <span class="html-italic">m</span>/<span class="html-italic">z</span> of bisphenols while the numbers plotted in (B) represent the patients name. 227—BPA, 249—BPS, 241—BPB, 199—BPF, 345—BPP, 213—BPE, 267—BPZ, 335—BPAP, BPAF—335, 358—BADGE, 376—BADGE•H<sub>2</sub>O, 394—BADGE•2H<sub>2</sub>O, 412—BADGE•H<sub>2</sub>O•HCl, and 430—BADGE•2HCl. CCS/central cord syndrome; CCTime/circulation time (min); CLCTime/clamp cap time (min); NTAA/No. of thoracic artery anastomoses; NVA/No. of venous anastomoses; NRAA/No. of radial artery anastomoses; CK24h/creatinine kinase (U/L), 24 h after the surgency; CK48h/creatinine kinase (U/L), 48 h after the surgency; Tr/I_24h/Troponin I (ng/L), 24 h after the surgency; Tr/I_48h/Troponin I (ng/L), 48 h after the surgency; Tr/I_HD/Troponin I (ng/L), Hospital discharge data.</p>
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<p>The flowchart of DLLME procedure.</p>
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31 pages, 724 KiB  
Review
A Review of the Mycotoxin Family of Fumonisins, Their Biosynthesis, Metabolism, Methods of Detection and Effects on Humans and Animals
by Christian Kosisochukwu Anumudu, Chiemerie T. Ekwueme, Chijioke Christopher Uhegwu, Chisom Ejileugha, Jennifer Augustine, Chioke Amaefuna Okolo and Helen Onyeaka
Int. J. Mol. Sci. 2025, 26(1), 184; https://doi.org/10.3390/ijms26010184 - 28 Dec 2024
Viewed by 417
Abstract
Fumonisins, a class of mycotoxins predominantly produced by Fusarium species, represent a major threat to food safety and public health due to their widespread occurrence in staple crops including peanuts, wine, rice, sorghum, and mainly in maize and maize-based food and feed products. [...] Read more.
Fumonisins, a class of mycotoxins predominantly produced by Fusarium species, represent a major threat to food safety and public health due to their widespread occurrence in staple crops including peanuts, wine, rice, sorghum, and mainly in maize and maize-based food and feed products. Although fumonisins occur in different groups, the fumonisin B series, particularly fumonisin B1 (FB1) and fumonisin B2 (FB2), are the most prevalent and toxic in this group of mycotoxins and are of public health significance due to the many debilitating human and animal diseases and mycotoxicosis they cause and their classification as by the International Agency for Research on Cancer (IARC) as a class 2B carcinogen (probable human carcinogen). This has made them one of the most regulated mycotoxins, with stringent regulatory limits on their levels in food and feeds destined for human and animal consumption, especially maize and maize-based products. Numerous countries have regulations on levels of fumonisins in foods and feeds that are intended to protect human and animal health. However, there are still gaps in knowledge, especially with regards to the molecular mechanisms underlying fumonisin-induced toxicity and their full impact on human health. Detection of fumonisins has been advanced through various methods, with immunological approaches such as Enzyme-Linked Immuno-Sorbent Assay (ELISA) and lateral flow immunoassays being widely used for their simplicity and adaptability. However, these methods face challenges such as cross-reactivity and matrix interference, necessitating the need for continued development of more sensitive and specific detection techniques. Chromatographic methods, including HPLC-FLD, are also employed in fumonisin analysis but require meticulous sample preparation and derivitization due to the low UV absorbance of fumonisins. This review provides a comprehensive overview of the fumonisin family, focusing on their biosynthesis, occurrence, toxicological effects, and levels of contamination found in foods and the factors affecting their presence. It also critically evaluates the current methods for fumonisin detection and quantification, including chromatographic techniques and immunological approaches such as ELISA and lateral flow immunoassays, highlighting the challenges associated with fumonisin detection in complex food matrices and emphasizing the need for more sensitive, rapid, and cost-effective detection methods. Full article
(This article belongs to the Special Issue Mycotoxins and Food Toxicology)
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<p>Chemical structures of the major fumonisins [<a href="#B68-ijms-26-00184" class="html-bibr">68</a>].</p>
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18 pages, 5813 KiB  
Article
Lipid Profile of Larix cajanderi Mayr in Adaptation to Natural Conditions in the Cryolithozone
by Vasiliy V. Nokhsorov, Tatiana D. Tatarinova, Lyubov V. Dudareva, Natalia V. Semenova and Trofim C. Maximov
Int. J. Mol. Sci. 2025, 26(1), 164; https://doi.org/10.3390/ijms26010164 - 28 Dec 2024
Viewed by 300
Abstract
The prevalence of coniferous trees in the forest landscapes of northeastern Siberia is conditioned by their high frost resistance. The Kajander larch (Larix cajanderi Mayr), which can survive under natural conditions (down to −60 °C) in the cryolithozone of Yakutia, is the [...] Read more.
The prevalence of coniferous trees in the forest landscapes of northeastern Siberia is conditioned by their high frost resistance. The Kajander larch (Larix cajanderi Mayr), which can survive under natural conditions (down to −60 °C) in the cryolithozone of Yakutia, is the dominant forest-forming species. We hypothesise that our study using HPTLC–UV/Vis/FLD, TLC–GC/FID, and GC–MS methods of seasonal features of the lipid profile of Kajander larch tissues will bring us closer to understanding the mechanisms of participation of lipid components in the adaptation of this valuable tree species to the cold climate of the cryolithozone. Rare delta5-unsaturated polymethylene-interrupted fatty acids (∆5-UPIFA) were identified in the fatty acids (FAs) of L. cajanderi shoots, including 18:2(Δ5.9) (taxoleic), 18:3(Δ5.9.12) (pinolenic), and 18:4(Δ5.9.12.15) (coniferonic). It was found that the content of ∆5-UPIFA in L. cajanderi shoots markedly increased (1.5-fold, representing up to 23.9% of sum FAs) during the autumnal transition of trees to dormancy. It was observed that the ranges of low temperatures experienced during the prolonged winter period primarily determined the structural diversity of membrane lipids and their constituent FAs during the cold adaptation of L. cajanderi. The results obtained can be used for the selection of molecular markers of cold tolerance in woody plants, including fruit trees. Full article
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Figure 1
<p><span class="html-italic">Larix cajanderi</span> Mayr (<b>A</b>), growing on the territory of the Botanical Garden in the cryolithozone of Yakutia (photo taken on June 2024); <span class="html-italic">Larix cajanderi</span> Mayr (<b>B</b>), shoots of the current year (photo taken on June 2024).</p>
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<p>The rate of average monthly air temperature (°C) and average precipitation (mm) (red dashed lines) in the cryolithozone.</p>
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<p>HPTLC profile of polar lipids in <span class="html-italic">L. cajanderi</span> shoots in a one-year cycle. Images were taken at (<b>A</b>) white light after derivatization; (<b>B</b>) 366 nm; (<b>C</b>) 254 nm; Track 1—January, Track 2—February, Track 3—March, Track 4—April, Track 5—May, Track 6—June, Track 7—July, Track 8—August, Track 9—September, Track 10—October, Track 11—November, Track 12—December. Different colors represent different lipid classes.</p>
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<p>Seasonal changes in the composition of membrane lipids in <span class="html-italic">L. cajanderi</span> shoots in the cryolithozone of Yakutia (% of lipid structures). The samples were selected at various points throughout the annual cycle. PC—phosphatidylcholine; PI—phosphatidylinositol; PE—phosphatidylethanolamine; PG—phosphatidylglycerol; PA—phosphatidic acid; DPG—diphosphatidylglycerol; GlCer—glycoceramide, DGDG—digalactosyldiglyceride, MGDG—monogalactosyldiglyceride, SQDG—sulfoquinovosyldiacylglycerol, PS—phosphatidylserine, NL—neutral lipid. Different letters above the bars indicate statistically significant differences at <span class="html-italic">p</span>-value &lt; 0.05 (<span class="html-italic">t</span>-test).</p>
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<p>Dynamics of PC/PE, PC + PI/PE + PA + DPG + PG, DGDG/MGDG, (DGDG + SQDG + PG + DPG + PA)/MGDG ratios in <span class="html-italic">L. cajanderi</span> shoots (% of lipid structures). Values are presented as the means ± SEMs. The significance of differences between the compared mean values was assessed Kruskal–Wallis ANOVA by ranks (<span class="html-italic">p</span> &lt; 0.05). Different superscript letters indicate significant differences of analyzed parameters.</p>
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<p>GC–MS chromatogram of fatty acid methyl esters (FAME) in the shoots of <span class="html-italic">L. cajanderi</span> growing in the cryolithozone of Yakutia. Peaks: 14:0 (1), 15:0 (2), 16:0 (3), 16:1n−9 (4), 17:0–a (5), 18:1–i (6), 18:0 (7), 18:1(n−9) (8), 18:1n−7 (9), 18:2∆5.9 (taxoleic) (10), 18:2n−6 (LA) (11), 18:3∆5.9.12 (pinolenic) (12), 18:3n−3 (ALA) (13), 18:4(∆5.9.12.15) (coniferonic) (14), 20:0 (15), 20:1n−9 (16), 20:2n−6 (17), 20:3(5.11.14) (sciadonic) (18), 20:3(∆7.11.14) (bis-homo-linolenic) (19), 22:0 (20), 23:0 (21).</p>
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<p>Heat map of the seasonal dynamics of FAs in the composition of total lipids in <span class="html-italic">L. cajanderi</span> shoots in the cryolithozone of Yakutia. The samples were collected at various points throughout the annual cycle.</p>
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<p>Desaturation ratios (<b>a</b>) and desaturation and elongation (<b>b</b>) of <span class="html-italic">L. cajanderi</span> shoots in spring, summer, autumn, and winter. SDR—stearic desaturation ratio; ODR—oleic desaturation ratio; LDR—linoleic desaturation ratio; DBI—double-bond index; UI—unsaturation index. Values are presented as the means ± SEMs. The significance of differences between the compared mean values was assessed using Kruskal–Wallis ANOVA by ranks (<span class="html-italic">p</span> &lt; 0.05). Different superscript letters indicate significant differences of analyzed parameters.</p>
Full article ">Figure 9
<p>PCA score plot of principal component analysis of FAs profiles in <span class="html-italic">L. cajanderi</span> shoots during the annual cycle.</p>
Full article ">
26 pages, 9841 KiB  
Article
Prostaglandins Differentially Regulate the Constitutive and Mechanosensitive Release of Soluble Nucleotidases in the Urinary Bladder Mucosa
by Alejandro Gutierrez Cruz, Mahsa Borhani Peikani, Tori D. Beaulac and Violeta N. Mutafova-Yambolieva
Int. J. Mol. Sci. 2025, 26(1), 131; https://doi.org/10.3390/ijms26010131 - 27 Dec 2024
Viewed by 253
Abstract
The urothelium and lamina propria (LP) contribute to sensations of bladder fullness by releasing multiple mediators, including prostaglandins (PGs) and adenosine 5′-triphosphate (ATP), that activate or modulate functions of cells throughout the bladder wall. Mediators that are simultaneously released in response to bladder [...] Read more.
The urothelium and lamina propria (LP) contribute to sensations of bladder fullness by releasing multiple mediators, including prostaglandins (PGs) and adenosine 5′-triphosphate (ATP), that activate or modulate functions of cells throughout the bladder wall. Mediators that are simultaneously released in response to bladder distention likely influence each other’s mechanisms of release and action. This study investigated whether PGs could alter the extracellular hydrolysis of ATP by soluble nucleotidases (s-NTDs) released in the LP of nondistended or distended bladders. Using an ex vivo murine detrusor-free bladder model to access the LP during bladder filling and a sensitive HPLC-FLD detection methodology, we evaluated the decrease in ATP and the increase in adenosine 5′-diphosphate (ADP), adenosine 5′-monophosphate (AMP), and adenosine by s-NTDs released in the LP. Endogenous PGE2 increased the spontaneous but not the distention-induced release of s-NTD via EP2 and EP3 prostanoid receptors, whereas exogenous PGE2 increased the spontaneous s-NTD release via EP3, EP4, and FP receptors and the distention-induced s-NTD release via EP1-4 and FP receptors. Endogenous PGF, PGD2, and PGI2 did not change the s-NTD release. Exogenous PGD2 increased the spontaneous s-NTD release via DP2 receptors and the distention-induced s-NTD release via DP1 and DP2 receptors. Exogenous PGF increased the spontaneous but not the distention-induced release of s-NTD via FP receptors. It is possible that higher concentrations of PGE2, PGF, and PGD2 (as expected in inflammation, bladder pain syndrome, or overactive bladder) potentiate the release of s-NTDs and the consecutive degradation of ATP as a safeguard mechanism to prevent the development of excessive bladder excitability and overactivity by high amounts of extracellular ATP. Full article
(This article belongs to the Special Issue Purinergic Signalling in Physiology and Pathophysiology 2.0)
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Figure 1
<p>Effects of EP prostanoid receptor antagonists on the eATP hydrolysis by spontaneously released s-NTDs. Original HPLC chromatograms showing the hydrolysis of eATP and formation of eADP, eAMP, and eADO after 60 min of contact of the eATP substrate with s-NTDs released in EL solutions of nondistended bladder preparations treated with either vehicle (i.e., DMSO 0.2%) or EP receptor antagonists (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) in the presence of vehicle (n = 6) or of the EP1 antagonist SC51322 (1 μM, n = 6) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the EP2 receptor antagonist PF04418948 (1 μM, n = 7) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the EP3 receptor antagonist L-798,106 (0.25 μM, n = 5) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the EP4 antagonist L-161,982 (1 μM, n = 6) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Each purine is expressed as a percentage of the total amount of purines detected in EL solutions at each time point of enzymatic reaction. Asterisks denote significant differences from the vehicle control. * <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, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Effects of EP prostanoid receptor antagonists on the eATP hydrolysis by s-NTDs released during distention of the bladder wall. Original HPLC chromatograms showing the hydrolysis of eATP and the formation of eADP, eAMP, and eADO after 60 min of contact of the eATP substrate with s-NTDs released in EL solutions of distended bladder preparations treated with either vehicle (i.e., DMSO 0.2%) or EP receptor antagonists (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) in the presence of vehicle (n = 6) or the EP1 antagonist SC51322 (1 μM, n = 6) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the EP2 receptor antagonist PF04418948 (1 μM, n = 7) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the EP3 receptor antagonist L-798,106 (0.25 μM, n = 5) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the EP4 antagonist L-161,982 (1 μM, n = 6) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Each purine is expressed as a percentage of the total amount of purines detected in EL solutions at each time point of enzymatic reaction. Asterisks denote significant differences from the vehicle control. * <span class="html-italic">p</span> &lt; 0.05.</p>
Full article ">Figure 3
<p>Effects of DP and FP prostanoid receptor antagonists on the eATP hydrolysis by spontaneously released s-NTDs. Original HPLC chromatograms showing the hydrolysis of eATP and formation of eADP, eAMP, and eADO after 60 min of contact of the eATP substrate with s-NTDs released in EL solutions of nondistended bladder preparations treated with either vehicle (i.e., DMSO 0.2%) or receptor antagonists (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) in the presence of vehicle (n = 6) or the DP1 antagonist S-5751 (1 μM, n = 4) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the DP2 receptor antagonist OC000459 (10 μM, n = 4) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the CRTH2/DP receptor antagonist AMG 853 (1 μM, n = 8) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the FP receptor antagonist AL8810 (10 μM, n = 6) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Each purine is expressed as a percentage of the total amount of purines detected in EL solutions at each time point of enzymatic reaction. Asterisks denote significant differences from the vehicle control. ** <span class="html-italic">p</span> &lt; 0.01, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
Full article ">Figure 4
<p>Effects of DP and FP prostanoid receptor antagonists on the eATP hydrolysis by s-NTDs released during distention of the bladder wall. Original HPLC chromatograms showing the hydrolysis of eATP and formation of eADP, eAMP, and eADO after 60 min of contact of the eATP substrate with s-NTDs released in EL solutions of distended bladder preparations treated with either vehicle (i.e., DMSO 0.2%) or receptor antagonists (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) in the presence of vehicle (n = 6) or the DP1 antagonist S-5751 (1 μM, n = 4) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the DP2 receptor antagonist OC000459 (10 μM, n = 4) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the DP1/DP2 receptor antagonist AMG 853 (1 μM, n = 8) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the FP receptor antagonist AL8810 (10 μM, n = 6) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Each purine is expressed as a percentage of the total amount of purines detected in EL solutions at each time point of enzymatic reaction.</p>
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<p>eATP hydrolysis by s-NTDs released in EL solutions of nondistended bladder preparations treated with exogenous PGE<sub>2</sub> in the absence or presence of EP prostanoid receptor antagonists. Original HPLC chromatograms showing the eATP degradation after 60 min of contact with the EL solutions (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) by PGE2 (10 μM) in the presence of vehicle (n = 8) or of the EP1 antagonist SC51322 (1 μM, n = 6) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the EP2 receptor antagonist PF04418948 (1 μM, n = 5) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the EP3 receptor antagonist L-798,106 (0.25 μM, n = 9) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the EP4 antagonist L-161,982 (1 μM, n = 4) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Asterisks denote significant differences from the vehicle control (n = 6). * <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, **** <span class="html-italic">p</span> &lt; 0.0001. Open circles denote significant differences of eATP degradation in PGE<sub>2</sub> alone vs. EP receptor antagonist + PGE<sub>2</sub>. <sup>o</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>oo</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>ooo</sup> <span class="html-italic">p</span> &lt; 0.001, <sup>oooo</sup> <span class="html-italic">p</span> &lt; 0.0001. Two-way ANOVA with Tukey’s multiple comparisons test.</p>
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<p>eATP hydrolysis by s-NTDs released in EL solutions of distended bladder preparations treated with exogenous PGE<sub>2</sub> in the absence or presence of EP prostanoid receptor antagonists. Original HPLC chromatograms showing the eATP degradation after 60 min of contact with the EL solutions (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>e</b>) and the increase in eADP (<b>f</b>–<b>i</b>), eAMP (<b>j</b>–<b>m</b>), and eADO (<b>n</b>–<b>q</b>) by PGE2 (10 μM) in the presence of vehicle (n = 8) or of the EP1 antagonist SC51322 (1 μM, n = 5) (<b>b</b>,<b>f</b>,<b>g</b>,<b>n</b>), the EP2 receptor antagonist PF04418948 (1 μM, n = 5) (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>), the EP3 receptor antagonist L-798,106 (0.25 μM, n = 9) (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>), and the EP4 antagonist L-161,982 (1 μM, n = 4) (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>). n, number of bladder preparations. Asterisks denote significant differences from the vehicle control (n = 6). * <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, **** <span class="html-italic">p</span> &lt; 0.0001. Open circles denote significant differences of eATP degradation in PGE<sub>2</sub> alone vs. EP receptor antagonist + PGE<sub>2</sub>. <sup>o</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>oo</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>ooo</sup> <span class="html-italic">p</span> &lt; 0.001, <sup>oooo</sup> <span class="html-italic">p</span> &lt; 0.0001. Two-way ANOVA with Tukey’s multiple comparisons test.</p>
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<p>eATP hydrolysis by s-NTDs released in EL solutions of nondistended or distended bladder preparations treated with exogenous PGE<sub>2</sub> or PGF<sub>2α</sub> in the absence or presence of an FP prostanoid receptor antagonist. Original chromatograms showing the eATP degradation after 60 min of contact with the EL solutions of nondistended and distended bladders (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease and the increase in eADP, eAMP, and eADO in EL solutions of nondistended (<b>b</b>,<b>f</b>,<b>j</b>,<b>n</b>) or distended (<b>c</b>,<b>g</b>,<b>k</b>,<b>o</b>) bladders treated with PGE<sub>2</sub> (n = 8) or AL8810 + PGE2 (n = 4). Effects of PGF<sub>2α</sub> (n = 6) or AL8810 + PGF<sub>2α</sub> (n = 4) on time courses of eATP hydrolysis to eADP, eAMP, and eADO in EL solutions of nondistended (<b>d</b>,<b>h</b>,<b>l</b>,<b>p</b>) or distended (<b>e</b>,<b>i</b>,<b>m</b>,<b>q</b>) bladders are shown in the panels to the right of the solid black line. n, number of bladder preparations. Asterisks denote significant differences vs. the vehicle controls (n = 6). * <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, **** <span class="html-italic">p</span> &lt; 0.0001. Open circles denote significant differences of eATP degradation in PG alone vs. AL8810 + PG. <sup>o</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>oo</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>ooo</sup> <span class="html-italic">p</span> &lt; 0.001, <sup>oooo</sup> <span class="html-italic">p</span> &lt; 0.0001. Two-way ANOVA with Tukey’s multiple comparisons test.</p>
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<p>eATP hydrolysis by s-NTDs released in EL solutions of nondistended bladder preparations treated with exogenous PGD<sub>2</sub> in the absence or presence of DP prostanoid receptor antagonists. Original HPLC chromatograms showing the eATP degradation after 60 min of contact with the EL solutions (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>d</b>) and the increase in eADP (<b>e</b>–<b>g</b>), eAMP (<b>h</b>–<b>j</b>), and eADO (<b>k</b>–<b>m</b>) by PGD2 (10 μM, n = 7) in the presence of vehicle or of the DP1 antagonist S-5751 (1 μM, n = 4) (<b>b</b>,<b>e</b>,<b>h</b>,<b>k</b>), the DP2 receptor antagonist OC000459 (10 μM, n = 4) (<b>c</b>,<b>f</b>,<b>i</b>,<b>l</b>), and the dual CRTH2/DP receptor antagonist AMG 853 (1 μM, n = 4) (<b>d</b>,<b>g</b>,<b>j</b>,<b>m</b>). n, number of bladder preparations. Asterisks denote significant difference from the vehicle control (n = 6). Black asterisks denote significant differences of PGD<sub>2</sub> effects from the vehicle control; colored asterisks denote significant differences of DP receptor antagonist + PGD<sub>2</sub> from the vehicle control. * <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, **** <span class="html-italic">p</span> &lt; 0.0001. Open circles denote significant differences of eATP degradation in PGD<sub>2</sub> alone vs. DP receptor antagonist + PGD<sub>2</sub>. <sup>o</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>oo</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>ooo</sup> <span class="html-italic">p</span> &lt; 0.001, <sup>oooo</sup> <span class="html-italic">p</span> &lt; 0.0001. Two-way ANOVA with Tukey’s multiple comparisons test.</p>
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<p>eATP hydrolysis by s-NTDs released in EL solutions of distended bladder preparations treated with exogenous PGD<sub>2</sub> in the absence or presence of DP prostanoid receptor antagonists. Original HPLC chromatograms showing the eATP degradation after 60 min of contact with the EL solutions (<b>a</b>). The scale in the first panel applies to all chromatograms. LU, luminescence units. Summarized results demonstrating time courses of the eATP decrease (<b>b</b>–<b>d</b>) and the increase in eADP (<b>e</b>–<b>g</b>), eAMP (<b>h</b>–<b>j</b>), and eADO (<b>k</b>–<b>m</b>) by PGD2 (10 μM, n = 7) in the presence of vehicle or of the DP1 antagonist S-5751 (1 μM, n = 4) (<b>b</b>,<b>e</b>,<b>h</b>,<b>k</b>), the DP2 receptor antagonist OC000459 (10 μM, n = 4) (<b>c</b>,<b>f</b>,<b>i</b>,<b>l</b>), and the dual CRTH2/DP receptor antagonist AMG 853 (1 μM, n = 4) (<b>d</b>,<b>g</b>,<b>j</b>,<b>m</b>). n, number of bladder preparations. Asterisks denote significant differences from the vehicle control (n = 6). Black asterisks denote significant differences of PGD<sub>2</sub> effects from the vehicle control; colored (red, blue, brown, green) asterisks denote significant difference of DP receptor antagonist + PGD<sub>2</sub> from the vehicle control. * <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, **** <span class="html-italic">p</span> &lt; 0.0001. Open circles denote significant differences of eATP degradation in PGD<sub>2</sub> alone vs. DP receptor antagonist + PGD<sub>2</sub>. <sup>o</sup> <span class="html-italic">p</span> &lt; 0.05, <sup>oo</sup> <span class="html-italic">p</span> &lt; 0.01, <sup>ooo</sup> <span class="html-italic">p</span> &lt; 0.001, <sup>oooo</sup> <span class="html-italic">p</span> &lt; 0.0001. Two-way ANOVA with Tukey’s multiple comparisons test.</p>
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19 pages, 1965 KiB  
Article
Purple Yampee Derivatives and Byproduct Characterization for Food Applications
by Sandra V. Medina-López, Cristian Molina García, Maria Cristina Lizarazo-Aparicio, Maria Soledad Hernández-Gómez and Juan Pablo Fernández-Trujillo
Foods 2024, 13(24), 4148; https://doi.org/10.3390/foods13244148 - 21 Dec 2024
Viewed by 578
Abstract
This study assessed the technological potential and bioactive compounds present in purple yampee (Dioscorea trifida L.f.) lyophilized powder, peeled and whole flour, as well as the tuber peel, starch residual fiber, and wastewater mucilage. Although most values approached neutrality, flour showed a [...] Read more.
This study assessed the technological potential and bioactive compounds present in purple yampee (Dioscorea trifida L.f.) lyophilized powder, peeled and whole flour, as well as the tuber peel, starch residual fiber, and wastewater mucilage. Although most values approached neutrality, flour showed a lower pH and high density, while greater acidity was observed in the mucilage. Color differed statistically and perceptibly between all samples, with similar values of °hue to purple flours from other sources, and the maximum chroma was found in lyophilized pulp and lightness in fiber. Average moisture levels around 7.2% and water activity levels of 0.303 (0.194 for whole flour) in fractions suggested favorable storability, while the interaction of the powders with water was similar to other root and tuber powdered derivatives. Yampee periderm had the highest swelling power, oil absorption capacity, water holding capacity, and absorption index and capacity. Mucilage had a higher solubility index and outstanding emulsion activity, greater than 90%. Twelve anthocyanins, with new reports of petunidin derivatives for the species, and more than 30 phytochemicals were identified through advanced liquid chromatography techniques. The greatest amounts of pinitol and myo-inositol were found in the mucilage, and sucrose, glucose, and fructose prevailed in the other powders. Successfully characterized yampee fractions showed high potential as functional food ingredients. Full article
(This article belongs to the Section Food Security and Sustainability)
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Graphical abstract

Graphical abstract
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<p>Photos of powdered fractions and simulated colors of (<b>a</b>) YSF, (<b>b</b>) YSM, (<b>c</b>) LYP, (<b>d</b>) YPF, (<b>e</b>) WTP, and (<b>f</b>) YPP.</p>
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<p>Amino acids in <span class="html-italic">D. trifida</span> mucilage (<b>upper</b> chromatogram) and lyophilized pulp (<b>under</b>) observed through HPLC-FLD.</p>
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<p>Amino acids in <span class="html-italic">D. trifida</span> mucilage (<b>upper</b> chromatogram) and lyophilized pulp (<b>under</b>) observed through HPLC-FLD.</p>
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<p>Main anthocyanin compounds identified at 520 nm through HPLC-DAD in <span class="html-italic">D. trifida</span> fractions after 20 days from their manufacture.</p>
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<p>Main anthocyanins quantified in <span class="html-italic">D. trifida</span> fractions mucilage YSM, lyophilized pulp LYP, starch fiber, flour, periderm, and whole flour from left to right, after 20-day storage. Main peonidin derivatives are depicted as follows: Peonidin 3-<span class="html-italic">O</span>-glucoside-5-<span class="html-italic">O</span>glucoside (Peonidin 1), Peonidin 3-O-feruloylglucoside-5-O-glucoside (Peonidin 2), and Peonidin 3-O-<span class="html-italic">p</span>-cumaroylglucoside-5-O-glucoside (Peonidin 3). The average concentration of the molecules (<span class="html-italic">n</span> = 3) is presented in milligrams per 100 g of sample, letters correspond to significant statistical differences among fractions (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>The evolution of sugars in time (day 43 -darker color- and 180 of storage) for each fraction depicted by individually quantified sugars (<b>a</b>) Myo-inositol, (<b>b</b>) Pinitol, (<b>c</b>) Glucose, (<b>d</b>) Fructose, (<b>e</b>) Sucrose. Concentrations of each measure are depicted as mean values with standard deviation error bars (<span class="html-italic">n</span> = 3). Means in a column followed by different lowercase letters (a–f) are significantly different at the 5% level at the initial time of measure. Means in the columns followed by different capital letters (A–E) are significantly different at the 5% level.</p>
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33 pages, 21111 KiB  
Review
A Review on Sheet Metal Forming Behavior in High-Strength Steels and the Use of Numerical Simulations
by Luis Fernando Folle, Tiago Nunes Lima, Matheus Passos Sarmento Santos, Bruna Callegari, Bruno Caetano dos Santos Silva, Luiz Gustavo Souza Zamorano and Rodrigo Santiago Coelho
Metals 2024, 14(12), 1428; https://doi.org/10.3390/met14121428 - 13 Dec 2024
Viewed by 615
Abstract
High-strength steels such as Dual Phase (DP), Transformation-Induced Plasticity (TRIP), and Twinning-Induced Plasticity (TWIP) steels have gained importance in automotive applications due to the potential for weight reduction and increased performance in crash tests. However, as resistance increases, there is also an increase [...] Read more.
High-strength steels such as Dual Phase (DP), Transformation-Induced Plasticity (TRIP), and Twinning-Induced Plasticity (TWIP) steels have gained importance in automotive applications due to the potential for weight reduction and increased performance in crash tests. However, as resistance increases, there is also an increase in springback due to residual stresses after the forming process. This is mainly because of the greater elastic region of these materials and other factors associated with strain hardening, such as the Bauschinger effect, that brings theory of kinematic hardening to mathematical modeling. This means that finite element software must consider these properties so that the simulation can accurately predict the behavior. Currently, this knowledge is still not widespread since it has never been used in conventional materials. Additionally, engineers and researchers use the Forming Limit Diagram (FLD) curve in their studies. However, it does not fully represent the actual failure limit of materials, especially in high-strength materials. Based on this, the Fracture Forming Limit Diagram (FFLD) curve has emerged, which proposes to resolve these limitations. Thus, this review aims to focus on how finite element methods consider all these factors in their modeling, especially when it comes to the responses of high-strength steels. Full article
(This article belongs to the Special Issue Modeling, Simulation and Experimental Studies in Metal Forming)
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Figure 1

Figure 1
<p>Advanced high-strength steels developed for automotive applications [<a href="#B20-metals-14-01428" class="html-bibr">20</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Example of springback in sheet metal bent at 90° [<a href="#B34-metals-14-01428" class="html-bibr">34</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Effect of springback on high-strength steels [<a href="#B35-metals-14-01428" class="html-bibr">35</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Springback effect after (<b>a</b>) bending in deep drawing [<a href="#B36-metals-14-01428" class="html-bibr">36</a>] and (<b>b</b>) V-bending. Reproduced with permission from Elsevier, 2024.</p>
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<p>Influence of bending and straightening on residual stresses during deep drawing of metallic sheets.</p>
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<p>(<b>a</b>) Standard geometry used for the study of springback; (<b>b</b>) measurements made on the part after bending [<a href="#B36-metals-14-01428" class="html-bibr">36</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Convergence analysis on the axial loading value (normalized) as a function of the density and the element type. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B39-metals-14-01428" class="html-bibr">39</a>].</p>
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<p>The error in the axial loading estimation as a function of the CPU time, for different element types and numbers of elements. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B39-metals-14-01428" class="html-bibr">39</a>].</p>
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<p>Shell element with integration points in the thickness.</p>
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<p>Strain stages in a tensile test for a conventional material.</p>
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<p>Types of localized failure that can occur through void nucleation: (<b>a</b>) Failure by localized shear plastic without necking, (<b>b</b>) Failure by localized shear plastic after necking and (<b>c</b>) Failure by void coalescence with obvious necking [<a href="#B53-metals-14-01428" class="html-bibr">53</a>]. Reproduced with permission from John Wiley and Sons, 2024.</p>
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<p>Examples of behavior under fracture of 3 metals [<a href="#B54-metals-14-01428" class="html-bibr">54</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Two types of mechanisms for void coalescence: (<b>a</b>) parallel connection between voids; (<b>b</b>) void shear connection [<a href="#B55-metals-14-01428" class="html-bibr">55</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Two failure mechanisms: necking for SPCC and SPRC and ductile fracture for other sheet metals. SPCC and SPRC are conventional carbon steels [<a href="#B56-metals-14-01428" class="html-bibr">56</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Forming Limit Diagram obtained by measuring the diffuse necking: (<b>a</b>) specimens, (<b>b</b>) fracture regions, and (<b>c</b>) plotted curve.</p>
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<p>Visualization of the circles used in the Nakajima test to obtain the main strains [<a href="#B57-metals-14-01428" class="html-bibr">57</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Location of positions where deformations can be measured. (<b>a</b>) In the necking zone. (<b>b</b>) Out of the necking zone. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B58-metals-14-01428" class="html-bibr">58</a>].</p>
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<p>Comparison between FLD (black and red) and FFLD (blue) curves: (<b>a</b>) in the space of major and minor principal strains; (<b>b</b>) in the space of stress triaxiality and equivalent strain to failure [<a href="#B76-metals-14-01428" class="html-bibr">76</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Global strain status, experimental FLC, and damage: (<b>a</b>) results at the integration points located on the negative surface; (<b>b</b>) results at the integration points located on the positive surface [<a href="#B76-metals-14-01428" class="html-bibr">76</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Comparison of the (<b>a</b>) experiment and (<b>b</b>) simulation [<a href="#B76-metals-14-01428" class="html-bibr">76</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Comparison between results obtained in a (<b>a</b>) simulation using the FLC curve and (<b>b</b>) a simulation using the MMC fracture criterion of an automotive front rail made from DP780 steel [<a href="#B73-metals-14-01428" class="html-bibr">73</a>]. Reproduced with permission from SAE international, 2024.</p>
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<p>Fracture strain versus stress triaxiality and Lode angle simulated. Figure reproduced under Creative Commons Attribution 3.0 International License from [<a href="#B88-metals-14-01428" class="html-bibr">88</a>].</p>
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<p>Mathematical adjustment curves for tensile testing. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B92-metals-14-01428" class="html-bibr">92</a>].</p>
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<p>Comparison of tensile test data with Bulge test. Figure reproduced under Creative Commons Attribution 3.0 International License from [<a href="#B93-metals-14-01428" class="html-bibr">93</a>].</p>
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<p>Three main directions of anisotropy measurements in the sheet rolling Direction.</p>
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<p>Compressed disk specimens of AA2090-T3 using different lubricants and at different thickness strains (ε<sub>z</sub>) [<a href="#B80-metals-14-01428" class="html-bibr">80</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Strains measured in samples after the disk compression test [<a href="#B80-metals-14-01428" class="html-bibr">80</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Calculation of the biaxial anisotropy coefficient. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B103-metals-14-01428" class="html-bibr">103</a>].</p>
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<p>Comparison of true stress–strain curves determined by uniaxial tension and Bulge test for 3 different steels [<a href="#B104-metals-14-01428" class="html-bibr">104</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Schematic representation of the Bauschinger effect.</p>
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<p>Typical tensile–compression test [<a href="#B104-metals-14-01428" class="html-bibr">104</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Stress–strain curves of the tensile test under loading–unloading–reloading condition for determination of Young’s modulus of elasticity at different pre-strains [<a href="#B104-metals-14-01428" class="html-bibr">104</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Young’s modulus change with plastic strain.</p>
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<p>Scheme of a tribological system in sheet forming. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B116-metals-14-01428" class="html-bibr">116</a>].</p>
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<p>The 3D images and mean roughness Rz values of bionic structures (<b>a</b>) St1, (<b>b</b>) St2, (<b>c</b>) St3, (<b>d</b>) St4 (<b>e</b>) St5, and (<b>f</b>) flat reference surface [<a href="#B118-metals-14-01428" class="html-bibr">118</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Friction coefficient results obtained [<a href="#B118-metals-14-01428" class="html-bibr">118</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Coefficient of friction under different contact pressures [<a href="#B120-metals-14-01428" class="html-bibr">120</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Friction variation with working temperature: (<b>a</b>) Variation curves of the friction coefficient with time under different temperatures; (<b>b</b>) Experimental friction coefficients at different temperatures. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B121-metals-14-01428" class="html-bibr">121</a>].</p>
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<p>Results of the coefficient of friction as a function of sliding speed and contact pressure. Figure reproduced under Creative Commons Attribution 4.0 International License from [<a href="#B122-metals-14-01428" class="html-bibr">122</a>].</p>
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<p>Comparison of springback for different mesh sizes in finite element simulation [<a href="#B38-metals-14-01428" class="html-bibr">38</a>]. Reproduced with permission from Springer Nature, 2024.</p>
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<p>Comparison of springback for different time steps in finite element simulation [<a href="#B38-metals-14-01428" class="html-bibr">38</a>]. Reproduced with permission from Springer Nature, 2024.</p>
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<p>The comparison of calculated springback between isotropic and kinematic hardening mode [<a href="#B38-metals-14-01428" class="html-bibr">38</a>]. Reproduced with permission from Springer Nature, 2024.</p>
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<p>Finite element simulation results for DP980 in a springback test: (<b>a</b>) θ<sub>1</sub>, (<b>b</b>) θ<sub>2</sub>, and (<b>c</b>) sidewall radius ρ [<a href="#B36-metals-14-01428" class="html-bibr">36</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Finite element simulation results for TWIP980 in a springback test: (<b>a</b>) θ<sub>1</sub>, (<b>b</b>) θ<sub>2</sub>, and (<b>c</b>) sidewall radius ρ [<a href="#B36-metals-14-01428" class="html-bibr">36</a>]. Reproduced with permission from Elsevier, 2024.</p>
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<p>Numerical simulation results for models with constant and variable friction [<a href="#B120-metals-14-01428" class="html-bibr">120</a>]. Reproduced with permission from Elsevier, 2024.</p>
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12 pages, 2329 KiB  
Article
Detection of Total Aflatoxins in Herbal Medicines Based on Lateral Flow Assay with Contamination Ratio Model
by Xiao-Ya Qin, Rui Feng, Heng Zhou, Hui-Qin Pan, Hao Wang, Xiao-Jing Huang, Jian-Ying Shen, Qing Hu and Shen Ji
Molecules 2024, 29(24), 5827; https://doi.org/10.3390/molecules29245827 - 10 Dec 2024
Viewed by 467
Abstract
In this study, we developed a colloidal gold immunochromatographic strip (CGIS) method that used the matrix-matched calibration curves of contamination ratio models to quantitatively determine the total aflatoxin in five herbal medicines. This approach addresses issues related to false results and poor accuracy [...] Read more.
In this study, we developed a colloidal gold immunochromatographic strip (CGIS) method that used the matrix-matched calibration curves of contamination ratio models to quantitatively determine the total aflatoxin in five herbal medicines. This approach addresses issues related to false results and poor accuracy associated with conventional methods. The CGIS was analyzed using a Vertu touch reader, and the matrix-matched calibration was established based on the absorbance ratios of the T and C lines, as well as the logarithmic values of the total aflatoxin concentrations. The total aflatoxins could be accurately and digitally detected from 2.5 to 40 μg/kg, and the LOD of total aflatoxins was 1 μg/kg in the five herbal medicines. The recovery rates from the spiked samples ranged from 65.1% to 98.6%, and the RSD was less than 16.9%. A total of 229 samples were analyzed by both CGIS and HPLC-FLD, with agreement ranging from 78.4% to 132.6% (Arecae semen), 82.6% to 133.0% (Nelumbinis semen), 79.9% to 117.9% (Coicis semen), 78.1% to 119.0% (Platycladi semen), and 76.1% to 123.0% (Ziziphi spinosae semen). This process for the discrimination of the CGIS results was established to assess if samples met the requirement of aflatoxin limits, which could save approximately 75% in time and reduce the workload of retesting by a designated confirmatory reference method to less than 10%. This study demonstrated that the application of matrix-matched calibration curves based on contamination ratio models to CGIS can effectively enhance the rapid quantitative determination capability of total aflatoxins in herbal medicine matrices. Full article
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<p>The agreements of <span class="html-italic">A. semen</span> samples were determined under different calibration curves.</p>
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<p>The agreements of <span class="html-italic">A. semen</span> samples were determined under different calibration curves.</p>
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<p>The distribution of the four types of aflatoxins in <span class="html-italic">A. semen</span> (<b>A</b>), <span class="html-italic">N. semen</span> (<b>B</b>), <span class="html-italic">C. semen</span> (<b>C</b>), <span class="html-italic">P. semen</span> (<b>D</b>), and <span class="html-italic">Z. spinosae semen</span> (<b>E</b>), respectively.</p>
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<p>The calibration curves for aflatoxin detection. The four-parametric logistic calibration curves were created by plotting the ratio of T and C against the concentration of aflatoxins (the calibration curve concentration was obtained by HPLC-FLD detection) in <span class="html-italic">A. semen</span> (<b>A</b>), <span class="html-italic">N. semen</span> (<b>B</b>), <span class="html-italic">C. semen</span> (<b>C</b>), <span class="html-italic">P. semen</span> (<b>D</b>), <span class="html-italic">Z. spinosae semen</span> (<b>E</b>), and the solvent standard (<b>F</b>), respectively.</p>
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<p>The flow chart for the process of judging the CGIS results. Sample results categorized as “uncertain” should be reinspected by HPLC-FLD or LC-MS/MS method for confirmation.</p>
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<p>The distribution of the AFs-positive rate (<b>A</b>), AFs-positive samples at different levels (<b>B</b>), and sample results categorized as qualified, unqualified and uncertain (<b>C</b>).</p>
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<p>Correlation between CGIS and HPLC-FLD results of <span class="html-italic">A. semen</span> (<b>A</b>), <span class="html-italic">N. semen</span> (<b>B</b>), <span class="html-italic">C. semen</span> (<b>C</b>), <span class="html-italic">P. semen</span> (<b>D</b>), and <span class="html-italic">Z. spinosae semen</span> (<b>E</b>) samples.</p>
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13 pages, 4786 KiB  
Article
Influence of Temperature on the Damping Properties of Selected Viscoelastic Materials
by Lucjan Witek and Piotr Łabuński
Materials 2024, 17(23), 5832; https://doi.org/10.3390/ma17235832 - 28 Nov 2024
Viewed by 563
Abstract
The paper presents results of experimental investigations of the influence of temperature on the effectiveness of passive vibration isolation. Two types of viscoelastic materials (butyl rubber and bituminous material) were tested. In the performed vibration analysis, the Oberst beam made out of aluminum [...] Read more.
The paper presents results of experimental investigations of the influence of temperature on the effectiveness of passive vibration isolation. Two types of viscoelastic materials (butyl rubber and bituminous material) were tested. In the performed vibration analysis, the Oberst beam made out of aluminum alloy with a damping material in a Free Layer Damping (FLD) configuration was used. The experimental modal analysis was performed using the Unholtz-Dickie UDCO TA-250 vibration system. To investigate the influence of temperature on the effectiveness of passive vibration isolation, an isothermal cooling chamber (using Peltier cells) was designed and constructed. The tests were carried out in a wide frequency range from 40 Hz to 4000 Hz, at a constant sweep rate, in a temperature range from −2 °C to 22 °C. Miniature piezoelectric acceleration sensors were used to determine the acceleration of the beam and the exciter head. The analysis of accelerations of both the object and the shaker head allowed for the determination of a Frequency Response Function (FRF) for the beam. The course of FRF was used to determine the resonance frequencies and the vibration amplitudes of the beam damped with bituminous material and butyl rubber at various temperatures. The loss factor η, calculated for each resonance using the generalized half-power method (n-dB method), was used as an indicator of damping intensity. The research results presented in this work (important from scientific point of view) also have utilitarian significance and can be used in the design of more quiet and comfortable motor vehicles, railway wagons and aircraft structures. Full article
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<p>Electromagnetic vibration shaker and amplifier used in experimental modal analysis.</p>
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<p>Diagram of the cooling chamber built above the vibration exciter.</p>
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<p>The interior of the cooling chamber with visible piezoelectric acceleration sensors, temperature sensor and the tested beam.</p>
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<p>Vibration exciter with a closed cooling chamber and a heat sink for cooling the hot side of the Peltier cells.</p>
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<p>Dimensions and structure of specimen.</p>
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<p>Frequency response curves of specimen damped by the butyl rubber in examined temperatures (frequency range of 40 Hz–4000 Hz).</p>
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<p>Frequency response curves of beam damped by the butyl rubber in examined temperatures (frequency range of 40 Hz–700 Hz, modes 2, 3, 4, 5).</p>
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<p>Loss factor η of beam damped by the butyl rubber as a function of temperature for selected modes (mode no. 2 (51.6 Hz–56.5 Hz) and mode no. 5 (467.2 Hz–598.9 Hz)).</p>
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<p>Frequency response curves of specimen damped by the bituminous material in the examined temperatures (frequency range of 40 Hz–4000 Hz).</p>
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<p>Frequency response curves of specimen damped by the bituminous material in the examined temperatures (frequency range of 40 Hz–1300 Hz, modes 2, 3, 4, 5).</p>
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<p>Loss factor η of beam damped by bituminous material as a function of temperature for selected modes (mode no. 2 (61.6 Hz–86.7 Hz) and mode no. 4 (338.4 Hz–531.4 Hz)).</p>
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25 pages, 8713 KiB  
Article
The Effect of Specimen Width on the Deformation Behavior and Formability of cp-Ti Grade 4 Sheets During Uniaxial and Cyclic Bending Under Tension Loading
by Desmond Mensah, Nicholas Pitkin, Michael P. Miles, David T. Fullwood, Marko Knezevic and Brad Kinsey
Materials 2024, 17(23), 5756; https://doi.org/10.3390/ma17235756 - 25 Nov 2024
Viewed by 592
Abstract
This study examines the specimen size-dependent deformation behavior of commercially pure titanium grade 4 (cp-Ti grade 4) sheets under tension, with strain paths between uniaxial tension (UT) and plane-strain tension and compares the results with cyclic bending under tension (CBT) data. Specimens of [...] Read more.
This study examines the specimen size-dependent deformation behavior of commercially pure titanium grade 4 (cp-Ti grade 4) sheets under tension, with strain paths between uniaxial tension (UT) and plane-strain tension and compares the results with cyclic bending under tension (CBT) data. Specimens of varying widths (11.7, 20, 60, 100, and 140 mm) were tested in both rolling (RD) and transverse (TD) directions. The research employed digital image correlation for full-field strain measurements, finite element simulations, and fracture surface thickness data. Contrary to traditional forming concepts, i.e., the forming limit diagram (FLD) has the lowest major strain at the plane-strain condition, and the fracture forming limit has decreased major strain with increasing (less negative) minor strain, wider specimens exhibited higher major strains at strain localization and fracture under UT. In contrast, CBT findings showed decreased formability with increasing width, i.e., closer to plane-strain deformation, as expected. Strain distribution analyses revealed a transition from nearly uniform deformation in narrow specimens to multiaxial strain states in wider specimens. Thickness measurements along the fracture surface revealed a steeper profile in UT compared to CBT, indicating more localized deformation and necking in UT. In comparison with AA6016-T4, the cp-Ti grade 4 showed greater thickness, suggesting lower susceptibility to localized thinning. Strong anisotropy was observed between the RD and TD, with TD specimens showing higher formability and steeper thickness gradients in UT. Strain fields, along with thickness reduction and adiabatic heating, are used to rationalize the observed width-sensitive deformation behavior of cp-Ti sheets. Notably, CBT improved overall formability compared to UT due to its ability to distribute strain more evenly and delay critical necking. The contrasting trends between simple UT and CBT emphasize the relationship between loading conditions, specimen geometry, and material behavior in determining formability. These findings highlight the ability of the CBT test to create known and desired deformation effects, i.e., lower major strain at failure with increasing specimen width, and more uniform deformation, i.e., consistent thinning across the specimen width, for cp-Ti. Given the observed effects of width in UT, the selection of the testing method is critical for cp-Ti to ensure that results reflect expected material behavior. Full article
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<p>Schematic representation of the principal strain space showing the forming limit curve (FLC), the fracture forming limit (FFL), and an idealized strain path with arrows obtained in a sheet metal formability test utilized for determining these limit curves [<a href="#B6-materials-17-05756" class="html-bibr">6</a>].</p>
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<p>Stress–strain curves of as-received 1 mm sheets of cp-Ti measured along the rolling (RD) and transverse (TD) directions during standard uniaxial tension under 0.001/s strain rate at room temperature.</p>
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<p>Geometries of the uniaxial tension specimens for all widths: <a href="#materials-17-05756-t003" class="html-table">Table 3</a> contains the dimensions for each sample and explanation of the alphabetical labels.</p>
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<p>Experimental setup in MTS with a DIC camera and light source for strain measurements.</p>
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<p>“Apparent” engineering stress–strain curves of uniaxial tension of cp-Ti grade 4 RD, cp-Ti grade TD, and AA6016-T4 RD at a strain rate of ~0.001/s.</p>
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<p>DIC strain contour plots at peak stress and just before fracture across different widths for (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade 4 TD, and (<b>c</b>) AA6016-T4 RD, as well as (<b>d</b>) a comparison between cp-Ti grade 4 RD experiments and simulations at peak stress.</p>
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<p>DIC strain contour plots at peak stress and just before fracture across different widths for (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade 4 TD, and (<b>c</b>) AA6016-T4 RD, as well as (<b>d</b>) a comparison between cp-Ti grade 4 RD experiments and simulations at peak stress.</p>
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<p>DIC strain contour plots at peak stress and just before fracture across different widths for (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade 4 TD, and (<b>c</b>) AA6016-T4 RD, as well as (<b>d</b>) a comparison between cp-Ti grade 4 RD experiments and simulations at peak stress.</p>
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<p>Strain paths to failure for all specimen widths of (<b>a</b>) cp-Ti grade 4 RD, cp-Ti grade TD, and AA6016-T4 RD under UT, and (<b>b</b>) cp-Ti grade 4 RD under UT and CBT loading.</p>
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<p>Strain paths to failure for all specimen widths of (<b>a</b>) cp-Ti grade 4 RD, cp-Ti grade TD, and AA6016-T4 RD under UT, and (<b>b</b>) cp-Ti grade 4 RD under UT and CBT loading.</p>
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<p>Effect of specimen width on engineering strain at fracture for cp-Ti grade 4 in UT the RD and TD, as well as the CBT RD, and the AA6016-T4 RD.</p>
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<p>Limit strains at peak engineering stress values, i.e., necking, for all specimen widths of (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade TD, and (<b>c</b>) AA6016-T4 RD; (<b>d</b>) major and minor limit strains at the center of specimens for all materials and direction.</p>
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<p>Fracture surface thickness variation across different widths for (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade 4 TD, (<b>c</b>) AA6016-T4 RD, and (<b>d</b>) cp-Ti grade 4 RD CBT.</p>
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<p>Evolution of center specimen thinning strain rate versus engineering strain for (<b>a</b>) cp-Ti grade 4 RD, (<b>b</b>) cp-Ti grade 4 TD, and (<b>c</b>) AA6016 RD with varying specimen widths from 11.7 mm to 140 mm.</p>
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<p>Stress triaxiality with equivalent plastic strain at peak stress (UTS) at two positions across specimen widths for cp-Ti grade 4 RD.</p>
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<p>(<b>a</b>) Schematic of the near-plane-strain specimen geometry and (<b>b</b>) comparison of strain paths between 100 mm wide near-plane-strain and uniaxial tension results for cp-Ti RD.</p>
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<p>Temperature evolution versus engineering strain for the cp-Ti grade 4 TD specimens of 11.7 and 100 mm widths, with inset thermal images showing heat distribution patterns at the final frame prior to fracture.</p>
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<p>Inverse pole figure (IPF) map of undeformed grain structure in cp-Ti grade 4 sheets [<a href="#B32-materials-17-05756" class="html-bibr">32</a>,<a href="#B33-materials-17-05756" class="html-bibr">33</a>].</p>
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<p>Stereographic pole figures showing texture in undeformed cp-Ti grade 4 sheets [<a href="#B32-materials-17-05756" class="html-bibr">32</a>,<a href="#B33-materials-17-05756" class="html-bibr">33</a>].</p>
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<p>FE meshes for one half of the 11.7 mm and 140 mm specimens consisting of C3D8R elements along with the boundary conditions constructed in Abaqus for simulating the uniaxial tensile tests.</p>
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<p>Photograph of cp-Ti grade 4 RD fractured specimens for all widths.</p>
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<p>Photograph of cp-Ti grade 4 TD fractured specimens for all widths.</p>
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<p>Photograph of AA6016-T4 RD fractured specimens for all widths.</p>
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15 pages, 2062 KiB  
Article
A Pre-Column Derivatization Method for the HPLC-FLD Determination of Dimethyl and Diethyl Amine in Pharmaceuticals
by Georgios Kamaris, Maria Tsami, Georgiana-Roxana Lotca, Sofia Almpani and Catherine K. Markopoulou
Molecules 2024, 29(23), 5535; https://doi.org/10.3390/molecules29235535 - 23 Nov 2024
Viewed by 905
Abstract
In recent years, the detection of nitrosamine precursors has become an important issue for regulatory authorities such as the European Medicines Agency (EMA) and the Food and Drug Administration (FDA). The present study provides a pre-column derivatization method for the analysis of dimethylamine [...] Read more.
In recent years, the detection of nitrosamine precursors has become an important issue for regulatory authorities such as the European Medicines Agency (EMA) and the Food and Drug Administration (FDA). The present study provides a pre-column derivatization method for the analysis of dimethylamine (DMA) and diethylamine (DEA) in pharmaceutical products using HPLC and a fluorescence detector. Appropriate chromatographic parameters, including mobile phase composition (organic solvent, buffer, pH), elution type, flow rate, temperature, and λexcitation/emission, were investigated. Analysis was performed at λexcitation = 450 nm and λemission = 540 nm on a C18 column (at 40 °C) using gradient elution as a mobile phase with Eluent A: Phosphoric Acid Buffer (20 mM, pH = 2.8) and Eluent B: methanol, with a flow of 0.8 mL/min. The method was validated according to ICH specifications in terms of linearity (0.5–10 ng/mL for DMA and 5–100 ng/mL for DEA), specificity, and robustness, as well as repeatability, intermediate precision (%RSD < 2.9), and accuracy (% recovery 98.2–102.0%). The derivatization process was optimized using the “Crossed D-Optimal” experimental design procedure, where one mixture component was cross-correlated with two factors. The stability of the samples was studied over a period of one month. To process the samples (pharmaceuticals), various purification techniques were tried using solid/liquid or liquid/liquid extraction with dichloromethane. Finally, a straightforward solid-phase extraction (SPE, C18) method was chosen prior to derivatization. The method was successfully applied, since the extraction recoveries were >81.6% for DMA (0.5 ppm) and >81.1% for DEA (5 ppm). Based on the results obtained and the available literature, the scientific community seeks, by proposing flexible analytical methods, to delimit the problem of nitrosamines. Full article
(This article belongs to the Special Issue Applications of Fluorescent Sensors in Food and Environment)
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<p>Reaction between NBD-Cl and (<b>a</b>) DMA, (<b>b</b>) DEA.</p>
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<p>Stability test for NBD-DMA (blue) and NBD-DEA (orange) derivatives.</p>
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<p>Chromatograms of blank (pink) and diluted standard mix (black) of DΜA and DΕA (C<sub>DMA</sub> = 10 ng/mL and C<sub>DMA</sub> = 100 ng/mL).</p>
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<p>Sample preparation steps.</p>
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<p>Chromatograms of (<b>A</b>) blank diluent (red), blank after SPE and derivatization (pink), unspike for Uniphyllin tablets (black) and spiked for Uniphyllin tablets (blue); (<b>B</b>) blank diluent (red), blank after SPE and derivatization (pink) unspike for Xylosan 2% (brown) and spiked for Xylosan 2% (blue).</p>
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11 pages, 2116 KiB  
Article
Enzymatic Oxidation of Aflatoxin M1 in Milk Using CotA Laccase
by Yongpeng Guo, Hao Lv, Zhiyong Rao, Zhixiang Wang, Wei Zhang, Yu Tang and Lihong Zhao
Foods 2024, 13(22), 3702; https://doi.org/10.3390/foods13223702 - 20 Nov 2024
Viewed by 606
Abstract
Aflatoxin M1 (AFM1) in milk poses a significant threat to human health. This study examined the capacity of Bacillus licheniformis CotA laccase to oxidize AFM1. The optimal conditions for the CotA laccase-catalyzed AFM1 oxidation were observed at [...] Read more.
Aflatoxin M1 (AFM1) in milk poses a significant threat to human health. This study examined the capacity of Bacillus licheniformis CotA laccase to oxidize AFM1. The optimal conditions for the CotA laccase-catalyzed AFM1 oxidation were observed at pH 8.0 and 70 °C, achieving an AFM1 oxidation rate of 86% in 30 min. The Km and Vmax values for CotA laccase with respect to AFM1 were 18.91 μg mL−1 and 9.968 μg min−1 mg−1, respectively. Computational analysis suggested that AFM1 interacted with CotA laccase via hydrogen bonding and van der Waals interactions. Moreover, the oxidation products of AFM1 mediated by CotA laccase were identified as the C3-hydroxy derivatives of AFM1 by HPLC-FLD and UPLC-TOF/MS. Toxicological assessment revealed that the hepatotoxicity of AFM1 was substantially reduced following oxidation by CotA laccase. The efficacy of CotA laccase in removing AFM1 in milk was further tested, and the result showed that the enzyme agent achieved an AFM1 removal rate of 83.5% in skim milk and 65.1% in whole milk. These findings suggested that CotA laccase was a novel AFM1 oxidase capable of eliminating AFM1 in milk. More effort is still needed to improve the AFM1 oxidase activity of CotA laccase in order to shorten the processing time when applying the enzyme in the milk industry. Full article
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<p>Enzymatic properties and kinetics of CotA laccase-mediated AFM<sub>1</sub> oxidation. Effect of pH (<b>A</b>), temperature (<b>B</b>), and metal ions (<b>C</b>) on CotA laccase-mediated AFM<sub>1</sub> oxidation. (<b>D</b>) Michaelis–Menten plot of CotA laccase-catalyzed AFM<sub>1</sub> oxidation.</p>
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<p>Identification of CotA laccase-mediated AFM<sub>1</sub> oxidation products. (<b>A</b>) HPLC chromatograms of AFM<sub>1</sub> and CotA laccase-mediated AFM<sub>1</sub> oxidation products. (<b>B</b>) Mass spectra analysis of AFM<sub>1</sub> and CotA laccase-mediated AFM<sub>1</sub> oxidation products. (<b>C</b>) The reaction scheme for AFM<sub>1</sub> oxidation by CotA laccase.</p>
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<p>Molecular docking analysis of AFM<sub>1</sub> with CotA laccase. (<b>A</b>) The two-dimensional interaction model of AFM<sub>1</sub> with CotA laccase. (<b>B</b>) The three-dimensional interaction model of AFM<sub>1</sub> with CotA laccase.</p>
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<p>Evaluation of the cytotoxic effects of AFM<sub>1</sub> and its oxidation products. (<b>A</b>) Viability of L-02 cells following exposure to 100 μΜ of AFM<sub>1</sub> and CotA laccase-catalyzed AFM<sub>1</sub> oxidation products. (<b>B</b>) LDH activity. (<b>C</b>,<b>D</b>) Apoptosis rate of L-02 cells. Different letters denote statistically significant differences between groups (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Elimination of AFM<sub>1</sub> in milk by CotA laccase. Effect of CotA laccase amount (<b>A</b>) and incubation time (<b>B</b>) on AFM<sub>1</sub> degradation rate in skim milk and whole milk.</p>
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11 pages, 865 KiB  
Article
The Influence of Extra-Fine Milling Protocol on the Internal Fit of CAD/CAM Composite and Ceramic Crowns
by João Paulo Mendes Tribst, Fatema Hosseini, Rafaela Oliveira Pilecco, Carlos Manuel Serrano, Cornelis Johannes Kleverlaan and Amanda Maria de Oliveira Dal Piva
Materials 2024, 17(22), 5601; https://doi.org/10.3390/ma17225601 - 15 Nov 2024
Viewed by 851
Abstract
This study aimed to evaluate the marginal and internal adaptation of CAD/CAM crowns milled using two different milling protocols (fine or extra-fine) within a 4-axis milling machine. The crowns were fabricated from lithium disilicate ceramic (IPS e.max CAD) and resin composite (Tetric CAD), [...] Read more.
This study aimed to evaluate the marginal and internal adaptation of CAD/CAM crowns milled using two different milling protocols (fine or extra-fine) within a 4-axis milling machine. The crowns were fabricated from lithium disilicate ceramic (IPS e.max CAD) and resin composite (Tetric CAD), assessing their fit in various regions. The crowns (N = 40, n = 10) were milled from lithium disilicate and resin composite using a CEREC Primemill unit. Four groups were formed based on the material and milling protocol: EFLD (extra-fine lithium disilicate), FLD (fine lithium disilicate), EFRC (extra-fine resin composite), and FRC (fine resin composite). The crowns were measured using the replica technique, evaluating internal and marginal adaptation in 18 measuring points per specimen. Data were statistically analyzed using ANOVA and Tukey’s test. Resin composite crowns demonstrated a significantly better internal fit compared to lithium disilicate (p < 0.001). Marginal and internal measurements for resin composites were consistently smaller across regions compared to lithium disilicate. No significant differences were found between milling protocols except for the axial wall region (p = 0.001), where extra-fine milling resulted in smaller values. Resin composite crowns exhibited superior internal fit compared to lithium disilicate, regardless of milling protocol. Both the fine and extra-fine milling protocols had minimal impact on adaptation, except at the axial wall region, with both protocols promoting adequate results overall. Full article
(This article belongs to the Special Issue From Conventional to Modern Biomaterials in Dentistry—2nd Edition)
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<p>Different measuring points on the sectioned impression: margin (M), cervical-axial angle (CAA), axial wall (AW), axio-occlusal angle (AOA), occlusal space (OS).</p>
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<p>Boxplot with internal and marginal crown preparation space in µm on the <span class="html-italic">y</span>-axis and material and milling protocol on the <span class="html-italic">x</span>-axis. The dashed line indicates the separation between extra-fine and fine milling protocols. Asterisks represent data values that are far away from others.</p>
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14 pages, 1972 KiB  
Article
Detection of Ochratoxin A in Maize and Its Potential Impact on Avian Pathology in Romanian Farms
by Silviu-Ionut Beia, Violeta Alexandra Ion, Elvira Gagniuc, Oana-Crina Bujor, Elena Ştefania Ivan, Andreea Barbu, Elena Pitoiu, Violeta Elena Beia and Liliana Bădulescu
Life 2024, 14(11), 1477; https://doi.org/10.3390/life14111477 - 13 Nov 2024
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Abstract
Ochratoxin A (OTA) is a nephrotoxic mycotoxin that commonly contaminates maize, posing significant health risks to both poultry and humans. In this study, a rapid and sensitive method utilizing ultra-performance liquid chromatography coupled with fluorescence detection (UPLC-FLD) was developed for the quantification of [...] Read more.
Ochratoxin A (OTA) is a nephrotoxic mycotoxin that commonly contaminates maize, posing significant health risks to both poultry and humans. In this study, a rapid and sensitive method utilizing ultra-performance liquid chromatography coupled with fluorescence detection (UPLC-FLD) was developed for the quantification of OTA levels in maize. The method utilizes immunoaffinity column purification for improved specificity. Accuracy and precision were validated in line with European Union Reference Laboratory (EURL-MP) guidelines, meeting regulatory standards for linearity, trueness, detection and quantification limits, precision, and uncertainty, as per European Commission Regulation (EC) No. 401/2006 and its amendments. The method demonstrated an average recovery rate of 116.78% for maize, with RSDwR values (within-laboratory reproducibility) of 12.72%. Furthermore, OTA occurrence and its possible effects were investigated in several farms in South Romania, where necropsy and histopathological analyses of poultry revealed severe kidney damage, including renal tubular degeneration. Full article
(This article belongs to the Special Issue Veterinary Pathology and Veterinary Anatomy: 2nd Edition)
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<p>Typical UPLC-FLD chromatograms of OTA: (<b>a</b>) reference standard solution (3 ng/mL), (<b>b</b>) QC (maize), and (<b>c</b>) maize sample (M3). * represents the OTA peak.</p>
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<p>Gross and histopathological lesions from Ross 308 gout-affected commercial broiler chickens after exposure to feed with mycotoxins. (<b>a</b>) Swollen kidneys full of chalky deposit and the dilatation of ureters; the kidneys are marked by dashed white-line box. (<b>b</b>) The kidneys are enlarged, degenerate, and filled with urates, with bilateral multifocal petechiae; the kidneys are marked by the dashed white-line box. (<b>c</b>) The gross examination of the bursa of Fabricius reveals significant atrophy, with a notable reduction in size and weight, and pale discoloration; the kidneys are marked by the dashed white-line box. (<b>d</b>) Visceral gout, observed in the transverse cross-section of the chicken kidney. Bluish-purple urate deposits in the lumen of renal tubules forming urate cylinders (arrows), HE stain. (<b>e</b>) Gout tophi (indicated by a white dashed circle and arrow), with cellular spicules surrounded by macrophages and multinucleated giant cells, moderate interstitial lymphocytic and histiocytic nephritis, tubular degeneration, and necrosis in the chicken kidney, HE stain; (<b>f</b>) Gout tophi (indicated by a white dashed circle and arrow), with interstitial fibrosis and urate deposits in the chicken kidney, HE stain.</p>
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19 pages, 3544 KiB  
Article
Deciphering Carotenoid and Flowering Pathway Gene Variations in Eastern and Western Carrots (Daucus carota L.)
by Sarvamangala S. Cholin, Chaitra C. Kulkarni, Dariusz Grzebelus, Rashmi Jakaraddi, Aishwarya Hundekar, B. M. Chandan, T. S. Archana, Nair R. Krishnaja, G. Prabhuling, Gabrijel Ondrasek and Philipp Simon
Genes 2024, 15(11), 1462; https://doi.org/10.3390/genes15111462 - 13 Nov 2024
Viewed by 844
Abstract
Background/Objectives: Carrot is a major root vegetable in the Apiaceae owing to its abundant carotenoids, antioxidants, vitamins, and minerals. The modern dark orange western carrot was derived from sequential domestication events from the white-rooted wild form to the pale orange-, purple-, or yellow-rooted [...] Read more.
Background/Objectives: Carrot is a major root vegetable in the Apiaceae owing to its abundant carotenoids, antioxidants, vitamins, and minerals. The modern dark orange western carrot was derived from sequential domestication events from the white-rooted wild form to the pale orange-, purple-, or yellow-rooted eastern carrot. Genetic and molecular studies between eastern and western carrots are meager despite their evolutionary relatedness. Methods: Twelve RNA seq libraries obtained from distinct eastern and western cultivars at vegetative and reproductive developmental stages were utilized to identify differentially expressed genes (DEGs) to decode the key molecular genetic changes in carotenoid and flowering pathways. Results: In the carotenoid pathway, an upregulation of the PSY, CRTISO, and LCYE genes was observed in the western cultivar, while the eastern cultivar exhibited a higher abundance of downstream enzymes, particularly CCD and NCED1. These later enzymes are crucial in linking apocarotenoids and xanthin-mediated ABA signaling. In the flowering pathway, we noted a greater expression of DEGs associated with the photoperiod and vernalization pathways in the western cultivar. In contrast, the eastern cultivar displayed a dominance of genes from the autonomous pathway (FLD, LD, FLK, and PEBP) that function to repress FLC. The experimental validation of 12 key genes through quantitative real-time PCR further confirms their functional role in carrots. Conclusions: The identified key regulatory genes in these major pathways are valuable for designing breeding strategies for manipulating carotenoid content and flowering time while developing climate-specific carrots. The knowledge of carotenoid and flowering pathways is advantageous in producing nutritionally improved roots and seeds in carrots across diverse climates. Full article
(This article belongs to the Collection Feature Papers: 'Plant Genetics and Genomics' Section)
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<p>Pair-wise comparison of up- and downregulated DEGs across tissues and cultivars (<span class="html-italic">p</span> = 0.01 and Log2FC |±2|). (<b>A</b>) DEGs up- and downregulated in western and eastern cultivars, respectively, in root tissue. (<b>B</b>) DEGs up- and downregulated in western and eastern cultivars, respectively, in FPL tissue. (<b>C</b>) DEGs up- and downregulated in FPL and root tissue, respectively, in western cv. (<b>D</b>) DEGs up- and downregulated in FPL and root tissue, respectively, in eastern cv.</p>
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<p>Pair-wise, unique, and common DEGs. (<b>A</b>) Number of DEGs identified for ‘root’ (eastern vs. western root) ‘FPL’ (eastern vs. western FPL), ‘western cv’ (root vs. FPL in western cv), and ‘eastern cv’ (root vs. FPL in eastern cv), represented in bar graphs. (<b>B</b>) The number of unique and common DEGs identified across tissues and cultivars.</p>
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<p>Details of BLAST hits of 17,566 DEGs with <span class="html-italic">p</span>-value 0.01 and Log2FC |±2|; (<b>A</b>) top five species BLAST hits; (<b>B</b>) species distribution of the BLAST hits.</p>
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<p>Classes of transcriptional factors differentially expressed across eastern and western cvs.</p>
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<p>(<b>A</b>) Heat map of key carotenoid pathway genes differentially expressed across eastern and western cv root and FPL tissues based on TPM values. (<b>B</b>) Putative carotenoid pathway highlighted with identified genes.</p>
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<p>(<b>A</b>) Heat map of key flowering genes identified in the present study based on TPM values. (<b>B</b>) Putative illustration of flowering pathway network proposed for eastern cv based on identified DEGs. Highlighted in the pink are genes that predominated especially in the eastern cv; genes highlighted in the green box are key flowering integrator genes critical for reproductive transition.</p>
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<p>Relative expression changes in 12 key flowering genes across eastern and western carrots in Log2FC from qRT PCR.</p>
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