[go: up one dir, main page]

 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (177,813)

Search Parameters:
Keywords = C3

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
8 pages, 1010 KiB  
Brief Report
A Comparison of Paddle Forces between Whitewater and Flatwater Training in C1 Canoe Slalom
by James M. Wakeling, Stanislava Smiešková, Matej Vajda and Jan Busta
J. Funct. Morphol. Kinesiol. 2024, 9(3), 167; https://doi.org/10.3390/jfmk9030167 (registering DOI) - 17 Sep 2024
Abstract
Background/Objectives: Becoming an elite canoe slalom athlete requires thousands of hours of training, spread over many years. It is difficult to assess the correct balance between flatwater and whitewater training because differences in the paddle forces on these terrains are not known. The [...] Read more.
Background/Objectives: Becoming an elite canoe slalom athlete requires thousands of hours of training, spread over many years. It is difficult to assess the correct balance between flatwater and whitewater training because differences in the paddle forces on these terrains are not known. The aim of this study was to describe paddle forces during canoe slalom training on flatwater and whitewater courses for the C1 canoe category. Methods: Paddle forces for twenty C1 canoe slalom athletes were quantified during all-out figure-of-eight tests on a flatwater course and during race simulations on a whitewater course. Paddle forces were measured using strain gauges embedded in the paddle shaft and quantified by their force, impulse, and stroke durations. Results: The mean force during the pull phase of the paddle strokes was not significantly different between the flatwater and whitewater courses; however, the longer pull phase durations led to a greater pull phase impulse when paddling on the whitewater course. Conclusions: This study indicates that training for all-out runs on a whitewater course is more demanding for canoe slalom athletes than performing all-out trials on a flatwater figure-of-eight course. This evidence may help to develop effective training plans that are essential to reach the highest levels of the sport. Full article
(This article belongs to the Special Issue Biomechanical Analysis in Physical Activity and Sports)
Show Figures

Figure 1

Figure 1
<p>Distribution of pull duration, transition time, impulse, and paddle force for the twenty athletes. Strokes for flatwater training are shown in black, and those for whitewater training are in grey.</p>
Full article ">Figure 2
<p>Mean stroke parameters (with standard error of mean). Strokes for flatwater training are shown in black, and those for whitewater training are in grey.</p>
Full article ">
11 pages, 610 KiB  
Article
Necessary and Sufficient Criteria for a Four-Weight Weak-Type Maximal Inequality in the Orlicz Class
by Erxin Zhang
Axioms 2024, 13(9), 635; https://doi.org/10.3390/axioms13090635 (registering DOI) - 17 Sep 2024
Abstract
Let Φi(i=1,2) be two N-functions, f be a μ-measurable function, and ωi(i=1,2,3,4) be four weight functions. This study presents necessary and [...] Read more.
Let Φi(i=1,2) be two N-functions, f be a μ-measurable function, and ωi(i=1,2,3,4) be four weight functions. This study presents necessary and sufficient conditions for weight functions (ω1,ω2,ω3,ω4) such that the inequality {x:Mf(x)>λ}Φ1(λω1(x))ω2(x)dμ(x)c1XΦ2(c1|f(x)|ω3(x))ω4(x)dμ(x) holds, which extends several established results. Full article
(This article belongs to the Special Issue Theory of Functions and Applications II)
Show Figures

Figure 1

Figure 1
<p>Equivalence relation graph.</p>
Full article ">
14 pages, 4623 KiB  
Article
Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous
by Gouthaman Siddan and Viswas Raja Solomon
Catalysts 2024, 14(9), 629; https://doi.org/10.3390/catal14090629 (registering DOI) - 17 Sep 2024
Abstract
SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in [...] Read more.
SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity. Full article
(This article belongs to the Special Issue Mesoporous Nanostructured Materials for Heterogeneous Catalysis)
Show Figures

Figure 1

Figure 1
<p>FT-IR spectra of (<b>a</b>) SBA-15 and (<b>b</b>) DABCOIL@SBA-15.</p>
Full article ">Figure 2
<p>CP/MAS <sup>13</sup>C NMR spectra of (<b>a</b>) DABCOIL@SBA-15 and (<b>b</b>) <sup>29</sup>Si NMR of DABCOIL@SBA-15.</p>
Full article ">Figure 3
<p>SEM images of (<b>a</b>) SBA-15 and (<b>b</b>) DABCOIL@SBA-15. TEM images of (<b>c</b>) SBA-15 and (<b>d</b>) DABCOIL@SBA-15.</p>
Full article ">Figure 4
<p>X-ray diffraction of (<b>a</b>) SBA-15 and (<b>b</b>) DABCOIL@SBA-15.</p>
Full article ">Figure 5
<p>Nitrogen adsorption/desorption isotherms of (<b>a</b>) SBA-15 and (<b>b</b>) DABCOIL@SBA-15.</p>
Full article ">Figure 6
<p>TGA analysis of (<b>a</b>) SBA-15 and (<b>b</b>) DABCOIL@SBA-15.</p>
Full article ">Figure 7
<p>Hammett plot for competitive reaction.</p>
Full article ">Scheme 1
<p>Synthesis of bi-functionalized ionic liquid grafted-SBA-15.</p>
Full article ">Scheme 2
<p>Synthesis of <span class="html-italic">N</span>-functionalized isatin derivatives.</p>
Full article ">Scheme 3
<p>Synthesis of <span class="html-italic">N</span>-alkyl isatin derivatives in optimized condition.</p>
Full article ">Scheme 4
<p><span class="html-italic">N</span>-alkylation on substituted isatins in optimized condition.</p>
Full article ">Scheme 5
<p>Synthesis of <span class="html-italic">N</span>-alkyl isatin with acyl bromide and Michael-type acceptors.</p>
Full article ">Scheme 6
<p>Synthesis of <span class="html-italic">N</span>-alkyl isatin with different acyl donors for α-oxoimide, Optimized condition.</p>
Full article ">Scheme 7
<p>Synthesis of <span class="html-italic">N</span>-alkyl bis-isatin with di-halo carbon tether, Optimized condition.</p>
Full article ">Scheme 8
<p>The proposed plausible mechanism for <span class="html-italic">N</span>-alkylated reaction.</p>
Full article ">
10 pages, 1547 KiB  
Article
Comparative Study of the Antioxidant Activity of the Conformers of C-tetra(4-methoxyphenyl)calix[4]resorcinarene
by Laura Angélica Maldonado-Sanabria, Ivette Nicole Rodriguez-Saavedra, Ingrid Valentina Reyes-Peña, Alver Castillo-Aguirre, Mauricio Maldonado, Almudena Crespo and Miguel A. Esteso
Int. J. Mol. Sci. 2024, 25(18), 10010; https://doi.org/10.3390/ijms251810010 (registering DOI) - 17 Sep 2024
Abstract
C-tetra(4-methoxyphenyl)calix[4]resorcinarene was synthesized by hydrochloric acid-catalysed cyclocondensation of resorcinol and 4-methoxybenzaldehyde. Under these conditions, the reaction produces a conformational mixture of crown and chair structural conformers, which were separated and characterized by chromatographic and spectroscopic techniques. The antioxidant activity of both conformers [...] Read more.
C-tetra(4-methoxyphenyl)calix[4]resorcinarene was synthesized by hydrochloric acid-catalysed cyclocondensation of resorcinol and 4-methoxybenzaldehyde. Under these conditions, the reaction produces a conformational mixture of crown and chair structural conformers, which were separated and characterized by chromatographic and spectroscopic techniques. The antioxidant activity of both conformers was measured by using the DPPH assay, through which it was observed that the chair conformer showed greater antioxidant activity (IC50 = 47.46 ppm) than the crown conformer (IC50 = 78.46 ppm). Additionally, it was observed that the mixture of both conformers presented lower antioxidant activity than either conformer in isolation. The results found suggest that the chair conformer has efficient antioxidant activity that makes it a potential target for further research. Full article
Show Figures

Figure 1

Figure 1
<p>Chromatograms of the separation, via HPLC, of <span class="html-italic">C</span>-tetra(4-methoxyphenyl)calix[4]resorcinarene: (<b>a</b>) the conformational mixture, (<b>b</b>) the <span class="html-italic">chair</span> conformer and (<b>c</b>) the <span class="html-italic">crown</span> conformer.</p>
Full article ">Figure 2
<p><sup>1</sup>H-NMR <span class="html-italic">C</span>-tetra(4-methoxyphenyl)calix[4]resorcinarene: <span class="html-italic">crown</span> conformer (<b>1a</b>) and <span class="html-italic">chair</span> conformer (<b>1b</b>). Signals a, b and c (in red) correspond to protons a, b and c of the resorcinol residue.</p>
Full article ">Figure 3
<p>DPPH free radical inhibition for 1:1 conformer mixture, individual <span class="html-italic">C</span>-tetra(4-methoxyphenyl)calix[4]resorcinarene conformers (<span class="html-italic">chair</span> and <span class="html-italic">crown</span>) and positive control (ascorbic acid).</p>
Full article ">Figure 4
<p>Fa–CI plot of the conformational mixture to evaluate antagonism. The combination index (CI) values are represented on the y-axis and the affected fraction (Fa) on the x-axis.</p>
Full article ">Figure 5
<p>Hydrogen bonding interactions for <b>1a</b> (<b>a</b>), <b>1b</b> (<b>b</b>) and the conformational mixture (<b>c</b>).</p>
Full article ">Scheme 1
<p>Synthesis of <span class="html-italic">C</span>-tetra(4-methoxyphenyl)calix[4]resorcinarene, including the <span class="html-italic">crown</span> (<b>1a</b>) and <span class="html-italic">chair</span> (<b>1b</b>) conformers.</p>
Full article ">
18 pages, 1763 KiB  
Article
In Vitro Study of Cyano-Phycocyanin Release from Hydrogels and Ex Vivo Study of Skin Penetration
by Daiva Galinytė, Jurga Bernatoniene, Modestas Žilius, Kristina Rysevaitė-Kyguolienė, Arūnas Savickas, Jūratė Karosienė, Vitalis Briedis, Dainius Haroldas Pauža and Nijolė Savickienė
Pharmaceuticals 2024, 17(9), 1224; https://doi.org/10.3390/ph17091224 (registering DOI) - 17 Sep 2024
Abstract
Background: This study explored the most suitable materials for incorporating cyano-phycocyanin (C-PC) into hydrogels, focusing on maintaining the C-PC’s long-term structural integrity and stabilityNext, the release of C-PC from the hydrogels and its skin penetration were investigated. Methods: A series of 1% ( [...] Read more.
Background: This study explored the most suitable materials for incorporating cyano-phycocyanin (C-PC) into hydrogels, focusing on maintaining the C-PC’s long-term structural integrity and stabilityNext, the release of C-PC from the hydrogels and its skin penetration were investigated. Methods: A series of 1% (w/w) C-PC hydrogels was prepared using various gelling agents and preservatives. Spectrophotometric measurements compared the amount of C-PC in the hydrogels to the initially added amount. After selecting the most suitable gelling agent and preservative, two C-PC hydrogels, with and without propylene glycol (PG) (Sigma-Aldrich, St. Louis, MO, USA), were produced for further testing. In vitro release studies utilized modified Franz-type diffusion cells, while ex vivo skin-permeation studies employed Bronaugh-type cells and human skin. Confocal laser scanning microscopy analyzed C-PC accumulation in the skin. Results: The findings demonstrated that sodium alginate (Sigma-Aldrich, St. Louis, MO, USA), hydroxyethyl cellulose (HEC) (Sigma-Aldrich, St. Louis, MO, USA), and SoligelTM (Givaudan, Vernier, Switzerland) are effective biopolymers for formulating hydrogels while maintaining C-PC stability. After 6 h, C-PC release from the hydrogel containing PG was approximately 10% or 728.07 (±19.35) μg/cm2, significantly higher than the nearly 7% or 531.44 (±26.81) μg/cm2 release from the hydrogel without PG (p < 0.05). The ex vivo qualitative skin-permeation study indicated that PG enhances C-PC penetration into the outermost skin layer. Conclusion: PG’s ability to enhance the release of C-PC from the hydrogel, coupled with its capacity to modify the skin barrier ex vivo, facilitates the penetration of C-PC into the stratum corneum. Full article
(This article belongs to the Special Issue Pharmaceutical Formulation Characterization Design)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>pH of hydrogels and determined concentrations of C-PC in the produced hydrogels with different gelling agents. An asterisk (*) indicates statistically significant differences between the added and determined concentrations of C-PC (<span class="html-italic">p</span> &lt; 0.05), evaluated using a paired-sample <span class="html-italic">t</span>-test. The means and standard deviations are presented. The experiment was repeated three times.</p>
Full article ">Figure 2
<p>Determined concentrations of C-PCs in hydrogels with different preservatives. Different letters denote statistically significant differences (<span class="html-italic">p</span> &lt; 0.05) in the C-PC concentrations among hydrogels containing the same gelling agent but different preservatives, as assessed using Bonferroni’s test. An asterisk (*) indicates statistically significant differences (<span class="html-italic">p</span> &lt; 0.05) between the initially added and the determined C-PC concentrations, evaluated using a paired-sample <span class="html-italic">t</span>-test. The means and standard deviations are presented. The experiment was repeated three times.</p>
Full article ">Figure 3
<p>The release of C-PC from hydrogels: C-PC PG hydrogel and C-PC hydrogel without PG (control). Different letters indicate statistically significant differences (<span class="html-italic">p</span> &lt; 0.05) determined by independent-samples <span class="html-italic">t</span>-test. Means and standard deviations are presented. The experiment was repeated 3 times.</p>
Full article ">Figure 4
<p>Confocal images of human skin autofluorescence (control) and human skin section after treatment with C-PC hydrogel and C-PC PG hydrogel. Scale bar 50 μm. The experiment was repeated 3 times.</p>
Full article ">
16 pages, 4776 KiB  
Article
Synergistic Antifungal Effect and In Vivo Toxicity of a Monoterpene Isoespintanol Obtained from Oxandra xylopioides Diels
by Orfa Inés Contreras-Martínez, Alberto Angulo-Ortíz, Gilmar Santafé Patiño, Jesus Sierra Martinez, Ricardo Berrio Soto, Joice Margareth de Almeida Rodolpho, Krissia Franco de Godoy, Fernanda de Freitas Aníbal and Bruna Dias de Lima Fragelli
Molecules 2024, 29(18), 4417; https://doi.org/10.3390/molecules29184417 (registering DOI) - 17 Sep 2024
Abstract
Candida sp. infections are a threat to global health, with high morbidity and mortality rates due to drug resistance, especially in immunocompromised people. For this reason, the search for new alternatives is urgent, and in recent years, a combined therapy with natural compounds [...] Read more.
Candida sp. infections are a threat to global health, with high morbidity and mortality rates due to drug resistance, especially in immunocompromised people. For this reason, the search for new alternatives is urgent, and in recent years, a combined therapy with natural compounds has been proposed. Considering the biological potential of isoespintanol (ISO) and continuing its study, the objective of this research was to assess the effect of ISO in combination with the antifungals fluconazole (FLZ), amphotericin B (AFB) and caspofungin (CASP) against clinical isolates of C. tropicalis and to evaluate the cytotoxic effect of this compound in the acute phase (days 0 and 14) and chronic phase (days 0, 14, 28, 42, 56, 70 and 84) in female mice (Mus musculus) of the Balb/c lineage. The results show that ISO can potentiate the effect of FLZ, AFB and CASP, showing synergism with these antifungals. An evaluation of the mice via direct observation showed no behavioral changes or variations in weight during treatment; furthermore, an analysis of the cytokines IFN-γ and TNF in plasma, peritoneal cavity lavage (PCL) and bronchoalveolar lavage (BAL) indicated that there was no inflammation process. In addition, histopathological studies of the lungs, liver and kidneys showed no signs of toxicity caused by ISO. This was consistent with an analysis of oxaloacetic transaminases (GOT) and pyruvic transaminases (GPT), which remained in the standard range. These findings indicate that ISO does not have a cytotoxic effect at the doses evaluated, placing it as a monoterpene of interest in the search for compounds with pharmacological potential. Full article
(This article belongs to the Section Natural Products Chemistry)
Show Figures

Figure 1

Figure 1
<p>Effect of ISO in combination with FLZ, AFB and CASP against <span class="html-italic">C. tropicalis</span>. The fractional inhibitory concentration indices (FICIs) of the different clinical isolates of <span class="html-italic">C. tropicalis</span> are shown.</p>
Full article ">Figure 2
<p>Global leukocyte count, acute phase (<b>A</b>–<b>C</b>) and chronic phase (<b>D</b>–<b>F</b>). (<b>A</b>) Acute phase: blood; (<b>B</b>) acute phase: PCL; (<b>C</b>) acute phase: BAL; (<b>D</b>) chronic phase: blood; (<b>E</b>) chronic phase: PCL; (<b>F</b>) chronic phase: BAL. Groups: G1: CTRL + water; G2: CTRL + oil; G3–G6: 25, 50, 100 and 200 mg/mL of ISO at 14 days. (*) vs. G1: *** <span class="html-italic">p</span> ≤ 0.001; **** <span class="html-italic">p</span> ≤ 0.0001. (°) vs. G2: ° <span class="html-italic">p</span> ≤ 0.05, °°° <span class="html-italic">p</span> ≤ 0.0001. The results are presented with the mean and standard deviation (<b>A</b>,<b>E</b>). The results are presented as the median with the upper and lower quartiles: Me [Q1; Q3] (<b>B</b>–<b>D</b>,<b>F</b>).</p>
Full article ">Figure 3
<p>Differential leukocyte count, acute phase. (<b>A</b>) Monocytes in PCL. (<b>B</b>) Mast cells in PCL. (<b>C</b>) Monocytes in BAL. (<b>D</b>) Monocytes in blood. (<b>E</b>) Neutrophils in blood. (<b>F</b>) Eosinophils in blood. Groups: G1: CTRL + water; G2: CTRL + oil; G3–G6: 25, 50, 100 and 200 mg/mL of ISO after 14 days. (*) vs. G1: * <span class="html-italic">p</span> ≤ 0.05; ** <span class="html-italic">p</span> ≤ 0.01; *** <span class="html-italic">p</span> ≤ 0.001; **** <span class="html-italic">p</span> ≤ 0.0001. (°) vs. G2: °° <span class="html-italic">p</span> ≤ 0.01; °°° <span class="html-italic">p</span> ≤ 0.001. The results are presented with the mean and standard deviation (<b>B</b>,<b>D</b>). The results are presented as the median with the upper and lower quartiles: Me [Q1; P3] (<b>A</b>,<b>C</b>,<b>E</b>,<b>F</b>).</p>
Full article ">Figure 4
<p>Differential leukocyte count, chronic phase. (<b>A</b>) Monocytes in PCL. (<b>B</b>) Monocytes in BAL (<b>C</b>) Neutrophils in BAL. (<b>D</b>) Neutrophils in blood. (<b>E</b>) Eosinophils in the blood. Groups: G1: CTRL + water; G2: CTRL + oil; G3–G6: 25, 50, 100 and 200 mg/mL of the ISO at 90 days. (*) vs. G1: * <span class="html-italic">p</span> ≤ 0.05; ** <span class="html-italic">p</span> ≤ 0.01; *** <span class="html-italic">p</span> ≤ 0.001. (°) vs. G2: ° <span class="html-italic">p</span> ≤ 0.05; °° <span class="html-italic">p</span> ≤ 0.01; °°° <span class="html-italic">p</span> ≤ 0.001, °°°° <span class="html-italic">p</span> ≤ 0.0001. The results are presented with the mean and standard deviation (<b>B</b>,<b>D</b>). The results are presented as the median with the upper and lower quartiles: Me [Q1; P3] (<b>A</b>–<b>E</b>).</p>
Full article ">Figure 5
<p>GOT and GPT doses in the acute and chronic phases. (<b>A</b>) Acute phase: GOT. (<b>B</b>) Acute phase: GPT. (<b>C</b>) Chronic phase: GPT. Groups: G1: CTRL + water; G2: CTRL + oil; G3–G6: 25, 50, 100 and 200 mg/mL of ISO after 14 days. (*) vs. G1: (°) vs. G2: ° <span class="html-italic">p</span> ≤ 0.05; °° <span class="html-italic">p</span> ≤ 0.01. The results are presented with the mean and standard deviation.</p>
Full article ">Figure 6
<p>Measurement of INF-γ and TNF cytokine levels in the acute and chronic phase. (<b>A</b>) Acute phase: IFN-γ. (<b>B</b>) Acute phase: TNF. (<b>C</b>) Chronic phase: IFN-γ. Groups: G1: CTRL + water; G2: CTRL + oil; G3–G6: 25, 50, 100 and 200 mg/mL of ISO after 14 days. The results are presented as the median with the upper and lower quartiles: Me [Q1; P3]. (*) vs. G1: * <span class="html-italic">p</span> ≤ 0.05; ** <span class="html-italic">p</span> ≤ 0.01; *** <span class="html-italic">p</span> ≤ 0.001.</p>
Full article ">Figure 7
<p>Histological sections of the kidneys in the acute (<b>a</b>) and chronic (<b>b</b>) phases. (A) Control G1 (water); (B) control G2 (oil); (C) G3 (25 mg/kg); (D) G4 (50 mg/kg); (E) G5 (100 mg/kg) and (F) G6 (200 mg/kg). The white arrows indicate areas of lymphoplasmacytic infiltrates; there were no changes in the groups represented by images (A), (B) or (F) in the chronic phase.</p>
Full article ">Figure 8
<p>Histological sections of the lungs in the acute (<b>a</b>) and chronic (<b>b</b>) phases. (A) Control G1 (water); (B) control G2 (oil); (C) G3 (25 mg/kg); (D) G4 (50 mg/kg); (E) G5 (100 mg/kg) and (F) G6 (200 mg/kg). Red arrows indicate foci of hemorrhage; white arrows show areas of lymphoplasmacytic infiltrates; and black arrows represent thickening in the alveolar septa.</p>
Full article ">Figure 9
<p>Histological sections of the liver in the acute (<b>a</b>) and chronic (<b>b</b>) phases. (A) Control G1 (water); (B) control G2 (oil); (C) G3 (25 mg/kg); (D) G4 (50 mg/kg); (E) G5 (100 mg/kg) and (F) G6 (200 mg/kg). White arrows indicate areas of lymphoplasmacytic infiltrates; yellow arrows indicate the presence of binucleated hepatocytes (a sign of regeneration); red marks refer to discrete foci of necrosis and black marks represent areas of granuloma.</p>
Full article ">Figure 10
<p>Experiment design. Female Balb/c mice received oral treatment with 100 μL of different concentrations of the ISO (25, 50, 100 and 2000 mg/mL) every 14 days in an acute (28 days) and chronic (98 days) phase study.</p>
Full article ">
22 pages, 2639 KiB  
Review
Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Cancer: Current Use and Future Prospects
by Henry Dickerson, Ahmad Diab and Othman Al Musaimi
Int. J. Mol. Sci. 2024, 25(18), 10008; https://doi.org/10.3390/ijms251810008 (registering DOI) - 17 Sep 2024
Abstract
Tyrosine kinase inhibitors (TKIs) have emerged as a leading targeted cancer therapy, reducing the side effects often seen with non-targeted treatments, especially the damage to healthy cells. To tackle resistance, typically caused by epidermal growth factor receptor (EGFR) mutations, four generations of TKIs [...] Read more.
Tyrosine kinase inhibitors (TKIs) have emerged as a leading targeted cancer therapy, reducing the side effects often seen with non-targeted treatments, especially the damage to healthy cells. To tackle resistance, typically caused by epidermal growth factor receptor (EGFR) mutations, four generations of TKIs have been developed. Each generation has shown improved effectiveness and fewer side effects, resulting in better patient outcomes. For example, patients on gefitinib, a first-generation TKI, experienced a progression-free survival (PFS) of 10 months compared to 5 months with conventional chemotherapy. Second-generation TKI afatinib outperformed erlotinib and extended PFS to 11.1 months compared to 6.9 months with cisplatin. Third-generation TKIs further increased survival to 38.6 months, compared to 31.8 months with first-generation TKIs. This progress demonstrates the ability of newer TKIs to overcome resistance, particularly the T790M mutation, while reducing adverse effects. Ongoing research focuses on overcoming resistance from newer mutations like C797S to further improve patient survival. These developments highlight the significant progress in TKI therapy and the continued effort to refine cancer treatment. Recent research in South Korea shows that third-generation TKIs are ineffective against non-small cell lung cancer (NSCLC) with the C797S mutation. Several trials have started showing promising in vitro and in vivo results, but more trials are needed before clinical approval. This review underscores notable advancements in the field of EGFR TKIs, offering a comprehensive analysis of their mechanisms of action and the progression of various TKI generations in response to resistance. Full article
Show Figures

Figure 1

Figure 1
<p>Chemical structure of Enhertu.</p>
Full article ">Figure 2
<p>EGFR structure, including domains, exons, and respective mutations.</p>
Full article ">Figure 3
<p>Molecular signaling of the EGFR and the resulting biological response, under pathological and treatment states [<a href="#B42-ijms-25-10008" class="html-bibr">42</a>].</p>
Full article ">Figure 4
<p>Schematic representation of gefitinib inside the EGFR-TK pocket.</p>
Full article ">Figure 5
<p>Resistance factors to first- and second-generation TKIs.</p>
Full article ">Figure 6
<p>Schematic representation of osimertinib bound to the active site of EGFR tyrosine kinase, with each amino acid involved and their interaction type [<a href="#B43-ijms-25-10008" class="html-bibr">43</a>].</p>
Full article ">Figure A1
<p>Chemical structures of all 12 EGFR TKIs used to treat NSCLC, separated into respective generations.</p>
Full article ">Figure A2
<p>Chemical structure of gefitinib; red, anilinoquinazoline core.</p>
Full article ">Figure A3
<p>Chemical structure of afatinib. Red, anilinoquinazoline core; blue, covalent warhead.</p>
Full article ">Figure A4
<p>Chemical structure of osimertinib. Red, pyrimidine-based core; blue, covalent warhead.</p>
Full article ">Figure A5
<p>Chemical structure of BBT-176. Red, pyrimidine-based core; blue, piperidine ring; green, sulfone.</p>
Full article ">
18 pages, 3144 KiB  
Article
Theoretical Study of the Effects of Different Coordination Atoms (O/S/N) on Crystal Structure, Stability, and Protein/DNA Binding of Ni(II) Complexes with Pyridoxal-Semi, Thiosemi, and Isothiosemicarbazone Ligand Systems
by Violeta Jevtovic, Aleksandra Rakić, Odeh A. O. Alshammari, Munirah Sulaiman Alhar, Tahani Alenezi, Violeta Rakic and Dušan Dimić
Inorganics 2024, 12(9), 251; https://doi.org/10.3390/inorganics12090251 (registering DOI) - 17 Sep 2024
Abstract
Nickel transition metal complexes have shown various biological activities that depend on the ligands and geometry. In this contribution, six Ni(II) nitrate complexes with pyridoxal-semi, thiosemi, and isothiosemicarbazone ligands were examined using theoretical chemistry methods. The structures of three previously reported complexes ([Ni(PLSC)(H [...] Read more.
Nickel transition metal complexes have shown various biological activities that depend on the ligands and geometry. In this contribution, six Ni(II) nitrate complexes with pyridoxal-semi, thiosemi, and isothiosemicarbazone ligands were examined using theoretical chemistry methods. The structures of three previously reported complexes ([Ni(PLSC)(H2O)3]∙2NO3, [Ni(PLTSC)2] ∙2NO3∙H2O, and [Ni(PLITSC)(H2O)3]∙2NO3) were investigated based on Hirshfeld surface analysis, and the most important stabilization interactions in the crystal structures were outlined. These structures were optimized at the B3LYP/6-311++G(d,p)(H,C,N,O,(S))/LanL2DZ(Ni) level of theory, and the applicability was checked by comparing theoretical and experimental bond lengths and angles. The same level of theory was applied for the optimization of three additional structures, ([Ni(PLSC)2]2+, [Ni(PLTSC)(H2O)3]2+, and [Ni(PLITSC)2]2+). The interactions between selected ligands and Ni(II) were examined using the Natural Bond Orbital (NBO) and Quantum Theory of Atoms in Molecules (QTAIM) approaches. Particular emphasis was placed on interactions between oxygen, sulfur, and nitrogen donor atoms and Ni(II). Human Serum Albumin (HSA) and the DNA-binding properties of these complex cations were assessed using molecular docking simulations. The presence of water molecules and various substituents in the thermodynamics of the processes was demonstrated. The results showed significant effects of structural parameters on the stability and reactivity towards important biomolecules. Full article
(This article belongs to the Special Issue Metal Complexes Diversity: Synthesis, Conformations, and Bioactivity)
Show Figures

Figure 1

Figure 1
<p>Complexation modes of neutral PLSC, PLTSC, and PLITSC ligands.</p>
Full article ">Figure 2
<p>Hirshfeld surfaces of different nickel(II) nitrate complexes included in this study.</p>
Full article ">Figure 3
<p>Optimized structures (at the B3LYP/6-311++G(d,p)(H,C,N,O,(S)/LanL2DZ(Ni) level of theory) of selected octahedral Ni(II) complexes. Carbon—gray; nitrogen—blue; oxygen—red; sulfur—yellow; nickel—teal; hydrogen atoms have been omitted for clarity.</p>
Full article ">Figure 4
<p>Structure of HSA with subdomains: IA in reddish, IB in yellow, IIA in green, IIB in orange, IIIA in lilac, and IIIB in pink. The active positions FA1–FA8 are denoted with the representation of myristic acids (yellow CPK model), commonly bound in the structures. The position of a fluorescent amino acid, Trp214, is depicted as dark green CPK balls, while [Ni(PLSC)<sub>2</sub>]<sup>2+</sup> is presented as purple CPK balls.</p>
Full article ">Figure 5
<p>The most important interactions between HSA and [Ni(PLSC)(H<sub>2</sub>O)<sub>3</sub>]<sup>2+</sup> (<b>left</b>) and [Ni(PLSC)<sub>2</sub>]<sup>2+</sup> (<b>right</b>) complexes, as obtained in the molecular docking simulations.</p>
Full article ">Figure 6
<p>The most important interactions between DNA and [Ni(PLSC)(H<sub>2</sub>O)<sub>3</sub>]<sup>2+</sup> (<b>left</b>) and [Ni(PLSC)<sub>2</sub>]<sup>2+</sup> (<b>right</b>) complexes, as obtained via the molecular docking simulations.</p>
Full article ">
8 pages, 422 KiB  
Article
Iron Supply of Multivitamins–Multiminerals Commercialized Online by Amazon in Western and Southern Europe: A Labeling Analysis
by Margherita G. M. Mattavelli, Giacomo Piccininni, Gabriel F. Toti, Mario G. Bianchetti, Luca Gabutti, Sebastiano A. G. Lava, Carlo Agostoni, Pietro B. Faré and Gregorio P. Milani
Nutrients 2024, 16(18), 3140; https://doi.org/10.3390/nu16183140 (registering DOI) - 17 Sep 2024
Abstract
Background. In high-income countries, shopping for non-prescription multivitamin–multimineral supplements has tremendously increased. Objective and Methods. The purpose of this labeling analysis is to inform on the daily elemental iron (with or without vitamin C) supply provided by multivitamin–multimineral supplements sold online by Amazon [...] Read more.
Background. In high-income countries, shopping for non-prescription multivitamin–multimineral supplements has tremendously increased. Objective and Methods. The purpose of this labeling analysis is to inform on the daily elemental iron (with or without vitamin C) supply provided by multivitamin–multimineral supplements sold online by Amazon in Western and Southern Europe (amazon.es®, amazon.de®, amazon.it®, and amazon.fr®). Results. We identified 298 iron-containing multivitamin–multimineral preparations sold by Amazon marketplaces: 153 preparations sourced from amazon.de®, 68 from amazon.fr®, 54 from amazon.it®, and 23 from amazon.es®. The daily iron dose provided by these preparations was 14 [5–14] mg (median and interquartile range), with no differences among the marketplaces. Approximately 90% (n = 265) of the preparations contained ferrous iron. Moreover, 85% (n = 253) of the preparations were fortified with vitamin C in a dose of 80 [40–100] mg daily. Conclusions. The median supply of iron (about 14 mg) and vitamin C (80 mg) in iron-containing multivitamin–multimineral preparations offered on Amazon platforms in Western and Southern Europe falls below that currently recommended for iron deficiency in review articles, namely 100 mg of iron and 500 mg of vitamin C per day. The iron supply of iron-containing multivitamin–multimineral preparations falls also below the dose of 30–60 mg advocated to prevent iron deficiency in menstruating women. Full article
(This article belongs to the Section Micronutrients and Human Health)
Show Figures

Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Daily iron supply provided by 298 iron-containing multivitamin–multimineral preparations sold by amazon.de<sup>®</sup>, amazon.fr<sup>®</sup>, amazon.it<sup>®</sup>, and amazon.es<sup>®</sup>. The preparations are subdivided into three different groups according to the suggested daily dose of iron, namely 2–9 mg, 10–19 mg, and 20–50 mg daily. Ferrous (Fe<sup>2+</sup>) iron- and ferric (Fe<sup>3+</sup>) iron-containing preparations are presented separately.</p>
Full article ">
15 pages, 2323 KiB  
Article
Novel Approach to Organization of Structured Cobalt-Based Fischer–Tropsch Catalyst
by Andrei Gorshkov, Lilia Sineva, Kirill Gryaznov and Vladimir Mordkovich
Catalysts 2024, 14(9), 628; https://doi.org/10.3390/catal14090628 (registering DOI) - 17 Sep 2024
Abstract
Structured Fischer–Tropsch synthesis catalysts were tested in tubular reactors of industry-standard diameters of 0.5 or 0.75 inches. The structured catalyst bed was manufactured by the obturation of a straight bunch of graphite-based extrudates (D = 1.5 mm, L = 30 mm). A conventional [...] Read more.
Structured Fischer–Tropsch synthesis catalysts were tested in tubular reactors of industry-standard diameters of 0.5 or 0.75 inches. The structured catalyst bed was manufactured by the obturation of a straight bunch of graphite-based extrudates (D = 1.5 mm, L = 30 mm). A conventional loose bed of granulated catalyst (D = 1.5 mm, L = 3 mm) was tested as a reference. In a 1000–3000 h−1 syngas space velocity range, structured and loose catalyst bed testing showed no significant differences in their main catalytic parameters. Nevertheless, their C5+ hydrocarbon group composition was quite different, i.e., the alkene fraction rose from 9 to 23%, while n-alkanes dropped from 81 to 64%. This could be a result of secondary reaction intensification in the conventional loose bed due to its zeolite acid site’s higher availability. Further FTS testing of the structured catalysts in 4000–6000 h−1 manifested distinctive limits in C5+ productivity for 0.5 and 0.75 inches of 512 kg C5+/(m3 reactor · h) and 362 kg C5+/(m3 reactor · h), respectively. This may be explained by limitations in structured bed thermal conductivity. It suggests that the arrangement of extrudates in the structured catalyst can significantly affect the reaction heat and mass transfer conditions and affords new opportunities for group composition control by means of catalyst bed organization. Full article
(This article belongs to the Section Catalysis in Organic and Polymer Chemistry)
23 pages, 3170 KiB  
Article
Biochemical Characterization and Disease Control Efficacy of Pleurotus eryngii-Derived Chitosan—An In Vivo Study against Monilinia laxa, the Causal Agent of Plum Brown Rot
by Ippolito Camele, Amira A. Mohamed, Amira A. Ibrahim and Hazem S. Elshafie
Plants 2024, 13(18), 2598; https://doi.org/10.3390/plants13182598 (registering DOI) - 17 Sep 2024
Abstract
Chitin (Ct) is a crucial biopolymer present in fungi, algae, arthropods, and is usually obtained from crustacean shells. Chitosan (Cs) is a derivative from Ct deacetylation, and possesses numerous uses in various agro-industrial fields. Research on fungal-derived Ct and Cs is mostly focused [...] Read more.
Chitin (Ct) is a crucial biopolymer present in fungi, algae, arthropods, and is usually obtained from crustacean shells. Chitosan (Cs) is a derivative from Ct deacetylation, and possesses numerous uses in various agro-industrial fields. Research on fungal-derived Ct and Cs is mostly focused on pharmaceutical uses, however their uses for plant disease control remain less explored. The main objective of the current study is to evaluate the possibility of using chitosan obtained from mushroom Pleurotus eryngii (Cs-Pe) for controlling some phytopathogens compared to commercial chitosan (C.Cs). This study is focused on the following key areas: (i) extracting Ct from P. eryngii mycelium and converting it to Cs through deacetylation, using both bleaching and non-bleaching methods; (ii) conducting a physico-chemical characterization and in vitro evaluation of the antimicrobial activity of the obtained Cs; (iii) performing an in vivo assessment of the phytotoxic and cytotoxic effects of Cs; and (iv) investigating in vivo the impact of the studied chitosan on fruit quality and its biocontrol efficacy against Monilinia laxa infections in plum fruits. Results showed that Cs-Pe, especially the unbleached one, displayed promising in vitro antimicrobial activity against the majority of tested pathogens. Regarding the cytotoxicity, the highest significant increase in cell abnormality percentage was observed in the case of C.Cs compared to Cs-Pe. In the in vivo study, Cs-Pe acted as a protective barrier, lowering and/or preventing moisture loss and firmness of treated plums. The studied Cs-Pe demonstrated notable efficacy against M. laxa which decreased the fruits’ percentage decline. These results strongly suggest that Cs derived from P. eryngii is a potential candidate for increasing plums’ shelf-life. This research shed light on the promising applications of P. eryngii-derived Cs in the agri-food field. Full article
(This article belongs to the Section Plant Protection and Biotic Interactions)
Show Figures

Figure 1

Figure 1
<p>Chemical structure of chitin (<b>A</b>) and chitosan (<b>B</b>).</p>
Full article ">Figure 2
<p>Chitin extracted from <span class="html-italic">P. eryngii</span> and deacetylated chitosan. (<b>A</b>) U.Ct.Pe; (<b>B</b>) B.Ct.Pe; (<b>C</b>) U.Cs.Pe; (<b>D</b>) B.Cs.Pe. Photos were taken by a Nikon Digital Camera (D5100) (Nikon Imaging Japan Inc., Tokyo, Japan).</p>
Full article ">Figure 3
<p>FT-IR spectrum of C.Cs (A), B.Cs.Pe (B), U.Cs.Pe (C), and Ct (D).</p>
Full article ">Figure 4
<p>Types of mitotic abnormality induced by treatment of <span class="html-italic">Vicia faba</span> root tips by different tested Cs. (<b>A</b>,<b>B</b>): micronucleus at interphase; (<b>C</b>): stickiness at metaphase; (<b>D</b>): disturbed metaphase; (<b>E</b>): non-congression at metaphase; (<b>F</b>,<b>G</b>): oblique at metaphase; (<b>H</b>,<b>I</b>): disturbed anaphase; (<b>J</b>): bridges at anaphase; (<b>K</b>): late separation at anaphase; (<b>L</b>,<b>M</b>): laggard at anaphase; (<b>N</b>,<b>O</b>): disturbed at telophase; (<b>P</b>,<b>Q</b>): late separation at telophase; (<b>R</b>): laggard at telophase; (<b>S</b>): bridge at telophase; and (<b>T</b>): diagonal telophase (X = 100).</p>
Full article ">Figure 5
<p>Weight loss of plums after coating treatment. Where: C + ve: control positive (fruits infected only with <span class="html-italic">M. laxa</span>); AA: acetic acid at 1%; Gly: glycerol. Bars with different letters for each period are significantly different at <span class="html-italic">p</span> &lt; 0.05. Data for each bar are expressed as the mean of three replicates ± SDs.</p>
Full article ">Figure 6
<p>Weight loss percentage of plums at the end of conservation period.</p>
Full article ">Figure 7
<p>Peel color change in plums after coating treatment. Bars with different letters for each period are significantly different at <span class="html-italic">p</span> &lt; 0.05 using the Tukey B test. Data for each bar are expressed as the mean of three replicates ± SDs.</p>
Full article ">Figure 8
<p>The firmness of plums after coating treatment at the end of the conservation period. Bars with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05. Data for each bar are expressed as the mean of three replicates ± SDs.</p>
Full article ">Figure 9
<p>The sugar content of plums after coating treatment at the end of the conservation period. Bars with different letters are significantly different at <span class="html-italic">p</span> &lt; 0.05. Data for each bar are expressed as the mean of three replicates ± SDs.</p>
Full article ">Figure 10
<p>The decay percentage of plums after coating treatment and artificial infection with <span class="html-italic">M. laxa</span>. Bars with different letters for each method are significantly different at <span class="html-italic">p</span> &lt; 0.05. Data are expressed as the mean of three replicates ± SDs.</p>
Full article ">
15 pages, 4909 KiB  
Article
Investigating the Effects of Transition Metals and Activated Carbon on Hydrogenation Characteristics of Severely Deformed ZK60 Processed by High-Energy Ball Milling
by Aqeel Abbas, Tzu-Chieh Hsu, Jhe-Yi Lin, Hung-Cheng Ho, Kun-Ming Lin and Hsin-Chih Lin
Materials 2024, 17(18), 4562; https://doi.org/10.3390/ma17184562 (registering DOI) - 17 Sep 2024
Abstract
The synergic effects of activated carbon and transition metals on the hydrogenation characteristics of commercial ZK60 magnesium alloy were investigated. Severe plastic deformation was performed using equal-channel angular pressing with an internal die angle of 120° and preheating at 300 °C. The ZK60 [...] Read more.
The synergic effects of activated carbon and transition metals on the hydrogenation characteristics of commercial ZK60 magnesium alloy were investigated. Severe plastic deformation was performed using equal-channel angular pressing with an internal die angle of 120° and preheating at 300 °C. The ZK60 alloy samples were processed for 12 passes using route BA. The deformed ZK60 alloy powder was blended with activated carbon and different concentrations of transition metals (Ag, Pd, Co, Ti, V, Ti) using high-energy ball milling for 20 h at a speed of 1725 rpm. The amount of hydrogen absorbed and its kinetics were calculated using Sievert’s apparatus at the higher number of cycles at a 300 °C ab/desorption temperature. The microstructure of the powder was analyzed using an X-ray diffractometer and scanning electron microscope. The results indicated that 5 wt% activated carbon presented the maximum hydrogen absorption capacity of 6.2 wt%. The optimal hydrogen absorption capacities were 7.1 wt%, 6.8 wt%, 6.7 wt%, 6.64 wt%, 6.65 wt%, and 7.06 wt% for 0.5 Ag, 0.3 Co, 0.1 Al, 0.5 Pd, 2 Ti, and 0.5 V, respectively. The hydrogen absorption capacities were reduced by 35.21%, 26.47%, 41.79%, 21.68%, 26.31%, and 26.34% after 100 cycles for 5C0.5Ag, 5C0.3Co, 5C0.1Al, 5C0.5Pd, 2Ti, and 5C0.5V, respectively. Hydrogen absorption kinetics were significantly improved so that more than 90% of hydrogen was absorbed within five minutes. Full article
(This article belongs to the Section Energy Materials)
Show Figures

Figure 1

Figure 1
<p>Hydrogen absorption performance of ZK60 alloy with different proportion of activated carbon.</p>
Full article ">Figure 2
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C+ different additives of Ag and (<b>b</b>) 5C + 0.5Ag at higher number of cycles.</p>
Full article ">Figure 3
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C + different additives of Co and (<b>b</b>) 5C + 0.3Co at higher number of cycles.</p>
Full article ">Figure 4
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C + different additives of Al and (<b>b</b>) 5C + 0.3Al at higher number of cycles.</p>
Full article ">Figure 5
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C + different additives of Pd and (<b>b</b>) 5C + 0.5Pd at higher number of cycles.</p>
Full article ">Figure 6
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C + different additives of Ti and (<b>b</b>) 5C + 2Ti at higher number of cycles.</p>
Full article ">Figure 7
<p>Hydrogen absorption performance of Zk60 with (<b>a</b>) 5C + different additives of V and (<b>b</b>) 5C + 0.5V at higher number of cycles.</p>
Full article ">Figure 8
<p>P-C-T curves for ZK60 alloy with the powders of different elements.</p>
Full article ">Figure 9
<p>XRD analysis of ZK60 with different additives.</p>
Full article ">Figure 10
<p>FESEM images of ZK60-5C with (<b>a</b>) 0.5Ag (<b>b</b>) 0.3Co (<b>c</b>) 0.3Al (<b>d</b>) 0.5Pd (<b>e</b>) 2Ti (<b>f</b>) 0.5V after dehydrogenation.</p>
Full article ">
11 pages, 1144 KiB  
Article
Dosimetric Comparison between the HyperArc and Conventional VMAT in Cervical Spine Stereotactic Radiosurgery
by Jeehoon Park, Byungdo Park and Jeongho Kim
J. Clin. Med. 2024, 13(18), 5497; https://doi.org/10.3390/jcm13185497 (registering DOI) - 17 Sep 2024
Abstract
Background: This research aims to evaluate the usability of the HyperArc (HA) technique in stereotactic radiosurgery for cervical spine metastasis by comparing the dosimetry of the target and organs at risk, specifically the spinal cord, between HA and VMAT and conventional volumetric modulated [...] Read more.
Background: This research aims to evaluate the usability of the HyperArc (HA) technique in stereotactic radiosurgery for cervical spine metastasis by comparing the dosimetry of the target and organs at risk, specifically the spinal cord, between HA and VMAT and conventional volumetric modulated arc therapy (VMAT). Methods: A RANDO® phantom and QFix EncompassTM and support system were used to simulate three target types (A, B, and C) based on RTOG0631 guidelines. Treatment plans included one VMAT and two HyperArc techniques with different SRS NTO values (100 and 250). Dosimetric parameters such as conformity index (CI), homogeneity index (HI), R50, and spinal cord sparing were analyzed. Gamma analysis was performed using portal dosimetry to validate the dose delivery accuracy. Results: HyperArc plans demonstrated higher conformity, sharper dose fall-off, and improved quality assurance (QA) results compared to VMAT plans. HA with SRS NTO 250 showed even better results in terms of conformity, dose fall-off, and spinal cord dose reduction (V10 and Dmax) compared to HA with SRS NTO 100. Although the mean gamma passing rates were slightly lower, all plans achieved rates above 95%. Conclusion: The findings suggest that HA provides superior dosimetric benefits over VMAT and could be effectively utilized for cervical spine radiation therapy. Full article
(This article belongs to the Topic Innovative Radiation Therapies)
Show Figures

Figure 1

Figure 1
<p>Target delineation for Types A, B, and C.</p>
Full article ">Figure 2
<p>Isodose curve for (<b>a</b>) HA (SRS NTO 250), (<b>b</b>) HA (SRS NTO 100), (<b>c</b>) VMAT (NTO 100), and (<b>d</b>) DVH.</p>
Full article ">Figure 3
<p>Dosimetric results for the target and spinal cord. The asterisks and circles represent outlier values, while the numbers denote the sample numbers.</p>
Full article ">
17 pages, 4052 KiB  
Article
Microplastics Can Inhibit Organic Carbon Mineralization by Influencing Soil Aggregate Distribution and Microbial Community Structure in Cultivated Soil: Evidence from a One-Year Pot Experiment
by Zonghai Chen, Quan Wan, Pengyu Zhou, Haochen Li, Yige Liu, Ying Lu and Bo Li
Agronomy 2024, 14(9), 2114; https://doi.org/10.3390/agronomy14092114 (registering DOI) - 17 Sep 2024
Abstract
Microplastics (MPs) pollution has become a global pollution problem, potentially affecting soil carbon cycling and structure stability in agricultural systems. However, the effects of MPs pollution on soil organic carbon fractions/transformation and soil aggregate stability remain unknown. Thus, a combination of one-year pot [...] Read more.
Microplastics (MPs) pollution has become a global pollution problem, potentially affecting soil carbon cycling and structure stability in agricultural systems. However, the effects of MPs pollution on soil organic carbon fractions/transformation and soil aggregate stability remain unknown. Thus, a combination of one-year pot and short-term mineralized incubation experiments that involved a reference (CK, with no MPs), different concentrations (0.1, 1, and 2 w/w % polyethylene (PE)), and types (0.1 w/w % PE, polypropylene (PP), and polyvinyl chloride (PVC)) of MPs were carried out to investigate the effects on the soil aggregate stability and organic carbon mineralization after one year of adding MPs. The results showed that the size distribution of the soil partial aggregates varied significantly as affected by the MP concentration and type (p ˂ 0.05). Compared with 0.1% PE, significant increases in the MWD (mean weight diameter) and GMD (geometric mean diameter) of 2% PE of 27.22% and 32.73%, respectively, were detected. In addition, high concentrations (>1%) of PE significantly decreased the dissolved organic carbon (DOC) (p ˂ 0.05), whereas they significantly increased the stable carbon fractions including the particulate organic carbon (POC) and mineral-bound organic carbon (MOC) (p ˂ 0.01). Meanwhile, compared with the CK, both MP types and doses significantly decreased the soil organic carbon mineralization rate (SOCMR) and cumulative mineralization amount (CM) (p ˂ 0.001). Moreover, the MPs significantly increased the total PLFA (phospholipid fatty acid) by 261.9–438.8% (p ˂ 0.01), and the soil pH and total PLFA were the dominant factors that affected the SOCMR as affected by MPs. Thus, a high concentration (>1%) of PE significantly decreased the SOCMR by influencing the soil pH, TN, and macroaggregate (R>0.25) content and microbial community composition. This study provided evidence of the feedback of MPs pollution on soil C dynamic and aggregates in cultivated soil in South China. Full article
Show Figures

Figure 1

Figure 1
<p>Soil physicochemical properties in different MP treatments. Note: (<b>A</b>) represents the pH; (<b>B</b>) represents the content of total nitrogen (TN); (<b>C</b>) represents the content of cation exchange (CEC); (<b>D</b>) represents the content of soil organic carbon (SOC); (<b>E</b>) represents the content of alkaline dissolved nitrogen (AN); (<b>F</b>) represents the content of soil effective phosphorus (AP); CK: treatment without MPs; C: concentration; T: type. MPs’ effects on soil physicochemical properties were analyzed using one-way ANOVA analysis. Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). *: <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; n. s.: indicates no significant difference.</p>
Full article ">Figure 2
<p>Soil water-stable aggregate stability in different MP treatments. Note: (<b>A</b>) represents the content of large aggregate (R <sub>&gt; 0.25</sub>); (<b>B</b>) represents the mean weight diameter (MWD); (<b>C</b>) represents the geometric mean diameter (GMD); (<b>D</b>) represents the fractal dimension (FD). Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). C: concentration; T: type. *: <span class="html-italic">p</span> &lt; 0.05; **: <span class="html-italic">p</span> &lt; 0.01; n. s.: indicates no significant difference.</p>
Full article ">Figure 3
<p>Soil enzyme activities in different MP treatments. Note: (<b>A</b>) represents the activity of polyphenol oxidase; (<b>B</b>) represents the activity of β-glucosidase; Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). ***: <span class="html-italic">p</span> &lt; 0.001; n. s. indicated no significant.</p>
Full article ">Figure 4
<p>Total phospholipid fatty acid (PLFA) contents (<b>A</b>), Gram-positive bacteria PLFA contents (<b>B</b>), Gram-negative bacteria PLFA contents (<b>C</b>) and their PLFA ratios (<b>D</b>), bacteria PLFA contents (<b>E</b>), fungal PLFA contents (<b>F</b>) and their PLFA ratios (<b>G</b>) in different MP treatments. Note: G+: Gram-positive bacteria; G-: Gram-negative bacteria; G+/G−: Gram-positive/Gram-negative bacteria ratio; C: concentration; T: type. Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). *: <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.</p>
Full article ">Figure 5
<p>Soil organic carbon fractions in different MP treatments. Note: (<b>A</b>) represents the content of particulate organic carbon (POC); (<b>B</b>) represents the content of mineral-associated organic carbon (MOC); (<b>C</b>) represents the content of easily oxidized organic carbon (EOC); (<b>D</b>) represents the content of microbial biomass carbon (MBC); (<b>E</b>) represents the content of hot water-soluble carbon (HWOC); (<b>F</b>) represents the content of dissolved organic carbon (DOC). CK: treatment without MPs. Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). C: concentration; T: type. *: <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; n. s.: indicates no significant difference.</p>
Full article ">Figure 6
<p>The SOC mineralization rate (<b>A</b>,<b>B</b>) and cumulative mineralization amount (<b>C</b>,<b>D</b>) in different MP treatments. Different lowercase letters indicate significant differences between different treatments (Duncan’s test, <span class="html-italic">p</span> &lt; 0.05). ***: <span class="html-italic">p</span> &lt; 0.001.</p>
Full article ">Figure 7
<p>Redundancy analysis (RDA) of the relationships between soil aggregate stability (<b>A</b>), SOC mineralization (<b>B</b>), and soil environment factor in MP treatments.</p>
Full article ">
17 pages, 6692 KiB  
Article
Detecting the Sigma Phase in Duplex Stainless Steel by Magnetic Noise and First Harmonic Analysis
by João Silva, Edgard Silva, Augusto Sampaio, Rayssa Lins, Josinaldo Leite, Victor Albuquerque Silva and João Manuel R. S. Tavares
Materials 2024, 17(18), 4561; https://doi.org/10.3390/ma17184561 (registering DOI) - 17 Sep 2024
Abstract
Non-destructive electromagnetic tests based on magnetic noise analysis have been developed to study, among others, residual stress, heat treatment outcomes, and harmful microstructures in terms of toughness. When subjected to thermal cycles above 550 °C, duplex stainless steels form an extremely hard and [...] Read more.
Non-destructive electromagnetic tests based on magnetic noise analysis have been developed to study, among others, residual stress, heat treatment outcomes, and harmful microstructures in terms of toughness. When subjected to thermal cycles above 550 °C, duplex stainless steels form an extremely hard and chromium-rich constituent that, if it is superior to 5%, compromises the steel’s corrosion resistance and toughness. In the present work, a study was carried out concerning the interaction of excitation waves with duplex stainless steel. Hence, by analyzing the magnetic noise and variations in the amplitude of the first harmonic of the excitation waves, the detection of the deleterious sigma phase in SAF 2205 steel is studied. To simplify the test, a Hall effect sensor replaced the pick-up coil placed on the opposite surface of the excitation coil. Sinusoidal excitation waves of 5 Hz and 25 Hz with amplitudes ranging from 0.25 V to 9 V were applied to samples with different amounts of the sigma phase, and the microstructures were characterized by scanning electron microscopy. The results show that the best testing condition consists of applying waves with amplitudes from 1 V to 2 V and using the first harmonic amplitude. Thus, the test proved effective for detecting the formation of the deleterious sigma phase and can follow the ability to absorb energy by impact and, thus, the material embrittlement. Full article
Show Figures

Figure 1

Figure 1
<p>Used experimental setup: (1) signal generator, (2) shielded cables, (3) excitation coil, (4) material sample, (5) Hall effect sensor, (6) test bench with Faraday cage, (7) acquisition board, and (8) computer.</p>
Full article ">Figure 2
<p>Representation of the histogram for two situations, H<sub>0</sub> and H<sub>a</sub>, where one seeks to know with an error α how precisely the two measurements differ.</p>
Full article ">Figure 3
<p>(<b>a</b>) The optical microscopy of the DSS structure in the as-received condition, where δ is the ferrite phase and γ the austenite, and (<b>b</b>) the magnetic flux density variation as a function of the rotation angle.</p>
Full article ">Figure 4
<p>(<b>a</b>) The scanning electron microscopy image (10% KOH attack, 1000x of magnification) and (<b>b</b>) the X-ray diffractogram of the as-received condition sample (δ—ferrite and γ—austenite).</p>
Full article ">Figure 5
<p>(<b>a</b>) The scanning electron microscopy image (10% KOH attack, 1000X of magnification) and (<b>b</b>) the X-ray diffractogram of the sample treated at 850 °C for ¼ h (δ—ferrite, γ—austenite, and σ—sigma).</p>
Full article ">Figure 6
<p>(<b>a</b>) The scanning electron microscopy image (10% KOH attack, 1000X of magnification) and (<b>b</b>) the X-ray diffractogram of the sample treated at 850 °C for 2 h (δ—ferrite, γ—austenite, and σ—sigma).</p>
Full article ">Figure 7
<p>(<b>a</b>) Magnetic noise, measured in the magnetic flux density, of the conditions without the sigma phase, as a function of the time, after applying the 50 Hz high-pass filter for an excitation wave of 5 Hz and 1 V. (<b>b</b>) Magnetic noise of the conditions with 5% of the sigma phase, as a function of time, after applying the 50 Hz high-pass filter, for an excitation wave of 5 Hz and 1 V.</p>
Full article ">Figure 8
<p>RMS of the signal acquired by the Hall sensor as a function of the amplitude of a 5 Hz excitation wave applied in samples with and without treatment and a cutoff of 50 Hz.</p>
Full article ">Figure 9
<p>RMS of the signal acquired by the Hall sensor as a function of the amplitude of the 5 Hz excitation wave applied in samples with and without treatment and a cutoff frequency of 250 Hz.</p>
Full article ">Figure 10
<p>Module of the difference in RMS as a function of the amplitude of the 5 Hz excitation wave and the two tested cutoff frequencies.</p>
Full article ">Figure 11
<p>RMS of the signal acquired by the Hall sensor as a function of the amplitude of the excitation wave applied to the samples with and without treatment for an excitation frequency of 25 Hz and a cutoff of 50 Hz.</p>
Full article ">Figure 12
<p>RMS of the signal acquired by the Hall sensor as a function of the amplitude of the excitation wave applied to the 8 mm samples with and without treatment with an excitation frequency of 25 Hz and a cutoff of 250 Hz.</p>
Full article ">Figure 13
<p>RMS difference module as a function of the wave amplitude of the applied 25 Hz transmitter wave and the two cutoff frequencies.</p>
Full article ">Figure 14
<p>RMS of the signal acquired by the Hall sensor as a function of the amplitude of the 5 Hz excitation wave applied to 8 mm samples for conditions with different amounts of the sigma phase and a cutoff of 50 Hz.</p>
Full article ">Figure 15
<p>RMS variation of the first harmonic as a function of the amplitude of the 5 Hz and 25 Hz excitation waves and samples with and without the sigma phase. The 25 Hz and 3 V excitation wave error range is shown.</p>
Full article ">Figure 16
<p>Differences in percentage between conditions without and with the sigma phase as a function of the amplitude of the 5 Hz and 25 Hz excitation waves.</p>
Full article ">Figure 17
<p>RMS variation of the first harmonic as a function of the treatment time for the 5 Hz and 25 Hz excitation waves. The 5 Hz and 1 V excitation wave error range is shown.</p>
Full article ">
Back to TopTop