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40 pages, 15661 KiB  
Review
Breath and Beyond: Advances in Nanomedicine for Oral and Intranasal Aerosol Drug Delivery
by Simeng Du, Zhiyang Wen, Jinghan Yu, Yingying Meng, Yuling Liu and Xuejun Xia
Pharmaceuticals 2024, 17(12), 1742; https://doi.org/10.3390/ph17121742 (registering DOI) - 23 Dec 2024
Abstract
Designing and standardizing drug formulations are crucial for ensuring the safety and efficacy of medications. Nanomedicine utilizes nano drug delivery systems and advanced nanodevices to address numerous critical medical challenges. Currently, oral and intranasal aerosol drug delivery (OIADD) is the primary method for [...] Read more.
Designing and standardizing drug formulations are crucial for ensuring the safety and efficacy of medications. Nanomedicine utilizes nano drug delivery systems and advanced nanodevices to address numerous critical medical challenges. Currently, oral and intranasal aerosol drug delivery (OIADD) is the primary method for treating respiratory diseases worldwide. With advancements in disease understanding and the development of aerosolized nano drug delivery systems, the application of OIADD has exceeded its traditional boundaries, demonstrating significant potential in the treatment of non-respiratory conditions as well. This study provides a comprehensive overview of the applications of oral and intranasal aerosol formulations in disease treatment. It examines the key challenges limiting the development of nanomedicines in drug delivery systems, formulation processes, and aerosol devices and explores the latest advancements in these areas. This review aims to offer valuable insights to researchers involved in the development of aerosol delivery platforms. Full article
(This article belongs to the Section Pharmaceutical Technology)
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<p>Aerosolized NDDS overcomes different physiological barriers. (<b>A</b>) Representative trajectories of α-lactalbumin-derived peptides in intestinal mucus for 2 and 10 s were observed using multiparticle tracking. The logarithmic distribution of the effective diffusion coefficient of individual particles over 1 s is demonstrated. In ex vivo experiments, Cy5-labeled α-lactalbumin-derived peptides (red) were co-incubated with Alexa Fluor 488-WGA-labeled intestinal mucus (green) to visualize the two-dimensional diffusive coverage of the peptides in the mucus. Three-dimensional distributional imaging after 3 h of permeabilization demonstrates the distribution within a depth of 0–30 μm. Adapted from ref. [<a href="#B63-pharmaceuticals-17-01742" class="html-bibr">63</a>] with permission. (<b>B</b>) Schematic representation of DNA tetrahedrons, triangle DNA origami nanostructures, and DNA nanoribbons dissociated into i-primary structures upon acidic stimulation (**: <span class="html-italic">p</span> &lt; 0.01, ****: <span class="html-italic">p</span> &lt; 0.0001). Adapted from ref. [<a href="#B64-pharmaceuticals-17-01742" class="html-bibr">64</a>] with permission.</p>
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<p>Strategies for providing extended retention of atomized NDDS. (<b>A</b>) Schematic diagram of the N-in-M system demonstrating the structure of the N-in-M system and showing the mechanism of nanoparticle release. Adapted from ref. [<a href="#B83-pharmaceuticals-17-01742" class="html-bibr">83</a>] with permission. (<b>B</b>) Synthesis route of PHCK and the principle of prolonged retention time and treatment of allergic rhinitis. Adapted from ref. [<a href="#B84-pharmaceuticals-17-01742" class="html-bibr">84</a>] with permission.</p>
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<p>The ability of atomized NDDS to modulate drug release. (<b>A</b>) Schematic representation of the responsiveness and pH-sensitive mechanism of mMMP13@RP/P-KGF to MMP-2 and transmission electron microscopy (TEM) images of mMMP13@RP/P-KGF, amMMP13@RP/P-KGF and their nanoparticles pretreated with MMP-2 at pH 7.4 or 5.5 conditions are shown, scale bar: 300 nm. The particle sizes and zeta potentials of mMMP13@RP, mMMP13@RP/P-N3, mMMP13@RP/P-KGF, and amMMP13@RP/P-KGF were measured by dynamic light scattering, and the cumulative releases of KGF from amMMP13@RP/P-KGF were also demonstrated after treatment with different concentrations of MMP-2. Error lines indicate standard deviation (n = 3). Adapted from ref. [<a href="#B110-pharmaceuticals-17-01742" class="html-bibr">110</a>] with permission. (<b>B</b>) Schematic diagram of the MPS/D-SEL system demonstrating its mucus penetration and sequential drug release mechanism. (<b>C</b>) After inhalation of MPS-loaded lipo, SEL, D-SEL, or the physical mixture of MPS/SEL and free DNase I, the levels of anti-inflammatory cytokines (IL-4 and IL-10) in BALF, the level of MUC5AC in BALF, AB-PAS staining images showing goblet cell metaplasia (scale bar = 50 μm), and H&amp;E staining images (scale bar = 100 μm; zoom-in images scale bar = 50 μm; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, NS: <span class="html-italic">p</span> &gt; 0.05). Adapted from ref. [<a href="#B113-pharmaceuticals-17-01742" class="html-bibr">113</a>] with permission.</p>
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<p>Targeting ability of aerosolized NDDS. (<b>A</b>) Biodistribution of inhaled PT-BsAb assessed by fluorescence imaging (*: <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). Adapted from ref. [<a href="#B125-pharmaceuticals-17-01742" class="html-bibr">125</a>] with permission. (<b>B</b>) Preparation and distribution of exosomes and liposomes (**: <span class="html-italic">p</span> &lt; 0.01, ****: <span class="html-italic">p</span> &lt; 0.0001); scale bar: 50 nm, 50 μm and 1000 μm. Adapted from ref. [<a href="#B139-pharmaceuticals-17-01742" class="html-bibr">139</a>] with permission.</p>
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<p>Effect of prescription process on atomization stability, deposition, and redispersion of NDDS. (<b>A</b>) Effect of compositional variations of different LNP formulations on mRNA delivery efficiency. By varying the molar ratio of ionizable lipids, auxiliary phospholipids, and cholesterol, 19 formulations of LNPs were prepared, and their encapsulation rates after nebulization and transfection efficiencies in A549 cells were determined. Adapted from ref. [<a href="#B150-pharmaceuticals-17-01742" class="html-bibr">150</a>] with permission. (<b>B</b>) Schematic of the preparation of hydrogel-LNPs, stability testing of LNPs during nebulized delivery, demonstrating TEM results before and after nebulization of liposomes, A-LNPs, and B-LNPs, scale bar: 200 nm, as well as DLS results before and after nebulization of liposomes, A-LNPs, and B-LNPs, and permeability changes. Adapted from ref. [<a href="#B160-pharmaceuticals-17-01742" class="html-bibr">160</a>] with permission. (<b>C</b>) This figure illustrates the process of nebulizing blank cationic liposomes (CL), Lpx, and HNPs by SMI. The particle size and PDI of these particles were measured both before and after nebulization (*: <span class="html-italic">p</span> &lt; 0.05, **: <span class="html-italic">p</span> &lt; 0.01). Adapted from ref. [<a href="#B162-pharmaceuticals-17-01742" class="html-bibr">162</a>] with permission. (<b>D</b>) Schematic diagram of the composition and redispersion of AZM@FDKP~E-MPs. Adapted from ref. [<a href="#B178-pharmaceuticals-17-01742" class="html-bibr">178</a>] with permission.</p>
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<p>Aerosolization devices to improve NDDS stability, deposition, and redispersion. (<b>A</b>) Schematic representation of individual LNP/mRNAs including PEG lipids (blue), ionizable lipids (green), structured lipids (pink), and cholesterol (yellow), demonstrating representative size distributions of LNP/mRNAs under different treatments: untreated (grey), vibrating mesh (red), and MAP (blue), as well as the particle sizes of the LNPs/mRNAs after aerosolization, the changes in zeta potentials, changes in encapsulation rate, and schematic diagrams and results of FRET-based lipid membrane fusion assay are shown. Adapted from ref. [<a href="#B188-pharmaceuticals-17-01742" class="html-bibr">188</a>] with permission. (<b>B</b>) Principle of NM atomization. Adapted from ref. [<a href="#B189-pharmaceuticals-17-01742" class="html-bibr">189</a>] with permission. (<b>C</b>) Demonstration of intranasal deposition after 2 min of administration using a conventional liquid spray pump and Opt-Powder by gamma camera image information. Adapted from ref. [<a href="#B197-pharmaceuticals-17-01742" class="html-bibr">197</a>] with permission. (<b>D</b>) demonstrated the concept of in-flight electrically neutralized electrospray, including its working principle, experimental images, simulation of spray morphology in DC and AC modes in comparison with experiment, and simulated time series of the neutralization process. Adapted from ref. [<a href="#B198-pharmaceuticals-17-01742" class="html-bibr">198</a>] with permission.</p>
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<p>Statistical trends in the development of OIADD. (<b>A</b>) Number of OIADD-related publications from 2004 to 2023. (<b>B</b>) Key focus areas in OIADD research. (<b>C</b>) Proportion of clinical formulation studies. (<b>D</b>) Number of OIADD-related drugs approved by the FDA from 2004 to 2023.</p>
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16 pages, 1297 KiB  
Article
The Comparison of Accuracy of Post Space Digital Impressions Made by Three Different Intraoral Scanners: An In Vitro Study
by Abdullah A. Meshni, Saurabh Jain, Hanan Nasser Marie Osaysi, Khadijah Nasser Hezam and Samar Samir Gomaan Adlan
Diagnostics 2024, 14(24), 2893; https://doi.org/10.3390/diagnostics14242893 (registering DOI) - 23 Dec 2024
Abstract
Background and Objectives: The present study aims to assess and compare the accuracy of post-space impressions captured by three different intraoral scanners (IOS) using various canal diameters. Methods: Three extracted natural maxillary central incisors were selected and prepared for a 1 mm wide [...] Read more.
Background and Objectives: The present study aims to assess and compare the accuracy of post-space impressions captured by three different intraoral scanners (IOS) using various canal diameters. Methods: Three extracted natural maxillary central incisors were selected and prepared for a 1 mm wide margin and a 3 mm ferrule. All steps required for the endodontic procedure were performed, and the post space was prepared using post drills. The post length was kept constant at 12 mm, whereas the width was varied (Group 1: 1.4 mm, Group 2: 1.6 mm, and Group 3: 1.8 mm). Three IOSs (Trios3, iTero2, and Medit i700) were used to acquire a digital impression of the prepared post space. Each tooth was scanned 10 times by each scanner. So, in the end, 90 digital images were recorded, and the STL files were stored. GC Pattern resin was used to fabricate resin post and core patterns, which were scanned using an extraoral scanner (EOS). The STL file obtained was used as the reference file. To evaluate the trueness of the tested IOSs, each three-dimensional scan from an IOS was superimposed on the reference scan with the help of the Medit Design software 2.1.4. The software generates color plots and gives numerical values as deviations in the Root mean square (RMS) for the variance between the two superimposed scans. The data collected was tabulated for statistical analysis. One Way ANOVA was used to test the significance difference between three different IOSs, followed by Bonferroni Post-hoc test pairwise test to identify the differences between every two different IOS. Statistical significance was set at p < 0.05. Results: The mean deviation for trueness in post space impression values recorded by the Medit i700 was highest among groups 1, 2, and 3 [0.825 (±0.071), 0.673 (±0.042) and 0.516 (±0.039), respectively], followed by iTero2 [0.738 (±0.081), 0.569 (±0.043) and 0.470 (±0.037), respectively] and Trios3 [0.714 (±0.062), 0.530 (±0.040) and 0.418 (±0.024), respectively]. Significant differences were found between the groups for all three IOSs (Trios3: p-value < 0.0001; iTero2: p-value < 0.0001; Medit i700: p-value < 0.0001). Conclusions: Within the limitations of this study, it can be concluded that Trios3 IOS has higher accuracy (as it exhibited minimal deviation for trueness) in recording post space, followed by iTero2 and Mediti700 IOS. As the diameter of the post space is increased, the accuracy of recording by IOS increases. For all the tested IOSs (except for Trios3 and iTero2, when used to record post space with 1.8 mm canal diameter), the deviations in trueness were higher than the clinically acceptable limits. Thus, IOSs should be used cautiously when recording impressions of post spaces. Full article
(This article belongs to the Section Point-of-Care Diagnostics and Devices)
14 pages, 2391 KiB  
Article
Facile Preparation Route of Cellulose-Based Flame Retardant by Ball-Milling Mechanochemistry
by Mohamed Aaddouz, Fouad Laoutid, Jerome Mariage, Jevgenij Lazko, Bopha Yada, El Miloud Mejdoubi, Antoniya Toncheva and Philippe Dubois
Molecules 2024, 29(24), 6065; https://doi.org/10.3390/molecules29246065 (registering DOI) - 23 Dec 2024
Abstract
In this study, a sustainable cellulose-based flame-retardant additive was developed, characterized, and incorporated into polypropylene (PP). Microcrystalline cellulose (Cel) was chemically modified with P₂O₅ using the solvent-free ball-milling mechanochemistry approach at room temperature. This modification enabled phosphorus grafting onto cellulose, significantly enhancing the [...] Read more.
In this study, a sustainable cellulose-based flame-retardant additive was developed, characterized, and incorporated into polypropylene (PP). Microcrystalline cellulose (Cel) was chemically modified with P₂O₅ using the solvent-free ball-milling mechanochemistry approach at room temperature. This modification enabled phosphorus grafting onto cellulose, significantly enhancing the cellulose charring ability and improving the thermal stability of the char as revealed by thermogravimetric analysis (TGA). The resulting product, Cel-P, containing 4.15 wt.% phosphorus, was incorporated and uniformly dispersed as a flame-retardant (FR) additive at 30 wt.% in PP through melt processing. The PP+30-Cel-P composite demonstrated improved char formation and FR properties, including reduction of both peak heat release rate (pHRR) and total heat release (THR) in mass loss cone calorimetry (MLC). Moreover, lower light absorptivity was obtained by smoke opacity tests as compared to PP filled with unmodified cellulose. Full article
(This article belongs to the Special Issue Advances in Polymer Materials Based on Lignocellulosic Biomass)
18 pages, 498 KiB  
Systematic Review
Behind the Scenes of Adaptive Learning: A Scoping Review of Teachers’ Perspectives on the Use of Adaptive Learning Technologies
by Patricia D. Simon and Lily Min Zeng
Educ. Sci. 2024, 14(12), 1413; https://doi.org/10.3390/educsci14121413 (registering DOI) - 23 Dec 2024
Abstract
Adaptive learning technologies are emerging educational tools that personalize instruction and tasks to meet students’ current ability levels. Despite their increasing prevalence, the present discourse on adaptive learning software focuses on the technical aspects of adaptive learning systems without accounting for other factors [...] Read more.
Adaptive learning technologies are emerging educational tools that personalize instruction and tasks to meet students’ current ability levels. Despite their increasing prevalence, the present discourse on adaptive learning software focuses on the technical aspects of adaptive learning systems without accounting for other factors that impact their use in classrooms. In acknowledgment of the importance of teachers’ roles in the implementation of educational tools, this review examined studies about teachers’ perspectives on the use of adaptive learning technologies in their courses. A systematic search was conducted in four databases (ERIC, Academic Search Complete, Google Scholar, and Taylor Francis Online). Twenty-nine full-text articles were retained for analysis. A hybrid of deductive and inductive approaches was applied to analyze the data, using the factors described in the Technology Acceptance Model and its extensions as a guide. The findings showed that teachers who saw the long-term benefits of using adaptive learning technologies were more willing to invest time and effort to learn and use the tools in their classes. Barriers identified were the scant professional development opportunities for teachers, the programs’ complexities, and the demands on teachers’ time. To make adaptive learning programs work, teachers must be on board as co-designers and content creators, and they require ongoing technical and institutional support and sufficient preparation in teacher education programs. Full article
(This article belongs to the Section Technology Enhanced Education)
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<p>Systematic search procedure.</p>
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15 pages, 11668 KiB  
Article
Analysis of the Properties of Anticorrosion Systems Used for Structural Component Protection in Truck Trailers
by Wojciech Skotnicki and Dariusz Jędrzejczyk
Materials 2024, 17(24), 6303; https://doi.org/10.3390/ma17246303 (registering DOI) - 23 Dec 2024
Abstract
The article compares the properties of coatings (cataphoretic, hot-dip zinc, and thermo-diffusion zinc) applied to steel components used in the automotive industry. The research focused on the analysis of corrosion resistance, hardness measurements, and tribological properties conducted on steel guides used in trailer [...] Read more.
The article compares the properties of coatings (cataphoretic, hot-dip zinc, and thermo-diffusion zinc) applied to steel components used in the automotive industry. The research focused on the analysis of corrosion resistance, hardness measurements, and tribological properties conducted on steel guides used in trailer and truck body structures as well as fasteners (M12 × 40 bolts). The base surfaces were cleaned chemically. Corrosion resistance was tested in a salt chamber, while coating thickness was measured using the magnetic induction method. Coating hardness (HV 0.02) was assessed with a microhardness tester, and tribological properties were tested under dry friction conditions. The results showed that the zinc coatings demonstrated corrosion resistance far superior to paint coatings. Full article
(This article belongs to the Special Issue Metal Coatings for Wear and Corrosion Applications (Second Edition))
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Figure 1
<p>Steel guide appearance with the applied bolt connection (the location where samples were taken for testing is marked with a white arrow).</p>
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<p>Microstructure observed on the cross-section of the tested coatings using a scanning microscope: (<b>a</b>)—thermo-diffusion zinc coating, (<b>b</b>,<b>d</b>)—hot-dip zinc coating, (<b>c</b>)—EDS analysis of thermo-diffusion coating’s cross section according to the green line, (<b>e</b>)—cataphoretic coating.</p>
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<p>Microstructure observed on the cross-section of the tested coatings using a scanning microscope: (<b>a</b>)—thermo-diffusion zinc coating, (<b>b</b>,<b>d</b>)—hot-dip zinc coating, (<b>c</b>)—EDS analysis of thermo-diffusion coating’s cross section according to the green line, (<b>e</b>)—cataphoretic coating.</p>
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<p>Change in hardness measured on the cross-section of the tested coatings.</p>
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<p>Comparison of the roughness of the tested coatings.</p>
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<p>An example of a roughness profile (<b>a</b>) and surface topography of a hot-dip zinc coating (<b>b</b>).</p>
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<p>The course of changes in the friction coefficient value during a single measurement.</p>
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<p>Comparison of the average friction coefficient values determined for the tested coatings.</p>
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<p>The cross-section microstructure of the coating after tribological tests: (<b>a</b>)—hot-dip coating, (<b>b</b>)—thermo-diffusion coating, (<b>c</b>)—cataphoretic coating.</p>
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<p>Sample surface after tribological test: (<b>a</b>)—hot-dip coating, (<b>b</b>)—thermodiffusion coating, (<b>c</b>)—cataphoretic coating.</p>
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<p>Tested elements after the corrosion test: (<b>a</b>)—guide; (<b>b</b>)—M12 × 40 bolts.</p>
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12 pages, 4405 KiB  
Article
Effect of Ion-Assisted Deposition Energy of RF Source on Optical Properties, Microstructure, and Residual Stress of HfO2 Thin Films
by Bo Wang, Jian Zhang, Hai Liu, Haigui Yang, Yanchao Wang, Haifeng Wang, Jingjie Pan, Zhen Liu, Zhenfeng Shen, Wenkai Gao, Hanwen Hu, Yi Zhao, Haolong Tang, Tongtong Wang and Xiaoyi Wang
Coatings 2024, 14(12), 1616; https://doi.org/10.3390/coatings14121616 - 23 Dec 2024
Abstract
HfO2 thin films were prepared using radio frequency (RF) ion source-assisted deposition, and the effects of auxiliary ion energy on the microstructure, optical properties, and residual stress of the films were systematically studied. The experimental results showed that when the auxiliary ion [...] Read more.
HfO2 thin films were prepared using radio frequency (RF) ion source-assisted deposition, and the effects of auxiliary ion energy on the microstructure, optical properties, and residual stress of the films were systematically studied. The experimental results showed that when the auxiliary ion energy increased, the extinction coefficient, compressive stress, and optical band gap were gradually increased. These changes were attributed to increased grain boundary defects, crystal structure disorder, and grain size decrease due to high-energy ion bombardment. The HfO2 films deposited at a lower ion energy (600 V) exhibited higher surface quality (RMS = 0.78 nm), better optical properties (k = 10⁻5), and lower residual stress (1.26 GPa). Full article
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<p>Schematic diagram of the RF source-assisted deposition system.</p>
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<p>(<b>a</b>) X-ray diffraction patterns of HfO<sub>2</sub> films deposited at varying auxiliary ion energies. (<b>b</b>) The calculated grain size of the (−111) crystal plane of HfO<sub>2</sub> films deposited under different negative bias voltages.</p>
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<p>Schematic diagram of the changes in the microstructure of HfO<sub>2</sub> samples under auxiliary ion energy.</p>
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<p>Surface AFM images of HfO<sub>2</sub> samples; ((<b>a</b>) 600 V, (<b>b</b>) 700 V, (<b>c</b>) 800 V, (<b>d</b>) 900 V, (<b>e</b>) 1000 V, (<b>f</b>) 1100 V).</p>
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<p>Surface roughness of HfO<sub>2</sub> films deposited at different auxiliary ion energies.</p>
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<p>Transmission spectra of HfO<sub>2</sub> thin films deposited on a quartz substrate at different assist ion energies. The bottom center inset shows the larger-scale transmission spectrum in the wavelength range of 480 to 580 nm.</p>
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<p>Refractive index (<b>a</b>) and extinction coefficient spectra (<b>b</b>) of HfO<sub>2</sub> films prepared under different ion-assisted energies. Refractive index (<b>c</b>) and extinction coefficient (<b>d</b>) of HfO<sub>2</sub> films at 532 nm as a function of ion-assisted energy.</p>
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<p>Optical band gap of HfO<sub>2</sub> films deposited at different auxiliary ion energies.</p>
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<p>Residual stress distribution of HfO<sub>2</sub> films prepared under different ion-assisted energies. From (<b>a</b>–<b>f</b>), they are 600 V, 700 V, 800 V, 900 V, 1000 V, and 1100 V, respectively.</p>
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<p>Changes in the average residual stress of HfO<sub>2</sub> films prepared under different ion-assisted energies.</p>
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13 pages, 3458 KiB  
Article
A Novel Polytetrahydrofuran-Based Shape Memory Polyurethane Enhanced by Polyglycolide-Block-Polytetrahydrofuran-Block-Polyglycolide Copolymer
by Xin Li, Lingchen Mao, Weiqian Li, Han Wu, Suyang Dai, Rui Xiao, Jiayi Huang, Guodong Liu, Keda Yang, Wensheng Bu, Ni Jiang, Zhihua Gan and Zhenbo Ning
Polymers 2024, 16(24), 3610; https://doi.org/10.3390/polym16243610 - 23 Dec 2024
Abstract
A series of polyurethanes (PU-GT) were prepared using polyglycolide-block-polytetrahydrofuran-block-polyglycolide (PGA-PTHF-PGA), polytetrahydrofuran homopolymer (PTHF), glycerol, and hexamethylene diisocyanate (HDI) by a one-pot synthesis method. The non-isothermal crystallization and subsequent heating curves showed that the PTHF component in these polyurethanes could crystallize in a temperature [...] Read more.
A series of polyurethanes (PU-GT) were prepared using polyglycolide-block-polytetrahydrofuran-block-polyglycolide (PGA-PTHF-PGA), polytetrahydrofuran homopolymer (PTHF), glycerol, and hexamethylene diisocyanate (HDI) by a one-pot synthesis method. The non-isothermal crystallization and subsequent heating curves showed that the PTHF component in these polyurethanes could crystallize in a temperature range of −11.5~2.6 °C during the cooling process, and the melting temperatures of PTHF crystallites were in the range of 24.0~26.9 °C. The WAXD results implied that a small content of PGA could crystallize in the membranes of PU-GT polyurethanes. And compared with PU-GT-100, which did not contain the PGA-PTHF-PGA block polymer, other PU-GT polyurethanes showed excellent mechanical properties because of the existence of the PGA component. Moreover, these polyurethanes had temperature-responsive shape memory properties due to the PTHF crystallites. The temporary shape could be fixed at −20 °C and recovered to the permanent shape at 37 °C. We conducted two kinds of conceptual experiments using PU-GT-50 polyurethane, which showed its great potential for medical applications in vascular and wound repair. Full article
(This article belongs to the Special Issue Polyurethane Materials for Multifunctional Applications)
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<p>The synthesis of PU-GT polyurethane. (<b>a</b>) <sup>1</sup>H NMR spectra of PTHF and PGA-PTHF-PGA. (<b>b</b>) GPC curves of PTHF and PGA-PTHF-PGA. (<b>c</b>) Synthetic route. (<b>d</b>) FTIR curves (3700–550 cm<sup>−1</sup>) of PU-GT polyurethanes with different compositions. (<b>e</b>) FTIR curves (1800–1600 cm<sup>−1</sup>).</p>
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<p>Crystallization behaviors of PU-GT polyurethanes with different compositions. (<b>a</b>) DSC curves of non-isothermal crystallization at a rate of 10 °C/min from 230 °C to −40 °C. (<b>b</b>) The subsequent heating curves at a rate of 10 °C/min from −40 °C to 230 °C. (<b>c</b>) Thermal properties obtained from the non-isothermal DSC analysis; <span class="html-italic">T</span><sub>m, PTHF</sub> is the melting temperature of PTHF component during the heating process, <span class="html-italic">T</span><sub>c, PTHF</sub> is the crystallization temperature of PTHF component during the cooling process, <span class="html-italic">ΔH</span><sub>c, PTHF</sub> is the exothermic enthalpy of PTHF component obtained from non-isothermal DSC analysis, and <span class="html-italic">ΔH</span><sub>m, PTHF</sub> is the fusion enthalpy of PTHF obtained from the heating process. (<b>d</b>) WAXD results of different PU-GT polyurethanes.</p>
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<p>The tensile properties of PU-GT polyurethanes with different compositions. (<b>a</b>) Representative strain–stress curves, (<b>b</b>) tensile breaking strength, (<b>c</b>) elongation at break, and (<b>d</b>) toughness. Each experiment was repeated five times, and (<b>a</b>) was plotted from the most representative results. The average of the five sets of test results was calculated to obtain (<b>b</b>–<b>d</b>), and the error bars indicate the standard deviation of each set of data from the average.</p>
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<p>Shape memory behavior of PU-GT polyurethanes. (<b>a</b>) The shape fixity ratio (<span class="html-italic">R</span><sub>f</sub>) and (<b>b</b>) the shape recovery ratio (<span class="html-italic">R</span><sub>r</sub>). (<b>c</b>) Digital photographs showing the shape memory behavior of PU-GT-50. (<b>d</b>) Illustration of the shape memory behavior of PU-GT polyurethane.</p>
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<p>Biocompatibility of the PU-GT polyurethane. (<b>a</b>) Cell proliferation and (<b>b</b>) viability of L929 osteoblast-like cells cultured with PU-GT polyurethane. (<b>c</b>) Illustration of the potential application of PU-GT-50 as vascular repair materials. (<b>d</b>) The structure of PU-GT-50/SA. (<b>e</b>) Adhesion experiment. (<b>f</b>) Shape memory behavior of the double-layer PU-GT polyurethane, showing the permanent shape, the temporary shape after the crystallization at 0 °C, and the restored permanent shape after melting at 37 °C. (<b>g</b>) Illustration of the potential application as wound dressing of PU-GT-50/SA.</p>
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13 pages, 992 KiB  
Review
The Application of Molecularly Imprinted Polymers in Forensic Toxicology: Issues and Perspectives
by Susan Mohamed, Simone Santelli, Arianna Giorgetti, Guido Pelletti, Filippo Pirani, Paolo Fais and Jennifer P. Pascali
Chemosensors 2024, 12(12), 279; https://doi.org/10.3390/chemosensors12120279 - 23 Dec 2024
Abstract
Molecularly imprinted polymers (MIPs) are synthetic receptors designed to selectively bind specific molecules, mimicking natural antibody–antigen interactions. Produced through polymerization around a target molecule (template), MIPs create imprints that confer high specificity and binding affinity upon template removal. Initially developed in the 1970s [...] Read more.
Molecularly imprinted polymers (MIPs) are synthetic receptors designed to selectively bind specific molecules, mimicking natural antibody–antigen interactions. Produced through polymerization around a target molecule (template), MIPs create imprints that confer high specificity and binding affinity upon template removal. Initially developed in the 1970s with organic polymers, MIPs now play critical roles in separation sciences, catalysis, drug delivery, and sensor technology. In forensic science, MIPs offer potential for sample preparation, pre-concentration, and analyte detection, especially with complex biological and non-biological matrices. They exhibit superior stability under extreme conditions, enabling their use in challenging forensic contexts such as detecting new psychoactive substances or trace explosives. Despite advantages like reusability and high selectivity, MIPs face limitations in forensic analysis due to their complex synthesis, potential template leakage, and non-specific binding. Moreover, the lack of standardized protocols limits their mainstream adoption, as forensic applications require validated, reproducible methods. This review systematically assesses MIPs in forensic toxicology, focusing on their current capabilities, limitations, and potential for broader integration into forensic workflows. Future research should address standardization and evaluate MIPs’ effectiveness in diverse forensic applications to realize their full potential. Full article
(This article belongs to the Special Issue Chemical Sensing and Analytical Methods for Forensic Applications)
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<p>PRISMA 2020 flow diagram for new systematic reviews, which included searches of databases and registers only. Source: [<a href="#B10-chemosensors-12-00279" class="html-bibr">10</a>] This work is licensed under CC BY 4.0. To view a copy of this license, visit <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a> (accessed on 17 September 2024). * Consider, if feasible to do so, reporting the number of records identified from each database or register searched (rather than the total number across all databases/registers). ** If automation tools were used, indicate how many records were excluded by a human and how many were excluded by automation tools.</p>
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18 pages, 1205 KiB  
Systematic Review
Dimensional Accuracy of Intraoral Scanners in Recording Digital Impressions of Post and Core Preparations: A Systematic Review
by Saeed M. Alqahtani, Mohammed Salman Almalki, Mai Almarzouki, Saad Saleh AlResayes, Nisreen Nabiel Hassan, Arwa Jaber I. Mohana, Majed S. Altoman and Mohammed E. Sayed
Diagnostics 2024, 14(24), 2890; https://doi.org/10.3390/diagnostics14242890 - 23 Dec 2024
Abstract
Background: This study aims to perform a review by selecting, analyzing, and evaluating articles that discuss the accuracy of intraoral scanners (IOSs) in recording post space compared to conventional impression-making techniques. Methods: The review question framed using the PITR framework (participant, index test, [...] Read more.
Background: This study aims to perform a review by selecting, analyzing, and evaluating articles that discuss the accuracy of intraoral scanners (IOSs) in recording post space compared to conventional impression-making techniques. Methods: The review question framed using the PITR framework (participant, index test, targeted condition, and reference standard) is as follows: What is the dimensional accuracy (T) of impressions made using intraoral scanners (I) for post space (P) compared to impressions made using conventional techniques and digitalized using extraoral scanners (R)? Four electronic databases were searched using pre-set keywords. The guidelines and strategies recommended by PRISMA formed the basis for planning, executing, and documenting this systematic review. QUADAS-2 was used to critically analyze the quality of all the selected articles. Results: After excluding ineligible articles, the end synthesis has nine studies (n = 9) for qualitative analysis. All nine evaluated studies were found to be at risk of bias, with high or unclear risk in one or more domains. Three out of nine evaluated studies had unclear concerns regarding the applicability, and the remaining six had low concerns. In all the included studies, the IOSs were reported to have deviations in accuracy compared to the conventional techniques for making digital impressions of post space. Conclusions: The accuracy of IOSs was found to be inversely proportional to the length of post space and directly proportional to the diameter of post space. IOSs, when used adequately in short post spaces, can be an alternative to conventional impression-making for making custom posts and cores. Full article
(This article belongs to the Special Issue New Possibilities for Digital Diagnosis and Planning in Dentistry)
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<p>Article selection strategy based on PRISMA guidelines.</p>
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<p>Graphical presentation of QUADAS-2 results.</p>
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<p>Research trends on IOS use in post and core impressions.</p>
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16 pages, 10339 KiB  
Article
Exploring the Application Method of Bamboo Powder in Promoting the Development of Sustainable Outdoor Furniture
by Yafei Fan, Ziqian Zhu, Jiacheng Luan and Yi Liu
Sustainability 2024, 16(24), 11282; https://doi.org/10.3390/su162411282 - 23 Dec 2024
Abstract
With the depletion of fossil fuels, more and more green products are appearing in daily necessities. Bamboo is a common sustainable biomaterial with the characteristics of fast growth, easy bending, low cost, and easy processing, and it is widely used in furniture design. [...] Read more.
With the depletion of fossil fuels, more and more green products are appearing in daily necessities. Bamboo is a common sustainable biomaterial with the characteristics of fast growth, easy bending, low cost, and easy processing, and it is widely used in furniture design. However, the poor aging resistance and UV resistance of natural bamboo materials limit their application in outdoor furniture. In order to improve the service life of outdoor bamboo furniture, this study prepared bamboo boards from bamboo powder and utilized them in the design of outdoor furniture. The research was conducted in two stages. In the first stage, functional modification was carried out on the surface of bamboo fibers (BF). Epoxy resin and UV absorber ZnO were introduced into the bamboo powder matrix, and a three-dimensional network structure of bamboo powder-based polymer material was formed by adjusting the material ratio and reaction conditions. With the increase of ZnO content, the absorption of moisture by the bamboo powder-based polymer materials decreased. The compressive strength of 1.5%ZnO-Board reached 36.8 MPa, exceeding the compressive strength of C30 concrete. In the second stage, 1.5% ZnO-Board was selected for solidification and demolding, and used as the seat surface for outdoor chairs. Through the car crushing experiment, the chair panel did not undergo significant deformation during the car crushing process. The anti-aging experiment showed that the structure and morphology of the panel would not be damaged by long-term UV irradiation. The panel did not show any weight changes in the anti-water-absorption experiment. By using low-contrast color combinations, the seats can be organically integrated into the environmental background, effectively enhancing the coordination and unity of the overall aesthetic harmony of the space. Compared with the commonly used plastic outdoor seats, the outdoor seats prepared in this study showed a 144% increase in carbon reduction effect. This study highlights the potential of modified bamboo powder for the design of outdoor furniture, which is of great significance to reducing outdoor plastic products and promoting sustainable life. Full article
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<p>Preparation process ((<b>a</b>) Bamboo powder raw material; (<b>b</b>) Pretreatment of bamboo powder; (<b>c</b>) Blending treatment of zinc oxide, pretreated bamboo powder, and epoxy resin; (<b>d</b>) Curing and demolding process of bamboo powder-based polymers) of bamboo powder-based composite materials.</p>
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<p>The microstructure of ZnO-Board.</p>
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<p>(<b>a</b>) FTIR image of ZnO-Board, (<b>b</b>) UV Visible Absorption Spectroscopy of ZnO-Board, (<b>c</b>) Thermogravimetric curve of ZnO-Board, (<b>d</b>) Thermal degradation rate of ZnO-Board.</p>
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<p>Water contact angle (<b>a</b>) 0% ZnO-Board, (<b>b</b>) 0.5% ZnO-Board, (<b>c</b>) 1% ZnO-Board, (<b>d</b>) 1.5% ZnO-Board.</p>
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<p>Water absorption curve of ZnO-Board.</p>
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<p>Compressive strength testing of ZnO-Board.</p>
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<p>(<b>a</b>) ZnO-Board morphology after compression test. Surface condition after compression test of (<b>b</b>) 0% ZnO-Board, (<b>c</b>) 0.5% ZnO-Board, (<b>d</b>) 1% ZnO-Board, (<b>e</b>) 1.5% ZnO-Board.</p>
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<p>Outdoor chair finished product image.</p>
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<p>(<b>a</b>) Surface of chair after UV aging, (<b>b</b>) comparison of UV visible spectra before and after aging experiment.</p>
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16 pages, 5584 KiB  
Article
Analyses of the Properties of the NiO-Doped Ga2O3 Wide-Bandgap Semiconductor Thin Films
by Cheng-Fu Yang, En-Chi Tsao, Yi-Wen Wang, Hsin-Pei Lin, Teen-Hang Meen and Shu-Han Liao
Coatings 2024, 14(12), 1615; https://doi.org/10.3390/coatings14121615 - 23 Dec 2024
Abstract
The study began by pre-sintering Ga2O3 powder at 950 °C for 1 h, followed by the preparation of a mixture of Ga2O3 and 12 at% NiO powders to fabricate a source target material. An electron beam (e-beam) [...] Read more.
The study began by pre-sintering Ga2O3 powder at 950 °C for 1 h, followed by the preparation of a mixture of Ga2O3 and 12 at% NiO powders to fabricate a source target material. An electron beam (e-beam) system was then used to deposit NiO-doped Ga2O3 thin films on Si substrates. X-ray diffraction (XRD) analyses revealed that the pre-sintered Ga2O3 at 950 °C exhibited β-phase characteristics, and the deposited NiO-doped Ga2O3 thin films exhibited an amorphous phase. After the deposition of the NiO-doped Ga2O3 thin films, they were divided into two portions. One portion underwent various analyses directly, while the other was annealed at 500 °C in air before being analyzed. Field-emission scanning electron microscopy (FESEM) was utilized to process the surface observation, and the cross-sectional observation was primarily used to measure the thickness of the NiO-doped Ga2O3 thin films. UV-Vis spectroscopy was used to calculate the bandgap by analyzing the transmission spectra, while the Agilent B1500A was employed to measure the I-V characteristics. Hall measurements were also performed to assess the mobility, carrier concentration, and resistivity of both NiO-doped Ga2O3 thin films. The first innovation is that the 500 °C-annealed NiO-doped Ga2O3 thin films exhibited a larger bandgap and better electrical conductivity. The manuscript provides an explanation for the observed increase in the bandgap. Another important innovation is that the 500 °C-annealed NiO-doped Ga2O3 thin films revealed a high-energy bandgap of 4.402 eV. The third innovation is that X-ray photoelectron spectroscopy (XPS) analyses of the Ga2p3/2, Ga2p1/2, Ga3d, Ni2p3/2, and O1s peaks were conducted to further investigate the reasons behind the enhanced electrical conductivity of the 500 °C-annealed NiO-doped Ga2O3 thin films. Full article
(This article belongs to the Special Issue Coatings for Advanced Devices)
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<p>Schematic diagram for the NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>Schematic diagram to obtain the various NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and the different analyses for the various NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>Surface morphologies of (<b>a</b>) un-annealed and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>c</b>) the cross-sectional image of the deposited NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>EDS analysis of the 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films: (<b>a</b>) analysis area and (<b>b</b>) analysis result.</p>
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<p>Tauc plots of (<b>a</b>) un-annealed, (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films, and (<b>c</b>) un-annealed and undoped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>SIMS analysis results of Ga, Ni, Si, and O elements of (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>Current–voltage properties of the un-annealed and 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>XPS spectra of the Ga<sub>2p3/2</sub> peaks and the Gaussian-resolved components (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>XPS spectra of the Ga<sub>2p1/2</sub> peaks and the Gaussian-resolved components (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>XPS spectra of the Ga<sub>3d</sub> peaks and the Gaussian-resolved components in (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>XPS spectra of the Ni<sub>2p3/2</sub> and Ni <sub>2p1/2</sub> peaks and the Gaussian-resolved components of (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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<p>XPS spectra of the O<sub>1s</sub> peaks and the Gaussian-resolved components in (<b>a</b>) un-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films and (<b>b</b>) 500 °C-annealed NiO-doped Ga<sub>2</sub>O<sub>3</sub> thin films.</p>
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17 pages, 2243 KiB  
Article
In Situ Preparation of Silver Nanoparticles/Organophilic-Clay/Polyethylene Glycol Nanocomposites for the Reduction of Organic Pollutants
by Amina Sardi, Bouhadjar Boukoussa, Aouicha Benmaati, Kheira Chinoune, Adel Mokhtar, Mohammed Hachemaoui, Soumia Abdelkrim, Issam Ismail, Jibran Iqbal, Shashikant P. Patole, Gianluca Viscusi and Mohamed Abboud
Polymers 2024, 16(24), 3608; https://doi.org/10.3390/polym16243608 - 23 Dec 2024
Abstract
This work focuses on the preparation and application of silver nanoparticles/organophilic clay/polyethylene glycol for the catalytic reduction of the contaminants methylene blue (MB) and 4-nitrophenol (4-NP) in a simple and binary system. Algerian clay was subjected to a series of treatments including acid [...] Read more.
This work focuses on the preparation and application of silver nanoparticles/organophilic clay/polyethylene glycol for the catalytic reduction of the contaminants methylene blue (MB) and 4-nitrophenol (4-NP) in a simple and binary system. Algerian clay was subjected to a series of treatments including acid treatment, ion exchange with the surfactant hexadecyltrimethylammonium bromide (HTABr), immobilization of polyethylene glycol polymer, and finally dispersion of AgNPs. The molecular weight of polyethylene glycol was varied (100, 200, and 4000) to study its effect on the stabilization of silver nanoparticles (AgNPs) and the catalytic activity of the resulting samples. The results showed that the catalyst with the highest molecular weight of polyethylene glycol had the highest AgNP content. Catalyst mass, NaBH4 concentration, and type of catalyst were shown to have a significant influence on the conversion and rate constant. The material with the highest silver nanoparticle content was identified as the optimal catalyst for the reduction of both pollutants. The measured rate constants for the reduction of methylene blue (MB) and 4-nitrophenol (4-NP) were 164 × 10−4 s−1 and 25 × 10−4 s−1, respectively. The reduction of MB and 4-NP in the binary system showed high selectivity for MB dye, with rate constants of 64 × 10−4 s−1 and 9 × 10−4 s−1 for MB and 4-NP, respectively. The reuse of the best catalyst via MB dye reduction for four cycles showed good results without loss of performance. Full article
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<p>XRD patterns of obtained Nano-1, Nano-2, and Nano-3 nanocomposites.</p>
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<p>FTIR spectra of obtained samples before and after modification.</p>
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<p>XPS spectra of different nanocomposites: (<b>a</b>) XPS survey spectra, (<b>b</b>) high-resolution Ag3d XPS, (<b>c</b>) high-resolution O1s XPS, and (<b>d</b>) high-resolution C1s XPS.</p>
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<p>Thermal analysis of different samples: (<b>a</b>) TGA curves; (<b>b</b>) DTG curves.</p>
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<p>TEM images of obtained Nano-1, Nano-2, and Nano-3 nanocomposites.</p>
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<p>(<b>a</b>–<b>c</b>) UV–vis of MB dye catalyzed by Nano-1 at different masses. (<b>d</b>) Conversion of MB dye as a function of time. (<b>e</b>) Correlation plot between Nano-1 catalyst mass and MB dye conversion. (<b>f</b>) Plot of ln(C<sub>t</sub>/C<sub>0</sub>) as a function of time.</p>
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<p>(<b>a</b>,<b>b</b>) UV–vis of MB dye catalyzed by Nano-1 catalyst at different concentrations of [NaBH<sub>4</sub>]. (<b>c</b>) Conversion of MB dye as a function of time. (<b>d</b>) Plot of Ln(C<sub>t</sub>/C<sub>0</sub>) as a function of time.</p>
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<p>(<b>a</b>–<b>c</b>) UV–vis of MB dye catalyzed by different catalysts. (<b>d</b>) Conversion of MB dye as a function of time. (<b>e</b>) Plot of Ln(C<sub>t</sub>/C<sub>0</sub>) as a function of time.</p>
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<p>(<b>a</b>) UV–vis of MB dye and 4-NP catalyzed by Nano-3 catalyst in binary system. (<b>b</b>) Zeta potential as a function of solution pH. (<b>c</b>) Conversion of MB dye and 4-NP as a function of time. (<b>d</b>) Plot of ln(C<sub>t</sub>/C<sub>0</sub>) as a function of time.</p>
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<p>Reuse of Nano-3 catalyst via MB dye reduction.</p>
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16 pages, 429 KiB  
Article
Exploring Sustainable Approaches to Improving Student Intelligence Through Basketball-Specific Means in Higher Education
by Cristiana Maria Porfireanu, Nicoleta Leonte, Ofelia Popescu, Alina Daniela Moanta and Mihaita Alin Saftel
Educ. Sci. 2024, 14(12), 1409; https://doi.org/10.3390/educsci14121409 - 23 Dec 2024
Abstract
Sustainable education involves educating young people about the importance of varied physical activities and developing long-term skills for an active lifestyle. We choose basketball as a method for sustainable education because it is a sport with diverse technical procedures and tactical actions anda [...] Read more.
Sustainable education involves educating young people about the importance of varied physical activities and developing long-term skills for an active lifestyle. We choose basketball as a method for sustainable education because it is a sport with diverse technical procedures and tactical actions anda game that plays a significant role in cognitive functional development. This study aims to modernize physical education and sports education to meet current trends and needs. A modern approach to lessons can contribute to the mental and motor development of young people, forming individuals who value movement for health and physical well-being. Thus, integrating VR into physical education lessons (using the means of basketball) represents a paradigm shift in how students prepare and improve their motor function. The study focuses on non-specialized higher education, combining the cognitive benefits of sports with sustainable practices, as we found his to be a gap in our literature review. The experimental program used Raven’s Progressive Matrices, a cognitive ability test, to measure general intelligence. The data were collected on two groups of children (control and experimental, at the beginning of the experiment and after 39 lessons of 100 min each). The t Test results applied in SPSS showed a significant increase in average scores for Raven’s Progressive Matrices after performing the motor program using basketball-specific means, especially for the experimental group. In conclusion, basketball can be a valuable tool for improving cognitive abilities, along with academic and social stimulation, being the key to complete intellectual development. Full article
(This article belongs to the Topic Recent Advances in Physical Education and Sports)
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<p>Research stages.</p>
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15 pages, 6531 KiB  
Article
Preparation and Performance Study of Novel Foam Vegetation Concrete
by Teng Zhang, Tianbin Li, Hua Xu, Mengyun Wang and Lingling Lu
Materials 2024, 17(24), 6295; https://doi.org/10.3390/ma17246295 (registering DOI) - 23 Dec 2024
Abstract
Vegetation concrete is one of the most widely used substrates in ecological slope protection, but its practical application often limits the growth and nutrient uptake of plant roots due to consolidation problems, which affects the effectiveness of slope protection. This paper proposed the [...] Read more.
Vegetation concrete is one of the most widely used substrates in ecological slope protection, but its practical application often limits the growth and nutrient uptake of plant roots due to consolidation problems, which affects the effectiveness of slope protection. This paper proposed the use of a plant protein foaming agent as a porous modifier to create a porous, lightweight treatment for vegetation concrete. Physical performance tests, direct shear tests, plant growth tests, and scanning electron microscopy experiments were conducted to compare and analyze the physical, mechanical, microscopic characteristics, and phyto-capabilities of differently treated vegetation concrete. The results showed that the higher the foam content, the more significant the porous and lightweight properties of the vegetation concrete. When the foam volume was 50%, the porosity increased by 106.05% compared to the untreated sample, while the volume weight decreased by 20.53%. The shear strength, cohesion, and internal friction angle of vegetation concrete all showed a decreasing trend with increasing foaming agent content. Festuca arundinacea grew best under the 30% foaming agent treatment, with germinative energy, germinative percentage, plant height, root length, and underground biomass increasing by 6.31%, 13.22%, 8.57%, 18.71%, and 34.62%, respectively, compared to the untreated sample. The scanning electron microscope observation showed that the pore structure of vegetation concrete was optimized after foam incorporation. Adding plant protein foaming agents to modify the pore structure of vegetation concrete is appropriate, with an optimal foam volume ratio of 20–30%. This study provides new insights and references for slope ecological restoration engineering. Full article
(This article belongs to the Special Issue Functional Cement-Based Composites for Civil Engineering (Volume II))
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<p>Vegetation concrete: (<b>a</b>) Vegetation concrete, (<b>b</b>) Consolidation of Vegetation concrete (Magnified view).</p>
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<p>Foam made by high-speed mixer: (<b>a</b>) High-speed mixer, (<b>b</b>) Foam.</p>
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<p>Sample preparation: (<b>a</b>) Add powdered components and stir; (<b>b</b>) Add water and stir; (<b>c</b>) Add foam. (<b>d</b>) Stirring, (<b>e</b>) Add larger granular components and stir; (<b>f</b>) Foam vegetation concrete.</p>
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<p>Vegetation concrete samples with different foam volumes: (<b>a</b>) 0%, (<b>b</b>) 10%, (<b>c</b>) 20%, (<b>d</b>) 30%, (<b>e</b>) 40%, (<b>f</b>) 50%.</p>
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<p>Change in volume weight and porosity of vegetation concrete with added foam volume.</p>
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<p>Shear strength of vegetation concrete at different ages.</p>
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<p>Influence of foam volume on cohesion and angle of internal friction of vegetated concrete.</p>
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<p>The growth conditions of <span class="html-italic">Festuca arundinacea</span> on vegetation concrete with different treatments: (<b>a</b>) 0%, (<b>b</b>) 10%, (<b>c</b>) 20%, (<b>d</b>) 30%, (<b>e</b>) 40%, (<b>f</b>) 50%.</p>
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<p>Influence of foam volume on the biomass of <span class="html-italic">Festuca arundinacea</span>.</p>
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<p>SEM images of vegetation concrete samples at ×2000 magnification: (<b>a</b>) 0%, (<b>b</b>) 10%, (<b>c</b>) 20%, (<b>d</b>) 30%, (<b>e</b>) 40%, (<b>f</b>) 50%.</p>
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<p>SEM images of vegetation concrete with 0% and 50% foam volume at ×5000 magnification: (<b>a</b>) 0%, (<b>b</b>) 50%.</p>
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19 pages, 5387 KiB  
Article
Cytotoxic Natural Products from Cryptomeria japonica (Thunb. ex L.) D.Don
by Bjørn Tobiassen Heieren, Anja Strandvoll Dyrdal, Lars Herfindal, Bjarte Holmelid, Cato Brede, Heidi Lie Andersen and Torgils Fossen
Int. J. Mol. Sci. 2024, 25(24), 13735; https://doi.org/10.3390/ijms252413735 - 23 Dec 2024
Abstract
Cryptomeria japonica is a commercially important tree native to Japan. The tree belongs to the ancient genus Cryptomeria and has found important uses as a medicinal plant, as well as a main source of timber in Japan. In recent years, there has been [...] Read more.
Cryptomeria japonica is a commercially important tree native to Japan. The tree belongs to the ancient genus Cryptomeria and has found important uses as a medicinal plant, as well as a main source of timber in Japan. In recent years, there has been an increased interest in discovering extended uses of C. japonica as a source of novel bioactive natural products with potential applications as lead compounds for active principles of future drugs. The compounds were isolated by a combination of two-phase extraction, XAD-7 Amberlite column chromatography, Sephadex LH-20 column chromatography and preparative High Performance Liquid Chromatography (HPLC). The structures were determined by a combination of several 1D and 2D Nuclear Magnetic Resonance (NMR) experiments and high-resolution mass spectrometry. Here, we report on the isolation and characterization of the novel biflavone glucoside hinokiflavone 7″-O-β-glucopyranoside, in addition to sixteen known compounds including the flavonols quercetin, quercetin 3-O-α-rhamnopyranoside and quercetin 3-O-β-galactopyranoside, the dihydroflavonols taxifolin 3-O-β-glucopyranoside, taxifolin 7-O-β-glucopyranoside, the flavanones naringenin, naringenin 7-O-β-galactopyranoside and eriodictyol 4′-O-β-glucopyranoside, the flavanol catechin, the biflavonoid amentoflavone, the dihydrochalcone phloretin 2′-O-β-glucopyranoside, the sesquiterpenoid roseoside, the polyphenolic compounds chlorogenic acid, methyl chlorogenate and the flavanocoumarins catechin-(7,8)-7″-(3,4 dihydroxyphenyl)-dihydro-8″(3H)-pyranone, and mururin A. The compounds exhibited low-to-moderate cytotoxic activity against MOLM-13 leukemia cells. Full article
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Figure 1

Figure 1
<p><span class="html-italic">Cryptomeria japonica</span> grown in the Arboretum of University of Bergen. Photo: Heidi Lie Andersen. Photo was taken on 14 November 2024.</p>
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<p>Molecular structures of quercetin (<b>1</b>), quercetin 3-<span class="html-italic">O</span>-<span class="html-italic">α</span>-rhamnopyranoside (<b>2</b>), quercetin 3-<span class="html-italic">O</span>-<span class="html-italic">β</span>-galactopyranoside (<b>3</b>), taxifolin 3-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>4</b>), taxifolin 7-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>5</b>), naringenin (<b>6</b>), naringenin 7-<span class="html-italic">O</span>-<span class="html-italic">β</span>-galactopyranoside (<b>7</b>), eriodictyol 4′-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>8</b>), catechin (<b>9</b>), amentoflavone (<b>10</b>), phloretin 2′-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>11</b>), roseoside (<b>12</b>), chlorogenic acid (<b>13</b>), and methyl chlorogenate (<b>13m</b>), in addition to the rare natural products catechin-(7,8)-7″-(3,4-dihydroxyphenyl)-dihydro-8″(3H)-pyranone (<b>14</b>), hinokiflavone 7″-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>15</b>), and Mururin A (<b>16</b>).</p>
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<p>Expanded regions of the 2D <sup>1</sup>H-<sup>13</sup>C HMBC spectrum (<b>left</b>) and the 2D <sup>1</sup>H-<sup>1</sup>H ROESY spectrum (<b>right</b>) of hinokiflavone 7″-<span class="html-italic">O</span>-<span class="html-italic">β</span>-glucopyranoside (<b>15</b>) showing important crosspeaks for determination of linkages between the substructures of the compound. Blue arrows highlight the observed correlations in the molecular structure.</p>
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