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15 pages, 4402 KiB  
Article
Electrophoretic Deposition of Chitosan Coatings on the Porous Titanium Substrate
by Julia Flesińska, Magdalena Szklarska, Izabela Matuła, Adrian Barylski, Sylwia Golba, Julia Zając, Maciej Gawlikowski, Przemysław Kurtyka, Barbara Ilnicka and Grzegorz Dercz
J. Funct. Biomater. 2024, 15(7), 190; https://doi.org/10.3390/jfb15070190 - 9 Jul 2024
Abstract
Medicine is looking for solutions to help implant patients recover more smoothly. The porous implants promote osteointegration, thereby providing better stabilization. Introducing porosity into metallic implants enhances their biocompatibility and facilitates osteointegration. The introduction of porosity is also associated with a reduction in [...] Read more.
Medicine is looking for solutions to help implant patients recover more smoothly. The porous implants promote osteointegration, thereby providing better stabilization. Introducing porosity into metallic implants enhances their biocompatibility and facilitates osteointegration. The introduction of porosity is also associated with a reduction in Young’s modulus, which reduces the risk of tissue outgrowth around the implant. However, the risk of chronic inflammation remains a concern, necessitating the development of coatings to mitigate adverse reactions. An interesting biomaterial for such modifications is chitosan, which has antimicrobial, antifungal, and osteointegration properties. In the present work, a porous titanium biomaterial was obtained by powder metallurgy, and electrophoretic deposition of chitosan coatings was used to modify its surface. This study investigated the influence of ethanol content in the deposition solution on the quality of chitosan coatings. The EPD process facilitates the control of coating thickness and morphology, with higher voltages resulting in thicker coatings and increased pore formation. Ethanol concentration in the solution affects coating quality, with higher concentrations leading to cracking and peeling. Optimal coating conditions (30 min/10 V) yield high-quality coatings, demonstrating excellent cell viability and negligible cytotoxicity. The GIXD and ATR-FTIR analysis confirmed the presence of deposited chitosan coatings on Ti substrates. The microstructure of the chitosan coatings was examined by scanning electron microscopy. Biological tests showed no cytotoxicity of the obtained materials, which allows for further research and the possibility of their use in medicine. In conclusion, EPD offers a viable method for producing chitosan-based coatings with controlled properties for biomedical applications, ensuring enhanced patient outcomes and implant performance. Full article
(This article belongs to the Special Issue Advances in Biomedical Alloys and Surface Modification)
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11 pages, 3218 KiB  
Article
Electrospinning Polyvinyl Alcohol Reinforced with Chitin: The Effect of the Degree of Acetylation
by Andres Krumme and James D. Mendez
Polymers 2024, 16(14), 1955; https://doi.org/10.3390/polym16141955 - 9 Jul 2024
Abstract
Nanocomposites made via electrospinning were constructed of polyvinyl alcohol (PVA) and chitin. Chitin was extracted from a natural source (Fomes fomentarius), which allowed for precise control of the chemical properties of the resulting material. Chitin was chosen as a filler due [...] Read more.
Nanocomposites made via electrospinning were constructed of polyvinyl alcohol (PVA) and chitin. Chitin was extracted from a natural source (Fomes fomentarius), which allowed for precise control of the chemical properties of the resulting material. Chitin was chosen as a filler due to its low cost and widespread availability. Increasing the degree of acetylation of the chitin increased the Young’s Modulus of the resulting fiber mats but only at relatively high levels. While composites at lower acetylation levels were stable, no increase in the Young’s Modulus was observed, presumably due to decreased intermolecular bonding among fibers. The results suggest that precise control of the degree of acetylation of chitin, more than the loading amount and dispersibility, significantly impacts composite formation. Full article
(This article belongs to the Special Issue Advances in Applications and Sustainability of Electrospinning)
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<p>Idealized forms of chitin (<b>left</b>) and chitosan (<b>right</b>).</p>
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<p>Characteristic stress/strain curve for chitin/chitosan and PVA electrospun films.</p>
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<p>Young’s Modulus of fiber mats with 7% PVA and varying concentrations of chitin with a 26.1% degree of acetylation.</p>
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<p>Young’s Modulus of fiber mats with 7% PVA and varying concentrations of chitin with a 35.5% degree of acetylation.</p>
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<p>Electrospun fiber mats composed of chitin with a DA of 26.1% showed beading at both 0.5% (<b>left</b>) and 2% loading (<b>right</b>).</p>
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<p>Electrospun fiber mats composed of chitin with a DA of 35.5% showed beading at 0.5% loading (<b>left</b>), similar to a lower DA, but smooth fibers were evident at 2% loading (<b>right</b>).</p>
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<p>Young’s Modulus of fiber mats containing 1% of chitin (DA 35.5%) and varying concentrations of PVA.</p>
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<p>Young’s Modulus of fiber mats containing 1% of chitin (DA 26.1%) and varying concentrations of PVA.</p>
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<p>Young’s Modulus of fiber mats comprises 10% PVA and 1% chitin with varying degrees of acetylation.</p>
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26 pages, 10235 KiB  
Article
In Vitro Evaluation of Colistin Conjugated with Chitosan-Capped Gold Nanoparticles as a Possible Formulation Applied in a Metered-Dose Inhaler
by Narumon Changsan, Apichart Atipairin, Poowadon Muenraya, Rutthapol Sritharadol, Teerapol Srichana, Neelam Balekar and Somchai Sawatdee
Antibiotics 2024, 13(7), 630; https://doi.org/10.3390/antibiotics13070630 - 6 Jul 2024
Viewed by 415
Abstract
Inhaled colistin is used to treat pneumonia and respiratory infections through nebulization or dry powder inhalers. Nevertheless, the development of a metered-dose inhaler (MDI) for colistin, which could enhance patient convenience and treatment efficacy, has not yet been developed. Colistin is known for [...] Read more.
Inhaled colistin is used to treat pneumonia and respiratory infections through nebulization or dry powder inhalers. Nevertheless, the development of a metered-dose inhaler (MDI) for colistin, which could enhance patient convenience and treatment efficacy, has not yet been developed. Colistin is known for its ability to induce cellular toxicity. Gold nanoparticles (AuNPs) can potentially mitigate colistin toxicity. Therefore, this study aimed to evaluate the antimicrobial effectiveness of colistin conjugated with chitosan-capped gold nanoparticles (Col-CS-AuNPs) and their potential formulation for use with MDIs to deliver the aerosol directly to the deep lung. Fourier-transform infrared spectroscopy, nuclear magnetic resonance, and elemental analysis were used to characterize the synthesized Col-CS-AuNPs. Drug release profiles fitted with the most suitable release kinetic model were evaluated. An MDI formulation containing 100 µg of colistin per puff was prepared. The aerosol properties used to determine the MDI performance included the fine particle fraction, mass median aerodynamic diameter, and geometric standard deviation, which were evaluated using the Andersen Cascade Impactor. The delivered dose uniformity was also determined. The antimicrobial efficacy of the Col-CS-AuNP formulation in the MDI was assessed. The chitosan-capped gold nanoparticles (CS-AuNPs) and Col-CS-AuNPs had particle sizes of 44.34 ± 1.02 and 174.50 ± 4.46 nm, respectively. CS-AuNPs effectively entrapped 76.4% of colistin. Col-CS-AuNPs exhibited an initial burst release of up to 60% colistin within the first 6 h. The release mechanism was accurately described by the Korsmeyer–Peppas model, with an R2 > 0.95. The aerosol properties of the Col-CS-AuNP formulation in the MDI revealed a high fine particle fraction of 61.08%, mass median aerodynamic diameter of 2.34 µm, and geometric standard deviation of 0.21, with a delivered dose uniformity within 75–125% of the labeled claim. The Col-CS-AuNP MDI formulation completely killed Escherichia coli at 5× and 10× minimum inhibitory concentrations after 6 and 12 h of incubation, respectively. The toxicity of CS-AuNP and Col-CS-AuNP MDI formulations in upper and lower respiratory tract cell lines was lower than that of free colistin. The stability of the Col-CS-AuNP MDI formulation was maintained for at least 3 months. The Col-CS-AuNP MDI formulation effectively eradicated bacteria over a 12-h period, showing promise for advancing lung infection treatments. Full article
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<p>The SEM images of CS-AuNPs (<b>A</b>) and Col-CS-AuNPs (<b>B</b>).</p>
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<p>Schematic diagram of the synthesis of colistin conjugated with chitosan-capped gold nanoparticles (Col-CS-AuNPs).</p>
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<p>Cumulative colistin release (%) from Col-CS-AuNPs over ten days (<b>A</b>). Colistin release from Col-CS-AuNPs was fitted to kinetic models (<b>B</b>–<b>E</b>). Colistin release was fitted to each kinetic model: zero-order kinetic model by plotting cumulative % drug release vs. time (<b>B</b>), first-order kinetic model by plotting the logarithmic value of the remaining percent drug release vs. time (<b>C</b>), simplified Higuchi model by plotting cumulative % drug release vs. the square root of time (<b>D</b>), and Korsmeyer–Peppas model by plotting the log-cumulative % drug release vs. log time (<b>E</b>). The Korsmeyer–Peppas model showed a high correlation with R<sup>2</sup> &gt; 0.95. Dots represent the drug released at a specified time point, and the dashed line represents the regression line, as shown in each graph.</p>
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<p>Colistin deposition (%) in each stage of the Andersen Cascade Impactor (ACI, USP apparatus 1) determined at an airflow rate of 28.3 L/min. Results are presented as mean ± SD, <span class="html-italic">n</span> = 6. Cut-off diameters are as follows: Stage 0 (9.0 μm), Stage 1 (5.8 μm), Stage 2 (4.7 μm), Stage 3 (3.3 μm), Stage 4 (2.1 μm), Stage 5 (1.1 μm), Stage 6 (0.7 μm), and Stage 7 (0.4 μm).</p>
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<p>A time-kill kinetics curve of Col-CS-AuNP product concentrate of MDI formulation against <span class="html-italic">E. coli</span> at concentrations of 1×, 5×, and 10× MIC values. The samples were incubated with the tested bacteria at specified intervals (<span class="html-italic">n</span> = 3). The asterisk (*) indicates significant differences (<span class="html-italic">p</span>-value &lt; 0.05) compared to treated and non-treated samples at the same intervals. The dashed line represents a limit of detection of 2 log CFU/mL.</p>
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<p>Percent viability of NCI-H358 cells (upper respiratory tract cell line) (<b>A</b>) and A549 cells (lower respiratory tract cell line) (<b>B</b>) to determine cytotoxic effect by MTT assay after incubation with colistin (orange bars), colistin conjugated with chitosan-capped gold nanoparticles metered-dose inhaler (Col-CS-AuNP MDI) formulation (red bars), and chitosan-capped gold nanoparticles (CS-AuNPs) used as blank (green bars). Data represent the mean ± standard deviation, <span class="html-italic">n</span> = 3. The asterisk (*) indicates significant differences (<span class="html-italic">p</span>-value &lt; 0.05) between the groups.</p>
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53 pages, 15874 KiB  
Review
How the Chemical Properties of Polysaccharides Make It Possible to Design Various Types of Organic–Inorganic Composites for Catalytic Applications
by Sandugash Akhmetova, Alima Zharmagambetova, Eldar Talgatov, Assemgul Auyezkhanova, Makpal Malgazhdarova, Murat Zhurinov, Arlan Abilmagzhanov, Aigul Jumekeyeva and Alima Kenzheyeva
Molecules 2024, 29(13), 3214; https://doi.org/10.3390/molecules29133214 - 6 Jul 2024
Viewed by 271
Abstract
Recently, the use of plant-origin materials has become especially important due to the aggravation of environmental problems and the shortage and high cost of synthetic materials. One of the potential candidates among natural organic compounds is polysaccharides, characterized by a number of advantages [...] Read more.
Recently, the use of plant-origin materials has become especially important due to the aggravation of environmental problems and the shortage and high cost of synthetic materials. One of the potential candidates among natural organic compounds is polysaccharides, characterized by a number of advantages over synthetic polymers. In recent years, natural polysaccharides have been used to design composite catalysts for various organic syntheses. This review is devoted to the current state of application of polysaccharides (chitosan, starch, pectin, cellulose, and hydroxyethylcellulose) and composites based on their catalysis. The article is divided into four main sections based on the type of polysaccharide: (1) chitosan-based nanocomposites; (2) pectin-based nanocomposites; (3) cellulose (hydroxyethylcellulose)-based nanocomposites; and (4) starch-based nanocomposites. Each section describes and summarizes recent studies on the preparation and application of polysaccharide-containing composites in various chemical transformations. It is shown that by modifying polysaccharides, polymers with special properties can be obtained, thus expanding the range of biocomposites for catalytic applications. Full article
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<p>Structure of a chitosan molecule.</p>
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<p>CS@Cu<sub>2</sub>O-catalyzed coupling reactions of (<b>a</b>) aryl bromide/chloride with phenols and (<b>b</b>) of <span class="html-italic">N</span>-heterocyclic amines with aryl bromide/iodides. Reprinted with permission from ref. [<a href="#B47-molecules-29-03214" class="html-bibr">47</a>]. Copyright 2019 Science China Press.</p>
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<p>The homocoupling of arylboronic acid reaction.</p>
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<p>Suzuki–Miyaura cross-coupling of phenylboronic acid with different aryl iodides/bromides.</p>
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<p>C-X amination of aryl halides with ammonia (<b>a</b>) and C-H oxidation of alkylarenes to ketones with tert-butyl hydroperoxide (TBHP) (<b>b</b>).</p>
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<p>Pd@25M18-catalyzed Mizoroki–Heck reaction of aromatic iodides with olefins.</p>
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<p>Preparation of the CSM@Cu<sup>0</sup> catalyst (<b>a</b>) and its application to the boron addition reactions (<b>b</b>). Reprinted from ref. [<a href="#B53-molecules-29-03214" class="html-bibr">53</a>].</p>
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<p>Schematic illustration outlining the preparation and structure of the CS<sub>x</sub>-BPA-PW catalysts [<a href="#B54-molecules-29-03214" class="html-bibr">54</a>].</p>
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<p>Reaction network of the dibenzothiophene (DBT) hydrodesulfurization process.</p>
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<p>Reaction network of n-hex-2-yne hydrogenation.</p>
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<p>Preparation of the Pd-Zn@CS/SiO<sub>2</sub> membrane catalyst (<b>a</b>) and its application for the reductive homocoupling of various aryl halides (<b>b</b>). Adapted from [<a href="#B58-molecules-29-03214" class="html-bibr">58</a>].</p>
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<p>Reductive decolorization of Congo red using NaBH<sub>4</sub> as a reductive agent in ambient conditions.</p>
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<p>Schematic diagram of a micro fluidic device [<a href="#B61-molecules-29-03214" class="html-bibr">61</a>].</p>
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<p>Plausible mechanism for the synthesis of 5-substituted hydantoins using Fe<sub>3</sub>O<sub>4</sub>-chitosan as a magnetic catalyst. Reaction conditions: aldehyde (1 mmol), ammonium carbonate (5 mmol), Zn(CN)<sub>2</sub> (1 mmol), catalyst (20 mg), and 60 °C. Reprinted with permission from ref. [<a href="#B64-molecules-29-03214" class="html-bibr">64</a>]. Copyright 2016 Oxford International Collaboration Centre Press.</p>
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<p>Two proposed mechanistic routes for the synthesis of 1,4-dihydropyridine derivatives using Fe<sub>3</sub>O<sub>4</sub>@chitosan as a catalyst. The first proposed mechanism: step 1; step 2; step 3. The second proposed mechanism: step 1′; step 2′; step 3′. Reprinted with permission from ref. [<a href="#B66-molecules-29-03214" class="html-bibr">66</a>]. Copyright 2016 Springer Nature.</p>
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<p>Schematic illustration of the synthesis of the mesoporous magnetic biomass-based acidic FCHC-SO<sub>3</sub>H catalyst [<a href="#B67-molecules-29-03214" class="html-bibr">67</a>].</p>
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<p>One-pot, three-component synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo-[α]xanthene-11-one derivatives. Adapted from [<a href="#B68-molecules-29-03214" class="html-bibr">68</a>].</p>
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<p>Preparation of HPA@Fe<sub>3</sub>O<sub>4</sub>-Al<sub>2</sub>O<sub>3</sub>/CS-CG (<b>a</b>) and its application in the synthesis of 6-amino-8-aryl-7-cyano-8<span class="html-italic">H</span>-[1,3] dioxolo-[4,5-g]-chromene (<b>b</b>). Reprinted from ref. [<a href="#B69-molecules-29-03214" class="html-bibr">69</a>].</p>
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<p>Synthetic procedure for the fabrication of Fe<sub>3</sub>O<sub>4</sub>@CS@MS@Ag as a catalyst. Reprinted from ref. [<a href="#B70-molecules-29-03214" class="html-bibr">70</a>].</p>
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<p>Preparation of MCS@PhTet@Cu(II) (<b>a</b>) and its application in the synthesis of 3-imino-2-phenylisoindolin-1-one derivatives (<b>b</b>). Reprinted from ref. [<a href="#B71-molecules-29-03214" class="html-bibr">71</a>].</p>
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<p>Transesterification reaction [<a href="#B73-molecules-29-03214" class="html-bibr">73</a>].</p>
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<p>Enantiomer-selective transesterification of racemic ethanols mediated by immobilized CaL-B.</p>
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<p>Schematic representation of <span class="html-italic">D</span>-glucose oxidation to <span class="html-italic">D</span>-gluconic acid in the presence of peroxidase (HRP) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS).</p>
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<p>The plausible mechanism for the cascade alcohol oxidation–Knoevenagel condensation reaction, highlighting the catalyst effect. Reprinted from ref. [<a href="#B82-molecules-29-03214" class="html-bibr">82</a>].</p>
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<p>Structural formula of pectin.</p>
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<p>Synthesis of tetrahydrobenzo[b]pyran and 3,4-dihydropyrano[c]chromene derivatives in the presence of pectin.</p>
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<p>Synthesis of dihydropyrano[2,3-c]pyrazole derivatives.</p>
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<p>Chemoselectivity in the oxidation of sulfides and the oxidative coupling of thiols (<b>a</b>), as well as the oxidative coupling of thiols by using γ-Fe<sub>2</sub>O<sub>3</sub>/Cu@HPECGs with H<sub>2</sub>O<sub>2</sub> (<b>b</b>).</p>
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<p>Scheme of the formation of a polymer-stabilized palladium catalyst deposited on a solid support for the process of acetylene compound hydrogenation.</p>
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<p>Synthesis of Plutella xylostella (<b>a</b>) and Cylas formicarius (<b>b</b>) pheromones.</p>
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<p>Buchwald–Hartwig cross-coupling reaction.</p>
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<p>Preparation of a Cu/Pectin@Fe<sub>3</sub>O<sub>4</sub> nanocomposite and its application for the synthesis of 1-substituted-1H tetrazoles. Reprinted from ref. [<a href="#B132-molecules-29-03214" class="html-bibr">132</a>].</p>
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<p>Preparation of Cu<sup>2+</sup>@Fe<sub>3</sub>O<sub>4</sub>–pectin and its application in regioselective three-component triazole synthesis.</p>
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<p>Structural formula of cellulose.</p>
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<p>Oxidation of sulfides and thiols.</p>
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<p>TEM (<b>a</b>) and SEM images (<b>b</b>) of Cel/Ben/V. Reprinted from ref. [<a href="#B137-molecules-29-03214" class="html-bibr">137</a>].</p>
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<p>Hydrogenation of chlorate on a Pd-Pt/CB-Fe<sub>2</sub>O<sub>3</sub> support.</p>
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<p>Synthesis of cyclic carbonate using various epoxides.</p>
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<p>Reaction of α,β-unsaturated compounds in the presence of a catalyst.</p>
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<p>Sonogashira cross-coupling reaction.</p>
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<p>Synthesis of 4-<span class="html-italic">H</span>-pyrimido[2,1-b]benzothiazole derivatives in the presence of Fe<sub>3</sub>O<sub>4</sub>@nanocellulose/Sb(V) under solvent-free conditions at 90 °C.</p>
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<p>Structural formula of an HEC monomer.</p>
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<p>Synthetic schemes for the preparation of HEC-NHC-Pd [<a href="#B158-molecules-29-03214" class="html-bibr">158</a>].</p>
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<p>Hydrogenation of α-pinene to cis-pinane and trans-pinane.</p>
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<p>Fischer–Tropsch synthesis to paraffins (<b>a</b>) and olefins (<b>b</b>).</p>
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<p>Supported on ZnO polysaccharide-stabilized palladium catalyst for the hydrogenation of acetylene compounds. Reprinted from ref. [<a href="#B22-molecules-29-03214" class="html-bibr">22</a>].</p>
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<p>Structure of amylose and amylopectin in starch. Reprinted from ref. [<a href="#B165-molecules-29-03214" class="html-bibr">165</a>].</p>
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<p>Dehydrogenation of d-DMAB in the absence of solvent.</p>
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<p>Synthesis of starch-crt@Au [<a href="#B173-molecules-29-03214" class="html-bibr">173</a>].</p>
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<p>Catalytic hydrogenation of <span class="html-italic">p</span>-nitroanisole to <span class="html-italic">p</span>-anisidine with NaBH<sub>4</sub> at room temperature.</p>
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<p>Schematic of the procedure for the preparation of the nanocomposite Talc\HWSS@Fe<sub>3</sub>O<sub>4</sub> (<b>a</b>) and its catalytic application in a three-component reaction (<b>b</b>). Adapted from ref. [<a href="#B175-molecules-29-03214" class="html-bibr">175</a>].</p>
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<p>Proposed mechanism of 4<span class="html-italic">H</span>-pyran and tetrahydro-4<span class="html-italic">H</span>-chromene synthesis in the presence of a Ag/Fe<sub>3</sub>O<sub>4</sub>@starch magnetic nanocatalyst. Reprinted from ref. [<a href="#B176-molecules-29-03214" class="html-bibr">176</a>].</p>
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<p>Suggested structure of the βCD-IL@M-Starch-catalyzed (<b>a</b>); synthesis of imidazo[2,1-b][1,3,4]thiadiazol-5-amine derivatives (<b>b</b>) [<a href="#B177-molecules-29-03214" class="html-bibr">177</a>].</p>
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<p>Iron–nitrogen heterocyclic carbene (Fe-NHC) on HACS and S350, catalyzing the dehydration of fructose to 5-(hydroxymethyl) furfural [<a href="#B179-molecules-29-03214" class="html-bibr">179</a>].</p>
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<p>Mechanism of sulfonated carbon-based solid acid catalyst synthesis: (<b>a</b>) the removal of water from the starch; (<b>b</b>) the dissociation of the (-C-O-C-) bond, forming polycyclic aromatic carbon sheets; (<b>c</b>) the sulfonation of the carbon sheets with sulfuric acid; (<b>d</b>) carbonization with the formation of larger layered polycyclic aromatic sheets. Adapted from ref. [<a href="#B180-molecules-29-03214" class="html-bibr">180</a>].</p>
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25 pages, 2695 KiB  
Article
Biological and Physicochemical Analysis of Sr-Doped Hydroxyapatite/Chitosan Composite Layers
by Maria Elena Zarif, Bogdan Bita, Sasa Alexandra Yehia-Alexe, Irina Negut, Gratiela Gradisteanu Pircalabioru, Ecaterina Andronescu and Andreea Groza
Polymers 2024, 16(13), 1922; https://doi.org/10.3390/polym16131922 - 5 Jul 2024
Viewed by 264
Abstract
In this work results are presented on the evaluation of HAp, HApSr, HAp_CS, and HApSr_CS layers deposited on Ti substrates regarding L929 cell viability and cytotoxicity as well as antimicrobial activity against Staphylococcus aureus, in connection with their physicochemical properties. The HAp [...] Read more.
In this work results are presented on the evaluation of HAp, HApSr, HAp_CS, and HApSr_CS layers deposited on Ti substrates regarding L929 cell viability and cytotoxicity as well as antimicrobial activity against Staphylococcus aureus, in connection with their physicochemical properties. The HAp and HApSr layers generated by radio-frequency magnetron sputtering technique were further covered with chitosan by a matrix-assisted pulsed laser evaporation technique. During the plasma depositions, the Ti substrates were heated externally by a home-made oven above 100 °C. The HApSr_CS layers generated on the unpolished Ti substrates at 100 °C and 400 °C showed the highest biocompatibility properties and antimicrobial activity against Staphylococcus aureus. The morphology of the layer surfaces, revealed by scanning electron microscopy, is dependent on substrate temperature and substrate surface roughness. The optically polished surfaces of Ti substrates revealed grain-like and microchannel structure morphologies of the layers deposited at 25 °C substrate temperature and 400 °C, respectively. Chitosan has no major influence on HAp and HApSr layer surface morphologies. X-ray photoelectron spectroscopy indicated the presence of Ca 2p3/2 peak characteristic of the HAp structure even in the case of the HApSr_CS samples generated at a 400 °C substrate temperature. Fourier transform infrared spectroscopy investigations showed shifts in the wavenumber positions of the P-O absorption bands as a function of Sr or chitosan presence in the HAp layers generated at 25, 100, and 400 °C substrate temperatures. Full article
(This article belongs to the Special Issue Recent Advances in Polymer Composites for Functional Applications)
22 pages, 5618 KiB  
Article
Evaluation of Different Pectic Materials Coming from Citrus Residues in the Production of Films
by Mónica Umaña, Susana Simal, Esperanza Dalmau, Christelle Turchiuli and Chloé Chevigny
Foods 2024, 13(13), 2138; https://doi.org/10.3390/foods13132138 - 5 Jul 2024
Viewed by 471
Abstract
This article explores the use of citrus residues as a source of different pectic materials for packaging film production: a water-soluble orange residue extract (WSE) (~5% pectin), semi-pure pectins extracted in citric acid (SP) (~50% pectin), and commercial pure citrus pectins (CP). First, [...] Read more.
This article explores the use of citrus residues as a source of different pectic materials for packaging film production: a water-soluble orange residue extract (WSE) (~5% pectin), semi-pure pectins extracted in citric acid (SP) (~50% pectin), and commercial pure citrus pectins (CP). First, these materials were characterized in terms of chemical composition. Then, films were produced using them pure or mixed with chitosan or glycerol through solvent-casting. Finally, antioxidant activity, functional properties (e.g., mechanical and gas barrier properties), and visual appearance of the films were assessed. WSE films showed the highest antioxidant activity but the lowest mechanical strength with the highest elongation at break (EB) (54%); incorporating chitosan increased the films’ strength (Young’s modulus 35.5 times higher). SP films showed intermediate mechanical properties, reinforced by chitosan addition (Young’s modulus 4.7 times higher); they showed an outstanding dry O2 barrier. CP films showed a similar O2 barrier to SP films and had the highest Young’s modulus (~29 MPa), but their brittleness required glycerol for improved pliability, and chitosan addition compromised their surface regularity. Overall, the type of pectic material determined the film’s properties, with less-refined pectins offering just as many benefits as pure commercial ones. Full article
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<p>Total phenolic content (TPC) and antioxidant activity according to the ABTS and FRAP methods of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 6).</p>
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<p>Moisture content (MC), solubility in water (S), and swelling capacity (SC) of the films produced with the water-soluble orange residue extract (WSE), semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 2).</p>
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<p>Thickness and mechanical properties: Young’s modulus (YM), maximum tensile strength (TS), and elongation at break (EB) of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 10 for the thickness, and n = 4 for the mechanical properties).</p>
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<p>Water vapor permeability (WVP) of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 2).</p>
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<p>Oxygen permeability (OP) of the films produced with the semi-pure pectin (SP) and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 2).</p>
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<p>SEM surface micrographs of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP) and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan).</p>
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<p>CIELab coordinates, white index (WI), and opacity of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan). Different letters in the same parameter indicate significant (<span class="html-italic">p</span> &lt; 0.05) differences among films (n = 3).</p>
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<p>Photographs of the films produced with the water-soluble orange residue extract (WSE), the semi-pure pectin (SP), and the commercial pure pectin (CP), alone (control) or in combination with chitosan (Chi) or glycerol (Gly) or only with chitosan (chitosan).</p>
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15 pages, 792 KiB  
Article
Chitosan–Gelatin Scaffolds Loaded with Different Antibiotic Formulations for Regenerative Endodontic Procedures Promote Biocompatibility and Antibacterial Activity
by Maha Alghofaily, Aljowhara Almana, Jenan Alrayes, Rhodanne Lambarte, Michael D. Weir and Fahd Alsalleeh
J. Funct. Biomater. 2024, 15(7), 186; https://doi.org/10.3390/jfb15070186 - 4 Jul 2024
Viewed by 310
Abstract
Background: This study investigated the biocompatibility and antibacterial efficacy of chitosan–gelatin (CH-G) scaffolds loaded with slow-releasing antibiotic formulations used in regeneration endodontic procedures (REPs). Methods: Scaffolds were fabricated using freeze drying and loaded with varying concentrations of augmentin or modified triple antibiotic [...] Read more.
Background: This study investigated the biocompatibility and antibacterial efficacy of chitosan–gelatin (CH-G) scaffolds loaded with slow-releasing antibiotic formulations used in regeneration endodontic procedures (REPs). Methods: Scaffolds were fabricated using freeze drying and loaded with varying concentrations of augmentin or modified triple antibiotic paste (mTAP). High-resolution scanning electron microscopy (SEM) was used to characterize the scaffold, while drug release was monitored via UV-Vis spectrophotometry. Immortalized human mesenchymal stem cells (hMSCs) were cultured on CH-G scaffolds alone (control), either 0.1 mg/mL or 1 mg/mL of augmentin or mTAP, and 10 mg/mL calcium hydroxide (Ca(OH)2). Cell viability and proliferation were assessed using the Alamar Blue assay and SEM, respectively, and live/dead staining further corroborated cell viability. Antibacterial activity against Enterococcus faecalis was evaluated using the MTT assay and confocal laser scanning microscopy (CLSM). Results: Augmentin at 0.1 mg/mL appeared to promote better cell growth and attachment within the scaffolds than all other formulations, exhibiting acceptable viability. SEM revealed improved cell attachment in augmentin and mTAP groups compared to the Ca(OH)2 group. Augmentin at 1 mg/mL and mTAP groups significantly reduced viable bacteria compared to controls. Augmentin groups and mTAP at 1 mg/mL were highly effective in eliminating E. faecalis biofilms, with mTAP potentially causing more cell death within the remaining biofilm structures. Conclusions: This study suggests that CH-G scaffolds loaded with augmentin and mTAP, particularly at a concentration of 1 mg/mL, offer promising advantages for REPs due to their biocompatibility, antibacterial efficacy, and ability to promote cell attachment. Further research may explore the long-term effects in clinical settings. Full article
(This article belongs to the Special Issue Advanced Materials for Clinical Endodontic Applications (2nd Edition))
16 pages, 3917 KiB  
Article
Chitosan-Integrated Curcumin–Graphene Oxide/Copper Oxide Hybrid Nanocomposites for Antibacterial and Cytotoxicity Applications
by Anandhavelu Sanmugam, Logesh Kumar Sellappan, Abbishek Sridharan, Swathy Manoharan, Ananda Babu Sairam, Abdulrahman I. Almansour, Subha Veerasundaram, Hyun-Seok Kim and Dhanasekaran Vikraman
Antibiotics 2024, 13(7), 620; https://doi.org/10.3390/antibiotics13070620 - 3 Jul 2024
Viewed by 328
Abstract
This study deals with the facile synthesis of a single-pot chemical technique for chitosan–curcumin (CUR)-based hybrid nanocomposites with nanostructured graphene oxide (GO) and copper oxide (CuO) as the antibacterial and cytotoxic drugs. The physicochemical properties of synthesized hybrid nanocomposites such as CS-GO, CS-CuO, [...] Read more.
This study deals with the facile synthesis of a single-pot chemical technique for chitosan–curcumin (CUR)-based hybrid nanocomposites with nanostructured graphene oxide (GO) and copper oxide (CuO) as the antibacterial and cytotoxic drugs. The physicochemical properties of synthesized hybrid nanocomposites such as CS-GO, CS-CuO, CS-CUR-GO, and CS-CUR-GO/CuO were confirmed with various advanced tools. Moreover, the in vitro drug release profile of the CS-CUR-GO/CuO nanocomposite exhibited sustained and controlled release during different time intervals. Also, the antibacterial activity of the CS-CUR-GO/CuO hybrid nanocomposite presented the maximum bactericidal effect against Staphylococcus aureus and Escherichia coli pathogens. The hybrid nanocomposites revealed improved cytotoxicity behaviour against cultured mouse fibroblast cells (L929) via cell adhesion, DNA damage, and proliferation. Thus, the chitosan-based hybrid nanocomposites offer rich surface area, biocompatibility, high oxidative stress, and bacterial cell disruption functionalities as a potential candidate for antibacterial and cytotoxicity applications. Full article
17 pages, 4094 KiB  
Article
Atomistic Modeling of Quaternized Chitosan Head Groups: Insights into Chemical Stability and Ion Transport for Anion Exchange Membrane Applications
by Mirat Karibayev, Bauyrzhan Myrzakhmetov, Dias Bekeshov, Yanwei Wang and Almagul Mentbayeva
Molecules 2024, 29(13), 3175; https://doi.org/10.3390/molecules29133175 - 3 Jul 2024
Viewed by 298
Abstract
The chemical stability and ion transport properties of quaternized chitosan (QCS)-based anion exchange membranes (AEMs) were explored using Density Functional Theory (DFT) calculations and all-atom molecular dynamics (MD) simulations. DFT calculations of LUMO energies, reaction energies, and activation energies revealed an increasing stability [...] Read more.
The chemical stability and ion transport properties of quaternized chitosan (QCS)-based anion exchange membranes (AEMs) were explored using Density Functional Theory (DFT) calculations and all-atom molecular dynamics (MD) simulations. DFT calculations of LUMO energies, reaction energies, and activation energies revealed an increasing stability trend among the head groups: propyl trimethyl ammonium chitosan (C) < oxy propyl trimethyl ammonium chitosan (B) < 2-hydroxy propyl trimethyl ammonium chitosan (A) at hydration levels (HLs) of 0 and 3. Subsequently, all-atom MD simulations evaluated the diffusion of hydroxide ions (OH) through mean square displacement (MSD) versus time curves. The diffusion coefficients of OH ions for the three types of QCS (A, B, and C) were observed to increase monotonically with HLs ranging from 3 to 15 and temperatures from 298 K to 350 K. Across different HLs and temperatures, the three QCS variants exhibited comparable diffusion coefficients, underlining their effectiveness in vehicular transport of OH ions. Full article
(This article belongs to the Special Issue Advances in the Theoretical and Computational Chemistry)
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<p>Depiction of <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="normal">S</mi> <mi mathvariant="normal">N</mi> </msub> <mn>2</mn> </mrow> </semantics></math> degradation reactions for QCS segments (<b>A</b>–<b>C</b>) at the HL 0.</p>
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<p>Depiction of <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="normal">S</mi> <mi mathvariant="normal">N</mi> </msub> <mn>2</mn> </mrow> </semantics></math> degradation reactions for QCS segments (<b>A</b>–<b>C</b>) at the HL 3.</p>
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<p>Representation of LUMO densities for the optimized ground state geometries of QCS segments, including (<b>A</b>) 2-hydroxy propyl trimethyl ammonium chitosan, (<b>B</b>) oxy propyl trimethyl ammonium chitosan, and (<b>C</b>) propyl trimethyl ammonium chitosan.</p>
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<p>RDFs for the correlation between the oxygen atom of <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ion and the nitrogen atom of QCS (types <b>A</b>–<b>C</b>) in the presence of explicit water molecules at the different HLs.</p>
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<p>MSD vs. time curves at different HLs for <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ions and <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="normal">H</mi> <mn>2</mn> </msub> <mi mathvariant="normal">O</mi> </mrow> </semantics></math> molecules in systems with QCS types (<b>A</b>–<b>C</b>), respectively.</p>
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<p>Snapshot of water clusters surrounding QCS types (<b>A</b>–<b>C</b>) AEMs at various HLs. Drawing method for water: Quick Surface and color scheme for water: blue; Drawing method for <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ion: VdW representation and color scheme for <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ion: yellow (oxygen), grey (hydrogen); Drawing method for QCS: CPK representation and color scheme for QCS: violet (carbon), grey (hydrogen), red (oxygen), blue (nitrogen).</p>
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<p>RDFs for the correlation between the oxygen atom of <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ion and the nitrogen atom of QCS (types <b>A</b>–<b>C</b>) in the presence of explicit water molecules at the different temperatures.</p>
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<p>MSD vs. time curves at different temperature values for <math display="inline"><semantics> <msup> <mi>OH</mi> <mo>−</mo> </msup> </semantics></math> ions and <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="normal">H</mi> <mn>2</mn> </msub> <mi mathvariant="normal">O</mi> </mrow> </semantics></math> in systems with QCS types (<b>A</b>–<b>C</b>), respectively.</p>
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<p>Representative structures of different QCS segments: (<b>A</b>) 2-hydroxy propyl trimethyl ammonium chitosan, (<b>B</b>) oxy propyl trimethyl ammonium chitosan, and (<b>C</b>) propyl trimethyl ammonium chitosan.</p>
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<p>Illustration of the representative segment of QCS (A) for the <math display="inline"><semantics> <mrow> <msub> <mi mathvariant="normal">S</mi> <mi mathvariant="normal">N</mi> </msub> <mn>2</mn> </mrow> </semantics></math> degradation reaction.</p>
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29 pages, 1050 KiB  
Review
Valorization of Seafood Waste for Food Packaging Development
by Zhijing Zhan, Yiming Feng, Jikai Zhao, Mingyu Qiao and Qing Jin
Foods 2024, 13(13), 2122; https://doi.org/10.3390/foods13132122 - 3 Jul 2024
Viewed by 654
Abstract
Packaging plays a crucial role in protecting food by providing excellent mechanical properties as well as effectively blocking water vapor, oxygen, oil, and other contaminants. The low degradation of widely used petroleum-based plastics leads to environmental pollution and poses health risks. This has [...] Read more.
Packaging plays a crucial role in protecting food by providing excellent mechanical properties as well as effectively blocking water vapor, oxygen, oil, and other contaminants. The low degradation of widely used petroleum-based plastics leads to environmental pollution and poses health risks. This has drawn interest in renewable biopolymers as sustainable alternatives. The seafood industry generates significant waste that is rich in bioactive substances like chitin, chitosan, gelatins, and alginate, which can replace synthetic polymers in food packaging. Although biopolymers offer biodegradability, biocompatibility, and non-toxicity, their films often lack mechanical and barrier properties compared with synthetic polymer films. This comprehensive review discusses the chemical structure, characteristics, and extraction methods of biopolymers derived from seafood waste and their usage in the packaging area as reinforcement or base materials to guide researchers toward successful plastics replacement and commercialization. Our review highlights recent advancements in improving the thermal durability, mechanical strength, and barrier properties of seafood waste-derived packaging, explores the mechanisms behind these improvements, and briefly mentions the antimicrobial activities and mechanisms gained from these biopolymers. In addition, the remaining challenges and future directions for using seafood waste-derived biopolymers for packaging are discussed. This review aims to guide ongoing efforts to develop seafood waste-derived biopolymer films that can ultimately replace traditional plastic packaging. Full article
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<p>Biopolymers derived from seafood waste with potential food packaging applications.</p>
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<p>(<b>a</b>) The chemical structure of chitin; (<b>b</b>) the molecular structure of two common crystal structures of α-chitin and β-chitin [<a href="#B29-foods-13-02122" class="html-bibr">29</a>]; (<b>c</b>) the chemical structure of chitosan; (<b>d</b>) the representative chemical structure of gelatin; (<b>e</b>) the chemical structure of alginate as a single unit; (<b>f</b>) the representative alginate chain.</p>
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17 pages, 3430 KiB  
Article
Chitosan-Based Films with Essential Oil Components for Food Packaging
by Magdalena Woźniak, Joanna Młodziejewska, Karolina Stefanowska, Lucyna Mrówczyńska, Anna Sip, Renata Dobrucka and Izabela Ratajczak
Coatings 2024, 14(7), 830; https://doi.org/10.3390/coatings14070830 - 3 Jul 2024
Viewed by 362
Abstract
Chitosan-based films show great potential in terms of application in food preservation and are also promising carriers of biologically active ingredients. This paper presents the potential use of chitosan-based films with the addition of essential oil components, e.g., carvacrol, eugenol, and isoeugenol, intended [...] Read more.
Chitosan-based films show great potential in terms of application in food preservation and are also promising carriers of biologically active ingredients. This paper presents the potential use of chitosan-based films with the addition of essential oil components, e.g., carvacrol, eugenol, and isoeugenol, intended for food packaging. The characteristics of the obtained films were determined, including antibacterial, mechanical, barrier, and structural parameters. In addition, the antibacterial and antioxidant effects of the essential oil components were assessed. Eugenol (44.41%) and isoeugenol (43.56%) showed high antiradical activities, similar to the activity of Trolox (44.33%), which is used as a standard antioxidant. In turn, carvacrol was characterized by the strongest effect against the examined strains of bacteria, both Gram-positive and Gram-negative. The chitosan film with carvacrol showed the most valuable antibacterial and mechanical properties (tensile strength and elongation at break). The antibacterial activities of the chitosan–carvacrol films were higher than that of the carvacrol solution. The inhibition zones of the chitosan–carvacrol films were in the range 29–41 mm (except for Enterococcus faecalis, with an inhibition zone of 15 mm) compared to the inhibition zones of the carvacrol solution (28 mm). The results showed that chitosan is an effective carrier of fragrance compounds, mainly carvacrol. However, all the tested chitosan-based films with the addition of fragrance compounds showed appropriate parameters (biological, mechanical, and barrier), which makes them an ecological alternative to plastics intended for food packaging. Full article
(This article belongs to the Special Issue Recent Advances in Food Bio-Preservation Films)
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<p>The chemical structures of the essential oil components.</p>
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<p>The antiradical activities of the tested compounds. Trolox was used as a standard antioxidant. Identical superscripts next to the results mean no significant difference (for <span class="html-italic">p</span> &lt; 0.05) between the mean values according to Tukey’s post hoc HSD test.</p>
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<p>The hemolytic activities of the tested compounds. Identical superscripts next to the results mean no significant difference (for <span class="html-italic">p</span> &lt; 0.05) between the mean values according to Tukey’s post hoc HSD test.</p>
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<p>The tensile strengths (<b>A</b>) and elongations at break (<b>B</b>) of the chitosan-based films (CHT—pure chitosan film; CHT-CAR—chitosan–carvacrol film; CHT-EUG—chitosan–eugenol film; CH-ISOEUG—chitosan–isoeugenol film). Identical superscripts next to the results mean no significant difference (for <span class="html-italic">p</span> &lt; 0.05) between the mean values according to Tukey’s post hoc HSD test.</p>
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<p>The water vapor transmission rates (WVTRs) determined for the tested chitosan-based films (CHT—pure chitosan film; CHT-CAR—chitosan–carvacrol film; CHT-EUG—chitosan–eugenol film; CH-ISOEUG—chitosan–isoeugenol film). Identical superscripts next to the results mean no significant difference (for <span class="html-italic">p</span> &lt; 0.05) between the mean values according to Tukey’s post hoc HSD test.</p>
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<p>The ATR-FTIR spectra of the chitosan-based films (CHT—pure chitosan film; CHT-CAR—chitosan–carvacrol film; CHT-EUG—chitosan–eugenol film; CH-ISOEUG—chitosan–isoeugenol film).</p>
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21 pages, 10322 KiB  
Article
The Effect of Nanoclay Type on the Mechanical Properties and Antibacterial Activity of Chitosan/PVA Nanocomposite Films
by Hadisehsadat Farrokhi, Mojtaba Koosha, Navid Nasirizadeh, Mahshid Salari, Majid Abdouss, Tianduo Li and Yinghua Gong
J. Compos. Sci. 2024, 8(7), 255; https://doi.org/10.3390/jcs8070255 - 2 Jul 2024
Viewed by 333
Abstract
Nanoclays are a class of nanomaterials extensively used to prepare polymer nanocomposites. In this study, four types of common nanoclays were selected to prepare chitosan–polyvinyl alcohol (CP) nanocomposite films. Montmorillonite cloisite Na+ (MMT), organically modified montmorillonite (OMMT), and bentonite (BNT), as layered [...] Read more.
Nanoclays are a class of nanomaterials extensively used to prepare polymer nanocomposites. In this study, four types of common nanoclays were selected to prepare chitosan–polyvinyl alcohol (CP) nanocomposite films. Montmorillonite cloisite Na+ (MMT), organically modified montmorillonite (OMMT), and bentonite (BNT), as layered aluminosilicates, and halloysite nanotubes (HNT), as a tubular nanoclay, were blended with CP films at concentrations of 1.5, 3 and 4.5%. The nanocomposite films were characterized by FTIR, XRD, SEM/EDX, AFM, tensile strength, and antibacterial tests. SEM/EDX results showed a more uniform distribution of the OMMT and HNT nanoclays in the polymer matrix. AFM images showed a rougher surface for nanocomposite films compared to CP film. Increasing the nanoclay concentration in the films from 1.5 to 4.5% resulted in higher tensile strength for HNT and MMT while the trend was reversed for OMMT and BNT. Among the samples, nanocomposite films composed of OMMT and BNT showed the highest tensile strength at the lowest concentrations (CP-OMMT1.5 99 ± 3.7 MPa, CP-B1.5 81 ± 1.5 MPa). The nanocomposite films prepared from OMMT showed the highest antibacterial activity against E. coli and S. aureus with an inhibition zone of 15 and 19 mm, respectively. The results of this study showed that BNT and OMMT are promising nanoclays for enhancing the mechanical properties and antibacterial activity of hydrophilic polymers. The results of this research can provide new insights into selecting suitable nanoclays for different applications. Full article
(This article belongs to the Special Issue Biopolymeric Matrices Reinforced with Natural Fibers and Nanofillers)
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<p>XRD patterns for (<b>A</b>) pure nanoclays and (<b>B</b>) CP film and its nanocomposites.</p>
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<p>XRD patterns for (<b>A</b>) pure nanoclays and (<b>B</b>) CP film and its nanocomposites.</p>
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<p>FTIR spectra of (<b>A</b>) HNT, BNT, MMT, and OMMT pure nanoclays, CP films (<b>B</b>), and their nanocomposite films with HNT (<b>B</b>), BNT (<b>C</b>), MMT (<b>D</b>), and OMMT (<b>E</b>).</p>
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<p>SEM images of the nanocomposite films: (<b>A</b>) CP, (<b>B</b>) CP-HNT3%, (<b>C</b>) CP-BNT3%, (<b>D</b>) CP-MMT3%, and (<b>E</b>) CP-OMMT3%.</p>
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<p>SEM/EDX mapping images for Si atom in the cross section of the nanocomposite films: (<b>A</b>) CP-HNT3%, (<b>B</b>) CP-BNT3%, (<b>C</b>) CP-MMT3%, and (<b>D</b>) CP-OMMT3%.</p>
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<p>AFM images, 2D (left) and 3D (right), of the surface of the films: (<b>A</b>) CP, (<b>B</b>) CP-HNT3%, (<b>C</b>) CP-BNT3%, (<b>D</b>) CP-MMT3%, and (<b>E</b>) CP-OMMT3%.</p>
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<p>Tensile strength of the films at room temperature at the extension rate of 10 mm/min (<span class="html-italic">p</span>-value &lt; 0.01, groups that do not share a letter are significantly different).</p>
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14 pages, 4625 KiB  
Article
Highly Sensitive Optical Fiber MZI Sensor for Specific Detection of Trace Pb2+ Ion Concentration
by Lijie Zhang, Hongbin He, Shangpu Zhang, Yanling Xiong, Rui Pan and Wenlong Yang
Photonics 2024, 11(7), 631; https://doi.org/10.3390/photonics11070631 - 2 Jul 2024
Viewed by 349
Abstract
A novel chitosan (CS) functionalized optical fiber sensor with a bullet-shaped hollow cavity was proposed in this work for the trace concentration of Pb2+ ion detection in the water environment. The sensor is an optical fiber Mach–Zehnder interferometer (MZI), which consists of [...] Read more.
A novel chitosan (CS) functionalized optical fiber sensor with a bullet-shaped hollow cavity was proposed in this work for the trace concentration of Pb2+ ion detection in the water environment. The sensor is an optical fiber Mach–Zehnder interferometer (MZI), which consists of a sequentially spliced bullet-shaped hollow-core fiber (HCF), thin-core fiber, and another piece of spliced bullet-shaped HCF. The hollow-core fiber is caused to collapse by adjusting the amount of discharge to form a tapered hollow cavity with asymmetric end faces. The bullet-like hollow cavities act as beam expanders and couplers for optical fiber sensors, which were symmetrically spliced at both ends of a section of thin core fiber. The simulation and experiments show that the bullet-like hollow-core tapered cavity excites more cladding modes and is more sensitive to variation in the external environment than the planar and spherical cavities. The ion-imprinted chitosan (IIP-CS) film was fabricated with Pb2+ ion as a template and uniformly coated on the surface for specific recognition of Pb2+. Experimental verification confirms that the developed sensor can achieve high-sensitivity Pb2+ ion detection, with a sensitivity of up to −12.68 pm/ppm and a minimum Pb2+ ion detection concentration of 5.44 ppb Meanwhile, the sensor shows excellent selectivity, repeatability, and stability in the ion detection process, which has huge potential in the direction of heavy metal ion detection in the future. Full article
(This article belongs to the Section Lasers, Light Sources and Sensors)
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<p>The schematic diagram of fiber axial coupling.</p>
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<p>Schematic diagram of ion imprinting and specific adsorption principle.</p>
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<p>Two−dimensional model structures (<b>a</b>–<b>c</b>) and light field distribution (<b>d</b>–<b>f</b>) of the plane−plane coupling cavities, concave–concave coupling cavities, and bullet-shaped coupling cavities of optical fiber sensors.</p>
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<p>Light field distribution in the coupling cavities with different lengths (<b>a</b>) 30 µm, (<b>b</b>) 50 µm, and (<b>c</b>) 100 µm.</p>
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<p>Transmission spectra of sensors with different lengths of TCF.</p>
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<p>The preparation processes of the bullet-like tapered fiber sensor.</p>
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<p>Schematic diagram of the experimental system.</p>
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<p>Transmission spectra of sensors before and after the application of a sensitive film. The inset is the stability of the sensor spectra in water over time.</p>
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<p>Optical fiber sensor for Pb<sup>2+</sup> ion detection. (<b>a</b>) Spectral shifts of the sensor with Pb<sup>2+</sup> ion concentration. (<b>b</b>) The linear fitting curves for different Pb<sup>2+</sup> ion concentrations.</p>
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<p>The maximum wavelength shifts of the sensor for different metal ions.</p>
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<p>Repeatability and stability of the sensor.</p>
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<p>Effect of different pH and temperature on sensor sensitivity.</p>
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21 pages, 2537 KiB  
Article
Mattel’s ©Barbie: Preventing Plasticizers Leakage in PVC Artworks and Design Objects through Film-Forming Solutions
by Andrea Macchia, Livia Marinelli, Francesca Irene Barbaccia, Tilde de Caro, Alice Hansen, Lisa Maria Schuberthan, Francesca Caterina Izzo, Valentina Pintus, Katiuscia Testa Chiari and Mauro Francesco La Russa
Polymers 2024, 16(13), 1888; https://doi.org/10.3390/polym16131888 - 1 Jul 2024
Viewed by 462
Abstract
The main conservation problem of p-PVC artworks is phthalate-based plasticizer migration. Phthalate migration from the bulk to the surface of the materials leads to the formation of a glossy and oily film on the outer layers, ultimately reducing the flexibility of the material. [...] Read more.
The main conservation problem of p-PVC artworks is phthalate-based plasticizer migration. Phthalate migration from the bulk to the surface of the materials leads to the formation of a glossy and oily film on the outer layers, ultimately reducing the flexibility of the material. This study aimed to develop a removable coating for the preservation of contemporary artworks and design objects made of plasticized polyvinyl chloride (p-PVC). Several coatings incorporating chitosan, collagen, and cellulose ethers were assessed as potential barriers to inhibiting plasticizer migration. Analytical techniques including optical microscopy (OM), ultraviolet/visible/near-infrared spectroscopy (UV/Vis/NIR), Fourier transform infrared spectroscopy with attenuated total reflection (FTIR-ATR), and scanning electron microscopy (SEM) were utilized to evaluate the optical and chemical stability of selected coating formulations applied to laboratory p-PVC sheet specimens. Subsequently, formulations were tested on a real tangible example of a design object, ©Barbie doll, characterized by the prevalent issue of plasticizer migration. Furthermore, the results obtained with the tested formulations were evaluated by a group of conservators using a tailored survey. Finally, a suitable coating formulation capable of safeguarding plastic substrates was suggested. Full article
(This article belongs to the Special Issue Polymeric Materials in Modern—Contemporary Art III)
Show Figures

Figure 1

Figure 1
<p>Transmission spectroscopy trends for both unaged (<b>a</b>) and aged (<b>b</b>) coatings subtracted from the p-PVC substrate spectrum, associated with standard deviation (light blue).</p>
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<p>Results of spectrocolorimetric analysis of unaged, aging, and variation between the coatings. Blue color represents ΔE of unaged coatings on p-PVC sheet, orange color represents ΔE of aging coating on p-PVC sheet, and grey represents the confront of the ΔE variation between unaged and aging coatings.</p>
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<p>Digital microscope images of the coatings applied to the p-PVC sheet before, and after artificial accelerated aging.</p>
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<p>Optical microscope images after 72 h. Final ATP (adenosine triphosphate) values expressed in BTU units and reported for each film’s surface.</p>
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<p>Digital microscopy images from visible light before and after aging treatment on the non-treated surface of the ©Barbie leg.</p>
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<p>SEM images of the Films applied on the surface of the ©Barbie leg before (<b>A</b>) and after (<b>B</b>) aging.</p>
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26 pages, 3941 KiB  
Review
Bio-Based Aerogels in Energy Storage Systems
by Vilko Mandić, Arijeta Bafti, Ivana Panžić and Floren Radovanović-Perić
Gels 2024, 10(7), 438; https://doi.org/10.3390/gels10070438 - 30 Jun 2024
Viewed by 410
Abstract
Bio-aerogels have emerged as promising materials for energy storage, providing a sustainable alternative to conventional aerogels. This review addresses their syntheses, properties, and characterization challenges for use in energy storage devices such as rechargeable batteries, supercapacitors, and fuel cells. Derived from renewable sources [...] Read more.
Bio-aerogels have emerged as promising materials for energy storage, providing a sustainable alternative to conventional aerogels. This review addresses their syntheses, properties, and characterization challenges for use in energy storage devices such as rechargeable batteries, supercapacitors, and fuel cells. Derived from renewable sources (such as cellulose, lignin, and chitosan), bio-based aerogels exhibit mesoporosity, high specific surface area, biocompatibility, and biodegradability, making them advantageous for environmental sustainability. Bio-based aerogels serve as electrodes and separators in energy storage systems, offering desirable properties such as high specific surface area, porosity, and good electrical conductivity, enhancing the energy density, power density, and cycle life of devices. Recent advancements highlight their potential as anode materials for lithium-ion batteries, replacing non-renewable carbon materials. Studies have shown excellent cycling stability and rate performance for bio-aerogels in supercapacitors and fuel cells. The yield properties of these materials, primarily porosity and transport phenomena, demand advanced characterization methods, and their synthesis and processing methods significantly influence their production, e.g., sol–gel and advanced drying. Bio-aerogels represent a sustainable solution for advancing energy storage technologies, despite challenges such as scalability, standardization, and cost-effectiveness. Future research aims to improve synthesis methods and explore novel applications. Bio-aerogels, in general, provide a healthier path to technological progress. Full article
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