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Gels, Volume 9, Issue 5 (May 2023) – 80 articles

Cover Story (view full-size image): The general theory is developed for the transient electrophoresis of a colloidal particle in a polymer gel medium. The Laplace transform of the particle electrophoretic mobility with respect to time is derived by considering the long-range hydrodynamic interaction between the particle and the polymer gel medium. According to the obtained Laplace transform, the transient gel electrophoretic mobility approaches the steady gel electrophoretic mobility as time approaches infinity. The present theory covers the transient free-solution electrophoresis. It is shown that the relaxation time for the transient gel mobility to reach its steady value is shorter than that of the transient free-solution mobility and becomes shorter as the Brinkman screening length decreases. View this paper
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39 pages, 1561 KiB  
Review
Application of Silk-Fibroin-Based Hydrogels in Tissue Engineering
by Yihan Lyu, Yusheng Liu, Houzhe He and Hongmei Wang
Gels 2023, 9(5), 431; https://doi.org/10.3390/gels9050431 - 22 May 2023
Cited by 21 | Viewed by 4773
Abstract
Silk fibroin (SF) is an excellent protein-based biomaterial produced by the degumming and purification of silk from cocoons of the Bombyx mori through alkali or enzymatic treatments. SF exhibits excellent biological properties, such as mechanical properties, biocompatibility, biodegradability, bioabsorbability, low immunogenicity, and tunability, [...] Read more.
Silk fibroin (SF) is an excellent protein-based biomaterial produced by the degumming and purification of silk from cocoons of the Bombyx mori through alkali or enzymatic treatments. SF exhibits excellent biological properties, such as mechanical properties, biocompatibility, biodegradability, bioabsorbability, low immunogenicity, and tunability, making it a versatile material widely applied in biological fields, particularly in tissue engineering. In tissue engineering, SF is often fabricated into hydrogel form, with the advantages of added materials. SF hydrogels have mostly been studied for their use in tissue regeneration by enhancing cell activity at the tissue defect site or counteracting tissue-damage-related factors. This review focuses on SF hydrogels, firstly summarizing the fabrication and properties of SF and SF hydrogels and then detailing the regenerative effects of SF hydrogels as scaffolds in cartilage, bone, skin, cornea, teeth, and eardrum in recent years. Full article
(This article belongs to the Special Issue Synthesis and Applications of Hydrogels)
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<p>SF hydrogel crosslinking methods include physical and chemical crosslinking. Methods used for physical crosslinking include temperature and ph-mediated self-assembly, ultrasonication, electric fields, etc. Methods used for chemical crosslinking include chemical cross-linking agents, photopolymerization, γ-Ray Irradiation, enzyme cross-linking, etc.</p>
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<p>In human tissues, SF-based hydrogels can be applied to bone, cartilage, skin and wound, cornea, teeth and tympanic membrane.</p>
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29 pages, 1817 KiB  
Review
A Critical Review on Classified Excipient Sodium-Alginate-Based Hydrogels: Modification, Characterization, and Application in Soft Tissue Engineering
by Rishav Sharma, Rishabha Malviya, Sudarshan Singh and Bhupendra Prajapati
Gels 2023, 9(5), 430; https://doi.org/10.3390/gels9050430 - 22 May 2023
Cited by 18 | Viewed by 4540
Abstract
Alginates are polysaccharides that are produced naturally and can be isolated from brown sea algae and bacteria. Sodium alginate (SA) is utilized extensively in the field of biological soft tissue repair and regeneration owing to its low cost, high biological compatibility, and quick [...] Read more.
Alginates are polysaccharides that are produced naturally and can be isolated from brown sea algae and bacteria. Sodium alginate (SA) is utilized extensively in the field of biological soft tissue repair and regeneration owing to its low cost, high biological compatibility, and quick and moderate crosslinking. In addition to their high printability, SA hydrogels have found growing popularity in tissue engineering, particularly due to the advent of 3D bioprinting. There is a developing curiosity in tissue engineering with SA-based composite hydrogels and their potential for further improvement in terms of material modification, the molding process, and their application. This has resulted in numerous productive outcomes. The use of 3D scaffolds for growing cells and tissues in tissue engineering and 3D cell culture is an innovative technique for developing in vitro culture models that mimic the in vivo environment. Especially compared to in vivo models, in vitro models were more ethical and cost-effective, and they stimulate tissue growth. This article discusses the use of sodium alginate (SA) in tissue engineering, focusing on SA modification techniques and providing a comparative examination of the properties of several SA-based hydrogels. This review also covers hydrogel preparation techniques, and a catalogue of patents covering different hydrogel formulations is also discussed. Finally, SA-based hydrogel applications and future research areas concerning SA-based hydrogels in tissue engineering were examined. Full article
(This article belongs to the Special Issue Alginate-Based Gels: Preparation, Characterization and Application)
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<p>Parameters for optimal hydrogels.</p>
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<p>Different methods for the preparation of hydrogel.</p>
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<p>The ssNMR method is an advanced technology tool for characterizing sustainable cellulose-based products.</p>
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<p>Schematics of alginate applications.</p>
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<p>Schematic of sodium alginate hydrogel modification, 3D bioprinting, and application.</p>
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12 pages, 2956 KiB  
Article
Mechanical and Physical Properties of an Experimental Chemically and Green-Nano Improved Dental Alginate after Proven Antimicrobial Potentials
by Lamia Singer and Christoph Bourauel
Gels 2023, 9(5), 429; https://doi.org/10.3390/gels9050429 - 21 May 2023
Cited by 4 | Viewed by 2013
Abstract
Objectives: Impression materials could be a source of cross-contamination due to the presence of microorganisms from blood and saliva inside the oral cavity. Nevertheless, routinely performed post-setting disinfection could compromise the dimensional accuracy and other mechanical properties of alginates. Thus, this study aimed [...] Read more.
Objectives: Impression materials could be a source of cross-contamination due to the presence of microorganisms from blood and saliva inside the oral cavity. Nevertheless, routinely performed post-setting disinfection could compromise the dimensional accuracy and other mechanical properties of alginates. Thus, this study aimed to evaluate detail reproduction, dimensional accuracy, tear strength, and elastic recovery of new experimentally prepared self-disinfecting dental alginates. Methods: Two antimicrobial-modified dental alginate groups were prepared by mixing alginate powder with 0.2% silver nitrate (AgNO3 group) and a 0.2% chlorohexidine solution (CHX group) instead of pure water. Moreover, a third modified group was examined by the extraction of Boswellia sacra (BS) oleoresin using water. The extract was used to reduce silver nitrate to form silver nanoparticles (AgNPs), and the mixture was used as well in dental alginate preparation (BS + AgNP group). Dimensional accuracy and detail reproduction were examined as per the ISO 1563 standard guidelines. Specimens were prepared using a metallic mold engraved with three parallel vertical lines 20, 50, and 75 µm wide. Detail reproduction was evaluated by checking the reproducibility of the 50 µm line using a light microscope. Dimensional accuracy was assessed by measuring the change in length between defined reference points. Elastic recovery was measured according to ISO 1563:1990, in which specimens were gradually loaded and then the load was released to allow for recovery from the deformation. Tear strength was evaluated using a material testing machine until failure at a crosshead speed of 500 mm/min. Results: The recorded dimensional changes between all tested groups were insignificantly different and within the reported acceptable values (between 0.037–0.067 mm). For tear strength, there were statistically significant differences between all tested groups. Groups modified with CHX (1.17 ± 0.26 N/mm) and BS + AgNPs (1.11 ± 0.24 N/mm) showed higher tear strength values compared to the control (0.86 ± 0.23 N/mm) but were insignificant from AgNO3 (0.94 ± 0.17 N/mm). All tested groups showed elastic recovery values that met both the ISO standard and ADA specifications for elastic impression materials and tear strength values within the acceptable documented ranges. Discussion: The CHX, silver nitrate, and green-synthesized silver nanoparticles could be promising, inexpensive alternatives for the preparation of a self-disinfecting alginate impression material without affecting its performance. Green synthesis of metal nanoparticles could be a very safe, efficient, and nontoxic method, with the advantage of having a synergistic effect between metal ions and active chemical constituents of plant extracts. Full article
(This article belongs to the Special Issue Physical and Mechanical Properties of Polymer Gels)
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<p>Interval plot illustrating the mean dimensional changes in millimeters in the vertical dimension and 95% confidence interval of all tested groups.</p>
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<p>Interval plot illustrating the mean dimensional changes in millimeters in the horizontal dimension and 95% confidence interval of all tested groups.</p>
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<p>Interval plot representing the mean tear strength (N/mm) values and 95% confidence interval of all tested groups. Groups that do not share a letter are significantly different.</p>
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<p>Interval plot representing the mean elastic recovery in % and 95% confidence interval of all tested groups. Groups that do not share a letter are significantly different.</p>
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<p>Detail reproduction metal mold with 20, 50, and 75 μm depth engraved lines.</p>
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<p>Schematic drawing of the stainless-steel analog indicating the lines measured between reference points X-X’ (Vertical dimension) and X’-Y (horizontal dimension).</p>
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<p>Tear strength specimen clamped in a Zwick testing machine.</p>
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<p>Copper split mold and a plastic fixation ring for elastic recovery testing.</p>
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17 pages, 4817 KiB  
Article
Polyurethane Shape Memory Polymer/pH-Responsive Hydrogel Hybrid for Bi-Function Synergistic Actuations
by Shuyi Peng, Xingyu Cao, Ye Sun, Lin Chen, Chao Ma, Lang Yang, Hongliang Zhao, Qijie Liu, Zhenzhong Liu and Chunxin Ma
Gels 2023, 9(5), 428; https://doi.org/10.3390/gels9050428 - 21 May 2023
Cited by 5 | Viewed by 2306
Abstract
Stimuli-responsive actuating hydrogels response to the external stimulus with complex deformation behaviors based on the programmable anisotropic structure design are one of the most important smart soft materials, which have great potential applications in artificial muscles, smart values, and mini-robots. However, the anisotropic [...] Read more.
Stimuli-responsive actuating hydrogels response to the external stimulus with complex deformation behaviors based on the programmable anisotropic structure design are one of the most important smart soft materials, which have great potential applications in artificial muscles, smart values, and mini-robots. However, the anisotropic structure of one actuating hydrogel can only be programmed one time, which can only provide single actuating performance, and subsequently, has severely limited their further applications. Herein, we have explored a novel SMP/hydrogel hybrid actuator through combining polyurethane shape memory polymer (PU SMP) layer and pH-responsive polyacrylic-acid (PAA) hydrogel layer by a napkin with UV-adhesive. Owing to both the super-hydrophilicity and super-lipophilicity of the cellulose-fiber based napkin, the SMP and the hydrogel can be bonded firmly by the UV-adhesive in the napkin. More importantly, this bilayer hybrid 2D sheet can be programmed by designing a different temporary shape in heat water which can be fixed easily in cool water to achieve various fixed shapes. This hybrid with a fixed temporary shape can achieve complex actuating performance based on the bi-functional synergy of temperature-triggered SMP and pH-responsive hydrogel. The relatively high modulus PU SMP achieved high to 87.19% and 88.92% shape-fixing ratio, respectively, correspond to bending and folding shapes. The hybrid actuator can actuate with the 25.71 °/min actuating speed. Most importantly, one SMP/hydrogel bi-layer hybrid sheet was repeatedly programmed at least nine times in our research to fix various temporary 1D, 2D and 3D shapes, including bending, folding and spiraling shapes. As a result, only one SMP/hydrogel hybrid can provide various complex stimuli-responsive actuations, including the reversable bending-straightening, spiraling-unspiraling. A few of the intelligent devices have been designed to simulate the movement of the natural organisms, such as bio-mimetic “paw”, “pangolin” and “octopus”. This work has developed a new SMP/hydrogel hybrid with excellent multi-repeatable (≥9 times) programmability for high-level complex actuations, including the 1D to 2D bending and the 2D to 3D spiraling actuations, which also provides a new strategy to design other new soft intelligent materials and systems. Full article
(This article belongs to the Special Issue Functional Gel Materials and Applications)
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<p>(<b>a</b>) The preparation diagram of the hybrid actuator. (<b>b</b>) SEM images of PAA hydrogel and polyurethane SMP. (<b>c</b>) Comparison of EDS-mapping images between blank hydrogel and PAA hydrogel. (<b>d</b>) The FTIR spectra of PAAm (blank hydrogel) and PAA hydrogel.</p>
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<p>(<b>a</b>) The shape fixing diagram of the polyurethane SMP. (<b>b</b>) The fixing rate of the polyurethane SMP. (<b>c</b>) The swelling ratio of different content AA hydrogels in the gradient increasing pH buffer solutions (IS = 0.1 mol/L). (<b>d</b>) The dynamic curve of the PAA-3 hydrogel swelling and shrinking.</p>
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<p>(<b>a</b>) SEM images of the actuator cross section (<b>b</b>) The SEM images of the cellulose-fiber based napkin. (<b>c</b>) The contact angle of the cellulose-fiber based napkin for water and UV glue. (<b>d</b>) The mechanical property of the PAA hydrogel, PU SMP and the hybrid actuator. (<b>e</b>) The fixing rate of the actuator. (<b>f</b>) The shape fixing cycle test of the actuator.</p>
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<p>(<b>a</b>) The bending angle of the actuator in different pH buffer solutions (IS = 0.1 mol/L). (<b>b</b>) The swelling process of the actuator in pH = 11 buffer solutions (IS = 0.1 mol/L). (<b>c</b>) The recovery process of the actuator in pH = 3 buffer solutions (IS = 0.1 mol/L). (<b>d</b>) The cycle test of the actuator under different pH buffer solutions (IS = 0.1 mol/L). All scale bars are 10 mm.</p>
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<p>(<b>a</b>) The actuation of the designed arc shape actuator with hydrogel outside. (<b>b</b>) The actuation of the designed arc shape actuator with hydrogel inside. (<b>c</b>) The actuation of the designed arc shape actuator with hydrogel inside. All scale bars are 10 mm.</p>
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<p>(<b>a</b>) The actuation of the designed right-angle shape actuator with hydrogel outside. (<b>b</b>) The actuation of the designed right-angle shape actuator with hydrogel inside. (<b>c</b>) The actuation of the designed “凵” shape actuator with hydrogel inside. (<b>d</b>) The actuation of the designed “M” shape actuator with hydrogel outside. All scale bars are 10 mm.</p>
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<p>(<b>a</b>) The actuation of the designed spiral shape actuator with hydrogel outside. (<b>b</b>) The actuation of the designed spiral shape actuator with hydrogel inside. All scale bars are 10 mm.</p>
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<p>(<b>a</b>) The standing process of the folding table. (<b>b</b>) The catching process of the paw-mimetic actuator. (<b>c</b>) The jacking up process of the pangolin-mimetic actuator. (<b>d</b>) The hunting process of the octopus-mimetic actuator.</p>
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<p>Schematic illustration of (<b>a</b>) structure of the hybrid actuator and (<b>b</b>) the actuations of the hybrid under programmable designed shapes.</p>
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12 pages, 3690 KiB  
Article
Experimental Study on Enhanced Oil Recovery of PPG/ASP Heterogeneous System after Polymer Flooding
by Yanfu Pi, Zailai Su, Ruibo Cao, Bo Li, Jinxin Liu, Xinyu Fan and Mingjia Zhao
Gels 2023, 9(5), 427; https://doi.org/10.3390/gels9050427 - 19 May 2023
Cited by 5 | Viewed by 1577
Abstract
Following the application of polymer flooding in Daqing Oilfield, the heterogeneity between different layers has intensified, resulting in the formation of more favorable seepage channels and cross-flow of displacement fluids. Consequently, the circulation efficiency has decreased, necessitating the exploration of methods to enhance [...] Read more.
Following the application of polymer flooding in Daqing Oilfield, the heterogeneity between different layers has intensified, resulting in the formation of more favorable seepage channels and cross-flow of displacement fluids. Consequently, the circulation efficiency has decreased, necessitating the exploration of methods to enhance oil recovery. This paper focuses on experimental research utilizing a newly developed precrosslinked particle gel (PPG) combined with alkali surfactant polymer (ASP) to create a heterogeneous composite system. This study aims to improve the efficiency of heterogeneous system flooding after polymer flooding. The addition of PPG particles enhances the viscoelasticity of the ASP system, reduces the interfacial tension between the heterogeneous system and crude oil, and provides excellent stability. The heterogeneous system has high resistance and residual resistance coefficients during the migration process in a long core model, achieving an improvement rate of up to 90.1% under the permeability ratio of 9 between high and low permeability layers. Employing heterogeneous system flooding after polymer flooding can increase oil recovery by 14.6%. Furthermore, the oil recovery rate of low permeability layers can reach 28.6%. The experimental results confirm that the application of PPG/ASP heterogeneous flooding after polymer flooding can effectively plug high-flow seepage channels and improve oil washing efficiency. These findings hold significant implications for further reservoir development after polymer flooding. Full article
(This article belongs to the Special Issue Polymer Gels for the Oil and Gas Industry)
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<p>Time-dependent curve of viscosity and interfacial tension.</p>
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<p>Flow rate and pressure curve of the double-tube parallel experiment.</p>
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<p>Pressure curve of PPG/ASP system.</p>
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<p>Production curves during PPG/ASP flooding: (<b>a</b>) Pressure, water cut, and oil recovery as a function of the injected pore volume of PPG/ASP flooding. (<b>b</b>) Displacement flow rate curves of the heterogeneous system.</p>
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<p>Profile control experiment and flow experiment setup.</p>
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<p>Connection diagram of oil displacement test device.</p>
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14 pages, 8800 KiB  
Article
Gamma Radiation-Induced Advanced 2,3-Dimethylacrylic Acid-(2-Acrylamido-2-methyl-1-propanesulfonic Acid) Superabsorbent Hydrogel: Synthesis and Characterization
by Md Murshed Bhuyan and Jae-Ho Jeong
Gels 2023, 9(5), 426; https://doi.org/10.3390/gels9050426 - 19 May 2023
Cited by 6 | Viewed by 1814
Abstract
Gamma radiation technique for the preparation of pure hydrogels is gaining popularity worldwide. Superabsorbent hydrogels play vital roles in different fields of application. The present work mainly focuses on the preparation and characterization of 2,3-Dimethylacrylic acid-(2-Acrylamido-2-methyl-1-propane sulfonic acid) (DMAA–AMPSA) superabsorbent hydrogel by applying [...] Read more.
Gamma radiation technique for the preparation of pure hydrogels is gaining popularity worldwide. Superabsorbent hydrogels play vital roles in different fields of application. The present work mainly focuses on the preparation and characterization of 2,3-Dimethylacrylic acid-(2-Acrylamido-2-methyl-1-propane sulfonic acid) (DMAA–AMPSA) superabsorbent hydrogel by applying gamma radiation and optimization of the proper dose. To prepare DMAA–AMPSA hydrogel, different doses ranging from 2 kGy to 30 kGy were imparted on the blend aqueous solution of the monomers. The equilibrium swelling increases with increasing radiation dose, followed by decreasing after reaching a certain level, and the highest result is found to be 26,324.9% at 10 kGy. Fourier Transform Infrared (FTIR) and Nuclear Magnetic Resonance (NMR) spectroscopy confirmed the formation of co-polymer by showing the characteristic functional groups and proton environment of the gel. X-ray Diffraction (XRD) pattern indicates the crystalline/amorphous nature of the gel. The Differential Scanning Calorimetry (DSC) and Thermogravimetry Analysis (TGA) revealed the thermal stability of the gel. The surface morphology and constitutional elements were analyzed and confirmed by Scanning Electron Microscopy (SEM) equipped with Energy Dispersive Spectroscopy (EDS). Finally, it can be stated that hydrogels can be usable in metal adsorption, drug delivery, and other relevant fields. Full article
(This article belongs to the Special Issue Advances in Responsive Hydrogels)
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<p>Effect of gamma radiation dose on equilibrium swelling of hydrogel.</p>
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<p>DMAA–AMPSA hydrogels (<b>a</b>) swelled hydrogels prepared at 2, 5, 10, 20, and 30 kGy. doses and (<b>b</b>) prepared at 10 kGy dose (before and after swelling).</p>
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<p>FTIR spectrum of (<b>a</b>) AMPSA powder and (<b>b</b>) DMAA-AMPSA gel.</p>
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<p>FTIR spectrum of (<b>a</b>) AMPSA powder and (<b>b</b>) DMAA-AMPSA gel.</p>
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<p><sup>1</sup>H NMR of DMAA–AMPSA hydrogel.</p>
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<p>XRD spectrum of DMAA–AMPSA hydrogel.</p>
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<p>(<b>a</b>) TGA and (<b>b</b>) DSC thermograms of DMAA-AMPSA gel prepared by 10 kGy radiation dose.</p>
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<p>(<b>a</b>) SEM and (<b>b</b>) EDS of DMAA–AMPSA hydrogel.</p>
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<p>Probable polymerization of DMAA–AMPSA hydrogel.</p>
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19 pages, 5150 KiB  
Article
Microbial Polysaccharide-Based Formulation with Silica Nanoparticles; A New Hydrogel Nanocomposite for 3D Printing
by Maria Minodora Marin, Ioana Catalina Gifu, Gratiela Gradisteanu Pircalabioru, Madalina Albu Kaya, Rodica Roxana Constantinescu, Rebeca Leu Alexa, Bogdan Trica, Elvira Alexandrescu, Cristina Lavinia Nistor, Cristian Petcu and Raluca Ianchis
Gels 2023, 9(5), 425; https://doi.org/10.3390/gels9050425 - 19 May 2023
Cited by 2 | Viewed by 2069
Abstract
Natural polysaccharides are highly attractive biopolymers recommended for medical applications due to their low cytotoxicity and hydrophilicity. Polysaccharides and their derivatives are also suitable for additive manufacturing, a process in which various customized geometries of 3D structures/scaffolds can be achieved. Polysaccharide-based hydrogel materials [...] Read more.
Natural polysaccharides are highly attractive biopolymers recommended for medical applications due to their low cytotoxicity and hydrophilicity. Polysaccharides and their derivatives are also suitable for additive manufacturing, a process in which various customized geometries of 3D structures/scaffolds can be achieved. Polysaccharide-based hydrogel materials are widely used in 3D hydrogel printing of tissue substitutes. In this context, our goal was to obtain printable hydrogel nanocomposites by adding silica nanoparticles to a microbial polysaccharide’s polymer network. Several amounts of silica nanoparticles were added to the biopolymer, and their effects on the morpho-structural characteristics of the resulting nanocomposite hydrogel inks and subsequent 3D printed constructs were studied. FTIR, TGA, and microscopy analysis were used to investigate the resulting crosslinked structures. Assessment of the swelling characteristics and mechanical stability of the nanocomposite materials in a wet state was also conducted. The salecan-based hydrogels displayed excellent biocompatibility and could be employed for biomedical purposes, according to the results of the MTT, LDH, and Live/Dead tests. The innovative, crosslinked, nanocomposite materials are recommended for use in regenerative medicine. Full article
(This article belongs to the Special Issue Hydrogels for 3D Printing)
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<p>Viscosity as a function of shear rate for S0, S1, S2, and S3 hydrogel-based inks.</p>
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<p>FTIR Spectra of the obtained samples.</p>
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<p>(<b>A</b>) Equilibrium swelling behavior in different pH media of the 3D printed samples. Statistical analysis (<b>A</b>): The influence of different pH media over the samples swelling degree; (<b>B</b>–<b>D</b>): The influence of composition for the samples kept in the same pH media ((<b>B</b>)-pH 5, (<b>C</b>)-pH 7.4, (<b>D</b>)-pH 11: The resulted values consist of average values with additional standard errors. Statistical significance: **** <span class="html-italic">p</span> &lt; 0.0001. ONE WAY ANOVA TEST.</p>
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<p>(<b>A</b>) Equilibrium swelling behavior in different pH media of the 3D printed samples. Statistical analysis (<b>A</b>): The influence of different pH media over the samples swelling degree; (<b>B</b>–<b>D</b>): The influence of composition for the samples kept in the same pH media ((<b>B</b>)-pH 5, (<b>C</b>)-pH 7.4, (<b>D</b>)-pH 11: The resulted values consist of average values with additional standard errors. Statistical significance: **** <span class="html-italic">p</span> &lt; 0.0001. ONE WAY ANOVA TEST.</p>
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<p>Thermal properties of the obtained sample, TGA.</p>
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<p>DMA analyses of the obtained hydrogels swelled at equilibrium; (<b>A</b>). Frequency sweep tests (filled symbols represent G′ and open symbols represent G″); (<b>B</b>). Stress-strain analyses.</p>
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<p>(<b>A</b>). SEM images showing the microstructure aspect of 3D printed scaffolds (30×, 50×, 250×); (<b>B</b>). The roundness of open pores is calculated using the Wadell equation. The resulting values consist of average values with additional standard errors. Statistical significance: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.005; *** <span class="html-italic">p</span> &lt; 0.0005. ONE WAY ANOVA TEST.</p>
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<p>TEM images of the nanocomposite sample (S3).</p>
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<p>Antimicrobial activity (<span class="html-italic">Staphylococcus aureus</span> and <span class="html-italic">Escherichia coli</span>) of the 3D printed samples. (<b>A</b>). Images with the seeded samples; (<b>B</b>). Inhibition zone diameters for the samples seeded with <span class="html-italic">Staphylococcus aureus</span>; (<b>C</b>). Inhibition zone diameters for the samples seeded with <span class="html-italic">Escherichia coli</span>. Statistical significance: ns <span class="html-italic">p</span> &lt; 0.5; ** <span class="html-italic">p</span> &lt; 0.005, **** <span class="html-italic">p</span> &lt; 0.0001. ONE WAY ANOVA TEST.</p>
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<p>Biological assessment of the 3D printed constructs. Results were obtained from: (<b>A</b>). MTT assay, (<b>B</b>). LDH tests and (<b>C</b>). Live/Dead tests (scale bar-200 µm).</p>
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<p>Schematic representation of the formation and characterization of the new polysaccharide-based nanocomposites.</p>
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21 pages, 2879 KiB  
Review
Coinage Metals Doped ZnO Obtained by Sol-Gel Method—A Brief Review
by Cristina Maria Vlăduț, Oana-Cătălina Mocioiu and Elena Mirabela Soare
Gels 2023, 9(5), 424; https://doi.org/10.3390/gels9050424 - 18 May 2023
Cited by 1 | Viewed by 1939
Abstract
ZnO is one of the most studied oxides due to its nontoxic nature and remarkable properties. It has antibacterial and UV-protection properties, high thermal conductivity, and high refractive index. Various ways have been used to synthesize and fabricate coinage metals doped ZnO, but [...] Read more.
ZnO is one of the most studied oxides due to its nontoxic nature and remarkable properties. It has antibacterial and UV-protection properties, high thermal conductivity, and high refractive index. Various ways have been used to synthesize and fabricate coinage metals doped ZnO, but the sol-gel technique has received a lot of interest because of its safety, low cost, and facile deposition equipment. Coinage metals are represented by the three nonradioactive elements of group 11 of the periodic table: gold, silver, and copper. This paper, which was motivated by the lack of reviews on the topic, provides a summary of the synthesis of Cu, Ag, and Au-doped ZnO nanostructures with an emphasis on the sol-gel process and identifies the numerous factors that affect the morphological, structural, optical, electrical, and magnetic properties of the produced materials. This is accomplished by tabulating and discussing a summary of a number of parameters and applications that were published in the existing literature over the previous five years (2017–2022). The main applications being pursued involve biomaterials, photocatalysts, energy storage materials, and microelectronics. This review ought to serve as a helpful reference point for researchers looking into the many physicochemical characteristics of coinage metals doped ZnO, as well as how these characteristics vary according to the conditions under which experiments are conducted. Full article
(This article belongs to the Special Issue Current and Future Trends in Supramolecular Gels)
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<p>Sol-gel process.</p>
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<p>Spin-coating technique.</p>
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<p>Dip-coating technique.</p>
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<p>X-ray diffraction peaks of pristine and Cu-doped ZnO nanoparticles (Reprinted with permission from Ref. [<a href="#B48-gels-09-00424" class="html-bibr">48</a>]. 2019, Elsevier from Journal of Alloys and Compounds).</p>
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<p>X-ray diffraction peaks of pristine and Cu-doped ZnO films deposited by sol−gel techniques (Reprinted with permission from Ref. [<a href="#B49-gels-09-00424" class="html-bibr">49</a>]. 2022, Creative Commons from ACS Omega).</p>
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<p>TEM micrograph of (<b>a</b>) ZnO and (<b>b</b>) Cu-ZO nanoparticles (Reprinted with permission from Ref. [<a href="#B48-gels-09-00424" class="html-bibr">48</a>]. 2019, Elsevier from Journal of Alloys and Compounds).</p>
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<p>FE-SEM images of pristine and Cu-doped ZnO thin films deposited by the sol−gel method (Reprinted with permission from Ref. [<a href="#B49-gels-09-00424" class="html-bibr">49</a>]. 2022, Creative Commons from ACS Omega).</p>
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<p>(<b>a</b>) Photocatalytic degradation of MB under the irradiation of visible light over the ZnO and Ag-doped ZnO nanoparticles without any catalysts,(<b>b</b>) plot of ln(C/C0) as a function of visible light irradiation time for the photocatalysis of MB containing ZnO and Ag-doped ZnO nanoparticles without any catalysts, and (<b>c</b>) variation of the observed kinetic constant for MB degradation during the photocatalytic reaction with different Ag contents (<b>d</b>) Proposed mechanism for the photocatalytic degradation of MB over the Ag-doped ZnO nanoparticles (Reprinted with permission from Ref. [<a href="#B54-gels-09-00424" class="html-bibr">54</a>]. 2019, AIP Conference Proceedings).</p>
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22 pages, 5010 KiB  
Review
Progress in Surface Modification of Titanium Implants by Hydrogel Coatings
by Huangqin Chen, Rui Feng, Tian Xia, Zhehan Wen, Qing Li, Xin Qiu, Bin Huang and Yuesheng Li
Gels 2023, 9(5), 423; https://doi.org/10.3390/gels9050423 - 18 May 2023
Cited by 21 | Viewed by 4079
Abstract
Although titanium and titanium alloys have become the preferred materials for various medical implants, surface modification technology still needs to be strengthened in order to adapt to the complex physiological environment of the human body. Compared with physical or chemical modification methods, biochemical [...] Read more.
Although titanium and titanium alloys have become the preferred materials for various medical implants, surface modification technology still needs to be strengthened in order to adapt to the complex physiological environment of the human body. Compared with physical or chemical modification methods, biochemical modification, such as the introduction of functional hydrogel coating on implants, can fix biomolecules such as proteins, peptides, growth factors, polysaccharides, or nucleotides on the surface of the implants, so that they can directly participate in biological processes; regulate cell adhesion, proliferation, migration, and differentiation; and improve the biological activity on the surface of the implants. This review begins with a look at common substrate materials for hydrogel coatings on implant surfaces, including natural polymers such as collagen, gelatin, chitosan, and alginate, and synthetic materials such as polyvinyl alcohol, polyacrylamide, polyethylene glycol, and polyacrylic acid. Then, the common construction methods of hydrogel coating (electrochemical method, sol–gel method and layer-by-layer self-assembly method) are introduced. Finally, five aspects of the enhancement effect of hydrogel coating on the surface bioactivity of titanium and titanium alloy implants are described: osseointegration, angiogenesis, macrophage polarization, antibacterial effects, and drug delivery. In this paper, we also summarize the latest research progress and point out the future research direction. After searching, no previous relevant literature reporting this information was found. Full article
(This article belongs to the Special Issue Hydrogel for Sustained Delivery of Therapeutic Agents)
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<p>Surface modification methods of titanium and its alloys [<a href="#B3-gels-09-00423" class="html-bibr">3</a>].</p>
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<p>Functional evaluation for BMDM polarization through surface biomarkers (<b>A</b>,<b>B</b>), inflammatory factor secreting pattern (<b>C</b>), and related gene expression levels (<b>D</b>). CCR7 and TNF-α served as the M1-polarized markers; CD206, IL-10, and Arg-1 served as the M2-polarized markers; OSM, BMP-6, and VEGF served as the pro-regeneration biomarker. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 [<a href="#B43-gels-09-00423" class="html-bibr">43</a>].</p>
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<p>Fibroblast activation, or fibroblast-myofibroblast transition, of NIH/3T3 cells after irradiation [<a href="#B50-gels-09-00423" class="html-bibr">50</a>]. (<b>A</b>) Representative fluorescence images of NIH/3T3 cells cultured with different samples for 2 days. The expression of α-SMA and Thy-1 was stained as green. (<b>B</b>) Cellular ATP level reflected by luminescence intensity after different treatments. (<b>C</b>) Western blotting detecting the expression of Thy-1, α-SMA, HSP70, HSP90, Smad-2, and p-Smad-2 after different treatments. a: TCPs; b: Ti/GelMAc/MPDA@Ce6; c: TCPs + Laser; d: Ti/GelMAc/MPDA@Ce6 + Laser. (<b>D</b>–<b>F</b>) Quantitative analysis according to Western blotting results. (n = 6, ** <span class="html-italic">p</span> &lt; 0.01, N.S.: no significance). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)</p>
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<p>Wettability and topography of the implant’s surface [<a href="#B77-gels-09-00423" class="html-bibr">77</a>]. (<b>a</b>) Contact angle values and water droplet images, (<b>b</b>,<b>c</b>) 2D and 3D AFM images, and (<b>d</b>) average maximum height of the profile (Rz) and the arithmetic mean roughness (Ra) of the synthesized samples (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Electrochemical construction of a catechol-grafted chitosan film for Cu<sup>2+</sup> incorporation [<a href="#B101-gels-09-00423" class="html-bibr">101</a>].</p>
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<p>Principle of hydrogel coating [<a href="#B105-gels-09-00423" class="html-bibr">105</a>]. (<b>a</b>) Formulation: monomer units and coupling agents copolymerize into polymer chains, but do not crosslink into a network, resulting in an aqueous solution. The solution may also contain other compounds for various functions but are not drawn here. (<b>b</b>) Substrate preparation: functional groups complementary to the coupling agents are imparted onto the surface of a substrate. (<b>c</b>) Paint: The aqueous solution is painted on the substrate by various operations. (<b>d</b>) Cure: The coupling agents react with each other to crosslink the polymer chains into network and react with the complementary functional groups to interlink the polymer network to the substrate.</p>
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<p>Layer-by-layer electrostatic self-assembly [<a href="#B112-gels-09-00423" class="html-bibr">112</a>].</p>
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<p>Hydrogel coatings on titanium bidirectionally regulate osteoclastic and osteogenic response behaviors [<a href="#B88-gels-09-00423" class="html-bibr">88</a>].</p>
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<p>Sustained release of VEGF promotes COL I (<b>A</b>) and CD 31 (<b>B</b>) expression in bone-surrounding scaffolds 6 and 12 weeks after implantation (n = 3) [<a href="#B44-gels-09-00423" class="html-bibr">44</a>].</p>
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<p>Fluorescence images of macrophage morphologies on dual-inflammatory cytokine (interferon-γ and IL-4)-coated TiO<sub>2</sub> nanotube surfaces [<a href="#B144-gels-09-00423" class="html-bibr">144</a>]. Activated macrophages are indicated by yellow arrows.</p>
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23 pages, 7527 KiB  
Article
Theoretical and Experimental Aspects of Sodium Diclofenac Salt Release from Chitosan-Based Hydrogels and Possible Applications
by Loredana Maria Himiniuc, Razvan Socolov, Irina Nica, Maricel Agop, Constantin Volovat, Lacramioara Ochiuz, Decebal Vasincu, Ana Maria Rotundu, Iulian Alin Rosu, Vlad Ghizdovat and Simona Ruxandra Volovat
Gels 2023, 9(5), 422; https://doi.org/10.3390/gels9050422 - 17 May 2023
Cited by 2 | Viewed by 1956
Abstract
Two formulations based on diclofenac sodium salt encapsulated into a chitosan hydrogel were designed and prepared, and their drug release was investigated by combining in vitro results with mathematical modeling. To understand how the pattern of drug encapsulation impacted its release, the formulations [...] Read more.
Two formulations based on diclofenac sodium salt encapsulated into a chitosan hydrogel were designed and prepared, and their drug release was investigated by combining in vitro results with mathematical modeling. To understand how the pattern of drug encapsulation impacted its release, the formulations were supramolecularly and morphologically characterized by scanning electron microscopy and polarized light microscopy, respectively. The mechanism of diclofenac release was assessed by using a mathematical model based on the multifractal theory of motion. Various drug-delivery mechanisms, such as Fickian- and non-Fickian-type diffusion, were shown to be fundamental mechanisms. More precisely, in a case of multifractal one-dimensional drug diffusion in a controlled-release polymer–drug system (i.e., in the form of a plane with a certain thickness), a solution that allowed the model’s validation through the obtained experimental data was established. The present research reveals possible new perspectives, for example in the prevention of intrauterine adhesions occurring through endometrial inflammation and other pathologies with an inflammatory mechanism background, such as periodontal diseases, and also therapeutic potential beyond the anti-inflammatory action of diclofenac as an anticancer agent, with a role in cell cycle regulation and apoptosis, using this type of drug-delivery system. Full article
(This article belongs to the Special Issue Synthesis and Applications of Hydrogels)
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<p>The FTIR spectra of the studied formulations and DCF.</p>
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<p>(<b>a</b>–<b>e</b>) Hydrogel state of the formulations proved by (<b>a</b>) the dependence of G’ and G’’ on the oscillatory frequency (black: G’; red: G’’; triangle: D1.5; circle: D2) and (<b>b</b>,<b>c</b>) inverted tube test; representative image of D1.5 hydrogel, (<b>d</b>) before and (<b>e</b>) after swelling in water.</p>
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<p>POM microphotographs (crossed polarizers): (<b>a</b>) D1.5 and (<b>b</b>) D2 formulations (magnification: 400×).</p>
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<p>SEM images of the (<b>a</b>) D1.5 and (<b>b</b>) D2 formulations (magnification: 5000×; scale bar: 20 μm).</p>
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<p>(<b>a</b>,<b>b</b>) Curves of the in vitro release of DCF from the chitosan-based matrix: (<b>a</b>) time (hours)–cumulative drug release (%); (<b>b</b>) cumulative drug release (%)–time (hours).</p>
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<p>Fractal fit of the in vitro release of diclofenac sodium salt from the chitosan hydrogel matrix. The release curve for the D1.5 formulation corresponds to a fractal degree of 1.3, whereas the release curve for the D2 formulation corresponds to a fractal degree of 1.7, implying the fact that the drug-release processes take place on two resolution scales.</p>
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<p>3D representation of drug-release correlative and non-correlative modes at global scale resolution (simultaneously differentiable and non-differentiable scale resolution) plotted in dimensionless coordinates through <math display="inline"><semantics> <mrow> <mfenced open="|" close="|" separators="|"> <mrow> <mi>h</mi> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>,</mo> <mi>t</mi> </mrow> </mfenced> </mrow> </mfenced> </mrow> </semantics></math> with <math display="inline"><semantics> <mrow> <mo>Φ</mo> <mo>≡</mo> <mn>2.35</mn> </mrow> </semantics></math>. Such a representation encompasses various types of drug-release processes.</p>
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<p>(<b>a</b>–<b>c</b>) 3D representations of drug-release correlative and non-correlative modes at global scale resolution (simultaneously differentiable and non-differentiable scale resolution) plotted in dimensionless coordinates through <math display="inline"><semantics> <mrow> <mfenced open="|" close="|" separators="|"> <mrow> <mi>h</mi> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>,</mo> <mi>t</mi> </mrow> </mfenced> </mrow> </mfenced> </mrow> </semantics></math> with <math display="inline"><semantics> <mrow> <mo>Φ</mo> <mo>≡</mo> <mn>2.35</mn> </mrow> </semantics></math>: (<b>a</b>) cellular-type structures (<math display="inline"><semantics> <mrow> <mo>Ω</mo> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>40</mn> <mo>,</mo> <mo> </mo> <mi>t</mi> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>60</mn> </mrow> </semantics></math>); (<b>b</b>) channel-type structures (<math display="inline"><semantics> <mrow> <mo>Ω</mo> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>150</mn> <mo>,</mo> <mo> </mo> <mi>t</mi> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>200</mn> </mrow> </semantics></math>); (<b>c</b>) mixed cellular-channel-type structures (<math display="inline"><semantics> <mrow> <mo>Ω</mo> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>300</mn> <mo>,</mo> <mo> </mo> <mi>t</mi> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>400</mn> </mrow> </semantics></math>).</p>
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<p>Graphical representation of compositions of the formulations and their codes.</p>
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<p>(<b>a</b>,<b>b</b>) Drug-release functional modes at differentiable scale resolution plot of <math display="inline"><semantics> <mrow> <mi>R</mi> <mi>e</mi> <mfenced open="[" close="]" separators="|"> <mrow> <mi>h</mi> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>,</mo> <mi>t</mi> </mrow> </mfenced> </mrow> </mfenced> </mrow> </semantics></math> with <math display="inline"><semantics> <mrow> <mo>Φ</mo> <mo>=</mo> <mn>2.35</mn> </mrow> </semantics></math>: (<b>a</b>) 3D and (<b>b</b>) 2D.</p>
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<p>(<b>a</b>,<b>b</b>) Drug-release functional modes at non-differentiable scale resolution plot of <math display="inline"><semantics> <mrow> <mi>I</mi> <mi>m</mi> <mfenced open="[" close="]" separators="|"> <mrow> <mi>h</mi> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>,</mo> <mi>t</mi> </mrow> </mfenced> </mrow> </mfenced> </mrow> </semantics></math> with <math display="inline"><semantics> <mrow> <mo>Φ</mo> <mo>=</mo> <mn>2.35</mn> </mrow> </semantics></math>: (<b>a</b>) 3D and (<b>b</b>) 2D.</p>
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<p>(<b>a</b>,<b>b</b>) 2D polymer–drug release dynamics at various scale resolution; plot of (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>R</mi> <mi>e</mi> <mfenced separators="|"> <mrow> <mi>h</mi> </mrow> </mfenced> </mrow> </semantics></math> and (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>I</mi> <mi>m</mi> <mo>(</mo> <mi>h</mi> <mo>)</mo> </mrow> </semantics></math> for <math display="inline"><semantics> <mrow> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>140</mn> <mo>,</mo> <mo> </mo> <mi>t</mi> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>200</mn> </mrow> </mfenced> <mo> </mo> <mi mathvariant="normal">a</mi> <mi mathvariant="normal">n</mi> <mi mathvariant="normal">d</mi> <mo> </mo> <mo>Φ</mo> <mo>=</mo> <mn>2.35</mn> </mrow> </semantics></math>.</p>
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<p>(<b>a</b>,<b>b</b>) 2D polymer–drug release dynamics at various scale resolution; plot of (<b>a</b>) <math display="inline"><semantics> <mrow> <mi>R</mi> <mi>e</mi> <mfenced separators="|"> <mrow> <mi>h</mi> </mrow> </mfenced> </mrow> </semantics></math> and (<b>b</b>) <math display="inline"><semantics> <mrow> <mi>I</mi> <mi>m</mi> <mo>(</mo> <mi>h</mi> <mo>)</mo> </mrow> </semantics></math> for <math display="inline"><semantics> <mrow> <mfenced separators="|"> <mrow> <mo>Ω</mo> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>275</mn> <mo>,</mo> <mo> </mo> <mi>t</mi> <mo>=</mo> <mn>0</mn> <mo>−</mo> <mn>400</mn> </mrow> </mfenced> <mo> </mo> <mi mathvariant="normal">a</mi> <mi mathvariant="normal">n</mi> <mi mathvariant="normal">d</mi> <mo> </mo> <mo>Φ</mo> <mo>=</mo> <mn>2.35</mn> </mrow> </semantics></math>.</p>
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32 pages, 2089 KiB  
Review
Composite Hydrogels with Included Solid-State Nanoparticles Bearing Anticancer Chemotherapeutics
by Alexandar M. Zhivkov, Trifon T. Popov and Svetlana H. Hristova
Gels 2023, 9(5), 421; https://doi.org/10.3390/gels9050421 - 17 May 2023
Cited by 4 | Viewed by 1751
Abstract
Hydrogels have many useful physicochemical properties which, in combination with their biocompatibility, suggest their application as a drug delivery system for the local and prorogated release of drugs. However, their drug-absorption capacity is limited because of the gel net’s poor adsorption of hydrophilic [...] Read more.
Hydrogels have many useful physicochemical properties which, in combination with their biocompatibility, suggest their application as a drug delivery system for the local and prorogated release of drugs. However, their drug-absorption capacity is limited because of the gel net’s poor adsorption of hydrophilic molecules and in particular, hydrophobic molecules. The absorption capacity of hydrogels can be increased with the incorporation of nanoparticles due to their huge surface area. In this review, composite hydrogels (physical, covalent and injectable) with included hydrophobic and hydrophilic nanoparticles are considered as suitable for use as carriers of anticancer chemotherapeutics. The main focus is given to the surface properties of the nanoparticles (hydrophilicity/hydrophobicity and surface electric charge) formed from metal and dielectric substances: metals (gold, silver), metal-oxides (iron, aluminum, titanium, zirconium), silicates (quartz) and carbon (graphene). The physicochemical properties of the nanoparticles are emphasized in order to assist researchers in choosing appropriate nanoparticles for the adsorption of drugs with hydrophilic and hydrophobic organic molecules. Full article
(This article belongs to the Special Issue Polymer Hydrogels for Cancer Therapy)
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<p>Chemical structures and abbreviations of some chemotherapeutics used as anticancer drugs by composition of hydrogel with included nanoparticles.</p>
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<p>Polymers most commonly used for composition hydrogels with included nanoparticles carrying different chemotherapeutics. * dendrimer.</p>
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<p>Polymers most commonly used for composition hydrogels with included nanoparticles carrying different chemotherapeutics. * dendrimer.</p>
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15 pages, 2616 KiB  
Article
Gel Properties and Structural Characteristics of Composite Gels of Soy Protein Isolate and Silver Carp Protein
by Li Zheng, Joe M. Regenstein, Linyi Zhou, Sayed Mohamed Mokhtar and Zhongjiang Wang
Gels 2023, 9(5), 420; https://doi.org/10.3390/gels9050420 - 17 May 2023
Cited by 3 | Viewed by 1722
Abstract
Problems with silver carp protein (SCP) include a strong fishy odor, low gel strength of SCP surimi, and susceptibility to gel degradation. The objective of this study was to improve the gel quality of SCP. The effects of the addition of native soy [...] Read more.
Problems with silver carp protein (SCP) include a strong fishy odor, low gel strength of SCP surimi, and susceptibility to gel degradation. The objective of this study was to improve the gel quality of SCP. The effects of the addition of native soy protein isolate (SPI) and SPI subjected to papain-restricted hydrolysis on the gel characteristics and structural features of SCP were studied. The β-sheet structures in SPI increased after papain treatment. SPI treated with papain was crosslinked with SCP using glutamine transaminase (TG) to form a composite gel. Compared with the control, the addition of modified SPI increased the hardness, springiness, chewiness, cohesiveness, and water-holding capacity (WHC) of the protein gel (p < 0.05). In particular, the effects were most significant when the degree of SPI hydrolysis (DH) was 0.5% (i.e., gel sample M-2). The molecular force results demonstrated that hydrogen bonding, disulfide bonding, and hydrophobic association are important molecular forces in gel formation. The addition of the modified SPI increases the number of hydrogen bonds and the disulfide bonds. Scanning electron microscopy (SEM) analysis showed that the papain modifications allowed the formation of a composite gel with a complex, continuous, and uniform gel structure. However, the control of the DH is important as additional enzymatic hydrolysis of SPI decreased TG crosslinking. Overall, modified SPI has the potential to improve SCP gel texture and WHC. Full article
(This article belongs to the Special Issue Food Gels: Structure and Properties)
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<p>(<b>A</b>) The hardness of cold-induced gels formed with SCP alone, with SCP, and N-SPI, and modified SCP with SPI modified with papain at different DH (0.1, 0.5, 1.0, 1.5, and 2.0); (<b>B</b>) the springiness of cold-induced gels; (<b>C</b>) the cohesiveness of cold-induced gels; and (<b>D</b>) the chewiness of cold-induced gels; different lowercase letters indicate significant differences <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of SPI modified with papain at different DH (0.1, 0.5, 1.0, 1.5, and 2.0%) combined with SCP on the WHC of compound gels. Different lowercase letters indicate significant differences <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The effect of the SPI modified with papain at different DH (0.1, 0.5, 1.0, 1.5, and 2.0%) combined with SCP on the whiteness of compound gels.</p>
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<p>Images of the compound gels.</p>
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<p>(<b>A</b>) The hydrophobic interactions of cold-induced gels formed with SCP alone, with SCP and N-SPI, and modified SCP with SPI modified with papain at different DH (0.1, 0.5, 1.0, 1.5, and 2.0); (<b>B</b>) the hydrogen bonds of cold-induced gels; (<b>C</b>) the disulfide bonds of cold-induced gels; and (<b>D</b>) the ionic bonds of cold-induced gels.</p>
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<p>Scanning electron microscope images of composite gel samples with SPI at different DH: (<b>A</b>) Control SCP gels; (<b>B</b>) SCP gels with N-SPI; (<b>C</b>) SCP gels at a DH of 0.1% SPI; (<b>D</b>) SCP gels with a DH of 0.5% SPI; (<b>E</b>) SCP gels with a DH of 1% SPI; (<b>F</b>) SCP gels with a DH of 1.5% SPI; and (<b>G</b>) SCP gels with a DH of 2% SPI.</p>
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13 pages, 3422 KiB  
Article
Graphene Oxide/Styrene-Butadiene Latex Hybrid Aerogel with Improved Mechanical Properties by PEI Grafted GO and CNT
by Zetian Zhao, Lina Zhang, Yinghu Song, Lichun Ma, Jialiang Li, Min Zhao, Xueliang Ji, Jianfei Gao, Guojun Song and Xiaoru Li
Gels 2023, 9(5), 419; https://doi.org/10.3390/gels9050419 - 16 May 2023
Cited by 3 | Viewed by 1915
Abstract
Graphene oxide aerogel (GOA) has wide application prospects due to its low density and high porosity. However, the poor mechanical properties and unstable structure of GOA have limited its practical applications. In this study, polyethyleneimide (PEI) was used to graft onto the surface [...] Read more.
Graphene oxide aerogel (GOA) has wide application prospects due to its low density and high porosity. However, the poor mechanical properties and unstable structure of GOA have limited its practical applications. In this study, polyethyleneimide (PEI) was used to graft onto the surface of GO and carbon nanotubes (CNTs) to improve compatibility with polymers. Composite GOA was prepared by adding styrene-butadiene latex (SBL) to the modified GO and CNTs. The synergistic effect of PEI and SBL, resulted in an aerogel with excellent mechanical properties, compressive resistance, and structural stability. When the ratio of SBL to GO and GO to CNTs was 2:1 and 7:3, respectively, the obtained aerogel performance was the best, and the maximum compressive stress was 784.35% higher than that of GOA. The graft of PEI on the surface of GO and CNT could improve the mechanical properties of the aerogel, with greater improvements observed with grafting onto the surface of GO. Compared with GO/CNT/SBL aerogel without PEI grafting, the maximum stress of GO/CNT–PEI/SBL aerogel increased by 5.57%, that of GO–PEI/CNT/SBL aerogel increased by 20.25%, and that of GO–PEI/CNT–PEI/SBL aerogel increased by 28.99%. This work not only provided a possibility for the practical application of aerogel, but also steered the research of GOA in a new direction. Full article
(This article belongs to the Special Issue Advances in Biopolymer Aerogels and Their Composites)
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<p>FT-IR spectra of various samples: (<b>a</b>) C/GO/GO–PEI, (<b>b</b>) O–CNT/CNT/CNT–PEI.</p>
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<p>Raman spectra of various samples: (<b>a</b>) C/GO/GO–PEI, (<b>b</b>) O–CNT/CNT/CNT–PEI.</p>
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<p>XPS survey spectra of various samples: (<b>a</b>) wide scan of GO–PEI, (<b>b</b>) C 1s of GO–PEI, (<b>c</b>) N 1s of GO–PEI, (<b>d</b>) wide scan of CNT–PEI, (<b>e</b>) C 1s of CNT–PEI, (<b>f</b>) N 1s of CNT–PEI.</p>
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<p>TEM images of (<b>a</b>) GO, (<b>b</b>) GO–PEI, (<b>c</b>) CNT, (<b>d</b>) CNT–PEI.</p>
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<p>SEM images of aerogels: (<b>a</b>–<b>c</b>) GO/CNT/SBL (SBL:GO = 2:1), (<b>d</b>–<b>f</b>) GO/CNT–PEI/SBL (SBL:GO = 2:1), (<b>g</b>–<b>i</b>) GO–PEI/CNT–PEI/SBL (SBL:GO = 2:1).</p>
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<p>Compression curves of (<b>a</b>) GOA, (<b>b</b>) SBL:GO = 1:2, (<b>c</b>) SBL:GO = 1:1, (<b>d</b>) SBL:GO = 2:1, (<b>e</b>) SBL:GO = 3:1, (<b>f</b>) EL curves at 50% compression.</p>
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<p>Compression curves of (<b>a</b>) GO/CNT/SBL, (<b>b</b>) GO/CNT–PEI/SBL, (<b>c</b>) GO–PEI/CNT/SBL, and (<b>d</b>) GO–PEI/CNT–PEI/SBL.</p>
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<p>Thermal analysis: (<b>a</b>) TGA and (<b>b</b>) DTG curves of samples of various mass ratios, (<b>c</b>) TGA and (<b>d</b>) DTG curves of samples grafted with PEI.</p>
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<p>Schematic of preparation for (<b>a</b>) GO–PEI, (<b>b</b>) CNT–PEI, (<b>c</b>) GO/CNT/SBL aerogel.</p>
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19 pages, 2332 KiB  
Review
Injectable Thermoresponsive Hydrogels for Cancer Therapy: Challenges and Prospects
by Sandrine Tanga, Marique Aucamp and Poornima Ramburrun
Gels 2023, 9(5), 418; https://doi.org/10.3390/gels9050418 - 16 May 2023
Cited by 14 | Viewed by 3754
Abstract
The enervating side effects of chemotherapeutic drugs have necessitated the use of targeted drug delivery in cancer therapy. To that end, thermoresponsive hydrogels have been employed to improve the accumulation and maintenance of drug release at the tumour site. Despite their efficiency, very [...] Read more.
The enervating side effects of chemotherapeutic drugs have necessitated the use of targeted drug delivery in cancer therapy. To that end, thermoresponsive hydrogels have been employed to improve the accumulation and maintenance of drug release at the tumour site. Despite their efficiency, very few thermoresponsive hydrogel-based drugs have undergone clinical trials, and even fewer have received FDA approval for cancer treatment. This review discusses the challenges of designing thermoresponsive hydrogels for cancer treatment and offers suggestions for these challenges as available in the literature. Furthermore, the argument for drug accumulation is challenged by the revelation of structural and functional barriers in tumours that may not support targeted drug release from hydrogels. Other highlights involve the demanding preparation process of thermoresponsive hydrogels, which often involves poor drug loading and difficulties in controlling the lower critical solution temperature and gelation kinetics. Additionally, the shortcomings in the administration process of thermosensitive hydrogels are examined, and special insight into the injectable thermosensitive hydrogels that reached clinical trials for cancer treatment is provided. Full article
(This article belongs to the Special Issue Gel-Based Drug Delivery Systems for Cancer Treatment)
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<p>Intravenous delivery and intratumoral delivery. (<b>A</b>). Intravenous delivery: the drug is systemically circulated throughout the body. (<b>B</b>). Intratumoral delivery: the drug remains localised within the tumour.</p>
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<p>Tumour structure showing hypoxic and acidic variations in different regions.</p>
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<p>Schematic representation of sol–gel transition mechanisms and hydrophobic drug loading of diblock and triblock copolymers. (<b>A</b>) Diblock copolymers (PEG-PLGA) gelate at higher temperatures with hydrophobic drugs bonded at hydrophobic core. (<b>B</b>) Triblock copolymers (PLGA-PEG-PLGA) gelate at increased temperatures with more hydrophilic linkages and less hydrophobic ends.</p>
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<p>(<b>A</b>) In vitro release profiles of the individual 5-fluorouracil and methotrexate from the modified hydrogel at 37 °C in PBS at 0.1% drug concentration, and (<b>B</b>) the release profile of 5-fluorouracil as a function of drug concentration in PBS at 37 °C [<a href="#B97-gels-09-00418" class="html-bibr">97</a>]. Reproduced with permission from Almawash, El Hamd, and Osman 2022 © Creative Commons CC BY 4.0.</p>
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<p>Drug release-dependent behaviour on mechanical strength for PTX-CD loaded hydrogels (<sup>*●</sup> <span class="html-italic">p</span> &lt; 0.01, CS/PVA/GA/GP vs. CS/PVA/GP, <sup>*♦</sup> <span class="html-italic">p</span> &lt; 0.01 and CS/PVA/GA/GP vs. CS/GP, <sup>**</sup> <span class="html-italic">p</span> &lt; 0.01) [<a href="#B93-gels-09-00418" class="html-bibr">93</a>]. Reproduced with permission from Elsevier B.V. Ltd. © 2016.</p>
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38 pages, 412 KiB  
Review
Recent Progress in Gels for Neuropathic Pain
by Ciprian Pușcașu, Anca Zanfirescu and Simona Negreș
Gels 2023, 9(5), 417; https://doi.org/10.3390/gels9050417 - 16 May 2023
Cited by 6 | Viewed by 4495
Abstract
Neuropathic pain is a complex and debilitating condition that affects millions of people worldwide. While several treatment options are available, they often have limited efficacy and are associated with adverse effects. In recent years, gels have emerged as a promising option for the [...] Read more.
Neuropathic pain is a complex and debilitating condition that affects millions of people worldwide. While several treatment options are available, they often have limited efficacy and are associated with adverse effects. In recent years, gels have emerged as a promising option for the treatment of neuropathic pain. Inclusion of various nanocarriers, such as cubosomes and niosomes, into gels results in pharmaceutical forms with higher drug stability and increased drug penetration into tissues compared to products currently marketed for the treatment of neuropathic pain. Furthermore, these compounds usually provide sustained drug release and are biocompatible and biodegradable, which makes them a safe option for drug delivery. The purpose of this narrative review was to provide a comprehensive analysis of the current state of the field and identify potential directions for future research in the development of effective and safe gels for the treatment of neuropathic pain, ultimately improving the quality of life for patients suffering from neuropathic pain. Full article
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26 pages, 36467 KiB  
Review
Recent Advances in Nanocellulose Aerogels for Efficient Heavy Metal and Dye Removal
by Azfaralariff Ahmad, Mohamad Anuar Kamaruddin, Abdul Khalil H.P.S., Esam Bashir Yahya, Syaifullah Muhammad, Samsul Rizal, Mardiana Idayu Ahmad, Indra Surya and C. K. Abdullah
Gels 2023, 9(5), 416; https://doi.org/10.3390/gels9050416 - 16 May 2023
Cited by 22 | Viewed by 3437
Abstract
Water pollution is a significant environmental issue that has emerged because of industrial and economic growth. Human activities such as industrial, agricultural, and technological practices have increased the levels of pollutants in the environment, causing harm to both the environment and public health. [...] Read more.
Water pollution is a significant environmental issue that has emerged because of industrial and economic growth. Human activities such as industrial, agricultural, and technological practices have increased the levels of pollutants in the environment, causing harm to both the environment and public health. Dyes and heavy metals are major contributors to water pollution. Organic dyes are a major concern because of their stability in water and their potential to absorb sunlight, increasing the temperature and disrupting the ecological balance. The presence of heavy metals in the production of textile dyes adds to the toxicity of the wastewater. Heavy metals are a global issue that can harm both human health and the environment and are mainly caused by urbanization and industrialization. To address this issue, researchers have focused on developing effective water treatment procedures, including adsorption, precipitation, and filtration. Among these methods, adsorption is a simple, efficient, and cheap method for removing organic dyes from water. Aerogels have shown potential as a promising adsorbent material because of their low density, high porosity, high surface area, low thermal and electrical conductivity, and ability to respond to external stimuli. Biomaterials such as cellulose, starch, chitosan, chitin, carrageenan, and graphene have been extensively studied for the production of sustainable aerogels for water treatment. Cellulose, which is abundant in nature, has received significant attention in recent years. This review highlights the potential of cellulose-based aerogels as a sustainable and efficient material for removing dyes and heavy metals from water during the treatment process. Full article
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<p>(<b>a</b>) Morphology illustration of plant cellulose fibers and their molecular structure. (<b>b</b>) Schematic of the preparation of cellulose micro/nano-crystals/fibers and derivatives.</p>
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<p>Common approach to preparing aerogels.</p>
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<p>(<b>a</b>) Cellulose aerogel gelling approach: coagulative regeneration and chemical agglomeration. (<b>b</b>) Different forms of cellulose aerogels: (<b>i</b>) monolith, (<b>ii</b>) beads, and (<b>iii</b>) microparticles; adapted from [<a href="#B39-gels-09-00416" class="html-bibr">39</a>,<a href="#B40-gels-09-00416" class="html-bibr">40</a>,<a href="#B41-gels-09-00416" class="html-bibr">41</a>].</p>
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<p>(<b>a</b>) Illustration of freeze-casting–freeze-drying principles. (<b>b</b>) Illustration of supercritical drying process using a two-component CO<sub>2</sub>–alcohol.</p>
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<p>Illustration of the health effects of water pollutants on human health.</p>
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<p>Schematic overview of the adsorption of dyes and heavy metal ions by a cellulose-based aerogel.</p>
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<p>Possible adsorbent–adsorbate interaction mechanisms for the decontamination of wastewater using a cellulose hydrogel or aerogel. Adapted from [<a href="#B98-gels-09-00416" class="html-bibr">98</a>].</p>
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22 pages, 5729 KiB  
Article
Alginate Hydrogel Formulation with Ketorolac for the Treatment of Pain Related Sialolithiasis
by Cristina Silva, Gladys Ramos-Yacasi, Mireia Mallandrich, Helena Colom-Codina, Joaquim Suñer-Carbó, Noelia Pérez-González, Ana Cristina Calpena and Francisco Fernández-Campos
Gels 2023, 9(5), 415; https://doi.org/10.3390/gels9050415 - 16 May 2023
Cited by 1 | Viewed by 1668
Abstract
Sialolithiasis mainly affects the oral salivary glands due to the presence of small stones that obstruct the secretion of saliva. The treatment and control of pain and inflammation during the course of this pathology is essential to guarantee the patient’s comfort. For this [...] Read more.
Sialolithiasis mainly affects the oral salivary glands due to the presence of small stones that obstruct the secretion of saliva. The treatment and control of pain and inflammation during the course of this pathology is essential to guarantee the patient’s comfort. For this reason, a ketorolac calcium cross-linked alginate hydrogel was developed, and it was then applied in the area of the buccal cavity. The formulation was characterized (swelling and degradation profile, extrusion, extensibility, surface morphology, viscosity, and drug release). The drug release was studied ex vivo in static Franz cells and with a dynamic ex vivo method under artificial saliva continuous flow. The product exhibits adequate physicochemical properties considering the intended purpose, and the drug concentrations retained in the mucosa were high enough to deliver a therapeutic local concentration able to reduce the pain associated with the patient’s conditions. The results confirmed the suitability of the formulation for application in the mouth. Full article
(This article belongs to the Special Issue Physically Cross-Linked Gels and Their Applications)
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<p>Layout of the salivary glands.</p>
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<p>Chemical structures of: (<b>a</b>) ketorolac tromethamine [<a href="#B17-gels-09-00415" class="html-bibr">17</a>] and (<b>b</b>) sodium alginate [<a href="#B18-gels-09-00415" class="html-bibr">18</a>].</p>
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<p>Appearance of KT alginate gels before reticulation (without the crosslinking agent CaCl<sub>2</sub>) (<b>A</b>), and G15 formulation, KT alginate gel cross-linked with the addition of CaCl<sub>2</sub> (<b>B</b>).</p>
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<p>FT-IR spectra for alginate gels: (<b>a</b>) red = dried placebo of KT alginate gel (prior reticulation) and blue = dried of KT alginate gel (prior reticulation); (<b>b</b>) red = dried placebo of KT G15 gel and blue = dried KT G15 gel; and (<b>c</b>) red = sodium alginate powder and blue = ketorolac powder.</p>
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<p>Extensibility of the formulation G15 depending on the weight applied fitting first-order kinetic model.</p>
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<p>Scanning electron microscopy images of KT hydrogel G15 at different magnifications: 2000× and scale bar of 50 µm (<b>A</b>) and 5000× and scale bar of 20 µm (<b>B</b>). The alginate and crosslinking agent (CaCl<sub>2</sub>) were mixed in a 1:1 for the final formulation.</p>
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<p>Swelling ratio of dried KT hydrogel G15 upon immersion in PBS at the different pH of the buccal cavity (<span class="html-italic">n</span> = 3 for each pH). The swelling ratio followed the hyperbola model.</p>
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<p>Degradation of G15 KT hydrogel in PBS pH 7.4, which fitted a zero-order kinetic model. Each value represents the mean ± SD (<span class="html-italic">n</span> = 3).</p>
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<p>Mucoadhesive force (mN/cm<sup>2</sup>) of hydrogel developed with porcine buccal mucosa and sublingual. Each value represents the mean ± SD (<span class="html-italic">n</span> = 3).</p>
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<p>Extrudability (g/cm<sup>2</sup>) behavior of hydrogel developed measured with a 2 mL syringe. Each value represents the mean ± SD (<span class="html-italic">n</span> = 3). * significant statistical difference <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Rheological behaviour of G15 KT hydrogel: (<b>a</b>) before being reticulated, (<b>b</b>) reticulated gel, and (<b>c</b>) extruded reticulated gel. Viscosity curve (blue line, right axis, η in Pa·s) and flow curve (red line, left axis, τ in Pa) of G15 Kt hydrogel as a function of shear rate (γ in s<sup>−1</sup>).</p>
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<p>Cumulative amount of ketorolac released from the hydrogel in artificial membranes, PES, and nylon.</p>
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<p>Cumulative amount of ketorolac permeated from the hydrogel through buccal and sublingual mucosae. Results are represented as the mean ± SD of six replicates.</p>
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<p>(<b>a</b>) Amount of ketorolac extracted from the buccal and sublingual mucosa after ex vivo dynamic study with a constant flow of artificial saliva, and (<b>b</b>) amount of KT dragged by the artificial saliva flow during the ex vivo dynamic study. * Statistical significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Histological sections of mucosae after the ex vivo permeation study: (<b>a</b>) Sublingual mucosa histology under basal conditions, without gel (100× magnification); (<b>b</b>) sublingual mucosa histology after gel exposure (100× magnification). (<b>c</b>) Buccal mucosa histology under basal conditions, without gel (100× magnification); (<b>d</b>) buccal mucosa histology after gel exposure (100× magnification). Scale bars = 100 µm.</p>
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<p>Simplified representation of the device to determine ex vivo mucoadhesion.</p>
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16 pages, 4176 KiB  
Article
Optimal Concentration and Duration of Endotracheal Tube Coating to Achieve Optimal Antimicrobial Efficacy and Safety Balance: An In Vitro Study
by Manar Fathy Al-Sayed, Mohamed Tarek El-Wakad, Mohammed A. Hassan, Ahmed M. Soliman and Amal S. Eldesoky
Gels 2023, 9(5), 414; https://doi.org/10.3390/gels9050414 - 16 May 2023
Cited by 2 | Viewed by 2219
Abstract
Background: Ventilator-associated pneumonia (VAP) is a common and genuine complication in fundamentally sick patients accepting mechanical ventilation. Silver nitrate sol-gel (SN) has been proposed as a potential preventative measure against VAP. Be that as it may, the arrangement of SN with distinctive concentrations [...] Read more.
Background: Ventilator-associated pneumonia (VAP) is a common and genuine complication in fundamentally sick patients accepting mechanical ventilation. Silver nitrate sol-gel (SN) has been proposed as a potential preventative measure against VAP. Be that as it may, the arrangement of SN with distinctive concentrations and pH values remains a basic factor influencing its effectiveness. Methods: Silver nitrate sol-gel was arranged with distinctive concentrations (0.1852%, 0.03496%, 0.1852%, and 0.01968%) and pH values (8.5, 7.0, 8.0, and 5.0) separately. The antimicrobial action of the silver nitrate and NaOH arrangements were assessed against Escherichia coli as a reference strain. The thickness and pH of the arrangements were measured, and biocompatibility tests were performed on the coating tube. The auxiliary changes in the endotracheal tube (ETT) tests after treatment were analyzed utilizing electron microscopy (SEM) and transmission electron microscopy (TEM). Results: The pH estimations of the diverse arrangements showed that the pH values shifted depending on the test conditions, with pH values extending from 5.0 to 8.5. The consistency estimations of the arrangements showed that the thickness values expanded as the pH values drew closer to 7.5 and diminished when the pH values went over 7.5. The antimicrobial action of the silver nitrate and NaOH arrangements were successful against Escherichia coli, with microbial checks decreasing in concentration (0.03496%, 0.1852% (pH: 8), and 0.01968%). The biocompatibility tests revealed tall cell reasonability rates, demonstrating that the coating tube was secure for therapeutic utilization and did not hurt typical cells. The SEM and TEM investigation gave visual proof of the antibacterial impacts of the silver nitrate and NaOH arrangements on the bacterial surface or interior of the bacterial cells. Moreover, the investigation revealed that a concentration of 0.03496% was the foremost successful in hindering the development of ETT bacterial colonization at the nanoscale level. Conclusions: We propose that cautious control and alteration of the pH and thickness of the arrangements are essential to guaranteeing the reproducibility and quality of the sol-gel materials. The silver nitrate and NaOH arrangements may serve as a potential preventative degree against VAP in sick patients, with a concentration of 0.03496% appearing to show the most elevated viability. The coating tube may serve as a secure and viable preventative measure against VAP in sick patients. Further investigation is required to optimize the concentration and introduction time of the arrangements to maximize their adequacy in avoiding VAP in real-world clinical settings. Full article
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<p>Error analysis for pH values of four samples.</p>
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<p>Error analysis for viscosity values of four samples.</p>
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<p>Cell viability of coated ETT with samples (1, 2, 3, and 4).</p>
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<p>Scanning electron microscope (SEM) images of samples (<b>a</b>) sample 1, (<b>b</b>) sample 2, (<b>c</b>) sample 3, and (<b>d</b>) sample 4.</p>
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<p>EDX analysis for elements in experiments.</p>
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<p>Transmission electron microscopy (TEM) images of samples (<b>a</b>) sample 1, (<b>b</b>) sample 2, (<b>c</b>) sample 3, and (<b>d</b>) sample 4.</p>
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<p>SN sol-gel prepared sequence.</p>
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<p>The dipping samples were in sol-gel for 24 h. (<b>a</b>) Silver concentration is 0.1852% (pH = 8.5), (<b>b</b>) silver concentration is 0.03496% (pH = 7), (<b>c</b>) silver concentration is 0.1852% (pH = 8), (<b>d</b>) silver concentration is 0.01968% (pH = 5).</p>
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<p>Gram-negative bacteria: <span class="html-italic">Escherichia coli</span> ATCC 25922 for all samples.</p>
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23 pages, 6859 KiB  
Review
Application and Research Prospect of Functional Polymer Gels in Oil and Gas Drilling and Development Engineering
by Yingrui Bai, Yuan Liu, Keqing Yang and Youming Lang
Gels 2023, 9(5), 413; https://doi.org/10.3390/gels9050413 - 16 May 2023
Cited by 9 | Viewed by 2092
Abstract
Polymer gel materials are formed by physically crosslinking and chemically crosslinking to form a gel network system with high mechanical properties and reversible performance. Due to their excellent mechanical properties and intelligence, polymer gel materials are widely used in biomedical, tissue engineering, artificial [...] Read more.
Polymer gel materials are formed by physically crosslinking and chemically crosslinking to form a gel network system with high mechanical properties and reversible performance. Due to their excellent mechanical properties and intelligence, polymer gel materials are widely used in biomedical, tissue engineering, artificial intelligence, firefighting and other fields. Given the current research status of polymer gels at home and abroad and the current application status of oilfield drilling, this paper reviews the mechanism of polymer gels formed by physically crosslinking and chemically crosslinking, summarizes the performance characteristics and the mechanism of action of polymer gels formed by non-covalent bonding, such as hydrophobic bonding, hydrogen bonding, electrostatic and Van der Waals interactions interactions, and covalent bonding such as imine bonding, acylhydrazone bonding and Diels-Alder reaction. The current status and outlook of the application of polymer gels in drilling fluids, fracturing fluids and enhanced oil recovery are also introduced. We expand the application fields of polymer gel materials and promote the development of polymer gel materials in a more intelligent direction. Full article
(This article belongs to the Special Issue Gels for Oil Drilling and Enhanced Recovery (2nd Edition))
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<p>(<b>a</b>) Schematic diagram of the structural model of a hydrophobic-conjugated hydrogel with a conjugated network. (<b>b</b>) Scanning electron micrographs of hydrophobic-conjugated composite and non-composite gels [<a href="#B24-gels-09-00413" class="html-bibr">24</a>].</p>
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<p>(<b>a</b>) Schematic molecular structure of CB[7]-PAAm gels. (<b>b</b>) Schematic diagram of the sol-gel phase transition of CB[7]-PAAm gels. (<b>c</b>) Effect of PH on the self-healing effect of CB[7]-PAAm gels(Red circles indicate gel self-healing joints) [<a href="#B33-gels-09-00413" class="html-bibr">33</a>].</p>
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<p>(<b>a</b>) Synthesis process and chemical structure of the hydrogel. (<b>b</b>) Demonstration of the presence of weak hydrogen bonds between acrylamide and acrylic acid and multiple strong hydrogen bonds between 2-ureido-4[1H]-pyrimidinone units in the hydrogel [<a href="#B35-gels-09-00413" class="html-bibr">35</a>].</p>
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<p>(<b>a</b>) Schematic diagram of the self-healing mechanism of polyampholytic electrolyte hydrogels. (<b>b</b>) Photographs of polyamphiphilic electrolytes polymerized with different total monomer concentrations. (<b>c</b>) Solvation volume ratio and Young’s modulus of amphiphilic electrolyte hydrogels with monomer concentration pair dependence. (<b>d</b>) Tensile behavior of polyamphiphilic electrolyte hydrogels with different monomer concentrations (The different color lines are the total molar concentrations of different ionic monomers) [<a href="#B37-gels-09-00413" class="html-bibr">37</a>,<a href="#B40-gels-09-00413" class="html-bibr">40</a>].</p>
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<p>Sol–gel transition under van der Waals interactions [<a href="#B42-gels-09-00413" class="html-bibr">42</a>].</p>
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<p>(<b>a</b>) Synthesis strategy of chitosan-based hydrogels. (<b>b</b>) Shape memory process of chitosan–polyacrylamide-based double network hydrogel in PBS solution (pH = 3). (<b>c</b>) Shape memory process of chitosan–polyacrylamide-based double network hydrogels in EDTA (0.1 M) aqueous solution [<a href="#B50-gels-09-00413" class="html-bibr">50</a>,<a href="#B52-gels-09-00413" class="html-bibr">52</a>].</p>
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<p>A model of dynamic covalent polymer networks crosslinking by acylhydrazone bonds (Different color lines indicate different polymer molecular chains) [<a href="#B57-gels-09-00413" class="html-bibr">57</a>].</p>
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<p>(<b>a</b>) Self-healing properties of hydrogels observed by direct visual observation. (<b>b</b>) Stress–strain curves of pristine and self-healing hydrogels at different healing times. (<b>c</b>,<b>d</b>) Self-repair efficiency of hydrogels tested by room temperature tensile [<a href="#B61-gels-09-00413" class="html-bibr">61</a>].</p>
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<p>Crosslinking density and mechanical properties of DN hydrogels can be controlled by varying the ratio of Fe<sup>3+</sup>-catechol and pH value. (<b>a</b>) The pictures from left to right, top to bottom, are SEM of SN hydrogels; SEM of Fe<sup>3+</sup>-catechol 1:1DN hydrogels; SEM of Fe<sup>3+</sup>-catechol 1:2DN hydrogels; SEM of Fe<sup>3+</sup>-catechol 1:3 DN hydrogels. (<b>b</b>) Possible crosslinking mechanism of hydrogels at different pH conditions [<a href="#B63-gels-09-00413" class="html-bibr">63</a>].</p>
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<p>(<b>a</b>) Plugging process of polymer self-healing gel. (<b>b</b>) SEM of modified ZIF particles. (<b>c</b>) SEM of modified ZIF particles after ageing. (<b>d</b>) Schematic diagram of the structure of modified ZIF [<a href="#B69-gels-09-00413" class="html-bibr">69</a>,<a href="#B70-gels-09-00413" class="html-bibr">70</a>].</p>
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<p>(<b>a</b>) Schematic diagram of the effect of surfactant on the stability of A surfactant with polyacrylamide, B surfactant with the associative polymer and C foam. (<b>b</b>) A and B are ESEM images before and after the addition of SDS to the solution of the associative polymer; C and D are ESEM images before and after the addition of crosslinking agent to the solution of guar gum [<a href="#B73-gels-09-00413" class="html-bibr">73</a>].</p>
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<p>Ultra-high-temperature-tolerant hydrogels (HT-PPGs). (<b>a</b>) General synthetic scheme for HT-PPG hydrogel synthesis. (<b>b</b>) Thermal stability evaluation of HT-PPG in 2% KCl at SR = 15 and 150 °C. HT-PPG recovered after 18 months of ageing and showed retention of structural integrity and gel particle morphology [<a href="#B84-gels-09-00413" class="html-bibr">84</a>].</p>
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<p>Mechanism of polymer self-healing gel plugging. (<b>a</b>) Gel particles circulate in the wellbore with the drilling fluid. (<b>b</b>) The gel particles are adsorbed and accumulated in the formation of fractures. (<b>c</b>) The gel particles are extruded and deformed to form a block gel to seal the fracture.</p>
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<p>Schematic diagram of the sol–gel conversion mechanism of polymeric fracturing fluid.</p>
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<p>Polymer gel for water conditioning and blocking mechanism.</p>
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21 pages, 3796 KiB  
Article
Clotrimazole-Loaded Borneol-Based In Situ Forming Gel as Oral Sprays for Oropharyngeal Candidiasis Therapy
by Nutdanai Lertsuphotvanit, Sarun Tuntarawongsa, Kritamorn Jitrangsri and Thawatchai Phaechamud
Gels 2023, 9(5), 412; https://doi.org/10.3390/gels9050412 - 15 May 2023
Cited by 3 | Viewed by 2443
Abstract
Oral candidiasis encompasses fungal infections of the tongue and other oral mucosal sites with fungal overgrowth and its invasion of superficial oral tissues. Borneol was assessed in this research as the matrix-forming agent of clotrimazole-loaded in situ forming gel (ISG) comprising clove oil [...] Read more.
Oral candidiasis encompasses fungal infections of the tongue and other oral mucosal sites with fungal overgrowth and its invasion of superficial oral tissues. Borneol was assessed in this research as the matrix-forming agent of clotrimazole-loaded in situ forming gel (ISG) comprising clove oil as the co-active agent and N-methyl pyrrolidone (NMP) as a solvent. Their physicochemical properties, including pH, density, viscosity, surface tension, contact angle, water tolerance, gel formation, and drug release/permeation, were determined. Their antimicrobial activities were tested using agar cup diffusion. The pH values of clotrimazole-loaded borneol-based ISGs were in the range of 5.59–6.61, which are close to the pH of 6.8 of saliva. Increasing the borneol content in the formulation slightly decreased the density, surface tension, water tolerance, and spray angle but increased the viscosity and gel formation. The borneol matrix formation from NMP removal promoted a significantly (p < 0.05) higher contact angle of the borneol-loaded ISGs on agarose gel and porcine buccal mucosa than those of all borneol-free solutions. Clotrimazole-loaded ISG containing 40% borneol demonstrated appropriate physicochemical properties and rapid gel formation at microscopic and macroscopic levels. In addition, it prolonged drug release with a maximum flux of 370 µg·cm−2 at 2 days. The borneol matrix generated from this ISG obsentively controlled the drug penetration through the porcine buccal membrane. Most clotrimazole amounts still remained in formulation at the donor part and then the buccal membrane and receiving medium, repectively. Therefore, the borneol matrix extended the drug release and penetration through the buccal membrane efficiently. Some accumulated clotrimazole in tissue should exhibit its potential antifugal activity against microbes invading the host tissue. The other predominant drug release into the saliva of the oral cavity should influence the pathogen of oropharyngeal candidiasis. Clotrimazole-loaded ISG demonstrated efficacious inhibition of growth against S. aureus, E. coli, C. albicans, C. krusei, C. Lusitaniae, and C. tropicalis. Consequently, the clotrimazole-loaded ISG exhibited great potential as a drug delivery system for oropharyngeal candidiasis treatment by localized spraying. Full article
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<p>Chemical structures of clotrimazole (<b>A</b>), NMP (<b>B</b>), and borneol (<b>C</b>).</p>
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<p>Rheological behavior of clotrimazole-loaded borneol-based ISG and related formulations, plotting between shear stress against shear rate (<b>A</b>) and relationship between viscosity and shear rate at room temperature (<b>B</b>).</p>
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<p>Wettability of clotrimazole-loaded borneol-based ISG and related formulations on the surface of the glass slide, agarose gel, and buccal porcine. Results are shown as mean values ± SD and demonstrated at room temperature (<span class="html-italic">n</span> = 3). * and # represent a significant difference (<span class="html-italic">p</span> &lt; 0.05) compared with ZCN.</p>
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<p>Interfacial tension and gel-formation behavior of clotrimazole-loaded borneol-based ISGs and borneol solution in PBS with pH 6.8.</p>
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<p>(<b>A</b>) Change of gel formation with time after contact with PBS with pH 6.8. (<b>B</b>) Morphological change of clotrimazole-loaded borneol-based ISG and related formulations after exposure with agarose gel containing PBS with pH 6.8.</p>
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<p>Percentage of water inducing a phase separation of clotrimazole-loaded borneol-based ISGs and borneol solution. Results are shown as mean values ± SD, (<span class="html-italic">n</span> = 3). * represents a significant difference (<span class="html-italic">p</span> &lt; 0.05) compared with 50BZCN.</p>
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<p>Clotrimazole release through (<b>A</b>) nylon membrane and (<b>B</b>) permeability through porcine buccal membrane from 40BZCN compared with ZN (<span class="html-italic">n</span> = 6).</p>
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<p>Photographs of the inhibition zone of ISG formulations containing 20–50% borneol (20BZCN-50BZCN) against <span class="html-italic">S. aureus</span> (<b>A</b>), <span class="html-italic">E. coli</span> (<b>B</b>), and <span class="html-italic">C. albicans</span> (<b>C</b>,<b>D</b>) (<span class="html-italic">n</span> = 3).</p>
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2 pages, 1916 KiB  
Correction
Correction: Jaik et al. Photomotion of Hydrogels with Covalently Attached Azo Dye Moieties—Thermoresponsive and Non-Thermoresponsive Gels. Gels 2022, 8, 541
by Thorben G. Jaik, Assegid M. Flatae, Navid Soltani, Philipp Reuschel, Mario Agio, Emiliano Descrovi and Ulrich Jonas
Gels 2023, 9(5), 411; https://doi.org/10.3390/gels9050411 - 15 May 2023
Viewed by 912
Abstract
In the original publication [...] Full article
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<p>Light microscopy images of pristine (left panels) and photoactuated regions (right panels) of gel layers prepared from (<b>a</b>,<b>b</b>) poly(HEAm<sub>96.5%</sub>-co-o-MREAm<sub>2.5%</sub>-co-BPAAm<sub>1%</sub>) P<sub>NR</sub>, swollen in water, (<b>c</b>,<b>d</b>) poly(NipAAm<sub>86.5%</sub>-HEAm<sub>10%</sub>-co-o-MREAm<sub>2.5%</sub>-co-BPAAm<sub>1%</sub>) P<sub>22°C</sub>, swollen in water, (<b>e</b>,<b>f</b>) the same polymer in isopropanol. Photoactuation was performed with a laser at λ = 532 nm and 2600 µW (irradiation region marked by a green spot). Red lines and arrows indicate notable gel features that were photoactuated. Videos of the photomotion are provided in the download section of the supporting information.</p>
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14 pages, 2613 KiB  
Article
Sodium Salt of Partially Carboxymethylated Sodium Alginate-g-Poly(acrylonitrile): I. Photo-Induced Synthesis, Characterization, and Alkaline Hydrolysis
by Jignesh Trivedi and Arvind Chourasia
Gels 2023, 9(5), 410; https://doi.org/10.3390/gels9050410 - 15 May 2023
Cited by 3 | Viewed by 1338
Abstract
An efficient redox initiating system, ceric ammonium nitrate/nitric acid, has been employed for the first time to carry out photo-induced graft copolymerization of acrylonitrile (AN) onto sodium salt of partially carboxymethylated sodium alginate, having an average degree of substitution value to be 1.10. [...] Read more.
An efficient redox initiating system, ceric ammonium nitrate/nitric acid, has been employed for the first time to carry out photo-induced graft copolymerization of acrylonitrile (AN) onto sodium salt of partially carboxymethylated sodium alginate, having an average degree of substitution value to be 1.10. The photo-grafting reaction conditions for maximum grafting have been systematically optimized by varying the reaction variables such as reaction time, temperature, the concentration of acrylonitrile monomer, ceric ammonium nitrate, and nitric acid, as well as the amount of the backbone. The optimum reaction conditions are obtained with a reaction time of 4 h, reaction temperature of 30 °C, acrylonitrile monomer concentration of 0.152 mol/L, initiator concentration of 5 × 10−3 mol/L, nitric acid concentration of 0.20 mol/L, amount of backbone of 0.20 (dry basis) and the total volume of the reaction system of 150 mL. The highest percentage of grafting (%G) and grafting efficiency (%GE) achieved are 316.53% and 99.31%, respectively. The optimally prepared graft copolymer, sodium salt of partially carboxymethylated sodium alginate-g-polyacrylonitrile (%G = 316.53), has been hydrolyzed in an alkaline medium (0.7N NaOH, 90–95 °C for ~2.5 h) to obtain the superabsorbent hydrogel, H–Na–PCMSA–g–PAN. The chemical structure, thermal characteristics, and morphology of the products have also been studied. Full article
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<p>The synthetic route for the photo-graft copolymer, Na–PCMSA–g–PAN, and its saponification for the formation of the superabsorbent hydrogel, H–Na–PCMSA–g–PAN.</p>
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<p>Influence of (<b>a</b>) amount of sodium salt of partially carboxymethylated sodium alginate (Na–PCMSA); (<b>b</b>) ceric ammonium nitrate (CAN) concentration; (<b>c</b>) nitric acid (HNO<sub>3</sub>) concentration; (<b>d</b>) acrylonitrile (AN) concentration; (<b>e</b>) reaction time and (<b>f</b>) reaction temperature on <span style="color:red">-●-</span> %G or <span style="color:blue">-■-</span> %GE.</p>
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<p>Influence of (<b>a</b>) amount of sodium salt of partially carboxymethylated sodium alginate (Na–PCMSA); (<b>b</b>) ceric ammonium nitrate (CAN) concentration; (<b>c</b>) nitric acid (HNO<sub>3</sub>) concentration; (<b>d</b>) acrylonitrile (AN) concentration; (<b>e</b>) reaction time and (<b>f</b>) reaction temperature on <span style="color:red">-●-</span> %G or <span style="color:blue">-■-</span> %GE.</p>
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<p>FTIR spectra of the following:(<b>a</b>) sodium salt of partially carboxymethylated sodium alginate (Na–PCMSA, (<math display="inline"><semantics> <mrow> <mover accent="true"> <mrow> <mi>DS</mi> </mrow> <mo stretchy="true">¯</mo> </mover> </mrow> </semantics></math> = 1.10); (<b>b</b>) Na-PCMSA–g–PAN (%G = 316.53); (<b>c</b>) PAN; (<b>d</b>) the superabsorbent hydrogel, H–Na–PCMSA–g–PAN.</p>
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<p>TG thermograms for (―) Na–PCMSA (<math display="inline"><semantics> <mrow> <mover accent="true"> <mrow> <mi>DS</mi> </mrow> <mo stretchy="true">¯</mo> </mover> </mrow> </semantics></math> = 1.10 (S<sub>1</sub>); (•••) Na–PCMSA–g–PAN (%G = 316.53) (S<sub>2</sub>) and (…) H–Na–PCMSA–g–PAN (S<sub>3</sub>) at 10 °C/min. The insert shows the first derivatives of the curves shown in the figure.</p>
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<p>Scanning electron micrographs of (<b>a</b>) Na–PCMSA (<math display="inline"><semantics> <mrow> <mover accent="true"> <mrow> <mi>DS</mi> </mrow> <mo stretchy="true">¯</mo> </mover> </mrow> </semantics></math> = 1.10) (500×), (<b>b</b>)Na–PCMSA–g–PAN (%G = 316.53) (500×), and (<b>c</b>) the superabsorbent hydrogel H–Na–PCMSA–g–PAN (500×).</p>
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<p>Detailed experimental setup for carrying out photo-graft copolymerization reaction.</p>
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14 pages, 2869 KiB  
Protocol
A LC-QTOF Method for the Determination of PEGDE Residues in Dermal Fillers
by Giuseppe Alonci, Anna Boussard, Martina Savona, Fabiana Cordella, Gaetano Angelici, Roberto Mocchi, Sabrina Sommatis and Damiano Monticelli
Gels 2023, 9(5), 409; https://doi.org/10.3390/gels9050409 - 13 May 2023
Viewed by 1744
Abstract
Hyaluronic acid is one of the most important ingredients in dermal fillers, where it is often cross-linked to gain more favorable rheological properties and to improve the implant duration. Poly(ethylene glycol) diglycidyl ether (PEGDE) has been recently introduced as a crosslinker because of [...] Read more.
Hyaluronic acid is one of the most important ingredients in dermal fillers, where it is often cross-linked to gain more favorable rheological properties and to improve the implant duration. Poly(ethylene glycol) diglycidyl ether (PEGDE) has been recently introduced as a crosslinker because of its very similar chemical reactivity with the most-used crosslinker BDDE, while giving special rheological properties. Monitoring the amount of the crosslinker residues in the final device is always necessary, but in the case of PEGDE, no methods are available in literature. Here, we present an HPLC-QTOF method, validated according to the guidelines of the International Council on Harmonization, which enables the efficient routine examination of the PEGDE content in HA hydrogels. Full article
(This article belongs to the Special Issue Advances in Hydrogels for Biomedical Applications)
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<p>(<b>A</b>). Overlayed TIC of PEGDE from BOC Science (black) and Blank solvent (blue). (<b>B</b>). Zoom on the PEGDE region of the TIC (top green line) and EIC of 11 PEGDE M + NH<sub>4</sub><sup>+</sup> ions.</p>
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<p>Py-GC/MS analysis of BOC Sciences PEGDE; (<b>A</b>) first shot: Split 1:100, T = 300 °C; (<b>B</b>) second shot: Split 1:200; T = 600 °C.</p>
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<p>Magnification of <sup>1</sup>H (<b>A</b>) and <sup>13</sup>C (<b>B</b>) NMR spectra in the 2–4.5 ppm and 60–80 ppm ranges, respectively. Chemical shift ranges were selected where PEGDE signals were registered.</p>
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<p>Overlayed EIC of the selected PEGDE oligomers from BOC Science. PEGDE is a mixture of different oligomers; 8 oligomers were selected for the determination.</p>
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<p>Comparison of the calibration curve of PEGDE in ACN (blue) and of standard PEGDE addition on a PEGDE-crosslinked HA hydrogel (orange).</p>
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<p>Comparison of calibration curve of spiked BDDE gel (blue) and PEGDE gel (orange).</p>
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<p>Calibration curve of PEGDE reference solutions.</p>
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<p>EIC of PEGDE 482 in reference solution (blue, RT = 6.09 min) and in PEGDE gel (red, RT = 6.09 min). In PEGDE gel, other impurity was observed and separated from PEGDE chromatographically. Only the EIC of PEGDE 482 is shown for clarity.</p>
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14 pages, 1404 KiB  
Article
Dielectric Study on Supramolecular Gels by Fiber Structure Formation from Low-Molecular-Weight Gelator/Water Mixtures
by Kenta Shimizu, Fumiya Abe, Yasuhiro Kishi, Rio Kita, Naoki Shinyashiki and Shin Yagihara
Gels 2023, 9(5), 408; https://doi.org/10.3390/gels9050408 - 12 May 2023
Cited by 2 | Viewed by 1701
Abstract
There are various types of gel materials used in a wide range of fields, and their gelation mechanisms are extremely diverse. Furthermore, in the case of hydrogels, there exist some difficulties in understanding complicated molecular mechanisms especially with water molecules interacting through hydrogen [...] Read more.
There are various types of gel materials used in a wide range of fields, and their gelation mechanisms are extremely diverse. Furthermore, in the case of hydrogels, there exist some difficulties in understanding complicated molecular mechanisms especially with water molecules interacting through hydrogen bonding as solvents. In the present work, the molecular mechanism of the structural formation of fibrous super-molecular gel by the low molecular weight gelator, N-oleyl lactobionamide/water mixture was elucidated using the broadband dielectric spectroscopy (BDS) method. The dynamic behaviors observed for the solute and water molecules indicated hierarchical structure formation processes in various time scales. The relaxation curves obtained at various temperatures in the cooling and heating processes showed relaxation processes respectively reflecting the dynamic behaviors of water molecules in the 10 GHz frequency region, solute molecules interacting with water in MHz region, and ion-reflecting structures of the sample and electrode in kHz region. These relaxation processes, characterized by the relaxation parameters, showed remarkable changes around the sol–gel transition temperature, 37.8 °C, determined by the falling ball method and over the temperature range, around 53 °C. The latter change suggested a structure formation of rod micelles appearing as precursors before cross-linking into the three-dimensional network of the supramolecular gels. These results clearly demonstrate how effective relaxation parameter analysis is for understanding the gelation mechanism in detail. Full article
(This article belongs to the Special Issue Shaping and Structuring of Polymer Gels)
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<p>Hierarchical structures of fiber-crosslinked supramolecular gels by rod micelle growth of low-molecular-weight gelators in water: (<b>a</b>) amphiphilic molecules, (<b>b</b>) rod micelles, (<b>c</b>) fiber elongation, (<b>d</b>) fiber crosslinking.</p>
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<p>Chemical structure of N-oleyl lactobionamide.</p>
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<p>Temperature dependence of the reciprocal of the fall time for descent of the ball in 5 wt% N-oleyl lactobion/water mixture. The solid line indicates a linear relationship between the experimental plot (<span style="color:#6495ED">●</span>) and temperature.</p>
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<p>Frequency dependences of the real and imaginary parts of the complex permittivity for 5 wt% N-oleyl lactobionamide/water mixtures at various temperatures from 25 °C to 70 °C in the cooling [left, (<b>a</b>)] and heating processes [right, (<b>b</b>)]. The plot colors correspond to temperatures indicated in the figure.</p>
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<p>Dielectric relaxation curve (thick orange solid line) of 5 wt% N-oleyl lactobionamide/water mixture at 70 °C and each relaxation process obtained by the fitting procedures with Equation (1). Dotted lines represent <span class="html-italic">h-</span>(red), <span class="html-italic">m</span>-(magenta), <span class="html-italic">l</span><sub>1</sub>-(blue) and <span class="html-italic">l</span><sub>2</sub>-(purple) processes with the dc conductivity contribution (green) and calculated total (black).</p>
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<p>Temperature dependences of ∆<span class="html-italic">ε<sub>h</sub></span>, <span class="html-italic">τ<sub>h</sub></span>, <span class="html-italic">β<sub>h</sub>.</span> dielectric relaxation parameters for the <span class="html-italic">h</span>-process (<span style="color:red">●</span>, <span style="color:red">○</span>) and those for ultrapure water (<span style="color:blue">●</span>). The closed and open symbols indicate cooling and heating processes, respectively. The vertical dashed lines indicate the sol–gel transition temperature, 37.8 °C. Numbers 1–3 in the figure indicate temperature regions. Temperature regions 1 and 2 are indicated by different colors as the higher and lower temperature regions of 52.5 °C where the relaxation parameter changes, and region 3 is the gel state temperature region below the sol–gel transition temperature.</p>
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<p>Temperature dependence of dielectric relaxation parameters, ∆<span class="html-italic">ε<sub>m</sub></span>, <span class="html-italic">τ<sub>m</sub></span> and <span class="html-italic">β<sub>m</sub></span> for <span class="html-italic">m</span>-process. The closed and open symbols indicate cooling and heating processes, respectively. The vertical dashed lines indicate the sol–gel transition temperature, 37.8 °C. Numbers 1–3 in the figure indicate temperature regions. Temperature regions 1 and 2 are indicated by different colors as the higher and lower temperature regions of 52.5 °C where the relaxation parameter changes, and region 3 is the gel state temperature region below the sol–gel transition temperature.</p>
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<p>Temperature dependences of dielectric relaxation parameters, ∆<span class="html-italic">ε</span>, <span class="html-italic">τ</span> and <span class="html-italic">β</span> for the <span class="html-italic">l</span><sub>1</sub>-process. The closed and open symbols indicate cooling and heating processes. The dashed lines indicate the sol–gel transition temperature. Numbers 1–3 in the figure indicate temperature regions. Temperature regions 1 and 2 are indicated by different colors as the higher and lower temperature regions of 52.5 °C where the relaxation parameter changes, and region 3 is the gel state temperature region below the sol–gel transition temperature.</p>
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17 pages, 8083 KiB  
Article
Sodium Salt of Partially Carboxymethylated Sodium Alginate-Graft-Poly(Acrylonitrile): II Superabsorbency, Salt Sensitivity and Swelling Kinetics of Hydrogel, H-Na-PCMSA-g-PAN
by Jignesh Trivedi and Arvind Chourasia
Gels 2023, 9(5), 407; https://doi.org/10.3390/gels9050407 - 12 May 2023
Cited by 7 | Viewed by 1464
Abstract
The water absorption measurements of a novel superabsorbent anionic hydrogel, H-Na-PCMSA-g-PAN, has been reported first time in water with a poor conductivity, 0.15 M saline (NaCl, CaCl2, and AlCl3) solutions, and simulated urine (SU) solutions at various times. The hydrogel [...] Read more.
The water absorption measurements of a novel superabsorbent anionic hydrogel, H-Na-PCMSA-g-PAN, has been reported first time in water with a poor conductivity, 0.15 M saline (NaCl, CaCl2, and AlCl3) solutions, and simulated urine (SU) solutions at various times. The hydrogel has been prepared by the saponification of the graft copolymer, Na-PCMSA-g-PAN (%G = 316.53, %GE = 99.31). Results indicated that as compared to the swelling capacity values evaluated in water with a poor conductivity, the ability of the hydrogel to swell in various saline solutions with the same concentration is significantly reduced at all different durations. The swelling tends to be Na+ > Ca2+ > Al3+ at the same saline concentration in the solution. Studies of the absorbency in various aqueous saline (NaCl) solutions also revealed that the swelling capacity decreased as the ionic strength of the swelling medium rose, which is consistent with the experimental results and Flory’s equation. Furthermore, the experimental results strongly suggested that second-order kinetics governs the swelling process of the hydrogel in various swelling media. The swelling characteristics and equilibrium water contents for the hydrogel in various swelling media have also been researched. The hydrogel samples have been successfully characterized by FTIR to show the change in chemical environment to COO and CONH2 groups after swelling in different swelling media. The samples have also been characterized by SEM technique. Full article
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<p>Saponification of Na-PCMSA-g-PAN to create superabsorbent hydrogel.</p>
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<p>Photograph of the superabsorbent hydrogel after 24 h of its immersion in water with a poor conductivity.</p>
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<p>Dynamic swelling curves for the superabsorbent hydrogel, in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution and (<b>e</b>) 0.15 M SU solution.</p>
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<p>Complexing capacity of H-Na-PCMSA-g-PAN, considering the relationship between the anionic groups of the hydrogel and multivalent metal cations (Ca<sup>2+</sup> and Al<sup>3+</sup>).</p>
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<p>Swelling capacity variation of H-Na-PCMSA-g-PAN hydrogel sample in NaCl solutions having different ionic strengths.</p>
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<p>Plots of t/S versus t for H-Na-PCMSA-g-PAN, in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution; (<b>e</b>) 0.15 M SU solution.</p>
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<p>Plots of t/S versus t for H-Na-PCMSA-g-PAN, in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution; (<b>e</b>) 0.15 M SU solution.</p>
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<p>FTIR spectra (lyophilized) H-Na-PCMSA-g-PAN sample after swelling in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution and (<b>e</b>) 0.15 M SU solution.</p>
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<p>Scanning Electron Microscopy pictures of the lyophilized hydrogel samples swollen in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution and (<b>e</b>) 0.15 M Simulated Urine (SU).</p>
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<p>Scanning Electron Microscopy pictures of the lyophilized hydrogel samples swollen in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution and (<b>e</b>) 0.15 M Simulated Urine (SU).</p>
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<p>Scanning Electron Microscopy pictures of the lyophilized hydrogel samples swollen in (<b>a</b>) water with a poor conductivity; (<b>b</b>) 0.15 M NaCl solution; (<b>c</b>) 0.15 M CaCl<sub>2</sub> solution; (<b>d</b>) 0.15 M AlCl<sub>3</sub> solution and (<b>e</b>) 0.15 M Simulated Urine (SU).</p>
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19 pages, 3542 KiB  
Article
Comparison of Different Aerogel Granules for Use as Aggregate in Concrete
by Torsten Welsch, Yannick Vievers, Martina Schnellenbach-Held, Danny Bialuschewski and Barbara Milow
Gels 2023, 9(5), 406; https://doi.org/10.3390/gels9050406 - 12 May 2023
Cited by 4 | Viewed by 2089
Abstract
In previous work of this group, a structural lightweight concrete was developed by embedding silica aerogel granules in a high-strength cement matrix. This concrete, called high-performance aerogel concrete (HPAC), is a lightweight building material characterized by its simultaneous high compressive strength and very [...] Read more.
In previous work of this group, a structural lightweight concrete was developed by embedding silica aerogel granules in a high-strength cement matrix. This concrete, called high-performance aerogel concrete (HPAC), is a lightweight building material characterized by its simultaneous high compressive strength and very low thermal conductivity. Besides these features, high sound absorption, diffusion permeability, water repellence and fire resistance qualify HPAC as an interesting material for the construction of single-leaf exterior walls without any further insulation. During the development of HPAC, the type of silica aerogel was found to majorly influence both fresh and hardened concrete properties. To clarify these effects, a systematic comparison of SiO2 aerogel granules with different levels of hydrophobicity as well as different synthesis methods was conducted in the present study. The granules were analyzed for their chemical and physical properties as well as their compatibility in HPAC mixtures. These experiments included determinations of pore size distribution, thermal stability, porosity, specific surface and hydrophobicity, as well as fresh/hardened concrete experiments such as measurements of compressive strength, flexural bending strength, thermal conductivity and shrinking behavior. It was found that the type of aerogel has a major influence on the fresh and hardened concrete properties of HPAC, particularly compressive strength and shrinkage behavior, whereas the effect on thermal conductivity is not very pronounced. Full article
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<p>Relation between compressive strength and thermal conductivity of aerogel (incorporated) concretes (AICs), aerogel composite concretes (AIC-composites) and high-performance aerogel concrete (HPAC) (Reprinted/adapted with permission from Ref. [<a href="#B5-gels-09-00406" class="html-bibr">5</a>], 2022, John Wiley and Sons).</p>
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<p>Pore distribution of selected samples in the meso- and lower macroporous regions.</p>
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<p>Temperature-dependent heat conductivity, example from sample P100.</p>
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<p>Mass loss of aerogels under air or nitrogen, with SUFA under nitrogen out of range (&gt;70%).</p>
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<p>(<b>a</b>) Compressive strength and (<b>b</b>) flexural bending strength of concrete specimen; average values and standard deviation of at least 3 specimens. <sup>1)</sup>: tested after 7d.</p>
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<p>(<b>a</b>) Compressive strength and (<b>b</b>) flexural bending strength of concrete specimen; average values and standard deviation of at least 3 specimens. <sup>1)</sup>: tested after 7d.</p>
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<p>Shrinkage value measured at a temperature of 25.0 °C and a humidity of 40.0%.</p>
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<p>Microscopic images of every HPAC mixture.</p>
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<p>Relation between water–cement ratio and (<b>a</b>) compressive strength and (<b>b</b>) flexural tensile strength.</p>
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<p>Relation between hardened concrete density and compressive strength.</p>
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<p>Relation between mass loss in thermogravimetric analysis at 800 °C (under air) and (<b>a</b>) compressive strength normalized to density of hardened concrete and (<b>b</b>) flexural tensile strength.</p>
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<p>Relation between mass loss in thermogravimetric analysis at 800 °C (under air) and water–cement ratio.</p>
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<p>Relation between bulk density and thermal conductivity.</p>
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<p>Relation between compressive strength and thermal conductivity.</p>
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13 pages, 2690 KiB  
Article
Superhydrophobic/Superoleophilic PDMS/SiO2 Aerogel Fabric Gathering Device for Self-Driven Collection of Floating Viscous Oil
by Feng Liu, Xin Di, Xiaohan Sun, Xin Wang, Tinghan Yang, Meng Wang, Jian Li, Chengyu Wang and Yudong Li
Gels 2023, 9(5), 405; https://doi.org/10.3390/gels9050405 - 12 May 2023
Viewed by 1694
Abstract
The persistent challenge of removing viscous oil on water surfaces continues to pose a major concern and requires immediate attention. Here, a novel solution has been introduced in the form of a superhydrophobic/superoleophilic PDMS/SiO2 aerogel fabric gathering device (SFGD). The SFGD is [...] Read more.
The persistent challenge of removing viscous oil on water surfaces continues to pose a major concern and requires immediate attention. Here, a novel solution has been introduced in the form of a superhydrophobic/superoleophilic PDMS/SiO2 aerogel fabric gathering device (SFGD). The SFGD is based on the adhesive and kinematic viscosity properties of oil, enabling self-driven collection of floating oil on the water surface. The SFGD is able to spontaneously capture the floating oil, selectively filter it, and sustainably collect it into its porous fabric interior through the synergistic effects of surface tension, gravity, and liquid pressure. This eliminates the need for auxiliary operations such as pumping, pouring, or squeezing. The SFGD demonstrates exceptional average recovery efficiencies of 94% for oils with viscosities ranging from 10 to 1000 mPa·s at room temperature, including dimethylsilicone oil, soybean oil, and machine oil. With its facile design, ease of fabrication, high recovery efficiency, excellent reclaiming capabilities, and scalability for multiple oil mixtures, the SFGD represents a significant advancement in the separation of immiscible oil/water mixtures of various viscosities and brings the separation process one step closer to practical application. Full article
(This article belongs to the Special Issue Gels for Removal and Adsorption)
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<p>(<b>a</b>) Schematic illustration of the construction process for the PDMS/SiO<sub>2</sub>-coated burlap fabric. (<b>b</b>) SEM images of the PDMS/SiO<sub>2</sub> composite aerogel coating on burlap fibers (left) with partial magnification (right). (<b>c</b>) Photographs of water contact angle (top) and oil contact angle (bottom) on the coated fabric surface in air conditions, respectively. (<b>d</b>) Photographs exhibiting the surface hydrophobicity of the water impacting test (left) and the water holding test (right).</p>
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<p>Photographs of (<b>a</b>–<b>f</b>) the underoil water-adhesion detection process on PDMS/SiO<sub>2</sub>-coated fabric surface and (<b>g</b>,<b>h</b>) water contact angles on the prepared surfaces under n-hexane and under dimethyl silicone oil, respectively.</p>
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<p>(<b>a</b>) XPS survey spectra of pristine burlap fabric, burlap fabric coated with PDMS only, and PDMS/SiO<sub>2</sub> composite aerogel coating. (<b>b</b>) FTIR spectra of pristine burlap fabric and burlap fabric coated with PDMS/SiO<sub>2</sub> composite aerogel coating.</p>
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<p>(<b>a</b>) Schematic Illustration of surface mechanical detection by an oscillating abrasion tester. (<b>b</b>) WCAs change of the burlap fabric by the PDMS/SiO<sub>2</sub> layer in the process of the abrasion test, and the SEM image after 1500 cycles and the corresponding insert SEM images of the pristine sample and the treated sample.</p>
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<p>Scheme for (<b>a</b>) assembling the superhydrophobic/superoleophilic aerogel fabric gathering device (SFGD) and (<b>b</b>) the process (<b>b<sub>1</sub></b>–<b>b<sub>5</sub></b>) of separating the immiscible viscous oil/water mixture.</p>
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<p>(<b>a</b>) Photographs for viscous oil removal from the water surface by SFGD. (<b>b</b>) The recovery of viscous silicone oil and the weighing difference of the sack before and after usage. (<b>c</b>) Recovery capacity and recovery efficiency of various kinds of viscous oils.</p>
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<p>Photographs for the collection process of an oil mixture from the water surface via SFGD. (<b>a</b>) SFGD, oil mixture, and water. (<b>b</b>–<b>e</b>) Oil collection process. (<b>f</b>) Cleaned water and recovered oil.</p>
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2 pages, 169 KiB  
Editorial
Editorial for the Special Issue “Advances in Colloidal Hydrogels”
by Fuguo Liu and To Ngai
Gels 2023, 9(5), 404; https://doi.org/10.3390/gels9050404 - 11 May 2023
Viewed by 993
Abstract
Hydrogels are three-dimensional polymer networks derived from hydrophilic macromonomers, which can be categorized as natural, synthetic, or hybrid hydrogels [...] Full article
(This article belongs to the Special Issue Advances in Colloidal Hydrogels)
23 pages, 4616 KiB  
Article
New Photocrosslinked 3D Foamed Scaffolds Based on GelMA Copolymers: Potential Application in Bone Tissue Engineering
by Jesús L. Pablos, Javier Jiménez-Holguín, Sandra Sánchez Salcedo, Antonio J. Salinas, Teresa Corrales and María Vallet-Regí
Gels 2023, 9(5), 403; https://doi.org/10.3390/gels9050403 - 11 May 2023
Cited by 8 | Viewed by 2227
Abstract
The production of customized polymeric hydrogels in the form of 3D scaffolds with application in bone tissue engineering is currently a topic of great interest. Based on gelatin methacryloyl (GelMa) as one of the most popular used biomaterials, GelMa with two different methacryloylation [...] Read more.
The production of customized polymeric hydrogels in the form of 3D scaffolds with application in bone tissue engineering is currently a topic of great interest. Based on gelatin methacryloyl (GelMa) as one of the most popular used biomaterials, GelMa with two different methacryloylation degrees (DM) was obtained, to achieve crosslinked polymer networks by photoinitiated radical polymerization. In this work, we present the obtention of new 3D foamed scaffolds based on ternary copolymers of GelMa with vinylpyrrolidone (VP) and 2-hydroxyethylmethacrylate (HEMA). All biopolymers obtained in this work were characterized by infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA), whose results confirm the presence of all copolymers in the crosslinked biomaterial. In addition, scanning electron microscopy (SEM) pictures were obtained verifying the presence of the porosity created by freeze-drying process. In addition, the variation in its swelling degree and its enzymatic degradation in vitro was analyzed as a function of the different copolymers obtained. This has allowed us to observe good control of the variation in these properties described above in a simple way by varying the composition of the different comonomers used. Finally, with these concepts in mind, biopolymers obtained were tested through assessment of several biological parameters such as cell viability and differentiation with MC3T3-E1 pre-osteoblastic cell line. Results obtained show that these biopolymers maintain good results in terms of cell viability and differentiation, along with tunable properties in terms of hydrophilic character, mechanical properties and enzymatic degradation. Full article
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<p>Scheme synthesis of GelMa monomers with two methacryloylation degrees and subsequent purification by reacting with methacrylic anhydride at basic pH. For GelMa purification, a dialysis tubing cellulose membrane (with 14 KDa molecular weight cut-off) was used, followed by its subsequent freeze and lyophilization.</p>
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<p><sup>1</sup>H NMR spectra of unmodified gelatin and methacrylated gelatin with two different methacrylation degrees (H-GelMa and L-GelMa). The signals of the acrylic protons and the methyl function of the introduced methacrylic groups are indicated (1.8–1.9 ppm and 5.3 ppm/6.2 ppm) together with the lysine methylene signals of gelatin at 2.9 ppm. DM was calculated following Equation (1): DM(%) = (1 − Area<sub>lys meth GelMa</sub>/Area<sub>lys meth Gelatin</sub>) × 100.</p>
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<p>Scheme of synthesis of biopolymers synthesized: Homogeneous solutions of GelMa and/or comonomers (VP and HEMA) to obtain by UV radical photopolymerization the crosslinked homopolymers and/or copolymers with vinylpyrrolidone and/or HEMA. It is also possible to observe the digital pictures of materials before and after lyophilization.</p>
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<p>FTIR spectra of GelMa monomer with two methacryloylation degrees (L-GelMa and H-GelMa samples). Inside are described the most relevant bands related to the GelMa monomer.</p>
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<p>(<b>A</b>,<b>B</b>) FTIR spectra of H-GelMa and L-GelMa biopolymer families copolymerized with vinylpyrrolidone (VP<sub>10/30</sub>), HEMA (HEMA<sub>10/30</sub>) and vinylpyrrolidone/HEMA (VP/HEMA<sub>10/30</sub>). (<b>A*</b>,<b>B*</b>) Expansion of the region between 1800 and 950 cm<sup>−1</sup>. Inside are described the most relevant bands related to the each comonomer present in every composition proposed.</p>
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<p>Degree of swelling of the different biopolymers after 24 h in different media: MiliQ water, PBS×1 and α-MEM. Data were calculated from Equation (2). Data were presented as mean ± standard deviation (SD). Error bars represented the SD of 3 independent samples. Statistical analysis was performed with the nonparametric Kruskal–Wallis test and post-hoc Dunn’s test. For all statistical tests, a value of <span class="html-italic">p</span> &lt; 0.05 was considered significant.</p>
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<p>SEM micrographs of foamed scaffolds (L-GelMa/H-GelMa and copolymers). Images have been obtained from their cross-sectional view.</p>
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<p>Enzymatic degradation of all different biopolymers synthesized. Collagenase type I degradation in all biopolymers synthesized in this work was studied at 2 h, 4 h, 7 h, 24 h, 48 h, 72 h, 96 h and 120 h. Results were analyzed in terms of their weight loss expressed as % weight loss, along with the weight loss of the dry initial sample and after 24 h of collagenase treatment. From left to right, (<b>A</b>). H-GelMa family and (<b>B</b>). L-GelMa family using a dilution of collagenase I (0.3 mg/mL) in DMEM for up to 24 h. (<b>C</b>). Determination of the dry weight of the biopolymers at zero time (100%) and after 24 h in terms of the remaining weight (%). Data were presented as mean ± standard deviation (SD). Error bars represented the SD of 3 independent samples.</p>
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<p>Rheological characterization of biomaterials in terms of storage modulus values (G′). (<b>A</b>,<b>C</b>) Frequency sweep sequence of biomaterials based on H-GelMa and L-GelMa, respectively. (<b>B</b>,<b>D</b>) Strain sweep sequence of biomaterials based on H-GelMa and. L-GelMa, respectively.</p>
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<p>Proliferation of MC3T3-E1 pre-osteblast-like cells as a function of culture time onto H-GelMa and L-GelMa scaffold families, after 1, 4 and 7 days. * Comparisons between each H-GelMa and L-GelMa with every series. Data are presented as mean ± standard deviation (SD). Error bars represented the SD of 3 independent samples. Statistical significance: * <span class="html-italic">p</span> &lt; 0.05 vs. H-GelMa or L-GelMa at 1, 4 and 7 days of culture.</p>
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<p>(<b>A</b>). Confocal laser scanning microscopy images of pre-osteoblast cultured onto scaffolds of L-GelMa family. (<b>B</b>). Histograms corresponding to the mineralization nodules of MC3T3-E1 stained with Alizarin-Red after being in contact with the biopolymers after 10 days of culture, respectively, on H-GelMa and L-GelMa families of biopolymers. Data are presented as mean ± standard deviation (SD). Error bars represented the SD of 3 independent samples. Statistical significance: * <span class="html-italic">p</span> &lt; 0.05 vs. H-GelMa or L-GelMa after 10 days of culture.</p>
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16 pages, 3856 KiB  
Article
Probing the Effect of Young’s Modulus on the Reservoir Regulation Abilities of Dispersed Particle Gels
by Zizhao Wang, Zhixuan Zhu, Tianyu Jiang, Jinming Liu, Yunbo Dong, Yining Wu, Mingwei Zhao, Caili Dai and Lin Li
Gels 2023, 9(5), 402; https://doi.org/10.3390/gels9050402 - 11 May 2023
Cited by 2 | Viewed by 1514
Abstract
The mechanical strength of dispersed particle gels (DPGs), which can be directly characterized by Young’s modulus, is an important parameter affecting reservoir regulation performance. However, the effect of reservoir conditions on the mechanical strength of DPGs, as well as the desired range of [...] Read more.
The mechanical strength of dispersed particle gels (DPGs), which can be directly characterized by Young’s modulus, is an important parameter affecting reservoir regulation performance. However, the effect of reservoir conditions on the mechanical strength of DPGs, as well as the desired range of mechanical strength for optimum reservoir regulation performance, have not been systematically studied. In this paper, DPG particles with different Young’s moduli were prepared and their corresponding migration performances, profile control capacities and enhanced oil recovery abilities were studied by simulated core experiments. The results showed that with increase in Young’s modulus, the DPG particles exhibited improved performance in profile control as well as enhanced oil recovery. However, only the DPG particles with a modulus range of 0.19–0.762 kPa could achieve both adequate blockage in large pore throats and migration to deep reservoirs through deformation. Considering the material costs, applying DPG particles with moduli within the range of 0.19–0.297 kPa (polymer concentration: 0.25–0.4%; cross-linker concentration: 0.7–0.9%) would ensure optimum reservoir control performance. Direct evidence for the temperature and salt resistance of DPG particles was also obtained. When aged in reservoir conditions below 100 °C and at a salinity of 10 × 104 mg·L−1, the Young’s modulus values of the DPG particle systems increased moderately with temperature or salinity, indicating a favorable impact of reservoir conditions on the reservoir regulation abilities of DPG particles. The studies in this paper indicated that the practical reservoir regulation performances of DPGs can be improved by adjusting the mechanical strength, providing basic theoretical guidance for the application of DPGs in efficient oilfield development. Full article
(This article belongs to the Special Issue Polymer Gels for the Oil and Gas Industry)
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<p>The interval distribution of the Young’s moduli of a representative DPG particle system (with 0.3% polymer + 0.8% cross-linker in this case).</p>
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<p>Migration performances of DPG particle systems with different Young’s moduli. (<b>a</b>) 0.2% polymer + 0.6% cross-linker, E = 0.082 kPa. (<b>b</b>) 0.25% polymer + 0.7% cross-linker, E = 0.19 kPa. (<b>c</b>) 0.3% polymer + 0.8% cross-linker, E = 0.257 kPa. (<b>d</b>) 0.35% polymer + 0.9% cross-linker, E = 0.762 kPa. (<b>e</b>) 0.4% polymer + 1.0% cross-linker, E = 1.222 kPa. (<b>f</b>) 0.45% polymer + 1.1% cross-linker, E = 1.723 kPa.</p>
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<p>Migration performances of DPG particle systems with different Young’s moduli. (<b>a</b>) 0.2% polymer + 0.6% cross-linker, E = 0.082 kPa. (<b>b</b>) 0.25% polymer + 0.7% cross-linker, E = 0.19 kPa. (<b>c</b>) 0.3% polymer + 0.8% cross-linker, E = 0.257 kPa. (<b>d</b>) 0.35% polymer + 0.9% cross-linker, E = 0.762 kPa. (<b>e</b>) 0.4% polymer + 1.0% cross-linker, E = 1.222 kPa. (<b>f</b>) 0.45% polymer + 1.1% cross-linker, E = 1.723 kPa.</p>
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<p>Profile control capacities of DPG particle systems with different Young’s moduli. (<b>a</b>) 0.2% polymer + 0.6% cross-linker, E = 0.082 kPa. (<b>b</b>) 0.25% polymer + 0.7% cross-linker, E = 0.19 kPa. (<b>c</b>) 0.3% polymer + 0.8% cross-linker, E = 0.257 kPa. (<b>d</b>) 0.35% polymer + 0.9% cross-linker, E = 0.762 kPa. (<b>e</b>) 0.4% polymer + 1.0% cross-linker, E = 1.222 kPa. (<b>f</b>) 0.45% polymer + 1.1% cross-linker, E = 1.723 kPa.</p>
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<p>Enhanced oil recovery abilities of DPG particles with different Young’s moduli. (<b>a</b>) 0.25% polymer + 0.7% cross-linker, E = 0.19 kPa. (<b>b</b>) 0.3% polymer + 0.8% cross-linker, E = 0.257 kPa. (<b>c</b>) 0.35% polymer + 0.9% cross-linker, E = 0.762 kPa.</p>
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<p>Patterns of change in the Young’s modulus of the DPG particle system at different temperatures.</p>
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<p>Patterns of change in the Young’s moduli of the DPG particle systems under different salinity conditions.</p>
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<p>Illustration of the multi-point pressure test setup.</p>
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<p>Section homogenization performance test device diagram.</p>
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