Preparation Of Hydrogels Research Articles

Laboratory synthesis and preparation of thermo-responsive polymeric micelle and hydrogel for resveratrol delivery and release

Laboratory synthesis and preparation of thermo-responsive polymeric micelle and hydrogel for resveratrol delivery and release

UTILIZATION OF CASSAVA PEEL AND CHITOSAN FOR THE PRODUCTION OF HYDROGEL AS A SUSTAINABLE SOLUTION FOR DOMESTIC WASTEWATER TREATMENT

Water pollution is a significant environmental issue, especially in developing countries where domestic wastewater often contains a high concentration of pollutants, posing risks to public health and the environment. Hydrogel from cassava peel and chitosan shows promise as a bioadsorbent for domestic wastewater treatment, but its capacity and optimal production temperature have not been fully studied. The study aimed to investigate the characteristics of hydrogel from cassava peel and chitosan, the optimal temperature for hydrogel production, and the efficacy of hydrogel as a bioadsorbent for domestic wastewater treatment. The study involved four stages: cellulose isolation, hydrogel preparation, wastewater treatment experimentation, and data analysis. The results showed that chitosan hydrogel synthesized at 750C had superior efficiency, achieving an optimal outcome of 88% in the treatment of household wastewater using a triad of chitosan hydrogel pellets. The degree of cross-linking in chitosan hydrogel diminished with an increase in heating temperature

Correction: Chen et al. Preparation and Photothermal Antimicrobial Performance of Triple Linkage Hydrogels. Coatings 2024, 14, 363

There were some errors in the original publication [...]

Nanocellulose‐reinforced, anti‐freezing, highly conductive ionic organic hydrogels for flexible electronic devices

AbstractCurrently, flexible electronic devices based on ionic conductive hydrogels are receiving widespread attention in the field of human health detection. In this paper, a facile one‐pot method is proposed for the preparation of ionic organic hydrogels, in which polyvinyl alcohol (PVA), cellulose nanofiber (CNF), and graphene oxide (GO) are dissolved in dimethyl sulfoxide‐water (DMSO/H2O), and the organic hydrogel is obtained by a freezing–thawing process. The ionic organic hydrogel with excellent properties is then prepared by soaking the hydrogel in a calcium chloride (CaCl2) solution using a salting‐out strategy. The ionic organic hydrogel possesses good tensile (283%) and strength (0.3 MPa), super electrical conductivity (7.72 S/m), and high strain sensitivity [gauge factor (GF) up to 5.22]. Meanwhile, it has excellent anti‐freezing and moisturizing properties. In addition, the ionic organic hydrogels can be used in flexible strain sensors and triboelectric nanogenerators to realize real‐time monitoring of human motion, traceless writing, and energy conversion. It is foreseen that the prepared ionic organic hydrogels provide a feasible method for realizing the long‐term use of wearable electronic devices in extreme environments and daily life.

A one-step polyvinyl alcohol/polyacrylamide/polyacrylic acid/dimethyl sulfoxide/CaCl2 hybrid hydrogel enabling anti-fatigue, anti-freeze and anti-dehydration for wearable strain sensor

Hydrogel with fatigue resistance, freezing tolerant and dehydration resistance are peculiarly attractive in strain sensors. The hydrogel soaked in organic solvent is an effective strategy to improve freezing resistance and dehydration resistance, while this may result in poor conductivity. Moreover, ion-incorporation is considered to be the most feasible method for solving above concern, while high concentration of salt ions will result in weak mechanical properties. Therefore, the facile preparation of anti-freezing and anti-dehydration hydrogels with excellent fatigue resistance remains a challenge. Herein, a polyvinyl alcohol/polyacrylamide/polyacrylic acid/dimethyl sulfoxide/CaCl2 hybrid hydrogel was designed and fabricated through a facile one-step method to balance a variety of outstanding properties. On account of the hybridization design of multi-materials, the hybrid hydrogel exhibited high ionic conductivity (∼0.2 S/m), strength (∼0.36 MPa) and stretchability (∼825 %). Meanwhile, the hybrid hydrogel demonstrated prominent freezing resistance, dehydration resistance and fatigue resistance. The mechanical properties almost no deterioration after 1000 stretching cycle at 100 % strain, exposure to environment for 30 days or freeze at low temperature. Besides, the hybrid hydrogel-based stain sensor showed a linear sensitivity (GF = 1.12 over 0–400 % strain), quickly responsivity (200 ms), and could monitor various human activities steadily, demonstrating distinguished potential for use in wearable health monitoring and flexible electric skins.

Preparation of nutrient hydrogels with core-shell structure for seed germination and seedling growth in high temperature saline environment.

Drought and soil degradation are the key factors in desertification control. How to improve the utilization efficiency of water and fertilizer has always been the focus of research in desert areas. The conventional hydrogel-loaded fertilizer is not suitable because of the high salinity and large temperature difference in sandy land. Therefore we prepared a novel temperature/pH-responsive core-shell structured hydrogel and loaded urea in three ways: in situ polymerization, encapsulation, and immersion, and germination and seedling growth experiments on Artemisia absinthium and Cabbage (Brassica campestris L. ssp. chinensis Makino) seeds. The results showed that the immersion hydrogel SAP4 (PCP-g-PAA/P(DMAEMA-co-AMPS))/urea had the best repetitive swelling performance, achieving 163.89 % of the original water absorption performance after 16 repetitions and the highest nitrogen release of 151.37 mg at 40 days. For A. desertorum, the treatment group applying the in situ composite hydrogel SAP2 (PCP-g-PAA/P(DMAEMA-co-AMPS)/urea) had the highest germination rate of 70 %; for B. campestris, the treatment groups applying SAP2, the encapsulated hydrogel SAP3 (PCP-g-PAA/urea/P(DMAEMA-co-AMPS)) and SAP4 hydrogels had higher germination rates, with SAP3 having a 100 % germination rate. This phenomenon suggests that the three urea-loaded temperature/pH-responsive core-shell structured hydrogels we have prepared are very promising as an aid to seed germination and seedling growth.

Rapid preparation of bioadhesive hydrogels containing catechol moieties at room temperature with reproducible adhesion to wet tissues, antimicrobial, antioxidant capacity for noncompressive hemostasis.

In order to cope with the massive tissue bleeding caused by sudden trauma and the demand for bioengineering materials with adjustable wet adhesion properties, this study formed the first layer of network by adding galactomannan (GG) and collagen (Col) structure, and then use the Fe3+-urushiol (UH) redox system to activate free radicals to initiate the polymerization of acrylic acid (AA) to quickly form an interpenetrating double network hydrogel. The cis hydroxyl group in GG and the hydroxyl group of UH form dynamic covalent borate ester bonds with borate ions in the borax solution, and use their responsiveness to pH to control the catechol group to achieve controllable adhesion. UH and Fe3+ endowed the hydrogel with excellent antibacterial ability, while adding Col enhanced the mechanical properties of the hydrogel. The elastic modulus and toughness increased from 4.32 kPa and 92.9 kJ/m3 to 18.90 kPa and 264.54 kJ/m3. In addition, due to the joint action of UH and Col, the hydrogel dressing can achieve rapid hemostasis within 20 s. In short, this hydrogel dressing has good biocompatibility, inherent antibacterial ability, adjustable moist tissue adhesion properties and rapid hemostatic ability, and is expected to become a candidate for wound hemostasis dressing.

Emissive glutathione modified sulphur quantum dots for the sensing of lemon yellow and luminescent hydrogels/films

Lemon yellow (LY) is an azo dye which is widely used as food colorant. The continuous consumption can result in the safety concerns for both human and environmental health. This study describes a new sulphur quantum dot (SQD) based fluorescent sensor, which was facilely prepared with oxidized-glutathione (GSSG) as passivator at mild condition of 75 °C. The obtained sulphur quantum dots (GSSG-SQDs) have a relative quantum yield of 0.25, which is 2–5 times that of most SQDs. GSSG-SQDs were used as a sensor for lemon yellow in the concentration range of 0.10–70 μM and the limit of detection of 60 nM. The application was verified with the real sensing of lemon yellow in the soft drinking and tap water, having the standard recovery from 92.5 % to 105 %. Given the great luminescence and photostability, GSSG-SQDs were used as a filler for the preparation of luminescent films and hydrogels as a promising material for a wide range of applications such as information encryption and bioengineering.

Progress in Protein-Based Hydrogels for Flexible Sensors: Insights from Casein.

In recent years, the rapid advancement of flexible sensors as the cornerstone of flexible electronics has propelled a flourishing evolution within the realm of flexible electronics. Unlike traditional flexible devices, hydrogel flexible sensors have characteristic advantages such as biocompatibility, adhesion, and adjustable mechanical properties and have similar properties to human skin. Especially, biobased hydrogels have become the preferred substrate material for flexible sensors due to increased environmental pressures caused by the scarcity of petrochemical resources. In this regard, proteins possess advantages such as diverse amino acid compositions, adjustable advanced structures, chemical modifiability, the application of protein engineering techniques, and the ability to respond to various external stimuli. These enable the hydrogels constructed from them to have greater designability, flexibility, and adaptability. As a result, their applications in manufacturing various types of sensors have experienced rapid growth. This work systematically reviews the sensing mechanism of protein-based hydrogels, focusing on the preparation of protein-based hydrogels and the optimization of flexible sensors mainly from the perspective of a typical type of animal-derived protein casein. In addition, while the potential of casein is recognized, the limitations of casein-based hydrogels in flexible sensor applications are explored, and insights are provided into the development trends of next-generation sensors based on casein-based hydrogel materials.

Preparation and characterization of bovine dental pulp-derived extracellular matrix hydrogel for regenerative endodontic applications: an in vitro study

BackgroundThe use of biological scaffolds in regenerative endodontics has gained much attention in recent years. The search for a new biomimetic scaffold that contains tissue-specific cell homing factors could lead to more predictable tissue regeneration. The aim of this study was to prepare and characterize decellularized bovine dental pulp-derived extracellular matrix (P-ECM) hydrogels for regenerative endodontic applications.MethodsFreshly extracted bovine molar teeth were collected. Bovine dental pulp tissues were harvested, and stored at -40º C. For decellularization, a 5-day protocol was implemented incorporating trypsin/EDTA, deionized water and DNase treatment. Decellularization was evaluated by DNA quantification and histological examination to assess collagen and glycosaminoglycans (GAGs) content. This was followed by the preparation of P-ECM hydrogel alone or combined with hyaluronic acid gel (P-ECM + HA). The fabricated scaffolds were then characterized using protein quantification, hydrogel topology and porosity, biodegradability, and growth factor content using Enzyme-linked immunosorbent assay (ELISA): transforming growth factor beta-1(TGF-β1), basic fibroblast growth factor (bFGF), bone morphogenetic protein 2 (BMP-2) and vascular endothelial growth factor (VEGF).ResultsDecellularization was histologically confirmed, and DNA content was below (50 ng/mg tissue). P-ECM hydrogel was prepared with a final ECM concentration of 3.00 mg/ml while P-ECM + HA hydrogel was prepared with a final ECM concentration of 1.5 mg/ml. Total protein content in P-ECM hydrogel was found to be (439.0 ± 123.4 µg/µl). P-ECM + HA showed sustained protein release while the P-ECM group showed gradual decreasing release. Degradation was higher in P-ECM + HA which had a significantly larger fiber diameter, while P-ECM had a larger pore area percentage. ELISA confirmed the retention and release of growth factors where P-ECM hydrogel had higher BMP-2 release, while P-ECM + HA had higher release of TGF-β1, bFGF, and VEGF.ConclusionsBoth P-ECM and P-ECM + HA retained their bioactive properties demonstrating a potential role as functionalized scaffolds for regenerative endodontic procedures.

The Utilization of Central Composite Design for the Production of Hydrogel Blends for 3D Printing

Central composite design (CCD) is a statistical experimental design technique that utilizes a combination of factorial and axial points to study the effects of multiple variables on a response. This study focused on optimizing hydrogel formulations for 3D printing using CCD. Three biopolymers were selected: sodium alginate (SA), gelatin (GEL), and carboxymethyl cellulose (CMC). The maximum and minimum concentrations of each polymer were established using a Google Scholar search, and CCD was employed to generate various combinations for hydrogel preparation. The hydrogels were characterized in accordance with their swelling degree (SD) in phosphate-buffered saline (PBS) and Dulbecco’s Modified Eagle Medium (DMEM), as well as their printability in 2D and 3D assays. The formulation consisting of 7.5% SA, 7.5% GEL, and 2.5% CMC exhibited the best swelling properties and exceptional printability, surpassing all other tested formulations. This study highlights the effectiveness of design of experiment methodologies in accelerating the development of optimized hydrogel formulations for various applications in 3D printing and suggests avenues for future research to explore their performance in specific biological contexts.

Preparation and characterization of functional dual network hydrogel for motion monitoring in smart bra

The smart bra is a kind of sports underwear with providing health monitoring and comfort protection for women breast in sports. Developing smart sensing materials that combine comfort and functionality for sensing breast condition remains a challenge. Here, natural polysaccharide sodium alginate (SA), acrylamide (AM) monomer and chitosan (CS) and polypyrrole (PPy) in-situ polymerized from pyrole (Py) monomer were used as raw materials to successfully synthesize double network conductive hydrogel by two-step method. The results show that in the hydrogels, the entanglement and interpenetration of macromolecules produce toughness (tensile/compressive strength is ∼0.248 MPa/∼2.836 MPa), elasticity (tensile/compression elastic recovery rate is∼94.06 %/∼98.41 %) and durability (after 30 tensile/compression cycles conducting at 25 %, 50 % and 100 % constant strain keep at high recovery rate). The rich moisture content provides its adhesion (adhesion strength ∼4.7557 kPa) and flexibility (bending stiffness 1.0843 cN cm∼), presenting sufficient adhesion reliability and robustness to different substrates. The addition of PPy enables the hydrogel to have conductivity (6.77 × 10−2 S cm−1) and sensing performance (tensile/compression sensitivity is ∼1.94/∼1.43). The conductive hydrogel, as a flexible strain sensor, shows good adhesion, flexibility, elasticity and sensitivity in application of sports smart bra, can detect both the tensile behavior of skin and the compression state of tissue through its mechano-electricity, and accurately sense the changes of physiological parameters during movement. The conductive hydrogel with high elasticity and strength has broad application prospects in smart bra.

A green strategy to realize the high value utilization of lignin for hydrogel formation

Grafting lignin extracted from pulping black liquor onto hydrogel not only endows hydrogel with strong adsorption capacity, but also realizes the high value utilization of lignin, thereby alleviating the environmental pressure caused by the exhaust gas generated by direct combustion of black liquor. However, those lignin fragments have lost generous active functional groups as the high temperature polycondensation during industrial production, restricting the improvement of lignin-based hydrogel adsorption capacity. Herein, we propose a strategy combining amination and oxidation to prepare lignin derivatives with low molecular weight and high activity groups. The introduced amino groups promote the Cα-Cβ cleavage of β-O-4 unit and the oxidation treatment converts S-unit hydroxyl to carboxyl. The hydrogel obtained by grafting aminated-oxidized-lignin shows satisfactory adsorption performance with a methylene blue adsorption capacity of 697.47 mg/g (vs. 195.12 mg/g for pristine hydrogel). The retention ability has also been greatly improved that only 0.43 % of the adsorbed methylene blue is released even after 96 h (vs. 5 % within just 12 h for pristine hydrogel). This work not only provides a new strategy for the high-value utilization of biomass resources, but also offers a new idea for the preparation of hydrogels with high adsorption performance.

Preparation and slow-release properties of nanocellulose composite hydrogels

Nanocellulose (CNF) was obtained from carrots using a combination of chemical treatment, mechanical milling, and ultrasonic treatment. Ultrafast preparation of maleic anhydride esterified nanocellulose was achieved by a hydrated hydrogen ion-driven dissociation, chemical cross-linking strategy based on a “one-pot” reaction method. Esterification modification with maleic anhydride reduced the crystallinity of nanocellulose and enhanced its thermal stability. High-strength drug-carrying hydrogels (MACNF/SA) with different drug loading capacities were prepared using cefixime (CFX) as a drug model and maleic anhydride esterified nanocellulose (MACNF) and sodium alginate (SA) as the main raw materials. The compressive strength of MACNF/SA hydrogels made from MACNF reached a maximum of 80.3 kPa when the mass ratio of CNF to MA was 2.5:12. Rheological property tests showed that the MACNF/SA hydrogels were pseudoplastic fluids with shear thinning. The drug release from the drug-carrying hydrogels followed non-Fickian diffusion.

Preparation and application of organic hydrogels incorporating polyacrylamide/sodium alginate/DMSO for enhanced anti-drying, anti-freezing, and self-healing properties

The double-network hydrogel comprises two asymmetrically structured cross-linked networks, demonstrating exceptional mechanical properties and possessing significant potential for application in the field of flexible sensors. However, conventional hydrogels primarily disperse in water as a medium and continuously lose moisture in natural environments, rendering them incapable of retaining hydration over extended periods and unsuitable for utilization under low-temperature conditions. In this study, we devised an organic hydrogel based on polyacrylamide (PAM), sodium alginate (SA), and dimethyl sulfoxide (DMSO). Through hydrogen bonding interactions among DMSO molecules, polyacrylamide, and sodium alginate, this organic hydrogel not only exhibits anti-drying and anti-freezing properties but also demonstrates self-healing characteristics. Moreover, the organic hydrogel showcases remarkable mechanical properties and conductivity capabilities that render it suitable for constructing flexible strain sensors to monitor human movements such as finger bending, elbow flexion, knee joint bending, and ankle extension. Additionally, the sensor exhibits excellent stability and durability.

The Characteristics Analysis of Hyaluronic Acid Modified By Cold Atmospheric Plasma and Its Performance in Hydrogel Preparation

ABSTRACTHyaluronic acid (HA) is extensively utilized in biomedical applications, and its functionality can be enhanced by introducing aldehyde groups (─CHO) through oxidation. In this study, cold atmospheric plasma (CAP) was used to treat aqueous HA solutions, resulting in the formation of plasma‐modified HA (PMHA) containing ─CHO groups. The free radicals generated from interactions between water molecules and CAP particles reacted with HA, leading to the oxidation of hydroxyl groups into ─CHO and the cleavage of glycosidic bonds, causing molecular depolymerization. The PMHA was then used to synthesize hydrogels in combination with carboxymethyl chitosan and ɛ‐polylysine. This study presents an effective approach for generating HA with aldehyde functionalities and offers insights into the interaction between CAP and polysaccharides.

Relation of acrylic acid polymerization behavior in deep eutectic solvent to water content: Computer simulation and experiment

Polymerizable deep eutectic solvents (DES) are promising starting materials for preparation of eutectogels and hydrogels that can be applied in drug delivery, as strain sensors and various components of soft electronics. However, the understanding of relationship between the molecular structure, physicochemical properties and polymerization behavior of such systems in pure state and in their mixtures with water is not well studied yet. In this work we report the results of both computer simulation and experimental investigations for polymerizable choline chloride/acrylic acid DES and its mixtures with water. Molecular dynamics was applied to reveal the influence of water on the structure of polymerizable DES at the molecular and supramolecular levels. The diffusion coefficients of DES components with different water content were measured using NMR. The course of photoinduced polymerization of DES/water mixtures was traced using FTIR spectroscopy, while the molar mass and hydrodynamic characteristics of obtained polyacrylic acid were studied by means of static and dynamic light scattering. It was found that addition of water leads to a gradual decrease in size of the acrylic acid clusters that exist in pure DES and is accompanied by an increase in orientation mobility and diffusion coefficients of components. The maximal molar mass was obtained for the polymer prepared by polymerization of DES with 5 wt% of water. This can be attributed to the optimal combination of acrylic acid clusters size and increased mobility of components.

Living Cell-Mediated Catalyst-Free Spontaneous Polymerization of Zwitterionic Methacrylates for Preparation of Probiotic-Loaded Hydrogels.

Living cell-mediated polymerization offers promising applications in biomaterials, yet its further biological utilization is hindered by the need for metal ions or radical initiators with available methods. In this study, we introduce a living cell-mediated polymerization that leverages the intrinsic metabolic activities of living cells to initiate and sustain free radical polymerization of zwitterionic methacrylates. The polymerization proceeded in the absence of transition metal catalysts, radical initiators, or light sources. The conversion of zwitterionic methacrylate strongly correlated with cellular activities and achieved a maximum conversion of 98% within 48 hours. Living cells efflux redox power across membranes through metabolism and that terminal electron fluxes are captured by zwitterionic methacrylates pre-assembled on the living cell surface to initiate radical polymerization reactions. The polymerization caused significant changes to the cell membrane surface and synthesized hydrogels with tailored mechanical properties. The polymer hydrogel obtained via probiotic E. coli Nissle 1917 was able to release the in-situ encapsulated molecules, which demonstrated living cell-mediated polymer hydrogel as a vehicle for the delivery of both cellular and molecular therapeutic agents. This research offered a green and efficient method for synthesizing bioactive materials and advancing the field of cellular therapeutics and drug delivery.

Preparation and properties of high-content carbon dots hydrogel based on amination modification

Preparation and properties of high-content carbon dots hydrogel based on amination modification

Preparation, Swelling, and Drug Release Studies of Chitosan-based Hydrogels for Controlled Delivery of Buspirone Hydrochloride.

Buspirone is used for the management of depression and anxiety disorders. Due to its short half-life and low bioavailability, it requires multiple daily doses and is associated with some side effects. This study aimed to develop chitosan-based hydrogels as drug-controlled release carriers. The objective of this study is to prepare chitosan-based hydrogels as controlled release carriers in order to overcome the side effects of buspirone HCl and improve patients' compliance and their life quality. Polymer chitosan was polymerized with two monomers, acrylic acid and itaconic acid, to synthesize pH-sensitive hydrogel. The Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) analysis were performed to confirm the structure formation and thermal stability. Water penetration capability and loading of the drug were performed by porosity and drug loading studies. The swelling and dissolution tests were performed to analyze the pH-sensitive nature of the developed hydrogels. FTIR, TGA, and DSC demonstrated that the chitosan-based hydrogels were successfully prepared. An increase in water penetration and drug loading into the hydrogel network was seen with the high incorporation of chitosan, acrylic acid, and itaconic acid. The swelling and dissolution studies revealed that prepared hydrogel offered the greatest swelling and drug release at a high pH of 7.4. The swelling and drug release from the hydrogel were affected by the concentrations of the incorporated contents. A controlled release of the drug was achieved by using chitosan-based hydrogel as a delivery carrier compared to commercial tablets of buspirone. The results showed that the developed chitosan-based hydrogel can be considered one of the most suitable drug carrier systems for the controlled delivery of buspirone.