Intervertebral disc degeneration (IVDD) is a globally prevalent disease, yet achieving dual repair of tissue and function presents significant challenges. Considering reactive oxygen species (ROS) is a primary cause of IVDD, and given the decrease of nucleus pulposus cells (NPCs) and extensive degradation of extracellular matrix (ECM) during IVDD development, the present study, inspired by the seeds-and-soil strategy, has developed NPCsloaded TBA@Gel&Chs hydrogel microspheres. These microspheres serve as exogenous supplements of NPCs and ECM analogs, replenishing seeds and soil for nucleus pulposus repair, and incorporating polyphenol antioxidant components to interrupt the oxidative stress-IVDD cycle, thereby constructing a microsphere system where NPCs and ECM support each other. Experiments proved that TBA@Gel&Chs exhibited significant extra-cellular ROS-scavenging antioxidant capabilities while effectively upregulating intracellular antioxidant proteins expression (Sirt3 and Sod2). This dual-action antioxidant capability effectively protects the vitality and physiological functions of NPCs. The therapeutic effects of microspheres on IVDD were also confirmed in rat models, which was found significantly restore histological structure and mechanical properties of degenerated discs. Additionally, RNA-seq results have provided evidences of antioxidant mechanism by which TBA@Gel&Chs protected NPCs from oxidative stress. Therefore, the NPCs-loaded TBA@Gel&Chs microspheres developed in this study have achieved excellent therapeutic effects, offering a paradigm using antioxidant biomaterials combined with cellular therapy for IVDD treatment.

The increasing demand for sustainable agricultural practices has intensified interest in soilless cultivation systems. However, hydroponics is unable to provide mechanical support for plant roots, and traditional soilless cultivation substrates mostly suffer from poor water retention capacity, rapid nutrient loss, and difficulty in precise control. Hydrogel-based soilless cultivation substrates show great potential for application due to their excellent water absorption, water retention and adjustable transparency. In this study, P(AM-co-NIPAM)/gelatin composite hydrogels with adjustable pore structures, mechanical strength and transparency were obtained by regulating the concentration of crosslinker. Soybean seedlings were grown on these substrates to evaluate the effects of hydrogel properties on root and shoot growth. The results demonstrate that hydrogels with optimized crosslink density possess superior mechanical properties, enhanced water retention capacity, and adequate transparency, facilitating both robust plant growth and high-resolution root system observation. We found that under the MBA content of 0.05 %, the hydrogel matrix could significantly promote the growth of aerial part and root system of soybean seedlings, and was conducive to the colonization of root bacteria. This work highlights the potential of controlled hydrogel matrices in soilless cultivation as a sustainable solution to improve root growth environments, enhance resource utilization, and enable dynamic root system studies. Given their adjustable structure and compatibility with plant growth, such hydrogels may also serve as promising candidates for future application in soilless crop production systems, particularly in scenarios where water and substrate optimization are critical to sustainable agricultural practices.

Hydrogel, as a typical representative of functional materials, constructs a three-dimensional network structure through physical or chemical cross-linking of hydrophilic polymer chains, which are rich in hydrophilic groups such as hydroxyl (-OH), carboxyl (-COOH), and amino (-NH2) on the molecular chain and exhibit excellent high water absorption (water absorption multiplication rate of 10-20 times and up to more than 500 times after nanocomposite modification). Studies have shown that the modified hydrogel removes more than 95 % of heavy metal ions (e.g., Pb2+, Cr3+) and possesses pH and temperature responsive swelling behavior. In response to the pressing problems faced by global agriculture, such as water scarcity, low fertilizer utilization, and soil heavy metal pollution, hydrogels show great potential for application in precision controlled release of fertilizers, water and moisture conservation, and pollution remediation. In this paper, we systematically review the performance characteristics of hydrogel, optimization strategies, and preparation methods, focusing on its innovative applications in agriculture and mechanistic role based on the environmental response mechanism to achieve the synergistic management of nutrients, water, and pollutants, which provides significant technological support for the development of sustainable agriculture.

The growing demand for sustainable and environment-friendly materials has driven extensive research on biopolymers for applications in agriculture, food science, and environmental remediation. Among these, nanocellulose-hydrogel hybrids (NC-HHs) have gained significant attention as an innovative class of bio-based materials that uniquely combine the remarkable physicochemical properties of nanocellulose with the functional versatility of hydrogels. These hybrids are characterised by exceptional water retention, mechanical strength and biodegradability, enabling advances in precision agriculture, smart food preservation and contaminant remediation. This review provides a comprehensive understanding of the synthesis, properties, and multifunctional applications of NC-HHs, emphasising their innovative role in sustainability. In agriculture, NCHHs enhance soil moisture retention, support plant growth, and serve as carriers for controlled-release fertilizers, optimizing water and nutrient use efficiency. In the food industry, they enable intelligent packaging solutions that extend shelf life, monitor food freshness, and inhibit microbial growth. Additionally, NC-HHs present groundbreaking strategies for environmental remediation by effectively immobilizing pollutants in water and soil. Beyond summarizing recent advances, this review presents an in-depth mechanistic perspective on the interactions between NC and HH, critically evaluating their structure-property relationships, functional adaptability and application-specific performance. By integrating recent advances in nanocellulose functionalisation, polymer chemistry and the development of responsive hydrogels, this review critically examines the key technological innovations and future prospects of NC-HHs, underscoring their transformative potential in addressing global challenges related to food security, environmental sustainability, and sustainable agricultural practices.

Gels are transversal materials with key applications in multiple scientific and technological sectors, including the preservation of Cultural Heritage that is a fundamental drive for socioeconomic resilience. Recently, the new class of twin-chain (TC) polymer gel networks was developed, using freeze-thaw (FT) cycles on solutions of polyvinyl alcohol (PVA) with two different hydrolysis degree and molar mass. Taking advantage of polymerpolymer phase separation in the pre-gel solutions, a sponge-like, interconnected porosity is templated in the hydrogels during FT, which concurs to boost the cleaning capability of the gels versus soil and aged coatings that jeopardize paintings and other iconic artworks. This review covers the latest developments in this new class of gels, and their use in the conservation of works of art. The TC gels allowed time-effective restoration of masterpieces (paintings by Picasso, Pollock, Lichtenstein), which would have been risky and time-consuming with conventional restoration materials in wet cleaning. The review discusses gelation mechanisms, the partial replacement or decoration of PVA with non-toxic synthetic or bio-based polymers, the counterintuitive role of gels' tortuosity in the cleaning process, and the upload of these gels with nanostructured cleaning fluids (microemulsions, micelles). Overall, the TC PVA hydrogels constitute an advanced tool to preserve Cultural Heritage and transfer it to future generations; moreover, they represent a class of sustainable soft matter materials with potential impact in several fields, spanning from detergency to the cosmetic, pharmaceutical and food industries, tissue engineering, and others.

Water scarcity is a critical problem around the world, and superabsorbent hydrogels has attracted growing attention in water management for handling water deficiency during agricultural and forestry practices. Herein, intending to apply gelatin hydrogel as soil conditioner, humic substances (HS) extracted from Chinese medicine residue compost were used to modify gelatin hydrogel through either physical mixing or chemical cross-linking. The results demonstrated that low level of HS could improve the hardness and rheological properties of the hydrogels, however, the gel strength significantly decreased when the concentration of HS rose up to 16 g/L. As revealed by TEM and XRD, chemical cross-linking reaction promoted the development of denser network structures, thereby improving the hardness and rheological properties of the hydrogels. Subsequently, applying HS at a concentration of 3 g/L was found to be preferable for enhancing the swelling ratio of the gelatin hydrogels, and lightweight substrates amended with the resultant hydrogels displayed superior water retention ratio (17.23 +/- 0.79 % for GelHS3 and 17.74 +/- 1.31 % for GelHS3-EDC). Furthermore, it was proved that HSincorporated hydrogels can effectively keep moisture for the growth of Melaleuca alternifolia (Maiden & Betche) Cheel saplings under drought stress. These findings suggest that humic substances can be utilized to modify hydrogels for use as soil conditioners.

Fogged surfaces, such as bathroom mirrors, quickly become a nuisance in everyday life, but are particularly problematic in safety-relevant and medical areas. Present approaches are often based on hydrophilic coatings, which can prevent fogging, but are not very durable. Surface-attached polymer networks that can be quickly and easily prepared from thin films of prepolymers by photochemical activation using brief irradiation with ambient light are presented. This novel photoreactive copolymer contains ionic, hydrophilic repeating units and hydrophilic nitro-substituted phenyl diazo ester moieties. The diazo groups in the prepolymer films form carbenes after excitation, which then bind to adjacent chains and to the substrate by C,H insertion cross-linking (CHic). The resulting surfaces exhibit excellent anti-fogging properties as they allow water to condense into a uniform thin film. The substrates remain highly transparent, even after frequent washing. In addition, the polymers can also be easily applied to previously damaged coatings by soiling in order to fully restore the anti-fog properties. Due to the solubility of the prepolymers in water, the easy cross-linking in sunlight, the durability of the coating, and the possibility of damage repair, the polymers are suitable for easy-use scenarios by non-professionals, which offers great potential for such an approach.

Superabsorbent nanocomposite hydrogels based on polyacrylamide (PAAm), cashew tree gum (CG), and laponite (LAP) were synthesized in different concentrations to investigate swelling, thermal, morphological and rheological properties. Vibrational modes confirmed the formation of hydrogels, while X-ray diffraction patterns reveal the semi-crystalline structure of the hydrogels. Thermal analysis showed that higher LAP content and CGLAP interactions improved the thermal stability of the hydrogels. Morphology analysis presented porous structures in CG-based hydrogels, contrasting with irregular plate-like structures in those without CG. The swelling capacity had better results in hydrogels with CG that were subjected to alkaline hydrolysis, mainly in a buffer solution with a pH > 4, due to the ionization of the hydrophilic groups. Hydrogels containing LAP maintained swelling degree stability at pH 10 and 12. In rheological tests, the addition of LAP increased the viscosity of the hydrogels, significantly improving the mechanical resistance of the hydrogels. Rheological parameters, such as the storage modulus (G ') and loss modulus (G ''), indicated that the materials exhibited predominantly solid behavior, particularly in CG-LAP-rich hydrogels. Low mortality of Artemia salina nauplii in toxicity tests confirmed material safety. The results indicate that CG-LAP hydrogels are promising for agricultural applications, offering optimized swelling properties, thermal stability, and mechanical strength.

Biodegradability and eco-friendliness are the most importance topic to consider in the development of new products. Commercial hydrogels for agriculture applications are made from fully synthetic polymers, which is non-biodegradable and harmful to environment. The utilization of polysaccharide in hydrogels production has sparked the rise of biodegradable hydrogels (BHs). However, using it alone results in poor mechanical properties and very fast degradation. Therefore, combining it with other materials as a composite is necessary. This article reviewed the development of BHs in the last 5 years. Classifications, materials resources, preparation methods, biodegradability of BHs, seeds germination and plant growth performance are critically investigated. Fundamental concepts such as definitions and application methods of BHs are described. Finally, important conclusions and outlook have been mentioned at the end of this article.

Phosphorus and potassium are essential macronutrients, and potassium dihydrogen phosphate, a compound containing both, plays a vital role in plant growth and reproduction. However, its rapid leaching poses significant environmental concerns, lessening its practical utility. To overcome this issue, a biodegradable hydrogel based on amla was synthesized through graft polymerization and evaluated as a water-retaining material for agricultural applications, specifically for the controlled release of fertilizers. The synthesized hydrogel was characterized using FTIR, SEM, XRD, and TGA. Its swelling properties, water retention capacity, porosity, and density were also examined. The biodegradable nature of the synthesized hydrogel was confirmed via soil burial and composting techniques, with FTIR used to validate the degradation. The hydrogel degraded almost entirely within 64 days in compost soil and 72 days in burial soil. Finally, potassium dihydrogen phosphate release studies were conducted, and the data were analyzed using Fick's law of diffusion and various kinetic models (zero order, first order, Higuchi, and Korsemers Peppas). The release pattern was measured via UV spectrophotometry over 45,000 min, demonstrating controlled nutrient delivery. These findings suggested that the synthesized hydrogel matrix has strong potential as an effective water retention system and for regulated nutrient release.