Search Results (406)

Polysaccharide-based wound dressings face challenges in mechanical properties and effective wound repair for infected wound surfaces. This study presents a novel polyvinyl alcohol (PVA)/Salecan (Sal) composite hydrogel dressing with high toughness, biocompatibility, and wound healing capabilities, developed using an interpenetrating polymer network strategy. The primary network was formed through electrostatic interactions between polydopamine (PDA) and biocompatible polysaccharide Salecan, followed by incorporation of AgNO₃, which was in situ reduced to silver nanoparticles within the hydrogel. PVA was introduced as a secondary matrix, further reinforcing the hydrogel network through cyclic freeze–thawing. The resulting hydrogel exhibited a tensile strength of 0.31 MPa, an elongation at break of 158.9%, and a toughness of 31.16 J·m⁻², demonstrating enhanced mechanical performance compared to both Salecan/PDA and previously reported Salecan/Fe³⁺ hydrogel. Co-culture experiments showed the hydrogel’s strong antibacterial effects, inhibiting 80.1% of Escherichia coli (E. coli) and 99.5% of Staphylococcus aureus (S. aureus). Fibroblast culture tests confirmed its excellent cytocompatibility. In vivo studies on infected wounds showed nearly complete healing in the S. aureus + hydrogel group within 12 days. Quantitative immunohistochemical analysis of CD31 revealed that hydrogel treatment significantly upregulated CD31 expression, indicating enhanced neovascularization. Complementary Western blot analysis further demonstrated that hydrogel-treated groups exhibited a marked downregulation of pro-inflammatory factors alongside CD31 upregulation. In summary, the PVA/Sal-based hydrogel represents a valuable strategy for reducing inflammation and promoting regeneration in the management of infected wounds. Full article

MXenes, a new family of two-dimensional transition-metal carbides and nitrides, have attracted significant interest in biomedicine because of their tunable surface groups and multifunctional properties. Hydrogels, with their three-dimensional polymeric networks rich in water, provide excellent biocompatibility and structural similarity to those of biological tissues. Although synthetic polymer–based MXene hydrogels are well studied, polysaccharide-based systems remain underexplored despite their biodegradability and biomedical relevance. In this work, MXene nanosheets were incorporated into a sodium alginate (ALG)–gellan gum (GG) polymeric blend to develop polysaccharide/MXene hydrogels. Two dehydration approaches, conventional drying and freeze-drying were used to evaluate their influence on the characteristics of the composite, including microstructure, surface roughness, compressive behavior, water states, and thermal stability. Conventionally dried polysaccharide/MXene nanocomposites with 1.0% wt. MXene have reduced the swelling ratio by ~60% and the volume change by 40% compared to polysaccharide blend. Freeze-dried polysaccharide/MXene nanocomposite hydrogels developed a porous, interconnected network, making them promising for applications requiring high surface area, such as adsorption and tissue engineering. In contrast, conventionally dried samples formed compact, smooth structures with improved barrier and mechanical performance. These results demonstrate that the dehydration strategy strongly governs the polymer network architecture, water states, and material functionality, offering pathways to tailor hydrogel modified with MXene for specific biomedical applications. Full article

In recent years, the sustained and even increasing interest in the development and application of novel composite materials based on the polysaccharide bacterial cellulose (BC) has been driven by the accumulation of experimental data and the emergence of analytical reviews that narratively summarize these findings. This review presents a comparative and critical analysis of various approaches to the fabrication of BC-based composites. Among them, in situ biosynthesis is highlighted as the most promising strategy. In this approach, different additives are introduced directly into the culture medium of BC-producing microorganisms, enabling the formation of materials with different mechanical and physicochemical properties. Such a method also allows imparting to the composites a range of properties that BC itself does not possess, including antibacterial and enzymatic activity, as well as electrical conductivity. During the so-called “cell weaving” stage, performed by BC-producing microorganisms, diverse substances and microorganisms can be incorporated into the cultivation medium. By varying the concentrations of the introduced compounds, their ratios to the synthesized BC, and by employing different BC-producing strains and substrates, it becomes possible to regulate the characteristics of the resulting composites. Special attention is given to the role of various polysaccharides that are either introduced into the medium during BC biosynthesis or co-synthesized alongside BC within the same environment. Depending on the mode of incorporation of these additional polysaccharides, the resulting materials demonstrate variations in Young’s modulus and tensile strength. Nevertheless, they almost invariably exhibit a decreased degree of BC crystallinity within the composite structure and an enhanced water absorption capacity compared to the pure polymer. Full article

Pollution of water resources with hazardous substances of anthropogenic origin (e.g., synthetic dyes, heavy metal ions) is currently one of the most important environmental issues, and the development of not only effective and economical but also eco-friendly methods of removing these substances from aqueous solutions is one of the greatest challenges. Among the various separation methods, techniques based on the utilization of different types of polymer membranes have gained increasing interest due to their usually high efficiency, the materials’ stability and reusability, and the possibility of using “green” components for their formation. Recent research efforts have been concentrated, inter alia, on the application of natural polysaccharide polymers (e.g., cellulose, alginates, starch, cyclodextrins) and their derivatives to produce well-performing membranes. Appropriately composed polysaccharide-based membranes under optimal process conditions enable effective separation of dyes, salts, and metal ions (e.g., often with a rejection rates of >95% for dyes and metal ions and <7% for salts). This review concerns the latest developments in the formation and utilization of novel polysaccharide-based membranes for the separation of synthetic dyes and metal ions from aqueous solutions and suspensions, with emphasis on their most important advantages, limitations, and potential impact on the environment and sustainability. Full article

Blow spinning is a low-cost and versatile method that permits the large-scale production of fibrous membranes. However, polysaccharides that show numerous merits such as biocompatibility and biodegradability often have a low spinnability due to their high chain rigidity and low ability to form sufficient entanglements. Here, we report the fabrication of polysaccharide micro-fibrous membranes from sodium alginate/polyethylene oxide solutions formulated in solvent mixtures of water and ethanol. The shear and extensional rheological responses of the solutions are characterized, and parameters including specific shear viscosity, reptation time, extensional relaxation time, and maximum stretch ratio are correlated with the concentrations of polymer, polyethylene oxide, and ethanol. It is found that flexible polyethylene oxide and poorer solvent ethanol can synergistically delay the chain relaxation during stretch and increase the stretchability of the solutions. A processability map of the solutions for blow spinning is constructed, enabling the fabrication of fibrous membranes with a fiber diameter of ~1 μm, tensile strength of 4.89 MPa, elongation at break of 15.24%, and Young’s modulus of 45.43 MPa. This study presents a new strategy to fabricate sodium alginate-based membranes, which should provide insights into the design of other polysaccharide membranes with specific functions and applications. Full article

Pediatric drug delivery presents unique challenges due to physiological and pharmacological differences across age groups, requiring specialized formulation approaches beyond simple dose adjustments of adult medications. This review synthesizes recent advances in polysaccharide-based pediatric drug delivery and highlights novel findings that may accelerate clinical translation. It summarizes how chitosan, alginate, hyaluronic acid, dextran, modified starches, and other polysaccharides are engineered into nanoparticles, hydrogels, films, and orodispersible/mini-tablet formulations to improve stability, bioavailability, taste masking, and controlled release across neonates to adolescents. These systems can accommodate developmental variations in absorption, distribution, metabolism, and excretion processes across pediatric subpopulations, with particular emphasis on oral and alternative administration routes. Evidence supporting unexpectedly high acceptability of mini-tablets, successful integration of modified polysaccharides in 3D-printed personalized low-dose therapies, and the emergence of blood–brain barrier-penetrating and RGD-functionalized polysaccharide nanocarriers for pediatric oncology are emphasized as novel, clinically relevant trends. This review also addresses regulatory considerations, safety profiles, and future perspectives. By integrating developmental insights with innovative formulation strategies, polysaccharide polymers offer promising solutions to improve medication adherence, safety, and efficacy across the pediatric age spectrum. Full article

Plant-based natural polymers are gaining attention as ecofriendly alternatives to synthetic materials with applications in food, biomedical, pharmaceutical, and environmental science. Tragacanth gum (TG), a natural exudate obtained from Astragalus species, represents a unique polysaccharide with a complex molecular structure and distinctive rheological properties. It has been traditionally used for centuries as a stabilizer and emulsifier. Recent advances highlight its potential as a multifunctional biopolymer with industrial and biomedical potential. This review explores the structural characteristics, physicochemical properties, and modification strategies of TG, comparing it with other plant derived gums. Special emphasis is given to its applications in drug delivery, tissue engineering, wound healing, biodegradable packaging, and functional food formulation. Strengths such as biocompatibility and gel-forming ability but challenges remain including variability in quality, limited standardization, and issues with large scale production. Emerging trends, such as nanoformulations, hybrid polymer composites, and smart hydrogels, are also discussed. By positioning TG within the broader context of sustainable biomaterials, this review identifies key research gaps and proposes future directions to advance its role in the green polymer economy. Full article

Polysaccharide-based edible coatings are increasingly explored as sustainable strategies for maintaining quality of fresh produce, acting as barriers to gas exchange while improving mechanical and optical properties. However, their effectiveness depends not only on the intrinsic features but also on the structural and physiological diversity of fruits and vegetables, which vary in peel composition, hydrophobicity, and texture. This study investigated plant-derived polysaccharide films (cassava starch, potato starch, corn starch, carboxymethylcellulose, hydroxypropylmethylcellulose, and pectin) characterized for moisture resistance, solubility, permeability, thermal stability, hydrophilicity, opacity, gloss, and mechanical strength. Concurrently, different fruits and vegetables (fruit, root, and tubers) were analyzed for their surface hydrophilicity to establish correlations between film properties and peel characteristics. The findings emphasize that no single polymer can be universally applied. In addition, the choice of matrix must be guided by both film functionality and produce surface traits. Starch-based films presented high hydrophilicity, suggesting better wettability, while pectin and cellulose derivatives presented distinct advantages for less hydrophilic peels. This work highlights the importance of tailoring edible coatings according to the physicochemical compatibility between films and fresh produce surfaces, providing insights for improving post-harvest preservation strategies and guiding the development of effective, sustainable coatings for diverse horticultural commodities. Full article

Food packaging serves a pivotal role in daily life, facilitating the efficient transportation of food and extending its shelf life. Petroleum-derived plastic packaging is extensively employed; however, its non-biodegradable nature poses significant environmental pollution and ecological degradation. Natural polymers (e.g., proteins such as gelatin and corn gluten protein; polysaccharides including pectin, chitosan, starch, cellulose, and alginate) and synthetic polymers (e.g., polyvinyl alcohol, polylactic acid, and polyhydroxyalkanoates) can be utilized to fabricate food packaging films, thereby achieving green and eco-friendly objectives. Nevertheless, the inferior mechanical strength and inadequate antibacterial activity of biopolymer-based packaging have restricted their practical applications. In recent years, nanomaterials (e.g., nanoparticles, nanotubes, nanofibers, and nanosheets) have been employed to enhance the performance of food packaging, emerging as a research hotspot. Notably, nanoparticles possess unique properties, including a high specific surface area, excellent dispersibility, and multifunctionality, which enables them to be easily incorporated into film matrices. Owing to their unique chemical structures, nanoparticles form strong interactions with film matrices, leading to a denser spatial structure. This not only markedly enhances the mechanical strength of the films, but also simultaneously improves their antibacterial and antioxidant capabilities. This review classifies and summarizes common nanomaterials based on their chemical compositions, providing a theoretical foundation and technical reference for the future development and application of nanomaterials in the field of bio-based active food packaging. Full article

Disposable diapers contribute significantly to municipal solid waste, with non-biodegradable polymers such as low-density polyethylene (LDPE) persisting in landfills for centuries. Biodegradable alternatives, including polylactic acid (PLA), poly(butylene adipate-co-terephthalate) (PBAT), bamboo, and organic cotton, offer reduced environmental persistence, although challenges remain regarding cost, mechanical performance, and scalability. This review synthesizes current literature on these materials, highlighting their properties, biodegradation mechanisms, environmental performance, and commercial feasibility. In addition, we examine emerging biodegradable superabsorbent polymers (SAPs), such as polysaccharide-based hydrogels, chitosan, and nanocellulose, essential for fully compostable diapers. Our review uniquely integrates material performance, tropical high-humidity degradation, cost considerations, and consumer acceptance, providing insights into both technological advances and barriers to adoption. Key challenges include high production costs, supply chain limitations, and maintaining performance parity with conventional diapers. Finally, we discuss sustainable waste management strategies, including industrial composting, and identify future research directions focused on optimizing biopolymer properties, safety, and life-cycle impacts. This synthesis informs researchers, industry stakeholders, and policymakers seeking to advance environmentally responsible diaper products. Full article

Biofilm growth on silicone (Si) medical devices is routinely treated with antibiotics or device removal; however, new approaches are needed. The current work evaluates photothermal therapy (PTT) to augment antibiotic efficacy or directly ablate Staphylococcus aureus biofilms. The semiconducting polymer, Poly [4,4-bis(2-ethylhexyl)-cyclopenta [2,1-b;3,4 b’]dithiophene-2,6-diyl-alt22,1,3-benzoselenadiazole-4,7-diyl] (PCPDTBSe), with a high photothermal conversion efficiency of 53.2%, was formulated into nanoparticles (BSe NPs) and incorporated into Si. Nanocomposites were stimulated with 800 nm light to generate mild hyperthermic conditions of 42 °C, or ablative temperatures above 50 °C. PTT, with or without antibiotics, was deployed against two strains of Staphylococcus aureus biofilms, Xen 29 and Xen 40, followed by an evaluation of bacterial survival, biofilm regrowth, and differential disruption of specific biofilm components. Mild hyperthermia was also used in an in vivo model of silicone implant infection. The results demonstrate a 55–59% reduction in S. aureus when PTT plus antibiotic was used in vitro, and a 51% reduction in vivo. Higher temperatures effectively eradicate both Xen 29 and Xen 40 strains, with a longer exposure time using lower laser power being optimal. Hyperthermia inhibited biofilm regrowth in both strains, resulting in a > 3 log reduction, plus increased dead cells, polysaccharides, and eDNA in treated Xen 40 biofilms. These experiments demonstrate that nanocomposite-based PTT can both reduce viable bacteria and alter individual biofilm components. Full article

Natural polysaccharides are used for very different applications and are particularly exploited for preparing hydrogel materials. For instance, gels based on different carbohydrate polymers have been applied to remove unwanted materials from the surface of cultural heritages items. This study was focused on the preparation of novel physical hydrogels suitable for the cleaning of sensitive materials like wood and paper, i.e., to remove the soil from their surface. For this purpose, alginate biopolymer was used and ionically crosslinked with six different amines, in the presence of N-hydroxysuccinimide as a co-gelling agent. All the synthetized gel materials were characterized by a multianalytical approach, using different techniques such as FT-IR, thermal analysis, SEM-EDS, mechanical tests, and evaluation of moisture properties. All the results showed that the introduction of the investigated amines improved the original properties of alginate and provided good cleaning properties when applied to sensitive surfaces. Full article

The morphology and composition of inorganic particles play a vital role in controlling the flame-retardant characteristics of polymers. Halogen-free flame-retardant polymers have also become a current research hotspot. Boron nitride (BN), phytic acid (PA), and chitosan (CS), a natural polysaccharide with a nitrogen content of approximately 6.8–7.5%, show great promise as flame retardants owing to their high thermal stability, P-based flame retardancy, and natural polysaccharide properties, respectively. In this study, BN (BN@PA-CS) particles coated with PA and CS were designed and prepared via a facile modification strategy. The effect of BN@PA-CS on the mechanical and flame-retardant properties of polyvinylidene fluoride (PVDF) was further investigated, and it was found that both characteristics were improved. Compared to pure PVDF, the PVDF composite films exhibited a significantly lower peak heat release rate and total heat release. With a BN@PA-CS content of 20%, the peak was the lowest at 18.25 W/g, corresponding to a decrease of 77.83%. This phenomenon may be attributed to the synergistic effect of the BN nanosheets and PA-CS in the BN@PA-CS particles. This work describes a facile and effective method of modifying the morphology and composition of inorganic particles, thereby controlling the properties of polymers, and provides a new approach to improving the safety of PVDF battery separators. Full article

The fields of healthcare and pharmaceutical science are increasingly focused on developing innovative and effective treatments. This trend is driven by a growing consumer demand for natural, sustainable, and highly functional polymer-based products. This study focuses on two biomaterials: chitosan and royal jelly. Chitosan, a linear polysaccharide derived from chitin, is well-regarded for its hemostatic and antimicrobial properties, making it an excellent candidate for wound healing applications. Royal jelly, a nutrient-rich secretion from honeybees, represents a complex mixture of proteins, lipids, vitamins, and antioxidants, notably 10-hydroxy-2-decenoic acid (10-H2DA). It is known for its anti-inflammatory, antioxidant, and regenerative effects on the skin. While the individual benefits of chitosan and royal jelly are well-documented, there is a significant research gap concerning their synergistic application in various treatments such as topical formulations, wound healing, regenerative medicine, and delivery transport processes. Ultimately, this review concludes that the synergistic effects of chitosan and royal jelly could provide a material platform with a superior dual-action profile, integrating the structural and antimicrobial benefits of chitosan with the powerful regenerative and anti-inflammatory effects of royal jelly. This synergy strongly supports their utility in developing next-generation, high-performance natural bioproducts for wound healing, bone regeneration, agriculture, or aquaculture applications. Full article

The shift towards renewable resources has positioned agar, a natural seaweed polysaccharide, as a pivotal and sustainable material for developing next-generation energy storage technologies. This review highlights the transformative role of agar-based composites as a game-changing and eco-friendly platform for supercapacitors, batteries, and fuel cells. Moving beyond the traditional synthetic polymers, agar introduces a novel paradigm by leveraging its natural gelation, superior film-forming ability, and inherent ionic conductivity to create advanced electrolytes, binders, and matrices. The novelty of this field lies in the strategic fabrication of synergistic composites with polymers, metal oxides, and carbon materials, engineered through innovative techniques like electrospinning, solvent casting, crosslinking, 3D printing, and freeze-drying. We critically examine how these innovative composites are breaking new ground in enhancing device efficacy, flexibility, and thermal stability. Ultimately, this analysis not only consolidates the current landscape but also charts future pathways, positioning agar-based materials as a pivotal and sustainable solution for powering the future. Full article