Search Results (338)

Modification of PLA with functional nanoparticles is a promising approach for imparting new properties to the material. In this work, titanium nanoparticles (Ti NPs) and titanium dioxide nanoparticles (TiO₂ NPs) were synthesized by laser ablation and characterized by dynamic light scattering, spectrophotometry, and transmission electron microscopy. The average hydrodynamic diameter of Ti NPs was 12 nm, while that of TiO₂ NPs was 24 nm; both dispersions possessed a positive zeta potential (23–27 mV) and spherical morphology. L-PLA composite films containing 0.1 wt.% Ti NPs or TiO₂ NPs were obtained by solution casting. Atomic force and modulation-interference microscopy confirmed the uniform distribution of nanoparticles within the polymer matrix, although partial aggregation was observed. The introduction of TiO₂ NPs increased the water contact angle. Mechanical testing revealed a significant reinforcing effect: the addition of 0.1 wt.% NPs increased the Young’s modulus by 62–68% and the ultimate tensile strength by 16–18% while maintaining a ductile fracture pattern with elongation at break up to ~8%. Both types of composites generated reactive oxygen species (ROS) in aqueous solutions: Ti NPs increased H₂O₂ production by 5.5 times and TiO₂ NPs by 4.9 times, and they also induced the formation of hydroxyl radicals. The accumulation of 8-oxoguanine in DNA and long-lived oxidized protein species confirmed the materials’ ability to cause oxidative damage to biomacromolecules. For E. coli, growth inhibition reached 40.5% (for composites with Ti NPs) and 71% (for composites with TiO₂ NPs). The effect was even more pronounced for S. aureus, where inhibition levels were approximately 70% and 80%, respectively; flow cytometry confirmed the strong bactericidal effect, showing that materials containing TiO₂ NPs increased the proportion of dead cells to 25% for E. coli and ~68% for S. aureus. Cytotoxicity assessment on human fibroblasts (HSF) demonstrated the high biocompatibility of neat L-PLA and composites with Ti NPs (viability > 95%) and with TiO₂ NPs (viability ~93%). The obtained results indicate that L-PLA-based composites with Ti NPs and TiO₂ NPs exhibit pronounced ROS-mediated antibacterial activity without additional UV irradiation. These findings position these materials as highly promising candidates for active biodegradable food packaging to extend shelf-life and for biomedical devices, such as wound dressings and implants, where reducing the risk of bacterial colonization is critical. Full article

Hydrogels constructed from natural biomacromolecules with multifunctional properties, such as improved mechanical strength, ionic stability, biocompatibility, and ionic conductivity, are highly desirable for advanced food and biomedical applications, yet remain challenging to design. Although alginate is one of the most widely used hydrogel-forming polysaccharides due to its biocompatibility and gelation ability, its intrinsic limitations often hinder the development of hydrogels with fully optimized performance. This review provides a systematic comparison of alginate-based composite hydrogels formed with complementary biopolymers, including whey proteins, gelatin, pectin, starch, and chitosan, focusing on their synergistic effects on structural, mechanical, and functional properties. Recent studies are critically analyzed to elucidate how polymer–polymer interactions influence gel network formation, environmental ionic stability, and encapsulation performance. Particular attention is given to fabrication strategies and formulation parameters that enhance the immobilization and controlled release of probiotics, vitamins, polyphenols, and other bioactive compounds. By integrating current knowledge on structure–function relationships and processing approaches, this review offers practical design guidelines for the development of multifunctional alginate-based hydrogel systems for applications in functional foods and nutraceutical delivery. Full article

Among the most structurally diverse biomacromolecules, polysaccharides have attracted increased attention as nanocarriers for precision medicine due to their inherent biocompatibility and versatility in functionalization. Molecular features, such as monomer composition, glycosidic linkages, charge density, and chemical modification, essentially determine the nanoscale assembly process of these biopolymers, as well as their biological compatibility. This review highlights the role of these properties in the assembly process of polysaccharide-based nanocarriers leading to a variety of self-assembled nanostructures, such as polyelectrolyte complexes, protein–polysaccharide complexes, amphiphilic micelles, vesicles, hybrid systems, and nanogels, which are extensively discussed throughout the review. This review also focuses on the structure–property–function relationships of nanocarriers as applied to the rapidly developing area of precision medicine, emphasizing the problems of sustainability and reproducibility. By combining the principles of molecular engineering, supramolecular assembly, and measurable properties, this work aims to present a unified view of the molecular engineering of polysaccharide-based nanocarriers for enhanced translation potential, as well as to outline a coherent framework for the rational development of next-generation polysaccharide-based nanocarriers with improved clinical relevance. Full article

Marine algae, microalgae, and Cyanophyceae emerge as sustainable and versatile sources of biomacromolecules for the fabrication of hydrogels with broad biomedical potential. Their phycocolloids, such as alginate, agar, carrageenan, ulvan, and extracellular polysaccharides (EPS), exhibit intrinsic biocompatibility, tunable gelation behavior, and bioactive sulfated structures that support cell viability, tissue regeneration, and therapeutic delivery. This review provides a comprehensive overview of hydrogel fabrication strategies, including physical, chemical, and hybrid crosslinking approaches, and highlights recent advances in composite systems incorporating proteins, glycosaminoglycans, and functional nanomaterials. Applications in skin repair, cartilage and bone regeneration, neural and cardiovascular engineering, and controlled drug delivery are examined, alongside the expanding role of marine-derived hydrogels as bioinks for 3D and 4D bioprinting. Despite their promise, challenges remain related to extract variability, purification complexity, mechanical limitations, and the need for standardized characterization. Future perspectives emphasize genetic engineering of algae and cyanobacteria, development of multifunctional hybrid hydrogels, sustainable large-scale production, and pathways toward clinical translation. Together, these insights position marine-derived hydrogels as next-generation biomaterials with significant potential for regenerative medicine and therapeutic innovation. Full article

Owing to their distinctive physicochemical features, their structural analogues of benzene ring bioisosteres, and their strong affinity for biomacromolecules, pyridine derivatives function both as core structural scaffolds in pharmacologically active compounds and as versatile elements for optimizing key drug-like properties, such as water solubility, membrane permeability, and metabolic stability. In this study, we synthesized five pyridine-fused heterocyclic compounds using common synthetic intermediates as precursors. Full article

Inspired by natural scaffolds, artificial scaffolds have garnered significant attention in recent years. Compared with synthetic scaffolds such as organic and polymer scaffolds, biological scaffolds from the foundational biomolecules nucleic acids (DNA/RNA) and proteins demonstrate distinct advantages in the assembly of inorganic nanoparticles and proteins, as well as in drug delivery. These advantages stem from their exquisite spatial structures, genetically encoded programmability, and their favorable biocompatibility, which is attributed to natural building blocks and degradable backbones that minimize long-term cytotoxicity. The intrinsic properties and structural symmetry of biomacromolecules as building blocks often determine the properties of the corresponding assemblies, and thus greatly influence their functions. In this review, we classify bottom-up constructed biological scaffolds according to these two primary constituent classes (nucleic acids and proteins) to examine their framework structures and key features. We also discuss the relevant applications of artificial bioscaffolds. As an emerging class of nanomaterial with precise structures and genetic programmability, biological scaffolds hold significant promise for future development. Full article

As a traditional dual-purpose ingredient for both medicine and food, the biomacromolecules in Panax ginseng include polysaccharides, pectin, exosomes, proteins and dietary fiber. Due to their unique chemical structures, physiological activities, and processing adaptability, these components have achieved diversified applications in the medical field, becoming one of the core raw materials for functional food development. Modern research shows that the biomacromolecules found in ginseng can regulate the body’s immunity, antioxidant and anti-tumor properties, as well as antibacterial properties and the ability to enhance the body’s metabolic capacity, demonstrating significant application potential in healthcare-related fields. Recent studies have found that in addition to the root, the stems, leaves, fruits and flowers of P. ginseng also contain various effective components such as ginseng polysaccharides and pectin, which have enhanced the utilization value of ginseng plant resources. Ginseng biomacromolecules can not only replace antibiotics but also improve the production performance of animals by influencing the structure of intestinal flora, providing raw materials for the selection and application of natural feed additives for animals. This review summarizes the latest research findings on the pharmacological properties and practical applications of ginseng-derived biomolecules. It primarily addresses the structural characteristics, pharmacological activities, and current applications in health and medicine of biomolecules such as ginseng polysaccharides, ginseng exosomes, ginseng proteins, and ginseng dietary fiber. It aims to provide a fresh perspective and a solid theoretical foundation for the in-depth development of ginseng in the fields of medicine and molecular biology. Full article

ILs have emerged as versatile formulation components in DDS due to their tunable physicochemical properties and ability to modulate biomolecular and interfacial interactions. This review examines IL-enabled DDS strategies across major delivery platforms, including nanocarrier-based systems, microtechnology-assisted devices, and biomacromolecule formulations, with emphasis on formulation design principles rather than administration route. We discuss how ILs enhance API solubility, stability, permeability, and formulation flexibility through API–IL complex formation and controlled membrane interactions and relate mechanistic insights into IL–membrane interactions to both delivery performance and safety via structure–activity relationships. Current limitations, including toxicity concerns, lack of standardized evaluation criteria, scalability challenges, and regulatory ambiguity, are critically assessed. Overall, this review positions ILs as formulation-enabling materials rather than standalone therapeutics and underscores the importance of rational design, standardized assessment, and early regulatory alignment for advancing IL-enabled DDS toward clinical translation. Full article

The industrial application of free sucrose phosphorylase (SPase) is significantly limited due to cost, stability issues, and poor reusability. In this study, we employed organic–inorganic hybrid nanoflowers to achieve cell immobilization by co-assembling metal ions with cells. The surface of cells was coated with nanoflowers via chitosan-regulated biomimetic mineralization, thereby enhancing the activity of immobilized cells while providing a protective structure to improve stability. The relative activity of the immobilized cells was 30% higher than that of the free cells. After placing at 4 °C in 15 days, the relative activity of immobilized cells (80%) was substantially higher than that of free cells (40%). Moreover, the immobilized cells retained approximately 85% of their relative activity after 10 cycles. In summary, the novel biocatalysts developed in this study combine high catalytic performance with excellent reusability, demonstrating significant advantages in E. coli cell immobilization and providing a solid foundation for their application in industrial biocatalysis and related fields. Full article

Human serum albumin (HSA) is one of the main proteins in human blood plasma and serves as a molecular “taxi” transporting various compounds, including organic compounds, drugs, metal ions, etc., through the circulatory system throughout the human body. As with any other proteins, HSA hydration plays an important role in maintaining its structure and functioning as well as influencing its ability to bind to ligands. This contribution presents, for the first time, a generalized picture of hydration of this biomacromolecule obtained within the framework of the 3D-RISM (three-dimensional Reference Interaction Site Model) theory of solvation. Based on 3D isodensity maps and structural parameters (hydration numbers, hydration layer thickness, fraction of hydrogen bonds, SASA, etc.), the most probable model of HSA hydration structure was reconstructed. With the description of HSA hydration, two important issues were also addressed in detail. The first is the correct determination of the hydration layer thickness, a common problem in protein science. The second is the possible state and behavior of hydration water in HSA–ligand binding. The presented results provide a deeper understanding of the relationship between solvent and HSA, which brings new knowledge to the understanding of protein hydration. Full article

While surface plasmon resonance (SPR) sensors serve as vital tools for biomolecular detection; conventional versions suffer from inherent limitations, including confined localized electromagnetic fields and inadequate sensitivity for detecting low-abundance analytes. Consequently, this paper reviews the progress of research in nanomaterial-enhanced SPR sensors to address these challenges. Initially, the review elaborates on the sensing principles and signal modulation strategies of SPR sensors. It systematically analyzes the enhancement mechanisms of noble metal nanoparticles (ranging from spherical 0D to advanced anisotropic 1D/2D nanostructures), magnetic nanoparticles (MNPs), and two-dimensional (2D) nanomaterials, alongside their applications in the detection of small molecules, nucleic acids, and biomacromolecules. Crucially, this review provides a comparative benchmarking of these materials, evaluating their trade-offs between sensitivity enhancement and practical stability. Furthermore, it identifies critical bottlenecks in industrialization, specifically addressing environmental challenges such as thermal cross-sensitivity and oxidative degradation, alongside issues of reproducibility and standardization. Finally, future research directions are proposed, including developing novel nanomaterials, exploring low-cost alternatives, and constructing flexible wearable sensing systems. Full article

Hydrogels based on gelatin–chitosan mixtures have great potential for practical application in the development of new materials in food technology and biomedicine. This study examines the effect of chitosan on the gelling properties, rheological, and structural characteristics of fish gelatin type A hydrogels in the acidic pH range of 3.2–3.9. It was shown that an increase in the chitosan-to-gelatin mass ratio up to 0.15 resulted in a growth in the hydrogel thermal stability and an increase in the elastic modulus, hardness, and yield stress. The structural strength of the fish gelatin–chitosan hydrogel increased due to the strengthening of the binding zones in the fish gelatin gel network in the presence of chitosan. According to scanning electron microscopy, the supramolecular microstructure of the gels demonstrated a significant compaction upon the addition of chitosan to fish gelatin. UV and IR spectroscopy data, as well as changes in zeta potential, showed the formation of supramolecular complexes of fish gelatin with chitosan as a result of hydrophobic interactions between biomacromolecules and the establishment of hydrogen bonds; in this case, electrostatic interactions between macromolecules of fish gelatin and chitosan are practically absent in the acidic pH region. The ability to form supramolecular complexes of different compositions at different mass ratios of polysaccharide-to-fish gelatin makes it possible to obtain hydrogels with high gelling properties, strength, elasticity, and thermal stability comparable to hydrogels of mammalian gelatin. Full article

Lignocellulosic biomass—the non-edible fraction of plants composed of cellulose, hemicellulose, and lignin—is the most abundant renewable carbon resource and a key lever for shifting from fossil to bio-based production. Agro-industrial residues (straws, cobs, shells, bagasse, brewery spent grains, etc.) offer low-cost, widely available feedstocks but are difficult to process because their polymers form a tightly integrated, three-dimensional matrix. Within this matrix, lignin provides rigidity, hydrophobicity, and defense, yet its heterogeneity and recalcitrance impede saccharification and upgrading. Today, most technical lignin from pulping and emerging biorefineries is burned for energy, despite growing opportunities to valorize it directly as a macromolecule (e.g., adhesives, foams, carbon precursors, UV/antioxidant additives) or via depolymerization to low-molecular-weight aromatics for fuels and chemicals. Extraction route and severity strongly condition lignin structure linkages (coumaryl-, coniferyl-, and sinapyl-alcohol ratios), determining reactivity, solubility, and product selectivity. Advances in selective fractionation, reductive/oxidative catalysis, and hybrid chemo-biological routes are improving yields while limiting condensation. Remaining barriers include feedstock variability, solvent and catalyst recovery, hydrogen and energy intensity, and market adoption (e.g., low-emission adhesives). Elevating lignin from fuel to product within integrated biorefineries can unlock significant environmental and economic benefits. Full article

The Transdermal Drug Delivery System (TDDS) offers several benefits, such as enhanced patient adherence, controlled release, reduced gastric irritation, and the bypassing of the first-pass metabolism. However, not all drugs can be delivered through this route in effective doses. Biodegradable microneedles (BMn) are designed to improve TDDS. This review outlines various types of BMn and their fabrication methods. BMn are produced in different forms, including hollow, solid, dissolve, and hydrogel-forming versions, which have garnered significant attention. These innovative BMn do not contain drugs themselves but instead absorb interstitial fluid to create continuous channels between the dermal microcirculation and a drug-containing patch. Several types of BMn have been tested and approved by regulatory bodies. The use of BMn technology is rapidly growing in point-of-care applications, attracting significant interest from both researchers and healthcare providers. BMn-based Point-of-care (POC) devices have high efficacy for finding various analytes of clinical interests and transdermal drug administration in a minimally invasive manner owing to BMn’ micro-size sharp tips and ease of use. Porous BMn technology may have a very rising future in the case of a vaccine delivery system. Full article

Collagen is a family of large, fibrous biomacromolecules common in animals, distinguished by unique molecular, structural, and functional properties. Despite the relatively low complexity of their sequences and the repetitive conformation of the triple helix, which is the defining feature of this family, unraveling sequence–stability and structure–function relationships in this group of proteins remains a challenging task. Considering the importance of the structural aspects in collagen chain recognition and selection, we reviewed our current knowledge of the heterotrimeric structures of non-collagenous (NC) regions that lack the triple helix sequence motif, Gly-X-Y, and are crucial for the correct folding of the functional states of these proteins. This study was conducted by simultaneously surveying the current literature, mining the structural database, and making predictions of the three-dimensional structure of these domains using highly reliable approaches based on machine learning techniques, such as AlphaFold. The combination of experimental structural data and predictive analyses offers some interesting clues about the structural features of heterotrimers formed by collagen NC regions. Structural studies carried out in the last decade show that for fibrillar collagens (types I, V, XI, and mixed V/XI), key factors include the formation of specific disulfide bridges and electrostatic interaction patterns. In the subgroup of collagens whose heterotrimers create supramolecular networks (types IV and VIII), available structural information provides a solid ground for the definition of the basis of the molecular and supramolecular organization. Very recent AlphaFold predictions and structural analyses of type VI collagen offer strong evidence of the specific domains in the NC region of the protein that are involved in chain selection and their staggering. Insightful crystallographic studies have also revealed some fundamental elements of the chain selection process in type IX collagen. Collectively, the data reported here indicate that, although some aspects (particularly the quantification of the relative contribution of the NC and triple helix regions to correct collagen folding) are yet to be fully understood, the available structural information provides a solid foundation for future studies aimed at precisely defining sequence–structure–function relationships in collagens. Full article