Macromol

UV radiation is responsible for acute and chronic adverse effects on the skin. In recent years, it has been shown that various phenolic acids, particularly cinnamic acid derivatives, prevent some of these effects. In the present study, the design and synthesis of three esters of ferulic acid, analogues of the octyl methoxycinnamate (OMC), one of the most commercially used filters, are presented. The esters were evaluated for their photoprotective activity against UVA and UVB radiation. The ester 3b exhibited an SPF of 9.22 and a λ_c value of 343.9, higher than the values of OMC (SPF value: 8.19, λ_c value: 337.7). The development and optimization of a novel encapsulation process of the synthesized esters in nanostructured lipid carriers (NLCs) and coating of the NLCs with chitosan was also performed. The optimization of the coating processes was performed using a Box–Behnken experimental design. The optimal nanosystems exhibited a size of 117.0 ± 5 nm, enhanced stability in dispersion, and 78% encapsulation efficiency. The nanoparticles were characterized by ATR/FT–IR, TGA, and TEM. Incorporation of the nanoparticle dispersions in a sunscreen formulation increased the SPF factor of the formulation up to 48%. The esters and nanosystems also showed a satisfactory ability to inhibit the peroxidation of linoleic acid (AAPH induced lipid peroxidation assay) (74–91% inhibition). Full article

In this work, the associative behavior of Gum Arabic in aqueous solutions was investigated through dynamic light scattering, nuclear magnetic resonance, and transmission and scanning electron microscopy. It was shown that in small associates, the spherical polysaccharide units have predominant sizes of 2–8 and 9–20 nm. The average hydrodynamic diameter of diffusing structural units, calculated on the basis of NMR experiment, turned out to be close to 20 nm, which corresponds with electron microscopy data. Based on geometric considerations and the composition and supramolecular structure of Gum Arabic, we calculated the parameters of branched chains of Gum Arabic. A possible “crown” model of polysaccharide chain association into spherical blocks is presented. The developed model allowed us to describe the effects observed during the time-extended association of Gum Arabic particles (molecules) in aqueous solutions, leading first to blocks’ swelling, then the appearance of local gelation, and only then to the creation of dense protective layers on the surfaces. It was established that the tendency of amphiphilic Gum Arabic molecules to form complexes both among themselves and with various surfaces and the possibility of forming viscous gel-like layers on the interfaces underly its use in many natural, food, technical, and technological applications, including emulsification. Full article

Additive manufacturing (AM) demands materials that combine precise printability with reliable thermal and mechanical performance. Polyglycerol (PG)-based macromolecular systems offer exceptional tunability through controlled architecture and chemical modification, enabling their use across both light-based and extrusion AM platforms. Strategic enhancements such as chemical functionalization, network formation, and hybrid reinforcement have expanded their capabilities from biomedical to structural applications, delivering improved stability, strength, and functionality. Despite these advances, performance-processing trade-offs and dispersion challenges remain barriers to widespread adoption. This review synthesizes current knowledge on PG-based materials in AM, mapping key structure-property-processing relationships and identifying strategies to advance their development as versatile and sustainable options for next-generation manufacturing. Full article

In an era defined by the imperative for sustainable, high-performance materials, this review examines the development and utility of key ester and ether derivatives from both cellulose and hemicellulose sourced from lignocellulosic biomass, with a special emphasis on waste feedstocks. Our findings indicate that these derivatives exhibit tunable physicochemical properties, enabling their broad use in established industrial sectors while also fueling the emergence of novel technological applications in nanotechnology, controlled delivery, tissue engineering, environmental remediation, electronics, and energy fields. This dual-polysaccharide platform demonstrates that underutilized biomass streams can be repurposed as valuable feedstocks, promoting a circular supply chain and supporting more sustainable solutions, thereby aligning with the goals of eco-friendly innovation in materials science. Future progress will likely depend on integrating green chemistry synthesis routes, optimizing waste-to-product conversion efficiency and scalability, and engineering derivatives for multifunctional performance, thus bridging the gap between commodity-scale use and high-tech material innovation. Full article

The present study focuses on the extraction, characterisation, and functional properties of pectin-like polymers from tomatoes. The results revealed that the highest pectin yield (35.5%) of the dry weight was extracted at pH 1, whilst the lowest yield (25.4%) was extracted at pH 3. Fourier Transform Infrared (FTIR) spectra displayed major peaks at 2900–3300 cm⁻¹ and 900–1100 cm⁻¹, which are typical of carbohydrate polymers. A compositional analysis revealed the presence of six monosaccharides (glucose, arabinose, fucose, galactose, mannose, and galacturonic acid) together with trace amounts of xylose, which are typical of pectin (or pectin-like) structures. This suggests that the pectin-like polymers have galactan and/or arabinan side chains. The emulsifying activities and stabilities were ≥50% and ≥96%, respectively. The pectin-like polymers also demonstrated notable antioxidant activities (70%) when determined using the 1-diphenyl-2-picrylhydrazyl (DPPH) assay. Full article

The most significant barrier against biopolymers’ commercialization is their sensitivity to external factors and poor material properties. In recent years, significant progress has been made to enhance these materials so that they are able to provide their unique physiological benefits while maintaining acceptable material performance. As these materials have developed, so too has their application in the food and medical industry, which often requires them to undergo sterilization. Sterilization is a process in which all microbial life and spores are removed from the surface and within materials and is a regulatory requirement for some food packaging products and all medical applications. Sterilization is carried out primarily using radiation, chemical, and heat treatment, which are all effective in disrupting cell regulation and causing cell death. These processes are known to induce structural and/or chemical changes in materials as well as potential migratory or leaching effects. This review aims to provide a comprehensive evaluation of these sterilization processes and the effects they have on polysaccharides, while established data is discussed that provides insight into their market viability post-sterilization and the importance of further characterization using sterilization. Full article

The rise in antifungal resistance among Candida species has prompted the search for alternative therapies, including plant-derived lectins with antimicrobial properties. This study evaluated the antifungal activity of Microgramma vacciniola frond lectin (MvFL) against clinically relevant Candida species and Nakaseomyces glabratus. MvFL exhibited fungistatic activity, with the lowest minimum inhibitory concentrations (MICs) of 0.625 μg/mL for N. glabratus and 1.25 μg/mL for Candida krusei. The minimal fungicidal concentrations (MFC) were not detected, indicating they are above 80 µg/mL. MvFL significantly reduced N. glabratus proliferation, disrupted lysosomal integrity, and affected mitochondrial membrane potential, indicating interference with key cellular processes. MvFL showed minimal activity against biofilm formation, only reducing Candida tropicalis biofilms at a subinhibitory concentration. Combination assays revealed additive or synergistic effects with fluconazole for C. krusei, C. tropicalis, and notably Candida parapsilosis, while antagonism was observed against Candida albicans and N. glabratus. These findings underscore the species-specific nature of lectin-drug interactions and the importance of evaluating such combinations carefully. Overall, MvFL demonstrates significant antifungal potential, particularly as an adjuvant to existing treatments. Its ability to inhibit growth and disrupt cellular function in yeasts supports the development of plant lectins as novel, safer antifungal agents in response to the growing challenge of antifungal resistance. Full article

Cancer represents a leading cause of mortality globally, with its complex biological nature posing significant challenges for treatment. Central to cancer progression are molecular pathways that govern cellular function, among which protein phosphatase 2A (PP2A) plays a vital role. As a serine/threonine phosphatase, PP2A maintains cellular homeostasis by dephosphorylating a broad range of protein substrates and has emerged as a key tumor suppressor. However, PP2A activity can be physiologically inhibited by endogenous regulators such as the SE Translocation (SET) protein. Overexpression of SET has been associated with the loss of PP2A function, promoting hallmark features of cancer. Interestingly, targeting the PP2A/SET interaction has shown therapeutic potential. Indeed, inhibiting SET to reactivate PP2A may restore cellular regulation, induce apoptosis in tumor cells, and attenuate cancer progression. Research efforts have explored compounds such as the endogenous D-erythro-C18-ceramide and the drug fingolimod (FTY720), both known for their ability to reactivate PP2A. In this work, PP2A/SET complex models were generated through a computational approach and, using molecular docking, the interaction of potential SET inhibitors from a library of 26 alkoxy phenyl 1-propan-one derivatives (APPDs) was characterized. Additionally, absorption, distribution, metabolism, and excretion (ADME) predictions were performed to assess pharmacokinetic properties and therapeutic potential. Eventually, the predicted binding affinities were then correlated with biological data to assess the reliability of the models. These findings provide valuable insights into molecule–receptor interactions and lay the groundwork for developing inhibitors with encouraging therapeutic implications. Full article

Compatibilizers that enhance sustainability and improve the miscibility of polymer blend components have garnered significant attention. This study investigates the difference between the synthetic chain extender Joncryl^® ADR 4468 and the natural epoxidized linseed oil (ELO) Merginat 8510100 as compatibilizers for thermoplastic starch/poly (butylene succinate) (TPS/PBS) blends. Blends containing 40% TPS and 60% PBS were prepared with 1, 3, and 5 phr of each compatibilizer, along with a reference with no additives. The properties of these blends were evaluated using tensile testing, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), rheology, and scanning electron microscopy (SEM). The findings indicate that while Joncryl^® ADR 4468 significantly improved tensile strength, it also resulted in a brittle fracture. In contrast, ELO batches exhibited greater ductility, albeit with lower tensile strength. These differences are attributed to the chain extension and minor cross-linking effects of Joncryl^® ADR 4468, compared to the increased chain mobility arising from ELO’s plasticizing and compatibilizing actions. Supporting evidence for these observations includes increased cold crystallization temperature (T_cc) and melting temperature (T_m), greater storage modulus along with higher complex viscosity, strengthened interfacial adhesion, and fewer morphological defects in Joncryl^® ADR 4468 blends. These results highlight the importance of selecting an appropriate compatibilizer based on specific application requirements. Overall, this study addresses the knowledge gap regarding the loadings of Joncryl^® ADR 4468 and ELO in TPS/PBS blends and provides a basis for further optimization strategies, such as the incorporation of binary compatibilizers, alternative grafting-based compatibilizers, and twin-screw blending modifications. Full article

Poly(butylene adipate-co-terephthalate) (PBAT) possesses mechanical properties and processing advantages comparable to low-density polyethylene (LDPE). However, its poor water vapor barrier properties (~2 orders of magnitude lower than LDPE) limit its applications in agricultural films and packaging. In this study, dodecenyl succinic anhydride (DDSA) was employed as a functional comonomer to synthesize DDSA-modified PBAT-based copolyesters (PBADT) with varying compositions via co-esterification and melt polycondensation, and the effects of the hydrophobic alkylene side chain on surface hydrophobicity, water vapor barrier property, and other physical and mechanical properties of PBADT were systematically investigated. Results indicate that the introduction of DDSA significantly enhanced the surface hydrophobicity and water vapor barrier properties of PBAT. As the DDSA content increased from 0 to 55 mol%, the water contact angle increased from 79° to 101°, and the water vapor barrier performance improved by nearly three times. Crucially, due to the chemical bonding of hydrophobic side chains to the main chains, the PBADT films exhibited excellent stability in its water vapor barrier performance under external mechanical friction. Furthermore, DDSA introduction markedly reduced haze and increased light transmittance, demonstrating improved optical clarity. On the other hand, the existence of the long alkylene side chain of DDSA also significantly inhibited the crystallization and mechanical properties of the copolyesters. Full article

Starch is one of the most abundant biopolymers in nature and is widely utilized across various industries, including food, pharmaceuticals, textiles, and packaging. Its attractiveness stems from its renewability, biodegradability, versatility, and abundance in nature. However, native starches have limitations, including poor solubility, thermal instability, retrogradation, and susceptibility to enzymatic degradation. Despite the broad range of applications of starch, challenges persist in optimizing its modifications, addressing cost constraints, and ensuring regulatory compliance in food and pharmaceutical applications. These shortcomings necessitate modifications to enhance their physicochemical and functional properties. Additionally, recent trends indicate a shift towards bioengineered starches with enhanced functional properties, utilizing artificial intelligence for process optimization, and expanded applications in advanced biomaterials to achieve sustainable development goals. Thus, this review delves into the diverse sources of starch, highlighting extraction techniques and comparing their characteristics. Additionally, the review examines various modification strategies and discusses their effects on starch structure, gelation, and industrial applications. Recent advancements in dual-modification approaches, nanotechnology integration, and eco-friendly modification techniques have been examined in the context of sustainable development. Moreover, this review highlights the role of modified starch in various pharmaceutical applications, including drug delivery systems and bioadhesives, as well as its importance in biodegradable plastics, food packaging, wastewater treatment, and bioethanol production. Full article

The growing threat of antimicrobial resistance drives the need for innovative and multifunctional therapeutic systems. In this study, a controlled-release system based on a bioactive film composed of gelatin, bacterial cellulose (BC), sericin, citric acid, PEG 400, and nisin was developed for topical applications in infected wound treatment. BC membranes were produced using Komagataeibacter xylinus and enzymatically treated to optimize dispersion within the polymer matrix. The resulting system exhibited a semi-rigid, homogeneous morphology with appropriate visual characteristics for dermatological use. Microbiological assays demonstrated significant antimicrobial activity against Gram-positive (Staphylococcus aureus) and resistant Gram-negative strains (Escherichia coli and Enterobacter cloacae), attributed to the synergistic action of nisin and citric acid, which enhanced bacterial outer membrane permeability. The antioxidant capacity was confirmed through DPPH radical scavenging assays, indicating a progressive release of bioactive compounds over time. Scanning electron microscopy (SEM) analyses revealed good integration of biopolymers within the matrix. These results suggest that the strategic combination of natural biopolymers and antimicrobial agents produced a functional system with improved mechanical properties, a broadened antimicrobial spectrum, and promising potential as a bioactive wound dressing for the treatment of infected skin lesions. Full article

Biodegradable polyesters have gained attention due to their sustainability benefits, considering the escalating environmental challenges posed by synthetic polymers. Advances in artificial intelligence (AI), including machine learning (ML) and deep learning (DL), are expected to significantly accelerate research in polymer science. This review article explores “bio” polymer informatics by harnessing insights from the AI techniques used to predict structure–property relationships and to optimize the synthesis of bioplastics. This review also discusses PolyID, a machine learning-based tool that employs message-passing graph neural networks to provide a framework capable of accelerating the discovery of bioplastics. An extensive literature review is conducted on explainable AI (XAI) and generative AI techniques, as well as on benchmarking data repositories in polymer science. The current state-of-the art in ML methods for ring-opening polymerizations and the synthesizability of biodegradable polyesters is also presented. This review offers an in-depth insight and comprehensive knowledge of current AI-based models for polymerizations, molecular descriptors, structure–property relationships, predictive modeling, and open-source benchmarked datasets for sustainable polymers. This study serves as a reference and provides critical insights into the capabilities of AI for the accelerated design and discovery of green polymers aimed at achieving a sustainable future. Full article

Carbohydrate-based hydrogels represent a new advancement in the development of multifunctional biomedical systems, thanks to their intrinsic biocompatibility, structural versatility, and capacity for functional modification. This review examines the latest progress made in employing these materials as intelligent theranostic platforms, with a particular focus on their role as biosensors and therapeutic drug delivery devices. Engineered to interact dynamically with the biological environment, carbohydrate hydrogels enable the site-specific release of therapeutic agents while simultaneously supporting the monitoring of key physiological markers. Their dual functionality offers significant advantages in managing complex pathologies such as cancer, metabolic disorders, and chronic inflammation, where personalized treatment and real-time feedback are essential. By exploring their biological application, this review underscores the pivotal role played by carbohydrate hydrogels in advanced therapeutic technologies. Full article

Alginate is a biomaterial that has demonstrated considerable potential and adaptability in the field of controlled drug delivery due to its unique physicochemical properties. Chemical modification of alginate has significantly enhanced its functionality, allowing the development of matrices with improved characteristics, such as increased affinity for hydrophobic drugs, sustained and controlled release, and improved cell and tissue adhesion. Hydrogels, microspheres, nanoparticles, and porous scaffolds are among the most extensively studied alginate-based drug delivery systems. It is estimated that over 50% of these systems have shown successful outcomes in in vitro testing, particularly in applications such as oral delivery of proteins and peptides, wound healing, tissue regeneration, and cancer therapy. Recent clinical advances involving alginate include the development of wound dressings, growth factor delivery systems, and cell-based therapies for treating degenerative diseases. Chemically modified alginate thus emerges as a highly adaptable and promising candidate for the design of advanced drug delivery systems across a wide range of biomedical applications. This review encompasses more than 100 research articles and aims to provide an updated overview of the current state of knowledge regarding the use of chemically modified alginate-based hydrogel systems in drug delivery. Full article

In this study, a series of copolymers was synthesized using the promising biodegradable polymers Poly(L-lactic acid) (PLLA), Poly(lactic-co-glycolic acid) (PLGA), and Poly(ethylene adipate) (PEAd), known for their high potential. PEAd was synthesized through a two-step melt polycondensation process and then used to prepare copolymers with PLLA (PLLA-co-PEAd) and PLGA (PLGA-co-PEAd) at weight ratios of 90/10 and 75/25, respectively. The synthesized materials, along with the starting polymers, were extensively characterized for their structure, molecular weight, crystallinity, and thermal behavior. These novel systems exhibit single thermal transitions, e.g., glass transition. The incorporation of PEAd into the copolymers induced a plasticizing effect, evidenced by a consistent decrease in the glass transition temperature. Due to the latter effect in combination with the M_w drop, the facilitation of crystal nucleation was observed. Finally, the results by dielectric spectroscopy on the local and segmental molecular mobility provided additional proof for the homogeneity of the systems, as manifested, e.g., by the recording of single segmental relaxation processes. Overall, the findings indicate that the PLLA-co-PEAd and PLGA-co-PEAd copolymers hold significant potential, and the use of complementary experimental techniques offers valuable insights and indirect indications of their properties. Full article

Since the mid-19th century, researchers have explored the potential of bio-based polymeric materials for diverse applications, with particular promise in medicine. This review provides a focused and detailed examination of natural and synthetic biopolymers relevant to tissue engineering and biomedical applications. It emphasizes the structural diversity, functional characteristics, and processing strategies of major classes of biopolymers, including polysaccharides (e.g., hyaluronic acid, alginate, chitosan, bacterial cellulose) and proteins (e.g., collagen, silk fibroin, albumin), as well as synthetic biodegradable polymers such as polycaprolactone, polylactic acid, and polyhydroxybutyrate. The central aim of this manuscript is to elucidate how intrinsic properties—such as molecular weight, crystallinity, water retention, and bioactivity—affect the performance of biopolymers in biomedical contexts, particularly in drug delivery, wound healing, and scaffold-based tissue regeneration. This review also highlights recent advancements in polymer functionalization, composite formation, and fabrication techniques (e.g., electrospinning, bioprinting), which have expanded the application potential of these materials. By offering a comparative analysis of structure–property–function relationships across a diverse range of biopolymers, this review provides a comprehensive reference for selecting and engineering materials tailored to specific biomedical challenges. It also identifies key limitations, such as production scalability and mechanical performance, and suggests future directions for developing clinically viable and environmentally sustainable biomaterial platforms. Full article

In recent years, pelvic organ prolapse (POP) cases have been rising, affecting women’s quality of life. Synthetic surgical transvaginal meshes used for POP treatment were withdrawn from the United States market in 2019 due to high risks, including infection, vaginal mesh erosion, and POP reoccurrence. Biodegradable mesh implants with three-dimensional printing technology have emerged as an innovative alternative. In this study, polycaprolactone (PCL) meshes for POP repair were fabricated using melt electrospinning writing (MEW) and mechanically evaluated through uniaxial tensile tests. Following this, they were coated with antibiotics—azithromycin, gentamicin sulfate, and ciprofloxacin—commonly used for genitourinary tract infections. Zone inhibition and biofilm assays evaluated antibiotic effectiveness in preventing mesh infections by Escherichia coli, and methicillin-susceptible (MSSA) and methicillin-resistant (MRSA) Staphylococcus aureus. The meshes presented a mechanical behavior closer to vaginal tissue than commercially available meshes. Fourier transform infrared analysis confirmed antibiotic incorporation. Ciprofloxacin demonstrated antibacterial activity against MRSA, with a 92% reduction in metabolic activity and a 99% biomass reduction. Gentamicin and ciprofloxacin displayed inhibitory activity against MSSA and E. coli. Scanning electron microscopy images support these conclusions. This methodology may offer a more effective, patient-friendly solution for POP repair, improving healing and the quality of life for affected women. Full article

The growing concern for environmental sustainability has led to an increased interest in biodegradable materials derived from renewable resources. This study explores the innovative use of residual biomass from the green photosynthetic microalga Chlamydomonas reinhardtii, left over after polysaccharide extraction, as a natural filler in the development of the compostable protein-based material SP-Milk^®. The microalgal biomass was characterized using Fourier transform infrared spectroscopy (FTIR) and UV-Visible Spectroscopy to assess its chemical and structural composition. Subsequently, it was incorporated into a biodegradable protein matrix, and the resulting biocomposites were evaluated for mechanical and thermal properties. The results demonstrate that the incorporation of algal filler improves the mechanical strength and elasticity of the material while reducing its glass transition temperature, highlighting its potential for use in sustainable applications as a possible substitute for conventional plastics. The biocomposite materials developed, based on the protein-based material SP-Milk^® and residual microalgal biomass, are environmentally friendly, contributing to the reduction in pollution and the risks associated with plastic accumulation. Thus, this study offers a simple, effective, and sustainable strategy for the valorization of microalgal biomass, enabling the production of biodegradable materials with enhanced mechanical performance, suitable for applications such as sustainable packaging within a circular economy framework. Full article