Wounds are highly prone to infection, which can delay healing and lead to severe complications such as gangrene and sepsis. Non-healing wounds significantly impact patients' physical and mental well-being and place a substantial financial burden on healthcare systems. Timely and effective treatment of wound infections is critical, but the rise of antibiotic-resistant pathogens complicates this process. In this study, we investigate a potent protease resistant antimicrobial peptide (AMP), PLNC8 αβ, for the treatment of wound infections and present a strategy for localized AMP delivery using functionalized advanced nanocellulose (NC) wound dressings. Two types of NC dressings were explored: bacterial cellulose (BC) and TEMPO-oxidized nanocellulose derived from wood powder (TC). In a porcine wound infection model, PLNC8 αβ exhibited high antimicrobial activity, successfully eradicating the infection while promoting wound re-epithelialization. To achieve controlled release of PLNC8 αβ from the NC dressings, the peptides were either physisorbed directly onto the nanofibrils or encapsulated within mesoporous silica nanoparticles (MSNs) that were incorporated into the dressings. The PLNC8 αβ functionalized dressings demonstrated low cytotoxicity toward human primary fibroblasts and keratinocytes. Both BC and TC dressings showed efficient contact inhibition of bacteria but were less effective in inhibiting bacteria in suspension. In contrast, MSN-functionalized dressings, displayed significantly enhanced peptide-loading and sustained release capacities, resulting in improved antimicrobial efficacy. These findings highlight the potential of PLNC8 αβ and PLNC8 αβ-functionalized nanocellulose wound dressings for the treatment of infected wounds, offering an effective alternative to conventional antibiotic therapies.

Underutilized co- and by-products are upgraded into materials with functional properties. The utilization of mushroom farming residues is investigated, specifically mushroom residues and spent mushroom substrate – whose chemical composition is determined – to produce cosmetic face masks, packaging films, and oil sorbents. Flexible mushroom sheets exhibit conformability and antioxidant activity between 82 and 94%, and better tensile strength in comparison with commercial cosmetic masks, making them suitable for such applications. Plasticization with glycerol increases the flexibility and tensile strain from ≈1 to 45% and moisture sorption from 32 to 100 wt.%. Spent mushroom substrate pulp yields stiff and strong rigid sheets with Young's moduli of 5 GPa and tensile strengths of 42 MPa. These sheets show 100% antioxidant activity, having hydrophobic behavior and oxygen barrier properties in dry conditions, and thus are promising for bioactive packaging applications. Foamed spent mushroom substrate sorbents demonstrate high affinity for both oil and water, with a water and oil uptake of 21 and 28 times their weight, respectively, while maintaining structural integrity. These properties make the foams viable as bio-based oil sorbents, highlighting the potential of by-products for advanced functional materials.

From an economic and environmental perspective, the use of less chemicals in the production of cellulose nanofibrils (CNFs) is advantageous. In this study, we investigated the oxidation (TEMPO/NaClO2/NaClO, pH 6.8) of softwood (SW) particles with varying amounts of TEMPO (16, 8 or 0 mg g−1 of wood). Following, TEMPO-oxidized SW nanofibrils (TO-SWNFs) were obtained by nanofibrillation and their size, morphology, and crystallite size were assessed. Hydrogel networks of TO-SWNFs were prepared and mechanical properties were measured in dH2O and phosphate buffered saline (PBS) to compare their performance for possible biomedical applications such as wound dressings. The results reveal that the presence of TEMPO is of importance for TO-SWNF network properties, presenting higher eq. H2O absorption (≈2500 %) and elongation at break (≈10 %) with good wet strength (≈180 kPa). In addition, a decrease in use of TEMPO catalyst from 16 to 8 mg g−1 of wood is possible, without detrimental effects on hydrogel network properties (dH2O absorption ≈ 2000 %, elongation at break ≈ 13 %, wet strength ≈ 190 kPa) related to applications as wound dressings.

Cellulose filaments with a unique microtape-like shape (width/thickness ratio ≈ 40) were studied for their potential as reinforcement in bio-epoxy resin with the hypothesis that their gross-sectional geometry would allow for efficient stress transfer and a higher transverse modulus. The microstructure of the spun filaments, orientation of the cellulose fibrils within them, and their mechanical properties were analyzed. Unidirectional (UD) composites with bio-epoxy resin were fabricated using vacuum infusion resulting in filament content of ≈ 23 vol% and low density 1.18 gcm−3.

Wide-angle X-ray scattering showed that the cellulose fibrils were relatively well aligned in the filament axis, having an orientation factor of 0.78. The axial filament modulus was measured to 33 GPa, the in-plane transverse modulus to 12 GPa and the axial strength was approx. 380 MPa. The longitudinal E-modulus of the UD composites was measured to 10 GPa and the strength to 120 MPa, both 3 times higher than the used bio-epoxy agreeing well with the estimated values. The transverse elongation at break of the UD composite was higher than typical values reported for glass-fiber epoxy composites, but the effect of filament shape on the transverse modulus was less significant than the predicted 4.5 GPa but still better than estimated for circular fibers. The lower property is likely due to the low filament content and the partially uneven in-plane filament arrangement. Simulations based on shear stress analysis suggest that the transverse properties of the UD composite could be improved by ensuring that the filament planes remain predominantly parallel in-plane during fabrication, and the overall mechanical properties could be improved by increasing the filament content.

Hierarchically porous, anisotropic, and green carbon aerogels (CAs) prepared from second most abundant and underutilized biopolymer lignin is used together with biobased epoxy resin to prepare green composite materials with superior mechanical properties. Green and facile preparation route involving ice-templating, lyophilization followed by carbonization was followed for the preparation of CAs. Ice-templating cooling rate is an important parameter in determining the porous structure of the CAs and by choosing a slower cooling rate bigger macropores can be achieved which facilitate the capillary impregnation of the epoxy resin through the CA structure. Hence in this study a cooling rate of 5 K/min was used and the CAs were prepared at 1000 °C from lignin/CNF suspensions containing 3, 5 and 7 wt% of total solid contents. Composites prepared using these CAs as reinforcements showed interesting morphologies which were analyzed using scanning electron microscopy and X-Ray microtomography. Prepared composites contained a mass fraction of 5–9 wt% of CAs. Composites showed remarkable 72 % higher dynamic mechanical properties compared to neat epoxy. Thus, this study introduces new synthesis strategy for carbon composites with completely biobased anisotropic CAs as oriented and strong reinforcements.

Wound infections result in delayed healing, morbidity, and increased risks of sepsis. Early detection of wound infections can facilitate treatment and reduce the need for the excessive use of antibiotics. Proteases are normally active during the healing process but are overexpressed during infection as part of the inflammatory response. Proteases are also produced by the bacteria infecting the wounds, making proteases a highly relevant biomarker for infection monitoring. Here, we show a fluorescence turn-on sensor for real-time monitoring of protease activity in advanced nanocellulose wound dressings for rapid detection of wound pathogens. Colloidal gold nanoparticles (AuNPs) were adsorbed on bacterial cellulose (BC) nanofibrils by using a carefully optimized self-assembly process. The AuNPs could either be homogeneously incorporated in BC dressings or 3D printed in wood-derived cellulose nanofiber (CNF) dressings using a BC-AuNP ink. The BC-adsorbed AuNPs were subsequently functionalized with fluorophore-labeled protease substrates. Cleavage of the substrates by proteases produced by the wound pathogens Staphylococcus aureus and Pseudomonas aeruginosa resulted in a significant increase in fluorescence that correlated with the growth phase of the bacteria. Wound dressing with integrated sensors for the detection of proteolytic activity can enable the sensitive and rapid detection of infections, allowing for optimization of treatment and reducing the risks of complications.

Bioflex is a biodegradable polymer blend combining poly(butylene adipate-co-terephthalate) (PBAT) and bio-based poly(lactic acid) (PLA), offering properties comparable to polyethylene. However, challenges like limited processability and low mechanical properties restrict its use to agricultural films. In this study, fibers from end-of-life textiles (polyester, viscose, cotton, and silk) are used to address these limitations, demonstrating a resource-efficient approach to reducing landfill deposits. Adding fibers to the polymer blend (30 wt%) visibly improves the melt strength. The end-of-life fibers affect the mechanical properties in different ways: polyester fibers almost double the tensile strength, viscose fibers triples flexural strength, and silk fibers lead to the highest compressive strength. The retained colors of the fibers further contribute to vibrant composites, making them ideal for cosmetics packaging, household goods, fashion accessories, and toys. Additionally, the composting test revealed varied disintegration behaviors. Cotton and silk began disintegrating first, viscose followed, while polyester showed no disintegration, extending the composite's durability in use. This study highlights the potential of end-of-life textiles as an excellent reinforcement for Bioflex copolymer blends, promoting efficient resource use, reducing environmental waste, and unlocking new application areas for biodegradable polymers.

Biocarbon being a highly demanding renewable source of carbon is important for many applications such as soil enrichment, electronic applications, etc. In this research, sustainable waste biomass-to-energy materials conversion, kinetic, thermodynamic and electronic properties of carbonized forest biomaterials were investigated to evaluate their high-potential in bipolar plate for fuel cell application. In thermogravimetric analysis, the lignin biocarbon showed the least activation energy of 95 KJ/mol compared to 127 and 145 KJ/mol for hardwood and softwood biocarbons respectively. The crystallographic nature of carbonized ligneous and cellulosic biomaterials was also investigated, showing its intrinsic properties and exotic functionality through semi-metallic properties determined from density function theory, transmission electron microscopy and UV–Vis absorption. Finally, the electrochemical properties of bio-carbon composites were examined to prove stability and corrosion resistance comparable to metallic plates. Biocarbon composites showed high polarization resistance up to 5.96 kΩ-cm2 with non-reactive properties, favorable to use in bipolar plates as an alternative to metallic plate which is expensive and prone to corrosion. Overall, sustainable biocarbon shows its ability as a high-performance functional material alternative to expensive nanofillers as well as to enhance the attributes of the bipolar plate composite by increasing connectivity between primary filler and insulating resin.