Cellulose‐Based Nanocomposites in Drug Delivery and Antimicrobial Therapies: Emerging Innovations and Translational Outlook

Exploring acid hydrolysis conditions and extended mechanical processing for producing cellulose nanocrystal and nanofibrils from pineapple leaf fibers.

Plant-derived nanocellulose particles, such as cellulose nanofibrils (CNFs) and cellulose nanocrystals (CNCs), are becoming increasingly popular for a wide range of applications. In particular, when they are employed as rheology modifiers and/or fillers, a choice between CNFs and CNCs is often not obvious. Here, we present the results of a comparative study on the rheological properties of suspensions and gels of carboxymethylated CNFs and CNCs with the same surface chemistry, surface density of charged groups, and thickness. We demonstrate that, at the same weight concentration, CNF suspensions have much higher viscosity and storage modulus, which is due to their longer length providing many entanglements. However, when comparing at the same nanoparticle concentration relative to C*, the situation is reversed: viscosity and storage modulus of CNCs appear to be much higher. This may be due in particular to the higher rigidity and intrinsic strength of highly crystalline CNCs. The gel points for CNF and CNC suspensions (without crosslinker) were compared for the first time. It was found that in the case of CNFs, the gel point occurs at a 3.5-fold lower concentration compared to that of CNCs. Hydrogels were also obtained by crosslinking negatively charged nanocellulose particles of both types by divalent calcium cations. For the first time, the thermodynamic parameters of the crosslinking of carboxymethylated CNFs by calcium ions were determined. Isothermal titration calorimetry data revealed that, for both CNFs and CNCs, crosslinking is endothermic and driven by increasing entropy, which is most likely due to the release of water molecules surrounding the interacting nanoparticles and Ca2+ ions. The addition of CaCl2 to suspensions of nanocellulose particles leads to an increase in the storage modulus; the increase being much more significant for CNCs. Physically crosslinked hydrogels of both CNFs and CNCs can be reversibly destroyed by increasing the shear rate and then quickly recover up to 85% of their original viscosity when the shear rate decreases. The recovery time for CFC networks is only 6 s, which is much shorter than that of CNC networks. This property is promising for various applications, where nanocellulose suspensions are subjected to high shear forces (e.g., mixing, stirring, extrusion, injection, coating) and then need to regain their original properties when at rest.

Recent progress in nanocellulose-based biocomposites for bone tissue engineering and wound healing applications.

Bacterial nanocellulose is a promising biomaterial extensively used in functional foods and for drug delivery. Moreover, its characteristics can further be potentialized whether coupled with natural bio-extracts to endow antibacterial activity. Persea americana or avocado seed extracts are rich in phytochemicals and have demonstrated their antioxidant, antimicrobial and enzymatic activities, therefore encapsulating them into bacterial nanocellulose (BNC) may offer a potential release system of antibacterial avocado seed compounds. Accordingly, this study explores the in-depth insight into the influence of different bacterial nanocellulose producing strains ( Komagataeibacter hansenii and Komagataeibacter xylinus ) and cultivation conditions (static and dynamic cultivation, fermentation time) on the bacterial nanocellulose productivity and characteristics. The obtained bacterial nanocellulose membranes and beads were characterized in terms of chemical structure, morphology and crystallinity. More profitable and productive K. xylinus was further selected for encapsulation (up to 72.89 mg) of avocado seed extracts into bacterial nanocellulose membranes and beads in order to comprehensively evaluate the kinetic release profiles and determine their antibacterial activity against Escherichia coli and Staphylococcus aureus. Results of the study show that the bacterial nanocellulose and avocado seed extracts biohybrids represent a promising immediate (up to 17.39 mg in 1 h) and sustained (up to 35.04 mg in 48 h) release systems. Kinetic release modeling and cytotoxicity assessments confirmed controlled release behavior and biocompatibility for safe antibacterial applications in cosmetics, functional foods and drug delivery.

Cellulose is the most venerable and essential natural polymer on the planet and is drawing greater attention in the form of nanocellulose, considered an innovative and influential material in the biomedical field. Because of its exceptional physicochemical characteristics, biodegradability, biocompatibility, and high mechanical strength, nanocellulose attracts considerable scientific attention. Plants, algae, and microorganisms are some of the familiar sources of nanocellulose and are usually grouped as cellulose nanocrystal (CNC), cellulose nanofibril (CNF), and bacterial nanocellulose (BNC). The current review briefly highlights nanocellulose classification and its attractive properties. Further functionalization or chemical modifications enhance the effectiveness and biodegradability of nanocellulose. Nanocellulose-based composites, printing methods, and their potential applications in the biomedical field have also been introduced herein. Finally, the study is summarized with future prospects and challenges associated with the nanocellulose-based materials to promote studies resolving the current issues related to nanocellulose for tissue engineering applications.

ABSTRACTThis review on bioactive Hydrogels (Bio‐HyGs) synthesizes current advancements in their design and utilization, particularly emphasizing their roles in drug delivery and wound healing. Bio‐HyGs, including gelatin methacrylate (GM), polyethylene glycol (PEG), and poly(vinyl alcohol) (PVA), are highlighted for their effectiveness in treating chronic wounds like diabetic and pressure ulcers, leveraging their moisture retention and tissue regeneration capabilities. These hydrogels are designed for the controlled release of bioactive compounds such as vascular endothelial growth factor (VEGF) and platelet‐derived growth factor (PDGF), thereby facilitating healing without the need for initial cell seeding. The review also covers hydrogels embedded with antimicrobial agents like silver nanoparticles and quaternized chitosan, which are crucial for managing infected wounds. Additionally, advancements in thermoresponsive hydrogels that respond to temperature changes and the application of self‐assembling peptides and 3D printing are discussed for their contributions to mimicking biological tissues, which enhance both drug delivery and wound healing. The review aims to provide a comprehensive understanding of structural and functional modifications in Bio‐HyGs, exploring their potential in transforming clinical outcomes in wound treatment and drug delivery systems.

Nanocellulose, a versatile platform: From the delivery of active molecules to tissue engineering applications

Porous nanocellulose gels and foams: Breakthrough status in the development of scaffolds for tissue engineering

Recent advances in nanoengineering cellulose for cargo delivery

14 - Nanocellulose nanocomposites for biomedical applications

ABSTRACTNanocellulose materials have undergone rapid development in recent years as promising biomedical materials because of their excellent physical and biological properties, in particular their biocompatibility, biodegradability, and low cytotoxicity. Recently, a significant amount of research has been directed toward the fabrication of advanced cellulose nanofibers with different morphologies and functional properties. These nanocellulose fibers are widely applied in medical implants, tissue engineering, drug delivery, wound‐healing, cardiovascular applications, and other medical applications. In this review, we reflect on recent advancements in the design and fabrication of advanced nanocellulose‐based biomaterials (cellulose nanocrystals, bacterial nanocellulose, and cellulose nanofibrils) that are promising for biomedical applications and discuss material requirements for each application, along with the challenges that the materials might face. Finally, we give an overview on future directions of nanocellulose‐based materials in the biomedical field. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41719.

Nanocellulose: Preparation, Functionalization and Applications

Nanocellulose obtained from renewable and abundant biomass has garnered significant attention as a sustainable material with exceptional properties and diverse applications. This review explores the key aspects of nanocellulose, focusing on its extraction methods, applications, and future prospects. The synthesis of nanocellulose involves mechanical, chemical, and biological techniques, each uniquely modifying the cellulose structure to isolate cellulose nanocrystals (CNCs), cellulose nanofibers (CNFs), or bacterial nanocellulose (BNC). These methods provide tailored characteristics, enabling applications across a wide range of industries. Nanocellulose’s remarkable properties, including high mechanical strength, large surface area, thermal stability, and biodegradability, have propelled its use in packaging, electronics, biomedicine, and environmental remediation. It has shown immense potential in enhancing the mechanical performance of composites, improving water purification systems, and serving as a scaffold for tissue engineering and drug delivery. However, challenges related to large-scale production, functionalization, regulatory frameworks, and safety concerns persist, necessitating further research and innovation. This review emphasizes the need for sustainable production strategies and advanced functionalization techniques to harness nanocellulose’s full potential. As an eco-friendly, high-performance material, nanocellulose presents a promising avenue for addressing global sustainability challenges while offering transformative solutions for various industries.

The aim of the study was to characterize and compare films made of cellulose nanocrystals (CNC), nano-fibrils (CNF), and bacterial nanocellulose (BNC) in combination with chitosan and alginate in terms of applicability for potential food packaging applications. In total, 25 different formulations were made and evaluated, and seven biopolymer films with the best mechanical performance (tensile strength, strain)—alginate, alginate with 5% CNC, chitosan, chitosan with 3% CNC, BNC with and without glycerol, and CNF with glycerol—were selected and investigated regarding morphology (SEM), density, contact angle, surface energy, water absorption, and oxygen and water barrier properties. Studies revealed that polysaccharide-based films with added CNC are the most suitable for packaging purposes, and better dispersing of nanocellulose in chitosan than in alginate was observed. Results showed an increase in hydrophobicity (increase of contact angle and reduced moisture absorption) of chitosan and alginate films with the addition of CNC, and chitosan with 3% CNC had the highest contact angle, 108 ± 2, and 15% lower moisture absorption compared to pure chitosan. Overall, the ability of nanocellulose additives to preserve the structure and function of chitosan and alginate materials in a humid environment was convincingly demonstrated. Barrier properties were improved by combining the biopolymers, and water vapor transmission rate (WVTR) was reduced by 15–45% and oxygen permeability (OTR) up to 45% by adding nanocellulose compared to single biopolymer formulations. It was concluded that with a good oxygen barrier, a water barrier that is comparable to PLA, and good mechanical properties, biopolymer films would be a good alternative to conventional plastic packaging used for ready-to-eat foods with short storage time.

Nanostructured materials made through flow-assisted assembly of proteinaceous or polymeric nanosized fibrillar building blocks are promising contenders for a family of high-performance biocompatible materials in a wide variety of applications. Optimization of these processes relies on improving our knowledge of the physical mechanisms from nano- to macroscale and especially understanding the alignment of elongated nanoparticles in flows. Here, we study the full projected orientation distributions of cellulose nanocrystals (CNCs) and nanofibrils (CNFs) in confined flow using scanning microbeam SAXS. For CNCs, we further compare with a simulated system of dilute Brownian ellipsoids, which agrees well at dilute concentrations. However, increasing CNC concentration to a semidilute regime results in locally arranged domains called tactoids, which aid in aligning the CNC at low shear rates, but limit alignment at higher rates. Similarly, shear alignment of CNF at semidilute conditions is also limited owing to probable bundle or flock formation of the highly entangled nanofibrils. This work provides a quantitative comparison of full projected orientation distributions of elongated nanoparticles in confined flow and provides an important stepping stone towards predicting and controlling processes to create nanostructured materials on an industrial scale.