ABSTRACT
Cellulose nanocrystals (CNCs) are unique and promising natural nanomaterials that can be extracted from native cellulose fibers by acid hydrolysis. In this study, we developed chemically modified CNC derivatives by covalent tethering of PEGylated biotin and perylenediimide (PDI)-based near-infrared organic dye and evaluated their suitability for labeling and imaging of different cell lines including J774A.1 macrophages, NIH-3T3 fibroblasts, HeLa adenocarcinoma cells, and primary murine dendritic cells. PDI-labeled CNCs showed a superior photostability compared to similar commercially available dyes under long periods of constant and high-intensity illumination. All CNC derivatives displayed excellent cytocompatibility toward all cell types and efficiently labeled cells in a dose-dependent manner. Moreover, CNCs were effectively internalized and localized in the cytoplasm around perinuclear areas. Thus, our findings demonstrate the suitability of these new CNC derivatives for labeling, imaging, and long-time tracking of a variety of cell lines and primary cells.
Subject(s)
Nanoparticles , Nanostructures , Animals , Cellulose , HeLa Cells , Humans , MiceABSTRACT
We report on gelatin films incorporating rosin-grafted cellulose nanocrystals (r-CNCs), which fulfill the most relevant requirements for antimicrobial packaging applications. Transparent gelatin/r-CNCs bionanocomposite films (0.5-6 wt% r-CNCs) were obtained by solution casting and displayed high UV-barrier properties, which were superior to the most used plastic packaging films. The gelatin/r-CNCs films exhibited a moderate water vapor permeability (0.09 g mm/m2 h kPa), and high tensile strength (40 MPa) and Young's modulus (1.9 GPa). The r-CNCs were more efficient in improving the optical, water vapor barrier and tensile properties of gelatin films than conventional CNCs. Grafting of rosin on CNCs resulted in an antimicrobial nanocellulose that inhibited the growth of Staphylococcus aureus and Escherichia coli. The antibacterial properties of r-CNCs were sustained in the gelatin films, as demonstrated by agar diffusion tests and proof-of-principle experiments involving cheese storage. Overall, the incorporation of r-CNCs as active fillers in gelatin films is a suitable approach for producing novel eco-friendly, antimicrobial packaging materials.
Subject(s)
Cellulose/chemistry , Food Packaging , Gelatin/chemistry , Resins, Plant/chemistry , Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Cellulose/pharmacology , Gelatin/chemical synthesis , Gelatin/pharmacology , Humans , Nanoparticles/chemistry , Permeability , Resins, Plant/chemical synthesis , Resins, Plant/pharmacology , Staphylococcus aureus/drug effects , Staphylococcus aureus/pathogenicity , Steam , Tensile StrengthABSTRACT
In this study, continuous casting is proposed as a suitable approach to scale up the production of gelatin-cellulose nanocrystals (CNCs) bionanocomposites. The processing conditions and bionanocomposite properties were established based on the ζ-potential and gelatin content, and CNCs concentration, respectively. Gelatin film-forming solution at 20â¯wt% was required for proper continuous casting processing, leading to a productivity of 0.20â¯m2 film/min, which was at least 1000-fold higher than that of the classical bench casting. The gelatin-CNCs bionanocomposites displayed transparency, flexibility, and improved UV-barrier and thermal properties. Adding only 0.5â¯wt% of CNCs resulted in an increase of 77 % and 48 % in the tensile strength and Young's modulus of gelatin, respectively. Comparison with previous nanocellulose-based nanocomposites pointed out the relatively superior performance of the gelatin-CNCs bionanocomposites obtained by continuous casting for various applications, including flexible food packaging.
