Evaluation of a novel nano-size collagenous matrix film cross-linked with gallotannins catalyzed by laccase.

The effect of hydrolysis degree of gallotannins (GT, 1 mg/g) on cross-linking of nano-size collagen catalyzed by laccase (12 U/g) was studied, and the antibacterial properties of GT hydrolysates (HGT)-laccase (Lac) collagen films on minced cod were also investigated. The results showed that the tensile strength of HGT-Lac films (87.23-100.77 MPa) was higher than those added HGT alone (85.59-95.58 MPa) under the same hydrolysis degree of GT. Compared to the denaturation temperature (78.05 °C) of pure nano-size collagen film without addition of HGT and laccase, the denaturation temperature of HGT (80.75-86.30 °C) and HGT-Lac (91.97-101.64 °C) films increased greatly, especially for HGT-Lac films. Moreover, both HGT and HGT-Lac films showed some mild antibacterial properties for minced cod during storage at 4 °C for 8 days. Therefore, the combination of HGT and laccase could improve the performance of nano-size collagen film and extend the application of collagen in biodegradable/edible packaging.

Incorporation of gelatin improves toughness of collagen films with a homo-hierarchical structure.

In this study, gelatin (type A and type B) with/without transglutaminase (TGase) were added to collagen fiber films to form hierarchical structure and its effects on the film were investigated. The analysis of mechanical properties indicate that gelatin significantly increased the toughness of the collagen film, where the 10 wt% type A gelatin -contained films had highest tensile strength, elongation at break and work of fracture. However, TGase crosslinking compromised the benefits of type A gelatin greatly, while type B gelatin showed a slight improvement, due to the difference in crosslinking activity between them. In the meantime, the hydrogen bonds were formed between the collagen and gelatin according to the results of the Fourier transformation infrared. In general, it is expected that the hierarchical structure formed in the collagen/gelatin films can be used as an effective strategy to enhance the collagen matrix films' mechanical properties.

Using cellulose nanofibers to reinforce polysaccharide films: Blending vs layer-by-layer casting.

Based on the electrostatic interaction mechanism, cellulose nanofiber (CNF) was utilized as reinforcing additives to fabricate polysaccharide films (alginate (Alg) or chitosan (CH)) by two methods: blending and layer-by-layer (LbL). Results showed that the addition of CNF led to higher tensile strength for all films than those without CNF addition, except for the blending CH film due to CNF agglomeration. The highest TS reached 140 MPa for the blending Alg film at 7 wt% CNF. Moreover, all CNF-reinforced films generally had lower water vapor permeability. The addition of CNF aggravated the opacity of all films, especially for the blending ones. Microstructure indicated that CNF were well dispersed in Alg-based films while aggregates were evident in the blending CH films. Interactions between CNF and Alg (or CH) and their relations on film performance were supported by FTIR and DSC of the resultant films, zeta-potential and turbidity of the film-forming solutions.

A top-down approach to improve collagen film's performance: The comparisons of macro, micro and nano sized fibers.

The severe reduction of mechanical strength of collagen once it is extracted or dissociated from animal tissues and no additional crosslinking approaches are conducted, impede its application in biodegradable and edible food packaging. Here, for the first time, high pressure homogenization (HPH) was used to prepare diverse sized fibers and the related fibers-composed films' performance were investigated. These fibers have a diversity of effects on film performance. The films prepared with smaller sized fibers had a more uniform and denser structure. The mechanical and the water barrier properties of the films improved significantly as the fiber size decreased. No obvious change in FTIR and thermal properties suggests that the improved film performance is mainly attributed to the physical entanglement and non-covalent bonds. Given the forementioned benefits of the films, control of fiber size can be a potential industrial approach for producing collagenous materials in edible food packaging.

Metal ions increase mechanical strength and barrier properties of collagen-sodium polyacrylate composite films.

From the previous experiment, it was confirmed that the incorporation of 0.3 wt% sodium polyacrylate (PAAS) into collagen (Co) fibers can improve the mechanical properties and thermal stability of the composite films. In this study, Ca2+, Fe3+ and Ag+ ranging 0.001-0.004 mol/g were used to improve the properties of Co-PAAS blend films based on the rationale of their potential electrostatic interaction with these biopolymers. As expected, Zeta-potential film-forming solutions was decreased to some extent with the addition of metal ions. SEM images presented that the surface of the composites became coarser and internal structure became more stratified as metal ion contents increased. Tensile strength was increased by the addition of these ions with a varied optimal concentration: Ca2+ (0.003 mol/g), Fe3+ (0.002 mol/g) and Ag+ (0.001 mol/g). Water vapor permeability (WVP), solubility and light transmission value of films while causing film thickness no obvious change. In addition, the differential scanning calorimetry (DSC) and thermo-gravimetric analysis (TGA) results indicated that the metal ions improved the thermal stability of the composite film. Therefore, Ca2+, Fe3+ and Ag+ with an appropriate addition amount can be used as a potential alternative to reinforce collagenous composite materials.