Collagen/functionalized cellulose nanofibril composite aerogels with pH-responsive characteristics for drug delivery system.

In this work, carboxylated and amination modified cellulose nanofibrils (CNFs) were fabricated via the TEMPO catalytic oxidation system and diethylenetriamine, and collagen composite aerogels were fabricated through a simple self-assembly pretreatment and directional freeze-drying technology. Morphology analysis showed that the collagen composite aerogels had distinct layered-oriented double network structures after the self-assembly pretreatment. The intermolecular interactions between the collagen fibrils and functionalized CNFs (fCNFs) on the structures and properties of the composite aerogels were also examined through various characterization techniques. Water contact angle tests demonstrated the pH-responsive characteristics of the collagen/fCNF composite aerogels. Using 5-fluorouracil as the model drug, the pH-response mechanism was revealed. These results indicated that the collagen/fCNF composite aerogels exhibited excellent pH-responsive drug release capacities. Therefore, these pH-responsive collagen composite aerogels might have potential applications in industrial production in the biomedical, drug delivery, and tissue engineering fields.

Self-assembly of collagen fibrils on graphene oxide and their hybrid nanocomposite films.

In order to explore the distribution, conformation and interaction of collagen on GO nanosheet surfaces, the mechanism of self-assembly of collagen was investigated in the presence of GO nanosheets. Atomic force microscopy (AFM) was employed to observe the conformation of self-assembled collagen fibrils on the GO nanosheets surfaces. The collagen concentration and incubation time mainly affect the size of the collagen fibrils while the pH of the dispersion determines the self-assembly sites of collagen fibrils on the GO nanosheets surfaces. This pH-dependent adsorption is attributed to the interfacial interactions between the tunable ionization of the collagen molecules and the amphiphilic GO nanosheets. Vacuum-assisted self-assembly technology confirmed that GO nanosheets can direct the self-assembly of collagen molecules and form nacre-like nanocomposites. The GO/collagen nanocomposite films combine the remarkable properties of GO nanosheets and collagen to form functional nanocomposites with well-ordered hierarchical structures. Further, strong interfacial interactions between GO nanosheets with collagen fibrils result in enhanced mechanical properties and biocompatibility of nanocomposite films, which is conducive to enhance the neuronal differentiation of SH-SY5Y cells. Overall, this work provides fresh insight into the interactions between GO and collagen, which is essential for the design and manufacture of bioinspired nanocomposites with tailored mechanical properties.

Effects of the aspect ratio of multi-walled carbon nanotubes on the structure and properties of regenerated collagen fibers.

Collagen is a natural one-dimensional nanomaterial. Multi-walled carbon nanotubes (MWNTs) have been previously shown to interact with biomolecules and to have promising applications in reinforced biopolymers for tissue engineering and regenerative medicine. In this work, collagen/MWNT composite fibers are prepared using dry-jet wet-spinning technology. Three types of MWNTs with aspect ratios of 40, 150, and 4000 are used to investigate the effects of the MWNT aspect ratio on the properties of the composite fibers. There results show that there are strong molecular interactions between the MWNTs and collagen molecules. The mechanical properties and thermal stability of the composite fibers are significantly improved compared to those of the collagen fibers. The diameter and aspect ratio of the MWNTs are the main factors affecting the self-assembled structure of the collagen molecules, the alignment of the microfibrils, and the mechanical and thermal performance of the composite fibers.