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.

Multifunctional Ti3C2Tx MXene/Silver Nanowire Membranes with Excellent Catalytic, Antifouling, and Antibacterial Properties for Nitrophenol-Containing Water Purification.

The uncontrolled release of nitrophenol and dye pollutants into water systems is an increasingly serious worldwide concern, and thus efficient wastewater treatment technologies are urgently needed. Herein we report a novel two-dimensional (2D) transition metal carbides and/or nitrides (Ti3C2Tx MXene) membrane modified with silver nanowires (AgNWs) by vacuum assisted filtration technology for the ultrafast nitrophenol catalysis and water purification applications. Regular and controllable membrane transport channels were constructed by stacking Ti3C2Tx MXene nanosheets. Furthermore, the intercalation of AgNWs into the Ti3C2Tx MXene interlayer greatly enlarged the interlayer spacing, resulting in more gaps for fast and selective molecular transport. The optimized Ti3C2Tx MXene@AgNWs (M@A) membrane exhibited a water flux up to ∼191.9 L/(m2 h) while maintaining a high bovine serum albumin (BSA) rejection of ∼95.4%. We emphatically used M@A membranes as efficient catalysts for the reduction of 4-nitrophenol (4-NP), and the results indicated that M@A-12% membrane exhibited the greatest catalytic reduction ability, and recycling utilization. M@A-12% membrane also had an antibacterial rate of more than 99% against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). This work provides a possibility to expand the application of 2D multifunctional M@A membranes in wastewater treatment and pollutant catalytic degradation.

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.

Synthesis of a starch-based sulfonic ion exchange resin and adsorption of dyestuffs to the resin.

A starch-based ion exchange resin (SIR) was synthesized by copolymerizing raw starch with sodium methallyl sulfonate and styrene. The structural and surface properties of the SIR were characterized by 13C nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, gel permeation chromatography, scanning electron microscopy, X-ray diffractometry, thermogravimetric analysis, Brunauer-Emmett-Teller surface area analysis, and laser particle size analysis. The SIR was physicochemically and thermally stable and resistant to acids, bases, and enzymes. In static adsorption tests, the SIR had decolorization ratios (DRs) for mixed dyestuffs in wastewater of up to 84.04%, which was higher than the DR for a synthetic ion exchange resin (001 × 7, DR 77.14%). In dynamic adsorption tests, the SIR bed had a DR of 99.85% and a wastewater handling capacity 25 times the column volume. After three adsorption-regeneration cycles, the DR of the resin bed had decreased by <7.5%. The properties of the SIR, particularly the adaptability of the SIR to continuous column adsorption, make the SIR suitable for removing dyestuffs from industrial wastewater and a potential substitute for traditional sorbents such as activated carbon and synthetic resins.

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.

Evaluation of PHBHHx and PHBV/PLA fibers used as medical sutures.

Two types of fibers were prepared by using bio-based materials: a mono-filament made from poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) and a multi-filament made from poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and polylactic acid (PLA) blend. The two fibers were evaluated for mechanical properties, biocompatibility and degradability for the potential application as medical sutures. The PHBHHx fiber showed remarkable biocompatibility by H.E. Stainning, with very little impact to the surrounding tissues. The degradation of the fiber was observed by SEM after implantation for 36 weeks, and the major degradation product was detected after 96 weeks. Consistently, the PHBHHx fiber maintained more than half of the mechanical properties after 96 weeks. The other fiber was prepared by twisting PHBV/PLA blend strands to a bunch, and showed high biocompatibility and relatively high degradability. The bunched structure loosed after 36 weeks of implantation. These low-cost and easily prepared fibers have great potential in medical applications, since they could avoid the formation of fibrous capsule, reduce the size of scar, and degrade into non-toxic and even beneficial products.