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Most of the series of nanochitins have been produced by the break-down process. In this study, chitin nanoparticles were prepared by a bottom-up process. Chitin was treated with sodium hydroxide to obtain an alkaline chitin aqueous solution. The alkaline chitin was regenerated by neutralization and then vigorously stirred to obtain chitin nanoparticles. The average particle size of the chitin nanoparticles was 7 nm. The individual particles were stably dispersed in water. Chitin nanoparticles had lower crystallinity than the raw material chitin and the surface of the chitin nanoparticles regenerated in water were presumed to be hydrophilic. The low crystallinity and the high hydrophilicity of the surface contributed to the high dispersibility of the chitin nanoparticles in water. Chitin nanoparticles had higher heat resistance than the raw material chitin, suggesting a large change in the higher-order structure associated with dissolution and subsequent regeneration of chitin. Since chitin nanoparticles interact with each other less than chitin nanofibers produced by mechanical treatment, the viscosity of nanoparticles was smaller than that of nanofibers. Therefore, it can be prepared at a high concentration. In addition, the chitin nanoparticles can be easily redispersed in water after being concentrated by centrifugation.

In this study, maleated chitin nanofibers (MCNFs)-poly (vinyl alcohol) (PVA) composite films were fabricated to evaluate the reinforcement effect of MCNFs to PVA. Maleated chitin nanofibers (MCNFs) were prepared by esterification of α-chitin powder with maleic anhydride and 2 passes grinder treatment. The average diameter of MCNFs was about 10 nm. The PVA-MCNF composites films were prepared by solution casting technique at 0, 1, 3, 5, 10 and 15 wt% of MCNFs. The FTIR and XRD analyses revealed that, there were strong interaction between MCNFs and PVA. The nanocomposite films displayed nearly similar transparency level of PVA film suggesting that the MCNFs were dispersed at the nanoscale range. Both the DSC and TGA analyses have shown that, thermal stability of PVA was significantly enhanced upon inclusion of MCNFs. The tensile testing data also indicated that, the Young’s modulus, tensile strength, elongation at break and toughness of PVA were increased by 71.87%, 41.47%, 49.10% and 261.20%, respectively through incorporation of 3 wt% MCNFs into the PVA matrix. The maximum swelling index of PVA film in deionized water (195%) was reduced to 141% for 3 wt% MCNFs containing composite film. The strong interfacial interactions between MCNFs and PVA were the decisive factors for the betterment of PVA properties. Generally, this study demonstrates a substantial approach in making thermo-mechanically stable and less water sensitive biodegradable nanocomposite films to be applied in making flexible packaging and biomedical materials.

Chitin, an N-acetyl-D-glucosamine polymer, has been known to enhance plant growth. However, this polysaccharide has not been used extensively in experimental work or agriculture practices because its hydrophobic nature makes it difficult to handle. Chitin nanofiber (CNF), which disperses well in water, can feasibly be used to evaluate the effect of chitin on the promotion of plant growth. In this study, we analysed the contents of inorganic elements and global gene expression to obtain an overview of the growth-promoting action of chitins in plants. Significant increases in the biomass of aerial parts and concentration of chlorophyll following treatment with CNF or short-chain chitin oligomers were observed in tomatoes that were hydroponically cultivated under ultralow nutrient concentrations. The results of the quantification of inorganic elements demonstrated that concentrations of nitrogen and carbon significantly increased in whole tomato plant under chitin treatment. Transcriptome analysis of CNF-treated tomatoes by RNA sequencing showed that the expression levels of genes related to nitrogen acquisition and assimilation, nutrient allocation and photosynthesis were altered. These results indicate that the growth-promoting action of chitin treatment is caused by an improvement in nitrogen uptake efficiency and that CNF could be a useful material for nutrient management in tomato production.

Fish collagen peptide (FCP) is a water-soluble polymer with easy accessibility, bioactivity, and reactivity due to its solubility. The gelation of FCP can be carried out by chemical crosslinking, but the mechanical strength of FCP hydrogel is very low because of its intrinsically low molecular weight. Therefore, the mechanical properties of FCP gel should be improved for its wider application as a biomaterial. In this study, we investigated the mechanical properties of M-FCP gel in the context of understanding the influence of chitin nanofibers (CHNFs) on FCP hydrogels. FCP with a number average molecular weight (Mn) of ca. 5000 was reacted with glycidyl methacrylate (GMA) and used for the preparation of photocrosslinked hydrogels. Subsequently, composite hydrogels of methacrylate-modified FCP (M-FCP) and CHNF were prepared by the photoirradiation of a solution of M-FCP containing dispersed CHNF at an intensity of ~60 mW/cm2 for 450 s in the presence of 2-hydroxy-1-[4-(hydroxyethoxy)phenyl]-2-methyl-1-propanone (Irgacure 2959) as a photoinitiator. Compression and tensile tests of the FCP hydrogels were carried out using a universal tester. The compression and tensile strength of the hydrogel increased 10-fold and 4-fold, respectively, by the addition of 0.6% CHNF (20% M-FCP), and Young’s modulus increased 2.5-fold (20% M-FCP). The highest compression strength of the M-FCP/CHNF hydrogel was ~300 kPa. Cell proliferation tests using fibroblast cells revealed that the hydrogel with CHNF showed good cell compatibility. The cells showed good adhesion on the M-FCP gel with CHNF, and the growth of fibroblast cells after 7 days was higher on the M-FCP/CHNF gel than on the M-FCP gel without CHNF. In conclusion, we found that CHNF improved the mechanical properties as well as the fibroblast cell compatibility, indicating that M-FCP hydrogels reinforced with CHNF are useful as scaffolds and wound-dressing materials.

Honeycomb-like porous chitosan (CS) films are attractive tools for developing functional materials for filters, catalyses, adsorbents, biomaterials, etc. A simple method for fabricating honeycomb-like porous CS films without special reagents, facilities, and techniques would make them accessible. Here we introduce an easily available method for fabricating honeycomb-like CS films without a strong acid/base, toxic reagents, or special facilities/techniques. An aqueous solution containing CS and poly(N-isopropylacrylamide) (PNIPAm) was allowed to stand at 25 °C to evaporate water. After 3 days, CS–PNIPAm composite films with homogenously phase-separated PNIPAm particles were obtained. The PNIPAm particles were removed by immersion in methanol, and the resulting films dried under reduced pressure to become honeycomb-like porous CS films. The pore size could be varied in the range of 0.5–3.0 μm by altering the CS concentration and the molecular weight of CS where the pore size was reduced under conditions with stronger interaction between CS molecules. We reveal that the key to success with this system is the decrease of lower critical solution temperature (LCST) of PNIPAm with water evaporation. In addition, we confirmed the removed PNIPAm was recyclable in this system. Furthermore, we found this method was also applicable to alginate. The proposed facile method for fabricating honeycomb-like porous polymeric films could provide various functional porous materials.

In this study, the effects of chitosan and surface-deacetylated chitin nanofibrils (SDACNFs) on hair growth were evaluated. In human follicle dermal papilla cells in vitro, chitosan and SDACNFs were shown to increase cell growth on day 3 after the initiation of treatment, together with an increase in the production of fibroblast growth factor-7 (FGF-7) by these cells on day 3. Furthermore, in an in vivo study in mice, chitosan and SDACNF application promoted hair growth. The number of anagen follicles significantly increased compared with that in the control group, whereas the number of telogen follicles significantly decreased in the chitosan and SDACNF groups. In the chitosan and SDACNFs groups, moreover, the expression levels of FGF-7 and Sonic hedgehog were significantly upregulated in hair follicles. Overall, our results demonstrated that chitosan and SDACNFs promoted hair growth and therefore may have applications as novel therapeutic agents for the treatment of hair loss in patients.

Pelleted preparations were formulated from sacran (Sac), an anionic, sulfated, carboxyl-containing polysaccharide, which is extracted from the Japanese indigenous cyanobacterium Aphanothece sacrum, and surface-deacetylated chitin nanofibers (SDACNF). The use of this material as an extended-release excipient for tetrahydrocurcumin (THC), a model drug that is used to treat wounds via its radical scavenging ability was examined. The THC used in the study was complexed with 2-hydroxypropyl-β-cyclodextrin (HP-β-CD), which increases its water solubility. The radical scavenging activity of the THC/HP-β-CD complex (molar ratio of 1:1) was significantly higher than the values for SDACNF or Sac alone. The rate of release of THC from the Sac/SDACNF pellets containing the THC/HP-β-CD complex decreased with increasing Sac content in the pellet, suggesting that Sac/SDACNF (1:1) and Sac alone pellets function as extended-release excipients for THC. The findings reported here indicate that this can be attributed to the ability of the Sac component to retain fluids, thus extending the effects of the drug. In view of the above experimental outcomes, i.e. wound healing efficacy, fluid absorption, retention and the extended drug release of the system indicates that this preparation, in the appropriate ratios, has the potential for use as a controlled-release drug in wound healing.

Crickets are gaining worldwide attention as a nutrient source with a low environmental impact. We considered crickets as a new source of chitin raw material. Chitin isolated from crickets was successfully converted to nanochitin by pulverization. First, chitin was obtained from cricket powder in a 2.6% yield through a series of chemical treatments. Chitin identification was confirmed by FT-IR and 13C NMR. The chitin had an α-type crystal structure and a deacetylation degree of 12%. Next, it was pulverized in a disk mill to obtain nanochitin. Cricket nanochitin was of a whisker shape, with an average fiber width of 10.1 nm. It was larger than that of crab shells, while the hydrodynamic diameter and crystal size were smaller. Such differences in shape affected the physical properties of the dispersion. The transmittance was higher than that of crab nanochitin due to the size effect, and the viscosity was smaller. Moreover, the dry non-woven cricket nanochitin sheets were more densely packed, and their modulus and breaking strength were greater.

Chitin nanofiber is a nanomaterial produced by pulverizing chitin, the main component of crab shells. Since it has excellent mechanical properties, it is expected to be used as a reinforcing material to strengthen materials. Chitin was mechanically ground in water using a ball mill to prepare nanofibers. The ball size, total ball weight, and milling time were varied, and the resulting water dispersion and the cast film were analyzed to optimize the conditions for efficient preparation. The length and width of the nanofibers were also measured by SEM and AFM observations. The size of the balls affected the level of grinding and the intensity of impact energy on the chitin. The most efficient crushing was achieved when the diameter was 1 mm. The total ball weight directly affects the milling frequency, and milling proceeds as the total weight increases. However, if too many balls occupy the container, the grinding efficiency decreases. Therefore, a total ball weight of 300 g was optimal. Regarding the milling time, the chitin becomes finer depending on the increase of that time. However, after a specific time, the shape did not change much. Therefore, a milling time of approximately 150 min was appropriate.

Surface wrinkling to fabricate hierarchical surface topographies has attracted much attention because of the potential and multifunctional applications of hierarchical surface wrinkles beyond uniform wrinkles. Although many reports have described the preparation of hierarchical wrinkles induced by mechanical stress and heat, fabrication through drying-induced shrinkage has hardly been reported. Here we introduce hierarchical surface wrinkles and bumps generated on a chitosan film via the preparation of double-skin layers with κ- and ι-carrageenans, respectively, and subsequent drying. Double-skin layers are fabricated on a swollen chitosan film, called a chitosan hydrogel film, that is soaked first in κ- or ι-carrageenan solution and then in water to remove excess adsorbed κ- or ι-carrageenan. After the film is dried, hierarchical microscopic surface architectures are observed. In the case of the κ-carrageenan system, the wrinkles are hierarchical, consisting of wrinkles (6.2 ± 2.8 μm) that have smaller buckles (0.23 ± 0.09 μm). We reveal that the wrinkles or the smaller buckles are caused by plane inhomogeneous shrinkage between the κ-carrageenan layer and the chitosan film or by the aggregation of the κ-carrageenan layer upon drying, respectively. Interestingly, the ι-carrageenan system showed hierarchical bumps consisting of semispherical bumps (5.6 ± 2.1 μm) that have smaller bumps (0.78 ± 0.27 μm). We reveal that the larger bumps are generated during the immersion of the chitosan hydrogel film into ι-carrageenan solution. The smaller bumps are generated by the aggregation of the ι-carrageenan layer that occurs during drying; this process requires the plane compression strain caused by the shrinkage of the chitosan hydrogel film.

Sorbitol polyglycidyl ether (SPE), which is a bio-based water-soluble epoxy resin, was cured with lysine (Lys) and arginine (Arg) as basic amino acids and with cysteine (Cys) as an acidic amino acid. Furthermore, biocomposites of the Lys- and Arg-cured SPE (SPE-Lys and SPE-Arg) and Cys-cured SPE (SPE-Cys) with chitin nanofiber (ChNF) not higher than 10 wt% were successfully prepared by compression molding and casting methods, respectively. Also, SPE-Cys biocomposites with chitosan nanofiber (CsNF) not higher than 2 wt% were successfully prepared by the casting method. The FT-IR spectral analysis of the cured resins suggested that the e-amino and carboxy groups of Lys, α-amino and carboxy groups of Arg, thiol group of Cys mainly reacted with epoxy groups of SPE. The FT-IR spectral analysis of the ChNF biocomposites suggested that a side reaction of SPE with acetic acid which was contained in ChNF suspension occurred. The dynamic mechanical analysis revealed that a higher order of the loss modulus peak temperature (Tα) was SPE-Lys (39 °C) > SPE-Arg (33 °C) > SPE-Cys (21 °C). Although Tαs of ChNF biocomposites were lower than those of the corresponding cured resins, Tαs of SPE-Cys/CsNF biocomposites were higher than that of SPE-Cys by the action of CsNF as a basic catalyst. The storage moduli over the range of 50–100 °C for SPE-Lys/ChNF, SPE-Cys/ChNF and SPE-Cys/CsNF biocomposites were much higher than those for the corresponding cured resins. SPE-Lys/ChNF and SPE-Cys/CsNF biocomposites exhibited higher tensile strengths and moduli than SPE-Lys and SPE-Cys did, respectively.

The development of chitin-based materials with favorable mechanical properties and biocompatibility is an important research goal owing to the wide-ranging practical applications. In this study, a composite film was prepared using chitin nanofibers and gelatin. The CNF/gelatin composite film was highly viscous and had a fine nanofiber structure. The transmittances indicated high transparency, regardless of nanofiber content. The water content of the CNF/gelatin composite film increased linearly as the gelatin content increased. Although the CNF/gelatin composite film did not induce severe inflammation, it strongly induced fibroblast proliferation, indicating high biocompatibility. Based on these results, the films are suitable for biological applications, e.g., tissue engineering, medicines, and cosmetics.

We previously developed bio-based wrinkled surfaces induced by wood-mimetic skins upon drying in which microscopic wrinkles were fabricated on a chitosan (CS) film by immersing it in a phenolic acid solution, followed by horseradish peroxidase (HRP)-catalyzed surface reaction and drying. However, the detailed structure of the resulting wood-mimetic skins, including crosslinking mode and thickness, has not been clarified due to the difficulty of the analysis. Here, we prepare wrinkled films using ferulic acid (FE), vanillic acid (VA), and homovanillic acid (HO) and characterize their structures to clarify the unknown characteristics of wood-mimetic skin. Chemical and structural analyses of wood-mimetic skins prepared using VA and HO indicate that the crosslinking structure in the skin is composed of ionic bonds between CS and an oligophenolic residue generated by the HRP-catalyzed reaction on the CS surface. Moreover, the quantity of these ionic bonds is related to the skin hardness and wrinkle size. Finally, SEM and TOF-SIMS analyses indicate that the skin thickness is on the submicron order (

Surface-deacetylated chitin nanofibers (SDACNFs) reinforced with a sulfobutyl ether β-cyclodextrin (SBE-β-CD) (NFs-CDs) gel were developed to obtain a controlled release carrier of prednisolone (PD) for the treatment of colitis. PD was released slowly from the gel at both pH 1.2 and 6.8. The in vitro slow release of PD from the NFs-CDs gel was reflected in the in vivo absorption of the drug after oral administration to rats. These results suggest that a simple gel composed of a mixture of SDACNFs and SBE-β-CD has the potential for use in the controlled release of PD. We also evaluated the therapeutic effects of the NFs-CDs gel containing PD on dextran sulfate sodium (DSS)-induced colitis model mice. The administration of the NFs-CDs gel at intervals of 3days from the beginning of the DSS treatment resulted in a significant improvement, not only in colitis symptoms but also histopathological changes in colon tissue. In addition, the therapeutic effects of the NFs-CDs gel on colitis can be attributed to decreased levels of neutrophil infiltration and the development of oxidative stress. These efficacy profiles of the NFs-CDs gel containing PD suggest that it has the potential for use in the treatment of, not only colitis, but also a variety of other disorders associated with inflammation and oxidative injuries.

The deproteinization is a major constraint for chitin recovery from crustacean wastes. In this work, high protein removal was achieved through the combination of two-stage solid state culture by Lactobacillus brevis and Rhizopus oligosporus . The first stage was carried out employing a heterofermentative starter ( L. brevis ) using glucose as sole carbon source. For the second stage, the inoculum levels of the food grade fungi were 10 3 , 10 5 or 10 7 spores/ml. The highest deproteinization (96% ± 0.43%) and demineralization (66.45 ± 2.14%) were achieved with 10 7 spores/ml. The protein removal was attributed to acid and neutral proteolytic activities, which highest activity during culture was determined at pH 5. Lactic acid was the main organic acid produced along with acetic, succinic and oxalic acids. The released protein hydrolysates (120.56 mg protein/g) displayed M W range between 25 × 10 3 and 11 × 10 3 Da. The highest concentration of astaxanthin extracted from liquid was 8.78 μg/g. Protein hydrolysates and astaxanthin showed radical scavenging activity with I C50 of 1.13 ± 0.03 mg/g and 2.02 ± 0.01 μg/g, respectively. The purified chitin presented molecular weight of 1313 × 10 3 Da, preserving high crystalline index (I CR of 87.5%) and 93.67% degree of acetylation.

In this study, we report that surface-deacetylated chitin nano-fibers (SDACNFs) are more effective in decreasing renal injury and oxidative stress than deacetylated chitin powder (DAC) in 5/6 nephrectomized rats. An oral administration of low doses of SDACNFs (40mg/kg/day) over a 4 week period resulted in a significant decrease in serum indoxyl sulfate, creatinine and urea nitrogen levels, compared with a similar treatment with DAC or AST-120. The SDACNFs treatment also resulted in an increase in antioxidant potential, compared with that for DAC or AST-120. Immunohistochemical analyses also demonstrated that SDACNFs treated CRF rats showed a decrease in the amount of accumulated 8-OHdG compared with the CRF group. These results suggest that the ingestion of SDCH-NF results in a significant reduction in the levels of pro-oxidants, such as uremic toxins, in the gastrointestinal tract, thereby inhibiting the subsequent development of oxidative stress in the systemic circulation.

A freeze-dried gel composed of surface-deacetylated chitin nanofibers (SDACNFs), reinforced with an anionic cyclodextrin, sulfobutyl ether β-cyclodextrin (SBE-β-CD) was evaluated for treating wounds in a rat model, and the results were compared with a SDACNFs gel without SBE-β-CD. The incorporation of prednisolone (PD), a poorly water-soluble drug, in both types of gels and its release from the gels were also compared. In both cases, wound areas were decreased and their effect was higher than that of commercially available wound dressings. The rate of release of PD from the freeze-dried SDACNFs/SBE-β-CD was much faster than that form SDACNFs alone without SBE-β-CD, due to fact that the PD is more soluble in the amorphous SBE-β-CD complex compared to the other preparations. The findings indicate that the freeze-dried SDACNFs/SBE-β-CD gel would be beneficial as a new biomaterial for the treatment of wounds and for preparing homogeneous high-content gels that contain poorly water-soluble drugs.

We evaluated the effect of chitin nanofibril (CNF) application via skin swabs on an experimental atopic dermatitis (AD) model. AD scores were lower, and hypertrophy and hyperkeratosis of the epidermis were suppressed after CNF treatment. Furthermore, inflammatory cell infiltration in both the epidermis and dermis was inhibited. CNFs also attenuated histological scores. The suppressive effects of CNFs were equal to those of corticosteroid application; however, chitin did not show these effects. CNF application might have anti-infllammatory effects via suppression of the activation of nuclear factor-kappa B, cyclooxygenase-2, and inducible nitric oxide synthase. In an early-stage model of experimental AD, CNFs suppressed AD progression to the same extent as corticosteroids. They also suppressed skin inflammation and IgE serum levels. Our findings indicate that CNF application could aid in the prevention or treatment of AD skin lesions.

Chitin (β-(1-4)-poly-N-acetyl-D-glucosamine) is widely distributed in nature. A method for the preparation of chitin nanofibers (CNFs) is reported. CNFs are considered to have several potential applications because they have useful properties such as high specific surface area and porosity. More recently, beneficial effects of CNF as functional foods were reported. First, the anti-inflammatory effect of oral administration of chitin CNFs was demonstrated in a mouse model of inflammatory bowel disease (IBD). It was found that CNFs improved clinical symptoms and suppressed IBD. CNFs decreased the areas with nuclear factor-κB (NF-κB) staining in colon tissue. Second, the anti-obesity effects of surface-deacetylated chitin nanofibers (SDACNF) in a mouse model of high-fat diet-induced obesity was evaluated. SDACNFs suppressed the increase in body weight produced by the high-fat diet; however, CNFs did not suppress such weight gain. SDACNFs decreased serum levels of leptin. These results suggest that CNF and SDACNF are promising functional foods for patients with IBD or obesity.

We previously reported a chitin nanofiber hydrogel from squid pen β-chitin by a simple NaOH treatment. In the present study, a calcium phosphate/chitin nanofiber hydrogel was prepared for bone tissue engineering. Calcium phosphate was mineralized on the hydrogel by incubation in a solution of diammonium hydrogen phosphate solution followed by calcium nitrate tetrahydrate. X-ray diffractometry and Fourier transform infrared spectroscopy showed the formation of calcium phosphate crystals. The morphology of the calcium phosphate crystals changed depending on the calcification time. After mineralization, the mechanical properties of the hydrogel improved due to the reinforcement effect of calcium phosphate crystal. In an animal experiment, calcium phosphate/chitin nanofiber hydrogel accelerated mineralization in subcutaneous tissues. Morphological osteoblasts were observed.

Chitosan produced by the deacetylation of chitin is a cationic polymer with antimicrobial properties. In this study, we demonstrate the improvement of chitosan properties by nanofibrillation. Nanofiber sheets were prepared from nanofibrillated chitosan under neutral conditions. The Young’s modulus and tensile strength of the chitosan NF sheets were higher than those of the chitosan sheets prepared from dissolving chitosan in acetic acid. The chitosan NF sheets showed strong mycelial growth inhibition against dermatophytes Microsporum and Trichophyton. Moreover, the chitosan NF sheets exhibited resistance to degradation by the fungi, suggesting potentials long-lasting usage. In addition, surface-deacetylated chitin nanofiber (SDCNF) sheets were prepared. The SDCNF sheet had a high Young’s modulus and tensile strength and showed antifungal activity to dermatophytes. These data indicate that nanofibrillation improved the properties of chitosan. Thus, chitosan NF and SDCNF sheets are useful candidates for antimicrobial materials.

This study evaluated the effects of oral administration of surface-deacetylated chitin nanofibers (SDACNFs) on hypercholesterolemia using an experimental model. All rats were fed a high cholesterol diet with 1% w/w cholesterol and 0.5% w/w cholic acid for 28 days. Rats were divided equally into four groups: the control group was administered 0.05% acetic acid dissolved in tap water, and the SDACNF, chitosan (CS), and cellulose nanofiber (CLNF) groups were administered 0.1% CNF, CS, or CLNF dissolved in the tap water, respectively, during the experimental period. Changes in body weight, intake of food and water, and organ weight were measured. Serum blood chemistry and histopathological examination of the liver were performed. Administration of SDACNF did not affect body weight change, food and water intake, or organ weights. Administration of SDACNF and CS decreased the diet-induced increase in serum total cholesterol, chylomicron, very-low-density lipoprotein, and phospholipid levels on day 14. Moreover, oral administration of SDACNFs suppressed the increase of alanine transaminase levels on day 29 and suppressed vacuolar degeneration and accumulation of lipid droplets in liver tissue. These data indicate that SDACNF has potential as a functional food for patients with hypercholesterolemia.

We have designed a novel 1,8-naphthalimide derivative with an open space for an anion. Computational calculation has predicted that the space could trap various anion species and photo-induced charge transfer depending on the anion's electrophilic properties. Indeed, the fluorescence behaviour of the 1,8-naphthalimide derivative complexes with each anion is consistent with the computational prediction.

Zwitterionic nanocrystals were prepared by TEMPO-mediated oxidation, partial deacetylation, and subsequent mechanical disintegration of α-chitin. The pH dependence of the morphology, transparency, and viscosity of the nanocrystals were evaluated. After those reactions, the carboxylate and amino group contents of the chitin derivative were 0.45 and 1.26 mmol/g, respectively. After mechanical treatment, the water dispersion consisted of nanocrystals approximately 250 nm long and 10nm thick. Under acidic and basic conditions, the water dispersions were highly transparent. On the other hand, under neutral conditions, the dispersion was turbid due to the ionic interaction between the cationic and anionic groups on the nanocrystal surface. Although the surface zwitterionic nanocrystals collected from acidic and basic dispersion were randomly oriented due to electrostatic repulsions, nanocrystals formed aggregates in neutral water due to the cationic and anionic interaction between them. Nanocrystals in neutral water had higher viscosity than those in acidic and basic water, since ionic interaction caused nanocrystal networks to form in water.

Chitin (β-(1-4)-poly-N-acetyl-D-glucosamine) is widely distributed in nature and is the second most abundant polysaccharide after cellulose. It is often converted to its more deacetylated derivative, chitosan. Previously, many reports have indicated the accelerating effects of chitin, chitosan, and its derivatives on wound healing. More recently, chemically modified or nano-fibrous chitin and chitosan have been developed, and their effects on wound healing have been evaluated. In this review, the studies on the wound-healing effects of chitin, chitosan, and its derivatives are summarized. Moreover, the development of adhesive-based chitin and chitosan are also described. The evidence indicates that chitin, chitosan, and its derivatives are beneficial for the wound healing process. More recently, it is also indicate that some nano-based materials from chitin and chitosan are beneficial than chitin and chitosan for wound healing. Clinical applications of nano-based chitin and chitosan are also expected.

Silver nanoparticles were prepared on chitin nanofiber surfaces by UV light reduction of silver ions. The chitin nanofibers could be efficient substrates to immobilize silver nanoparticles with stable dispersion states. The dispersion and the nanocomposite film with acrylic resin showed characteristic absorption property in the visible light region due to the effect of the silver nanoparticles. Silver nanoparticles endowed strong antifungal activity to chitin nanofibers.

Composite materials reinforced with microfibrillated cellulose (MFC) fibers were prepared and characterized in terms of their mechanical properties. The surface of the MFC fibers was treated with a silane coupling reagent having an NH2 functional group to improve fiber-matrix adhesion. Due to the unique structure of the MFC, which consists of nano-order-scale interconnected fibrils and microfibrils with greatly expanded surface area and submicron pore size compared to conventional cellulose, it was possible to enhance the effect of silane coupling agent and thereby improve the compatibility between the fibers and matrix and also the dispersibility of fibers. The Young's modulus was significantly increased to more than 70%.

Fully biobased nanoparticles harnessed from the lignification of wood are introduced in this paper. A phenolic oligomer is produced by the horseradish peroxidase-catalyzed polymerization of ferulic...

A new and simple approach for surface wrinkling inspired by polymer assemblies in wood fibers is introduced. A hard skin is synthesized on a linear polysaccharide support that resembles the structural units of the cell wall. This skin, a wood mimetic layer, is produced through immersion in a solution containing phenolic precursor and subsequent surface reaction by horseradish peroxidase. A patterned surface with micron-scale wrinkles is formed upon drying and as a result of inhomogeneous shrinkage. We demonstrate that the design of the wrinkled surfaces can be controlled by the molecular structure of the phenolic precursor, temperature, and drying stress. It is noteworthy that this is a totally bio-based system involving green materials and processes.

Chitosan nanofibers were easily prepared from fully deacetylated chitosan dry powder using a high-pressure waterjet system. From SEM observation, after 10 cycles of treatment, most of the chitosan had been reduced to homogeneous nanofibers measuring tens of nanometers. On the other hand, further mechanical treatment did not show a significant change. Relative crystallinity of chitosan nanofibers gradually decreased as the number of passes increased since high-pressure waterjet treatment damaged the crystalline region of chitosan nanofibers. The transmittance of the chitosan nanofiber slurry increased steeply, as the number of passes increased, indicating that the chitosan fibers were disintegrated effectively. Viscosity of chitosan nanofiber slurry also showed that the chitosan disintegrated well into nanofibers up to 10 passes. Above 10 passes, disintegration efficiency was saturated. The molecular weights of the nanofibers steeply decreased due to the depolymerization of chitosan by mechanical disintegration. The Young's modulus and tensile strength of chitosan nanofiber sheets were improved as the number of treatments increased, but further treatments deteriorated the tensile strength.

N-halamine chitin nanofiber (NF) film was prepared by the reaction of chitin NF film with sodium hypochlorite solution to endow the film with antibacterial and antifungal activities. The amount of active chlorine content loaded on the chitin NF film depended on the sodium hypochlorite concentration and reaction time. FT-IR, UV-vis, XRD, and TG analyses showed that the N-H bond was substituted to the N-Cl bond and that the reaction took place at the chitin NF surface. After chlorination, the characteristic nanochitin morphology was maintained. Although the active chlorine content of the film gradually decreased by disassociation of the N-Cl bond, chlorine was rechargeable into chitin NF by another sodium hypochlorite solution treatment. The chlorinated chitin NF film showed strong efficacies against Gram-negative and -positive bacteria of Escherichia coli and Staphylococcus aureus, respectively. Moreover, the films showed 100% and 80% inhibition of spore germination when faced against Alternaria alternata and Penicillium digitatum fungi, respectively.

Poly(p-phenylene benzobisoxazole) (PBO) nanofibers were prepared from commercially available PBO fiber by a simple downsizing process for the first time. Partial alkaline hydrolysis of the oxazole ring brought ionic functional groups onto the fiber surface, enabling the disintegration of the PBO fiber into nanofibers with the help of an electrostatic repulsive force. The obtained nanofibers, whose average diameter was 24 nm, were characterized by SEM, FT-IR, ζ-potential analysis, XRD, and TGA. They dispersed homogeneously in water due to the surface charges. Filtration allowed a PBO nanofiber sheet to be easily prepared from the homogeneous dispersion in water.

A protein–chitin nanofiber complex was successfully prepared from crab shells by a mechanical treatment after the removal of CaCO3. One step in the conventional series of treatments—i.e., the removal of proteins—was omitted to bring down the production cost of the nanofibers. The obtained protein–chitin nanofibers had uniform width of approximately 20 nm and a high aspect ratio. These characteristics were similar to conventional chitin nanofibers. The optically transparent protein–chitin nanofiber composite was fabricated with acrylic resin. The nanofibers reinforced the acrylic resin film and thereby increased its mechanical properties. Proteins on the chitin nanofiber surface affected the biomineralization of CaCO3 in the crab shell. Mineralization of CaCO3 on the protein–chitin nanofiber was carried out by the gas-diffusion method. Protein molecules on the chitin NFs increased the chances for biomineralization to occur. The protein molecules stabilized the formation of vaterite and inhibited the transformation of vaterite to calcite.

Surface N -maleylation and N -naphthaloylation of chitin nanofiber (NF) were achieved by reaction with maleic and naphthalic anhydrides in water, respectively. Maleyl and naphthaloyl groups were sufficiently introduced to an amino group on a surface-deacetylated chitin NF. The characteristic nanofiber morphology was maintained after maleylation and naphthaloylation. These NFs were homogeneously dispersed in several organic solvents. Especially, naphthaloyl chitin NF was dispersed even in aromatic solvents, owing to the high level of solvation interactions with the naphthaloyl group. The NF dispersions in those aromatic solvents exhibited a dispersive-to-precipitate transition response at approximately 29 °C. Moreover, the naphthaloyl chitin NF dispersion cut harmful ultraviolet light. The maleyl chitin NF formed a self-standing gel after cross-linking polymerization.

We prepared a gel starting from deacetylated chitin nanofibers by utilizing electrostatic interactions with an anionic cyclodextrin, sulfobutyl ether β-cyclodextrin (SBE-β-CyD). Among the various C...

We previously reported a xanthan gum (Xan) hydrogel showing excellent mechanical properties. Mineralization of hydroxyapatite (Hap) upon the Xan hydrogel would provide a unique biomaterial applicable for bone tissue engineering. Here, we show the mineralization of Hap upon the Xan hydrogel by means of an alternate soaking process. Hap was gradually grown upon the Xan-matrix surface with increasing number of soaking cycles due to the ionic interactions between calcium cations and carboxyl groups. Interestingly, the mineralization induced a microstructure change in the gel-matrix from a layered structure to a porous structure. The mechanical properties of the resulting Hap–Xan composite hydrogels were further investigated by a tensile test, where the Hap–Xan composite hydrogel with an appropriate amount of Hap (Xan/Hap = 2.7) was capable of approximately 370% elongation.

We introduce a simple preparation procedure for aramid nanofibers from Twaron fibers by using a downsizing process. Alkaline hydrolysis pretreatment brings ionic charges on the fiber surface, allowing facile disintegration of Twaron into nanofibers by virtue of the electrostatic repulsive force. Since the nanofibers can be dispersed homogeneously in water, the processability and formability of the polymer were improved. The resulting aramid nanofibers, having a high degree of physical performance, a uniform nanosized morphology, and a high surface-to-volume ratio, will expand the range of novel applications of aramid fibers.