Search

Diabetic wounds are prone to recurrent infections, often leading to delayed healing. To address this challenge, we developed a chitin-copper sulfide (CuS@CH) composite sponge, which combines bacterial trapping with near-infrared (NIR) activated phototherapy for treating infected diabetic wounds. CuS nanoparticles were synthesized and incorporated in situ within the sponge using a chitin assisted biomineralization strategy. The positively charged chitin surface effectively adhered bacteria, while NIR irradiation of CuS generated reactive oxygen species (ROS) heat and Cu 2+ to rapidly damage the trapped bacteria. This synergistic effect resulted in an exceptional antibacterial performance against E. coli (∼99.9%) and S. aureus (∼99.3%). The bactericidal mechanism involved NIR-induced glutathione oxidation, membrane lipid peroxidation, and increased membrane permeability. In diabetic mouse models, the CuS@CH sponge accelerated the wound healing of S. aureus infected wounds by facilitating collagen deposition and reducing inflammation. Furthermore, the sponge demonstrated good biocompatibility. This dual-functional platform integrating bacterial capture and NIR-triggered phototherapy shows promise as an antibacterial wound dressing to promote healing of infected diabetic wound.

The cellulose nanofibers (CNFs) based pH-sensitive indicator films were developed by mixing guar gum (GG) with bromothymol blue-anchored chitin (BTB-Chitin) as an indicator to monitor shrimp freshness. The BTB-Chitin was prepared by grafting hydroxypropyltriethylamine groups (HPTA) to chitin first, then anchoring bromothymol blue (BTB) to prepare intelligent pH response BTB-Chitin. The 0.08 BTB-Chitin films had a good tensile strength of 11.76 MPa and the water contact angle values were 125°, which displayed obvious color response to pH buffers and acid base volatile gas. Besides, the homogeneous and flexible composite films showed good color stability and reversibility. The released amount of BTB was very low from the BTB-Chitin films in heptane and corn oil. The composite films had been degraded completely in 15 days in soil. The pH and volatile base nitrogen were measured to determine the degree decay of shrimp (Litopenaeus vannamei), and the prepared pH-sensitive films changed from yellow (fresh) to cyan (spoiled) with the freshness of shrimp decreased, indicating the BTB-Chitin films could detect the shrimp freshness in real-time and high visibility., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Natural polysaccharides show enviable advantages for preparation of sustainable hybrid materials. However, in most cases, complex chemical modifications of natural polysaccharides are required, which not only causes changes of the inherent properties of polysaccharides, but also increases the manufacturing costs of the final materials. Therefore, it is highly desired to develop efficient and low-cost ways to access polysaccharides-containing hybrid materials. In this work, we report the environmentally friendly preparation of a new kind of polysaccharide-based materials, called polysaccharide-vitrimer hybrid materials, for the first time. The vitrimer synthesis and hybridization with polysaccharides can be achieved via a convenient one-pot method in absence of solvent and catalyst. In addition, time-consuming and labor-intensive physical/chemical modifications of natural polysaccharides are completely avoided. The resultant hybrid materials show good mechanical performance (tensile toughness is up to 13.7 MJ/m 3 ), high thermal stability (T d,max is up to 457 °C), fast self-healing ability (self-healing efficiency is up to 99 % within 20s at 80 °C) and excellent reprocessability and recyclability (at least three cycles). Especially, conductive polysaccharide-vitrimer hybrid materials could be readily prepared from the resultant materials, exhibiting novel applications as flexible sensors and electromagnetic shielding materials (the EMI SE is up to 24.93 dB)., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Conductive hydrogel flexible sensors have attracted considerable research interest because of their good conductivity, flexibility, and biocompatibility. However, conventional hydrogels suffer from dehydration under ambient environments and freezing at low temperatures. Herein, we prepared a chitin/polyacrylamide organohydrogel with highly stretchable, anti-freezing, and anti-drying properties. This organohydrogel was creatively prepared by one-step radical polymerization in the chitin and calcium chloride/methanol (Ca solvent) aqueous solution. Benefiting from the chitin/Ca solvent system, the organohydrogel shows relatively high stretchability (improve ~5 times), excellent anti-freezing (up to -80 °C) upon long-term storage, and anti-drying (67 days under normal environment) performance. What's more, the reversible noncovalent bonds in the organohydrogel endow it with repeatable multi-purpose adhesion and rapid self-healing, while the abundant free ions grant it good conductivity to be a flexible sensor. Therefore, it is promising that this chitin-based conductive organohydrogel with multifunctionality would provide wide application scopes of flexible electronic devices., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Biobased N-doped hierarchically porous carbon (N-HPC) electrodes were successfully prepared by utilizing marine crustacean derivatives and chitin nanofibers (ChNF), as versatile bio-templates of zeolitic imidazolate frameworks (ZIF-8) to form ChNF@ZIF-8 nanocomposites, followed by a subsequent carbonization process. The ZIF-8 nanoparticles were in situ synthesized on ChNF surfaces to avoid fragmentation for fabricating hierarchically porous carbon structure (N-HPC), which is efficiently doped with rich nitrogen content that originates in ChNF and ZIF-8. The results show that N-HPC electrodes demonstrate improved electrochemical performance and the constructed symmetric supercapacitor assembled with N-HPC exhibits enhanced capacitive performance of specific capacity (128.5 F·g -1 at 0.2 A·g -1 ) and excellent electrochemical stability even after 5000 cycles. This facile and effective preparation method of N-HPC electrodes derived from marine crustacean nanomaterials will have great potential in the construction of next-generation electrochemical energy-storage devices with excellent capacitance performance., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this study, a series of conductive composite wires were successfully prepared by combining dispersions of multi-wall carbon nanotubes (MWCNTs) and TEMPO-oxidized cellulose nanofibers (TOCNFs) with different MWCNTs contents into a dispersion of partially deacetylated α-chitin nanofibers (α-DECHNs) followed with a drying process. The TOCNFs/MWCNTs/α-DECHNs composite wires were prepared by extruding the negatively charged TOCNFs/MWCNTs dispersion into the positively charged α-DECHNs dispersion. The contact of the positively charged α-DECHNs and the negatively charged TOCNFs/MWCNTs triggers the electrostatic interaction (heterocoagulation) resulting in wire-shaped conductive composites. The SEM analysis indicates this conductive composite material has a wire-like shape with a rough but tight surface. The properties of samples were characterized by a zeta potential analyzer (Zetasizer Nano), a four-probe, an electrochemical workstation, a Fourier transform infrared spectroscopy (FTIR), an X-ray diffractometer (XRD), and a thermogravimetric analyzer (TG). Besides, the conductivity and the AC impedance of TOCNFs/MWCNTs/α-DECHNs composite wires with different MWCNTs contents were also analyzed. The conductivity of the composite wire increases from 9.98 × 10 - 6  S∙cm - 1 to 1.56 × 10 - 3  S∙cm - 1 as the MWCNTs content raises from 3.0 wt% to 14.0 wt%. When the MWCNTs content reaches 14.0 wt%, the prepared composite wire can light up LED at a voltage of 5 V, indicating the great potential of this biomass-based conductive composite in conductive material application., (Copyright © 2019 Elsevier B.V. All rights reserved.)

In this paper, nanochitin was used as an alternative natural nanomaterial to combine with cellulose fibers for fabricating high-strength paper. Two typical chitin nanowhiskers having contrasting sign of surface charge were compared to evaluate the enhancement performance on paper in details. The results show that nanochitin with positive charges on the surface has a significant effect on the strength properties of the prepared paper, especially on wet strength. When the dosage of chitin nanowhiskers was 2%, the wet strength index was increased to 2.48 N·m/g, which is important for paper-based analytical devices with the common use in liquid analysis. Typical colorimetric glucose assays were successfully performed, suggesting the improved analytical performance on these prepared paper., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020. Published by Elsevier B.V.)

The effects of gelatin-carboxymethyl cellulose (Gel-CMC) based films containing chitin nano fiber (CHNF) and Trachyspermum ammi essential oil (Ajowan), on the shelf life extension of the raw beef at refrigerated temperature (4 °C) over a 12-day period were evaluated. Ajowan essential oil (AJEO) and CHNF were added to the films at 0.24, 0.64 and 1% v/v; and 2 and 4 wt%, respectively. The microbiological (total viable count, psychrotrophic count, Pseudomonas spp., Staphylococcus aureus, lactic acid bacteria, molds and yeasts), the chemical (pH, thiobarbituric acid and total volatile basic nitrogen), color and sensory properties of the packaged samples were evaluated periodically. Bacteria grew the most quickly in the control samples, followed by those wrapped with the Gel-CMC films; The lowest microbial counts, the least change in the chemical properties and the highest sensory scores after 12 days of storage were obtained for the samples wrapped in the films incorporated with 1% AJEO and 4 wt% CHNF., Competing Interests: Declaration of competing interest We wish to confirm that there are no known conflicts of interest associated with this publication and there has been no significant financial support for this work that could have influenced its outcome. We confirm that the manuscript has been read and approved by all named authors and that there are no other persons who satisfied the criteria for authorship but are not listed. We further confirm that the order of authors listed in the manuscript has been approved by all of us. We confirm that we have given due consideration to the protection of intellectual property associated with this work and that there are no impediments to publication, including the timing of publication, with respect to intellectual property. In so doing we confirm that we have followed the regulations of our institutions concerning intellectual property., (Copyright © 2019. Published by Elsevier B.V.)

This paper reports a green nanocomposite made by simply blending chitin nanofibers and bamboo cellulose nanofibers without chemically dissolving chitin and cellulose raw materials. Good biodegradability and biocompatibility of chitin in conjunction with good mechanical properties of cellulose are beneficial for developing green nanocomposite applicable for food packaging. The bamboo cellulose nanofiber (BACNF) is isolated by using a TEMPO-oxidation followed by an aqueous counter collision (ACC) method. Chitin nanofiber (CTNF) is isolated by using the ACC method. A simple blending is used to prepare the nanocomposite with different CTNF and BACNF concentration. Morphologies, mechanical properties, chemical interactions, thermal properties, water contact angles and biodegradability of the nanocomposite are investigated. The tensile strength and Young's modulus of the prepared nanocomposite increased up to 3 and 1.3 times, respectively as the BACNF concentration increase. The nanocomposite exhibites better thermal stability than the pure BACNF. Furthermore, the nanocomposite is fully biodegradable within a week. Good mechanical, thermal properties as well as biodegradability of the nanocomposite are promising for possible food packaging application., (Copyright © 2019 Elsevier B.V. All rights reserved.)

A series of highly porous and biocompatible poly (vinyl alcohol) (PVA) hydrogels containing partially deacetylated α-chitin nanowhiskers (ChWs) were fabricated by the double-cross-link (DC) with glutaraldehyde (GA) and repeating freeze-thawing cycle. Then these hydrogels were used as carrier for bovine serum albumin (BSA), which served as the model drug. The nanowhiskers worked effectively to raise the mechanical property of the PVA/ChWs hydrogels. This property increased significantly from 1.55 to 26.59 MPa with the increase of the ratio of ChWs to PVA from 0% to 40%. Additionally, the morphological properties of the gel matrix were comprehensively investigated. The results showed that the novel ChWs/PVA hydrogels were facilely constructed from sequential chemical cross-linking and physical cross-linking with GA. The hydrogel with the ChWs to PVA weight ratios of 40% achieved the highest equilibrium swelling ratio, and could release more than 80% of the BSA from its gel matrix within 75 h., (Copyright © 2019 Elsevier B.V. All rights reserved.)

A carboxylate chitooligomer (C-COS) containing carboxyl groups attached to chitooligomer (COS) molecules has been prepared by laccase/2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) system, which is a green-chemistry method. Several experiments were designed to evaluate inhibition effects on melanin and mechanisms of C-COS. The results indicated that C-COS exhibited more distinct anti-melanogenic effects compared to COS. C-COS inhibits melanin production with tyrosine (Tyr) and DOPA as the substrate of melanin formation, and the inhibition rates are, respectively, 89.07% and 84.45%, which reach 1.4-2 times those of COS. UV-vis spectroscopy was used to elucidate the interaction mechanism between C-COS and tyrosinase (TYR). It is C-COS chelating with metal Cu ions in tyrosinase (TYR) that decreases the enzyme activity. Half-maximal inhibitory concentrations (IC 50 ) of C-COS were calculated as 13.49 and 4.07 mg/mL for monophenolase (cresolase) and diphenolase (catecholase), respectively., (Copyright © 2018. Published by Elsevier Ltd.)

Natural hydrogels have attracted extensive research interest and shown great potential for many biomedical applications. In this study, a series of biocompatible hydrogels was reported based on the self-assembly of positively charged partially deacetylated α-chitin nanofibers (α-DECHN) and negatively charged 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibers (TOCNF) for anticancer drug delivery. The formation mechanisms of the α-DECHN/TOCNF hydrogels with different mixing proportions were studied, and their morphological, mechanical, and swelling properties were comprehensively investigated. Additionally, the drug delivery performance of the hydrogels was compared via sustained release test of an anticancer drug (5-fluorouracil). The results showed that the hydrogel with higher physical cross-linking degree exhibited a higher drug loading efficiency and drug release percentage.

Thermogravimetric characteristics of chitin and chitosan and their potentials to produce value-added organonitrogen chemicals were separately evaluated via TG/DSC-FTIR and Py-GC/MS. Results shown that chitin had the better thermal stability and higher activation energy than chitosan because of the abundant acetamido group. Furthermore, the dominated volatilization in active pyrolysis of chitin contributed to its endothermic property, whereas the charring in chitosan led to the exothermal. During fast pyrolysis, the acetamido group in chitin and chitosan was converted into acetic acid or acetamide. Typical products from chitosan pyrolysis were aza-heterocyclic chemicals, i.e. pyridines, pyrazines, and pyrroles, with the total selectivity of 50.50% at 600°C. Herein, selectivity of pyrazine compounds was up to 22.99%. These aza-heterocyclic chemicals came from the nucleophilic addition reaction of primary amine and carbonyl. However, main reaction during chitin pyrolysis was ring-opening degradation, which led to the formation of acetamido chemicals, especially acetamido acetaldehyde with the highest selectivity of 27.27% at 450°C. In summary, chitosan had the potential to produce aza-heterocyclic chemicals, and chitin to acetamido chemicals., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Immobilized silver nano-particles (Ag NPs) possess excellent antimicrobial properties due to their unique surface characteristics. In this paper, immobilized silver nano-particles were synthesized in the presence of chitin nano-crystals (CNC) based on the Tollens mechanism (reduction of silver ion by aldehydes in the chitosan oligosaccharides (COS)) under microwave-assisted conditions. The prepared Ag NPs-loaded CNC nano-composites were then applied onto the paper surface via coating for the preparation of antibacterial paper. Fourier transform infrared (FT-IR) and X-ray diffraction (XRD) results confirmed that the Ag NPs were immobilized onto the CNC. The transmission electron microscope (TEM) and scanning electron microscopy (SEM) results further revealed that the spherical Ag NPs (5-12nm) were well dispersed on the surface of CNC. The coated paper made from the Ag NPs-loaded CNC nano-composites exhibited a high effectiveness of the antibacterial activity against E. coli or S. aureus., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Structured biofoams with aligned porous structures were fabricated from nanosized chitin by employing a directional freeze-casting technique. The effects of the freezing conditions and slurry formulation on nanochitin foam morphology were investigated. The morphology of obtained foams was characterized using scanning electron microscopy (SEM). It was found that the pore structure of the obtained foams was a likewise of the ice crystals formed during the directional freezing. The results indicate that directional freeze-casting protocol can significantly influence the morphological features and microstructures of the obtained biofoams which could have numerous applications, including engineered carriers, scaffolds, filters and specifically as a template for potential multi-layered composites after infusion with a second phase., (Copyright © 2014 Elsevier Ltd. All rights reserved.)