Chitosan Nanocomposite Research Articles

Enhancing bacterial control and daylight-driven water remediation with chitosan-impregnated MoC nanosheets.

The functionalization of nanoparticles with 2D nanosheets is an effective approach to enhance their functional properties for pollutant removal. This research outlines the synthesis of a 2D-delaminated molybdenum carbide (MXene) chitosan nanocomposite (2D-d-Mo2CTx-Cs NC) with bacterial control and photocatalytic properties for dye adsorption. The nanocomposite includes Tx-surface terminating groups O, OH, and F. In this investigation, the composite was synthesized using the etching method and its formation was confirmed through UV spectra at 288nm. It was characterized through FTIR, XRD, Particle size, Zetapotential, FESEM, HRTEM, EDAX, and XPS analyses. FTIR spectral analysis of NC suggests that amines are formed through a Schiff base reaction between glutaraldehyde and Cs, or through the interaction of terminal aldehydes and carbonyl groups. The XRD analysis confirmed the crystalline structure of the composite. FESEM images revealed irregularly structured nanosheets (NSs) material in the prepared 2D-d-Mo2CTx-Cs NC samples. HRTEM images revealed 2D-d-Mo2CTx NSs impregnated onto Cs with an average size of 50nm, as confirmed by a particle size analyzer, with a zeta potential value of -15mV. Additionally, Mo, C, N, and O are the most significant elements present in the NC, as confirmed by EDAX and XPS analyses. Further, biocompatibility testing of 2D-d-Mo2CTx-Cs NC yielded positive results. Moreover, under sunlight, the composites effectively adsorbed methylene blue with a 90% adsorption capacity, as confirmed by kinetic studies. Furthermore, the synergistic effect of Cs and d-Mo2CTx NSs resulted in significant antibacterial (50-200µl of 1mg/ml) and antibiofilm activity (100µl of 1mg/ml) against pathogenic bacteria. Furthermore, this study represents the first report on the use of 2D-d-Mo2CTx-Cs NC for daylight-influenced photocatalytic applications with a bacteria-controlling effect.

Facile synthesis of copper nitroprusside chitosan nanocomposite and its catalytic reduction of environmentally hazardous azodyes

One of the biggest issues affecting the entire world currently is water contamination caused by textile industries’ incapacity to properly dispose their wastewater. The presence of toxic textile dyes in the aquatic environment has attracted significant research interest due to their high environmental stability and their negative effects on human health and ecosystems. Therefore, it is crucial to convert the hazardous dyes such as methyl orange (MO) azo dye into environmentally safe products. In this context, we describe the use of Copper Nitroprusside Chitosan (Cu/SNP/Cts) nanocomposite as a nanocatalyst for the chemical reduction of azodyes by sodium borohydride (NaBH4). The Cu/SNP/Cts was readily obtained by chemical coprecipitation in a stoichiometric manner. The X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FT-IR) spectroscopy were applied to investigate chemical, phase, composition, and molecular interactions. Additionally, Scanning electron microscope (SEM) was used to examine the nanomaterial's microstructure. UV–vis spectroscopy was utilized for studying the Cu Nitroprusside Chitosan's catalytic activity for the reduction of azodye. The Cu/SNP/Cts nanocomposite demonstrated outstanding performance with total reduction time 160 s and pseudo-first order constant of 0.0188 s−1. Additionally, the stability and reusability study demonstrated exceptional reusability up to 5 cycles with minimal activity loss. The developed Cu/SNP/Cts nanocomposite act as efficient nanocatalysts for the reduction of harmful Methyl orange azodye.

Nanoarchitectonics and Biological Properties of Nanocomposite Thermosensitive Chitosan Hydrogels Obtained with the Use of Uridine 5'-Monophosphate Disodium Salt.

Currently, an important group of biomaterials used in the research in the field of tissue engineering is thermosensitive chitosan hydrogels. Their main advantage is the possibility of introducing their precursors (sols) into the implantation site using a minimally invasive method-by injection. In this publication, the results of studies on the new chitosan structures in the form of thermosensitive hydrogels containing graphene oxide as a nanofiller are presented. These systems were prepared from chitosan lactate and chitosan chloride solutions with the use of a salt of pyrimidine nucleotide-uridine 5'-monophosphate disodium salt-as the cross-linking agent. In order to perform the characterization of the developed hydrogels, the sol-gel transition temperature of the colloidal systems was first determined based on rheological measurements. The hydrogels were also analyzed using FTIR spectroscopy and SEM. Biological studies assessed the cytotoxicity (resazurin assay) and genotoxicity (alkaline version of the comet assay) of the nanocomposite chitosan hydrogels against normal human BJ fibroblasts. The conducted research allowed us to conclude that the developed hydrogels containing graphene oxide are an attractive material for potential use as scaffolds for the regeneration of damaged tissues.

Development of silver-doped copper oxide and chitosan nanocomposites for enhanced antimicrobial activities.

Antimicrobial resistance (AMR) has emerged as a significant and pressing public health concern, posing serious challenges to effectively preventing and treating persistent diseases. Despite various efforts made in recent years to address this problem, the global trends of AMR continue to escalate without any indication of decline. As AMR is well-known for antibiotics, developing new materials such as metal containing compounds with different mechanisms of action is crucial to effectively address this challenge. Copper, silver, and chitosan in various forms have demonstrated significant biological activities and hold promise for applications in medicine and biotechnology. Exploring the biological properties of these nanoparticles is essential for innovative therapeutic approaches in treating bacterial and fungal infections, cancer, and other diseases. To this end, the present study aimed to synthesize silver@copper oxide (Ag@CuO) nanoparticles and its chitosan nanocomposite (Chi-Ag@CuO) to investigate their antimicrobial efficacy. Various established spectroscopic and microscopic methods were employed for characterization purposes, encompassing scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). Subsequently, the antimicrobial activity of the nanoparticles was assessed through MIC (minimum inhibitory concentration), MBC (minimum bactericidal concentration), and well-disk diffusion assays against Pseudomonas aeruginosa, Acinetobacter baumannii Staphylococcus aureus, Staphylococcus epidermidis, and Candida albicans. The size of the CuO-NPs, Ag@CuO, and Chi-Ag@CuO NPs was found to be 70-120 nm with a spherical shape and an almost uniform distribution. The nanocomposites were found to possess a minimum inhibitory concentration (MIC) of 5 μg/mL and a minimum bactericidal concentration (MBC) of 250 μg/mL. Moreover, these nanocomposites generated varying clear inhibition zones, with diameters ranging from a minimum of 9±0.5 mm to a maximum of 25±0.5 mm. Consequently, it is evident that the amalgamation of copper-silver-chitosan nanoparticles has exhibited noteworthy antimicrobial properties in the controlled laboratory environment, surpassing the performance of other types of nanoparticles.

Recent Advancements in Metallic Au- and Ag-Based Chitosan Nanocomposite Derivatives for Enhanced Anticancer Drug Delivery

The rapid advancements in nanotechnology in the field of nanomedicine have the potential to significantly enhance therapeutic strategies for cancer treatment. There is considerable promise for enhancing the efficacy of cancer therapy through the manufacture of innovative nanocomposite materials. Metallic nanoparticles have been found to enhance the release of anticancer medications that are loaded onto them, resulting in a sustained release, hence reducing the dosage required for drug administration and preventing their buildup in healthy cells. The combination of nanotechnology with biocompatible materials offers new prospects for the development of advanced therapies that exhibit enhanced selectivity, reduced adverse effects, and improved patient outcomes. Chitosan (CS), a polysaccharide possessing distinct physicochemical properties, exhibits favorable attributes for controlled drug delivery due to its biocompatibility and biodegradability. Chitosan nanocomposites exhibit heightened stability, improved biocompatibility, and prolonged release characteristics for anticancer medicines. The incorporation of gold (Au) nanoparticles into the chitosan nanocomposite results in the manifestation of photothermal characteristics, whereas the inclusion of silver (Ag) nanoparticles boosts the antibacterial capabilities of the synthesized nanocomposite. The objective of this review is to investigate the recent progress in the utilization of Ag and Au nanoparticles, or a combination thereof, within a chitosan matrix or its modified derivatives for the purpose of anticancer drug delivery. The research findings for the potential of a chitosan nanocomposite to deliver various anticancer drugs, such as doxorubicin, 5-Fluroacil, curcumin, paclitaxel, and 6-mercaptopurine, were investigated. Moreover, various modifications carried out on the chitosan matrix phase and the nanocomposite surfaces to enhance targeting selectivity, loading efficiency, and pH sensitivity were highlighted. In addition, challenges and perspectives that could motivate further research related to the applications of chitosan nanocomposites in cancer therapy were summarized.

Microwave-assisted green synthesis of silver nanoparticles and chitosan nanocomposites for the removal of reactive blue-19

Microwave-assisted green synthesis of silver nanoparticles and chitosan nanocomposites for the removal of reactive blue-19

Efficient 2-Nitrophenol determination based on ultra-sonochemically prepared low-dimensional Au-nanoparticles decorated ZnO-chitosan nanocomposites by linear sweep voltammetry

In this study, linear sweep voltammetry (LSV) was implemented for the sensitive detection of 2-nitrophenol (2-NP) in phosphate buffer solution (PBS) at pH 7.00 with lab-made nanocomposite materials for environmental remediation. Initially, a flat glassy carbon electrode (GCE) modified using the inorganic-organic binary Au-NPs@ZnO/CTSN(Chitosan) nanocomposites (NCs) was used as a working electrode (WE). The NCs of Au NPs@ZnO/CTSN were basically prepared by an ultra-sonochemical process and fabricated on a GCE using conducting coating binder such as PEDOT:PSS. Before the electrochemical examination, the Au NPs@ZnO/CTSN NC was fully characterized by Fourier Transform Infrared Spectroscopy (FTIR), Field Emission Scanning Electron Microscopy (FESEM), Energy-dispersive X-ray Spectroscopy (EDS), Brunauer-Emmett-Teller (BET), X-Ray Diffraction analysis (XRD), High-Resolution Transmission Electron Microscopy (HRTEM), and X-Ray Photoelectron Spectroscopy (XPS) to analyze the functional, morphological, structural, elemental, surface area, crystallinity, and binding energy analyses. A linear concentration range (LDR) of 2-NP from 15⁓150 μM was evaluated by LSV in room conditions. From the slope of the calibration curve, the sensor sensitivity was calculated and found to be 20.9905 μAμM−1cm−2. At signal/noise ratio of 3, the lower limit of detection (LOD) is obtained as 0.45 ± 0.023 μM. Additionally, pH optimization, sensor-probe characterization, stability, and validity are fully analyzed in identical conditions by LSV. Besides this, the assembled 2-NP sensor probe as Au NPs@ZnO/CTSN NCs/PEDOT:PSS/GCE for validity test was performed elaborately and found the reliable and satisfactory results. This is a new approach to the development of electrochemical sensors for environmental chemical analysis using an electrochemical process with gold-nanoparticle decorated ZnO-chitosan for the safety of environmental and healthcare fields on a broad scale.

Iron-Based Nanoparticles Synthesis, Characterization, and Antimicrobial Effectiveness

Background: Antimicrobial resistance (AMR) has emerged as a significant and pressing public health concern, posing serious challenges to effectively preventing and treating persistent diseases. Developing new antibiotics with different mechanisms of action is crucial to effectively address challenges in treating infections. A lot of work has already been done on mono-metallic nanoparticles to address the issue.Methods: This study aimed to synthesize multi-metallic iron, silver, and chitosan-embedded nanoparticles using a green approach. Iron, silver, chitosan nanoparticles, and a composite of iron–silver–chitosan was also synthesized. The synthesized nanoparticles and composites were characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier Transform Infrared Spectroscopy (FTIR) to evaluate their structural parameters. Their antimicrobial efficacy was investigated through MIC (minimum inhibitory concentration), MBC (minimum bactericidal concentration), and well-disk diffusion assays against Pseudomonas aeruginosa, Acinetobacter baumannii, Staphylococcus aureus, Staphylococcus epidermidis and Candida albicans.Results: The size of the Cu-NPs, Cu-Ag NPs, and Cu-Ag-CS NPs were found to be in the range of 32-40 nm size with a spherical shape. The nanocomposites' MIC and MBC were calculated to be 125 μg/mL and 500 μg/mL, respectively. The nanocomposites exhibited a range of clear inhibition zones, with a minimum diameter of 12 ± 0.5 mm and a maximum diameter of 22 ± 0.5 mm. Conclusion: The iron–silver–chitosan nanocomposite has been shown to have significant antimicrobial effects in the laboratory environment compared to other nanoparticles hence can be applied as potential biomedical/biological candidates in future.Keywords: Antibacterial; Antifungal Agents; Iron; Silver; Chitosan; Nanoparticles

Exploring the biomedical potential of chitosan‐ceria nanocomposites: synthesis and characterizations

The objective of this study was to synthesize and evaluate the biological effectiveness of cerium oxide (CeO2) against various bacterial and fungal strains. The chitosan‐CeO2 nanocomposite was comprehensively characterized. The Fourier transform infrared (FTIR) spectra displayed a combination of bands that provided evidence for the existence of a composite complex between the chitosan (CS) structure and the Ce–O bands originating from CeO2 nanoparticles. SEM measurements showed uniform dispersion across the whole CS surface, and the morphological changes were clearly observed as the CeO2 nanoparticle content was increased. In contrast, CS‐CeO2 demonstrates enhanced antibacterial efficacy against both Gram‐positive and Gram‐negative pathogens. The MTT method was utilized to assess the cytotoxicity of the examined CS‐CeO2, with the aim of evaluating the cell viability of various cancer cell lines under varying ultraviolet (UV) exposures. The enhanced penetration of CS and CeO2 nanocomposites into cancer cells during their anticancer activity, even in the absence of UV light, led to an increased rate of cell death. The administration of greater dosages of CS and its CeO2 nanocomposites led to an increased generation of reactive oxygen species (ROS), which was observed to be associated with an enhancement in the efficacy of anticancer activity. The impact was additionally amplified through exposure to UV radiation. The nanocomposite thin films demonstrated much higher antioxidant activity against the DPPH radical as compared to ordinary vitamin C. The aforementioned observation was derived from an evaluation of the antioxidant properties of the subject utilizing the DPPH free radical scavenging technique.

Chitosan-Loaded Lagenaria siceraria and Thymus vulgaris Potentiate Antibacterial, Antioxidant, and Immunomodulatory Activities against Extensive Drug-Resistant Pseudomonas aeruginosa and Vancomycin-Resistant Staphylococcus aureus: In Vitro and In Vivo Approaches.

Antimicrobial resistance poses considerable issues for current clinical care, so the modified use of antimicrobial agents and public health initiatives, coupled with new antimicrobial approaches, may help to minimize the impact of multidrug-resistant (MDR) bacteria in the future. This study aimed to evaluate the antimicrobial, antioxidant, and immunomodulatory activities of Lagenaria siceraria, Thymus vulgaris, and their chitosan nanocomposites against extensive drug-resistant (XDR) Pseudomonas aeruginosa and vancomycin-resistant Staphylococcus aureus (VRSA) using both in vitro and in vivo assays. The in vitro antimicrobial susceptibilities of P. aeruginosa and VRSA strains revealed 100% sensitivity to imipenem (100%). All P. aeruginosa strains were resistant to cefoxitin, cefepime, trimethoprim + sulfamethoxazole, and fosfomycin. However, S. aureus strains showed a full resistance to cefoxitin, amoxicillin, ampicillin, erythromycin, chloramphenicol, and fosfomycin (100% each). Interestingly, all S. aureus strains were vancomycin-resistant (MIC = 32-512 μg/mL), and 90% of P. aeruginosa and S. aureus strains were XDR. The antimicrobial potential of Lagenaria siceraria and Thymus vulgaris nanocomposites with chitosan nanoparticles demonstrated marked inhibitory activities against XDR P. aeruginosa and VRSA strains with inhibition zones' diameters up to 50 mm and MIC values ranging from 0.125 to 1 μg/mL and 1 to 8 μg/mL, respectively. The results of the in vivo approach in male Sprague Dawley rats revealed that infection with P. aeruginosa and S. aureus displayed significant changes in biochemical, hematological, and histopathological findings compared to the negative control group. These values returned to the normal range after treatment by chitosan nanoparticles, either loaded with Lagenaria siceraria or Thymus vulgaris. Real-time quantitative polymerase chain reaction (RT-qPCR) findings presented significant upregulation of the relative expression of the IL10 gene and downregulation of the IFNG gene throughout the experimental period, especially after treatment with chitosan nanoparticles loaded either with Lagenaria siceraria or Thymus vulgaris in comparison to the positive control groups. In conclusion, this is the first report suggesting the use of Lagenaria siceraria and Thymus vulgaris nanocomposites with chitosan nanoparticles as a promising contender for combating XDR P. aeruginosa and VRSA infections as well as a manager for inflammatory situations and oxidative stress-related disorders.

Polyphenol assisted nano-reinforced chitosan films with antioxidant and antimicrobial properties

Active packaging with nano-reinforcement has appeared as an emerging strategy to replace the conventional plastic packaging films. In this contribution, Quercetin/rutin/vanillic acid incorporated chitosan nanocomposites with a reinforcement effect of cellulose derived cellulose nanocrystals (CNC) or chicken feather derived nano-keratin (NK) were developed using solvent casting method. Polyphenol incorporated CNC reinforced films displayed 69% increase in tensile strength whereas only 38% rise in strength was depicted by nano-keratin reinforcement. Quercetin incorporated CNC reinforced films exhibited 22% decline in film's permeability to water vapors and almost 38% upsurge in opacity. The crosslinking between hydroxyl, amino and carboxyl groups of polyphenols, Chitosan and CNC respectively was confirmed by FTIR. XRD and SEM analysis suggested dispersed nano fillers in chitosan matrix and depicted intercalated morphologies with rough surface. The thermal transitions of prepared films were found to be comparable to chitosan control. Quercetin incorporated CNC reinforced films exhibited 70% DPPH free radical scavenging activity with highest phenolic content. Quercetin and rutin incorporated CNC composites showed anti-microbial activity which may be due to polyphenols in the film's structure. Moreover, baby carrots wrapped with quercetin incorporated CNC reinforced chitosan films exhibited least weight loss and maintained overall acceptability over one-week storage. Comparatively, among all blends, combining quercetin and chitosan along with CNC reinforcement, can aid in development of active films with improved mechanical strength, enhanced UV protection, free radical scavenging ability and antimicrobial properties appropriate for food preservation.

Hydrophobic and antibacterial properties of textiles using nanocomposite chitosan and SiO2 from rice husk ash as-coating

This research aims to develop hydrophobic and antibacterial properties of textiles using chitosan and silica oxide (SiO2) nanocomposite coating. SiO2 was extracted from rice husk ash and chitosan from crustacean shells. SiO2 and chitosan powder were pulverized using High Energy Milling (HEM). The nanocomposite was synthesized using the sol-gel method with concentration variations of 0.2 %:0.4 %, 0.4 %:0.6 %, 0.6 %:0.8 %, and 0.8 %:1 %. Textile coating was carried out by dip coating method with variations of 1x, 2x, 3x, and 4x dyeing. The crystal structure and size of the nanocomposites were obtained using X-ray Diffraction (XRD). Surface morphology and particle size were obtained using a Scanning Electron Microscope (SEM). The contact angle was measured using the sessile drop method. The bacterial activity tests were conducted by measuring the surface temperature of textiles with a thermal camera after being irradiated with UV-C. The ability of textiles to inhibit bacterial growth was tested using Staphylococcus aureus bacteria. The results showed that the smallest crystal size obtained was 30.21 nm. The amount of particle size and contact angle are significantly influenced by the quality of Citosan-SiO2 and coloring changes. The smallest particle size obtained is 32 nm. The highest value of contact angle obtained was 161° The average surface temperature of the textile after being irradiated with UV-C reached 40.7 °C. The highest zone of inhibition obtained was 17 mm and is in the strong category. This research shows that textiles coated with chitosan-SiO2 can inhibit bacterial growth and have potential applications in the clothing industry.

Physicochemical and photocatalytic properties of biogenic ZnO and its chitosan nanocomposites for UV-protection and antibacterial activity on coated textiles

The textiles for medical use and the purification of textile factory effluents have become the most crucial part of the human healthcare sector. In this study bioactive compounds produced by four distinct plant extracts were used for the synthesis of zinc oxide nanoparticles. The four different ZnO nanoparticles were comprehensively characterized by different analytical techniques. XRD analysis revealed the crystalline nature and phase purity of the ZnO nanoparticles. FTIR spectra provided information on the function of plant extracts in the stabilization or capping process. The size distribution and morphological diversity of the nanoparticles were further clarified by SEM and TEM images. The photocatalytic degradation activity of the four ZnO nanoparticles on two different dyes showed that ZnO nanoparticles prepared from A. indica were most effective for the degradation of 98 % and 91 % of Rhodamine B and Alizarin red dye respectively. The selected ZnO nanoparticles from A. indica were used to prepare ZnO-chitosan nanocomposites before coating on cotton fabrics. The hydrophobicity, UV protection factor, and antibacterial activity of ZnO-chitosan nanocomposites, when coated on cotton fabrics, were also examined. The overall results demonstrated the ZnO and ZnO-chitosan nanocomposite prepared in the present study as a promising material for environmental remediation application.

Cu@Ag–CeO2/Chitosan Nanocomposite: Green Catalyst for Synthesis of 4-Arylidene-isoxazolidinones and Amidoalkyl Naphthols with Density Functional Theory and Antimicrobial Studies

Cu@Ag–CeO₂/Chitosan Nanocomposite: Green Catalyst for Synthesis of 4-Arylidene-isoxazolidinones and Amidoalkyl Naphthols with Density Functional Theory and Antimicrobial Studies

Synthesis, characterization, pharmacological and computational evaluation of hyaluronic acid modified chebulinic acid encapsulated chitosan nanocomposite for cancer therapy

The purpose of this study was to produce hyaluronic acid customized nanoparticles with chitosan for the delivery of chebulinic acid (CLA) to enhance its anticancer potential against breast cancer. A significant portion of CLA was encapsulated (89.72 ± 4.38 %) and loaded (43.15 ± 5.61 %) within hybrid nanoparticles. The colloidal hybrid nanoparticles demonstrated a polydispersity index (PDI) of about 0.379 ± 0.112, with zeta capacitance of 32.69 ± 5.12 (mV), and an average size of 115 ± 8 (nm). It was found that CLA-CT-HA-NPs had stronger anticancer effects on MCF-7 cells (IC50 = 8.18 ± 3.02 μM) than pure CLA (IC50 = 17.15 ± 5.11 μM). The initial cytotoxicity findings were supported by additional investigations based on comet assay and flow cytometry analysis. Tumor remission and survival were evaluated in five separate groups of mice. When juxtaposed with pure CLA (3.17 ± 0.419 %), CLA-CT-HA-NPs improved survival rates and reduced tumor burden by 3.76 ± 0.811(%). Furthermore, in-silico molecular docking investigations revealed that various biodegradable polymers had several levels of compatibility with CLA. The outcomes of this study might potentially served as an effective strategy for delivering drugs in the context of breast cancer therapy.

MoS2 nanoflower decorated bio-derived chitosan nanocomposites for sustainable energy storage: Structural, optical and electrochemical studies

Bio-derived chitosan-molybdenum di sulfide (Cs–MoS2) nanocomposites are prepared by a simple and economical aqueous casting method with varying concentrations of MoS2. The structural, surface morphological, optical, and electrochemical properties of the nanocomposites were studied. FTIR analysis reveals the strong interaction between Cs and MoS2. FESEM micrograph showed an increment of the surface roughness due to the incorporation of MoS2 layers into Cs. The surface wettability of the nanocomposites was found to be decreased from 73° to 33° due to the incorporation of MoS2 into the chitosan. UV–vis spectroscopy study demonstrates a reduction of optical bandgap from 4.29 to 3.44 eV as the nanofiller, MoS2, introduces localized states within the forbidden energy bandgap. The incorporation of MoS2 was found to increase the specific capacitance of Cs from 421 mFg−1 to 1589 mFg−1 at a current density of 100 μAg-1. The EIS analysis revealed an increase in the pseudo-capacitance from 0.09 μF to 4.13 μF and a reduction of charge transfer resistance that comes from the nanofiller contribution. MoS2 nanoflower introduces more active sites and expands the electroactive zone, thus improving the charge storage property of Cs. The Cs–MoS2 may offer a new route for the synthesis of eco-friendly, biodegradable, and electrical storage devices.

Bifunctional of Fe3O4@chitosan nanocomposite as a clarifying agent and cationic flocculant on different sugar solutions as a comprehensive semi industrial application

In the sugar industry, eliminating side impurities throughout the manufacturing process is the most significant obstacle to clarifying sugar solutions. Herein, magnetic chitosan (MCS) nanocomposite was Fabricated to be used as a biodegradable, environmentally friendly clarifying agent throughout the cane juice and sugar refining processes. Fe3O4 was synthesized using the coprecipitation procedure, and then MCS was combined using a cross-linking agent. Furthermore, 14.76 emu g−1 was the maximum saturation magnetization (Ms) value. Because MCS is magnetically saturated, it may be possible to employ an external magnetic field to separate the contaminant deposited on its surface. Additionally, zeta potential analysis showed outstanding findings for MCS with a maximum value of (+) 20.7 mV, with improvement in color removal % up to 44.8% using MCS with more than 24% in color removal % compared to the traditional clarification process. Moreover, utilizing MCS reduced turbidity from 167 to 1 IU. Overall, we determined that MCS nanocomposite exhibits considerable effectiveness in the clarifying process for different sugar solutions, performing as an eco-friendly bio-sorbent and flocculating material.

Development of polysaccharide-coated layered double hydroxide nanocomposites for enhanced oral insulin delivery

Oral insulin (INS) is predicted to have the most therapeutic advantages in treating diabetes to repress hepatic glucose production through its potential to mimic the endogenous insulin pathway. Many oral insulin delivery systems have been investigated. Layered double hydroxide (LDH) as an inorganic material has been widely used in drug delivery thanks to its appealing features such as good biocompatibility, low toxicity, and excellent loading capability. However, when used in oral drug delivery, the effectiveness of LDH is limited due to the acidic degradation in the stomach. In this study, to overcome these challenges, chitosan (Chi) and alginate (Alg) dual-coated LDH nanocomposites with the loading of insulin (Alg-Chi-LDH@INS) were developed by the layered-by-layered method for oral insulin delivery with dynamic size of ~ 350.8 nm, negative charge of ~ − 13.0 mV, and dispersity index 0.228. The insulin release profile was evaluated by ultraviolet–visible spectroscopy. The drug release profiles evidenced that alginate and chitosan coating partially protect insulin release from a burst release in acidic conditions. The analysis using flow cytometry showed that chitosan coating significantly enhanced the uptake of LDH@INS by Caco-2 cells compared to unmodified LDH and free insulin. Further in the in vivo study in streptozocin-induced diabetic mice, a significant hypoglycemic effect was maintained following oral administration with great biocompatibility (~ 50% blood glucose level reduction at 4 h). This research has thus provided a potential nanocomposite system for oral delivery of insulin.Graphical

Chitosan, chitosan derivatives, and chitosan-based nanocomposites: eco-friendly materials for advanced applications (a review).

For many years, chitosan has been widely regarded as a promising eco-friendly polymer thanks to its renewability, biocompatibility, biodegradability, non-toxicity, and ease of modification, giving it enormous potential for future development. As a cationic polysaccharide, chitosan exhibits specific physicochemical, biological, and mechanical properties that depend on factors such as its molecular weight and degree of deacetylation. Recently, there has been renewed interest surrounding chitosan derivatives and chitosan-based nanocomposites. This heightened attention is driven by the pursuit of enhancing efficiency and expanding the spectrum of chitosan applications. Chitosan's adaptability and unique properties make it a game-changer, promising significant contributions to industries ranging from healthcare to environmental remediation. This review presents an up-to-date overview of chitosan production sources and extraction methods, focusing on chitosan's physicochemical properties, including molecular weight, degree of deacetylation and solubility, as well as its antibacterial, antifungal and antioxidant activities. In addition, we highlight the advantages of chitosan derivatives and biopolymer modification methods, with recent advances in the preparation of chitosan-based nanocomposites. Finally, the versatile applications of chitosan, whether in its native state, derived or incorporated into nanocomposites in various fields, such as the food industry, agriculture, the cosmetics industry, the pharmaceutical industry, medicine, and wastewater treatment, were discussed.

Effects of oregano essential oil Pickering emulsion and ZnO nanoparticles on the properties and antibacterial activity of konjac glucomannan/carboxymethyl chitosan nanocomposite films.

Green and environmentally friendly natural bio-based food packaging films are increasingly favored by consumers. This study incorporated carboxylated-cellulose nanocrystal stabilized oregano essential oil (OEO) Pickering emulsion and ZnO nanoparticles (ZNPs) into konjac glucomannan (KGM)/carboxymethyl chitosan (CMCS) complexes to develop active food packaging films. The effects of OEO Pickering emulsion and ZNPs on the physical, structural, and antimicrobial activities of the nanocomposite films were evaluated. The OEO Pickering emulsion had a droplet size of 48.43 ± 3.56 μm and showed excellent dispersion and stability. Fourier transform infrared and X-ray diffraction analyses suggested that the interactions between the Pickering emulsion, ZNPs and KGM/CMCS matrix were mainly through hydrogen bonding. SEM observations confirmed that the Pickering emulsion and ZNPs were well incorporated into the KGM/CMCS matrix, forming tiny pores within the nanocomposite films. The incorporation of the OEO Pickering emulsion and/or ZNPs obviously increased the light and water vapor barrier ability, thermal stability, mechanical strength and antimicrobial properties of the KGM/CMCS nanocomposite film. Notably, KGM/CMCS/ZNPs/OEO Pickering emulsion films exhibited the highest barrier, and mechanical and antimicrobial activities due to the synergistic effect between the OEO Pickering emulsion and ZNPs. These results suggest that KGM/CMCS/ZNPs/OEO Pickering emulsion films can be utilized as novel active food packaging materials to extend the shelf life of packaged foods.