High Molecular Weight Chitosan Research Articles

Synthesis, properties and applications of new hybrid material based on native/magnetically modified sepiolite and chitosans

The study introduces novel hybrid materials containing native and magnetite-containing sepiolite (Sep, SepM respectively) and chitosans (Ch) of different molecular weights. The main objective of this work was to determine the properties of these materials, including the different types of stability (colloidal, gravitational and thermal) in systems containing sepiolite, in order to obtain effective, stable and easily producible hybrid materials with great potential for water and wastewater treatment. The following measurements and methods were performed to characterize the investigated system: low-temperature nitrogen adsorption–desorption, zeta potential analysis, UV–Vis, FT-IR, XRD, XRF, SEM-EDS, TGA, DSC and DTG. It was found that the complexes with high molecular weight chitosan exhibited the best stability of the systems. The same tendency was observed for the concentration dependence: the higher the chitosan concentration, the better the stabilization of the composites. Overall, this study shows that chitosan effectively improves the colloidal and gravitational stability of the composites. Due to its unique structure, the synthesized magnetic hybrid material has shown great advantages in the adsorptive removal of textile dyes such as anionic acid red 88 (AR88) and cationic methylene blue (MB) which can be easily removed from the dye solutions after its use using an external magnetic field.

Analysis of molecular structure and topological properties of chitosan isolated from crab shell and mushroom

This investigation aimed to scrutinize the chemical and structural analogies between chitosan extracted from crab exoskeleton (High Molecular Weight Chitosan, HMWC) and chitosan obtained from mushrooms (Mushroom-derived Chitosan, MRC), and to assess their biological functionalities. The resulting hydrolysates from the hydrolysis of HMWC by chitosanase were categorized as chitosan oligosaccharides (csCOS), while those from MRC were denoted as mrCOS. The molecular weights (MW) of csCOS and mrCOS were determined using Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) mass spectrometry. Furthermore, structural resemblances of csCOS and mrCOS were assessed utilizing X-ray powder diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy. Intriguingly, no apparent structural disparity between csCOS and mrCOS was noted in terms of the glucosamine (GlcN) and N-acetylglucosamine (GlcNAc) composition ratios. Consequently, the enzymatic activities of chitosanase for HMWC and MRC exhibited remarkable similarity. A topological examination was performed between the enzyme and the substrate to deduce the alteration in MW of COSs following enzymatic hydrolysis. Moreover, the evaluation of antioxidant activity for each COS revealed insignificance in the structural disparity between HMWC and MRC. In summary, grounded on the chemical structural similarity of HMWC and MRC, we propose the potential substitution of HMWC with MRC, incorporating diverse biological functionalities.

Chitosan-(poly)acrylic acid polyelectrolyte complexes: Enhanced mucoadhesion and sustained drug release in vaginal tablets

Polyelectrolyte complexes (PECs) have emerged as promising vehicles for medical applications, attributable to their non-toxicity, non-immunogenicity, and ability for controlled drug release. Notably, their inherent mucoadhesive properties are being leveraged for sustained drug delivery across mucosal barriers, including vaginal, ocular, nasal, and buccal membranes. This study delves into the formulation and effects of chitosan-(poly)acrylic acid-based PEC for vaginal tablet applications. A comparative analysis of various polymer combinations was conducted, emphasizing the differential impacts of low versus high-molecular weight chitosan. Results highlighted that PECs augmented the flowability of powder mixtures and bolstered the tablets' physical properties. Moreover, PEC-enhanced formulations exhibited a pronounced increase in swelling efficiency, with swelling index values reaching up to 92.67 % ± 1.90, ensuring structural integrity during dissolution. In ex vivo mucoadhesion tests, tablets from PEC mixes demonstrated extended adhesion, surpassing 48 h for certain formulations. The optimized PEC formulation successfully achieved sustained drug release while retaining tablet adhesion for the duration of the release period.

3D-Printed Chitosan-Based Scaffolds with Scutellariae baicalensis Extract for Dental Applications.

The plant material Scutellariae baicalensis radix, which is rich in flavones (baicalin), possesses antibacterial, antifungal, antioxidant, and anti-inflammatory properties. This work aimed to develop a 3D-printed chitosan-based hydrogel rich in Scutellariae baicalensis extract as an innovative approach for the personalized treatment of periodontal diseases. Chitosan-based hydrogels were prepared, and the printability of the prepared hydrogels was determined. The hydrogel with 2.5% w/v of high molecular-weight chitosan (CS), 2% w/v gelatin (Gel), and 10% w/w of extract (Ex) presented the best printability, producing smooth and uniform scaffolds. It was proved that the CS/Gel/Ex hydrogel was stabilized by hydrogen bonds and remained in amorphous dispersion in the 3D-printed structures (confirmed by ATR-FTIR and XRPD). Due to the amorphization of the active substance, a significant increase in the release of baicalin in vitro was observed. It was demonstrated that there was an initial burst release and a continuous release profile (n = 3). Higuchi kinetic was the most likely baicalin release kinetic. The second fit, the Korsmeyer-Peppas kinetics model, showed coupled diffusion of the active ingredient in the hydrated matrix and polymer relaxation regulated release, with n values ranging from 0.45 to 0.89. The anti-inflammatory properties of 3D-printed scaffolds were assessed as the ability to inhibit the activity of the hyaluronidase enzyme. Activity was assessed as IC50 = 63.57 ± 4.98 mg hydrogel/mL (n = 6). Cytotoxicity tests demonstrated the biocompatibility of the material. After 24 h of exposure to the 2.5CS/2Gel/10Ex scaffold, fibroblasts migrated toward the scratch, closed the "wound" by 97.1%, and significantly accelerated the wound healing process. The results render the 3D-printed CS/Gel/extract scaffolds as potential candidates for treating periodontal diseases.

Reinforced hydrogel building via formation of alginate-chitosan double network with pH & salt-responsiveness and electric conductivity for soft actuators

Aiming at green and friendly environmental protection, polyvinyl alcohol/sodium alginate/chitosan (PSCS) double network hydrogel was successfully prepared through diffusing the high molecular weight chitosan into PVA/sodium alginate (PS) hydrogel without any other toxic reagents. The polyanion hydrogels could be significantly enhanced by immersing the polyanion hydrogel in high molecular weight chitosan solution without requiring specific structure. The PSCS hydrogel had a compact and rough surface structure with the smaller porosities and larger crystallization degree compared with polyvinyl alcohol/sodium alginate hydrogels and polyvinyl alcohol/sodium alginate/Ca2+ (PSCa) hydrogels. The PSCS hydrogel possessed excellent hydrolysis resistance, the significant pH-sensitive and salt-sensitive swelling. In addition, the flexibility, Young's modulus and mechanical properties of PSCS hydrogel can be adjusted through the changing the content of sodium alginate. Moreover, PS, PSCa and PSCS had electric conductivity, and PSCS showed twice the conductivity compared to PS hydrogel. Based on differences of swelling ratio, a PSCS bilayer hydrogel was designed and showed excellent pH-driven deformation ability. The PSCS hydrogel is expected to expand the application of hydrogels in conditions involving stimulus response, and might serve as a promising intelligent actuators or soft robots.

Synthesis and comprehensive characterization with anticancer activity assessment of salicylaldehyde and 2-acetylphenol based chitosan thiosemicarbazones and their copper(II) complexes

Functionalization of chitosan as salicylaldehyde and 2-acetylphenol-based chitosan thiosemicarbazone involving amino group at C2 position of pyranose ring was confirmed by comprehensive characterization by spectroscopic and analytical ways. Both the low molecular weight (Mw) chitosan oligosaccharide (CS) (Mw < 3000 Da, degree of deacetylation (DDA) = 87 %) and the crab shell chitosan (CCS) (Mw = 350 kDa, DDA = 67 %) functionalized thiosemicarbazones behaved as ONS tridentate ligand to form the square planar copper(II) complexes with a chloride ion as an additional ligand to satisfy the co-ordination sphere. All the derivatives were found thermally stable till the commencement of chitosan backbone disruption at 200 °C. The MTT assay profiles showed a conspicuous enhancement in the in vitro antitumorigenic and anticancer activity of native chitosan upon its functionalization as phenolic carbaldehyde chitosan thiosemicarbazones. Further, the assays more often revealed a further lowering of cell viability with chitosan oligosaccharide derivatives in comparison to high molecular weight chitosan derivatives, and a lower viability of the MCF-7 cancer cells than the tumorigenic MDCK cells. Both the low Mw chitosan with high DDA and high Mw chitosan with low DDA, the chitosan-functionalized salicylaldehyde based thiosemicarbazones, and their copper(II) chitosan thiosemicarbazone complexes were found to have minimal toxicity with IC50 >600 μgmL−1 against the mouse embryonic normal fibroblast NIH3T3 cells. These results were indicatives of more protonation and enhanced anticancer activity of chitosan oligosaccharide derivatives, and preferential cytotoxicity of chitosan biomaterials against the tumorigenic and cancer cells with more negatively charged cell surfaces.

Improvement of Osteogenic Differentiation of Mouse Pre-Osteoblastic MC3T3-E1 Cells on Core-Shell Polylactic Acid/Chitosan Electrospun Scaffolds for Bone Defect Repair.

Electrospun hybrid scaffolds composed of synthetic and natural polymers have gained increasing interest in tissue engineering applications over the last decade. In this work, scaffolds composed of polylactic acid electrospun fibers, either treated (P-PLA) or non-treated (PLA) with air-plasma, were coated with high molecular weight chitosan to create a core-shell microfibrous structure. The effective thickness control of the chitosan layer was confirmed by gravimetric, spectroscopic (FTIR-ATR) and morphological (SEM) investigations. The chitosan coating increased the fiber diameter of the microfibrous scaffolds while the tensile mechanical tests, conducted in dry and wet environments, showed a reinforcing action of the coating layer on the scaffolds, in particular when deposited on P-PLA samples. The stability of the Chi coating on both PLA and P-PLA substrates was confirmed by gravimetric analysis, while their mineralization capacity was evaluated though scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) after immersing the scaffolds in simulated body fluids (SBF) at 37 °C for 1 week. Sample biocompatibility was investigated through cell viability assay and SEM analysis on mouse pre-osteoblastic MC3T3-E1 cells grown on scaffolds at different times (1, 7, 14 and 21 days). Finally, Alizarin Red assay and qPCR analysis suggested that the combination of plasma treatment and chitosan coating on PLA electrospun scaffolds influences the osteoblastic differentiation of MC3T3-E1 cells, thus demonstrating the great potential of P-PLA/chitosan hybrid scaffolds for bone tissue engineering applications.

The effects of ketogenic and chitosan-based diets on submandibular salivary gland in rat model: a comparative histological study

ObjectiveThis study was carried out in the submandibular salivary glands (SSGs) of rats to demonstrate the effect of a ketogenic diet (KD) in comparison with dietary chitosan supplementation.MethodEighteen albino rats were randomly divided into three equal groups of six animals each. Rats in Group I were fed a balanced diet and considered controls. Meanwhile, those of Groups II and III were fed a KD, a balanced diet with high molecular weight chitosan, respectively. After 45 days, rats were euthanized, and the SSGs were dissected carefully for staining with hematoxylin and eosin (H&E), alpha-smooth muscle actin (α-SMA) immunohistochemical staining, and Congo red special stain. Quantitative data from α-SMA staining and Congo red staining were statistically analyzed using one-way ANOVA followed by Tukey’s multiple comparisons post hoc test.ResultsRegarding Congo red and α-SMA staining, one-way ANOVA revealed a significant difference between the three groups. For α-SMA staining and Congo red staining, Group II had the highest mean values of 91.41 ± 3.30 and 68.10 ± 5.04, respectively, while Group I had the lowest values of 56.13 ± 3.96 and 16.87 ± 2.19, respectively. Group III had mean values of 60.70 ± 3.55 for α-SMA and 19.50 ± 1.78 for Congo red. Tukey’s multiple comparisons post hoc test revealed significant differences between groups I & II and between groups II & III (P < 0.05). Meanwhile, there was a nonsignificant difference between groups I and III (P > 0.05).ConclusionA KD has a deleterious effect on rats’ SSG whatever the test we used, and dietary chitosan supplementation ameliorates these damaging effects.

Evaluation of fungicidal efficacy of free and nano-encapsulated chitosan against &lt;i&gt;Aspergillus flavus&lt;/i&gt; isolated from rice (&lt;i&gt;Oryza sativa&lt;/i&gt;) seed

Grains are exposed to contamination by mycotoxins, both in the field and during storage. Aflatoxins produced by Aspergillus species are the most harmful and carcinogenic mycotoxins in grains. Synthetic fungicides are widely used for the control of mycotoxigenic fungi in grains. However, rising public awareness about the toxicological effects of fungicides on human health necessitates the development of non-toxic bio-fungicides. In this connection, reports have shown that chitosan synthesized from shell waste has the potential to serve as an alternative fungicide. Therefore, this study investigated the fungicidal efficacy of free and nano-encapsulated chitosan against aflatoxigenic fungus (Aspergillus flavus). High molecular weight chitosan was purchased, and the in-vitro antifungal efficacy of chitosan against A. flavus was tested using the food poisoning method. Nano-encapsulated chitosan was synthesized using the ionic gelation method, the particle size was determined, and invitro inhibition against A. flavus was investigated. The results revealed that nano-encapsulated chitosan with particle sizes of 525.4 nm, 468.3 nm, and 711.7 nm were obtained. In-vitro mycelial A. flavus growth inhibition of 100% was recorded at 1.5% and 2.0% of free chitosan, while at 0.5% and 1.0% of free chitosan, 45% and 75% inhibition were observed, respectively. Nano-encapsulated chitosan with particle size (nm) of 525.4, 468.3, and 711.7 at 0.50% recorded 61%, 84% and 87% inhibition, respectively. However, at 0.25%, the rate of inhibition was 64%, 78% and 67%, respectively. This study showed that free chitosan and nano-encapsulated chitosan are potential antifungal agents for the control of A. flavus.

Ocular Mucoadhesive and Biodegradable Sponge-Like Inserts for the Sustained and Controlled Delivery of Voriconazole; Preparation, D-optimal Factorial Optimization and in-vivo Evaluation

The aim of this study was to formulate and optimize by statistical means mucoadhesive and biodegradable sponge-like inserts loaded with voriconazole (VCZ) which increases the contact time of the drug with the eye and sustain its release from the formula in a controlled manner. This avoids the pulsed effect reported for the drug suspension and results in reducing the number of drug instillations in the eye with the result of enhancing the patient compliance. Also, the sponge like nature of the insert reduces the foreign body sensation caused by other ocular solid dosage forms. They were prepared using casting/freeze-drying technique using five polymers namely high molecular weight chitosan (CH), sodium alginate (AL), sodium carboxy methyl cellulose (CMC), gellan gum (GG) and xanthan gum (XG). The prepared inserts were subjected to evaluations of their visual appearance, weight variation, drug content, surface pH, in-vitro release (percent drug released after 1h (Q1 (%)), mean dissolution time (MDT) and dissolution efficiency (DE)) in addition to kinetic analysis of the release data, water uptake, mucoadhesion and rheology of the forming plain polymer solution at the maximum rate of shear. The independent variables of the D-optimal factorial design were the polymer type and concentration while Q1 (%), MDT, DE, % water uptake after 15 minutes and rheology at the maximum rate of shear were chosen as dependant variables. The performed optimization process using design expert software showed an optimum formula consisting of 2 % GG. It showed slow release behavior compared to the drug suspension. FTIR and DSC studies showed that there is no interaction between VCZ and GG. The optimum formula has good in-vitro mucoadhesive properties and pH in the safe ocular range. Moreover, it showed promising in-vivo results of rapid hydration and gelling in addition to good mucoadhesive behavior when instilled in the eye, high ocular safety and biocompatibility, sustained antifungal activity in comparison to the drug suspension and finally biodegradation. So, it may be taken into consideration as an outstanding carrier for the ocular delivery of VCZ.

Effects of chitosan with different molecular weights on storage quality and fungi inhibition of mini-cucumber

The effect of low (LWC, 30 kD), medium (MWC, 150 kD) and high molecular weight chitosan (HWC, 300 kD) coatings on storage quality and fungi inhibition of mini-cucumber was evaluated. Chitosan coatings significantly reduced the weight loss, and delayed the color change and sensory score of mini-cucumber when compared with the control. Chitosan coatings significantly retarded the decrease of DPPH free radical scavenging rate and total phenol content, and inhibited the total number of bacterial colonies and the viable numbers of yeast and molds in mini-cucumber. Chitosan coatings also significantly reduced the disease incidence and disease severity of mini-cucumber artificial inoculated with Botrytis cinerea. LWC coating showed superior preservation effectiveness and antifungal activity to MWC and HWC coating. Compared with the control, LWC coating prolonged the shelf life by 6 days which was evaluated by sensory score, and reduced the total number of bacterial colonies and viable numbers of yeast and molds in mini-cucumber by 4.20 log10 CFU/g and 2.72 log10 CFU/g, respectively. These results suggested that chitosan molecular weights affected preservation effectiveness and antifungal activity against B. cinerea and LWC could be used to prolong the shelf life of mini-cucumber and maintain its quality after harvest.

&lt;i&gt;Agaricus bisporus&lt;/i&gt; chitosan influences the concentrations of caftaric acid and furan-derived compounds in Pinot noir juice and base wine

Chitosan is a fining agent used in winemaking, although its use in juice and wine beyond fining has been limited until now. Therefore, this study's first aim was to determine if chitosan derived from Agaricus bisporus (button mushrooms) could reduce caffeic and caftaric acid concentrations in Pinot noir grape juice (Study A). The second aim was to determine if chitosan, when added to base wine, could influence the synthesis of furan-derived compounds during storage (Study B). In Study A, Pinot noir grape juice was stored at 10 °C for 18 hours after the following treatments: control (no addition), bentonite/activated charcoal (BAC), low molecular weight (&lt; 3 kDa; LMW) chitosan, med. MW (250 kDa; MMW) chitosan, and high MW (422 kDa; HMW) chitosan (all 1 g/L additions). Caftaric acid was decreased, and total amino acid concentration was increased in the LMW chitosan-treated juice, while the estimated total hydroxycinnamic acid content, turbidity, and browning were decreased in the MMW chitosan-treated juice compared to the control. In Study B, Pinot noir base wine destined for sparkling wine was stored at 15 and 30 °C for 90 days with the following treatments: control (no addition), LMW chitosan, MMW chitosan, and HMW chitosan (all 1 g/L additions). The three chitosan treatments stored at 30 °C had increased furfural, homofuraneol, and 5-methylfurfural formation in the base wine compared to the control. At 15 °C, furfural and homofuraneol had greater concentrations in all chitosan-treated wines after 90 days of storage. Our results demonstrate the potential of mushroom-derived chitosan to remove caftaric acid from grape juice and suggest that chitosan can influence the synthesis of furan-derived compounds in wine after short-term storage.

Enhancing stability of liposomes using high molecular weight chitosan to promote antioxidative stress effects and lipid-lowering activity of encapsulated lutein in vivo and in vitro

Lutein is an antioxidant with multiple beneficial functions. However, its therapeutic potential is hampered by its low water solubility and bioavailability. The goal of this study is to compare the stability of lutein-loaded liposomes (Lu-lip) and low (LC)/high molecular weight (HC) chitosan-coated Lu-lip, along with their antioxidant capacity using H2O2-induced HepG2 cells and their lipid-lowering activity using high-fat diet mice. Both LC and HC reduced the lutein degradation rate by 17.5 % and 26.72 % in a challenging environment at pH 6 and T = 4 °C. Compared to LC, the HC coating improved the size- and zeta-potential-stability of Lu-lip at 5 < pH < 7, with the best performance at pH 6. The HC coating prolonged the lutein release profile, increased the cellular uptake of Lu-lip, and reduced the reactive oxygen species (ROS) levels and the H2O2-induced necrotic cell ratios by increasing the activities of catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px). Animal experiments have shown that oral administration of LC and HC coated Lu-lip can significantly reduce body weight levels, total triglycerides (TG), total cholesterol (TC), and non-high-density lipoprotein (n-HDL-C) in high-fat diet mice while significantly increasing the levels of CAT, SOD and GSH-Px in the liver of mice. LC and HC coated Lu-lip can reduce fat accumulation in the liver and epididymal adipose tissue.

Highly efficient production of N,N'-diacetylchitobiose according to substrate modification and changes in enzyme kinetics

The purpose of this study is to improve the method for characterizing the kinetics of enzymes on chitin and to improve the inconvenience of colloidal chitin production and use. Therefore, we prepared a low molecular weight (MW) substrate by partially hydrolyzing and acetylating high molecular weight chitosan (HMWC) with chitosanase. The activity of chitinase was confirmed under optimal reaction conditions using acetylated low molecular weight chitin (AcCOS). In the hydrolysates of AcCOS, N, N′-diacetylchitobiose (GlcNAc)2 was identified as the main product under optimal reaction conditions using TLC. Residual N-acetylglucosamine (GlcNAc), which could not be sufficiently identified by the sensitivity of TLC, was confirmed by Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) mass spectrometry. However, from a quantitative point of view, the TLC results suggest that the content of (GlcNAc)2 is much higher than that of GlcNAc. These results are significant for use as a specific substrate capable of evaluating the reaction rate of a chitinase substrate. Taken together, our results provide novel results for the highly efficient production of (GlcNAc)2 and the evaluation of its biological activity by chemical modification of the substrate.

Synthesized carboxymethyl-chitosan variant composites for cyclic adsorption-desorption based removal of Fe, Pb, and Cu

The global issue of environmental contamination from industrial wastewater comprising Cu, Fe and Pb demands effective treatment strategies. In this article, a functional composite sorbent was devised to selectively remove copper, iron, and lead from a real-world mimicking wastewater system. For the purpose, high, medium, and low molecular weight chitosan with amine and hydroxyl functional groups were used as a substrate, and glutaraldehyde was used to anchor the organic compound with carboxymethyl groups. Characterization with X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray analyzer accompanied by field emission scanning electron microscope, and Brunauer-Emmett-Teller were conducted for the synthesized adsorbent. Accordingly, the properties of the adsorbent were evaluated to infer that the synthesis assured a purified and functionalized system. The surface area of the medium carboxymethyl chitosan derivative was analyzed as 31.43 m2 g−1. Various adsorption parameters were examined methodically to assess upon optimal removal requirements. The effect of adsorbent dosage, contact time and concentration on the adsorption of the studied metal ions were conducted and the optimum values were achieved at pH 3.82, 540 min contact duration and 1.2 g L−1 sorbent dose. Maximum adsorbent capacities of 344.83 mg g−1, 9.59 mg g−1, and 90.09 mg g−1 were realized for Cu, Pb, and Fe, respectively. The experimental measurements of the studied heavy metal ions inferred the best fitness of Langmuir isotherm equilibrium and pseudo second order kinetic models. Further, elution studies with easy-to-deploy low-cost acidic and basic eluents (HCl, HNO3, H2SO4, KOH, and NaOH) were conducted with cyclic adsorption-desorption strategies. These investigations confirmed the adsorbent's good reusability up to 3 cycles of adsorption and its proximity to serve as a potential material for multi-heavy metal ions elimination from complex adsorbate systems.

Heterogeneous Radioinduced Graft Copolymerization of Caprolactone in Nanochitosan

This work focus on the chitosan-caprolactone graft copolymers’ (Ch-g-CL) synthesis through Radio Induced Grafting (RIG) of heterogeneous blends of solid chitosan polymers (particulated and nanoprecipitated) and liquid ε-caprolactone monomer, without the need of further reagents nor dissolution. The irradiation process was conducted at room temperature with gamma radiation from 60Co, followed in air and also under vacuum. Commonly applied sterilization doses of 25 and 45 kGy were used. The samples were analyzed, before and after irradiation, through FTIR-ATR, elemental analysis, scanning electron microscopy, 1H-NMR and size exclusion chromatography (SEC). It was found that copolymerization was successful on the blends with nanochitosan, due to a drastic increase in the active surface of the biopolymer. It was observed that the incorporation was better at higher doses and while irradiated on air, with up to 29% caprolactone incorporation. FTIR studies, along with elemental analysis and SEC, indicate that the most probable reaction is caprolactone grafting from/onto chitosan's amine groups. It was also observed that the incorporation increased in the higher molecular weight chitosan, which also has higher amine content. Practically, copolymers with 5–10% grafting sites with CL side chains of up to nine units, were obtained depending on the case. These RIG syntheses showed to lead to tunable Ch-g-CL structures of interest for biomedical applications as tissue scaffolds and drug delivery systems.

Structural, thermal, optical, and mechanical properties of composite films developed from the button mushroom (Agaricus bisporus)-sourced high molecular weight chitosan and potato starch

Films were fabricated using the button mushroom (Agaricus bisporus) sourced high molecular weight chitosan with or without potato starch using the casting method. Glycerol was used as the plasticizer. Chitosan content in the film-forming solution (FFS) was varied (0.5, 0.75 and 1.0% w/v of FFS) while potato starch (1.0% of FFS) and glycerol (25% of the total solid content in the solution) contents were not varied. The control sample contained only chitosan (1.0% of the FFS) and glycerol. The effect of increasing the content of chitosan on the rheological properties of FFS and the properties of the films were investigated. The FFS's shear viscosity and shear modulus (elastic and viscous components) increased with increasing chitosan content. Morphological examination revealed that the films exhibited a compact structure devoid of large pores and cracks. Surface roughness captured with an atomic force microscope was reduced (19-6 nm) with increasing content of chitosan in the film. The films exhibited two hydrated crystalline phases at 9 and 20o. Light transmittance and glossiness of the films were enhanced with increasing chitosan content. FTIR analysis indicated the increasing availability of reactive sites with the increasing content of chitosan leading to an enhanced hydrogen bonds network and increased cohesion of the film structure. This may be the reason for improved mechanical properties and reduced water vapour permeability of the films with increasing chitosan content.

Chitosan: Properties and Its Application in Agriculture in Context of Molecular Weight.

Chitosan is a naturally occurring compound that can be obtained from deacetylated chitin, which is obtained from various sources such as fungi, crustaceans, and insects. Commercially, chitosan is produced from crustaceans. Based on the range of its molecular weight, chitosan can be classified into three different types, namely, high molecular weight chitosan (HMWC, >700 kDa), medium molecular weight chitosan (MMWC, 150-700 kDa), and low molecular weight chitosan (LMWC, less than 150 kDa). Chitosan shows several properties that can be applied in horticultural crops, such as plant root growth enhancer, antimicrobial, antifungal, and antiviral activities. Nevertheless, these properties depend on its molecular weight (MW) and acetylation degree (DD). Therefore, this article seeks to extensively review the properties of chitosan applied in the agricultural sector, classifying them in relation to chitosan's MW, and its use as a material for sustainable agriculture.

Quaternization of high molecular weight chitosan for increasing intestinal drug absorption using Caco-2 cells as an in vitro intestinal model

Potential use of a quaternized chitosan (MW 600 kDa) with 65% of 3-chloro-2-hydroxypropyltrimethylammonium (600-HPTChC65) as an absorptive enhancer was investigated in Caco-2 monolayers. 600-HPTChC65 (0.005% w/v) quickly reduced transepithelial electrical resistance (TEER) to the maximum level in 40 min with full recovery within 6 h after removal. Its TEER reduction was corresponded to increased FD4 transport across the monolayers and disrupted localization of tight junction proteins ZO-1 and occludin at the cell borders. 600-HPTChC65 was densely localized at the membrane surface and intercellular junctions. This chitosan (0.08–0.32% w/v) reduced the efflux ratio of [3H]-digoxin by 1.7- 2 folds, suggesting an increased [3H]-digoxin transport across the monolayers. Its binding with P-gp on Caco-2 monolayer increased the signal of fluorescence-labeled anti-P-gp (UIC2) reactivity due to conformational change. 600-HPTChC65 (0.32% w/v) had no effect on P-gp expression in the Caco-2 monolayers. These results suggest that 600-HPTChC65 could enhance drug absorption through tight junction opening and decreased P-gp function. Its interaction with the absorptive barrier mainly resulted in disrupting ZO-1 and occludin organization as well as changing in P-gp conformation.

Comparison of shrimp waste-derived chitosan produced through conventional and microwave-assisted extraction processes: Physicochemical properties and antibacterial activity assessment

Depending on its physicochemical properties and antibacterial activities, chitosan can have a wide range of applications in food, pharmaceutical, medicine, cosmetics, agriculture, and aquaculture. In this experimental study, chitosan was extracted from shrimp waste through conventional extraction, microwave-assisted extraction, and conventional extraction under microwave process conditions. The effects of the heating source on the physicochemical properties and antibacterial activity were investigated. The results showed that the heating process parameters affected the physicochemical properties considerably. The conventional procedure yielded high molecular weight chitosan with a 12.7 % yield, while the microwave extraction procedure yielded a porous medium molecular weight chitosan at 11.8 %. The conventional extraction under microwave process conditions led to medium molecular weight chitosan with the lowest yield (10.8 %) and crystallinity index (79 %). Antibacterial assessment findings revealed that the chitosan extracted using the conventional method had the best antibacterial activity in the agar disk diffusion assay against Listeria monocytogenes (9.48 mm), Escherichia coli. (8.79 mm), and Salmonella Typhimurium (8.57 mm). While the chitosan obtained by microwave-assisted extraction possessed the highest activity against E. coli. (8.37 mm), and Staphylococcus aureus (8.05 mm), with comparable antibacterial activity against S. Typhimurium (7.34 mm) and L. monocytogenes (6.52 mm). Moreover, the minimal inhibitory concentration and minimal bactericidal concentration assays demonstrated that among the chitosan samples investigated, the conventionally-extracted chitosan, followed by the chitosan extracted by microwave, had the best antibacterial activity against the target bacteria.