High Molecular Weight Chitosan Research Articles

<i>Agaricus bisporus</i> 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 (< 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.

Biocatalysts based on papain associates with chitosan nanoparticles

The research purpose was to develop and study biocatalysts based on papain associates with chitosan nanoparticles. We obtained medium and high molecular weight chitosan nanoparticles, both with and without ascorbic acid . When the papainna-noparticles complexes with ascorbic acid were formed, the catalytic activity of the enzyme increased by 3 % for medium molecular weight chitosan and by 16 % for high molecular weight chitosan. After 168 hours of incubation in 0.05 M of Tris-HCl buffer (pH 7.5) at 37 °C, the free enzyme retained 15 % of its catalytic activity, whereas its associates with chitosan nanoparticles exhibited ~ 30 %. The papain complex with chitosan nanoparticles and ascorbic acid exhibited 40 % of the enzyme catalytic activity. We simulated the bonds and interactions within the chitosan-ascorbic acid-papain complex. The proposed biocatalysts have high prospects for effective use in cosmetology, biomedicine, and pharmacy.

Cyclic desorption based efficacy of polyvinyl alcohol-chitosan variant resins for multi heavy-metal removal

The simultaneous removal of Cu, Pb and Fe from water bodies has been targeted in this work with polyvinyl alcohol (PVA) and chitosan (low, medium, and high molecular weight) derivative and with cyclic desorption efficacy target. For a varied range of adsorbent loading (0.2–2 g L−1), initial concentration (187.7–563.1 mg L−1 for Cu, 5.2–15.6 mg L−1 for Pb, and 61.85–185.55 mg L−1 for Fe), and resin contact time (5 to 720 min), batch adsorption-desorption studies were conducted. After first adsorption-desorption cycle, the optimum absorption capacity was 6.85 mg g−1 for Pb, 243.90 mg g−1 for Cu, and 87.72 mg g−1 for Fe for the high molecular weight chitosan grafted polyvinyl alcohol resin (HCSPVA). The alternate kinetic and equilibrium models were analyzed along with the interaction mechanism between metal ions and functional groups. The cyclic desorption studies were carried out with simple eluent systems such as HCl, HNO3, H2SO4, KOH, and NaOH. The experiments revealed that the HCSPVA derivative has been an impressive, reusable, and effective sorbent for the mitigation of Pb, Fe, and Cu in complex wastewater systems. This is due to its easy synthesis, excellent adsorption capacity, quick sorption rate, and remarkable regeneration capabilities.

Controlled Chitosan Molecular Weight Reduction by Mechanochemical and Aging-Based Phosphoric Acid Hydrolysis

Chitosan is typically produced by the deacetylation of the chitin biopolymer. Its molecular weight (Mw) is a function of the chitin source and the deacetylation conditions. It remains a challenge to both control the Mw of chitosan and obtain good monodispersity, which are essential for optimal function of chitosan in different applications. This study explores the use of mechanochemistry and aging as effective methods toward the controlled reduction of the Mw of commercial high Mw chitosan (HMwChs) with phosphoric acid, where Mw was measured by gel permeation chromatography (GPC). In comparison to conventional solution-based methods, this new mechanochemical method features improved process mass intensity in comparison to conventional techniques and affords low Mw chitosan (LMwChs) samples in a range of 200 to 19.5 kDa, with a polydispersity down to1.8.

A Strategical Improvement in the Performance of CO2/N2 Gas Permeation via Conjugation of L-Tyrosine onto Chitosan Membrane

Rubbery polymeric membranes, containing amine carriers, have received much attention in CO2 separation because of their easy fabrication, low cost, and excellent separation performance. The present study focuses on the versatile aspects of covalent conjugation of L-tyrosine (Tyr) onto the high molecular weight chitosan (CS) accomplished by using carbodiimide as a coupling agent for CO2/N2 separation. The fabricated membrane was subjected to FTIR, XRD, TGA, AFM, FESEM, and moisture retention tests to examine the thermal and physicochemical properties. The defect-free dense layer of tyrosine-conjugated-chitosan, with active layer thickness within the range of ~600 nm, was cast and employed for mixed gas (CO2/N2) separation study in the temperature range of 25-115 °C in both dry and swollen conditions and compared to that of a neat CS membrane. An enhancement in the thermal stability and amorphousness was displayed by TGA and XRD spectra, respectively, for the prepared membranes. The fabricated membrane showed reasonably good CO2 permeance of around 103 GPU and CO2/N2 selectivity of 32 by maintaining a sweep/feed moisture flow rate of 0.05/0.03 mL/min, respectively, an operating temperature of 85 °C, and a feed pressure of 32 psi. The composite membrane demonstrated high permeance because of the chemical grafting compared to the bare chitosan. Additionally, the excellent moisture retention capacity of the fabricated membrane accelerates high CO2 uptake by amine carriers, owing to the reversible zwitterion reaction. All the features make this membrane a potential membrane material for CO2 capture.

Using Different Surface Energy Models to Assess the Interactions between Antiviral Coating Films and phi6 Model Virus.

High molecular weight chitosan (HMWCh), quaternised cellulose nanofibrils (qCNF), and their mixture showed antiviral potential in liquid phase, while this effect decreased when applied to facial masks, as studied in our recent work. To gain more insight into material antiviral activity, spin-coated thin films were prepared from each suspension (HMWCh, qCNF) and their mixture with a 1:1 ratio. To understand their mechanism of action, the interactions between these model films with various polar and nonpolar liquids and bacteriophage phi6 (in liquid phase) as a viral surrogate were studied. Surface free energy (SFE) estimates were used as a tool to evaluate the potential adhesion of different polar liquid phases to these films by contact angle measurements (CA) using the sessile drop method. The Fowkes, Owens-Wendt-Rabel-Kealble (OWRK), Wu, and van Oss-Chaudhury-Good (vOGC) mathematical models were used to estimate surface free energy and its polar and dispersive contributions, as well as the Lewis acid and Lewis base contributions. In addition, the surface tension SFT of liquids was also determined. The adhesion and cohesion forces in wetting processes were also observed. The estimated SFE of spin-coated films varied between mathematical models (26-31 mJ/m2) depending on the polarity of the solvents tested, but the correlation between models clearly indicated a significant dominance of the dispersion components that hinder wettability. The poor wettability was also supported by the fact that the cohesive forces in the liquid phase were stronger than the adhesion to the contact surface. In addition, the dispersive (hydrophobic) component dominated in the phi6 dispersion, and since this was also the case in the spin-coated films, it can be assumed that weak physical van der Waals forces (dispersion forces) and hydrophobic interactions occurred between phi6 and the polysaccharide films, resulting in the virus not being in sufficient contact with the tested material during antiviral testing of the material to be inactivated by the active coatings of the polysaccharides used. Regarding the contact killing mechanism, this is a disadvantage that can be overcome by changing the previous material surface (activation). In this way, HMWCh, qCNF, and their mixture can attach to the material surface with better adhesion, thickness, and different shape and orientation, resulting in a more dominant polar fraction of SFE and thus enabling the interactions within the polar part of phi6 dispersion.

Benzoxaborole-grafted high molecular weight chitosan from prawn: Synthesis, characterization, target recognition and antibacterial properties

Boronated polymers are in the focus of dynamic functional materials due to the versatility of the B-O interactions and accessibility of precursors. Polysaccharides are highly biocompatible, and therefore, an attractive platform for anchoring boronic acid groups for further bioconjugation of cis-diol containing molecules. We report for the first time the introduction of benzoxaborole by amidation of the amino groups of chitosan improving solubility and introducing cis-diol recognition at physiological pH.The chemical structures and physical properties of the novel chitosan-benzoxaborole (CS-Bx) as well as two phenylboronic derivatives synthesized for comparison, were characterized by nuclear magnetic resonance (NMR), infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), dynamic light scattering (DLS), rheology and optical spectroscopic methods. The novel benzoxaborole grafted chitosan was perfectly solubilized in an aqueous buffer at physiological pH, extending the possibilities of boronated materials derived from polysaccharides. The dynamic covalent interaction between boronated chitosan and model affinity ligands, was studied by means of spectroscopy methods. A glycopolymer derived from poly(isobutylene-alt-anhydride) was also synthesized to study the formation of dynamic assemblies with benzoxaborole-grafted chitosan. A first approximation to apply fluorescence microscale thermophoresis for the interactions of the modified polysaccharide is also discussed. Additionally, the activity of CSBx against bacterial adhesion was studied.

Evaluation of antifungal efficacy of chitosan against Aspergillus fumigatus of stored rice (Oryza sativa)

Contamination of stored rice with fungal pathogens results in rice of poor quality and economic value, and may also have harmful effects on human and animal health. This study aimed at evaluating the antifungal efficacy of chitosan against Aspergillus fumigatus of stored rice (Oryza sativa). Four forms of chitosan were used in this study viz; Purchased Low, Medium and high molecular weight chitosan and chitosan synthesized from Crab Shell using deproteinization, demineralization, decolouration and deacetylation. Degree of deacetylation of the synthesized chitosan was determined using Fourier transform infrared (FTIR) analysis. The in vitro antifungal activity of all forms of chitosan were determined using food poisoning method against Aspergillus fumigatus isolated from stored rice seeds using agar plate methods. The percentage inhibition of mycelial radial growth Aspergillus fumigatus by the different forms of chitosan was determined. Fourier Transfrom InfraRed Spectra of synthesized chitosan showed major absorption bands from 3444.72, 2966.17, 2512.60, 2144.84, 1429.74, 1258.12, 1160.05, 1025.2, 869.92, 710.50, 608.40 to 559.36. Absorption peak at 559 was assigned to glucopyranose ring in the chitosan matrix. Degree of deacetylation of synthesized chitosan was at 98.6% degree. Highest mycelia radial growth of 8.00 cm was recorded in control, while 2.00, 0.00, 5.23, and 1.33cm were recorded in 2.0% concentration of High Molecular Weight Chitosan (HMWC), Medium Molecular Weight Chitosan (MMWC), Low Molecular Weight Chitosan (LMWC) and Chitosan synthesized from Crab shell (CSCS) treatment respectively. The result of the percentage inhibition reveals that A. fumigatus had 100% inhibition in 1.5% HMWC and 2.0% MMWC while 85% inhibition in 2.0% CSCS which were significantly different from 2.0% LMWC with 36.5% inhibitions. Results obtained from this study has shown the effectiveness of chitosan as an effective antifungal agent which can improve and maintain the quality of stored rice and ensure a safer environment due to its nontoxic and environmental friendly properties.

Advances in the structure and function of chitosanase

Chitosanases represent a class of glycoside hydrolases with high catalytic activity on chitosan but nearly no activity on chitin. Chitosanases can convert high molecular weight chitosan into functional chitooligosaccharides with low molecular weight. In recent years, remarkable progress has been made in the research on chitosanases. This review summarizes and discusses its biochemical properties, crystal structures, catalytic mechanisms, and protein engineering, highlighting the preparation of pure chitooligosaccharides by enzymatic hydrolysis. This review may advance the understandings on the mechanism of chitosanases and promote its industrial applications.

Screen-printing of chitosan and cationised cellulose nanofibril coatings for integration into functional face masks with potential antiviral activity

Masks proved to be necessary protective measure during the COVID-19 pandemic, but they provided a physical barrier rather than inactivating viruses, increasing the risk of cross-infection. In this study, high-molecular weight chitosan and cationised cellulose nanofibrils were screen-printed individually or as a mixture onto the inner surface of the first polypropylene (PP) layer. First, biopolymers were evaluated by various physicochemical methods for their suitability for screen-printing and antiviral activity. Second, the effect of the coatings was evaluated by analysing the morphology, surface chemistry, charge of the modified PP layer, air permeability, water-vapour retention, add-on, contact angle, antiviral activity against the model virus phi6 and cytotoxicity. Finally, the functional PP layers were integrated into face masks, and resulting masks were tested for wettability, air permeability, and viral filtration efficiency (VFE). Air permeability was reduced for modified PP layers (43 % reduction for kat-CNF) and face masks (52 % reduction of kat-CNF layer). The antiviral potential of the modified PP layers against phi6 showed inhibition of 0.08 to 0.97 log (pH 7.5) and cytotoxicity assay showed cell viability above 70 %. VFE of the masks remained the same (~99.9 %), even after applying the biopolymers, confirming that these masks provided high level of protection against viruses.

Modified atmosphere packaging with chitosan coating to prevent deterioration of fresh in-hull Badami’s pistachio fruit

BackgroundFresh in-hull pistachio fruits are very perishable and hence have a limited storage life, with marketers and customers wishing for a longer shelf life. The present research was performed to explore the combined effects of different packaging conditions (ambient atmospheric condition, and passive- and active-modified atmosphere packaging) as well as chitosan coating (0, 1, and 1.5%w/v) on postharvest quality of fresh in-hull pistachios stored at 5 °C and 85–90% relative humidity for 45 days. The efficacy of treatments in prolongation of pistachio fruit shelf life was evaluated by determining weight loss, kernel firmness, acid (AV) and peroxide values (PV), mold and yeast count, aflatoxin content, and hull color parameters (L*, a*, b*, C*, h°, and BI) at 0, 15, 30 and 45 days of storage. In addition, O2 and CO2 concentrations in MAP headspace were monitored.ResultsBy applying high molecular weight chitosan coatings and MAP conditions, PV and AV values, microbial growth, aflatoxin B1 production, and weight loss values were inhibited, as well as kernel firmness reduction and hull color deterioration during storage were controlled. Active-MAP treatments in most cases performed better than passive-MAP treatments in this regard (P < 0.05). Combining chitosan coating with MAP demonstrated additive synergistic effects. At the end of storage, 1.5% chitosan-coated treatment under active-MAP maintained firmness (87% of the control treatment), hull lightness (76% of the control treatment), and microbial count (similar to the control treatment). It also maintained minimum weight loss (6.39%), acid (0.91 meq O2 kg−1 oil) and peroxide (0.49 goleic acid/100 goil) values compared to other treatments, proving that chitosan coating combined with MAP was more effective in preserving pistachio quality parameters. The equilibrium O2 and CO2 levels of passive-MAP treatments were maintained at higher values than those of active-MAP treatments which indicated that passive-MAP treatments had higher respiration rates than those of active-MAP treatments during storage.ConclusionsThe results revealed that applying the combination technique of MAP and chitosan coating effectively preserved the quality attributes and lengthened the shelf life of fresh in-hull pistachios. Therefore, it could potentially be commercialized as a new approach for future industry application.Graphical

Влияние наполнителей на механические свойства силоксановых пленок медицинского назначения

Preliminary results of studying the use efficiency of low molecular weight siloxane rubber SKTN-A as a matrix for a thin-film drug coating of implantable stents are presented. The porous structure of the films was formed by introducing intermediate (removable) fillers, such as ethyl alcohol, sodium bicarbonate and high molecular weight chitosan. The tensile strength and relative elongation of the obtained films were studied. It has been established that the strength of films formed using ethyl alcohol is practically similar to the strength of pure siloxane, while their relative elongation is 10% lower. The use of sodium bicarbonate makes it possible to increase the strength of the films by 37% (up to 0.22 MPa) and the relative elongation — up to 93%. When using chitosan, the strength of the films almost doubles (up to 0.28 MPa) and their plasticity is similar to that of pure siloxane and is approximately 40%.