Chitosan Mw Research Articles

Effect of molecular weight of chitosan on quercetin-loaded chitosan nanoparticles.

The widespread use of quercetin is limited by its instability, low solubility and poor oral bioavailability. Encapsulation of quercetin using a nanoparticle delivery system is an effective way to overcome these drawbacks. The effect of the molecular weight (Mw) of chitosan (CS) (100, 200, 500 and 1000 kDa) on quercetin-loaded chitosan nanoparticles (QCNPs) was investigated. The structure, stability, release properties and antioxidant activities of the nanoparticles (QCNP-10, QCNP-20, QCNP-50 and QCNP-100) were assessed. Particle size of QCNPs decreased and polydispersity index increased with the increasing Mw of CS. The main forces involved in the formation of QCNPs were hydrogen bonding and hydrophobic interaction. X-ray diffraction verified that quercetin was loaded into CS nanoparticles. The photostability and thermal stability of QCNPs increased with increasing Mw of CS. QCNP-100 exhibited the lowest release rate in a mixture of water and anhydrous ethanol. The antioxidant activities of QCNPs were enhanced with increasing Mw of CS, and QCNP-100 possessed the highest antioxidant activities, which might be relevant to its smallest particle size. Overall, these results revealed that the Mw of CS affected the properties of QCNPs, and QCNP-100 possessed the smallest particle, best stability, lowest release rate and highest antioxidant activities. © 2024 Society of Chemical Industry.

INFLUENCES OF CROSSLINKER AND MOLECULAR WEIGHT OF CHITOSAN ON PHYSICO-CHEMICAL PROPERTIES OF ANTIBACTERIAL TREATED COTTON FABRICS

This study investigated the influences of crosslinking agent and molecular weight on the surface and comfort properties of cotton fabrics treated by chitosan. Two types of chitosan, with molecular weight (2.6 kDa and 187 kDa), with deacetylation degree (DD) of 75%, were used, along with two types of crosslinking agents: citric acid (CA) and dimethylol dihydroxyethyleneurea (DMDHEU). These agents were applied to cotton fabrics for antibacterial treatments. The treated cotton fabrics were evaluated using several quality indicators related to physico-chemical properties, including whiteness (according to ISO 105 J02), breathability (according to ASTM D737:2004), moisture (according to ASTM D 2495-87), and thermal and moisture resistance under steady-state conditions (according to ISO 11092). Moreover, surface features of treated samples were observed through SEM images. The results showed that the antibacterial treatment of fabrics with lower molecular weight (Mw) chitosan was more favorable for the finishing processes, although the whiteness of the treated samples was quite low. Additionally, cotton fabrics treated with the CA agent exhibited better hygroscopicity and vapor transmission, but tended to have more pronounced yellow color, compared to those treated with the DMDHEU agent. These physico-chemical findings clarified the bonding mechanism of cellulose–crosslinker–chitosan in antibacterial treated cotton fabrics.

Stretchable hydrogels of chitosan/hyaluronic acid induced by polyelectrolyte complexation around neutral pH

In this work, we propose the formation of stretchable hydrogels at neutral pH from the physical crosslinking of chitosan (CS) and hyaluronic acid (HA) by polyelectrolyte complexation. A mixture of CS (Mw ≈ 600 kg/mol, degree of acetylation ≈ 50 %) solution and HA (Mw ≈ 77 kg/mol) solution was prepared with an excess of salts screening the electrostatic interactions CS/HA. In a controlled manner, the polyelectrolyte complexation was induced through the progressive dialysis of the salted polymer mixture against a sodium acetate solution (AcONa, 0.01 M) for 7 days. Depending on [HA], various materials were obtained: viscous solutions at [HA] = 0.75 % (w/v); hydrogels at [HA] = 1.50–2.24 % (w/v) with Young modulus of 14 kPa and stretchable to 200 %. The small angle X-ray scattering characterization of the hydrogels revealed a multiscale organization related to the conformation of the polymers induced by the physical interactions. The dialysis process with AcONa was optimized by adding a dialysis step against a zinc acetate solution containing Zn2+. The combination of polyelectrolyte complexation between CS/HA and metal complexation between Zn2+ and the polymers led to an enhancement of the hydrogel stretchability up to 400 %.

The effect of molecular weight of chitosan on the size of chitosan-Cu2+ complex-stabilized sulfur nanoparticles

Chitosan (CS) samples with average molecular weight (Mw) of 80.4, 61.8, and 45.2 kDa were prepared by the heterogeneous degradation of CS using 1% H2O2 solution under ambient conditions. The degree of deacetylation (DD) of the resultant CS was almost unchanged compared with that of the original CS. The sulfur nanoparticles (SNPs) were prepared by acidification of sodium thiosulfate (Na2S2O3) in a CS-Cu2+ complex solution. The influence of Mw CS on the size of SNPs was investigated. The average size of the SNPs/CS-Cu2+ complexes measured through Transmission electron microscopy (TEM) images was 25.1, 32.3, and 48.3 nm for using CS with Mw of 80.4, 61.8, and 45.2 kDa, respectively. The obtained SNPs/CS-Cu2+ complexes were also characterized by Ultraviolet-visible (UV-Vis), Fourier-transform infrared (FTIR), and x-ray diffraction (XRD) measurements. The synthetic method is favorable for large-scale production. Furthermore, the SNPs/CS-Cu2+ complex can be used as an agent for controlling plant disease in agriculture.

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.

Development of alginate beads for precise environmental release applications: A design of experiment based approach and analysis

Controlled release of active ingredients are important for drug delivery and more recently environmental applications including modulated dosing of chemical and biological controls. This study demonstrates the importance of investigating various material science factors that can influence the diffusion rates of alginate beads to improve and tune their performance for marine environmental applications. This investigation aimed to design a rational workflow to aid in leveraging alginate bead use as a carrier matrix for releasing a specific active agent into water. Experiments were conducted to focus on the narrow a large list of relevant material formulation parameters, which included chitosan molecular weight, chitosan concentration, calcium concentration, drop height, and bead size. Once the most relevant material preparation methods were screened, a more robust statistic Design of Experiments approach was performed and results determined the important (and unimportant) factors for increasing dye release kinetics in marine water. The process was further streamlined by narrowing the critical experimental factors to a three-level based on the prior analysis: chitosan MW, chitosan concentration, and bead size. Analysis of the collected data indicated that while chitosan MW had a negligible impact (Fstatistic = 0.22), bead size (Fstatistic = 60.33) significantly influenced the diffusion rates based on surface area. However, chitosan MW had minor effects where lower chitosan MW enabled higher product release rates. This case investigation was a novel application of the design of experiment approach towards environmental applications to understand differences in release rates to marine waters for the first time and the workflow provided also serve as the basis for researchers to optimize other environmental applications requiring optimization when it is unknown how a large number of formulation variables will impact performance in different environmental scenarios.

&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.

Effect of molecular weight and drying temperature on the physicochemical properties of chitosan edible film

AbstractBackgroundChitosan is the second most abundant polysaccharide abundant in nature after cellulose. In this study chitosan edible films with three different molecular weights (low [LMW], medium [MMW] and high [HMW] molecular weights) were prepared by drying them at room (21°C), 40 and 50°C and their physicochemical properties were characterized.ResultsMolecular weight had a positive effect on the thickness, tensile strength (TS), elongation at break (EAB) and swelling ability (SA) of the films. However, film solubility(S) and water vapor permeability (WVP) were negatively affected. Higher drying temperatures increased the TS of the films whereas lower drying temperatures increased the MC, S, WVP and the EAB of the films. All the films prepared were transparent; however, films made with LMW chitosan were yellowish color. FTIR spectra of the films were influenced by the molecular weight of chitosan and the drying temperature, which revealed that there was an interaction between MW and the drying temperature.ConclusionThis study demonstrated that films made with medium MW chitosan by drying at room temperature had the most favorable properties for food packaging applications.

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.

Graphene Oxide-Carbamoylated Chitosan Hydrogels with Tunable Mechanical Properties for Biological Applications.

Chitosan (CH)-based hydrogels have been extensively researched in numerous biological applications, including drug delivery, biosensing, wound healing, and tissue engineering, to name a few. Previously, modified CH hydrogels by carbamoylation, using potassium cyanate (KCNO) as the cross-linker, have shown improvement in viscoelastic properties and biocompatibility. In this study, graphene oxide (GO) nanofillers are added to carbamoylated CH to form a nanocomposite hydrogel and study the influence of CH molecular weight (Mw) and GO loading concentrations on hydrogel properties. The physical properties (swelling, degradation, and porous structure) of the hydrogels can be tuned as required for cell attachment and spreading by varying both the GO concentration and the Mw of CH. Rheological characterization showed an improvement in the mechanical properties (storage modulus, yield stress, and viscosity) of the synthesized CH-GO hydrogels with an increase in the Mw of CH and the GO concentration. Human retinal pigmented epithelial-1 (RPE-1) cells seeded onto the prepared hydrogel scaffolds showed good cell viability, adhesion, and cell spreading, confirming their cytocompatibility, with dependence on both Mw of CH and GO loading.

The Immobilization of Laccase on Mixed Polymeric Microspheres for Methyl Red Decomposition

Means of eliminating water pollutants or transforming them into less hazardous compounds by green catalysis are desired. The current work was developed with the goal of discovering supports suited for laccase (Lc) immobilization. The effect of the chitosan (CS) molecular weight (Mw) or the polyacrylic acid (PAA) addition was evaluated in microsphere formulation and enzyme immobilization by ESEM, rheology, operational stability, and kinetics. As a practical application, the synthesized products were tested in the methyl red (MR) decomposition and the product identification was performed by high-resolution mass spectrometry. Depending on the required properties, the laccase activity profile (pH, temperature, storage, and Michaelis–Menten parameters) and rheological strength can be modulated by varying the molecular mass of CS or by adding PAA in the support formulation. The immobilized products having the best features regarding MR degradation and recycling abilities were the medium Mw CS microspheres and the system with low Mw CS complexed by PAA, respectively. The degradation mechanism of the dye was proposed accordingly with the identified products by mass spectroscopy. The findings emphasize the potential of the proposed immobilization products to be exploited as viable biocatalysts for dye-contaminated water.

Assessment of the Antibiofilm Performance of Chitosan-Based Surfaces in Marine Environments

Marine biofouling is a natural process often associated with biofilm formation on submerged surfaces, creating a massive economic and ecological burden. Although several antifouling paints have been used to prevent biofouling, growing ecological concerns emphasize the need to develop new and environmentally friendly antifouling approaches such as bio-based coatings. Chitosan (CS) is a natural polymer that has been widely used due to its outstanding biological properties, including non-toxicity and antimicrobial activity. This work aims to produce and characterize poly (lactic acid) (PLA)-CS surfaces with CS of different molecular weight (Mw) at different concentrations for application in marine paints. Loligo opalescens pens, a waste from the fishery industry, were used as a CS source. The antimicrobial activity of the CS and CS-functionalized surfaces was assessed against Cobetia marina, a model proteobacterium for marine biofouling. Results demonstrate that CS targets the bacterial cell membrane, and PLA-CS surfaces were able to reduce the number of culturable cells up to 68% compared to control, with this activity dependent on CS Mw. The antifouling performance was corroborated by Optical Coherence Tomography since PLA-CS surfaces reduced the biofilm thickness by up to 36%, as well as the percentage and size of biofilm empty spaces. Overall, CS coatings showed to be a promising approach to reducing biofouling in marine environments mimicked in this work, contributing to the valorization of fishing waste and encouraging further research on this topic.

Effect of Different Molecular Weights of Chitosan on Formulation and Evaluation of Allopurinol-Loaded Nanoparticles for Kidney Targeting and in Management of Hyperuricemic Nephrolithiasis.

Present research study was conducted to formulate kidney-targeted allopurinol (AO)-loaded chitosan nanoparticles (ANPs) for management of hyperuricemic related nephrolithiasis. Different molecular weights of chitosan were used for fabricating ANP formulation by adopting modified ionotropic gelation method. The prepared batches were than evaluated for particle size analysis, entrapment efficiency, transmission electron microscopy, X-ray diffraction, Differential Scanning Calorimetry, in vitro release and in vivo animal study. The in vivo study depicted that post 2 h of administration of different formulations and pure drug; ANPs prepared from low molecular weight chitosan showed maximum concentration of AO in kidney signifying successful kidney targeting of drug (25.92 fold) whereas no or very less amount of AO was seen in other animal groups. Effectiveness (p < 0.01) of formulation in management of hyperuricemia-associated nephrolithiasis was also evaluated via estimation of urine pH and serum and urine uric acid levels of mice. Further histological study was also performed on kidney samples which again affirmed these results. Present investigation demonstrated that ANPs prepared from low MW chitosan depicted maximum kidney-targeting ability that might be due to its specific uptake by the kidneys as well as its higher solubility than other two polymers, which results in enhanced release rate from the formulation and also offers an efficient strategy for the management of hyperuricemic nephrolithiasis.

Morphological Study of Bio-Based Polymers in the Consolidation of Waterlogged Wooden Objects.

The removal of water from archaeological wooden objects for display or storage is of great importance to their long-term conservation. Any mechanical instability caused during drying can induce warping or cracking of the wood cells, leading to irreparable damage of the object. Drying of an object is commonly carried out in one of three ways: (i) air-drying with controlled temperature and relative humidity, (ii) drying-out of a non-aqueous solvent or (iii) freeze-drying. Recently, there has been great interest in the replacement of the standard, but limited, polyethylene glycol with biopolymers for wood conservation; however, their behaviour and action within the wood is not completely understood. Three polysaccharides—low-molar-mass (Mw) chitosan (Mw ca. 60,000 g/mol), medium-molar-mass alginate (Mw ca. 100,000 g/mol) and cellulose nanocrystals (CNCs)-are investigated in relation to their drying behaviour. The method of drying reveals a significant difference in the morphology of these biopolymers both ex situ and within the wood cells. Here, the effect these differences in structuration have on the coating of the wood cells and the biological and thermal stability of the wood are examined, as well as the role of the environment in the formation of specific structures. The role these factors play in the selection of appropriate consolidants and drying methods for the conservation of waterlogged archaeological wooden objects is also investigated. The results show that both alginate and chitosan are promising wood consolidants from a structural perspective and both improve the thermal stability of the lignin component of archaeological wood. However, further modification would be necessary to improve the biocidal activity of alginate before it could be introduced into wooden objects. CNCs did not prove to be sufficiently suitable for wood conservation as a result of the analyses performed here.

Development of Chitosan-Based Surfaces to Prevent Single- and Dual-Species Biofilms of Staphylococcus aureus and Pseudomonas aeruginosa.

Implantable medical devices (IMDs) are susceptible to microbial adhesion and biofilm formation, which lead to several clinical complications, including the occurrence of implant-associated infections. Polylactic acid (PLA) and its composites are currently used for the construction of IMDs. In addition, chitosan (CS) is a natural polymer that has been widely used in the medical field due to its antimicrobial and antibiofilm properties, which can be dependent on molecular weight (Mw). The present study aims to evaluate the performance of CS-based surfaces of different Mw to inhibit bacterial biofilm formation. For this purpose, CS-based surfaces were produced by dip-coating and the presence of CS and its derivatives onto PLA films, as well surface homogeneity were confirmed by contact angle measurements, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The antimicrobial activity of the functionalized surfaces was evaluated against single- and dual-species biofilms of Staphylococcus aureus and Pseudomonas aeruginosa. Chitosan-based surfaces were able to inhibit the development of single- and dual-species biofilms by reducing the number of total, viable, culturable, and viable but nonculturable cells up to 79%, 90%, 81%, and 96%, respectively, being their activity dependent on chitosan Mw. The effect of CS-based surfaces on the inhibition of biofilm formation was corroborated by biofilm structure analysis using confocal laser scanning microscopy (CLSM), which revealed a decrease in the biovolume and thickness of the biofilm formed on CS-based surfaces compared to PLA. Overall, these results support the potential of low Mw CS for coating polymeric devices such as IMDs where the two bacteria tested are common colonizers and reduce their biofilm formation.

Fabrication of chitosan-gallic acid conjugate for improvement of physicochemical stability of β-carotene nanoemulsion: Impact of Mw of chitosan

In this research, three various Mw of chitosan (CS)-gallic acid (GA) conjugates were synthesized, characterized, and used for improvement of physicochemical stability of β-carotene (BC) nanoemulsion (NE) by layer-by-layer technique. GA conjugation degrees were in the following order: HCS (125.6 mg/g) > MCS (102.3 mg/g) > LCS (74.6 mg/g) at GA:CS mass ratio of 0.5:1. Three varying Mw of CS-GA conjugates exhibited pronouncedly higher antioxidant abilities than native CS. For native CS, antioxidant abilities increased with the decrease of Mw. However, HCS-GA conjugate showed the highest antioxidant activity, due to the higher GA conjugation degrees and decreased intramolecular hydrogen bonds and crystallinity in HCS-GA conjugate. CS-GA conjugates substantially improved BC chemical stability in NE than CS and BC retentions were in the following order: HCS-GA (76.8%) > MCS-GA (68.3%) > LCS-GA (53.4%) after 30 days storage. The results obtained may provide some useful information for the applications of CS-GA conjugates for nutraceuticals stabilization in food systems.

Evaluation of α-Chitosan from Crab Shell and β-Chitosan from Squid Gladius Based on Biochemistry Performance

The objective of this study is to innovatively evaluate the biochemistry performance of α-chitosan from Portunus trituberculatus shell and β-chitosan from Illex argentinus squid gladius by using the weighted composite index method, and provide a theoretical basis for better development and utilization of chitosan biomedical materials. To build a composite evaluation system, seven key indicators, including molecular weight (Mw), deacetylation degree (DD), water binding capacity (WBC), fat binding capacity (FBC), thermal stability (TS), primary structure and secondary structure, which significantly affect chitosan biochemical characteristics, were determined and analyzed. The viscosity average Mw of chitosan was in the range of 22.5–377.1 kDa, and the DD was 83.4–97.8%. Thermogravimetric (TG) and differential scanning calorimetry (DSC) analyses of commercial chitosan (CS), crab chitosan (CSC) and squid chitosan (CSS) showed a downward trend in TS, while WBC and FBC showed an obvious upward trend. FT-IR had a similar profile in peak shape, but the peak position slightly shifted. CD indicated that chitosan maintained the double helix structure and multiple secondary structural elements. The composite weighted index values of CS, CSC and CSS were 0.85, 0.94 and 1.31 respectively, which indicated that the CSS biochemistry performance was significantly better than CSC, and β-chitosan has great potential in biomedical materials.

Squid pen chitosan nanoparticles: small size and high antibacterial activity

Chitosan nanoparticles (CSNs) have widely studied for many potential applications as a bioactive nanomaterial because of their excellent properties, such as quantum size effect, large surface area, high mobility, and high permeability. In this study, various CSNs prepared from squid pen chitosan with different molecular weight (Mw) and degree of deacetylation (DD). The lower Mw and higher DD of initial chitosan used, the smaller size of CSNs obtained. Small size CSNs (about 30 nm) are formed from the initial chitosan (Mw of 8 kDa, DD of 96%). In vitro tests, all as-prepared CSNs showed high antibacterial activity against Salmonella sp. and Staphylococcus aureus. In particular, the lowest CSNs concentration of 50 ppm, which was prepared from chitosan with a low Mw of 8 kDa and high DD of 96%, showed the highest activity. Besides, by using the similar initial chitosans, CSNs prepared from squid pens exhibit higher antibacterial activity than that one from shrimp shells. This study presents high potential applications of CSNs prepared from squid pen chitosan with small size and excellent antibacterial activity for various fields.

Effect of glucose-induced Maillard reaction on physical, structural and antioxidant properties of chitosan derivatives-based films

This work focused on studying the physicochemical and antioxidant properties changes of varying molecular weight (Mw) chitosan-depolymerization products (CDP)-based films occurring after crosslinking by heat-treatment and Maillard reaction (MR). Based on color properties and browning index, an enhancement of films properties was observed after treatment at 90 °C with a reduction in their water content, solubility and contact angle. Brown MR products were developed in heated films containing glucose thus improving their barrier properties. This effect was more pronounced in lower Mw-CDP based films. In addition, according to TGA, EAB and TS analyses an improvement in heat-treated films thermal stability and mechanical properties was detected and further confirmed through FTIR, X-ray and SEM analyses. The evaluation of the antioxidant potential through four different assays allowed to conclude that glucose addition, thermal treatment and the use of low Mw-CDP highly enhanced the MR-modified films antioxidant capacity. Consequently, MR crosslinked chitosan-based films could be potentially used as an alternative for bioactive and functional packaging effective in food oxidation inhibition, especially using low Mw chitosan derivatives.

The growth promotion effect of microelement fertilizers containing low molecular weight chitosan and xanthan on radish (Raphanus sativus L.)

The effects of gamma radiation on viscosity and molecular weight (Mw) of chitosan and xanthan were studied to utilize them as components that can induce plant growth promotor (PGP) effect and prolong the contact of agrochemicals with crop in the foliar microelement fertilizers. Various fertilizers were prepared from two formulations of microelements, radiation degraded low molecular weight (Mw) chitosan (LCST) and xanthan (LXT) and their effects on the growth, yield and quality of radish grown on alluvial soil were measured. The experiment was arranged in randomized complete block design (RCBD) with 3 replications in experiment station. The results revealed that all development parameters of radish were much improved by foliar application of microelements and low Mw polysaccharides. The highest yield of radish root obtained with the plants treated with lower microelements and higher chitosan content (MF2). There are insignificant differences in total soluble solids, sugar and vitamin C content in the root harvested from the plants treated with the formulations supplementing the same amount of LCST, but the fertilizer composed of higher amount of microelements and chitosan (MF4) reduced nitrate residue in the root. It can be concluded that foliar microelement fertilizer containing low Mw polysaccharide can be applied to improve the growth, yield and quality of radish.