Higher Chitosan Concentration Research Articles

Impact of Molar Composition on the Functional Properties of Glutinous Rice Starch-Chitosan Blend: Natural-Based Active Coating for Extending Mango Shelf Life.

This study investigates natural-based blends of glutinous rice starch (GRS) and chitosan (CS), varying their molar composition (0:100, 30:70, 50:50, 70:30, and 100:0) to explore their interaction dynamics. Our findings illustrate the versatility of these blends in solution and film forms, offering applications across diverse fields. Our objective is to understand their impact on coatings designed to extend the post-harvest shelf life of mangoes. Results reveal that increasing chitosan content in GRS/CS blends enhances mechanical strength, hydrophobicity, and resistance to Colletotrichum gloeosporioides infection, a common cause of mango anthracnose. These properties overcome limitations of GRS films. Advanced techniques, including FTIR analysis and stereo imaging, confirmed robust interaction between GRS/CS blend films and mango cuticles, improving coverage with higher chitosan content. This comprehensive coverage reduces mango dehydration and respiration, thereby preserving quality and extending shelf life. Coating with a GRS/CS blend containing at least 50% chitosan effectively prevents disease progression and maintains quality over a 10-day storage period, while uncoated mangoes fail to meet quality standards within 2 days. Moreover, increasing the starch proportion in GRS/CS blends enhances film density, optical properties, and reduces reliance on acidic solvents, thereby minimizing undesirable changes in product aroma and taste.

Construction of oleogels based on emulsion gels stabilized by glycyrrhizic acid and chitosan

Liquid oils can be converted into elastic solids by preparing oleogels using an emulsion-templated approach. In this study, we prepared emulsion gels using a layer-by-layer (LBL) electrostatic deposition approach. These emulsion gels were then used as templates to prepare oleogels. Initially, oil-in-water emulsion gels were formed using glycyrrhizic acid (GA) as a natural anionic surfactant to form and stabilize the oil droplets. Cationic chitosan (CS) was then added to these emulsions to form a biopolymer coating around the oil droplets. The GA/CS ratio in these emulsion gels played a critical role in determining the physical stability of the oleogels created from them. At a sufficiently high chitosan concentration (3% CS for samples with 1% GA, 2% CS for samples with 2% GA), the emulsion gels were resistant to destabilization during drying, which was attributed to the formation of a thick chitosan coating around the oil droplets. The oil loss from the optimized oleogels (GCOs1-3, GCOs2-2, GCOs2-3) during drying was relatively low (0.41%–1.08%), indicating their strong oil binding capacity. In contrast, non-optimized oleogels (2% GA, 1% CS) were prone to droplet coalescence and oil loss (74.2% ± 1.3%) during drying. The optimized oleogels (GCOs1-3, GCOs2-2, GCOs2-3) all had relatively high storage modulus (∼150 kPa) at a frequency of 1 rad/s. Overall, the interfacial engineering strategy used in this study may be useful for converting liquid oils into semi-solid materials, which may be useful for several applications in the food and other industries.

Clinical Investigation of Valsartan Sustained-Release Matrix Tablets: Formulation Design and Performance Evaluation

The primary objective of this main study is to develop and assess the sustained-release matrix tablets containing Valsartan, an angiotensin II receptor type 1 antagonist. The powder mixtures underwent a thorough examination of pre-compression parameters and observed angle of repose, bulk density, tapped density, and Carr’s index, all of which exhibited satisfactory results. Following compression, the tablets were subjected to post-compression evaluations, including weight variation, thickness, hardness, friability, drug content, in-vitro dissolution, and stability studies. In-vitro dissolution investigations are conducted over 24 hours, employing 0.1 N HCL for the initial 2 hours and pH 6.8 phosphate buffer for the subsequent 24 hours. Notably, formulations F4 and F7 demonstrated promising dissolution profiles, effectively controlling the release of the drug. These formulations, enriched with higher concentrations of chitosan and sodium alginate in addition to other polymers, successfully sustained the drug release for the entire 24-hour duration. The compatibility of the drug, polymers, and other excipients was meticulously assessed using FT-IR Spectroscopy, affirming the harmonious interaction among these components. Further analysis involved fitting the release data to various mathematical models, including Zero-order, First-order, Higuchi equation, and Korsmeyer-Peppas model, to ascertain the kinetics and mechanisms governing drug release. Results indicated that the drug release adhered to first-order kinetics, with a non-Fickian mechanism prevailing. Stability studies conducted for 3 months provided reassurance regarding the stability of the selected formulations (F4 and F7), bolstering confidence in their potential for sustained release of Valsartan.

ISOLATION AND CHARACTERIZATION OF CHITOSAN NANOPARTICLES FROM CRAB SHELL WASTE (PORTUNUS PELAGICUS)

Objective: The purpose of this study was to isolate and characterize of chitosan nanoparticles derived from Portunus pelagicus shell waste. Methods: Chitosan was isolated by deproteination, demineralization, and deacetylation methods. Furthermore, nanoparticles (NPs) were made by the ionic gelation method by dissolving chitosan in a mixture of acetic acid and sodium tripolyphosphate. The particle size analyzer and Fourier Transform Infrared Spectroscopy were used to measure the particle size of NPs and determine the functional group and degree of deacetylation. Results: The yield percentage of chitosan was 90.7%. The size of chitosan nanoparticles based on the highest intensity is 15.05 nm with a polydispersity index (PDI) value of 0.1140 at a concentration of 1%. Based on the degree of deacetylation of chitosan nanoparticles, it was found to be 84.98% at 1% concentration. Conclusion: The conclusion of this study is the formation of chitosan nanoparticles (1-100 nm) isolated from Portunus pelagicus shell waste. Based on the degree of deacetylation, chitosan nanoparticles with high chitosan content (>75%) were obtained.

Gas foamed scaffolds as smart 3D structures in skin tissue engineering

Globally, wound care is a major problem that poses big issues for national healthcare systems. Consequently, the development of wound dressings, systems applied over a wound to prevent complications and speed up recovery, is receiving increasing attention. Electrospun nanofibrous scaffolds gained great interest in the medical field due to their many advantages and beneficial characteristics. However, they are formed by of densely packed fiber layers, which render the available space between adjacent fibers minimal. In this study, nanometric fibers from pullulan polymeric blends were developed using cricket powder as novel component, due to its high chitin and chitosan content. Hydroxyapatite was also added due to its biocompatibility and capability to interact with the host tissues. The 2D mats based on electropsun fibers in membrane were converted to a 3D structure by gas foaming, involving NaBH4. The obtained 3D systems were characterized for their morphology and composition, and mechanical properties. The scaffolds biocompatibility was tested on normal human dermal fibroblasts and mesenchymal stem cells, and cell adhesion was assessed. TNF-α secretion was thereafter characterized to evaluate the anti-inflammatory effects of the scaffolds on macrophages, and their antioxidant activity was also investigated. Finally, an evaluation of the scaffolds’ safety and efficacy in vivo on a murine incisional and burn model was performed. The results obtained not only revealed greater structural and mechanical integrity of the gas-foamed scaffolds containing cricket powder, but also higher cytocompatibility towards different cell lines together with anti-inflammatory and antioxidant properties, thereby making them innovative tools to improve the process of wound healing.

Phenylalanine Ammonia-Lyase-Mediated Differential Response of Tomato (Solanum lycopersicum L.) Cultivars with Different Stress Tolerance to Treatment with Low-Molecular-Weight Chitosan

The latest research has shown that chitosan acts as a growth stimulator and elicitor in plants, including resistance to biotic and abiotic factors. However, increasing concentrations could possibly make chitosan a source of stress for plants. In this study, we investigated the effect of low-molecular-weight chitosan hydrolysate on the root development of tomato (Solanum lycoperscum) cultivars Red Cherry, Lel, and Tytan. The growth rate change, together with total phenolic content, phenylalanine ammonia-lyase (PAL) activity, and gene expression, were studied in relation to tomatoes. High concentrations of chitosan negatively affect the growth of tomato seedlings and contribute to changes in the tropism of the seedling roots. After the addition of chitosan hydrolysate, the PAL activity and the total phenolic content decreased 24 h later. PAL is a key enzyme in the biosynthesis of many plant stress factors. An analysis of the tomato PAL gene family was carried out. The SlPAL gene expression in the seedlings of cv. Cherry increased 1.5 times after 48 h, while in cv. Lel, the expression stably decreased in the presence of chitosan. The obtained results are supposed to aid our understanding of the mechanisms underlying the effects of chitosan on plant development and further its successful application in agriculture as well as in research on plant stress.

Utilizing chitosan and pullulan for the encapsulation of Lactiplantibacillus plantarum ZJ316 to enhance its vitality in the gastrointestinal tract

Lactiplantibacillus plantarum ZJ316 has demonstrated effective alleviation of gastritis and colitis, making it crucial to improve its viability within the gastrointestinal tract. In this study, Chitosan (CS) and pullulan (PUL) encapsulated nanofibers of ZJ316 were prepared using electrospinning, considering both the synergistic effects of prebiotics and probiotics and their protective effects. We found that increasing the CS ratio resulted in elevated conductivity of the polymer solution, while decreasing viscosity and pH. Scanning electron microscopy showed that at a CS: PUL ratio of 1:135, polymer filaments were difficult to form, and nanofiber diameter decreased with higher CS content. X-ray diffraction analysis confirmed the miscibility of CS and PUL, while ATR-FTIR demonstrated the presence of hydrogen bonding interactions between the two materials. Thermal analysis indicated that an increased CS concentration improved the thermal stability of the nanofibers. Based on these findings, the optimal CS:PUL ratio for electrospinning was determined to be 1:60. Encapsulation of ZJ316 in the nanofibers significantly enhanced its survival rate in simulated gastrointestinal fluid compared to free bacteria, with survival rates of 87.24 % (gastric) and 79.71 % (intestinal), respectively. This study provides valuable insights for the development of probiotic functional foods.

Formulation and In-Vitro evaluation of Nortriptyline Hydrochloride mucoadhesive buccal films

This contemporaneous research was aimed to formulate buccal mucoadhesive DDS to enhance bioavailability and avoid pre systemic metabolism. The mucoadhesive film was fabricated by solvent casting method with base polymer chitosan and a combination of hydrophilic polymer like PVP or Gelatin. The films were then evaluated. All the formulations were found to have optimum strength to withstand folding endurance. The films' consistent size, thickness, and weight variation were discovered. The drug content uniformity of films was exceptionally well. Given that the film's surface pH falls between 6.6 and 6.7, buccal administration is appropriate for it. The pH near to the neutral region decreases the chances of mucosal irritation. The invitro adhesion ability of the formulations were affected by the composition of chitosan and PVP or Gelatin. The lower and higher concentration of chitosan was not sufficient for invitro adhesion of films. The formulation having chitosan and hydrophilic polymers in the ratio 1:1.5 showed strong invitro adhesion. The invitro bioadhesion time of the formulations containing chitosan and gelatin or PVP was less due to poor ionization of gelatin. On increasing the concentration of hydrophilic polymers, the invitro bioadhesion time increased. The highest concentration of the polymers decreased the adhesion time. The formulation NF5 with chitosan and gelatin within the proportion of 1:1.5 exhibited drug release of 98.1% at 6 hours. The sole purpose of this work is to adhere the buccal film with the mucosa, hence formulation NF5 was selected as best formulation. Thus, current investigation's goal to develop a buccal mucoadhesive drug delivery was fulfilled.
 Keywords: Buccal film, Nortriptyline HCl, depression, in vitro studies, mucoadhesive

DEVELOPMENT AND EVALUATION OF NANOSPHERES CONTAINING CARBIMAZOLE

Objective: To develop and evaluate polymeric nanospheres of Carbimazole using Nano-precipitation method. Methods: The polymeric nanospheres of Carbimazole were prepared employing the nano-precipitation method using a varied concentration of Chitosan (polymer). The prepared formulations were characterized for several parameters such as SEM, Particle size, Micromeritic properties, Encapsulation efficiency, Degree of swelling, Percentage moisture loss, drug content, and in vitro drug release and release kinetics. Results: Carbimazole-loaded polymeric nanospheres were developed, and the evaluation parameters depicted results within an acceptable range. The result of FTIR studies shows that there is no interaction between drug and excipients. The melting point, obtained as per the reference standard (122-125 °C) depicted the purity and authenticity of the drug. The micromeritics studies also supported the characterization of drug and excipients. The drug content was found to be in the range of 80.3±0.65 to 99.5±0.81 for all six formulations. The entrapment efficacy was obtained for all six formulations and ranged from 82.17 to 99.56. The release parameters were also observed for all formulations, and they were determined in the range of 82.5±0.4 for formulation NS6 (12 h) to 98.6±0.9 for formulation NS4 (24 h). Conclusion: The results revealed thatthe formulation containing a higher concentration of Chitosan and a lower concentration of Tween 80 showed prolonged in vitro drug release in a controlled manner. Hence, On the basis of all formulation results, the NS4 was the best formulation among all.

Investigating the Correlation Between Drug Physical Properties and Physical Characteristics and Drug Entrapment Efficiencies of Chitosan-TPP Nanoparticles

Chitosan nanoparticles (NPs) have been the subject of intensive research. This study aimed to determine how different drug characteristics such as molecular weights, drug solubility in the processing medium, and drug ionization/charge state affected chitosan NPs particularly their percentage entrapment efficiency (% EE) and mean hydrodynamic diameters (MHDs). Drugs with varying molecular weights but of similar aqueous solubilities were chosen and were dissolved in a 2% chitosan-acetic acid solution. Chitosan NPs were formed using by ionic gelation technique using sodium tripolyphosphate (TPP) at specific concentration and volume ratios of chitosan to TPP. NPs containing Enalapril and Paracetamol displayed better short-term stability in terms of MHDs. A direct relationship between MHDs of NPs and chitosan concentrations was found. In comparison, at both low and high admixed drug concentrations and at high chitosan concentration, larger NPs sizes were associated with the lower molecular weight drug (Paracetamol). However, the study did not demonstrate a direct relationship between NPs characteristics such as MHDs and drugs molecular weights. The ZP of Paracetamol-loaded NPs was lowest at high drug concentrations at all chitosan concentrations compared to other drugs-loaded NPs. When compared to drugs with high and low molecular weights, medium molecular weight Atenolol showed the highest % EE. This clearly indicated that there was no direct correlation between drug molecular weight and % EE, but rather other factors influenced on % EE. Nevertheless, an inverse linear relationship with high correlation coefficients was only found when % EE was plotted against each drug molecular weight divided by the ratio of drugs solubilities in acetic acid to their employed concentrations, however the correlation was inconsistent between drugs of varying molecular weights.

Effects of carboxymethyl cellulose fiber formations with chitosan incorporation via coating and mixing processes

To date, the utilization of carboxymethyl cellulose (CMC) fibers are only restricted to weak mechanical application such as wound dressing. Physically, CMC has a weak mechanical strength due to the high hydrophilicity trait. However, this flaw was saved by the extensive number of reactive functional groups, allowing this macromolecule to form linkages with chitosan to ensure its versatility. This work successfully fabricated CMC-chitosan fiber via dissolution, crosslinking, dry-jet wet-spinning extrusion, and coagulation processes. Chitosan was constituted with CMC fiber in two approaches, coating, and inclusion at various concentrations. Morphologically, chitosan incorporation has triggered agglomerations and roughness toward CMC fibers (CMCF). Chemically, the interaction between CMC and chitosan was proved through FTIR analysis at peaks 1245 cm−1 (ECH covalent crosslinking), while 3340 cm−1 and 1586 cm−1 were due to ionic and hydrogen bonding. The result from analysis showed that at higher chitosan concentrations, the chitosan-included CMC fiber (CMCF-I) and chitosan-coated CMC fiber (CMFC) were mechanically enhanced (up to 86.77 and 82.72 MPa), thermally more stable (33 % residual mass), and less hydrophilic compared to the plain CMCF. The properties of CMC-chitosan fibers have opened up vast possible applications, especially as a reinforcement in a watery medium such as a hydrogel.

Chitosan polyplexes: Energetics of formation and conformational changes in DNA upon binding and release

Energetics of chitosan (CS) polyplexes and conformational stability of bound DNA were studied at pH 5.0 by ITC and HS–DSC, respectively. The CS–DNA binding isotherm was well approximated by the McGhee–von Hippel model suggesting the binding mechanism to be a cooperative attachment of interacting CS ligands to the DNA matrix. Melting thermograms of polyplexes revealed the transformation of different conformational forms of bound DNA in dependence on the CS/DNA weight ratio rw. At 0<rw<0.7 two conformational forms were observed and assigned, respectively, to the intact (free) and globular (bound) DNA. A contribution of the globular DNA to the melting enthalpy approached 100 % at the equivalent weight CS content. At higher CS contents a further stabilization of the globular DNA conformation was detected and assigned to the DNA globules in overcharged polyplexes. The polyplex dissociation was studied at pH 7.4 under conditions of zero and a physiological concentration of NaCl. Phase separation of the system was observed in both cases. DNA was almost completely immobilized in the lower phase enriched with CS. At physiological ionic strength, DNA converted from the globular to the intact form although remained to be immobilized in the CS phase.

Enhancing the properties of date palm fibre reinforced bio-epoxy composites with chitosan – Synthesis, mechanical properties, and dimensional stability

The present work deals with the mechanical behavior of dual bonding filler; chitosan (CTS) and date palm (DP) fibre in bio-epoxy composites. The primary objective of this research was to find out if the addition of CTS particles to a DP/bio-epoxy composite could enhance its mechanical properties. Bio-composites are being developed to better understand and manipulate the unique features of these versatile polysaccharides. CTS was included into the bio-epoxy matrix through solution mixing. Bio-epoxy composites with 40% DP fibre loading were developed by dispersing different CTS filler ratios - 5%, 10%, 15%, and 20%. For the purpose of comparison, a control sample was prepared without the inclusion of the CTS filler. The mixture was then manually disseminated for 7–10 min before being uniformly drenched into a steel cast mould with dimensions of 150 mm (width) 150 mm (length) 3 mm (thickness) and taken to the hot press, after which it underwent heating at a temperature of 110 °C for a duration of 10 minutes, while being subjected to a significant pressure of 250 bar. Tensile properties, impact properties, flexural properties, morphological characterization, water absorption, and thickness swelling were all measured on the prepared bio-composites. Among the CTS fractions, DP/CTS20 has the highest tensile strength (24.04 MPa) and tensile modulus (4.93 GPa), flexural strength (45.11 MPa), and impact strength (2.70 J/m2). The scanning electron microscope exposes the properties of fibres and polymers, as well as the reason for tensile test deficiency. Remarkably, bio-composites with higher CTS content have elevated moisture content and dimensional instability. Generally, we diagnosis that DP/CTS20 had the best tensile, flexural, and impact properties, as well as the highest water absorption and thickness swelling of any CTS compositions. The discovery improved our knowledge of bio-composite implementation trends, allowing us to assess their potential for more dependable implementations of much more sustainable green products. Furthermore, material enhancements such as bio-epoxy toughening to change the ductility behavior to improve energy absorption or natural fibre pretreatment can improve interbonding between the matrix and filler.

Strong tissue adhesive polyelectrolyte complex powders based on low molecular weight chitosan for acute hemorrhage control

Self-gelling and bioadhesive powders offered promising effective hemostats to suit irregularly shaped, complex and non-compressible wounds for clinical applications. In the current study, chitosan based polyelectrolyte complex coacervate were simply prepared by mixing high concentrations (10 %) of low molecular weight chitosan (CS) and polyacrylic acid (PAA) solutions. Obtained by lyophilization, the physical cross-linked polyelectrolyte complex powders would form a gel within 5 s upon hydration, which demonstrated excellent mechanical properties, significant antibacterial activities, strong and lasting adhesion on wet tissues in physiological environment. In vitro blood clotting assays showed that the CS/PAA powders could remarkably aggregate blood cells and accelerate blood clotting process. As studied by diverse hemorrhage models, including rat tail, liver and heart injuries and dog incision, CS/PAA powders significantly facilitated the decrease of blood loss as well as hemostatic time by creating robust physical barriers and promoting blood clot formation on the bleeding sites. These outstanding properties in terms of easy preparation, rapid self-gelling, strong wet adhesion, effective hemostasis and shape-adaptability endowed CS/PAA polyelectrolyte complex powders with great potential in managing acute hemorrhage of non-compressible trauma.

Optimization of Chitosan-Decorated Solid Lipid Nanoparticles for Improved Flurbiprofen Transdermal Delivery.

Transdermal delivery is a potential alternative route to oral administration for drugs associated with stomach discomfort, such as flurbiprofen, a widely nonsteroidal anti-inflammatory drug (NSAID). This study aimed to design solid lipid nanoparticle (SLN) transdermal formulations of flurbiprofen. Chitosan-coated SLNs were prepared by the solvent emulsification method, and their properties and permeation profiles across the excised rat skin were characterized. The particle size of uncoated SLNs was at 695 ± 4.65 nm, which increased to 714 ± 6.13, 847 ± 5.38, and 900 ± 8.65 nm upon coating with 0.05, 0.10, and 0.20% of chitosan, respectively. The drug association efficiency was improved when a higher concentration of chitosan was employed over SLN droplets that endowed a higher affinity of flurbiprofen with chitosan. The drug release was significantly retarded as compared to the uncoated entities and followed non-Fickian anomalous diffusion that was depicted by "n" values of >0.5 and <1. Also, the total permeation of chitosan-coated SLNs (F7-F9) was significantly higher than that of the noncoated formulation (F5). Overall, this study has successfully designed a suitable carrier system of chitosan-coated SLNs that provide insight into the current conventional therapeutic approaches and suggest new directions for the advancements in transdermal drug delivery systems for improved permeation of flurbiprofen.

Effect of Plasticizer Addition on The Characteristics of Chitosan-Alginate Edible Film

&lt;p&gt;The edible film of chitosan-alginate in this study showed characteristics of the physical and mechanical properties when various plasticizers of polyethylene glycol/PEG, polyvinyl alcohol/PVA, and glycerol were added into the origin film. It was also found that chitosan content in the edible film contributed to the change in the physical properties and the conductivity of the film. The general effect on the film because of the addition of plasticizers was the decrease of the tensile strength, the increase of the films' elongation, and the increase of the water vapor permeability (WVP). Among other plasticizers, PEG attracted the most attention in which it affected the most significant change on the properties. Meanwhile, the higher chitosan content in the chitosan-alginate film affected the increase of the tensile strength and the decrease of the elongation value, and the decrease of the WVP on the film. Characterization using FT-IR spectrophotometer showed that no chemical interaction was formed due to the mixing of alginate-chitosan in the film. Instead, only the physical blending of chitosan-alginate was formed in the edible film.&lt;/p&gt;

Chitosan as a Polyfunctional Crosslinker for a Renewable-Based Resorcinol Diglycidyl Ether

Chitosan is an abundant renewable biopolymer, insufficiently valorized, which is suitable for the development of sustainable and fully biobased materials. In this study, we combined it with the resorcinol diglycidyl ether, a biobased monoaromatic diepoxide. Formulations with a high chitosan content of up to 44 wt % were investigated and showed high reactivity and appropriate intervals of polymerization, ranging from 75 to 125 or 155 °C. The in situ Fourier transform infrared (FTIR) spectroscopy analysis confirmed that the two compounds reacted via an anionic polymerization mechanism combined with polyaddition reactions, proving that the chitosan acts as a polyfunctional crosslinker. The obtained thermoset resins have tan δ values ranging between 79 and 73 °C and storage moduli increasing with chitosan content (E′ ∼3.5–4.2 GPa), together with high crosslinking densities (15.65–27 mmol·cm–3).

Functional properties and characterization of maize starch films blended with chitosan

The preparation of biodegradable composite films from blending chitosan in maize starch via solution casting was explored and the effect of the ratio of chitosan/starch on the physicochemical, mechanical properties and antimicrobial activity of the films was investigated. The interaction through hydrogen bonding between starch molecules and chitosan and the reduction of crystallinity in blend films were revealed in FTIR and XRD results. The blend films with incorporation of proper amounts of chitosan to a maize starch matrix displayed an enhancement in tensile properties and water vapor barrier performance, an improvement in rigidity and antimicrobial activity accompanied by higher transparency. The film with 1/3 of chitosan/starch ratio appeared homogeneous structure, 21.54 ± 0.78 MPa of tensile strength and (2.81 ± 0.26)×10−10 g·m−1·s−1·Pa−1 of water vapor permeability which were 1.52 times higher and 60.9% lower than those of starch film, respectively. The deteriorated comprehensive performance of the films could be caused by excessively high chitosan content because of an incomplete miscibility between starch and chitosan. The chitosan/starch blend film possessed reasonable thermal stability and it could potentially be useful for food packaging applications.

Chitosan/NC Based Bio Composite Membrane: An Impact of Varying Amount of Chitosan on Filtration Ability for the Malachite Green Dye

This study is generally focused on knowing about which appropriate quantityof chitosan with cellulose nanocrystal gives best output in terms of strengthand potential to bear vaccum pressure during filtration study. It was observedthat membrane MIII showed best results in filtering out the malachite greendye present in the aqueous solution of 50 PPM taken during study. Thefiltration study was observed under three different pH values i.e. 2.0, 5.0and 9.0 and recorded results depicted that the first five cycles significantlyremove the dye concentration ranging from 32-13 PPM, 27-7 PPM and33-14 PPM respectively. The contact angle results for all the membraneshowed hydrophilic behaviour. The thickness and the swelling behaviour alsoanalysed and it was observed that membrane MV showed highest thickness (0.56 mm) as well as highest swelling behaviour (1.5) due to presence of highchitosan content in its composition

Influence of Chitosan Concentration on Characteristic of Microspheres Delivery System Prepared from Eleutherine palmifolia (L.) Merr. Extract

Background: Eleutherine palmifolia (L.) Merr. (E.palmifolia) is a medicinal plant containing naphthoquinone, isoliquiritigenin, and oxyresveratrol compound. This study aims to formulate and characterize the E. palmifolia microspheres delivery system using chitosan variation as the polymer. Methods: The preparation method was the solvent evaporation method. The microspheres delivery system was performed by variation of chitosan concentration in each formulation 0.637% (F1), 1.275% (F2), and 1.912% (F3). The physical and chemical characterizations include Entrapment Efficiency (EE), yield percentage, particle size, particle morphology, FTIR analysis, X-Ray Diffraction (XRD) analysis, and Differential Thermal Analysis (DTA) had been evaluated. Results: The results showed that chitosan concentration variation affected the microsphere's physical and chemical characteristics. Variations in the concentration of chitosan polymer (0.637%, 1.275% and 1.912%) had an effect on the physical characteristics of the microspheres of the resulting Dayak onion bulb extract. The higher the concentration of chitosan used, the higher the entrapment efficiency and the yield yield will increase. Meanwhile, in observing the particle size, the higher the concentration of chitosan used, the smaller the particle size produced. The optimal concentration of chitosan as a polymer at concentration variations of 0.637%, 1.275% and 1.912% to provide good physical characteristics of the Dayak onion bulb extract microspheres was shown in formula 3 with a chitosan concentration of 1.912%. Conclusion: The better characteristic was obtained upon higher chitosan concentration. The best physical characteristics of E.palmifolia extract microspheres were obtained from chitosan concentration at 1.912% (F3).