Solvent Casting Method Research Articles

Structural and Physiochemical Properties of Polyvinyl Alcohol-Succinoglycan Biodegradable Films.

Polyvinyl alcohol (PVA)-bacterial succinoglycan (SG) biodegradable films were developed through a solvent-casting method. Effects of the PVA/SG ratio on the thickness, transmittance, water holding capacity, and structural and mechanical properties were investigated by various analytical methods. All the prepared films were transparent and uniform, and XRD and FTIR analyses confirmed that PVA was successfully incorporated into SG. The films also showed excellent UV-blocking ability: up to close to 80% with increasing SG concentration. The formation of effective intermolecular interactions between these polymers was evidenced by their high tensile strength and moisture transport capacity. By measuring the biodegradation rate, it was confirmed that films with high SG content showed the fastest biodegradation rate over 5 days. These results confirm that PVA/SG films are eco-friendly, with both excellent biodegradability and effective UV-blocking ability, suggesting the possibility of industrial applications as a packaging material in various fields in the future.

Fabrication and characterization of bio-nanocomposite from sweet potato starch and Moringa oleifera leaf extract loaded with carbon quantum dots from Coffea arabica grounds

The study aims to generate and characterize a bio-nanocomposite film derived from sweet potato starch and Moringa oleifera leaf extract and carbon quantum dots (CQDs) derived from Arabica coffee grounds employing the solvent casting method. The effect of various concentrations of CQDs (0–400 ppm) was investigated on the physicochemical properties, UV-barrier, antioxidant properties, and biodegradability of the bionanocomposite (BNC) films. The morphological surface of the bio-nanocomposite was examined using scanning electron microscopy (SEM). Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were performed to evaluate the thermal stability of the samples. Mechanical properties, including tensile strength (TS) and elongation at break (EB), were also assessed. The results show that the incorporation of CQDs with starch-based biofilms had a remarkable impact on the properties of BNC. SEM images confirm the homogeneous structure of the films with slight granulations. Colorimetric analysis indicates the increase in color difference of BNCs as the concentration of CQDs varied. The BNC100 formulation confirmed batter opacity, transparency, and UV-barrier properties while BNC50 possessed significant improvement in tensile, elongation as well as a substantial increase in the melting point. FTIR and XRD analysis confirmed proper chemical interactions among the components within the polymeric structure of the BNC film. In addition, CQD integration has also steadily enhanced the antioxidant properties and biodegradability of BNC films. The fabricated films with CQDs have demonstrated a better quality in terms of optical properties, physical properties, thermomechanical properties, biodegradation rate, and antioxidant behavior that suggest the film's application in food packaging or other relevant fields.

Preparation and Characterization of Febuxostat Nanosuspension as Fast Dissolving Oral Film

Background: Quickly dissolved oral films are a widely accepted method of delivering drugs and help patients adhere to treatment regimens. Nanosuspensions (NS) are colloidal dispersions of drug particles with a submicron size, and their large surface area enhances the solubility and dissolution of low-water-soluble drugs. Febuxostat (FXT) is a non-purine xanthine oxidase inhibitor with a low dissolution rate that limits its absorption. Objective: To develop fast-dissolving oral films (FDOFs) containing FXT NS and convert NS into solid dosage forms to ease administration and accelerate drug release. Methods: FXT NS was prepared using Soluplus as a stabilizer and Tween80 as a co-stabilizer through an anti-solvent precipitation technique. We prepared FDOFs using a solvent casting method, utilizing hydrophilic polymers like pullulan, polyvinyl alcohol (PVA), gelatin, and plasticizers like polyethylene glycol (PEG400) and glycerin. The study assessed the film's thickness, weight, folding endurance, drug content, disintegration time, and drug release. We validated the drug's compatibility using FTIR, and conducted a crystallinity study using DSC and X-ray powder diffraction. Results: F4 was the optimized formula prepared using PVA and PEG400. In just three minutes, the F4 dissolution rate increased significantly (99.63% vs. 11.23%) compared to the FXT ordinary film. Also, it had good mechanical properties. Conclusions: FXT NS were successfully loaded into FDOFs with accepted properties.

Carboxymethyl Cellulose-Blended Films from Rice Stubble as a New Potential Biopolymer Source to Reduce Agricultural Waste: A Mini Review

The vegetative part of the rice plant, Oryza sativa L., that remains after paddy fields have been cleared during harvest or afterward is known as rice stubble. Carboxymethyl Cellulose from Rice Stubble (CMCr) is a promising biopolymer source that can be made from rice stubble waste. Carboxymethyl cellulose was synthesized from rice stubble by a solvent-casting method. Various types of plasticizers (glycerol and olive oil) and the components they contain provide flexibility for use as a material for food packaging. The films' moisture barrier was enhanced by the olive oil content while their extensibility was enhanced by the glycerol content. Indonesia is known as a country with the majority of the population working as farmers. Along with the increase in rice harvested area each year, agricultural waste in the form of rice stubble is also increasing. In the future, the application of CMCr in food packaging has the potential to revolutionize sustainable practices in Indonesia's agricultural sector. By leveraging CMCr's unique properties, such as enhanced moisture barrier and increased extensibility, there is an opportunity to develop eco-friendly packaging solutions. This innovation not only addresses the challenge of rising rice stubble waste but also contributes to the reduction of environmental pollution, offering a greener and more sustainable approach to packaging in the country.

One-pot synthesis of Li3xLa2/3−xTiO3/PVA composite with high tunable electrical attributes governed by the Li+ content

The primary goal of this study is to elucidate the structural and electrical characteristics, alongside potential applications, of ceramic-polymeric composites. These composites are achieved by incorporating lithium-lanthanum titanates (Li3xLa2/3−xTiO3 - LLTO) into a polyvinyl alcohol polymeric matrix (PVA). The synthesis of lithium-lanthanum titanates occurred through high-energy ball milling method. Then, three types of composites were produced using the solvent casting method: a sample of pure Poly (vinyl alcohol) polymer (PVA), a second PVA composite with the addition of La0·59Li0·24TiO3 (Li-0.24) and a third sample with La0·56Li0·33TiO3 (Li-0.33). SEM and AFM analyzes revealed notable changes in the morphology and 3D spatial patterns of the films upon incorporating lithium-lanthanum titanates into the PVA matrix. The PVA film presents a topography featuring a more evenly distributed range of topographic heights, indicating a smoother surface structure. With varying LLTO content, the morphology of the PVA composite underwent changes. The lower roughness of the PVA surface is evident from its measured average roughness value (Ra = 1.9 ± 0.5 nm). Upon incorporating LLTO, the surfaces displayed increased roughness, measuring specifically at 40.1 ± 7.3 nm (Li-0.24) and 22.7 ± 5.5 nm (Li-0.33). Notably, there was an approximately 43 % reduction in the average roughness value from Li-0.24 to Li-0.33. The analysis by Raman allowed the identification of functional groups of the PVA polymeric chain, in addition to the presence of some vibrational modes related to the structure of lithium-lanthanum titanates for the sample with the highest content of Li+ ions (Li-0.33). Finally, the sample Li-0.33 showed the lowest value of electrical resistance (67 kΩ) and of phase angle (16°), compared to the PVA (100 MΩ and 90°). These results show that the presence of the LLTO changed the insulating behavior of the PVA matrix changed and improved potential to electronic applications.

Bilayer Scaffolds of PLLA/PCL/CAB Ternary Blend Films and Curcumin-Incorporated PLGA Electrospun Nanofibers: The Effects of Polymer Compositions and Solvents on Morphology and Molecular Interactions.

Tissue engineering scaffolds have been dedicated to regenerating damaged tissue by serving as host biomaterials for cell adhesion, growth, differentiation, and proliferation to develop new tissue. In this work, the design and fabrication of a biodegradable bilayer scaffold consisting of a ternary PLLA/PCL/CAB blend film layer and a PLGA/curcumin (CC) electrospun fiber layer were studied and discussed in terms of surface morphology, tensile mechanical properties, and molecular interactions. Three different compositions of PLLA/PCL/CAB-60/15/25 (TBF1), 75/10/15 (TBF2), and 85/5/10 (TBF3)-were fabricated using the solvent casting method. The electrospun fibers of PLGA/CC were fabricated using chloroform (CF) and dimethylformamide (DMF) co-solvents in 50:50 and 60:40 volume ratios. Spherical patterns of varying sizes were observed on the surfaces of all blend films-TBF1 (17-21 µm) > TBF2 (5-9 µm) > TBF3 (1-5 µm)-caused by heterogeneous surfaces inducing bubble nucleation. The TBF1, TBF2, and TBF3 films showed tensile elongation at break values of approximately 170%, 94%, and 43%, respectively. The PLGA/CC electrospun fibers fabricated using 50:50 CF:DMF had diameters ranging from 100 to 400 nm, which were larger than those of the PLGA fibers (50-200 nm). In contrast, the PLGA/CC electrospun fibers fabricated using 60:40 CF:DMF had diameters mostly ranging from 200 to 700 nm, which were larger than those of PLGA fibers (200-500 nm). Molecular interactions via hydrogen bonding were observed between PLGA and CC. The surface morphology of the bilayer scaffold demonstrated adhesion between these two solid surfaces resembling "thread stitches" promoted by hydrophobic interactions, hydrogen bonding, and surface roughness.

An in vitro evaluation of Hypericum perforatum loaded-chitosan nanoparticle/agarose film as a Wound dressing

Wound dressing materials are crucial for accelerating the healing period of chronic wounds. In this study, chitosan nanoparticles loaded with Hypericum perforatum (Hp) were modified with agarose to create wound-healing films and their antimicrobial potential was investigated in vitro. Chitosan (CS) nanoparticles and Hp-loaded nanoparticles were prepared using the ionic gelation method. The synthesized Hp-loaded CS nanoparticles were modified with agarose by the solvent-casting method. Antimicrobial assays were performed using the disk diffusion method and agar well diffusion method. The characterization of nanoparticles and films was performed by UV–Vis spectrophotometry, Dynamic Light Scattering (DLS), Fourier Transform Infrared Spectroscopy (FT-IR), mechanical testing, and swelling testing. The results showed that Hypericum perforatum was loaded into chitosan nanoparticles with a 90.1 ± 2.53 % yield. The sizes of the Hypericum perforatum-loaded chitosan nanoparticles and chitosan nanoparticles were 156 ± 22 nm and 69 ± 4.2 nm, respectively. The CS-Hp/Agarose film showed no cytotoxic effect on L929 fibroblast cells and maintained cell viability for 72 h. These results indicate that Hp might be used in wound healing due to its antimicrobial and cell growth-promoting properties.

Assessing the reinforcement effect by response surface methodology of holocellulose from spent coffee grounds on biopolymeric films as food packaging materials.

The pollution caused by petroleum-derived plastic materials has become a major environmental problem that has encouraged the development of new compostable and environmentally friendly materials for food packaging based on biomodified polymers with household residues. This study aims to design, synthesize, and characterize a biobased polymeric microstructure film from polyvinyl alcohol and chitosan reinforced with holocellulose from spent coffee grounds for food-sustainable packaging. Chemical isolation with a chlorite-based solution was performed to obtain the reinforced holocellulose from the spent coffee ground, and the solvent casting method was used to obtain the films to study. Physicochemical and microscopic characterizations were conducted to identify and select the best formulations using a simplex-centroid design analysis. The response surface methodology results indicate that the new packaging material obtained with equal amounts of polymers and reinforced material (1:1:1) possesses the appropriate barrier properties and microstructural character to prevent water attack and hydrophobic behavior and thus could be used as an alternative for food packaging materials.

Numerical and experimental investigation into tool-workpiece interaction in flexible abrasive tool finishing

The present work examines the finishing performance of oxygen-free high conductivity (OFHC) copper using a fabricated flexible abrasive tool. It is challenging to finish soft materials like copper and aluminium using traditional finishing techniques due to frequent scratching. Flexible finishing tool can protect the surface integrity of the workpiece samples during finishing action. Flexible abrasive tools are fabricated using solvent casting method. This method fabricates the flexible tools with homogeneous abrasive dispersion and an open-cell porous structure. The developed tool is self-sharpening and self-lubricating and can finish soft materials efficiently. The flexible abrasive tools can be fabricated in different shapes and sizes to finish internal features and complex shapes. The interaction between the tool and workpiece is examined by the forces exerted by the flexible tool on the workpiece. The areal surface roughness of the finished surface is reduced to 33 nm from its initial roughness of 937 nm after 20 min of finishing a pre-defined region. Theoretical analysis is carried out to estimate contact pressure using Hertz contact theory. The results obtained from numerical and theoretical analysis have a close correlation with the experimental results. The maximum deviation of peak contact pressure obtained in theoretical estimation and numerical analysis from experimental results is found to be 20.73 % and 12.83 %, respectively. As the model includes the basic physics of the tool-workpiece interaction, the results can be improved with the inclusion of micro-level analysis of fluid-filled flexible abrasive tools with embedded abrasives.

Starch/chitosan nanoparticles bionanocomposite membranes for methylene blue dye removal

This research aims to develop relatively new membranes from starch biopolymer incorporated with different concentrations (0, 5, 10, 15, 20% w/w of solid starch) of chitosan nanoparticles (CNP) that can be used for water treatment. The membranes were fabricated using the solvent casting method while the CNP was produced using the ionic gelation method. The membranes were characterized in terms of morphology, porosity, water vapor permeability (WVP), and water contact angle. The application of the membranes to treat water was demonstrated on methylene blue solution because methylene blue is a commonly used dye in many industries. It was found that the starch/10% CNP membrane was the optimum membrane for methylene blue dye treatment because the membrane exhibits a smooth surface, high WVP (1.67 × 10−10 g Pa−1 h−1 m−1), high porosity (59.92%), low water contact angle value (44.8°), and resulted in the highest percentage removal of methylene blue (94.0%) after the filtration. After filtration, the starch/10% CNP membrane was still in good condition without breakage. In conclusion, the starch/CNP membranes produced in this study are promising for sustainable and environmentally friendly water treatment, especially for water containing methylene blue dye. This research aligns with current thematic trends in bionanohybrid composite materials utilization, offering innovative solutions for addressing water pollution challenges.

Preparation of High-Toughness Cellulose Nanofiber/Polylactic Acid Bionanocomposite Films via Gel-like Cellulose Nanofibers.

This study demonstrates a procedure for preparing gel-like cellulose nanofibers (CNFs) in polyethylene glycol (PEG) to toughen polylactic acid (PLA) nanocomposite films. A well-dispersed solution of CNFs in ethanol was produced from microcrystalline cellulose by using a high-pressure microfluidizer. The fiber diameter of CNFs was found to be in the range of 80-100 nm. Ethanol was replaced by PEG using a rotary evaporator to obtain gel-like CNFs/PEG. PLA/PEG/CNF films were prepared using the solvent casting method, with the CNF content varying from 0.15 to 5 phr. The effect of CNFs on the mechanical, morphological, and thermal properties of PLA nanocomposite films was investigated. The results demonstrate that the addition of CNFs improved Young's modulus and toughness of PLA/PEG films. In contrast, a slight decrease in mechanical properties was observed when the content of CNFs reached 0.83 phr. Considère's constructions are used to explain the neck phenomena and cold drawing of nanocomposite films. The crystallization and thermal stability of PLA nanocomposite films were enhanced, with a slight decrease in cold-crystalline temperature (T cc) and an increase in decomposition temperature (T d).

Assessment of Alginate Gel Films as the Orodispersible Dosage Form for Meloxicam.

The aim of this study was to obtain films based on sodium alginate (SA) for disintegration in the oral cavity. The films were prepared with a solvent-casting method, and meloxicam (MLX) as the active ingredient was suspended in a 3% sodium alginate solution. Two different solid-dosage-form additives containing different disintegrating agents, i.e., VIVAPUR 112® (MCC; JRS Pharma, Rosenberg, Germany) and Prosolve EASYtabs SP® (MIX; JRS Pharma, Rosenberg, Germany), were used, and four different combinations of drying time and temperature were tested. The influence of the used disintegrant on the properties of the ODFs (orodispersible films) was investigated. The obtained films were studied for their appearance, elasticity, mass uniformity, water content, meloxicam content and, finally, disintegration time, which was studied using two different methods. The films obtained with the solvent-casting method were flexible and homogeneous in terms of MLX content. Elasticity was slightly better when MIX was used as a disintegrating agent. However, these samples also revealed worse uniformity and mechanical durability. It was concluded that the best properties of the films were achieved using the mildest drying conditions. The type of the disintegrating agent had no effect on the amount of water remaining in the film after drying. The water content depended on the drying conditions. The disintegration time was not affected by the disintegrant type, but some differences were observed when various drying conditions were applied. However, regardless of the formulation type and manufacturing conditions, the analyzed films could not be classified as fast disintegrating films, as the disintegration time exceeded 30 s in all of the tested formulations.

Chitosan, Poly(vinyl alcohol) and Chitosan/Poly(vinyl alcohol) based active films loaded with white turmeric powder for food packaging applications

In recent years packaging materials made of biodegradable polymers received considerable attention. The packaging system containing antimicrobial agents was one of the new methods that have an advantage over the conventional system. This work aims to fabricate and characterize antibacterial films based on chitosan (CS) and poly(vinyl alcohol) (PVA) incorporated with white turmeric powder (WT) for food packaging applications. The active films of chitosan/cetrimide/white turmeric (CCW), poly(vinyl alcohol)/cetrimide/white turmeric (PCW) and PVA/CS/CT/WT (PCCW) with varied concentrations of WT were prepared by solvent casting method. The influence of WT on the physical and structural properties of the prepared films were studied using different analytical techniques. The results of SEM analysis indicated interactions of polymer matrix with WT contributed to homogeneous, compact and smooth surface morphology. The Fourier Transform Infrared (FTIR) Spectroscopy and X-ray diffraction (XRD) analysis revealed hydrogen bond formation with a polymer matrix that improved the physical and thermal properties. The research findings revealed that there was an improvement in the tensile strength, moisture adsorption, solubility and hydrophobicity of CCW active films with an increase in WT content. At the same time, there was an improvement in inhibiting bacterial growth with increasing concentration of WT for all the fabricated films. The results showed better mechanical and antibacterial properties for PCCW films. All the films exhibited biodegradation under environmental conditions. All these results suggested WT incorporated CS and PVA based films can be used in the food packaging industry to enhance the safety and quality of the packaging material.

The effect of methyl yellow concentrations on the optical properties of polyvinyl chloride-methyl yellow film as a radiation dosimeter

A dosimetry system's ability to monitor absorbed doses is crucial for the quality assurance and control of products that have been exposed to radiation. Here, we propose a polyvinyl chloride (PVC)-methyl yellow (MY) film as a potential dosimeter for irradiation facilities. The PVC-MY film was prepared with a simple solvent-casting method at different MY concentrations from 0.3 to 1.2 mM. To evaluate the dosimeter's performance, the film was exposed to gamma-irradiation with irradiation doses of 0–25 kGy. The optical characteristics of the films examined using a UV–Vis spectrophotometer showed that the color of the films changed from yellow to red with increasing irradiation doses, and the color change sensitivity of the films increased with increasing MY concentrations. The absorption spectra of the irradiated PVC-MY films showed three maximum absorption peaks at 417, 522, and 547 nm. As irradiation doses increased, the film absorption at 417 nm decreased, while the film absorption at 522 and 547 nm increased. The film's stability studies suggest storage of the irradiated film in a cold-dark conditions is recommended to prevent damage and maintain response stability. The findings in this study emphasize the potential of the PVC-MY film as a dosimeter for irradiation facilities.

Influence of Dry-Mixing and Solvent Casting Blending Techniques on the Mechanical and Biological Behavior of Novel Biocompatible Poly(ε-caprolactone)/Alumina-Toughened Zirconia Scaffolds Obtained by 3D Printing

This work focuses on the study and comparison of two mixing methods for the dispersion of Alumina-Toughened Zirconia (ATZ) within the polymer matrix of Poly(ε-caprolactone) (PCL). The dry-mixing method using solvent-free impact milling (M) and the solvent casting method with chloroform (SC) were investigated. Samples were produced by 3D printing, and specimens were printed at increasing ATZ loadings (namely, 10, 20, and 40 wt.%). The chemico-physical, mechanical, and cell interaction characteristics of the materials prepared with both mixing methods were studied. Solvent mixing allowed better dispersion of the ATZ in the polymer matrix with respect to dry mixing. In addition, dry mixing affected the molecular weight of the PCL/ATZ composites much more than the solvent casting method. For these reasons, materials obtained by solid mixing exhibited the worst mechanical performance with respect to those obtained by solvent casting, which showed increased Young’s moduli with increasing ATZ amounts. The in vitro biological response elicited in a mesenchymal stem cell model seemed to be influenced by the mixing method, with a preference for the composites obtained through solvent mixing and containing 20 or 40 wt.% of ATZ.

Structural, morphological, and dielectric properties of poly(vinylidene fluoride)/(Bi0.5Ba0.25Sr0.25) (La0.5Ti0.5) O3 composites

AbstractFerroelectric flexible polymer composite films of poly(vinylidene fluoride) (PVDF) with different weight percentages (10.0%, 20.0%, 30.0%, 40.0%, and 50.0%) of (Bi0.5Ba0.25Sr0.25) (La0.5Ti0.5) O3 were synthesized by solvent casting method. Analysis using the x‐ray diffractometer and Fourier transform infrared spectroscopy tools revealed the presence of the different phases (α, β) of PVDF. Scanning electron microscope morphology illustrates the homogenous dispersion of ceramics particles in the matrix. The differential scanning calorimetry curve (under 25–400°C) gives the value of melting temperature (Tm=169.98°C) and percentage crystallinity is about 29.45% for 50 wt.% composite. The findings demonstrated that the composite has good thermal stability up to 169.98°C. Dielectric analysis shows ferroelectric and dielectric behavior and also distinguishes α and β phases of PVDF. It was found that the composite film containing 50 wt.% (Bi0.5Ba0.25Sr0.25) (La0.5Ti0.5) O3 had a dielectric constant (εr) of 38 (at 100 Hz) and dielectric loss of 0.059, which are the maximum among the samples. The relative permittivity rises with an increase in filler content due to electrostatics and interfacial polarization between PVDF (CH2CF2 dipole) and ceramic. The real and imaginary part of impedance spectroscopy with frequency (Cole–Cole plots) for composite (10.0–50.0 wt.%) at 25°C are also investigated. The current study provides a fresh perspective on the fact that PVDF‐(Bi0.5Ba0.25Sr0.25) (La0.5Ti0.5) O3 composite system has improved thermal stability and dielectric characteristics.

Maleic acid crosslinked starch/polyvinyl alcohol blend films with improved barrier properties for packaging applications

Incorporating starch, which is a potential biodegradable substitute for petroleum-based polymers, into conventional polymers is challenging owing to limitations in processability and weak-performing resulting materials. Herein, corn starch/polyvinyl alcohol (PVA) blend films (starch: PVA ratio of 50:50) were prepared via the solvent casting method using glycerol as a plasticizer and with varying concentrations of maleic acid as the crosslinking agent. Fourier transform infrared spectroscopy revealed the molecular interactions of the maleic acid crosslinker with the polymeric network of starch and PVA through an ester linkage. The properties of the films were strongly dependent on the maleic acid concentration. An increasing maleic acid concentration imparted hydrophobicity to the film; therefore, water swelling was significantly reduced, and water resistance was enhanced. The film containing 20 wt% maleic acid exhibited excellent barrier properties, with the lowest oxygen and water vapor transmission rates of 0.5 ± 0.2 cc/m2⋅day and 232.3 ± 5.4 g/m2⋅day, respectively. Moreover, the mechanical properties of the film improved with increasing crosslinking. This study demonstrates that the addition of maleic acid leads to an improvement in the overall performance of starch/PVA blend films. Therefore, maleic acid-crosslinked films can be used as barrier materials in food packaging applications.

Nanocrystalline cellulose as a reinforcing agent for poly (vinyl alcohol)/ gellan-gum-based composite film for moxifloxacin ocular delivery

Nanocrystalline cellulose (NCC) is a star material in drug delivery applications due to its good biocompatibility, large specific surface area, high tensile strength (TS), and high hydrophilicity. Poly(Vinyl Alcohol)/Gellan-gum-based innovative composite film has been prepared using nanocrystalline cellulose (PVA/GG/NCC) as a strengthening agent for ocular delivery of moxifloxacin (MOX) via solvent casting method. Impedance analysis was studied using the capacitive sensing technique for examining new capacitance nature of the nanocomposite MOX film. Antimicrobial properties of films were evaluated using Pseudomonas aeruginosa and Staphylococcus aureus as gram-negative and gram-positive bacteria respectively by disc diffusion technique. XRD revealed the characteristic peak of NCC and the amorphous form of the drug. Sustained in vitro release and enhanced corneal permeation of drug were noticed in the presence of NCC. Polymer matrix enhanced the mechanical properties (tensile strength 22.05 to 28.41 MPa) and impedance behavior (resistance 59.23 to 213.23 Ω) in the film due to the presence of NCC rather than its absence (16.78 MPa and 39.03 Ω respectively). Occurrence of NCC brought about good antimicrobial behavior (both gram-positive and gram-negative) of the film. NCC incorporated poly(vinyl alcohol)/gellan-gum-based composite film exhibited increased mechanical properties and impedance behavior for improved ocular delivery of moxifloxacin.

Transdermal Delivery of Niacin Through Polysaccharide Films Ameliorates Cutaneous Flushing in Experimental Wistar Rats.

Niacin, an established therapeutic for dyslipidemia, is hindered by its propensity to induce significant cutaneous flushing when administered orally in its unmodified state, thereby constraining its clinical utility. This study aimed to fabricate, characterize, and assess the in-vitro and in-vivo effectiveness of niacin-loaded polymeric films (NLPFs) comprised of carboxymethyl tamarind seed polysaccharide. The primary objective was to mitigate the flushing-related side effects associated with oral niacin administration. NLPFs were synthesized using the solvent casting method and subsequently subjected to characterization, including assessments of tensile strength, moisture uptake, thickness, and folding endurance. Surface characteristics were analyzed using a surface profiler and scanning electron microscopy (SEM). Potential interactions between niacin and the polysaccharide core were investigated through X-ray diffraction experiments (XRD) and Fourier transform infrared spectroscopy (FTIR). The viscoelastic properties of the films were explored using a Rheometer. In-vitro assessments included drug release studies, swelling behavior assays, and antioxidant assays. In-vivo efficacy was evaluated through skin permeation assays, skin irritation assays, and histopathological analyses. NLPFs exhibited a smooth texture with favorable tensile strength and moisture absorption capabilities. Niacin demonstrated interaction with the polysaccharide core, rendering the films amorphous. The films displayed slow and sustained drug release, exceptional antioxidant properties, optimal swelling behavior, and viscoelastic characteristics. Furthermore, the films exhibited biocompatibility and non-toxicity towards skin cells. NLPFs emerged as promising carrier systems for the therapeutic transdermal delivery of niacin, effectively mitigating its flushing-associated adverse effects.

DESIGN AND OPTIMIZATION OF ESCITALOPRAM OXALATE ORAL DISSOLVING FILMS BY RESPONSE SURFACE METHODOLOGY

Objective: To develop and optimise the oral dissolving films of escitalopram oxalate by response surface methodology. Methods: Oral dissolving film compositions were optimized by central composite design. The films are prepared by solvent casting method. Initially, different polymers were screened and based on the results polyvinyl alcohol was selected as polymer, propylene glycol was selected as plasticizer. Concentration of polymer and concentration of plasticizer were fixed as independent variables; tensile strength, percent elongation, elastic modulus and amount dissolved up to 5 min (%D5 min) were taken as responses. Results: The prepared films exhibited good surface characteristics. The thickness, uniformity of weight, surface pH and drug content are within acceptable range. The mechanical properties like tensile strength, folding endurance, percent elongation and elastic modulus were determined. The statistical analysis showed that polymer concentration has a positive effect on disintegration time and the plasticizer concentration has a significant effect on folding endurance. The prepared film relesases nearly 95% at the end of 5 min. The design space was used to optimize the quantities of polymer and plasticizer. The comparison of checkpoint experiment batch responses are corelating with the predicted responses. Conclusion: Escitalopram oxalate oral dissolving films was successfully designed and optimized by response surface method. It was concluded that the prepared films exhibit good mechanical properties and maximum release within 10 min.