Monvisade, Pathavuth
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Preferred name
Monvisade, Pathavuth
Alternative Name
Monvisade, P.
Main Affiliation
Email
pathavuth.mo@kmitl.ac.th
29 results
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Item type:Publication, Colorimetric Screen-Printed Label Using Low Molecular Weight Chitosan Grafted with Rosolic Acid for pH and Ammonia Gas Sensing(2024-10-15) ;Ronte, Arnat ;Chalitangkoon, JongjitColorimetric sensing technologies are valued for their simplicity and adaptability, yet their large-scale production remains economically challenging. This study presents a cost-effective colorimetric pH sensor developed from low molecular weight chitosan (LC) grafted with rosolic acid (LCRA), engineered as a pH-sensitive colorant for screen-printing inks. LCRA was synthesized via a Mannich reaction and characterized using<sup>1</sup> H NMR, FT-IR, and UV-Vis spectroscopy. LCRA showed reduced crystallinity and thermal stability alongside notable improvements in water solubility compared to its LC precursor. The LCRA ink displayed compatibility with various substrates, including polypropylene spun bond, filter paper, and cotton, applying easily via screen printing without any dye leaching. Notably, it exhibited a responsive color change from orange-yellow to pink-red in response to pH adjustments between 4.0 and 12.0 and upon exposure to ammonia gas. These findings position the LCRA label as a versatile and efficient solution for visual pH detection across various applications. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Photocrosslinked Poly(Vinyl Alcohol)–Tung Oil–Natural Rubber Films: A Sustainable Solution for Enhanced Water Resistance and Mechanical Properties in Biodegradable Packaging(2025-06-20); ;Jianprasert, Apichaya ;Sintoppun, Tanaporn ;Yamaguchi, MasayukiThis study introduces a novel approach to addressing the water resistance limitations of poly(vinyl alcohol) (PVA)-based biodegradable films by developing a ternary blend system incorporating tung oil (T) and natural rubber (R), forming PTR films. Photocrosslinking, combined with thermal and redox catalytic systems, facilitated the creation of enhanced network structures, as confirmed by FTIR analysis, particularly at tung oils conjugated double bonds. Dynamic mechanical analysis (DMA) revealed significant shifts in glass transition temperatures (T<inf>g</inf>), signifying enhanced crosslink density and interconnectivity between the components. The resulting PTR films demonstrated remarkable improvements in water resistance, evidenced by higher solid remain percentages, reduced water absorption, and significantly lower water vapor permeability (WVP). Mechanical properties, including tensile strength and Youngs modulus, improved by up to 150% (from 6.6 MPa of PT0R15-r-np to 16.3 MPa of PT0R15-r-p30) and 870% (from 6.6 MPa of PT0R15-r-np to 16.3 MPa of PT0R15-r-p30), respectively, due to the formation of robust network structures. Contact angle measurements and reduced moisture content further underscored the enhanced hydrophobic and moisture barrier properties. These findings establish photocrosslinked PTR films as a sustainable and high-performance option for biodegradable packaging applications, offering practical advantages such as reduced processing temperatures and production times. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Bacterial cellulose and bacterial cellulose/chitosan films containing mangosteen pericarp extract for wound dressings(2021-01-01) ;Moonsungnoen, Pronpatsorn; Appropriate wound dressings for maintaining a moist wound environment, inducing re-epithelialization and protection from infection have been widely developed. Recently, many biocompatible polymers and bioactive substances have been extensively used for wound healing applications. In this study, bacterial cellulose film (BC-MPE film) and bacterial cellulose/chitosan film (BC/CH-MPE film) containing 1.56 mg/mL of mangosteen pericarp extract (MPE) were prepared. Antibacterial activity, cytotoxicity, physical and mechanical properties of the dry films were investigated. The BC film with MPE presented non-cytotoxic effect after 20 h of exposure to mouse fibroblast cell line (L929). The prepared films performed carrier of bioactive compounds that exhibited antibacterial activity against bacterial infection in burn wounds. The morphology of the films showed the characteristic of ultra-fine network structures with the entrapment of compounds. In addition, the compact structure was observed due to the rapid moisture loss during vacuum drying process. SEM images also showed that BC/CH-MPE film formed layers with chitosan entrapment causing the film to become thicker than BC-MPE film. The formation of MPE and chitosan in modified films was also confirmed by FTIR. The compact structure of BC/CH-MPE film led to the decrease in cumulative release of xanthone, WVTR and WAC. Moreover, the existence of chitosan in BC layers provided more flexible properties than the non-chitosan film. The chitosan addition demonstrated an influence of barrier film to protect the wound. Therefore, BC and chitosan were considered as suitable candidates for wound dressing material and xanthone content of MPE promoted wound healing as an effective therapeutic agent. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Antimicrobial nanolayer films of chloroxylenol–carboxyethylchitosan–modified silver nanoparticles for enhanced surgical suture performance(2024-07-20) ;Chittratan, Pakawat; ;Chalitangkoon, Jongjit; Antimicrobial surgical suture materials incorporating chloroxylenol-carboxyethylchitosan-modified silver nanoparticles (CECSX-AgNPs) were successfully prepared using the Layer-by-Layer (LbL) deposition technique. Chitosan (CS) was covalently affixed with chloroxylenol as hydrophobic functional groups (PCMX), yielding chloroxylenol-chitosan (CSX) and later hydrophilic acrylic acid onto the CSX skeleton, providing a novel water-soluble antimicrobial agent of chloroxylenol-carboxyethylchitosan (CECSX). <sup>1</sup>H NMR confirmed the successful substitution of PCMX and acrylic acid onto CS, with %DS<inf>PCMX</inf> and %DS<inf>AA</inf> of 8.0 and 33.0, respectively. CECSX successfully stabilized AgNPs via the chemical reduction method, resulting in CECSX modified AgNPs. The colloidal solution exhibited a yellowish hue, spherical shape, monodispersity with an average particle size of 4.8 ± 2.4 nm, and a zeta potential value of −20.97 ± 0.03 mV. Minimum inhibitory concentration (MIC) values for CECSX-AgNPs against E. coli (ATCC25922), S. aureus (ATCC25923), and A. baumanii (ATCC19606) were determined as 25, 12.5, and 1.56 mg/L, respectively. Using the LbL deposition technique, CECSX-AgNPs were successfully deposited onto various suture materials including cotton, polyamide, and polypropylene. Remarkably, CECSX-AgNPs coated surgical sutures exhibited the highest bacterial reduction of 99.99 %. These findings underscore the efficacy of CECSX as a high-performance stabilizing agent for AgNPs production, providing outstanding antibacterial activity on diverse surgical suture materials and promoting the wound healing process. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Development of Bilayer Chitosan–Carrageenan Hydrogel Film for Enhanced Controlled Release of Turmeric–β-Cyclodextrin Complex in Wound Dressings(2025-11-01); ;Sintoppun, Tanaporn ;Chantaranara, Prapassorn ;Punpairoj, PrapapornDeatvakkanee, PitchapaThis study presents the development and evaluation of a bilayer hydrogel film designed for controlled drug delivery in wound dressing applications. The outer layer, composed of chitosan and glycerol, exhibited excellent water resistance, flexibility, and favorable moisture-handling properties, including high water vapor permeability and moisture absorption, which are critical factors for maintaining an optimal wound environment. The inner drug-loaded layer, formulated with carrageenan and loaded with either free turmeric or turmeric–β-cyclodextrin inclusion complex (TCD), served as the drug reservoir. Films incorporating TCD exhibited significantly enhanced turmeric solubility and drug release efficiency compared to those containing uncomplexed turmeric. Among the tested formulations, CS-TCD1, which featured a thinner drug-loaded layer, achieved the highest performance, with approximately 68% cumulative release over four days. While the release kinetics showed a strong correlation with the Higuchi kinetic model (R<sup>2</sup> = 0.9927), further analysis using the Akaike Information Criterion (AIC) and the Korsmeyer–Peppas model indicated an anomalous (non-Fickian) transport mechanism, governed by both diffusion and matrix swelling or erosion. These results highlight the importance of matrix architecture and drug solubilization strategies in the design of hydrogel-based drug delivery systems for wound care. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, New Chitosan-Grafted Thymol Coated on Gold Nanoparticles for Control of Cariogenic Bacteria in the Oral Cavity(2022-08-02) ;Chittratan, Pakawat ;Chalitangkoon, Jongjit; ; Chitosan-grafted thymol (CST) coated on gold nanoparticles has been synthesized and characterized for the design of antimicrobial materials. CST was synthesized via adapting the Mannich reaction, and it acted as the capping agent for the synthesis of gold nanoparticles (AuNPs). The grafting of thymol onto the side chain of chitosan has provided a degree of substitution value (%DS<inf>NMR</inf>) of 10.0%, calculated by nuclear magnetic resonance spectroscopy. UV-visible spectrometry and elemental analysis were used to confirm the successful synthesis of CST through adapting the Mannich reaction. The appropriate concentration of CST for AuNP synthesis was found to be 0.020%w/v. A red-wine colloidal AuNP solution of 2.41-3.30 nM particle size exhibits a strong surface plasmon resonance at 502 nm, which shows negative charges at pH = 9 of -36.37 mV. This result evidenced that the AuNPs showed electrostatic repulsion and CST played a role as a capping agent to provide a good dispersion and stability state. CST coated on the AuNP surface was successfully utilized for the control of cariogenic bacteria in the oral cavity. The results obtained from this study show that the tuning of the capping agent used in the synthesis step strongly influences the latter antimicrobial activity of the nanoparticles against Streptococcus mutans ATCC 25175 and Streptococcus sobrinus ATCC 33402 activity, with an inhibition zone of 15.90 and 14.25 mm, respectively. The average minimum inhibitory concentration values against S. mutans ATCC 25175 and S. sobrinus ATCC 33402 were found to be 25 and 100 mg/L, respectively, whereas the minimum bactericidal concentration values were 100 and 200 mg/L, respectively. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Silver loaded hydroxyethylacryl chitosan/sodium alginate hydrogel films for controlled drug release wound dressings(2020-09-15) ;Chalitangkoon, Jongjit ;Wongkittisin, MarisaWound dressings composed of hydroxyethylacryl chitosan (HC) and sodium alginate (SA) were developed with antibacterial activity by loading Ag particles. The formation of Ag particle in the HC/SA films was achieved by an immersion method through in situ chemical reduction of AgNO<inf>3</inf> solution and confirmed by FTIR, SEM-EDS, XRD and XRF techniques. The effect of Ag loading in the Ca-crosslinked HC/SA films with different crosslinking density was studied on swelling behavior, mechanical properties, cytotoxicity, antibacterial activity and drug release behavior. The results showed that Ag loading increased swelling degree in phosphate buffer and enhanced mechanical properties. The HC/SA films with Ag loading exhibited antibacterial activity against E. coli and S. aureus as well as no toxicity on Vero cell. In vitro drug release profiles of the films were examined using para-acetylaminophenol, as a soluble model drug. The increase in crosslinking density and Ag loading prolonged drug releasing rate and almost the films showed linearity profiles. It can be concluded that the HC/SA films with Ag loading have a promising potential in modern wound dressings with antibacterial property and controlled drug release. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Enhancing chitosan solubility in alcohol: water mixtures for film-forming systems releasing with turmeric extracts(2021-06-01) ;Huaytragul, Janjira ;Chalitangkoon, Jongjit; Background: Film-forming system (FFS), a non-solid dosage form, are attractive drug delivery system for the topical drug administration due to ability to form a film in situ on a skin after spraying or applying. To minimize drying time, alcohol is often used as a solvent in the system. The aim of this research was to enhance chitosan solubility in alcoholic solution by chemical modification of chitosan, i.e., reductive amination and Michael addition reaction, for film-forming systems with efficient releasing of turmeric extract. Methods: Alcoholic-soluble chitosan derivative (CBA) was synthesized by reductive amination, followed by a Michael reaction. Its structure was investigated by FT-IR, <sup>1</sup>H NMR and XRD techniques. The CBA was incorporated with β-cyclodextrin encapsulated turmeric extract (CDTE) to prepare film-forming solution. Significant Findings: The results confirmed that the CBA was successful prepared, as the new peaks were observed by FT-IR and <sup>1</sup>H NMR, with good solubility in 50% aqueous alcoholic solution. The CBA-based film, derived from the solvent evaporation, exhibited nontoxic to HaCaT cells. Moreover, the films containing CDTE had smooth surfaces and released turmeric extract (74%) more effectively than films containing the extract alone (43%). The CBA-based ethanolic solution (30–50%v/v ethanol) could dry within ~6–9 min and form a thin film on human skin. Conclusions: Thus, the CBA-based solution with CDTE has potential as a film-forming system based on natural products. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Development of a pH-responsive intelligent label using low molecular weight chitosan grafted with phenol red for food packaging applications(2024-05-01) ;Ronte, Arnat ;Chalitangkoon, Jongjit ;Foster, E. JohanIn this study, we successfully developed a screen-printed pH-responsive intelligent label using low molecular weight chitosan grafted with phenol red (LCPR) as a colorant for screen printing ink. The LCPR was synthesized via a Mannich reaction, and its successful grafting was confirmed through FT-IR, UV–vis, and NMR spectroscopy. The LCPR exhibited lower crystallinity and thermal stability compared to low molecular weight chitosan (LC) and demonstrated zwitterionic behavior. To create intelligent labels, the LCPR-based ink was efficiently printed on cotton substrates with high resolution. The label exhibited remarkable sensitivity to buffer pH solutions and ammonia gas, leading to distinctive color changes from orange to red to purple. Additionally, the label showed excellent reversibility, storage stability, and leaching resistance to different food simulant solutions. The label was utilized to monitor shrimp freshness, successfully detecting a noticeable color shift upon spoilage. These findings highlight the significant potential of the LCPR-based label as an intelligent food packaging solution, offering pH-responsiveness and color stability for qualitative freshness detection of protein-rich food. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Dual covalent and ionic crosslinked xanthan gum–PVA hydrogel films for enhanced drug release performance(2025-11-01); ;Napradit, Sasipa ;Sintoppun, TanapornYamaguchi, MasayukiThis study presents the development and characterization of dual crosslinked xanthan gum–polyvinyl alcohol (XP) hydrogel films for potential use in controlled drug delivery applications. Hydrogel films were synthesized using glutaraldehyde for covalent crosslinking and Cu<sup>2+</sup> ions for ionic crosslinking, with varying polymer ratios and crosslinker concentrations. The swelling behavior and gel content were evaluated in both distilled water at 25 °C and simulated body fluid (SBF) at 37 °C, revealing that dual crosslinking significantly enhanced structural integrity and swelling resistance, with gel content reaching up to 98%. Thermal analysis using DSC and DMA confirmed increased glass transition temperatures, indicating reduced polymer chain mobility due to denser crosslinking networks. Mechanical tests showed that the films possessed high tensile strength (60–62 MPa), with stiffness increasing alongside Cu<sup>2+</sup> concentration and xanthan content. Cytocompatibility was validated through MTT assays on Vero cells, with all formulations exceeding 80% viability, thus classified as non-cytotoxic according to ISO 10993-5:2009 guidelines. Drug release studies using para-acetylaminophenol demonstrated sustained release behavior, achieving 50% release over 6 h in SBF. Kinetic analysis revealed that the release followed zero-order kinetics (R² = 0.9986) and case-II transport (n = 1.0396), indicating that release was governed by matrix swelling and erosion. These findings highlight the potential of XP dual crosslinked hydrogels as effective and biocompatible platforms for sustained drug delivery, particularly in wound care applications.
