Monvisade, Pathavuth
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Preferred name
Monvisade, Pathavuth
Alternative Name
Monvisade, P.
Main Affiliation
Email
pathavuth.mo@kmitl.ac.th
48 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) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Preparation of hydroxyapatite/poly(methyl methacrylate) and calcium silicate/poly(methyl methacrylate) interpenetrating hybrid composites(2007-10-01); ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Hydrothermal growth of ZnO nanostructures from nano-ZnO seeded in P(MMA-co-BA) matrix(2011-11-01); ; Nookaew, JitiNano-ZnO synthesized by hydrothermal reaction were embedded in poly(methyl methacrylate-co-butyl acrylate) matrix (P(MMA-co-BA)) to produce the nano-ZnO/P(MMA-co-BA) nanocomposites via in-situ polymerization at 85 °C. The nano-ZnO/P(MMA-co-BA) nanocomposites were hydrothermal treated in the mixture solution of Zn(NO <inf>3</inf>) <inf>2</inf>•6H <inf>2</inf>O and NH <inf>4</inf>OH at 90 °C under various pH (i.e.7, 8, 9 and 10) and treatment time (i.e. 4, 6, 8, 10, 12 and 24 hrs). The nano-ZnO could act as seeding particles for hydrothermal growth of ZnO nanostructures on the surfaces of nanocomposites. The higher pH of basic solutions used in the hydrothermal treatment, the higher amount of Zn(OH) <inf>4</inf> <sup>2-</sup> nuclei would be created, leading to a modification of the ZnO morphology from nano-nuclei to nanorods, nanorods bushes (flower-like nanostructure) and nanofibers with nanospine. The increase of hydrothermal treatment time resulted in the increases of amount and length of multidirectional grown ZnO nanorods. Data of the contact angle measurement exhibited the increase of hydrophobicity of the nano-ZnO/P(MMA-co-BA) nanocomposites after hydrothermal growth of ZnO nanostructures. The nanocomposites treated at pH∈=∈10 for 24 hrs shows the highest hydrophobicity with the contact angle of 121. In addition, the thermal stability of the nano-ZnO/P(MMA-co-BA) could be improved by the formation of hydrothermal grown ZnO nanostructure on the nanocomposite surface. © 2011 Springer Science+Business Media B.V. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Preparation and characterization of hydroxyapatite/poly(ethylene adipate) hybrid composites(2008-06-01); Hydroxyapatite/poly(ethylene adipate) (HAp/PEA) composites were prepared by in situ ring-opening polymerization of cyclic oligo(ethylene adipate) (C-OEA) within the porous HAp templates. HAp was firstly prepared by a co-precipitation method using calcium hydroxide and phosphoric acid and then shaped as a rectangular porous template. PEA precursor was synthesized by bulk polymerization of dimethyl adipate and ethylene glycol in the presence of tetraisopropyl orthotitanate. C-OEA was obtained by cyclo-depolymerization of the PEA precursor under high dilution condition using dibutyl tinoxide as a catalyst. The HAp/PEA composites were prepared by immersing the porous HAp templates in the mixture solution of C-OEA and dibutyl tinoxide catalyst overnight and ring-opening polymerizing at 180, 200 and 220°C for 24 h. The ring-opening polymerized PEA formed as a thin film coating on the surface of porous HAp template. The HAp/PEA composites contained PEA in the range of 20-26 wt%. The weight-average molecular weights of ring-opening polymerized PEA were in the range of 3800-4450 g/mol. Compressive strength of the HAp/PEA composite was significantly increased from 25 MPa in the porous HAp template to 140 MPa in the composite. © 2008 VSP. - 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); - 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); 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, In vitro drug release profiles of pH-sensitive hydroxyethylacryl chitosan/sodium alginate hydrogels using paracetamol as a soluble model drug(2017-06-01) - 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); ; 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, Study on Crosslinked Structure and Thermal Properties of Polymer Networks Based on Tung Oil and PVA with Different Catalytic Systems(2017-04-01); Yamaguchi, MasayukiThis work focuses on the effect of different catalytic systems on network structures and thermal properties of the polymer networks from poly(vinyl alcohol) (PVA) and Tung oil. The polymer networks based on Tung oil and PVA using potassium persulfate (KPS) as a thermal catalyst or KPS and sodium thiosulfate as a redox catalyst were performed at 60 °C and 80 °C. FTIR results confirmed that Tung oil could be crosslinked by both catalysts. Moreover, at 60 °C, it can be seen that the crosslinking reaction with the redox catalyst could occur better than with the thermal catalyst. To prove the crosslinking reaction of PVA in the polymer networks, water resistance of the polymer networks was also investigated. It was found that the PVA was successfully crosslinked by thermal catalyst but was not by redox catalyst. Besides, from this result, it could be suggested that, in the redox system, structure of the polymer networks was mainly formed by Tung oil. From DMA results, T<inf>g</inf> of PVA with the thermal catalyst is higher than that with the redox catalyst because of the network formation of PVA in thermal catalytic system. While the T<inf>g</inf> of Tung oil in the polymer networks with the redox catalyst is higher than that with the thermal catalyst. This is reasonable because the crosslinking reaction of Tung oil with the redox catalyst could easily occur better than with the thermal catalyst. Altogether, crosslink structure of Tung oil exhibited major influence on properties of PVA/Tung oil polymer network. - 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);