Suvimol Surassmo

Antibacterial effect of apatite-coated titanium dioxide for textiles applications.

An antibacterial activity of apatite-coated titanium dioxide (TiO2) against four types of bacteria (Staphylococcus aureus, Escherichia coli, methicillin-resistant Staphylococcus aureus (MRSA), and Micrococcus luteus) was investigated. Its antibacterial performance was observed under black light, visible light, and dark conditions. The number of viable bacteria decreased with irradiation time and became most prominent at 24 hours. Distortion of bacterial cells by the nanoparticles was demonstrated by scanning electron microscopy. Apatite-coated TiO2 was fixed on cotton textiles by dip-coat technique, and the antimicrobial properties of corresponding fabrics were then investigated. The effect of irradiation source on antimicrobial activity of coated cotton fabrics was examined, wherein black-light irradiation demonstrated higher antibacterial activity than either visible-light irradiation or dark conditions. Microbial populations of coated cotton fabrics decreased with increasing irradiation intensity. Coated cotton fabrics have been shown to be nontoxic to human dermal fibroblasts. Our findings suggest that the presence of apatite-coated TiO2 shows antibacterial activity in the presence of black light or visible light, suggesting its potential use in reducing the risk of microorganism transmission for textile applications.

Antibacterial activity of Thai medicinal plants against methicillin-resistant Staphylococcus aureus.

Methicillin-resistant Staphylococcus aureus (MRSA) is a major nosocomial pathogen which causes severe morbidity and mortality worldwide. Seventeen Thai medicinal plants were investigated for their activity against MRSA. Garcinia mangostana was identified as the most potent plant, and its activity was traced to the prenylated xanthone, alpha-mangostin (MIC and MBC values of 1.95 and 3.91 microg/ml, respectively).

Physicothermal Properties of Freeze-Dried Fish Oil Nanocapsules Frozen under Different Conditions

This research compared the effects of vacuum freeze drying (VFD) and conventional freeze drying (CFD) processes on the stability of fish oil–loaded nanocapsules (NCs). For CFD, the NCs showed aggregation that was dependent on the freezing temperature. The encapsulation efficiency of CFD was greater than that of VFD, except at the freezing temperature of −30°C. From differential scanning calorimetry (DSC) analysis and scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images, it was concluded that the CFD process was more effective in the oxidative stability of the fish oil–loaded NCs. In addition, the vacuum-freezing process may affect the fragility of the poly-ϵ-caprolactone membrane due to its low encapsulation efficiency and aggregation of particles. No differences in Z-potential values between the CFD samples were observed, whereas in the VFD samples, it became increased in the negative charge when decreasing the cooling temperature of the fish oil–loaded nanocapsules for the freeze-drying procedure. Regarding the observation of surface tension, CFD samples presented lower values than VFD samples at given freezing temperature.

Surface modification of PLGA nanoparticles by carbopol to enhance mucoadhesion and cell internalization

Mucoadhesive poly (lactic-co-glycolic acid) (PLGA) nanoparticles having a modified shell-matrix derived from polyvinyl alcohol (PVA) and Carbopol (CP), a biodegradable polymer coating, to improve the adhesion and cell transfection properties were developed. The optimum formulations utilized a CP concentration in the range of 0.05-0.2%w/v, and were formed using modified emulsion-solvent evaporation technique. The resulting CP-PLGA nanoparticles were characterized in terms of their physical and chemical properties. The absorbed CP on the PLGA shell-matrix was found to affect the particle size and surface charge, with 0.05% CP giving rise to smooth spherical particles (0.05CP-PLGA) with the smallest size (285.90 nm), and strong negative surface charge (-25.70 mV). The introduction of CP results in an enhancement of the mucoadhesion between CP-PLGA nanoparticles and mucin particles. In vitro cell internalization studies highlighted the potential of 0.05CP-PLGA nanoparticles for transfection into SiHa cells, with uptake being time dependent. Additionally, cytotoxicity studies of CP-PLGA nanoparticles against SiHa cancer cells indicated that low concentrations of the nanoparticles were non-toxic to cells (cell viability >80%). From the various formulations studied, 0.05CP-PLGA nanoparticles proved to be the optimum model carrier having the required mucoadhesive profile and could be an alternative therapeutic efficacy carrier for targeted mucosal drug delivery systems with biodegradable polymer.

Surface modification of nanostructure lipid carrier (NLC) by oleoyl-quaternized-chitosan as a mucoadhesive nanocarrier

A nanostructure lipid carrier (NLC) composed of solid, and liquid lipid as a core has been developed as a delivery system for hydrophobic drug molecules. The aim of this research was to fabricate an oleoyl-quaternized-chitosan (CS)-coated NLC, where the mucoadhesive property of nanoparticles is enhanced for more efficient drug delivery. NLC loaded with alpha-mangostin (AP), a model hydrophobic drug, were fabricated using a high pressure homogenization process and subsequently coated with CS. The fabricated nanoparticles showed particle sizes in the range of 200-400nm, with low polydispersity, high physical stability and excellent encapsulation efficiency (EE>90%). Additionally, in vitro viability, cytotoxicity and ability of NLC and CS-NLC to affect apoptosis in carcinoma Caco-2 cells were determined using the Triplex assay. Gene expressiom analysis were performed using quantitative reverse transcription Polymerase Chain Reaction (RT-qPCR). Moreover, in vivo toxicological testing of NLCs was conducted in zebrafish embryos. Results indicated that CS-NLC provieded high cytotoxicity than NLC itself. In the case of AP loaded nanoparticles, NLC loaded with AP (AP-NLC), and CS-NLC loaded with AP (CS-AP-NLC) exhibited higher cytotoxicity to Caco-2 over Hela cells. These results indicate that CS-NLC shows enhanced cellular uptake but increased cytotoxicity characteristics over NLC and therefore careful optimization of dosage and loading levels in CS-NLC is needed to allow cancer cell targeting, and for exploiting the potential of these systems in cancer therapy.

Physical and biological characterization of sericin-loaded copolymer liposomes stabilized by polyvinyl alcohol.

Sericin protein (SP) is widely used as a nutrient biomaterial for biomedical and cosmeceutical applications although it shows low stability to heat and light. To overcome these problems and add value to wastewater from the silk industry, sericin protein was recovered as sericin-loaded copolymer-liposomes (SP-PVA-LP), prepared through thin film hydration. The size and morphology of the liposomes were investigated using dynamic light scattering (DLS), and electron microscopy (SEM and TEM). The particle size, liposome surface morphology and encapsulation efficiency of SP were dependent on PVA concentration. The hydrodynamic size of the nanoparticles was between 200 and 400nm, with the degree of negative charge contingent on sericin loading. SEM and TEM images confirmed the mono-dispersity, and spherical nature of the particles, with FTIR measurements confirming the presence of surface bound PVA. Exposure of liposomes to 500ppm sericin highlighted a dependence of encapsulation efficiency on PVA content; 2% surface PVA proved the optimal level for sericin loading. Cytotoxicity and viability assays revealed that SP-loaded surface modified liposomes promote cellular attachment and proliferation of human skin fibroblasts without adverse toxic effects. Surface modified copolymer liposomes show high performance in maintaining structural stability, and promoting enhancements in the solubility and bio-viability of sericin. Taken together, these biocompatible constructs allow for effective controlled release, augmenting sericin activity and resulting in effective drug delivery systems.

Influence of High Hydrostatic Pressure on the Capsicum Oleoresin Encapsulated by Globular Protein

We studied herein the effects of high hydrostatic pressure on the physical properties of capsicum oleoresin encapsulated with globular protein, such as whey protein isolates (WPI), soybean protein isolates (SPI), and casein protein (CSP). After pressurization at 0.1, 100, 200, and 300 MPa with various concentrations (0.1, 1, 2, and 5 wt%) of proteins, the particle size, ζ-potential, and interface tension were evaluated. Furthermore, the encapsulation efficiency (EE), release study, and morphology were investigated to study the effects of high hydrostatic pressurization upon emulsion stability. While the pressurized emulsion droplet size of capsicum oleoresin emulsion with the protein decreased, the 0.1 wt% concentration of SPI presented the smallest size at 257.37 nm. The interface tension of all protein emulsions decreased slightly after high-pressure treatment according to the increment of the pressure level. EE (%) of the WPI, SPI, and CSP emulsions increased when the pressure level increased. The lowest EE 48.91% was presented in pressurized WPI emulsion at 0.1 MPa while CSP emulsion at 300 MPa showed the highest EE about 65.76%. Over twelve hours, the core material of the pressurized protein emulsions was released slowly compared to non-pressurized conditions with the WPI and CSP emulsions. At the end of the storage of the WPI and CSP non-pressured emulsions, the remaining amount of encapsulated capsicum oleoresin was only 10% and 40%, respectively, less than emulsions treated under high pressurization. Thus, the high pressurized protein could be a candidate for the encapsulation of the capsicum oleoresin.

Stabilization of Microcapsules Using a Freeze-Dried Gelatin Matrix: Aqueous Redispersibility and the Ingredient Activity

Microcapsules are of great interest to the food and pharmaceutical industries as vehicles to deliver active ingredients to the gastrointestinal tract. Drying plays an important role in stabilizing microcapsules to prolong their lifetime; however, drying often produces undesirable changes in the microcapsules, such as irreversible aggregation of the microcapsules and activity loss of the encapsulated ingredient. In this work, poly(epsilon-caprolactone) microcapsules containing a model bioactive compound (tocopherol) were prepared and stabilized in a freeze-dried gelatin matrix. This dried product was rehydrated and the aqueous redispersibility of the microcapsules and the tocopherol activity were investigated. The experimental results suggested that a kinetic balance between dehydration (caused by freezing) and gel network formation is a critical factor that affects the redispersibility and ingredient activity of the products. It was further suggested that a hydrogel-based product could be strategically fr...

Efficiency of resveratrol-loaded sericin nanoparticles: Promising bionanocarriers for drug delivery

Sericin protein nanoparticles are a biocompatible, bio-viable class of nanocarriers gaining prominence in drug delivery system. This research aimed to investigate the suitability fabrication of silk protein (SP) nanoparticles for loading with resveratrol (RSV) via a solventless precipitation technique. The addition of 0.5% (w/v) pluronic surfactant proved optimal for SP nanoparticle fabrication, with obtained nanoparticles being spherical, mono-dispersed and having mean size of approximately 200-400 nm. All exhibited negative surface charges, the extent of which being dependent on the SP concentration, and were non-toxic to normal skin fibroblasts (CRL-2522). Loading of RSV, a promising which poorly soluble multi-targeted anti-oxidative and anti-inflammatory natural polyphenol, into SP nanoparticles proved feasible, with encapsulation levels of 71-75% for 0.6% and 1.0% (w/v) nanoparticle formulations, respectively. Resveratrol-loaded SP nanoparticles strongly inhibited growth of colorectal adenocarcinoma (Caco-2) cells although proved non-cytotoxic to skin fibroblasts, as indicated by cell viability assays. Cellular internalization of SP nanoparticles proved facile and dependent on incubation time; transfection of these carriers, in vitro results indicating sustained release of RSV (over 72 h), and drug solubility enhancements on encapsulation highlight their potential in therapeutic and pharmaceutical applications. Thus, SP nanoparticles is a promising approach to be potential bio-nanocarrier for drug delivery system.

Controllable encapsulation of α-mangostin with quaternized β-cyclodextrin grafted chitosan using high shear mixing

In this study, the inclusion complex formation between α-mangostin and water-soluble quaternized β-CD grafted-chitosan (QCD-g-CS) was investigated. Inclusion complex formation with encapsulation efficiency (%EE) of 5, 15 and 75% can be varied using high speed homogenizer. Tuning %EE plays a role on physicochemical and biological properties of α-mangostin/QCD-g-CS complex. Molecular dynamics simulations indicate that α-mangostin is included within the hydrophobic β-CD cavity and being absorbed on the QCD-g-CS surface, with these results being confirmed by Fourier transform infrared (FTIR) spectroscopy. Probing the release characteristics of the inclusion complex at various %EE (5%, 15% and 75%) in simulated saliva (pH 6.8) demonstrated that α-mangostin release rates were dependent on % EE (order 5% > 15% > 75%). Additionally, higher antimicrobial and anti-inflammation activities were observed for the inclusion complex than those of free α-mangostin due to enhance the solubility of α-mangostin through the inclusion complex with QCD-g-CS.