ABSTRACT
The modified agars were prepared using H2O2 in ethanol solution at appropriate pH conditions. Some interesting physical and chemical properties of modified agar were determined and characterized compared with those of raw agar, and the underlying mechanisms were preliminarily studied. Results showed that the maximum gel strength of the modified agar was 1068 g/cm2, which increased by 30.9% compared with that of raw agar (816 g/cm2), and the minimum sulfate content of the modified agar was 0.21%, which decreased by 73.4% compared with that of raw agar (0.79%). Moreover, the viscosity, molecular weight, gelling temperature and melting temperature all decreased, whereas the whiteness and transparency increased after modification. Fourier transform infrared spectroscopy, scanning electron microscopy and thermogravimetric analysis indicated that the spatial structure of agar have changed after treated with H2O2. Taken together, the results demonstrated that the desulfation of agar with H2O2 is a promising approach with practical significance.
Subject(s)
Agar/chemistry , Hydrogen Peroxide/chemistry , Agar/ultrastructure , Chemical Phenomena , Galactose/chemistry , Molecular Structure , Molecular Weight , Spectroscopy, Fourier Transform Infrared , Sulfates/chemistry , Temperature , Thermogravimetry , Transition Temperature , ViscosityABSTRACT
Cellulose nanocrystals (CNCs) were prepared by acid hydrolysis of cotton linter pulp fibers and three different purification methods, i.e., without post purification (CNC1), dialyzed against distilled water (CNC2), and neutralized with NaOH (CNC3), and their effect on film properties was evaluated by preparation of agar/CNCs composite films. All the CNCs were rod in shape with diameter of 15-50 nm and length of 210-480 nm. FTIR result indicated that there was no distinctive differences in the chemical structure between CNCs and cotton linter cellulose fiber. No significant relationship was observed between the sulfate content and crystallinity index of CNCs. The CNC3 showed higher thermal stability than the other type of CNCs due to the less adverse effect on the thermal stability of sulfate groups induced by the neutralization with NaOH. The tensile strength (TS) of agar film increased by 15% with incorporation of 5 wt% of CNC3, on the contrary, it decreased by 10% and 15% with incorporation of CNC1 and CNC2, respectively. Other performance properties of agar/CNCs composite films such as optical and water vapor barrier properties showed that the CNC3 was more effective filler than the other CNCs. In the range of concentration of CNC3 tested (1-10 wt%), inclusion of 5 wt% of CNC3 was the maximum concentration for improving or maintaining film properties of the composite films. The neutralization of acid hydrolyzed cellulose using NaOH was simple and convenient for the preparation of CNC and bionanocomposite films.
Subject(s)
Agar/chemistry , Cellulose/chemistry , Cotton Fiber/methods , Gossypium/chemistry , Nanocomposites/chemistry , Nanoparticles/chemistry , Agar/ultrastructure , Cellulose/ultrastructure , Elastic Modulus , Nanocomposites/ultrastructure , Nanoparticles/ultrastructure , Permeability , Spectroscopy, Fourier Transform Infrared , Steam , Sulfates/analysis , Temperature , X-Ray DiffractionABSTRACT
Photothermal therapy using (Near Infrared) NIR region of EM spectrum is a fast emerging technology for cancer therapy. Different types of nanoparticles may be used for enhancing the treatment. Though the treatment protocols are developed based on experience driven estimated temperature increase in the tissue, it is not really known what spatiotemporal thermal behavior in the tissue is. In this work, this thermal behavior of tissue models is investigated with and without using nanoparticles. An increased temperature inside tissue compared to surface is observed which is counter intuitive from the present state of knowledge. It is shown from fiber level microstructure that this increased temperature leads to enhanced damage at the deeper parts of biomaterials. Nanoparticles can be utilized to control this temperature increase spatially. A multiple scattering based physical model is proposed to explain this counterintuitive temperature rise inside tissue. The results show promising future for better understanding and standardizing the protocols for photothermal therapy.
Subject(s)
Hyperthermia, Induced/standards , Infrared Rays/therapeutic use , Phototherapy/standards , Temperature , Agar/chemistry , Agar/radiation effects , Agar/ultrastructure , Animals , Cattle , Collagen/chemistry , Collagen/radiation effects , Collagen/ultrastructure , Computer Simulation , Gels , Hyperthermia, Induced/adverse effects , Hyperthermia, Induced/methods , Phototherapy/adverse effects , Phototherapy/methodsABSTRACT
The chemical structure of the agar obtained from Gelidium sesquipedale (Rhodophyta) has been determined by (13)C nuclear magnetic resonance ((13)C NMR) and Fourier transform infrared spectroscopy (FTIR). Agar (AG) films with different amounts of soy protein isolate (SPI) were prepared using a thermo-moulding method, and transparent and hydrophobic films were obtained and characterized. FTIR analysis provided a detailed description of the binding groups present in the films, such as carboxylic, hydroxyl and sulfonate groups, while the surface composition was examined using X-ray photoelectron spectroscopy (XPS). The changes observed by FTIR and XPS spectra suggested interactions between functional groups of agar and SPI. This is a novel approach to the characterization of agar-based films and provides knowledge about the compatibility of agar and soy protein for further investigation of the functional properties of biodegradable films based on these biopolymers.
Subject(s)
Agar/chemistry , Biocompatible Materials/chemistry , Rhodophyta/chemistry , Soybean Proteins/chemistry , Agar/isolation & purification , Agar/ultrastructure , Hydrophobic and Hydrophilic Interactions , Microscopy, Electron, Scanning , Photoelectron Spectroscopy , Spectroscopy, Fourier Transform Infrared , Surface Properties , Tensile StrengthABSTRACT
Synthesis of graft copolymers under the influence of microwave radiation alone is a rapid, efficient, clean, cheap, convenient, energy-saving and green method. Grafting of poly(2-hydroxyethylmethacrylate) on agar backbone was carried out under the influence of microwave radiation. The synthesis is optimized in terms of percentage grafting and intrinsic viscosity, by varying the microwave irradiation time and monomer (2-hydroxyethylmethacrylate) concentration. The synthesized graft copolymers have been characterized by intrinsic viscosity measurement, FTIR spectroscopy, UV-spectroscopy, elemental analysis (C, H, N, & S), thermal studies and scanning electron microscopy (SEM). Flocculation efficacy of the synthesized graft copolymers was studied in 0.25% kaolin and 1% coal fine suspension, through 'jar test' procedure. Further, flocculation efficacy of the best grade, coagulant (alum) and agar were studied for possible application in remediation of metals from river water.
Subject(s)
Agar/chemistry , Methacrylates/chemistry , Agar/chemical synthesis , Agar/ultrastructure , Biocompatible Materials/chemical synthesis , Biocompatible Materials/chemistry , Materials Testing , Microwaves , Molecular Structure , Spectroscopy, Fourier Transform Infrared , ViscosityABSTRACT
There has been a considerable interest in recent years in developing polymer gel matrices for many important applications such as 2DE for quantization and separation of a variety of proteins and drug delivery system to control the release of active agents. However, a well-defined knowledge of the ultrastructures of the gels has been elusive. In this study, we report the characterization of two different polymers used in 2DE: Gelatin, a naturally occurring polymer derived from collagen (protein) and agar, a polymer of polysaccharide (sugar) origin. Low-temperature SEM is used to examine the internal structure of these gels in their frozen natural hydrated states. Results of this study show that both polymers have an array of hollow cells that resembles honeycomb structures. While agar pores are almost circular, the corresponding Gaussian curve is very broad exhibiting a range of radii from nearly 370 to 700 nm. Gelatin pores are smaller and more homogeneous reflecting a narrower distribution from nearly 320 to 650 nm. Overall, these ultrastructural findings could be used to correlate with functions of the polymers.
Subject(s)
Agar/chemistry , Cryoelectron Microscopy/methods , Gelatin/chemistry , Agar/ultrastructure , Gelatin/ultrastructure , Microscopy, Electron, Scanning , Particle Size , Polymers/chemistry , PorosityABSTRACT
Agar-based nanocomposite films with different types of nanoclays, such as Cloisite Na+, Cloisite 30B, and Cloisite 20A, were prepared using a solvent casting method, and their tensile, water vapor barrier, and antimicrobial properties were tested. Tensile strength (TS), elongation at break (E), and water vapor permeability (WVP) of control agar film were 29.7±1.7 MPa, 45.3±9.6%, and (2.22±0.19)×10(-9) g·m/m2·s·Pa, respectively. All the film properties tested, including transmittance, tensile properties, WVP, and X-ray diffraction patterns, indicated that Cloisite Na+ was the most compatible with agar matrix. TS of the nanocomposite films prepared with 5% Cloisite Na+ increased by 18%, while WVP of the nanocomposite films decreased by 24% through nanoclay compounding. Among the agar/clay nanocomposite films tested, only agar/Cloisite 30B nanocomposite film showed a bacteriostatic function against Listeria monocytogenes.
Subject(s)
Agar/chemistry , Aluminum Silicates/chemistry , Food Packaging , Nanocomposites/chemistry , Agar/metabolism , Agar/ultrastructure , Aluminum Silicates/metabolism , Aluminum Silicates/pharmacology , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bentonite/chemistry , Bentonite/metabolism , Bentonite/pharmacology , Chemical Phenomena , Clay , Color , Listeria monocytogenes/drug effects , Mechanical Phenomena , Metal Nanoparticles/chemistry , Metal Nanoparticles/ultrastructure , Microscopy, Atomic Force , Microscopy, Electron, Scanning , Nanocomposites/ultrastructure , Permeability , Steam , Surface Properties , Tensile Strength , Water/chemistry , X-Ray DiffractionABSTRACT
PURPOSE: To study at the ultrastructural level which part of the skin is associated with percutaneous iodide transport by passive diffusion and iontophoresis. METHODS: Following passive diffusion or iontophoresis of iodide, the morphology and the ion distribution of the skin was preserved by rapid freezing. The skin was kept frozen until and during examination by transmission electron microscopy (TEM) and X-ray microanalysis (XRMA). The intrinsic electron absorbing characteristics of cryopreserved skin allow direct TEM examination without additional staining. XRMA can be used to obtain in a relatively nondestructive way in situ information on ion distributions across the skin. RESULTS: After passive diffusion, iodide was mainly found in the stratum corneum (SC), whereas there was little iodide in the viable epidermis. Iontophoresis up to 300 microA/cm2 did not significantly affect this distribution. With iontophoresis at 1,000 microA/cm2, the amount of iodide increased dramatically and was equally distributed over the SC and viable epidermis. The presence of iodide in the SC suggests that iodide is present inside corneocytes. CONCLUSIONS: Iontophoresis up to 300 microA/cm2 does not significantly perturb skin structures in contrast to iontophoresis at 1,000 microA/cm2. The presence of iodide inside corneocytes suggests the possibility of transcellular percutaneous iodide transport.