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Polyacrylic Acid (polyacrylic + acid)
Selected AbstractsSustained ophthalmic in situ gel of ketorolac tromethamine: rheology and in vivo studiesDRUG DEVELOPMENT RESEARCH, Issue 6 2009A.S. Manjappa Abstract Most ocular diseases are treated with topical eye drops. The poor bioavailability and therapeutic response exhibited by these conventional eye drops due to rapid precorneal elimination of the drug may be overcome by the use of in situ gelling systems that are instilled as drops into the eye and undergo a sol-to-gel transition in the cul-de-sac. The present work describes the formulation and evaluation of an ophthalmic delivery system of the nonsteroidal anti-inflammatory drug (NSAID), ketorolac tromethamine, based on the concept of pH-triggered in situ gelation. Polyacrylic acid (Carbopol® 934) was used as the gelling agent in combination with hydroxypropylmethylcellulose (Methocel E15LV), which acted as a viscosity enhancer. The prepared formulations were characterized for clarity, pH, drug content, rheology, and in vivo drug release. Clarity, pH, and drug content of the developed formulations were found to be satisfactory. The developed formulation showed pseudo-plastic rheology. The formulation with benzalkonium chloride and edetate disodium improved the rate of corneal absorption but not the extent. The developed formulation is a viable alternative to conventional eye drops by virtue of its ability to enhance bioavailability through its longer precorneal residence time and ability to sustain drug release. Also importantly is the ease of instillation afforded and decreased frequency of instillation resulting in better patient acceptance. Drug Dev Res, 2009. © 2009 Wiley-Liss, Inc. [source] Improvement of the Dispersion of Al2O3 Slurries Using EDTA-4NaJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2006Jingxian Zhang Polyacrylic acid (PAA) is known to be an effective dispersant for Al2O3 powder in aqueous media. However, at high solid loading (>55 vol%), the dispersion of the Al2O3 suspensions became difficult with only PAA as a dispersant. In this paper, ethylenediaminetetraacetic acid, tetrasodium salt, dihydrate (EDTA-4Na) was introduced to improve the dispersion of the Al2O3 suspensions. With the aid of EDTA-4Na, the adsorption amount of sodium polyacrylic acid (PAA-Na) increased, while the apparent viscosity of 60 vol% Al2O3 slurries decreased significantly. Particle size measurements showed that EDTA-4Na could help to reduce larger agglomerates, possibly by modifying the adsorbed layer thickness. The interactions between EDTA-4Na and PAA-Na were studied using Fourier-transform infrared spectroscopy analysis. Results showed that it was possible to introduce EDTA-4Na as the second dispersant to improve the dispersion of high solid content Al2O3 slurries. [source] Suitability of Stripping Chronopotentiometry for Heavy Metal Speciation Using Hydrogen Peroxide as Oxidant: Application to the Cd(II)-EDTA-PMA SystemELECTROANALYSIS, Issue 24 2005Núria Serrano Abstract The possibilities of stripping chronopotentiometry (SCP) for heavy metal speciation have been tested in the modality of chemical oxidation using the model systems Cd(II)-polyacrylic acid (PMA), Cd(II)-EDTA and Cd(II)-PMA-EDTA. The use of 0.03% H2O2 as a chemical oxidant provides reliable results from transition times, but peak potentials are dramatically affected by the presence of this reagent. The study suggests that chemical-oxidation SCP can be a technique complementary to other stripping modalities in the study of inert and macromolecular labile metal complexes. [source] Influence of the pulpal components on human dentine permeability in vitroINTERNATIONAL ENDODONTIC JOURNAL, Issue 3 2005P. Puapichartdumrong Abstract Aim, To examine the influence of the retained pulpal components on permeability of human dentine by monitoring drug diffusion. Methodology, Twelve intact dentine discs were prepared from freshly extracted human third molars. The dentine surface on the enamel side was etched with 10% polyacrylic acid for 30 s. The drug diffusion test was carried out before and after removal of the retained pulpal components. Each dentine disc was inserted between two plastic chambers; enamel- and pulpal-side chambers, which were filled with 0.05 mol L,1 naproxen sodium (NA) and phosphate-buffered saline (PBS), respectively. After 10 min, the solution on the pulpal-side chamber was collected to determine the concentration of NA using a spectrophotometer. To remove the retained pulpal components and residual NA, the pulp chamber of each disc was washed out with PBS and placed in an ultrasonic cleaner. After removal of these components and the residual NA, the drug diffusion test was repeated. The inner surface of the pulp chamber was observed using scanning electron microscopy (SEM) before and after the removal of the retained pulpal components. Results, The amount of NA that diffused through dentine into the pulp was significantly higher after the pulp chamber was washed out with PBS (paired t -test, P < 0.05). SEM observation demonstrated the presence of the retained pulpal components, odontoblastic layer and some parts of subodontoblastic zone, covering the surface of predentine. These components were removed after the pulp chamber was washed out with PBS followed by cleaning in an ultrasonic cleaner. Conclusions, The presence of retained pulpal components had a significant influence on drug diffusion through dentine discs. [source] Possibilities of polymer-aided dyeing of cotton fabric with reactive dyes at neutral pHJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2010B. J. Agarwal Abstract Water-soluble polymers have versatile application, viz., water-soluble polyacrylates have been widely used in the reactive dyeing of cellulosic fibers and the related soaping as an important component of the leveling and washing agent. In this article, one such water-soluble polymer, polyacrylic acid has been synthesized, characterized, and applied in conjunction with various types of reactive dyes, namely triazinyl, vinyl sulfone, high exhaustion, and bifunctional reactive dyes, along with crosslinking agents, namely glycerol 1,3-dichlorohydrin and hexamethylene tetramine-hydroquinone, respectively. One of the crosslinking agents (the former one) has been synthesized in the laboratory. Crosslinking agent is necessary to adhere the dye molecule onto the cellulose macromolecule. Different process sequences have been formulated and explored for dyeing purpose. All such dyeings were carried out at neutral pH. The dyed samples were assessed through color strength in terms of K/S values and their fastness properties were assessed by standard methods. All such dyeings were compared with conventional dyed samples. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Synthesis of processible doped polyaniline-polyacrylic acid compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2009Bhavana Gupta Abstract Processible composites of emeraldine salt form of polyaniline (PANI) with polyacrylic acid (PAA) are synthesized and studied for their structural, electrical, mechanical, thermal, and electrochemical properties. The processible conducting composites of various weight percentage from 20 wt % to 90 wt % (of PANI) have been prepared by mixing the PANI and PAA under vigorous stirring and sonication conditions. Self-standing films of electroactive homogeneous composites are obtained by solution casting method. A significant improvement in processibility, crystallinity, and thermal stability is observed in the composites; however, the electrical conductivity decreased remarkably as the percentage of PANI is decreased in the composites. The 60 wt % PANI-PAA composite showed crystalline structural property with orthorhombic crystal system and cell parameters as a = 5.93Å, b = 7.57Å, and c = 10.11Å. The 60 wt % PANI-PAA composite also showed better thermal stability and highest capacitance amongst all the composites and used as an active material for development of electrochemical capacitors (parallel plate assembly). The processible composites based electrochemical capacitors using 0.5 M NaClO4 -Acetonitril electrolyte showed super capacitance with ease in fabrication and cost effectiveness in comparison to other similar materials based capacitors. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Cation exchange finishing of nonwoven polyester with polycarboxylic acids and cyclodextrinsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007L. Ducoroy Abstract We describe a chemical method for the finishing of polyester nonwoven fabrics that aimed to obtain ion exchange textiles. This approach was based on the use of polycarboxylic acids (PCA) and cyclodextrins as carbohydrate compounds and finishing agents, respectively. It was observed that the reaction between these reactants yielded a crosslinked polymer that was physically anchored onto the fibers. This polymer can be considered as a resin issued from the esterification between the COOH groups of the PCA with the OH groups of the carbohydrate. As the esterification reaction was not complete, many free carboxylic groups remained on the surface of the coating polymer. This feature offered the ion exchange properties to the textile support. In this article, we described the pad-dry-cure process and showed the influence of the curing parameters (time and temperature), the nature, and the concentration of the components and the pH of the impregnating bath. The grafting rate (in wt %) and the ion exchange capacity (IEC) were observed in parallel. First, it was observed that the best IEC capacity (that could reach 1 mmol/g) was obtained when an ideal compromise was applied between time and temperature of curing. We also evidenced that IEC depended on the nature and on the concentration of the PCA (chosen among citric acid, 1,2,3,4-butanetetracarboxylic acid, and polyacrylic acid) and on the pH of the impregnating bath. Finally, it was observed that cyclodextrins were more appropriate than starch as finishing coreactants. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3730,3738, 2007 [source] Self-assembly of well-defined amphiphilic polymeric miktoarm stars, dendrons, and dendrimers in water: The effect of architectureJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2009Daria E. Lonsdale Abstract Five polymeric architectures with a systematic increase in architectural complexity were synthesized by "click" reactions from a toolbox of functional linear polymers and small molecule linkers. The amphiphilic architectures ranged from a simple 3-miktoarm star block copolymer to the more complex third generation dendrimer-like block copolymer, consisting of polystyrene (PSTY) and polyacrylic acid (PAA). Micellization of these architectures in water at a pH of 7 under identical ionic strength gave spherical micelles ranging in size from 9 to 30 nm. Subsequent calculations of the PSTY core density, average surface area per PAA arm on the corona-core interface, and the relative stretching of the PAA arms provided insights into the effect of architecture on the self-assembly processes. A particular trend was observed that with increased architectural complexity the hydrodynamic diameter, radius of the core in the dry state and the aggregation number also increased with the exception of the third generation dendrimer. On the basis of these observations, we postulate that thermodynamic factors controlling self-assembly were the entropic penalty of forming PSTY loops in the core counterbalanced by the reduction in repulsive forces through chain stretching. This results in a greater number of aggregating unimers and consequently larger micelle sizes. The junction points within the architecture also play an important role in controlling the self-assembly process. The G3 dendrimer showed results contradictory to the aforementioned trend. We believe that the self-assembly process of this architecture was dominated by the increased attractive forces due to stretching of the PSTY core chains to form a more compact core. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6292,6303, 2009 [source] Humic acid metal cation interaction studied by spectromicroscopy techniques in combination with quantum chemical calculationsJOURNAL OF SYNCHROTRON RADIATION, Issue 2 2010M. Plaschke Humic acids (HA) have a high binding capacity towards traces of toxic metal cations, thus affecting their transport in aquatic systems. Eu(III),HA aggregates are studied by synchrotron-based scanning transmission X-ray microscopy (STXM) at the carbon K -edge and laser scanning luminescence microscopy (LSLM) at the 5D0,7F1,2 fluorescence emission lines. Both methods provide the necessary spatial resolution in the sub-micrometre range to resolve characteristic aggregate morphologies: optically dense zones embedded in a matrix of less dense material in STXM images correspond to areas with increased Eu(III) luminescence yield in the LSLM micrographs. In the C 1s -NEXAFS of metal-loaded polyacrylic acid (PAA), used as a HA model compound, a distinct complexation effect is identified. This effect is similar to trends observed in the dense fraction of HA/metal cation aggregates. The strongest complexation effect is observed for the Zr(IV),HA/PAA system. This effect is confirmed by quantum chemical calculations performed at the ab initio level for model complexes with different metal centres and complex geometries. Without the high spatial resolution of STXM and LSLM and without the combination of molecular modelling with experimental results, the different zones indicating a `pseudo'-phase separation into strong complexing domains and weaker complexing domains of HA would never have been identified. This type of strategy can be used to study metal interaction with other organic material. [source] Orientation-Control Synthesis of KTa0.25Nb0.75O3 NanorodsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 3 2010Yong-Ming Hu Single-crystalline KTa0.25Nb0.75O3 (KTN) nanorods with an orthorhombic perovskite structure were synthesized via a polymer-assisted hydrothermal method. The preferred crystallographic orientation of the nanorods were found to be controllable by using different types of polymers in the process; that is, [001]-oriented KTN were obtained upon the use of polyvinyl alcohol (PVA) and [110]-oriented ones were formed with the use of a combination of polyacrylic acid and PVA. The two types of nanorods showed different properties. The [110]-oriented nanorods exhibited a better photocatalytic decolorization efficiency but very likely a lower thermal conductivity (as indicated by the Raman spectrum measurements) than the [001] nanorods. [source] Controlled Crystallization of Calcite Under Surface Electric Field Due to Polarized Hydroxyapatite CeramicsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2009Norio Wada We examined effects of surface electric fields for the crystallization of calcite on polarized hydroxyapatite ceramics with and without polyacrylic acid (PAA) as soluble additive. Both on negatively and positively charged surfaces without PAA, the only precipitates were rhombohedra calcite crystals with the face of the {10.4} plane favorably oriented parallel to the surfaces. This oriented growth was explained by the nucleation theory in the presence of an external electric field. However, the addition of PAA drastically changed the situation of the calcite crystals, i.e., the crystallites were the hemispheric aggregates of calcite needles with a facetted rhombohedral {10.4} end face and flat island-shaped aggregates of ones with a rough (00.1) end face having a triangular shape. The calcite needles grew along the crystallographic [00.1] axis. This oriented growth was explained by epitaxy on the PAA,Ca2+ complexes adsorbing on the surfaces. The morphology of the PAA,Ca2+ complex assemblies adsorbing on the surfaces before the calcite nucleation was an important factor to control the structure of calcite aggregates formed following. This morphology was controlled by properties of the surface electric field and the spatial distribution of the negatively and positively charged sites in the PAA,Ca2+ complexes. [source] Improvement of the Dispersion of Al2O3 Slurries Using EDTA-4NaJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2006Jingxian Zhang Polyacrylic acid (PAA) is known to be an effective dispersant for Al2O3 powder in aqueous media. However, at high solid loading (>55 vol%), the dispersion of the Al2O3 suspensions became difficult with only PAA as a dispersant. In this paper, ethylenediaminetetraacetic acid, tetrasodium salt, dihydrate (EDTA-4Na) was introduced to improve the dispersion of the Al2O3 suspensions. With the aid of EDTA-4Na, the adsorption amount of sodium polyacrylic acid (PAA-Na) increased, while the apparent viscosity of 60 vol% Al2O3 slurries decreased significantly. Particle size measurements showed that EDTA-4Na could help to reduce larger agglomerates, possibly by modifying the adsorbed layer thickness. The interactions between EDTA-4Na and PAA-Na were studied using Fourier-transform infrared spectroscopy analysis. Results showed that it was possible to introduce EDTA-4Na as the second dispersant to improve the dispersion of high solid content Al2O3 slurries. [source] Enzyme immobilization on ultrafine cellulose fibers via poly(acrylic acid) electrolyte graftsBIOTECHNOLOGY & BIOENGINEERING, Issue 4 2005Hong Chen Abstract Ultrafine cellulose fiber (diameter 200,400 nm) surfaces were grafted with polyacrylic acid (PAA) via either ceric ion initiated polymerization or methacrylation of cellulose with methacrylate chloride (MACl) and subsequent free-radical polymerization of acrylic acid. PAA grafts by ceric ion initiated polymerization increased with increasing reaction time (2,24 h), monomer (0.3,2.4 M), and initiator (1,10 mM) concentrations, and spanned a broad range from 5.5,850%. PAA grafts on the methacrylated cellulose fibers also increased with increasing molar ratios of MACl to cellulosic hydroxyl groups (MACl/OH, 2,6.4) and monomer acrylic acid (AA) to initiator potassium persulfate (KPS) ratios ([AA]/[KPS], 1.5,6), and were in a much narrower range between 12.8% and 29.4%. The adsorption of lipase (at 1 mg/ml lipase and pH 7) and the activity of adsorbed lipase (pH 8.5, 30°C), in both cases decreased with increasing PAA grafts. The highest adsorption and activity of the lipase on the ceric ion initiated grafted fibers were 1.28 g/g PAA and 4.3 U/mg lipase, respectively, at the lowest grafting level of 5.5% PAA, whereas they were 0.33 g/g PAA and 7.1 U/mg lipase, respectively, at 12.8% PAA grafts on the methacrylated and grafted fibers. The properties of the grafted fibers and the absorption behavior and activity of lipase suggest that the PAA grafts are gel-like by ceric-initiated reaction and brush-like by methacrylation and polymerization. The adsorbed lipase on the ceric ion-initiated grafted surface possessed greatly improved organic solvent stability over the crude lipase. The adsorbed lipases exhibited 0.5 and 0.3 of the initial activity in the second and third assay cycles, respectively. © 2004 Wiley Periodicals, Inc. [source] Interactions between Brushlike Polyacrylic Acid Side Chains on a Polyacrylate Backbone in Dioxane,WaterCHEMPHYSCHEM, Issue 2 2005Fengjun Hua Dr. Abstract Densely grafted polyacrylic acids (d-PAAs) with overcrowded PAA side chains on the polyacrylate main chains were synthesized and characterized. Acryloyl poly(tert -butyl acrylate) macromonomer [M-P(tert- BA)] was prepared with a definite chain length (n=29) by atom-transfer radical polymerization (ATRP), then homopolymerization was carried out to produce densely grafted P(tert- BA)s with polyacrylate main chains of two different lengths (m=27 and 161). The two d-PAAs were obtained by hydrolyzing d-P(tert- BA)s in the presence of trifluoroacetic acid (TFA). The d-PAAs exhibit intermolecular and intramolecular hydrogen bonding between the carboxylic groups of PAA side chains in dioxane and pyridine; both were investigated using proton nuclear magnetic resonance (1H NMR) spectroscopy. The intermolecular hydrogen bonding was found to be dependent on polymer concentration, temperature, and water content. The intramolecular association between the PAA side chains was found to produce a contraction of the hydrodynamic volume of the d-PAA. Intermolecular hydrogen bonding produces aggregates, as demonstrated by dynamic light scattering (DLS). The clusters were found to shrink as the overall water concentration decreased, and this effect is tentatively explained by considering the gradient in chemical potential of water inside the clusters in comparison with the solvent phase. [source] | ||||||||||||||||