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Ionic Polymers (ionic + polymer)
Selected AbstractsThermogravimetric investigation of the hydration behaviour of hydrophilic matricesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 4 2010Lorena Segale Abstract This article proposes thermogravimetric analysis (TGA) as a useful method to investigate the hydration behaviour of hydrophilic matrix tablets containing hydroxypropylmethylcellulose (HPMC), sodium carboxymethylcellulose (NaCMC) or a mixture of these two polymers and four drugs with different solubility. The hydration behaviour of matrix systems was studied as a function of the formulation composition and of the dissolution medium pH. TGA results suggest that the hydration of matrices containing HPMC is pH-independent and not affected by the characteristics of the loaded drug; this confirms HPMC as a good polymer to formulate controlled drug delivery systems. On the other hand, the performances of NaCMC matrix tablets are significantly affected by the medium pH and the hydration and swelling of this ionic polymer is influenced by the loaded drug. For systems containing the two polymers, HPMC plays a dominant role in the hydration/dissolution process at acidic pH, while at near neutral pH both the cellulose derivatives exert a significant influence on the hydration performance of systems. The results of this work show that TGA is able to give quantitative highlights on the hydration behaviour of polymeric materials; thus this technique could be a helpful tool to support conventional hydration/swelling/dissolution studies. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 2070,2079, 2010 [source] Recent progress in the use of soluble ionic polymers as pseudostationary phases for electrokinetic chromatographyELECTROPHORESIS, Issue 23-24 2004Christopher P. Palmer Abstract This review concerns the development, characterization, and application of soluble ionic polymeric materials as pseudostationary phases for electrokinetic chromatography since 2002. Cationic polymers, anionic siloxanes, polymerized surfactants (micelle polymers), and chiral polymers are considered. The use of stable suspensions of polymer nanoparticles in electrokinetic chromatography is also reviewed. [source] Proton Transfer on the Molecular Surface of Proteins and Model SystemsISRAEL JOURNAL OF CHEMISTRY, Issue 2 2009Ran Friedman Proton transfer (PT) reactions take place on the molecular surface of proteins, membranes, ionic polymers, and other molecules. The rates of the reactions can be followed experimentally, while the atomistic details can be elucidated by molecular modeling. This manuscript gives a brief overview of the use of computer simulations and molecular modeling, in conjuction with experiments, to study PT reactions on the surface of solvated molecules. An integrative approach is discussed, where molecular dynamics simulations are performed with a protein, and quantum-mechanics-based calculations are performed on a small molecule. The simulation results allow the identification of the necessary conditions that yield PT reactions on the molecular surface. The reactions are efficient when they involve a donor and acceptor located a few Å apart and under the influence of a negative electrostatic field. In proton-pumping proteins, it is possible to identify such conditions a priori and locate proton-attracting antenna domains without the need to mutate each potential donor and acceptor. Based on density functional theory calculations, the arrangement of water molecules that interconnect the donor and acceptor moieties is suggested as the rate-limiting step for proton transfer on the molecular surface. [source] Characterization of the interactions between polymethacrylate-based aqueous polymeric dispersions and aluminum lakesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 12 2001Nasser Nyamweya Abstract Instability in film coating formulations can arise from interactions between aluminum lake pigments and aqueous polymeric dispersions. The purpose of this study was to characterize the interactions between three polymethacrylate-based aqueous polymeric dispersions (Eudragit® RS 30 D, Eudragit® L 30 D-55, and Eudragit® NE 30 D) and aluminum lakes. Particle size measurements, pH stability profiles, zeta potential measurements, and microscopy were used to study mixed dispersions of the polymeric latices and the lakes. Interactions leading to dispersion instability were related to the surface charge of the components in the formulation. Interactions between the ionic polymers and the lakes arose from instability of the lakes outside a certain pH range resulting in the release of electrolytes, which led to aggregation of the polymeric particles. Interactions between the nonionic polymer and the lakes were related to the polymer modifying the surface charge of the lakes, resulting in aggregation of the pigment particles. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:1937,1947, 2001 [source] Patterned Co-Culture of Primary Hepatocytes and Fibroblasts Using Polyelectrolyte Multilayer TemplatesMACROMOLECULAR BIOSCIENCE, Issue 3 2007Srivatsan Kidambi Abstract This paper describes the formation of patterned cell co-cultures using the layer-by-layer deposition of synthetic ionic polymers and without the aid of adhesive proteins/ligands such as collagen or fibronectin. In this study, we used synthetic polymers, namely poly(diallyldimethylammonium chloride) (PDAC) and sulfonated polystyrene (SPS) as the polycation and polyanion, respectively, to build the multilayer films. We formed SPS patterns on polyelectrolyte multilayer (PEM) surfaces either by microcontact printing PDAC onto SPS surfaces or vice-versa. To create patterned co-cultures on PEMs, we capitalize on the preferential attachment and spreading of primary hepatocytes on SPS as opposed to PDAC surfaces. In contrast, fibroblasts readily attached to both PDAC and SPS surfaces, and as a result, we were able to obtain patterned co-cultures of fibroblast and primary hepatocytes on synthetic PEM surfaces. We characterized the morphology and hepatic-specific functions of the patterned cell co-cultures with microscopy and biochemical assays. Our results suggest an alternative approach to fabricating controlled co-cultures with specified cell,cell and cell,surface interactions; this approach provides flexibility in designing cell-specific surfaces for tissue engineering applications. [source] Multilayer Thin Films by Layer-by-Layer Assembly of Hole- and Electron-Transport Polyelectrolytes: Optical and Electrochemical PropertiesMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 20 2006Kyungsun Choi Abstract Summary: In this paper, we present the synthesis of a series of p-type and n-type semiconducting polyelectrolytes with triarylamine, oxadiazole, thiadiazole and triazine moieties. The synthesized polymeric hole and electron transport materials were examined optically and electrochemically using UV/Vis spectroscopy, PL spectroscopy and CV. Based on the optical and electrochemical data, each of the energy levels were calculated and all values suggested that they were promising hole- (p-type) or electron-transport (n-type) materials for devices. Moreover, the synthesized ionic polymers were suitable for LBL thin film deposition from dilute polymer solutions and the multilayers were fully characterized by UV/Vis, PL spectroscopy and CV. [source] Ionic polymer-metal composites as multifunctional materialsPOLYMER COMPOSITES, Issue 1 2003Mohsen Shahinpoor This paper presents a description and a set of experimental results on Ionic Polymer-Metal Composites (IPMC's) as dynamic sensors, transducers, and actuators. Strips of IPMC can exhibit large dynamic deformation if placed in a time-varying electric field of the order of 10's of volts/mm. Conversely, dynamic deformation and flexing of such ionic polymers produces dynamic electric fields that closely follow the form of the electric signal. The underlying principle of such a mechanoelectric effect in IPMC's can be explained by the linear irreversible thermodynamics in which ion and solvent transport are the fluxes and electric field and solvent pressure gradient are the forces. Important parameters include the material conductance and the solvent permeability. The dynamic sensing, transduction, and actuation responses of a strip of IPMC under an impact-type loading is also discussed. When a cantilever strip of IPMC is flipped, a damped oscillatory electric response is produced across a pair of electrodes placed at the cantilever of the strip, which is highly repeatable with a broad frequency range above 104 Hz. Such direct mechanoelectric responses of IMPC's are related to the endo-ionic mobility due to stresses imposed. Imposition of a finite solvent flux without allowing a current flux causes the material to create a certain conjugate electric field that can be dynamically monitored and measured. IPMC's are shown to be highly capacitive at low frequencies while they are highly resistive under high frequency excitations. IN a sending mode, IPMC strips can also sense chemical environments and humidity. These types of sensors/transducers/actuators conceivably can replace piezoresistive and piezoelectric sensors with just one sensor for broad ranges of frequencies. [source] | |||||||||||||