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Query: HUMANGGP:003721 (Poly)
 11,742 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Poly(3,4-ethylenedioxy)thiophene-poly(styrene sulfonate) (PEDOT-PSS) was used as the conductive component in a matrix of chemically different insulating polymers to form an array of vapor detectors. Such composites produced larger relative differential resistance responses when exposed to polar analytes than did the corresponding carbon black filled polymer composite detectors. However, the PEDOT-PSS composites produced smaller responses than carbon black composites when exposed to nonpolar analytes. The resolving power of a PEDOT-PSS detector array was compared to that of a carbon black composite array for a broadly construed set of organic vapors. The PEDOT-PSS array exhibited better, on average, discrimination between pairs of polar analytes and polar/nonpolar analytes than did the carbon black composite array. The carbon black composite array out-performed the PEDOT-PSS array in discriminating between nonpolar compounds. The addition of PEDOT-PSS composites to an array of carbon black composite detectors therefore can produce improved overall discrimination in a vapor sensor system when used in tasks to differentiate between of a broad set of analyte vapors.
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PMID:Preparation and properties of vapor detector arrays formed from poly(3,4-ethylenedioxy)thiophene-poly(styrene sulfonate)/insulating polymer composites 1093 85

A self-assembly approach to the preparation of nanocomposite siliceous thin films by using oligosilsesquioxanes as building blocks is presented. Poly(styrene-4-sulfonate), PSS, and octa(3-aminopropyl)silsesquioxane, NSi8, were layer-by-layer (LbL) assembled onto planar substrates and polystyrene (PS) particles, thus forming composite multilayers. We have clarified the binding properties of NSi8 to PSS by examining the pH influence on film buildup by microelectrophoresis (zeta-potential) and quartz crystal microgravimetry (QCM). The regular growth of PSS/NSi8 multilayers on planar supports was confirmed by surface plasmon resonance (SPR) spectroscopy and QCM. By applying the LbL coating procedure to spherical templates, we prepared compact, microporous hollow silica spheres by calcining PS spheres coated with (poly(allylamine hydrochloride) (PAH)/PSS)(2)/(NSi8/PSS)(n) (n varying from 3 to 12), at 750 degrees C, because of sintering of the octameric clusters (NSi8). Hollow spheres derived from coatings with n = 3 drastically altered in size (relative to the template core), depending on the size of the PS particles used. The novelty of this method for the nanofabrication of siliceous films stems from the use of well-defined and discrete building blocks, such as NSi8, leading to homogeneous organic-silica composite films as well as individual siliceous particles of variable size and shape.
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PMID:Oligosilsesquioxanes as versatile building blocks for the preparation of self-assembled thin films. 1209 63

The structural transformation of cytochrome c (cyt c) and its heme-free precursor, apo cyt c, induced by negatively charged sulfonated polystyrene (SPS) with different charge density (degree of sulfonation) and chain length was studied to understand the factors that influence the folding and unfolding of the protein. SPS forms stable transparent nanoparticles in aqueous solution. The hydrophobic association of the backbone chain and phenyl groups is balanced by the electrostatic repulsion of the sulfonate groups on the particle surface. The binding of cyt c to negatively charged SPS particles causes an extensive disruption of the native compact structure of cyt c: the cleavage of Fe-Met80 ligand, about 40% loss of the helical structure, and the disruption of the asymmetry environment of Trp59. On the other hand, SPS particle-bound apo cyt c undergoes a conformational change from the random coil to alpha-helical structure. The folding of apo cyt c in SPS particles was influenced by pH and ionic strength of the solution, SPS concentration, and the degree of sulfonation and chain length of SPS. The folding can reach more than 90% of the alpha-helix content of native cyt c in solution. Poly(sodium 4-styrenesulfonate) (PSS), which is 100% sulfonated polystyrene and cannot form hydrophobic cores in the solution, induces only two-thirds of the alpha-helix content compared with SPS. It appears that the electrostatic interaction between PSS/SPS and apo cyt c induces an early partially folded state of apo cyt c. The hydrophobic interaction between nonpolar residues in apo cyt c and the hydrophobic cores in SPS particles extends the alpha-helical structure of apo cyt c.
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PMID:Structural transformation of cytochrome c and apo cytochrome c induced by sulfonated polystyrene. 1295 97

Poly(4-styrenesulfonate) (PSS) has been used to ionically cross-link (glue together) single Langmuir-Blodgett bilayers derived from 1,2,4,5-tetrakis[N,N-dimethyl-N-(1-hexadecyl)-ammoniummethyl]benzene (2a) and tris(N,N-dimethyl-N-hexadecylammoniummethyl)mesitylene (3). The resulting films are of high quality as judged by He/N2 permeation selectivities of ca. 100. Such selectivity is well in excess of the Knudsen diffusion limit of 2.6 and approaches that which has been found for glued bilayers of 5,11,17,23,29,35-hexakis[(N,N,N-trimethylamonium)-N-methyl-37,38,39,40,41,42-hexakis-n-hexamedecyloxy-calix[6]arene hexachloride (1). The significance of these findings to LB technology, in general, is briefly discussed.
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PMID:Glued Langmuir-Blodgett bilayers from porous versus nonporous surfactants. 1530 54

Poly(diallyldimethylammonium chloride) (PDADMAC) and poly(sodium 4-styrenesulfonate) (PSS) have been consecutively adsorbed onto 1.5-microm charged silica (SiO2) particles. Time-dependent adsorption studies indicate that, due to the strong ionic charge of the dissociated polycation in water, adsorption is complete in less than 30 min. Indications of the maximum adsorption density, changes in surface charge, and stability of the layered particles are demonstrated through adsorption isotherms and electrophoretic mobility (EPM) measurements. Further stability of the PDADMAC layer is demonstrated through multiwashing with ultra pure deionized water. Preliminary desorption studies of the PSS layer also illustrate a stabilized two-layer system. Due to the nature of the electrostatic charges on the surface of the SiO2 core particles and both polyelectrolytes in aqueous media, the use of polyelectrolytes as layering elements serves as a model for the assembly of time-released drug delivery particle systems.
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PMID:Preparation and characterization of polymer composite multilayers on SiO2. 1584 21

Multilayer architectures of polyelectrolytes fabricated by the layer-by-layer technique (LbL) on pretreated polymeric and inorganic substrates were studied by contact angle measurements. Poly(diallyldimethylammonium chloride), PDADMAC, and poly(sodium 4-styrenesulfonate), PSS, were used as polyelectrolytes. Contact angle data were used to calculate the van der Waals and Lewis acid-base components of the surface tension of the investigated surfaces. Knowledge of these quantities provides valuable information on surface composition, coating density, and possible interactions of the surface with other substances. Unusual wetting behavior of PDADMAC layers upon prewetting of the multilayer surfaces was found and described in terms of surface tension changes. A model of polymer chain rearrangement upon wetting was proposed to explain this behavior.
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PMID:Surface thermodynamic properties of polyelectrolyte multilayers. 1584 36

We demonstrate the use of aqueous-based layer-by-layer (LbL) processing and in situ nanoreactor chemistry for creating polyelectrolyte multilayer (PEM) nanocomposites in which the concentration of a nanoparticle species is modulated throughout the depth of the film in a complex way. Using the in situ growth of silver nanoparticles to selectively increase the refractive index of precisely defined regions of the PEM film, we have produced a digitized rugate filter, a special type of dielectric mirror possessing many thin layers that approximate a continuous, periodic refractive index profile. The design of the digital rugate from an initial smooth index profile was aided by a computer, and construction of the device was accomplished entirely by automated means. Poly(allylamine hydrochloride) (PAH) and poly(acrylic acid) (PAA) bilayer regions within the film supported subsequent nanoreactor chemistry and created the high refractive index regions of the film, while PAH and poly(styrenesulfonate) (PSS) bilayer regions remained unmodified and served as the low index regions. Spectroscopic results obtained from the assembled device confirm the presence of a reflection band that grows in amplitude with increasing silver incorporation, reaching a peak reflectance of 75% after five silver loading and exchange cycles. The rugate structure suppresses reflection sidebands, features common to Bragg reflectors and simpler dielectric mirror designs. Cross-sectional TEM reveals nanoscale control of the size and location of silver-containing domains within the PEM film. The ability of this method to control the placement of nanoparticles within PEMs enables the inexpensive, easy production of conformable optical coatings with tunable properties. In addition, these nanocomposite films may have applications in a number of other fields where precise control of effective gradients in physical properties throughout thin films has been shown to affect the overall performance in a desirable way.
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PMID:Creating effective refractive index gradients within polyelectrolyte multilayer films: molecularly assembled rugate filters. 1587 62

Poly(3,4-ethylene dioxythiophene):poly(styrene sulfonic acid) (PEDOT:PSS) films exhibit a complex structure of interconnected conductive PEDOT domains in an insulating PSS matrix that controls their electrical properties. This structure is modified by a water rinse, which removes PSS with negligible PEDOT loss. Upon PSS removal, film thickness is reduced by 35%, conductivity is increased by 50%, and a prominent dielectric relaxation is eliminated. These results suggest that the removed PSS is not associated with PEDOT and that the conductive domain network is not substantially altered by the removal of a significant fraction of insulator. The removal of PSS may benefit organic light emitting diode fabrication by reducing acid attack on indium tin oxide electrodes and lead to more robust performance in switching circuits by extending the working frequency range.
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PMID:Influence of a water rinse on the structure and properties of poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) films. 1628 29

Poly(L-lactide) (PLLA) surface was modified via aminolysis by poly(allylamine hydrochloride) (PAH) at high pH and subsequent electrostatic self-assembly of poly(sodium styrenesulfonate) (PSS) and PAH, and the process was monitored by X-ray photoelectron spectroscopy (XPS) and contact angle measurement. These modified PLLAs were then used as charged substrates for further incorporation of gelatin to improve their cytocompatibility. The amphoteric nature of the gelatin was exploited and the gelatin was adsorbed to the negatively charged PLLA/PSS and positively charged PLLA/PAH at pH=3.4 and 7.4, respectively. XPS and water contact angle data indicated that the gelatin adsorption at pH=3.4 resulted in much higher surface coverage by gelatin than at pH=7.4. All the modified PLLA surfaces became more hydrophilic than the virgin PLLA. Chondrocyte culture was used to test the cell attachment, cell morphology and cell viability on the modified PLLA substrates. The results showed that the PAH and PSS modified PLLA exhibited better cytocompatibility than virgin PLLA, and the incorporation of the gelatin on these modified PLLA substrates further improved their cytocompatibility, with the PLLA/PSS substrate treated with the gelatin at pH=3.4 being the best, exceeding the chondrocyte compatibility of the tissue culture polystyrene.
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PMID:Surface modification of poly(L-lactic acid) to improve its cytocompatibility via assembly of polyelectrolytes and gelatin. 1670 73

Poly (3,4-ethylene dioxythiophene) (PEDOT): Poly (styrene sulfonate) (PSS) has attracted a lot of interest for application in organic electronics due to good stability and high electronic conductivity in its doped state. Indeed, thin layers of PEDOT:PSS was regularly used in light emitting diodes (PLEDs) as hole injection and transportation layer. Here, Doping and dedoping states of PEDOT:PSS were studied by absorbance spectra and Raman spectra. A new absorption band centered at 620 nm was observed on dedoped PEDOT:PSS. Consistently, Raman signals of dedoped PEDOT:PSS are resonantly intensified since the Raman excitation wavelength (633 nm) is set in the enhanced absorption band. So it gives a sensitive way to study the doping and dedoping states of PEDOT:PSS. Furthermore, for the encapsulated polymer light-emitting diodes, Raman spectroscopy is a powerful way to study the polymer layers inside the devices.
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PMID:[Study of poly (3,4-ethylene dioxythiophene) : poly (styrene sulfonate) by in-situ resonance Raman spectroscopy]. 1683 30


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