Search results for "Polystyrene"

showing 10 items of 349 documents

Characterization of cell wall proteins of yeast and hydrophobic mycelial cells of Candida albicans

1991

Cell surface hydrophobicity (CSH) of blastoconidia and blastoconidia bearing germ tubes of Candida albicans ATCC 26555 was monitored by assessing attachment of polystyrene microspheres to the cell surface, and we found that mature hyphae were significantly hydrophobic. Treatment of intact cells with low concentrations of beta-glucanase (Zymolyase 20T) or proteases abolished or significantly reduced attachment of latex beads to hyphae. This effect paralleled an obvious reduction in CSH of the entire cell population, as measured by an aqueous-hydrocarbon biphasic partitioning assay. Analysis of the cell wall material released by Zymolyase and adsorbed on polystyrene microspheres indicated tha…

HydrolasesImmunologyPopulationGerm tubeBiologyMicrobiologyBlastoconidiumFungal ProteinsCell wallCell WallCandida albicansCandida albicanseducationMercaptoethanolLatex beadsFungal proteineducation.field_of_studybiology.organism_classificationMicrospheresYeastMolecular WeightInfectious DiseasesSolubilityBiochemistryPolystyrenesParasitologyAdsorptionResearch ArticleInfection and Immunity
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Construction and characterization of models of hypercrosslinked polystyrene

2012

A simple algorithm involving classical molecular dynamics (MD) simulations is here suggested to build up models of hypercrosslinked polystyrene showing macroporous structure. The algorithm is composed by three consecutive stages: MD simulation of a single polystyrene coil, crosslink formation, and finally relaxation of the structure. The models, which are differentiated by the crosslinker concentration in the initial polystyrene chain, can be characterized by employing tools of the small angle neutron scattering analysis and procedures associated to the crosslinking algorithm, which allows one to discriminate among the different kinds of crosslinks between phenyl rings and to calculate the …

Hypercrosslinked polystyrene crosslinking degree molecular dynamicsMaterials sciencePolymers and PlasticsRelaxation (NMR)Substrate (chemistry)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesSmall-angle neutron scattering0104 chemical sciencesCharacterization (materials science)chemistry.chemical_compoundMolecular dynamicsColloid and Surface ChemistryChemical engineeringchemistryPolymer chemistryMaterials ChemistryPolystyrenePhysical and Theoretical Chemistry0210 nano-technologySIMPLE algorithmMacromoleculeColloid and Polymer Science
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Ion-exchange high-performance liquid chromatography of nucleotides and polypeptides on new types of ion-exchange sorbents, based on polystyrene-coate…

1991

A novel type of ion exchanger was prepared by multipoint covalent binding of polystyrene chains onto the surface of porous silica followed by polymer-analogous modification of the bonded layer. Both anion and cation exchangers were synthesized and examined in the separation of nucleotides and proteins. Rapid and efficient separation of basic polypeptides on strong anion exchangers and that of acidic polypeptides on strong cation exchangers could be achieved. For the separation of complete mixtures of polypeptides the application of zwitter-ionic ion exchangers can be recommended.

Inorganic chemistryCovalent bindingBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryIonchemistry.chemical_compoundAnimalsHumansNucleotidePorosityChromatography High Pressure Liquidchemistry.chemical_classificationChromatographyIon exchangeNucleotidesOrganic ChemistryGeneral MedicineChromatography Ion ExchangeSilicon DioxidechemistryPolystyrenesCattlePolystyreneIon Exchange ResinsPeptidesLayer (electronics)Journal of chromatography
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The calculation of the number-average degree of polymerization starting from intrinsic viscosity and overall rate

1962

The relation between the intrinsic viscosity [η] and the number-average degree of polymerization Pn is a function of the molecular weight distribution of the polymer. In a polymer in which the termination of polymer radicals occurs partly by combination of two growing chains, this molecular weight distribution depends on number and extent of additional reactions such as chain transfer; i.e., it is variable. Therefore Pn of such polymers cannot be obtained from intrinsic viscosity measurements by means of an equation of the type [η] = KPna. A new method is proposed which allows the evaluation of Pn in these cases, without necessity of osmotic (or related) measurements or fractionation. The v…

Kinetic chain lengthchemistry.chemical_classificationchemistry.chemical_compoundchemistryPolymerizationIntrinsic viscosityPolymer chemistryThermodynamicsMolar mass distributionChain transferPolystyrenePolymerDegree of polymerizationJournal of Polymer Science
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Lanthanide molecular oxohydroxides: Synthesis and characterisation of [Y4(μ4-O)(μ-OEt)2(μ,η2-AAA)2(η2-AAA)3]2(μ3-OH)4(μ3-OEt)2 (HAAA = allylacetatoac…

2007

International audience; The reaction between Y5O(OPri)13 and allylacetatoacetate or 2-(methacryloyloxy)ethyl acetatoacetate in 1:5 stoichiometry afforded octanuclear oxohydroxo species. Structural characterization was achieved for the allylacetatoacetate derivative homo and copolymerisation reactions with styrene were evaluated for doping of polystyrene. Hydoxo species, Y4(OH)2(AAA)10, where also obtained by reacting Y[N(SiMe3)]3 and HAAA.

LanthanideInorganic chemistrychemistry.chemical_element02 engineering and technologyAlkoxides010402 general chemistry01 natural sciences"Polymerizable ligands"StyreneInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryYttriumPhysical and Theoretical ChemistryPolymerizable ligands"Alkoxides"Doping"X-ray structure"Yttrium[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnology[SDE.ES]Environmental Sciences/Environmental and Society0104 chemical scienceschemistryPolystyreneX-ray structure0210 nano-technology"Yttrium"Derivative (chemistry)Stoichiometry
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Estimation of the size of liposomes by modified HDC

1991

Internal calibration in modified hydrodynamic chromatography has been realized by the approach of Prieve and Hoysan, i.e. the use of polystyrene monodisperse latexes to evaluate the equivalent capillary radius, R. The value obtained has been used to estimate the average sizes of a variety of liposome samples from egg yolk lecithin.

Liposomefood.ingredientChromatographyGeneral Chemical EngineeringDispersitySize-exclusion chromatographySynthetic membraneAnalytical chemistryLecithinCapillary radiuschemistry.chemical_compoundfoodchemistryembryonic structuresCalibrationPolystyreneJournal of High Resolution Chromatography
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Stationary–mobile phase distribution coefficient for polystyrene standards

2002

The measured shifts of the retention volume V R of polystyrene (PS) towards lower values in benzene–methanol (Bz–MeOH), and towards higher values in butanone–heptane (But–Hep) are in agreement with our theoretical model, in which both MeOH and But are adsorbed on Lichrospher. This paved way for us to model the chromatographic stationary (s)-phase as MeOH and the mobile (m)-phase as Bz–MeOH, and to calculate the distribution coefficients for PS. For But–Hep, the s-phase has been modeled as But, and the m-phase as But–Hep. A linear relation for the experimental equilibrium distribution P sm of PS is shown between the s- and m- phases in Bz–MeOH and But–Hep vs. the logarithm of the molecular m…

LogarithmChemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringAnalytical chemistryFiltration and SeparationGeneral ChemistryPartition coefficientchemistry.chemical_compoundAdsorptionVolume (thermodynamics)Phase (matter)Linear relationPolystyreneSeparation Science and Technology
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Untersuchungen zu den orientierungs- und dichtefluktuationen in amorphen polymeren mit hilfe der lichtstreuung

1976

Es wurden mit einem Lichtstreuphotometer die Orientierungs- und Dichtefluktuationen in den amorphen Polymeren «Polycarbonat» (Poly(oxycarbonyloxy-1,4-phenylenisopropyliden-1,4-phenylen)) und Polystyrol in Abhangigkeit von der Temperatur untersucht. Ferner fuhrten wir erganzende Messungen an Oligomeren des Polystyrols und an der flussig-kristallinen Verbindung 4-Butyl-N-(p-methoxybenzyliden)anilin (MBBA) in der isotropen Phase durch. Aus der Hohe der depolarisierten Lichtstreuung ergab sich, das eine Orientierungskorrelation, wie sie fur einige Bundelmodelle vorgeschlagen wurde, nicht auftritt. Besonders detaillierte Aussagen konnten fur Polystyrol gemacht werden. Die depolarisierte Lichtstr…

MBBAchemistry.chemical_compoundAngular rangeMonomerchemistryPolymer chemistryPolystyreneRandom coilLight scatteringDie Makromolekulare Chemie
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How Low Can You Go? Low Densities of Poly(ethylene glycol) Surfactants Attract Stealth Proteins.

2018

It is now well-established that the surface chemistry and “stealth” surface functionalities such as poly(ethylene glycol) (PEG) chains of nanocarriers play an important role to decrease unspecific protein adsorption of opsonizing proteins, to increase the enrichment of specific stealth proteins, and to prolong the circulation times of the nanocarriers. At the same time, PEG chains are used to provide colloidal stability for the nanoparticles. However, it is not clear how the chain length and density influence the unspecific and specific protein adsorption keeping at the same time the stability of the nanoparticles in a biological environment. Therefore, this study aims at characterizing the…

Magnetic Resonance SpectroscopyPolymers and PlasticsNanoparticleBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene Glycolsnanocarriers; poly(ethylene glycol); protein corona; stealth effect; surfactantsBiomaterialschemistry.chemical_compoundColloidMicePlasmaSurface-Active AgentsAdsorptionPEG ratioMaterials ChemistryAnimalsHumansColloidsChemistrySodium Dodecyl Sulfate021001 nanoscience & nanotechnology0104 chemical sciencesClusterinRAW 264.7 CellsChemical engineeringNanoparticlesPolystyrenesProtein CoronaAdsorptionNanocarriers0210 nano-technologyEthylene glycolBiotechnologyProtein adsorptionMacromolecular bioscience
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Disulfide-crosslinked hyaluronan-gelatin hydrogel films: a covalent mimic of the extracellular matrix for in vitro cell growth

2003

A new disulfide crosslinking method was developed for the preparation of blended hyaluronan (HA)-gelatin hydrogels to form a synthetic, covalently linked mimic of the extracellular matrix (ECM). The HA and gelatin were chemically modified using 3,3′-dithiobis(propionic hydrazide) (DTP). After reduction with dithiothreitol (DTT), the thiol derivatives of HA (HA-DTPH) and gelatin (gelatin-DTPH) were obtained and characterized. To minimize interference with biological function, the degree of substitution of HA-DTPH and gelatin-DTPH was kept below 50%. Solutions of HA-DTPH and gelatin-DTPH in varying blends (20%, 40%, 60%, 80% gelatin) were prepared in 1% w/v NaCl and crosslinked by disulfide b…

Magnetic Resonance SpectroscopyTime FactorsBiocompatible MaterialsSodium ChlorideGelatinHydrogel Polyethylene Glycol DimethacrylateDithiothreitolCell growthMicechemistry.chemical_compoundHyaluronic acidDisulfidesHyaluronic Acidchemistry.chemical_classificationMice Inbred BALB CBiomaterialHydrogels3T3 CellsMethylgalactosidesExtracellular MatrixCross-Linking ReagentsMechanics of MaterialsCovalent bondSelf-healing hydrogelsThiolCell DivisionBiotechnologyfood.ingredientMaterials scienceCell SurvivalBiomedical EngineeringBiophysicsHyaluronoglucosaminidaseBioengineeringmacromolecular substancesIn Vitro TechniquesHydrazideBiomaterialsDisulfidefoodPolymer chemistryCell AdhesionAnimalsSulfhydryl Compoundstechnology industry and agricultureFibroblastsBiomaterialDithiothreitolModels ChemicalchemistryCeramics and CompositesGelatinPolystyrenesBiomaterials
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