Search results for "quantitative"

showing 10 items of 2409 documents

Characterization of the Cyclodextrin−Surfactant Interactions by Volume and Enthalpy

2003

Volume and enthalpy of transfer of hydroxypropyl-α-cyclodextrin (HP-α-CD) and hydroxypropyl-γ-cyclodextrin (HP-γ-CD) from water to the aqueous solutions of sodium alkanoates (sodium hexanoate, sodium decanoate and sodium dodecanoate) were determined at 298 K. The cyclodextrin concentration was kept constant, and that of the surfactant was varied in order to analyze both the pre- and postmicellar regions. The experimental data in the premicellar region were consistent with the formation of 1:1 and 1:2 (1 cyclodextrin:2 surfactants) inclusion complexes, with the exception of the HP-α-CD/sodium dodecanoate system which presented only the 1:1 complexes. The mechanism of the 1:2 complexes format…

chemistry.chemical_classificationAqueous solutionCyclodextrinChemistrySodiumEnthalpyInorganic chemistrychemistry.chemical_elementSodium decanoateSurfaces Coatings and Filmschemistry.chemical_compoundPulmonary surfactantMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryQuantitative analysis (chemistry)The Journal of Physical Chemistry B
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Simulation and theory of fluid demixing and interfacial tension of mixtures of colloids and nonideal polymers.

2005

An extension of the Asakura-Oosawa-Vrij model of hard sphere colloids and non-adsorbing polymers, that takes polymer non-ideality into account through a repulsive stepfunction pair potential between polymers, is studied with grand canonical Monte Carlo simulations and density functional theory. Simulation results validate previous theoretical findings for the shift of the bulk fluid demixing binodal upon increasing strength of polymer-polymer repulsion, promoting the tendency to mix. For increasing strength of the polymer-polymer repulsion, simulation and theory consistently predict the interfacial tension of the free colloidal liquid-gas interface to decrease significantly for fixed colloi…

chemistry.chemical_classificationBinodalQuantitative Biology::BiomoleculesMaterials scienceThermodynamicsFOS: Physical sciencesPolymerCondensed Matter - Soft Condensed MatterAtomic packing factorSurface tensionCondensed Matter::Soft Condensed MatterColloidchemistrySoft Condensed Matter (cond-mat.soft)Density functional theoryPair potentialGrand canonical monte carloPhysical review. E, Statistical, nonlinear, and soft matter physics
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Surface anchoring on liquid crystalline polymer brushes

2002

We present a Monte Carlo study of the surface anchoring of a nematic fluid on swollen layers of grafted liquid crystalline chain molecules. The liquid crystalline particles are modeled by soft repulsive ellipsoids, and the chains are made of the same particles. An appropriately modified version of the configurational bias Monte Carlo algorithm is introduced, which removes and redistributes chain bonds rather than whole monomers. With this algorithm, a wide range of grafting densities could be studied. The substrate is chosen such that it favors a planar orientation (parallel to the surface). Depending on the grafting density, we find three anchoring regimes: planar, tilted, and perpendicula…

chemistry.chemical_classificationCondensed Matter - Materials ScienceQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyAnchoringPolymerSubstrate (electronics)Condensed Matter - Soft Condensed MatterCondensed Matter::Soft Condensed MatterPlanarchemistryHardware and ArchitectureLiquid crystalChemical physicsPerpendicularSoft Condensed Matter (cond-mat.soft)Monte Carlo algorithmComputer Physics Communications
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Studying the role of protein dynamics in an SN2 enzyme reaction using free-energy surfaces and solvent coordinates

2013

Conformational changes are known to be able to drive an enzyme through its catalytic cycle, allowing, for example, substrate binding or product release. However, the influence of protein motions on the chemical step is a controversial issue. One proposal is that the simple equilibrium fluctuations incorporated into transition-state theory are insufficient to account for the catalytic effect of enzymes and that protein motions should be treated dynamically. Here, we propose the use of free-energy surfaces, obtained as a function of both a chemical coordinate and an environmental coordinate, as an efficient way to elucidate the role of protein structure and motions during the reaction. We sho…

chemistry.chemical_classificationFlexibility (engineering)Quantitative Biology::BiomoleculesChemistryQuantitative Biology::Molecular NetworksGeneral Chemical EngineeringProtein dynamicsProteinsGeneral ChemistryCatalysisQuantitative Biology::Subcellular ProcessesSolventCrystallographyEnzymeChemical physicsSolventsThermodynamicsSN2 reactionProteïnesEnergy (signal processing)
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Determination of Plasma Lipid Hydroperoxides by an NADPH/NADP + Coupled Enzyme Reaction System. Evaluation of a Method

1998

Summary: Several techniques based on different principles have been proposed to measure lipid hydroperoxides. Enzymatic methods are sensitive and can be quite specific but they are subject to interference by inhibitors and not all are stoichiometric. The present work proposes some modifications of the Heath & Tappel (Anal Biochem 1976; 7:184—91) enzymatic method of determination of lipid hydroperoxides in order to standardize and automate it and to meet the analytical criteria required for a biological assay. The proposed new protocol and the automated assay give acceptable within-run and between-run precisions, with coefficients of variation of 3.34% and 5.80%, respectively, at the usual p…

chemistry.chemical_classificationGlutathione PeroxidaseLipid PeroxidesChromatographyChemistryBiochemistry (medical)Clinical BiochemistryReproducibility of ResultsSystem evaluationGeneral MedicineBiological fluidAutomationKineticsGlutathione ReductaseInvestigation methodsEnzymeBiochemistrySpectrophotometryNadph nadpPlasma lipidsHumansQuantitative analysis (chemistry)NADPcclm
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Quantitative analysis of broad molecular weight distributions obtained by matrix-assisted laser desorption ionisation-time-of-flight mass spectrometry

1996

In order to quantify the error of matrix-assisted laser desorption ionisation (MALDI) time-of-flight (TOF) mass spectrometry in the determination of broad molecular weight distributions, different mixtures by weight of two poly(methyl methacrylate) standards were prepared. These mixtures, with well-defined bimodal molecular weight distributions were analysed by MALDI-TOF mass spectrometry using different matrices (2,4,6-trihydroxyacetophenone and 2,5-dihydroxybenzoic acid) and different cations (Li+, Na+, K+, Rb+ and Cs+) for doping the analyte. From the MALDI-TOF mass spectrometric data, the weight fractions of the two polymers of all mixtures were determined and compared to the values mea…

chemistry.chemical_classificationMALDI imagingChemistryDesorptionAnalytical chemistryPolymerTime-of-flight mass spectrometryMass spectrometryQuantitative analysis (chemistry)Capillary electrophoresis–mass spectrometrySpectroscopySurface-enhanced laser desorption/ionizationEuropean Journal of Mass Spectrometry
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Calculation of the Phase Behavior of Lipids

1998

The self-assembly of monoacyl lipids in solution is studied employing a model in which the lipid's hydrocarbon tail is described within the Rotational Isomeric State framework and is attached to a simple hydrophilic head. Mean-field theory is employed, and the necessary partition function of a single lipid is obtained via a partial enumeration over a large sample of molecular conformations. The influence of the lipid architecture on the transition between the lamellar and inverted-hexagonal phases is calculated, and qualitative agreement with experiment is found.

chemistry.chemical_classificationPartition function (quantum field theory)Quantitative Biology::BiomoleculesStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsChemistryFOS: Physical sciencesThermodynamics02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular conformationLarge sampleQuantitative Biology::Subcellular ProcessesCondensed Matter::Soft Condensed MatterHydrocarbonPhase (matter)0103 physical sciencesLamellar structurelipids (amino acids peptides and proteins)Lipid bilayer phase behavior0210 nano-technologyCondensed Matter - Statistical Mechanics
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Influence of polymer flexibility on nanoparticle dynamics in semidilute solutions

2018

The hierarchical structure and dynamics of polymer solutions control the transport of nanoparticles (NPs) through them. Here, we perform multi-particle collision dynamics simulations of solutions of semiflexible polymer chains with tunable persistence length lp to investigate the effect of chain stiffness on NP transport. The NPs exhibit two distinct dynamical regimes - subdiffusion on short time scales and diffusion on long time scales. The long-time NP diffusivities are compared with predictions from the Stokes-Einstein relation (SER), mode-coupling theory (MCT), and a recent polymer coupling theory (PCT). Increasing deviations from the SER as the polymer chains become more rigid (i.e. as…

chemistry.chemical_classificationPersistence lengthCouplingQuantitative Biology::BiomoleculesFlexibility (anatomy)Materials scienceDiffusionStiffnessNanoparticle02 engineering and technologyGeneral ChemistryVolume viscosityPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesCondensed Matter::Soft Condensed Mattermedicine.anatomical_structurechemistryChemical physicsmedicinemedicine.symptom0210 nano-technologySoft Matter
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Standard Definitions of Persistence Length Do Not Describe the Local “Intrinsic” Stiffness of Real Polymer Chains

2010

On the basis of extensive Monte Carlo simulations of lattice models for linear chains under good and Θ solvents conditions, and for bottle-brush polymers under good solvent conditions, different me...

chemistry.chemical_classificationPersistence lengthPhysics::Biological PhysicsQuantitative Biology::BiomoleculesPolymers and PlasticsOrganic ChemistryMonte Carlo methodStiffnessPolymerCondensed Matter::Soft Condensed MatterInorganic ChemistrychemistryLattice (order)Materials ChemistrymedicineStatistical physicsPhysics::Chemical Physicsmedicine.symptomWorm-like chainMacromolecules
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Structure of bottle brush polymers on surfaces: weak versus strong adsorption.

2011

Large-scale Monte Carlo simulations are presented for a coarse-grained model of cylindrical molecular brushes adsorbed on a flat structureless substrate, varying both the chain length N of the side chains and the backbone chain length N(b). For the case of good solvent conditions, both the cases of weak adsorption (only 10 to 15% of the monomers being bound to the surface) and strong adsorption (~40% of the monomers being bound to the surface, forcing the bottle brush into an almost 2D conformation) are studied. We focus on the scaling of the total linear dimensions of the cylindrical brush with both chain lengths N and N(b), demonstrating a crossover from rod-like behavior (for not very la…

chemistry.chemical_classificationPersistence lengthQuantitative Biology::BiomoleculesChemistryMonte Carlo methodBrushBackbone chainPolymerSurfaces Coatings and Filmslaw.inventionCondensed Matter::Soft Condensed Matterchemistry.chemical_compoundAdsorptionChemical physicslawPolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryScalingThe journal of physical chemistry. B
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