Search results for "Spheres"

showing 10 items of 329 documents

Immobilization and controlled release of prostaglandin E2 from poly-L-lactide-co-glycolide microspheres.

2009

Prostaglandin E(2) (PGE(2)) is an arachidonic acid metabolite involved in physiological homeostasis and numerous pathophysiological conditions. Furthermore, it has been demonstrated that prostaglandins have a stimulating effect not only on angiogenesis in situ and in vitro but also on chondrocyte proliferation in vitro. Thus, PGE(2) represents an interesting signaling molecule for various tissue engineering strategies. However, under physiological conditions, PGE(2) has a half-life time of only 10 min, which limits its use in biomedical applications. In the present study, we investigated if the incorporation of PGE(2) into biodegradable poly-L-lactide-co-glycolide microspheres results in a …

Materials scienceMetabolitemedicine.medical_treatmentKineticsBiomedical EngineeringProstaglandinDinoprostoneBiomaterialschemistry.chemical_compoundmedicineProstaglandin E2Particle SizePolyglactin 910ChromatographyMetals and AlloysControlled releaseIn vitroMicrospheresKineticschemistryBiochemistryDelayed-Action PreparationsCeramics and Compositeslipids (amino acids peptides and proteins)Arachidonic acidProstaglandin Emedicine.drugJournal of biomedical materials research. Part A
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Crystallization in suspensions of hard spheres: a Monte Carlo and molecular dynamics simulation study

2011

The crystallization of a metastable melt is one of the most important non-equilibrium phenomena in condensed matter physics, and hard sphere colloidal model systems have been used for several decades to investigate this process by experimental observation and computer simulation. Nevertheless, there is still an unexplained discrepancy between the simulation data and experimental nucleation rate densities. In this paper we examine the nucleation process in hard spheres using molecular dynamics and Monte Carlo simulation. We show that the crystallization process is mediated by precursors of low orientational bond-order and that our simulation data fairly match the experimental data sets.

Materials scienceMonte Carlo method: Physics [G04] [Physical chemical mathematical & earth Sciences]NucleationFOS: Physical sciencesMolecular Dynamics SimulationCondensed Matter - Soft Condensed Matterlaw.inventionMolecular dynamicsSuspensionslawMetastabilityComputer SimulationGeneral Materials ScienceParticle SizeCrystallizationCondensed Matter - Statistical MechanicsStatistical Mechanics (cond-mat.stat-mech)Hard spheresCondensed Matter Physics: Physique [G04] [Physique chimie mathématiques & sciences de la terre]Chemical physicsScientific methodSoft Condensed Matter (cond-mat.soft)ThermodynamicsSPHERESCrystallizationMonte Carlo MethodJournal of Physics: Condensed Matter
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Hard sphere fluids at a soft repulsive wall: A comparative study using Monte Carlo and density functional methods

2011

Hard-sphere fluids confined between parallel plates at a distance D apart are studied for a wide range of packing fractions including also the onset of crystallization, applying Monte Carlo simulation techniques and density functional theory. The walls repel the hard spheres (of diameter σ) with a Weeks-Chandler-Andersen (WCA) potential V(WCA)(z) = 4ε[(σ(w)/z)(12) - (σ(w)/z)(6) + 1/4], with range σ(w) = σ/2. We vary the strength ε over a wide range and the case of simple hard walls is also treated for comparison. By the variation of ε one can change both the surface excess packing fraction and the wall-fluid (γ(wf)) and wall-crystal (γ(wc)) surface free energies. Several different methods t…

Materials scienceMonte Carlo methodGeneral Physics and AstronomyHard spheresAtomic packing factorMolecular physicsSurface energylaw.inventionSurface tensionCrystallawDensity functional theoryPhysical and Theoretical ChemistryCrystallizationThe Journal of Chemical Physics
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Cylindrical morphologies in asymmetric ABC triblock copolymers

1997

In asymmetric ABC triblock copolymers with C being the matrix-forming majority component, the formation of cylindrical morphologies is governed by the sum of the volume fractions of the components A and B (Φ A + Φ B ) as well as by their ratio (Φ B /Φ A ). The paper describes the morphologies of various polystyrene-block-polybutadiene-block-poly(methyl methacrylate) (SBM) and polystyrene-block-poly(ethylene-co-butylene)-block-poly(methyl methacrylate) block copolymers (SEBM) in dependence on these parameters. In addition to previously reported cylinder in cylinder (c i c, core shell) and helical (hel) morphologies, new microphase separated structures as cylinders at cylinder (c a c), undula…

Materials scienceMorphology (linguistics)Polymers and PlasticsOrganic ChemistryCondensed Matter PhysicsCore shellchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerCylinderSPHERESPhysical and Theoretical ChemistryMethyl methacrylateMacromolecular Chemistry and Physics
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Nucleation in suspensions of anisotropic colloids

2005

We report Monte Carlo studies of liquid crystal nucleation in two types of anisotropic colloidal systems: hard rods and hard ellipsoids. In both cases we find that nucleation pathways differ strongly from the pathways in systems of spherical particles. Short hard rods show an effect of self-poisoning. This part of the article is based on a previous publication [T. Schilling, D. Frenkel, Self-poisoning of crystal nuclei in hard-rod liquids, Phys. Rev. Lett. 92 (2004) 085505]. When a crystallite forms, its surfaces are covered preferentially by rods which align perpendicular to the surface. Therefore subsequent growth is stunted. Hard, almost spherical ellipsoids can be compressed to very hig…

Materials scienceNucleationGeneral Physics and AstronomyHard spheresScheikundeRodReaction coordinateCrystalHardware and ArchitectureChemical physicsLiquid crystalStatistical physicsCrystallitesense organsAnisotropyComputer Physics Communications
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Heterogeneous and homogeneous crystal nucleation in colloidal hard-sphere like microgels at low metastabilities

2011

We studied the crystallization kinetics of the homogeneous bulk as well as of the heterogeneous wall crystallization in a colloidal hard sphere model system within the fluid crystal coexistence region. Using time resolved static light scattering and Bragg microscopy we determined several parameters characterizing the crystallization process (induction times, growth coefficients, nucleation rate densities,…). By performing further analysis according to classical nucleation theory we can show that wall crystallization is favored by a vanishing nucleation barrier height leading to the conclusion that a hard sphere crystal completely wets a structureless hard wall.

Materials scienceNucleationPhysics::OpticsCrystal growthGeneral ChemistryHard spheresCondensed Matter Physicslaw.inventionCrystalColloidCrystallographylawChemical physicsStatic light scatteringClassical nucleation theoryCrystallizationSoft Matter
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Crystallization kinetics of colloidal binary mixtures with depletion attraction.

2014

In this work the crystallization kinetics of colloidal binary mixtures with attractive interaction potential (Asakura–Oosawa) has been addressed. Parameters such as fraction of crystals, linear crystal dimension and crystal packing have been quantified in order to understand how the crystal formation is driven in terms of the depth of the attractive potential and the composition of the binary mixture (described by the number ratio). It was found that inside the eutectic triangle, crystallization is mainly governed by nucleation and the crystal packing is close to the close-packing of hard spheres. Moving out from the eutectic triangle towards small component results in the crystallization o…

Materials scienceNucleationPhysics::OpticsGeneral ChemistryHard spheresCondensed Matter Physicslaw.inventionCondensed Matter::Soft Condensed MatterCrystalchemistry.chemical_compoundCrystallographyColloidchemistryChemical physicslawCondensed Matter::SuperconductivityStatic light scatteringPolystyreneCrystallizationEutectic systemSoft matter
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Solidification of a colloidal hard sphere like model system approaching and crossing the glass transition

2014

We investigated the process of vitrification and crystallization in a model system of colloidal hard spheres. The kinetics of the solidification process was measured using time resolved static light scattering, while the time evolution of the dynamic properties was determined using time resolved dynamic light scattering. By performing further analysis we confirm that solidification of hard sphere colloids is mediated by precursors. Analyzing the dynamic properties we can show that the long time dynamics and thus the shear rigidity of the metastable melt is highly correlated with the number density of solid clusters (precursors) nucleated. In crystallization these objects convert into highly…

Materials scienceNumber densityNucleationGeneral ChemistryHard spheresCondensed Matter Physicslaw.inventionCondensed Matter::Soft Condensed MatterCrystallographyDynamic light scatteringChemical physicslawMetastabilityStatic light scatteringCrystallizationGlass transitionSoft Matter
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Amoxicillin-loaded polyethylcyanoacrylate nanoparticles: influence of PEG coating on the particle size, drug release rate and phagocytic uptake.

2001

Polyethyleneglycol (PEG)-coated polyethylcyanoacrylate (PECA) nanoparticles loaded with amoxicillin were prepared and the influence of the PEG coating on the particle size, zeta potential, drug release rate and phagocytic uptake by murine macrophages was studied. Experimental results show that this colloidal drug delivery system could be useful for intravenous or oral administration. The profile of amoxicillin release from PECA nanoparticles system was studied under various conditions similar to those of some corporeal fluids. In all these experiments, amoxicillin release in the free form was studied by HPLC analysis. Experimental results showed that at pH 7.4 drug release rises when molecu…

Materials sciencePhagocytosisBiophysicsNanoparticleBioengineeringBiocompatible MaterialsIn Vitro TechniquesPolyethylene GlycolsBiomaterialsMiceDrug Delivery SystemsDrug StabilityPhagocytosisOral administrationPEG ratioZeta potentialAnimalsHumansCyanoacrylatesParticle SizeChromatographyMacrophagesAmoxicillinHydrogen-Ion ConcentrationUreaseMicrospheresBioavailabilityBiochemistryMechanics of MaterialsDrug deliveryCeramics and CompositesParticle sizeBiomaterials
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Polymeric nanospheres as strategy to increase the amount of triclosan retained in the skin: passive diffusion vs. iontophoresis

2012

The aim of this study was to evaluate the passive and iontophoretic permeation of triclosan in human skin using a triclosan solution and triclosan-loaded cationic nanospheres in order to determine which of the two strategies is more effective in allowing the deposition of triclosan within the skin. Triclosan-loaded nanospheres were prepared by the emulsification-solvent displacement technique using aminoalkyl methacrylate (Eudragit® RL 100) as polymer matrix. Nanospheres of 261.0 ± 15.1 nm with a positive surface charge (Ψz = 26.0 ± 3.2 mV) were obtained. Drug loading was 62.0 ± 1.7%. Results demonstrated that the amount of triclosan retained within the skin was significantly greater (8.5-f…

Materials sciencePharmaceutical ScienceBioengineeringHuman skinMethacrylateDiffusionchemistry.chemical_compoundColloid and Surface ChemistryParticle SizePhysical and Theoretical ChemistrySolubilityChromatography High Pressure LiquidSkinChromatographyIontophoresisOrganic ChemistryCationic polymerizationIontophoresisPermeationControlled releaseTriclosanTriclosanSolubilitychemistryMicroscopy Electron ScanningNanospheresJournal of Microencapsulation
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