Search results for "2-Dipalmitoylphosphatidylcholine"

showing 8 items of 18 documents

Membrane fluidity and the surface properties of the lipid bilayer: ESR experiment and computer simulation

2009

Penetration of the liposome membranes formed in the gel phase from DPPC (DPPC liposomes) and in the liquid-crystalline phase from egg yolk lecithin (EYL liposomes) by the TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) and 16 DOXYL (2-ethyl-2-(15-methoxy-oxopentadecyl)-4,4-dimethyl-3-oxazolidinyloxy) spin probes has been investigated. The penetration process was followed by 120 hours at 24(0)C, using the electron spin resonance (ESR) method. The investigation of the kinetics of the TEMPO probe building into the membranes of both types of liposomes revealed differences appearing 30 minutes after the start of the experiment. The number of TEMPO particles built into the EYL liposome membranes beg…

Liposomefood.ingredient12-DipalmitoylphosphatidylcholineMembrane FluiditySurface PropertiesChemistryBilayerLipid BilayersElectron Spin Resonance SpectroscopyAnalytical chemistryPharmaceutical SciencePenetration (firestop)Lecithinlaw.inventionCyclic N-OxidesMembranefoodlawMembrane fluidityComputer SimulationSpin LabelsLipid bilayerElectron paramagnetic resonanceMonte Carlo MethodJournal of Liposome Research
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Influence of different parameters on drug release from hydrogel systems to a biomembrane model. Evaluation by differential scanning calorimetry techn…

2000

A comparative study on the drug release capacity of four water swellable polymeric systems was carried out by differential scanning calorimetry (DSC). The polymeric systems chosen were alpha,beta-polyaspartahydrazide (PAHy) crosslinked by glutaraldehyde (GLU) (PAHy-GLU) or by ethyleneglycoldiglycidylether (EGDGE), (PAHy-EGDGE), polyvinylalcohol (PVA) crosslinked by glutaraldehyde (PVA-GLU) and alpha,beta-poly(N-hydroxyethyl)-DL-aspartamide (PHEA) by gamma irradiation (PHEA-gamma matrices). The degree of crosslinking for PAHy-GLU, PAHy-EGDGE and PVA-GLU samples was about 0.4 and 0.8. These hydrogels were characterized as free of drugs and were loaded with diflunisal (DFN) (approximately 2.5%…

Materials science12-DipalmitoylphosphatidylcholinePolymersBiophysicsDiflunisalBioengineeringBiocompatible Materialsmacromolecular substancesBiomaterialschemistry.chemical_compoundDifferential scanning calorimetryDrug Delivery SystemsPolymer chemistryMaterials TestingmedicinePolyhydroxyethyl MethacrylateLiposomeCalorimetry Differential ScanningEpoxy ResinsVesicletechnology industry and agricultureHydrogelsMembranes ArtificialDiflunisalControlled releaseNylonsCross-Linking ReagentsHydrazineschemistryChemical engineeringMechanics of MaterialsGlutaralDipalmitoylphosphatidylcholineDelayed-Action PreparationsPolyvinyl AlcoholSelf-healing hydrogelsLiposomesCeramics and CompositesGlutaraldehydemedicine.drug
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Effect of cholesterol on the physical properties of pulmonary surfactant films: Atomic force measurements study

2006

International audience; Atomic force measurements were performed on supported pulmonary surfactant (PS) films to address the effect of cholesterol on the physical properties of lung surfactant films. We recently found that cholesterol in excess of a physiological proportion abolishes surfactant function, and is the reason that surfactant fails to lower the surface tension upon compression. In this study, we investigated how the loss of mechanical stability observed earlier is related to the local mechanical properties of the film by local force measurements. The presence of 20% of cholesterol in bovine lipid extract surfactant (BLES) resulted in a decrease of the observed adhesive interacti…

Models Molecular12-DipalmitoylphosphatidylcholineSurface PropertiesFunctional failureLipid BilayersAnalytical chemistryMicroscopy Atomic ForceSurface tensionchemistry.chemical_compoundRigidity (electromagnetism)Pulmonary surfactantAnimalsSurface TensionInstrumentationAtomic force microscopyCholesterolPulmonary SurfactantsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCholesterol[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]chemistryMechanical stabilityPhosphatidylcholinesBiophysicsCattleAdhesiveUltramicroscopy
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Dynamics of surface of lipid membranes: theoretical considerations and the ESR experiment.

2016

The effect of the surface layer of model membranes on their physical properties was discussed in this paper. The research involved a physical ESR experiment with the use of spin probes and computer simulation based on the Monte Carlo technique. Liposomes formed during the process of sonication of lecithin were scanned in an ESR spectrometer. The membrane surface layer model, represented by the system of electric dipoles arranged in rectangular or hexagonal matrices, was studied. The final states of computer simulations were presented as textures. It was found that in the gel phase some ordered domain structures are formed, while in the liquid–crystal phase we got complex textures comprising…

Models MolecularPhase transition12-DipalmitoylphosphatidylcholineSurface PropertiesMonte Carlo methodBiophysicsAnalytical chemistryMolecular Conformation02 engineering and technologyPhase Transition03 medical and health sciencesSonication0302 clinical medicinePhase (matter)Lipid membraneSurface layerMembrane fluidityLipid bilayerMonte Carlo simulationChemistryCell MembraneElectron Spin Resonance SpectroscopyTemperatureGeneral MedicineHydrogen-Ion ConcentrationESR probe021001 nanoscience & nanotechnologyElectric dipole momentDipoleKineticsMembraneChemical physics030220 oncology & carcinogenesisLiposomesOriginal Article0210 nano-technologyMonte Carlo MethodEuropean biophysics journal : EBJ
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Hydrolytic action of phospholipase A2 in monolayers in the phase transition region: direct observation of enzyme domain formation using fluorescence …

1990

Phospholipase A2, a ubiquitous lipolytic enzyme highly active in the hydrolysis of organized phospholipid substrates, has been characterized optically in its action against a variety of phospholipid monolayers using fluorescence microscopy. By labeling the enzyme with a fluorescent marker and introducing it into the subphase of a Langmuir film balance, the hydrolysis of lipid monolayers in their liquid-solid phase transition region could be directly observed with the assistance of an epifluorescence microscope. Visual observation of hydrolysis of different phospholipid monolayers in the phase transition region in real-time could differentiate various mechanisms of hydrolytic action against …

Phase transition12-DipalmitoylphosphatidylcholineStereochemistryBiophysicsPhospholipidBiochemistryPhospholipases Achemistry.chemical_compoundPhospholipase A2Phase (matter)MonolayerEnzyme StabilityFluorescence microscopeLipid bilayer phase behaviorParticle SizePhospholipidsFluorescent DyesElapid VenomsPhospholipase ABinding SitesbiologyHydrolysisPhosphatidylethanolaminesCell BiologyImage EnhancementPhospholipases A2chemistryMicroscopy FluorescencePhospholipasesBiophysicsbiology.proteinlipids (amino acids peptides and proteins)DimyristoylphosphatidylcholineBiochimica et biophysica acta
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Investigation of Temperature-Induced Phase Transitions in DOPC and DPPC Phospholipid Bilayers Using Temperature-Controlled Scanning Force Microscopy

2004

Under physiological conditions, multicomponent biological membranes undergo structural changes which help define how the membrane functions. An understanding of biomembrane structure-function relations can be based on knowledge of the physical and chemical properties of pure phospholipid bilayers. Here, we have investigated phase transitions in dipalmitoylphosphatidylcholine (DPPC) and dioleoylphosphatidylcholine (DOPC) bilayers. We demonstrated the existence of several phase transitions in DPPC and DOPC mica-supported bilayers by both atomic force microscopy imaging and force measurements. Supported DPPC bilayers show a broad L(beta)-L(alpha) transition. In addition to the main transition …

Steric effectsPhase transition12-DipalmitoylphosphatidylcholineBiophysicsPhospholipid02 engineering and technologyMicroscopy Atomic Force010402 general chemistry01 natural sciencesPhase TransitionQuantitative Biology::Subcellular Processeschemistry.chemical_compoundTransition TemperaturePhospholipidsPhysics::Biological PhysicsMembranesBilayerTransition temperaturedigestive oral and skin physiologyBiological membrane021001 nanoscience & nanotechnology0104 chemical sciencesCondensed Matter::Soft Condensed MatterCrystallographyMembranechemistryChemical physicsDipalmitoylphosphatidylcholineAluminum Silicateslipids (amino acids peptides and proteins)0210 nano-technologyBiophysical Journal
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Size influences the effect of hydrophobic nanoparticles on lung surfactant model systems

2013

Item does not contain fulltext The alveolar lung surfactant (LS) is a complex lipid protein mixture that forms an interfacial monolayer reducing the surface tension to near zero values and thus preventing the lungs from collapse. Due to the expanding field of nanotechnology and the corresponding unavoidable exposure of human beings from the air, it is crucial to study the potential effects of nanoparticles (NPs) on the structural organization of the lung surfactant system. In the present study, we investigated both, the domain structure in pure DPPC monolayers as well as in lung surfactant model systems. In the pure lipid system we found that two different sized hydrophobic polymeric nanopa…

Systems BiophysicsPhase transitionPulmonary Surfactant-Associated ProteinsMaterials science12-DipalmitoylphosphatidylcholineSwineVesicleBiophysicstechnology industry and agricultureNanoparticleMembranes ArtificialNanotechnologyBiological membraneModels BiologicalPhase TransitionSurface tensionPulmonary surfactantChemical engineeringPhase (matter)MonolayerAnimalsNanoparticlesHydrophobic and Hydrophilic InteractionsNanomedicine Radboud Institute for Molecular Life Sciences [Radboudumc 19]
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Mixtures of lecithin with polymerizable derivatives of cholesterol. A monolayer film balance study.

1986

One of the best investigated binary lipid mixtures is the lecithin-cholesterol system. We show here that it is possible to modify the cholesterol in such a way that it can be polymerized without changing its behaviour in mixtures with lecithin. The polymerizable derivatives exhibit a very similar phase diagram in the mixture with dipalmitoyl-phosphatidylcholine as the cholesterol itself. This is demonstrated by filmbalance measurements.

food.ingredient12-DipalmitoylphosphatidylcholinePolymersUltraviolet RaysBiophysicsMembrane biologyLecithinchemistry.chemical_compoundMembrane LipidsfoodMonolayerPhase diagramCholesterolBalance studyViscositytechnology industry and agricultureWaterGeneral MedicineCholesterolchemistryChemical engineeringPolymerizationModels ChemicalThermodynamicslipids (amino acids peptides and proteins)Cholesterol EstersEuropean biophysics journal : EBJ
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