Search results for "Phosphatidylcholine"

showing 10 items of 221 documents

Macromolecules in ordered media VIII. High-performance size-exclusion chromatography as a technique for characterizing the interaction between polyan…

1997

Abstract The association of polyanions with liposomes based on dimyristoyl phosphatidyl choline and stearylamine at a ratio of 50:50 was investigated in terms of the binding model and, to a lesser extent, of the partition model. Aqueous size-exclusion chromatography has been proposed as a major technique for monitoring the interactions between liposomes and polyelectrolytes and the results were compared with those obtained by fluorescence spectroscopy. Quantitatively, the extent of the association follows the order: Sodium poly(styrene sulfonate) ( K A = 10 000 M −1 ), poly (acrylic acid) ( K A = 2000 M −1 ) and poly ( l -glutamic acid) ( K A = 700 M −1 ). Also, the effect of the ionic stre…

LiposomeChromatographyOrganic ChemistrySize-exclusion chromatographyFluorescence spectrometryGeneral MedicineBiochemistryPolyelectrolyteAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundchemistryIonic strengthPhosphatidylcholineAcrylic acidJournal of Chromatography A
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Electrically induced deformation of giant liposomes monitored by thickness shear mode resonators.

2006

Thickness shear mode resonators are capable of registering small changes in the thickness and viscoelastic properties of ultrathin films attached to their surface. It was found that it is possible to monitor the deformation of surface-bound giant liposomes by applying an electric field with small amplitudes. Changes in the apparent height of attached vesicles in the nanometer range were easily detected as a function of lipid composition. Increasing the bending modulus by adding cholesterol results in a significantly reduced deformation from 16.8 nm (5% cholesterol) down to 3.2 nm (20% cholesterol), rendering this new method a robust and sensitive tool to detect the bending elasticity of lip…

LiposomeMaterials scienceFlexural modulusbusiness.industrySurface PropertiesVesicleLipid BilayersSurfaces and InterfacesCondensed Matter PhysicsViscoelasticityElasticityResonatorOpticsCholesterolShear (geology)Electric fieldLiposomesElectrochemistryPhosphatidylcholinesGeneral Materials ScienceNanometreComposite materialbusinessSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Macromolecules in ordered media: 7. Influence of ionic strength and bilayer composition on the association of polyelectrolytes to mixed liposomes

1997

The effect of both the phospholipid composition of the bilayer and the ionic strength of the medium on the association between poly(2-vinyl pyridine) and mixed liposomes based on dimyristoyl phosphatidic acid and dimyristoyl phosphatidil choline was investigated using fluorescence spectroscopy. Intensity changes upon addition of vesicles have allowed us to estimate the extent of the association and data have been processed as association isotherms. We found that the association is enhanced by increasing both the ionic strength and the anionic phospholipid fraction. However, whereas the negative net charge of the bilayer strongly enhances the interaction, the presence of more and more electr…

LiposomePolymers and PlasticsBilayerVesicleOrganic Chemistrytechnology industry and agriculturePhospholipidElectrolytePolyelectrolytechemistry.chemical_compoundchemistryChemical engineeringIonic strengthPhosphatidylcholineMaterials ChemistryOrganic chemistrylipids (amino acids peptides and proteins)Polymer
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INTERACTION OF MACROMOLECULAR PRO-DRUGS WITH LIPID MODEL MEMBRANE - CALORIMETRIC STUDY OF 4-BIPHENYLACETIC ACID LINKED TO ALPHA,BETA-POLY(N-HYDROXYET…

1990

The effect of 4-biphenylacetic acid (BPAA) covalently linked to α,β-poly(N-hydroxyethyl)-dl-aspartamide (PHEA) on the thermotropic properties of dipalmitoylphosphatidylcholine (DPPC) liposomes was investigated by differential scanning calorimetry (DSC). Addition of increasing amounts of PHEA-BPAA adduct to a suspension of phospholipid vesicles modified the thermotropic gel-to-liquid crystalline phase transition by decreasing the enthalpy changes ΔH with concomitant broadening of the peak without variations in the transition temperature (Tm). These effects are interpreted in terms of a deep interaction of BPAA bound to the polymer with the apolar moiety of the lipid bilayer. The amount of dr…

LiposomeStereochemistryVesiclePhospholipidPharmaceutical ScienceThermotropic crystalCrystallographychemistry.chemical_compoundDifferential scanning calorimetrychemistryDipalmitoylphosphatidylcholinePhosphatidylcholinelipids (amino acids peptides and proteins)Lipid bilayer
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Development and characterization of liposomes containing glycols as carriers for diclofenac

2009

® Propylene glycol Permeation enhancer vesicles abstract This paper focuses on the preparation and characterization of new, stable phospholipid formulations as carriers for dermal delivery of diclofenac (DCF). To prepare these vesicles two water miscible permeation enhancers (PE) with glycol group: diethyleneglycol monoethyl ether (Transcutol ® , Trc) and propylene glycol (PG), were added at different concentrations (10%, 20%, 30%, 40%, 50%) during the preparation of diclofenac loaded soy lecithin (SL) liposomes. We added Transcutol ® or propylene glycol to the hydrophilic phase in order to obtain new systems able to enhance the skin delivery of diclofenac thanks to the synergic effect of g…

Liposomechemistry.chemical_compoundColloid and Surface ChemistryChromatographyLamellar phaseChemistryVesiclePhosphatidylcholineZeta potentialPhospholipidPermeationApparent viscosityColloids and Surfaces A: Physicochemical and Engineering Aspects
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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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Predicting the in vivo release from a liposomal formulation by IVIVC and non-invasive positron emission tomography imaging

2010

This study aimed to predict the in vivo performance from the in vitro release of a low-molecular weight model compound, [(18)F]-2-fluoro-2-deoxy-d-glucose ([(18)F]FDG), from liposomes and by means of positron emission tomography (PET). Liposomes composed of hydrogenated phosphatidylcholine (HPC) were prepared by a freeze-thaw method. Particle size distribution was measured by dynamic light scattering (DLS). In vitro release was examined with a dispersion method detecting the radioactivity of [(18)F]FDG. In vivo release of [(18)F]FDG, following i.p. injection of the liposomes in rats, was determined by using a Micro-PET scanner. Convolution was performed to predict the in vivo profiles from …

Liposomemedicine.diagnostic_testbusiness.industryPharmaceutical SciencePharmaceutical formulationModified Release Dosage FormRatschemistry.chemical_compoundIVIVCchemistryDynamic light scatteringFluorodeoxyglucose F18Positron emission tomographyIn vivoPositron-Emission TomographyPhosphatidylcholineLiposomesmedicineAnimalsParticle SizeNuclear medicinebusinessBiomedical engineeringEuropean Journal of Pharmaceutical Sciences
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Partitioning of Pyrene-Labeled Phospho- and Sphingolipids between Ordered and Disordered Bilayer Domains

2004

AbstractHere we have studied how the length of the pyrene-labeled acyl chain (n) of a phosphatidylcholine, sphingomyelin, or galactosylceramide affects the partitioning of these lipids between 1), gel and fluid domains coexisting in bovine brain sphingomyelin (BB-SM) or BB-SM/spin-labeled phosphatidylcholine (PC) bilayers or 2), between liquid-disordered and liquid-ordered domains in BB-SM/spin-labeled PC/cholesterol bilayers. The partitioning behavior was deduced either from modeling of pyrene excimer/monomer ratio versus temperature plots, or from quenching of the pyrene monomer fluorescence by spin-labeled PC. New methods were developed to model excimer formation and pyrene lipid quenchi…

Macromolecular SubstancesMembrane FluidityLipid BilayersMolecular ConformationBiophysicsPhase Transition03 medical and health scienceschemistry.chemical_compoundMembrane MicrodomainsPhosphatidylcholineMembrane fluidityFluorometryLipid bilayerPhospholipids030304 developmental biologySphingolipids0303 health sciencesPyrenesMembranesQuenching (fluorescence)Staining and LabelingChemistry030302 biochemistry & molecular biologyTemperatureBiological membraneModels ChemicalBiochemistryDipalmitoylphosphatidylcholineLiposomesBiophysicsPyrenelipids (amino acids peptides and proteins)SphingomyelinBiophysical Journal
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DIFFERENTIAL SCANNING CALORIMETRY STUDY ON DRUG RELEASE FROM AN INULIN-BASED HYDROGEL AND ITS INTERACTION WITH A BIOMEMBRANE MODEL:pH AND LOADING EFF…

2008

Inulin has been derivatized with methacrylic anhydride (MA) and succinic anhydride (SA) to obtain a methacrylated/succinilated derivative (INU-MA-SA) able to produce a pH sensitive hydrogel after UV irradiation. The hydrogel was characterized and loaded with diflunisal (10.4, 17 and 24%, w/w) chosen as a model drug. The drug release from INU-MA-SA-based hydrogel to a biomembrane model made by unilamellar vesicles of dimyristoylphosphatidyl-choline (DMPC) was investigated at pH 4.0 and 7.4 by differential scanning calorimetry (DSC) that appears to be a suitable technique to follow the transfer kinetics of a drug from a controlled release system to a biomembrane model. The drug release from t…

Magnetic Resonance SpectroscopyINULIN HYDROGELS DRUG RELEASE DIFFERENTIAL SCANNING CALORIMETRYPharmaceutical ScienceDiflunisalMethacrylic anhydrideCentrifugationInsulysinDosage formchemistry.chemical_compoundDifferential scanning calorimetryX-Ray DiffractionSpectroscopy Fourier Transform InfraredmedicineHypoglycemic AgentsChromatography High Pressure LiquidChromatographyCalorimetry Differential ScanningVesicleAnti-Inflammatory Agents Non-Steroidaltechnology industry and agricultureSuccinic anhydrideInulinHydrogelsMembranes ArtificialSuccinatesHydrogen-Ion ConcentrationDiflunisalControlled releaseMolecular WeightchemistryChemical engineeringSolubilitySelf-healing hydrogelsSpectrophotometry UltravioletChromatography Thin LayerDimyristoylphosphatidylcholinemedicine.drug
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Interactions of α-tocopherol with biomembrane models: Binding to dry lecithin reversed micelles

2005

Abstract The state of α-tocopherol (Vitamin E) in solutions of dry lecithin reversed micelles dispersed in an apolar medium has been investigated as a function of the Vitamin E to surfactant molar ratio (RVE) at fixed surfactant concentration by FT-IR, 1H NMR and SAXS with the aim to emphasize the role played by anisotropic intermolecular interactions and confinement effects as driving forces of its partitioning between apolar bulk solvent and polar nanodomains and of mutual Vitamin E/reversed micelle effects. It has been found that its binding strength to reversed micelles, triggered by steric and orientational constrains, is mainly regulated by specific interactions between the hydrophili…

Magnetic Resonance Spectroscopyfood.ingredientreversed micelleChemistry Pharmaceuticalmedicine.medical_treatmentPharmaceutical Sciencevitamin EMicelleLecithinDrug IncompatibilitySurface-Active Agentschemistry.chemical_compoundfoodPulmonary surfactantalpha-tocopherolPhosphatidylcholineSpectroscopy Fourier Transform InfraredmedicineOrganic chemistryTocopherolCarbon TetrachlorideMicellesVitamin EBiological membraneVitaminsintermolecular interactionlecithinchemistryPhosphatidylcholinesBiophysicslipids (amino acids peptides and proteins)solubilization.alpha-TocopherolInternational Journal of Pharmaceutics
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