Search results for " MICE"

showing 10 items of 558 documents

Interaction of polyelectrolytes with oppositely charged micelles studied by fluorescence and liquid chromatography

2005

It is studied by spectrofluorimetry the association of ionized cationic micelles (cetyltrimethylammonium bromide, CTAB) with oppositely charged polyelectrolyte [sodium poly(styrenesulfonate), PSSNa]. CTAB provokes a change in the fluorescence intensity emitted by PSSNa. The investigated surfactants form micelle-like aggregates before critical micellar concentration (CMC). Two approaches (binding and partition equilibrium) are used to obtain the association constant, KA, number of CTAB molecules in a binding site, N, and apparent partition coefficient, Γ. Analysis of the parameters as a function of polymer concentration and ionic strength μ is performed. The effect of μ shows an enhancement …

ChromatographyAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyMicellePolyelectrolytePartition coefficientchemistry.chemical_compoundBromideIonic strengthPartition equilibriumCritical micelle concentrationMaterials ChemistryEuropean Polymer Journal
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Compared effects of synthetic and natural bile acid surfactant on xenobiotic absorption. II. Studies with sodium glycocholate to confirm a hypothesis

1994

Abstract The effects of sodium glycocholate (SGC) on the intestinal absorption of drug-related xeriobiotics are investigated, on the basis of previously established absorption/partition relationships. Six phenylalkylcarboxylic acids, closely related to nonsteroid anti-inflammatory drugs in structure and constituting a true homologous series, were used as test compounds through an in situ rat gut technique, using the whole colon as nonspecialized absorption membrane model. Whereas the synthetic surfactants (i.e., polysorbates and laurylsulphates) at the critical micelle concentration have been shown to disrupt the aqueous boundary layer adjacent to the membrane, SGC does not; in contrast, it…

ChromatographyBile acidmedicine.drug_classSodiumPharmaceutical Sciencechemistry.chemical_elementMicelleIntestinal absorptionchemistry.chemical_compoundchemistryCritical micelle concentrationLipophilicitymedicineAbsorption (chemistry)XenobioticInternational Journal of Pharmaceutics
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Influence of the addition of modifiers on solute-micelle interaction in hybrid micellar liquid chromatography

1998

In reversed-phase micellar liquid chromatography (MLC) organic modifiers are usually added to the mobile phase to modify the eluent strength and to increase the efficiency of the chromatographic peaks. The effect of the modifiers methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, acetonitrile and tetrahydrofuran on the critical micelle concentration (cmc) of the anionic surfactant sodium dodecylsulphate (SDS) has been studied to enable understanding of the interactions between solute, micelles and bulk liquid in such hybrid eluents. Methanol, acetonitrile and tetrahydrofuran increased thecmc, whereas the other alcohols reduced its value. For butanol and pentanol, which partition into the…

ChromatographyButanolOrganic ChemistryClinical BiochemistryThermodynamics of micellizationAlcoholBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationChromatographia
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Retention mechanisms in micellar liquid chromatography.

2008

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode with mobile phases containing a surfactant (ionic or non-ionic) above its critical micellar concentration (CMC). In these conditions, the stationary phase is modified with an approximately constant amount of surfactant monomers, and the solubilising capability of the mobile phase is altered by the presence of micelles, giving rise to diverse interactions (hydrophobic, ionic and steric) with major implications in retention and selectivity. From its beginnings in 1980, the technique has evolved up to becoming a real alternative in some instances (and a complement in others) to classical RPLC with hydro…

ChromatographyChemistryOrganic ChemistrySolvationIonic bondingGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryMicelleAnalytical ChemistrySilanolchemistry.chemical_compoundSurface-Active AgentsModels ChemicalSolubilityMicellar liquid chromatographyPhase (matter)Critical micelle concentrationSolventsAdsorptionHydrophobic and Hydrophilic InteractionsAlgorithmsMicellesChromatography LiquidJournal of chromatography. A
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Ionic liquids in separation techniques.

2007

The growing interest in ionic liquids (ILs) has resulted in an exponentially increasing production of analytical applications. The potential of ILs in chemistry is related to their unique properties as non-molecular solvents: a negligible vapor pressure associated to a high thermal stability. ILs found uses in different sub-disciplines of analytical chemistry. After drawing a rapid picture of the physicochemical properties of selected ILs, this review focuses on their use in separation techniques: gas chromatography (GC), liquid chromatography (LC) and electrophoretic methods (CE). In LC and CE, ILs are not used as pure solvents, but rather diluted in aqueous solutions. In this situation IL…

ChromatographyChromatography GasOrganic ChemistryElectrophoresis CapillaryIonic LiquidsGeneral MedicineReversed-phase chromatographyBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundChaotropic agentCapillary electrophoresisCountercurrent chromatographychemistryLyotropicIonic liquidSolventsGas chromatographyCountercurrent DistributionChromatography LiquidChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Modelling of retention behaviour of solutes in micellar liquid chromatography

1997

In micellar liquid chromatography (MLC), the resolution for a given multi-component mixture can be optimized by changing several variables, such as the concentrations of surfactant and organic modifier, the pH and temperature. However, this advantage can only be fully exploited with the development of mathematical models that describe the retention and the separation mechanisms. Several reports have appeared recently on the possibilities of accurately predicting the solute retention in MLC. Although the retention and selectivity may strongly change with varying concentrations of surfactant, organic modifier and/or pH, the observed changes are very regular, and are well described by simple m…

ChromatographyMathematical modelResolution (mass spectrometry)ChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPulmonary surfactantMicellar liquid chromatographyIonic strengthCritical micelle concentrationSelectivityJournal of Chromatography A
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High Submicellar Liquid Chromatography

2013

Surfactant addition above the critical micellar concentration (CMC), in reversed-phase liquid chromatography (RPLC), was proposed as a way to modify the selectivity and analysis time, giving rise to a chromatographic mode called micellar liquid chromatography (MLC). However, solutions containing only surfactant are too weak and yield poor peak shape. This was remediated by the addition of a small amount of organic solvent. To preserve the existence of micelles, in MLC high contents of organic solvent are avoided. Nevertheless, there is no reason to neglect the potentiality of mobile phases containing a surfactant above its CMC in water and a high organic solvent content (without micelles). …

Chromatographycolumn interactionsElutionChemistryHydrophilic interaction chromatographyAnalytical chemistryFiltration and Separationmacromolecular substancesReversed-phase chromatographyMicelleAnalytical Chemistryreversed-phase liquid chromatographyCountercurrent chromatographyPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationchromatographic performancesubmicellar liquid chromatographySeparation & Purification Reviews
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Biopartitioning micellar chromatography to pedict mutagenicity of aromatic amines

2007

[EN] Mutagenicity is a toxicity endpoint associated with the chronic exposure to chemicals. Aromatic amines have considerable industrial and environmental importance due to their widespread use in industry and their mutagenic capacity. Biopartitioning micellar chromatography (BMC), a mode of micellar liquid chromatography that uses micellar mobile phases of Brij35 in adequate experimental conditions, has demonstrated to be useful in mimicking the drug partitioning process into biological systems. In this paper, the usefulness of BMC for predicting mutagenicity of aromatic amines is demonstrated. A multiple linear regression (MLR) model based on BMC retention data is proposed and compared wi…

Chronic exposureQuantitative structure–activity relationshipPredictive capabilityQuantitative Structure-Activity RelationshipAromatic aminesHigh-performance liquid chromatographyModels BiologicalMutagenicityDrug DiscoveryQUIMICA ANALITICAOrganic chemistryComputer SimulationAminesLeast-Squares AnalysisMicellesPharmacologychemistry.chemical_classificationChromatographyChromatographyOrganic ChemistryAromatic amineGeneral MedicineBiopartitioning micellar chromatographychemistryMicellar liquid chromatographyMutagenesisQuantitative retentione-activity relationships
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Confinement of chiral molecules in reverse micelles: FT-IR, polarimetric and VCD investigation on the state of dimethyl tartrate in sodium bis(2-ethy…

2008

Abstract The state of d and l -dimethyl tartrate confined within dry sodium bis(2-ethylhexyl) sulfosuccinate (AOT) reverse micelles dispersed in CCl 4 has been investigated by FT-IR spectroscopy, polarimetry, and vibrational circular dichroism (VCD). Measurements have been performed at 25 °C as a function of the solubilizate-to-surfactant molar ratio ( R ) at a fixed AOT concentration (0.158 M). The analysis of experimental data is consistent with the hypothesis that both enantiomers of dimethyl tartrate are mainly entrapped in the reverse micelles and located in proximity to the surfactant head-group region. The formation of this interesting self-organized chiral nanostructure involves som…

Circular dichroismInorganic chemistryInfrared spectroscopyTartrateMicellechemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPulmonary surfactantVibrational circular dichroismPhysical chemistryEnantiomerDimethyl tartrate Sodium bis(2-ethylhexyl) sulfosuccinate Reverse micelles Chiral nanostructures FT-IR spectroscopy Vibrational circular dichroism Optical rotationColloids and Surfaces A: Physicochemical and Engineering Aspects
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Confinement effects on the interactions of native DNA with Cu(II)-5-triethyl ammonium methyl salicylidene orto-phenylendiiminate in C12E4 liquid crys…

2008

Confinement effects of native calf thymus DNA interacting with the complex Cu(ii)-5-(triethylammoniummethyl)salicylidene ortho-phenylendiiminate (CuL(2+)) perchlorate in tetraethylene glycol monododecyl ether (C(12)E(4)) liquid crystals have been investigated by UV absorption spectrophotometry, circular dichroism (CD) and small angle X-ray scattering (SAXS). The results indicate the occurrence of dramatic structural changes of both the DNA and the CuL(2+)-DNA system, when going from aqueous solution to C(12)E(4) liquid crystals, due to confinement constrains imposed by the closed structure of C(12)E(4) reverse micelles. Further marked departures from the behaviour observed in aqueous soluti…

Circular dichroismIntracellular SpaceMicelleAbsorptionPolyethylene GlycolsInorganic ChemistryPerchloratechemistry.chemical_compoundX-Ray DiffractionLiquid crystalScattering Small AngleOrganometallic CompoundsAnimalsSettore CHIM/02 - Chimica FisicaAqueous solutionSmall-angle X-ray scatteringCircular DichroismWaterDNALiquid CrystalsCrystallographychemistrySettore CHIM/03 - Chimica Generale E InorganicaX-ray crystallographyCattleSpectrophotometry UltravioletAbsorption (chemistry)DNA intercalation reverse micelles
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