Search results for "critical micelle concentration"

showing 10 items of 64 documents

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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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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Surfactant Association: Recent Theoretical and Experimental Developments

1991

A theoretical model describing the association of ionic surfactants into rod-shaped micelles is combined with an approximate formula for the viscosity increase induced by rod-shaped aggregates. It is shown that most of the thermodynamic parameters of the association model can be obtained from viscosity measurements. The approach is applied to micellar solutions of hexadecylpyridinium salts. The pronounced effect of counter-ion concentration on the growth of rod-shaped micelles can be attributed to a slightly higher degree of counter-ion association in the cylindrical part than in the end portions. An attempt is made to explain the finding that the degree of counter-ion association is virtua…

Cloud pointViscosityPulmonary surfactantChemistryCritical micelle concentrationAssociation (object-oriented programming)Micellar solutionsIonic bondingThermodynamicsMicelle
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Soil remediation: humic acids as natural surfactants in the washings of highly contaminated soils

2005

The remediation of the highly contaminated site around the former chemical plant of ACNA (near Savona) in Northern Italy is a top priority in Italy. The aim of the present work was to contribute in finding innovative and environmental-friendly technology to remediate soils from the ACNA contaminated site. Two soils sampled from the ACNA site (A and B), differing in texture and amount and type of organic contaminants, were subjected to soil washings by comparing the removal efficiency of water, two synthetic surfactants, sodium dodecylsulphate (SDS) and Triton X-100 (TX100), and a solution of a natural surfactant, a humic acid (HA) at its critical micelle concentration (CMC). The extraction …

Conservation of Natural ResourcesOctoxynolSoil textureEnvironmental remediationHealth Toxicology and MutagenesisSettore AGR/13 - Chimica AgrariaThiophenesToxicologyHydrocarbons Aromaticcomplex mixturesSoilSonicationSurface-Active AgentsSoil PollutantsHumic acidHumic Substanceschemistry.chemical_classificationSoil-remediation Soil-washing Soxhlet Sonication Contaminated soilsExtraction (chemistry)Sodium Dodecyl SulfateWaterGeneral MedicineContaminationPollutionSoil contaminationItalychemistryChemical IndustryCritical micelle concentrationEnvironmental chemistrySoil waterEnvironmental Pollution
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α, ω-Dipolar amphiphiles: Influence of rigid and flexible units on aggregation behavior

1993

Mono- and α,ω-dipolar amphiphiles with hydrophilic pyridinium head groups, and flexible and rigid hydrophobic parts have been synthesized. Surface tension and conductivity measurements proved that micellar aggregates for amphiphiles 1–4 are formed. The incorporation of rigid units leads to a decrease in the critical micellar concentration (CMC): the rigid monopolar amphiphile 2 aggregates at lower concentration than the flexible monopolar amphiphile 1. A similar decrease was observed when chain ends were connected: the flexible α,ω-dipolar amphiphile 3 has a lower CMC than the flexible monopolar amphiphile 1. The more flexible amphiphiles 1–3 allow the formation of micelles of different sha…

CrystallographyLiquid crystalChemistryCritical micelle concentrationLyotropicAmphiphileMesophaseOrganic chemistryMicellar cubicLamellar structureGeneral ChemistryMicelleRecueil des Travaux Chimiques des Pays-Bas
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Direct injection of physiological fluids in micellar liquid chromatography

2000

Abstract Micellar liquid chromatography (MLC), which uses mobile phases of surfactants above the critical micellar concentration, provides a solution to the direct injection of physiological samples by solubilizing the protein components, and coating the analytical column with surfactant monomers to avoid clogging. A review showing the advantages and limitations of this technique over other chromatographic techniques used in drug analysis, working protocols, and examples of application is presented. The possibility of direct sample introduction simplifies and greatly expedites the treatments with reduced cost, improving the accuracy of the procedures. Surfactant monomers and micelles appear…

Doping in SportsChromatographyChemistryGeneral ChemistryMass spectrometryMicelleAmperometryFluorescence spectroscopyBody FluidsSurface-Active AgentsPharmaceutical PreparationsPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationHumansAnalytical proceduresMicellesChromatography LiquidProtein BindingJournal of Chromatography B: Biomedical Sciences and Applications
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Green Synthesis, Molecular Characterization and Associative Behavior of Some Gemini Surfactants without a Spacer Group.

2013

A series of new gemini surfactants without a spacer group, disodium 2,3-dialkyl-1,2,3,4-butanetetracarboxylates, were synthesized in a green chemistry context minimizing the use of organic solvents and applying microwaves (MW) when activation energy was required. Once the desired architecture was confirmed by means of the nuclear magnetic resonance technique (1H-NMR, 1H-1H COSY) for all the studied surfactants, the critical micellization concentration was determined by conductance measurements. The diffusion coefficient of micelles formed by the four compounds was characterized using pulsed field gradient (PFG)-NMR. Diffusion coefficients were found to be dependent on the concentration and …

Green chemistrygemini surfactantsmicrowavecritical micelle concentrationDiffusionContext (language use)cosmetic detergentlcsh:TechnologyMicelleArticlegreen synthesigemini surfactants green synthesis microwave cosmetic detergents critical micelle concentration PFG-NMR diffusion coefficientOrganic chemistryMoleculeGeneral Materials Sciencediffusion coefficientlcsh:MicroscopyAlkyllcsh:QC120-168.85Settore CHIM/02 - Chimica Fisicachemistry.chemical_classificationgemini surfactantcosmetic detergentslcsh:QH201-278.5lcsh:TChemistrygreen synthesisChemical engineeringlcsh:TA1-2040Critical micelle concentrationPFG-NMRlcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringlcsh:Engineering (General). Civil engineering (General)Pulsed field gradientlcsh:TK1-9971gemini surfactants; green synthesis; microwave; cosmetic detergents; critical micelle concentration; PFG-NMR; diffusion coefficientMaterials (Basel, Switzerland)
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