Search results for "Micellar"

showing 10 items of 185 documents

Development of a method to determine axitinib, lapatinib and afatinib in plasma by micellar liquid chromatography and validation by the European Medi…

2017

A method based on micellar liquid chromatography to quantify the tyrosine kinase inhibitors axitinib, lapatinib and afatinib in plasma is reported. The sample pretreatment was a simple 1/5-dilution in a pure micellar solution, filtration and direct injection, without requiring extraction or purification steps. The three drugs were resolved from the matrix in 17 min, using an aqueous solution of 0.07 M sodium dodecyl sulfate – 6.0% 1-pentanol, buffered at pH 7 with 0.01 M phosphate salt as mobile phase, running under isocratic mode at 1 mL/min through a C18 column. The detection was performed by absorbance at 260 nm. An accurate mathematical relationship was established between the retention…

0301 basic medicineretentionBioanalysisIndazolesAxitinibbioanalysisClinical BiochemistryAntineoplastic AgentsAfatinib01 natural sciencesBiochemistryMicelleAnalytical ChemistryMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compoundDrug StabilityPulmonary surfactantLimit of DetectionNeoplasmsdirect injectionHumansSodium dodecyl sulfateMicellesDetection limitAqueous solutionChromatographyChemistry010401 analytical chemistryImidazolesReproducibility of ResultsmodelingLapatinibCell BiologyGeneral Medicine0104 chemical sciences030104 developmental biologyanti-cancer drugMicellar liquid chromatographyLinear ModelsQuinazolinesoptimizationChromatography LiquidJournal of Chromatography B
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Polymeric Nanoparticles with Neglectable Protein Corona

2020

Small : nano micro 16(18), 1907574 (2020). doi:10.1002/smll.201907574

540 Chemistry and allied sciencesDispersity610 Medizinmicellar structuresNanoparticleProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialschemistry.chemical_compoundAdsorption610 Medical sciencesHumansGeneral Materials ScienceParticle SizeGel electrophoresisChemistryasymmetrical flow field-flow fractionationSarcosineGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineering540 Chemiedrug deliveryNanoparticlesParticleProtein CoronaParticle sizePeptides0210 nano-technologyHydrophobic and Hydrophilic InteractionsEthylene glycolBiotechnologySmall
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Isocratic and gradient elution in micellar liquid chromatography with Brij-35

2015

Polyoxyethylene(23)lauryl ether (known as Brij-35) is a nonionic surfactant, which has been considered as an alternative to the extensively used in micellar liquid chromatography anionic surfactant sodium lauryl (dodecyl) sulfate, for the analysis of drugs and other types of compounds. Brij-35 is the most suitable nonionic surfactant for micellar liquid chromatography, owing to its commercial availability, low cost, low toxicity, high cloud temperature, and low background absorbance. However, it has had minor use. In this work, we gather and discuss some results obtained in our laboratory with several β-blockers, sulfonamides, and flavonoids, concerning the use of Brij-35 as mobile phase mo…

Absorbancechemistry.chemical_compoundChromatographyAqueous solutionPulmonary surfactantchemistryMicellar liquid chromatographyPhase (matter)Filtration and SeparationEtherAcetonitrileMicellar electrokinetic chromatographyAnalytical ChemistryJournal of Separation Science
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Micellar liquid chromatography for prediction of drug transport.

2000

Abstract The vast majority of well absorbed drugs are transported passively across the cell membranes. Physicochemical descriptors of drug molecules that are believed to influence transcellular transport are routinely used to predict drug absorption by means of complex mathematical models. In this paper, a new in vitro method, based on the retention data in micellar liquid chromatography (MLC), is validated for the prediction of passive drug absorption. The retention of a heterogeneous drugs set in MLC using Brij 35 as surfactant in the mobile phase is compared with the retention data reported in literature obtained in red cell membrane lipid liposomes, human red cell membranes vesicles (ve…

Absorption (pharmacology)LiposomeChromatographyChemistryVesicleOrganic ChemistryCell MembraneAdministration OralGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMembranePulmonary surfactantMicellar liquid chromatographyParacellular transportHumansPharmacokineticsSpectrophotometry UltravioletMicellesChromatography LiquidJournal of chromatography. A
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Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
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Peak half-width plots to study the effect of organic solvents on the peak performance of basic drugs in micellar liquid chromatography.

2009

The addition of the anionic surfactant sodium dodecyl sulphate (SDS) to hydro-organic mixtures of methanol, ethanol, propanol or acetonitrile with water yielded enhanced peak shape (i.e. increased efficiencies and symmetrical peaks) for a group of basic drugs (β-blockers) chromatographed with a Kromasil C18 column. The effect can be explained by the thin layer of surfactant associated to the hydrocarbon chain on the stationary phase in the presence of the organic solvents, which covers the free silanols on the siliceous support avoiding their interaction with the cationic basic drugs. These instead interact with the anionic head of the surfactant increasing their retention and allowing a mo…

AcetonitrilesInorganic chemistryAdrenergic beta-AntagonistsBiochemistryMicelleAnalytical ChemistryPropanolchemistry.chemical_compoundPulmonary surfactantBasic compoundsSodium dodecyl sulphatePeak performanceSodium dodecyl sulfateAcetonitrileMicelleschemistry.chemical_classificationChromatographyOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineOrganic solventsHydrocarbonchemistryMicellar liquid chromatographyAlcoholsLinear Modelsβ-BlockersMethanolMicellar liquid chromatographyPeak half-widthsChromatography LiquidJournal of chromatography. A
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Thermodynamic properties of N-octyl- and N-dodecylnicotinamide chlorides in water

1990

Densities, heat capacities and enthalpies of dilution at 25°C and osmotic coefficients at 37°C were measured for N-octyl- and N-dodecylnicotinamide chlorides in water over an extended concentration region. Partial molar volumes, heat capacities, relative enthalpies and nonideal free energies and entropies at 25°C were derived as a function of the surfactant concentration. For both surfactants, plots of volumes, enthalpies and free energies vs. concentration are regular whereas those of heat capacities and entropies present anomalies at about 0.8 and 0.1m for the octyl and dodecyl compounds, respectively. Changes in the slope of a plot of osmotic coefficients times molality vs. molality were…

Activity coefficientMolalityChemistryThermodynamics of micellizationEnthalpyBiophysicsThermodynamicsBiochemistryHeat capacityMicelleMicellar solutionsOsmotic coefficientPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Interpretive search of optimal isocratic and gradient separations in micellar liquid chromatography in extended organic solvent domains

2020

Abstract Micellar liquid chromatography (MLC) is a reversed-phase mode with mobile phases containing an organic solvent and a micellised surfactant. Most procedures developed in MLC are implemented in the isocratic mode, since the general elution problem in chromatography is less troublesome. However, gradient elution may be still useful in MLC to analyse mixtures of compounds within a wide range of polarities, in shorter times. MLC using gradients is attractive to determine by direct injection moderate to low polar compounds in physiological samples. In these analyses, the use of initial micellar conditions (isocratic or gradient) with a fixed amount of surfactant above the critical micell…

Adrenergic beta-Antagonists1-Propanol010402 general chemistry01 natural sciencesBiochemistryMicelleChemistry Techniques AnalyticalAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantHumansMicellesChromatographyElutionChemistryChemical polarity010401 analytical chemistryOrganic ChemistrySodium Dodecyl SulfateGeneral Medicine0104 chemical sciencesSolventMicellar liquid chromatographyCritical micelle concentrationSolventsIndicators and ReagentsAdsorptionChromatography LiquidJournal of Chromatography A
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Micellar Liquid Chromatography:  A Worthy Technique for the Determination of β-Antagonists in Urine Samples

1998

Several beta-antagonists (acebutolol, atenolol, celiprolol, labetalol, metoprolol, nadolol, propranolol) were determined in urine samples with fluorometric detection after direct injection, in less than 15 min, with a micellar mobile phase of 0.1 M sodium dodecyl sulfate (SDS), 15% propanol, and 1% triethylamine at pH 3. The limits of detection (38 criterion) were usually between 3 and 30 ng/mL. The addition of propanol and triethylamine and the reduction of the pH of the mobile phase improved the efficiency of the chromatographic peaks that was rather low in pure micellar eluents. The selection of the composition of the mobile phase was easily performed through the use of an interpretive p…

Adrenergic beta-Antagonists1-PropanolHigh-performance liquid chromatographyAnalytical ChemistryPropanolSurface-Active Agentschemistry.chemical_compoundEthylaminesmedicineHumansSodium dodecyl sulfateTriethylamineMicellesDetection limitChromatographySodium Dodecyl SulfateHydrogen-Ion ConcentrationAtenololPropranololAcebutololSpectrometry FluorescenceAtenololchemistryMicellar liquid chromatographyChromatography LiquidMetoprololmedicine.drugAnalytical Chemistry
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Thermodynamic properties of alcohols in a micellar phase. Binding constants and partial molar volumes of pentanol in sodium dodecylsulfate micelles a…

1984

Densities of the ternary system water-sodium dodecylsulfate (NaDS)-pentanol and of the binary systems butanol-octane and pentanol-octane were measured at 15, 25, and 35 °C. The apparent molar volume of pentanol in the ternary system was analyzed using a mass-action model for the alcohol distribution in micellar solutions. The partial molar volume of alcohol bound to the micelles and the ratio between the binding constant and the aggregation number of the surfactant are calculated. The partial molar volume binding constant, is discussed in terms of solubilization sites of the alcohol in the micelles whereas the binding constant is compared with that derived from the Nernstian partition const…

Aggregation numberTernary numeral systemChemistryInorganic chemistryBiophysicsPartial molar propertyBiochemistryBinding constantMicelleMolar volumeCritical micelle concentrationMicellar solutionsPhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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