Search results for "cellar"

showing 10 items of 230 documents

Performance of short-chain alcohols versus acetonitrile in the surfactant-mediated reversed-phase liquid chromatographic separation of β-blockers

2010

Organic solvents are traditionally added to micellar mobile phases to achieve adequate retention times and peak profiles, in a chromatographic mode which has been called micellar liquid chromatography (MLC). The organic solvent content is limited to preserve the formation of micelles. However, at increasing organic solvent contents, the transition to a situation where micelles do not exist is gradual. Also, there is no reason to neglect the potentiality of mobile phases containing only surfactant monomers instead of micelles (high submicellar chromatography, HSC). This is demonstrated here for the analysis of β-blockers. The performance of four organic solvents (methanol, ethanol, 1-propano…

Chromatography Reverse-PhaseAcetonitrilesChromatographyElutionAdrenergic beta-AntagonistsOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyMicelleAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundModels ChemicalchemistryPulmonary surfactantMicellar liquid chromatographyAlcoholsData Interpretation StatisticalMethanolAcetonitrileAlgorithmsMicellesJournal of Chromatography A
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Comparison of surfactant-mediated liquid chromatographic modes with sodium dodecyl sulphate for the analysis of basic drugs

2020

In reversed-phase liquid chromatography (RPLC), basic drugs are positively charged at the usual working pH range and interact with free anionic silanols present in conventional silica-based stationary phases. This translates into stronger retention and tailed and broadened peaks. This problem can be resolved by the addition of reagents to the mobile phase that are adsorbed on the stationary phase, avoiding the access of solutes to silanols. Among these additives, surfactants under micellar conditions have provided good silanol suppressing potency through the technique known as micellar liquid chromatography (MLC). The most common example of this is anionic sodium dodecyl sulphate (SDS). Whe…

Chromatography Reverse-PhaseAqueous solutionChromatographyChemistryGeneral Chemical Engineering010401 analytical chemistryGeneral EngineeringSodium Dodecyl Sulfate02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMicelle0104 chemical sciencesAnalytical ChemistrySurface-Active AgentsSilanolchemistry.chemical_compoundPulmonary surfactantMicellar liquid chromatographyReagentPhase (matter)Microemulsion0210 nano-technologyMicellesChromatography LiquidAnalytical Methods
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Implementation of gradients of organic solvent in micellar liquid chromatography using DryLab®: Separation of basic compounds in urine samples

2014

In micellar liquid chromatography (MLC), chromatographic peaks are more evenly distributed compared to conventional reversed-phase liquid chromatography (RPLC). This is the reason that most procedures are implemented using isocratic elution. However, gradient elution may be still useful in MLC to analyse mixtures of compounds within a wide range of polarities, decreasing the analysis time. Also, it benefits the determination of moderately to low polar compounds in physiological fluids performing direct injection: an initial micellar eluent with a low organic solvent content, or a pure micellar (without surfactant) solution, will provide better protection of the column against the proteins i…

Chromatography Reverse-PhaseChromatographyChemistryElutionChemical polarityAdrenergic beta-AntagonistsOrganic ChemistryAnalytical chemistryGeneral MedicineBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compound1-PropanolColumn chromatographyPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationSolventsHumansIndicators and ReagentsAnalytical proceduresMicellesSoftwareJournal of Chromatography A
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Volumes and compressibilities of pentanol in aqueous dodecyltrimethylammonium bromide solutions at 15, 25 and 35°C

1990

Ultrasonic velocities and densities of the water-dodecyltrimethylammonium bromide (DTAB)-pentanol (PentOH) ternary system were measured at 15, 25 and 35°C as a function of the surfactant and alcohol concentrations. The apparent molar volumes and isentropic compressibilities of PentOH were calculated. The standard partial molar volumes increase with surfactant concentration continuously whereas the standard partial molar isentropic compressibilities show sharp changes in slope at about 0.25 mol-kg−1 DTAB, which can be ascribed to a micellar structural transition. The volume data for alcohol in micellar solutions were treated by a model reported for the distribution of polar additives between…

ChromatographyAqueous solutionIsentropic processChemistryDistribution constantBiophysicsConcentration effectThermodynamicsBiochemistryMicelleMolar volumePulmonary surfactantMicellar solutionsPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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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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Chromatographic Efficiency in Micellar Liquid Chromatography: Should it Be Still a Topic of Concern?

2013

Micellar liquid chromatography (MLC) was first proposed as an attractive alternative to avoid the use of organic solvents. It was soon apparent that pure micellar solutions yield poor efficiencies. This problem was remediated by the addition of a small amount of an organic solvent. However, the general opinion of the poor peak shape has prevailed as a handicap for MLC, in spite of the fact that the hybrid mode often offers similar or even improved efficiencies (for basic compounds) relative to that attained in the hydro-organic mode. Only the efficiencies for apolar non-ionizable compounds are still clearly inferior. This work describes the type of interactions and polarity changes with org…

ChromatographyChemistryHydrophilic interaction chromatographyAnalytical chemistryFiltration and SeparationSilanol effect suppressionAnalytical ChemistryAdsorptionHybrid mobile phasesPulmonary surfactantMicellar liquid chromatographyYield (chemistry)Mass transferBand broadeningMicellar solutionsMass transferenceWettingMicellar liquid chromatographyStationary phase architecture and wettingSeparation & Purification Reviews
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Comparison of the performance of non-ionic and anionic surfactants as mobile phase additives in the RPLC analysis of basic drugs

2011

Surfactants added to the mobile phases in reversed-phase liquid chromatography (RPLC) give rise to a modified stationary phase, due to the adsorption of surfactant monomers. Depending on the surfactant nature (ionic or non-ionic), the coated stationary phase can exhibit a positive net charge, or just change its polarity remaining neutral. Also, micelles in the mobile phase introduce new sites for solute interaction. This affects the chromatographic behavior, especially in the case of basic compounds. Two surfactants of different nature, the non-ionic Brij-35 and the anionic sodium dodecyl sulfate (SDS) added to water or aqueous-organic mixtures, are here compared in the separation of basic …

ChromatographyChemistryIonic bondingFiltration and SeparationReversed-phase chromatographyMicelleAnalytical Chemistrychemistry.chemical_compoundAdsorptionPulmonary surfactantChemical engineeringMicellar liquid chromatographyPhase (matter)Sodium dodecyl sulfateJournal of Separation Science
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On the measurement of consistent long-term retention factor values in micellar liquid chromatography

2007

Abstract In the field of the quantitative structure–retention and retention–activity relationships (QRAR and QSRR) is crucial to obtain consistent retention factors (k). For this purpose, two unbiased approaches to estimate k are used: (i) the IUPAC approach (based on the extra-column time correction) and (ii) the ‘2-references’ approach (based on the k estimation respect to two prefixed reference k values). Three reference chemicals were selected attending to their retention time, chemical stability and non-ionic character. Consistent retention factor values for these references were estimated for C18 chromatographic columns and Brij35 solutions as mobile phases after statistical analysis.…

ChromatographyChemistryLong term retentionChemical nomenclatureThermodynamicsBiochemistryAnalytical ChemistryColumn chromatographyMicellar liquid chromatographyEnvironmental ChemistryStatistical analysisPhase analysisRetention timeSpectroscopyAnalytica Chimica Acta
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Quantitative Retention−Structure and Retention−Activity Relationship Studies of Local Anesthetics by Micellar Liquid Chromatography

2011

The retention of compounds in micellar liquid chromatography (MLC) is governed by hydrophobic and electrostatic forces. For ionic compounds, both interactions should be considered. The present report offers a novel retention model that includes the hydrophobicity of compounds and the molar fraction of the charged form of compounds and compares it with other previously reported models. High correlations between the logarithm of capacity factors and these structural parameters were obtained for local anesthetics with different degrees of ionization using a nonionic surfactant solution as mobile phase. Modeling the retention of compounds as a function of physicochemical parameters and experime…

ChromatographyChemistryMicellar liquid chromatographyPhase (matter)Linear regressionAnestheticmedicineIonic bondingNonionic surfactantMole fractionQuantitative analysis (chemistry)Analytical Chemistrymedicine.drugAnalytical Chemistry
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Quantitative structure-retention and retention-activity relationships of beta-blocking agents by micellar liquid chromatography.

2001

Abstract Sixteen β-blocking agents (acebutolol, alprenolol, atenolol, bisoprolol, carteolol, celiprolol, esmolol, labetalol, metoprolol, nadolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) showing a large range of hydrophobicity (octanol–water partition coefficients, log P between −0.026 and 2.81) were subjected to micellar liquid chromatography with sodium dodecyl sulfate as micelle forming agent, and n-propanol as organic modifier. The correlation between log P and the retention factor extrapolated to a mobile phase free of micelles and organic modifier was investigated. The use of an interpolated retention factor or the retention factor for specific individual exp…

ChromatographyChemistryOrganic ChemistryAdrenergic beta-AntagonistsQuantitative Structure-Activity RelationshipGeneral MedicineBiochemistryMicelleAcebutololMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundMicellar liquid chromatographyOxprenololmedicineAlprenololSodium dodecyl sulfateMicellescirculatory and respiratory physiologymedicine.drugChromatography LiquidJournal of chromatography. A
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