Search results for "DSO"

showing 10 items of 1609 documents

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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Profiling of endogenous peptides by multidimensional liquid chromatography: On-line automated sample cleanup for biomarker discovery in human urine.

2009

A simple and flexible system, employing a column switching technique, has been designed to allow the analysis of peptides and proteins smaller than 15 kDa by molecular weight in filtered urine samples by performing a direct on-column injection utilising simultaneous sample clean-up and trace enrichment. The positively charged peptides and small proteins in the sample are attracted to the inner, negatively charged pore structure of the RAM-SCX column while the larger proteins and uncharged or negatively charged compounds are excluded. After preconditioning with the biological sample, large amounts of sample can be injected. Several important and adjustable parameters for the proper use of a …

ChromatographyChemistryIon chromatographyAnalytical chemistryReproducibility of ResultsFiltration and SeparationHydrogen-Ion ConcentrationMass spectrometryHigh-performance liquid chromatographyAnalytical ChemistryDilutionSpecimen HandlingMolecular WeightMatrix-assisted laser desorption/ionizationAdsorptionSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationHumansSample preparationSolid phase extractionPeptidesBiomarkersChromatography LiquidJournal of separation science
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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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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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Thin-layer chromatography of 2-methyl-4-chlorophenoxyacetic acid and its soil metabolites

1980

Abstract The thin-layer chromatography of 2-methyl-4-chlorophenoxyacetic acid, 4-chloro- o -cresol and 3-methyl-5-chlorocatechol and their pentafluorobenzyl derivatives has been studied on silica gel as adsorbent with 19 solvent systems. The best separation of the individual components occurred with toluene-benzene-acetic acid (2:2:1). Chloroform-diethyl ether-toluene (1:1:1) was suitable for the group separation of the pentafluorobenzyl derivatives.

ChromatographyChemistrySilica gelHydrophilic interaction chromatographyOrganic ChemistryGeneral MedicineCresolBiochemistryHigh-performance liquid chromatographyThin-layer chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyAdsorptionmedicineChromatography columnmedicine.drugJournal of Chromatography A
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Porous fractal gels: secondary effects in SEC

1992

Abstract The fractal nature of porous silica gels, Spherosil XOA 200 and of a Lichrospher mixture, has been tested through size exclusion chromatography of polystyrene in pure and mixed eluents. Fractal parameters, D f and L , depend on eluent with D f values close to 2.0 for Spherosil and higher than 2.0 for Lichrospher. D f and L changes with eluent have been related to secondary separation effects and partition and adsorption contributions have been evaluated.

ChromatographyChemistrySize-exclusion chromatographyAnalytical chemistryCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsFractal naturechemistry.chemical_compoundAdsorptionFractalColumn chromatographyMaterials ChemistryCeramics and CompositesPartition (number theory)PolystyrenePorosityJournal of Non-Crystalline Solids
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Determination of triazines and organophosphorus pesticides in water samples using solid-phase extraction.

1991

Abstract Octadecyl (C 18 )-bonded porous silica was evaluated for the extraction of triazine and organophosphorus pesticides from natural water. The extraction results showed an effective performance when 1 l of water was passed through small glass columns containing 500 mg of 50–100-μm C 18 bonded porous silica. The absorbed compounds were removed with ethyl acetate, evaporated to 200 μl and determined by gas chromatography. The overall average recoveries were greater than 85% except for dimethoate and trichlorfon. Application of this procedure to the analysis of natural water samples gave results that agree well with those obtained by solvent extraction methods.

ChromatographyChromatography GasChemistryTriazinesOrganic ChemistryExtraction (chemistry)Ethyl acetateGeneral MedicineBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundAdsorptionOrganophosphorus CompoundslawFlame ionization detectorGas chromatographySolid phase extractionPesticidesDimethoateWater Pollutants ChemicalTriazineJournal of chromatography
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Effect of solute association on the apparent adsorption isotherm. A model of the separation of non-racemic mixtures of enantiomers in achiral chromat…

1996

This article discusses the effect of solute association on the apparent adsorption isotherm and on the chromatographic peak profile. The modelling performed has shown that dimerization of a solute in a chromatographic system gives rise to an apparent adsorption isotherm of the non-linear type. This results first of all in peak broadening. Tailing or a fronting can be observed depending on the relative retention of the monomer and the dimer. Secondly, the retention of the solute depends on the amount of sample because of the non-linear character of the adsorption isotherm. As a result, an excess of one of two analytes with absolutely identical adsorption properties i.e. optical isomers, can …

ChromatographyElutionDimerOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundMonomerAdsorptionchemistrySorption isothermEnantiomerEquilibrium constantChromatographia
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Solid-phase extraction of quaternary ammonium herbicides

2000

This paper highlights recent advances in the solid-phase extraction (SPE) of quaternary ammonium herbicides in water, soil, plant and biological samples. After a brief introduction summarizing the properties of quaternary ammonium herbicides and the difficulties involved in measuring them, attention is paid primarily to solid supports used for isolation and concentration, pre-treatments required for the different matrices, and eluents applied for quantitative desorption of these analytes. The determination techniques used after SPE and applications of the proposed SPE methodology are also briefly discussed.

ChromatographyEnvironmental analysisHerbicidesChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundAdsorptionDesorptionSample preparationTrace analysisAmmoniumSolid phase extractionChromatography LiquidJournal of Chromatography A
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Clay-biosurfactant materials as functional drug delivery systems: Slowing down effect in the in vitro release of cinnamic acid

2017

Abstract The main objectives of the present paper were the preparation and characterization of new surfactant-modified clays and the evaluation of their potential applicability as drug delivery systems for the oral administration of the cinnamic acid (CA) drug. The organoclays (OC) were prepared by loading different amounts of the biocompatible nonionic polyoxyethylene sorbitan monolaurate surfactant (Tween20) onto K10 montmorillonite (Mt) clay and characterized through the construction of the adsorption isotherms by means of the spectrophotometric method. The performance of the prepared material was verified by gathering the adsorption isotherms of the cinnamic acid onto the Mt/Tween20 org…

ChromatographyIntercalation (chemistry)020101 civil engineeringGeology02 engineering and technologyPharmaceutical formulation021001 nanoscience & nanotechnologyCinnamic acid0201 civil engineeringchemistry.chemical_compoundMontmorilloniteAdsorptionadsorptionHill isothermCinnammic acidMontmorillonitePolyoxyethylene sorbitan monolaurateTween 20Drug delivery systemsPulmonary surfactantchemistryGeochemistry and PetrologyDrug deliveryOrganoclay0210 nano-technologyNuclear chemistry
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