Search results for "Reversed-phase chromatography"

showing 10 items of 187 documents

High-performance liquid chromatographic determination of Maillard compounds in store-brand and name-brand ultra-high-temperature-treated cows' milk.

2000

Furosine and furfural products of the Maillard reaction are used as specific indicators of the effect of heating treatments on milk quality. Their contents were measured in representative samples of store- and name-brand ultra-high-temperature-treated milks using RP-HPLC with UV detection. Furosine contents ranged from 40.32 to 50.67 and from 65.48 to 310.58 mg/100 g protein in name- and store-brand milks, respectively. Of the furfurals, only hydroxymethylfurfural was detected. The free hydroxymethylfurfural contents of store-brand milks ranged from 0.22 to 1.70 mg/100 g protein. Total hydroxymethylfurfural contents ranged from 0.29 to 0.41 and from 0.72 to 2.21 mg/100 g protein, for name- …

ChromatographyHot TemperatureOrganic ChemistryFood composition dataGeneral MedicineReversed-phase chromatographyFurfuralBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMaillard Reactionchemistry.chemical_compoundMaillard reactionsymbols.namesakeMilkchemistrysymbolsAnimalsCattleSpectrophotometry UltravioletUv detectionQuantitative analysis (chemistry)HydroxymethylfurfuralChromatography High Pressure LiquidJournal of chromatography. A
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Determination of hydroquinone and metal in photographic developer by reversed-phase ion-pair chromatography with amperometric detection

1988

Abstract Sodium 1-heptanesulphonate is used as an ion-pair reagent for the chromatographic separation of the two developing agents on a phenylsilica micro-column, with amperometric detection at an applied potential of + 0.75 V (vs. Ag/AgCl). No pretreatment of the developer is necessary. Linear calibration graphs were obtained in the range 10 −5 -1.5 × 10 −4 M.

ChromatographyHydroquinoneChemistrySodiumIon chromatographychemistry.chemical_elementReversed-phase chromatographyBiochemistryAmperometryPhotographic developerAnalytical ChemistryMetalchemistry.chemical_compoundvisual_artReagentvisual_art.visual_art_mediumEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Error analysis and performance of different retention models in the transference of data from/to isocratic/gradient elution.

2003

The transferability of retention data among isocratic and gradient RPLC elution modes is studied. For this purpose, 16 beta-blockers were chromatographed under both isocratic and gradient elution with acetonitrile-water mobile phases. Taking into account the elution mode where the experimental data come from, and the mode where the retention should be predicted, the following combinations are possible: isocratic predictions from (i) isocratic or (ii) gradient experimental designs; and gradient predictions from (iii) isocratic or (iv) gradient data. Each of these possibilities was checked using three retention models that relate the logarithm of the retention factor: (a) linearly and (b) qua…

ChromatographyLogarithmChemistryElutionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)Phase (matter)Volume fractionConfidence IntervalsGradient elutionChromatography LiquidJournal of chromatography. A
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Micellar Liquid Chromatography: Method Development and Applications

2015

ChromatographyMicellar liquid chromatographyChemistryReversed-phase chromatographyMethod development
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Interpretive optimisation of organic solvent content and flow-rate in the separation of β-blockers with a Chromolith RP-18e column

2009

The chromatographic performance of a Chromolith RP-18e column was comprehensively examined for a group of basic drugs (beta-blockers), eluted with isocratic ACN-water mixtures at increasing flow-rate up to 6 mL/min. As the flow-rate increases at fixed mobile phase composition, peak distribution (selectivity) is maintained, but the relative peak widths increase. This reduces the resolution below satisfactory values for closely eluting compounds. With the monolithic column, flow-rate becomes thus an important factor to be optimised, in addition to the mobile phase composition. Since, theoretically, retention factors (k) are independent of the flow-rate, the classical quadratic model relating …

ChromatographyMonolithic HPLC columnResolution (mass spectrometry)ChemistryElutionAdrenergic beta-AntagonistsAnalytical chemistryFiltration and SeparationReversed-phase chromatographyHigh-performance liquid chromatographyAnalytical ChemistryVolumetric flow rateSolventModels ChemicalSolventsOrganic ChemicalsSelectivityChromatography High Pressure LiquidJournal of Separation Science
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Impact of pore structural parameters on column performance and resolution of reversed-phase monolithic silica columns for peptides and proteins

2007

In this work, monolithic silica columns with the C4, C8, and C18 chemistry and having various macropore diameters and two different mesopore diameters are studied to access the differences in the column efficiency under isocratic elution conditions and the resolution of selected peptide pairs under reversed-phase gradient elution conditions for the separation of peptides and proteins. The columns with the pore structural characteristics that provided the most efficient separations are then employed to optimize the conditions of a gradient separation of a model mixture of peptides and proteins based on surface chemistry, gradient time, volumetric flow rate, and acetonitrile concentration. Bo…

ChromatographyMonolithic HPLC columnSilicon dioxideElutionOrganic ChemistryAnalytical chemistryProteinsReproducibility of ResultsGeneral MedicineReversed-phase chromatographySilicon DioxideBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryVolumetric flow ratechemistry.chemical_compoundchemistryPhase (matter)PeptidesMesoporous materialPorosityChromatography LiquidJournal of Chromatography A
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Quantitative retention–structure and retention–activity relationships of barbiturates by micellar liquid chromatography

1998

Abstract Studies on the structural requirements of chromatographic surfaces to emulate in vitro the partitioning process in biomembranes are of great interest. The use of micellar mobile phases in RPLC modifies the hydrophobicity of the stationary phase and provides hydrophobic and electrostatic sites of interaction as a consequence of the adsorption of surfactant monomers to the chromatographic surface. Modified stationary phases in MLC could be structurally similar to biomembranes, but thorough studies are necessary to confirm this. In this paper we focus our attention on barbiturates. The influence of the nature and concentration of the surfactant (Brij 35, SDS and CTAB) and the mobile p…

ChromatographyOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundAdsorptionMonomerPulmonary surfactantchemistryStationary phaseMicellar liquid chromatographyPhase (matter)Journal of Chromatography A
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Limits of multi-linear gradient optimisation in reversed-phase liquid chromatography

2005

Abstract The concept of limiting peak purity was applied to quantify the degree of completion of the separation capability of a chromatographic system using multi-linear gradients. The objective was to check whether the complexity of a gradient program deserves be increased to enhance resolution by inserting more linear segments, or on the contrary, no significant improvements can be expected under more complex gradients. A set of 19 isoindole derivatives of primary amino acids was selected to test the performance of isocratic, single linear and multi-linear gradients. Accurate simulated chromatograms were obtained via numerical integration of the general equation of gradient elution, using…

ChromatographyResolution (mass spectrometry)ChemistryElutionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryNumerical integrationChemometricschemistry.chemical_compoundDerivatizationChromatography LiquidSpectral purityJournal of Chromatography A
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Models and objective functions for the optimisation of selectivity in reversed-phase liquid chromatography.

2006

Interpretive methodologies are the most efficient tools for finding the optimal conditions in chromatography. These methodologies are supported by models or algorithms able to infer the system behaviour upon changes in the experimental factors. Once the models are built with data obtained from sets of carefully designed experiments, molecular modelling or other approaches, they can be applied to predict the performance of new conditions. The different elements involved in these methodologies, for both isocratic and gradient elution, are given. Special attention is devoted to the description of retention, owing to its major impact on the prediction of chromatographic resolution. Several mode…

ChromatographyResolution (mass spectrometry)ElutionChemistryEnvironmental ChemistryGradient elutionReversed-phase chromatographyBiological systemBiochemistrySpectroscopyAnalytical ChemistryAnalytica chimica acta
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Reversed-phase high-performance liquid chromatography of proteins and polypeptides on polystyrene-coated silica supports

1990

Abstract A new type of hydrolytically stable reversed-phase packing material prepared by multi-point covalent binding of polystyrene chains onto the surface of porous silica was examined in the high-performance liquid chromatography of proteins and polypeptides. Whereas wide-pore material was shown to give a rapid and efficient resolution of proteins, packings with smaller pores provided better selectivities for peptides.

ChromatographyResolution (mass spectrometry)Organic ChemistryCovalent bindingGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)PolystyrenePorositySelectivityJournal of Chromatography A
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