Search results for "Column chromatography"

showing 10 items of 143 documents

Chromatographic and mass spectrometric characterization of the structures of the polypeptide antibiotics samarosporin and stilbellin and identity wit…

1983

The structural identity of the polypeptide antibiotics, samarosporin I(II) and stilbellin I(II) with emerimicin IV(III) has been established by thin-layer chromatography, quantitative amino acid analysis by ion-exchange chromatography, gas-liquid chromatography of the N-pentafluoropropionyl amino acid n-propyl esters and N,O-bis-pentafluoropropionyl phenylalaninol with quartz capillaries coated with the chiral stationary phase N-propionyl-L-valine-tert-butylamide, and determination of the relative molecular masses and sequence-specific fragments by field desorption fast atom bombardment mass spectrometry. The separation of closely related sequence analogues of the above polypeptides could b…

chemistry.chemical_classificationAqueous solutionChromatographyChemistryOrganic ChemistryClinical BiochemistryPeptaibolFast atom bombardmentMass spectrometryBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundColumn chromatographyIsovalineMoleculeOrganic chemistryChromatographia
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Chromatography of metal chelates

1973

The chromatographic behavior of metal bis(ethoxyethyl)dithiocarbamate was investigated. The chelates of 14 elements (V, Cr, Co, Ni, Cu, Zn, Se, Mo, Cd, Te, Hg, Tl, Pb and Bi) could be preconcentrated from water with an on-line system and were shown to be suitable for C18-reversed-phase liquid chromatography. A quaternary solvent mixture with admixture of a surfactant was used as eluent, UV-detection was performed at 254 nm. Thermostating the column to 40° C resulted in a significant increase in chromatographic resolution and in a decrease of analysis time. The recovery of the chelates from the aqueous solutions as well as reproducibility of the results are very sensitive to pH changes.

chemistry.chemical_classificationAqueous solutionChromatographyResolution (mass spectrometry)Clinical BiochemistryGeneral MedicineBiochemistryAnalytical ChemistryMetalSolventColumn chromatographychemistryPulmonary surfactantvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceChelationDithiocarbamateFresenius' Zeitschrift f�r Analytische Chemie
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Life-time studies with capillary electrochromatography columns operated under different conditions.

2000

A test system has been established to permit the monitoring of the life-time performance of several reversed- phase capillary electrochromatography (CEC) columns. The retention factors, k(cec), peak symmetry coefficients, lambda(sym), and column efficiencies, N, of three neutral n-alkylbenzene analytes, namely ethyl-, n-butyl- and n-pentylbenzenes, were determined for Hypersil 3 microm n-octylsilica and n-octadecylsilica packed into CEC capillary columns of 100 microm I.D., with a packed length of 250 mm, and a total length of 335 mm. The performances of these CEC capillary columns were examined for a variety of eluents with pH values ranging between pH 2.0 - 8.0, similar to those employed …

chemistry.chemical_classificationCapillary electrochromatographyChromatographyCapillary actionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyHydrocarbonchemistryElectrochromatographyAlkylbenzenesTheoretical plateChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Capillary electrochromatography analysis of hormonal cyclic and linear peptides.

2001

The retention behavior of linear and cyclic peptides has been studied by capillary electrochromatography (CEC) with a variety of different n-alkyl silica reversed-phase sorbents and also with mixed-mode phases containing both strong cation-exchange (sulfonic acid) and n-alkyl groups bonded onto the silica surface, using eluents ranging from pH 2.0 to pH 5.0. Depending upon the amino acid sequence, electrochromatographic retention of the peptides was strongly affected by the composition of the eluent, its pH value, and the choice of sorbent packed into the capillaries. The dominant separation processes operating with these charged analytes could be modulated inter alia by the content of orga…

chemistry.chemical_classificationCapillary electrochromatographyChromatographySilicon dioxideSulfonic acidSilicon DioxidePeptides CyclicCyclic peptideHormonesAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyCapillary electrophoresischemistryElectrochromatographyAcetonitrileOligopeptidesChromatography Micellar Electrokinetic CapillaryAnalytical chemistry
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Solution properties of polyelectrolytes

1991

Abstract Chromatographic data for sodium polystyrene sulphonate were obtained on both silica- and polymer-based size-exclusion supports using mobile phases of various pH and ionic strength. Deviations of the elution volume were observed towards both lower and higher values relative to the reference calibration graph obtained with uncharged standards. An empirical correlation is proposed in order to account for all the secondary effects observed. The general applicability of this correlation was further tested for chromatographic data obtained for a series of peptides and proteins on a silica-based support under very different eluent conditions. Deviations from ideal elution behaviour such a…

chemistry.chemical_classificationChromatographyAqueous solutionCalibration curveChemistryElutionSodiumSize-exclusion chromatographyOrganic ChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicinePolymerBiochemistryPolyelectrolyteAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyIonic strengthSodium nitratePhase (matter)Ideal (ring theory)Sodium polystyrene sulphonateJournal of Chromatography A
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Separation of unmodified α-amino acid enantiomers by reverse phase HPLC

1980

A novel chiral phase system is presented for the resolution of unmodified α-amino acid racemates which is composed of a reverse phase packing coated with N-alkyl-L-hydroxyproline (where alkyl is n-C7H15-, n-C10H21- and n-C16H33-) and a hydro-organic eluent containing copper(II)acetate. The factors controlling retention and enantioselectivity such as concentration of Cu(II)ion and pH of the eluent, addition of NH4Ac to the eluent, type and content of organic solvent of hydro-organic eluent and column temperature were examined. The extremely high enantioselectivity observed (α up to 16) is assumed to be caused by a three site sorbate-sorbent interaction involving bidentate coordination of two…

chemistry.chemical_classificationChromatographyChemistryOrganic ChemistryClinical BiochemistryReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryAmino acidColumn chromatographySide chainEnantiomerSelectivityAlkylChromatographia
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Effect of the hydrophobic spacer in bonded [Cu(l-hydroxyprolyl)alkyl]+ silicas on retention and enantioselectivity of α-amino acids in high-performan…

1983

Abstract The following chiral ligands were bonded to silica: [Cu( l -hydroxyprolyl)methyl) + on LiChrosorb Si 60 (1), [Cu( l -hydroxyprolyl)methyl] + on LiChrosorb Si 100 (2) and [Cu( l -hydroxyprolyl) n -octyl] + on LiChrosorb Si 100 (3). The packings contained residual iodomethyl- and ω-iodooctyl groups at the surface. Studies on packing 1 and 2 under comparable conditions in eluents containing 10 -4 M copper acetate showed a higher retention on 1 than on 2 but a much better enantioselectivity in the latter case. The retention of enantiomers on all packings examined was found to be governed by the eluent pH and methanol content as well as by the concentration of ammonium acetate. The vari…

chemistry.chemical_classificationChromatographyChemistryOrganic Chemistrychemistry.chemical_elementGeneral MedicineBiochemistryHigh-performance liquid chromatographyCopperAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundColumn chromatographyMethanolEnantiomerAmmonium acetateAlkylJournal of Chromatography A
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Chiral separation of ephedrines by liquid chromatography using β-cyclodextrins

2001

β-cyclodextrins (β-CDs) have been evaluated as chiral recognition agents for the enantioseparation of ephedrines by liquid chromatography (LC). The compounds tested were norephedrine, ephedrine, pseudoephedrine, N-methylephedrine and N-methylpseuoephedrine. Two possibilities have been investigated, the employment of a chiral stationary phase consisting of immobilized β-cyclodextrin, and the addition of the chiral selector to the mobile phase. In the latter approach the following chiral agents have been assayed, native β-cyclodextrin (β-CD), methyl-β-cyclodextrin (M-β-CD), carboxyethyl-β-cyclodextrin (CE-β-CD), carboxymethyl-β-cyclodextrin (CM-β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD)…

chemistry.chemical_classificationChromatographyCyclodextrinBiochemistryAnalytical ChemistryNasal decongestantChiral column chromatographySolventchemistryIonic strengthmedicineEnvironmental ChemistryEphedrineEnantiomerChiral derivatizing agentSpectroscopymedicine.drugAnalytica Chimica Acta
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Separation of polycyclic aromatic hydrocarbons under isocratic conditions by a column switching technique

1994

A simple and efficient method of separating a 20-component PAH-mixture (RSM 1647 standard mixture +benzene, toluene, perylene and coronene) by RP-HPLC is described. Separation was by using two Superspher-100 RP-18 cartridges thermostatted at different temperatures under isocratic conditions with water-acetonitrile eluent. The analysis time with complete resolution of all components can be reduced to 15 min.

chemistry.chemical_classificationChromatographyOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryTolueneHigh-performance liquid chromatographyCoroneneAnalytical Chemistrychemistry.chemical_compoundCartridgeColumn chromatographyHydrocarbonchemistryBenzenePeryleneChromatographia
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Application of CEC procedures for the analysis of synthetic peptides: characterization of linear immunogenic peptides that mimic a HIV-1 gp120 epitope

2002

In this study, we describe the application of a new analytical procedure based on capillary electrochromatographic(CEC) techniques for the characterization of different basic and acidic peptides using isocratic eluent conditions containing acetonitrile and ammonium acetate buffers of different molarities between pH 3.8 and 5.2. In particular,10 immunogenic peptide analogs with isoelectric points ranging from 3.7 to 10.1 were investigated; nine of these peptides, 1-9, were truncated analogs of the parent peptide, 10, which is a peptidomimetic related to a HIV-1 gp120 epitope. Several of these peptides have the propensity to form alpha-helical secondary structures in solution. Electrochromato…

chemistry.chemical_classificationChromatographyPeptidomimeticElutionPeptideBiochemistrychemistry.chemical_compoundElectrophoresisEndocrinologyIsoelectric pointColumn chromatographychemistryPeptide synthesisAmmonium acetateThe Journal of Peptide Research
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