Search results for "Column chromatography"

showing 10 items of 143 documents

Assessment and optimization of system parameters in size exclusion separation of proteins on diol-modified silica columns

1981

Abstract On diol-modified silica columns the retention of proteins is governed by a size exclusion effect, but superimposed on this are some secondary effects, i.e. , ionic and diol-ligand interactions which can be controlled and adjusted reproducibly by varying the eluent composition. The eluent composition also affects the column efficiency and peak shape. Both dependences can be employed to obtain a better resolution of proteins than can be expected from size exclusion alone.

ChromatographyResolution (mass spectrometry)fungiOrganic ChemistrySize-exclusion chromatographyDiolAnalytical chemistryfood and beveragesIonic bondingGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistrySystem parametersJournal of Chromatography A
researchProduct

Hydrolytically stable chemically bonded silica supports with metal complexating ligands: Synthesis, characterization and use in high-performance liga…

1982

A silica of 14 nm pore size was reacted according to two procedures with the following silanes: γ-aminopropyltriethoxysilane (1), N-aminoethyl-N′-aminopropyltrimethoxysilane (2), N-aminoethyl-N′-aminoethyl-N″-aminopropyltrimethoxysilane (3), N-(3-triethoxysilanepropyl)-N, N-diacetic dimethylester (4), N-(3-trisodiumsilanolatepropyl)-N, N-diacetic acid disodium salt (5) and N-(3-trisodiumsilanolatepropyl)-ethylenediamine-N, N′, N′-triacetic acid trisodium salt (6). The reaction of silanes 1–4 with the silica was carried out under anhydrous conditions (procedure A). Silanes 1–6 were subjected to surface modification under essentially hydrous conditions applying a two-step procedure (procedure…

ChromatographySilanesChemistryLigandOrganic ChemistryClinical BiochemistryInorganic chemistrySorptionBiochemistrySilaneAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyIonic strengthAnhydrousSurface modificationChromatographia
researchProduct

Classification of vegetable oils according to their botanical origin using n-alkane profiles established by GC-MS.

2013

n-Alkane profiles established by gas chromatography-mass spectrometry (GC-MS) were used to classify vegetable oils according to their botanical origin. The n-alkanes present in corn, grapeseed, hazelnut, olive, peanut and sunflower oils were isolated by means of alkaline hydrolysis followed by silica gel column chromatography of the unsaponifiable fractions. The n-alkane fraction was constituted mainly of n-alkanes in the range C8-C35, although only those most abundant (15 n-alkanes, from 21 to 35 carbon No.) were used as original variables to construct linear discriminant analysis (LDA) models. Ratios of the peak areas selected by pairs were used as predictors. All the oils were correctly …

ChromatographySilica gelFraction (chemistry)General MedicineAlkaline hydrolysis (body disposal)SunflowerGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistryUnsaponifiableAlkanesPlant OilsGas chromatographyGas chromatography–mass spectrometryFood ScienceFood chemistry
researchProduct

Determination of benperidol and its reduced metabolite in human plasma by high-performance liquid chromatography and electrochemical detection.

1991

An isocratic high-performance liquid chromatographic method with electrochemical detection for the quantification of benperidol and its suggested reduced metabolite TVX Q 5402 in human plasma is described. The method included a two-step solid-phase extraction on reversed-phase and cation-exchange material, followed by separation on a cyanopropyl silica gel column (5 microns; 250 mm x 4.6 mm I.D.). The eluent was 0.15 M acetate buffer (pH 4.7) containing 25% acetonitrile (w/w). Spiperone served as internal standard. The inclusion of the cation-exchange step provided sample purity higher than those achieved with other methods. After extraction of 1 ml of plasma, concentrations as low as 0.5 n…

ChromatographySilica gelMetaboliteBenperidolExtraction (chemistry)General ChemistryHigh-performance liquid chromatographychemistry.chemical_compoundBenperidolColumn chromatographychemistryBlood plasmamedicineElectrochemistryHumansAcetonitrileChromatography High Pressure Liquidmedicine.drugJournal of chromatography
researchProduct

Thin-layer chromatography of chlorinated anisoles and veratroles

1989

The thin-layer chromatography of chlorinated anisoles (methoxybenzenes) and veratroles (1,2-dimethoxybenzenes) has been examined on silica gel G60 and RP-18 thin-layer plates. More than fifty solvent systems were screened and some of them recommended for particular separations. Acetone was shown to be suitable for group separation of both chlorinated anisoles and veratroles on a silica gel G60 stationary phase having a very narrow range of RF values. On the other hand, benzene, dichloromethane and the various mixtures of light petroleum (b.p. 40–60°C) and a more polar eluent (such as diethyl ether, acetone or ethyl acetate) were recommended for separation of certain individual isomers. The …

ChromatographySilica gelOrganic ChemistryClinical BiochemistryEthyl acetateReversed-phase chromatographyBiochemistryThin-layer chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistryAcetoneDiethyl etherDichloromethaneChromatographia
researchProduct

Determination of usnic and perlatolic acids and identification of olivetoric acids in Northern reindeer lichen (Cladonia stellaris) extracts

2010

AbstractThe ecologically important lichen Cladonia stellaris forms thick carpets in boreal forest floors. In addition to affecting temperature and water conditions in the soil underneath, the secondary metabolites formed by the lichen layer are of ecological interest. In this paper, we investigated the distribution of lichen acids in C. stellaris collected at different latitudes in Finland and developed methods to quantify the two optical enantiomers of usnic acid separately. The lichen extracts were analysed by high-performance liquid chromatography (HPLC) with UV and mass spectrometric (MS) detection and by gas chromatography with flame ionization (GC-FID) and MS detection. Usnic acid and…

ChromatographybiologyChemistryUsnic acidCladonia stellarisbiology.organism_classificationHigh-performance liquid chromatographyThallusChiral column chromatographychemistry.chemical_compoundBotanyGas chromatographyGas chromatography–mass spectrometryLichenEcology Evolution Behavior and SystematicsThe Lichenologist
researchProduct

Strong circularly polarized luminescence of an octahedral chromium(iii) complex

2019

The chiral spin-flip luminophore [Cr(ddpd)2]3+ can be resolved into enantiopure material by chiral HPLC. The corresponding enantiomers show very high luminescence dissymmetry factors of up to ∣glum ∣≈ 0.093 in circularly polarized luminescence (CPL) measurements for the "ruby-like" phosphorescence transition 2E/2T1 → 4A2 in the near-IR region around λ ≈ 775 nm.

ChromiumLuminescenceMaterials scienceLuminescent MeasurementsMolecular Conformationchemistry.chemical_element010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundChromiumCoordination ComplexesMaterials ChemistryDensity Functional Theory010405 organic chemistryMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChiral column chromatographyCrystallographyEnantiopure drugchemistryLuminescent MeasurementsCeramics and CompositesLuminophoreEnantiomerLuminescencePhosphorescenceChemical Communications
researchProduct

Reversed Phase Liquid Chromatography

2015

Countercurrent chromatographyChromatographyColumn chromatographyAqueous normal-phase chromatographyChemistryHydrophilic interaction chromatographySupercritical fluid chromatographyAnalytical chemistryReversed-phase chromatographyChromatography columnHigh-performance liquid chromatography
researchProduct

Novel σ1 antagonists designed for tumor therapy: Structure – activity relationships of aminoethyl substituted cyclohexanes

2021

Abstract Depending on the substitution pattern and stereochemistry, 1,3-dioxanes 1 with an aminoethyl moiety in 4-position represent potent σ1 receptor antagonists. In order to increase the stability, a cyclohexane ring first replaced the acetalic 1, 3-dioxane ring of 1. A large set of aminoethyl substituted cyclohexane derivatives was prepared in a six-step synthesis. All enantiomers and diastereomers were separated by chiral HPLC at the stage of the primary alcohol 7, and their absolute configuration was determined by CD spectroscopy. Neither the relative nor the absolute configuration had a large impact on the σ1 affinity. The highest σ1 affinity was found for cis-configured benzylamines…

DU145 tumor cellsCachannelPrimary alcohol01 natural sciencesAminoethylcyclohexanes; Antagonistic activity; Biotransformation; Ca; 2+; influx assay; Calculated free energy of binding; CD spectroscopy; Chiral HPLC; DU145 tumor cells; Inhibition of human prostate tumor cell growth; Lipophilicity; Molecular dynamics simulations; Molecular interactions; per-residue binding free energy; Selectivity; Stereochemistry; Structure affinity relationships; Voltage gated Ca; 2+; channel; σ receptors; σ; 1; receptor affinityInhibition of human prostate tumor cell growthStereochemistryDrug DiscoveryMoietySelectivityBiotransformationσ receptor0303 health sciencesChemistryAminoethylcyclohexanesCD spectroscopyAbsolute configurationAminoethylcyclohexaneMolecular interactionGeneral MedicineAntagonistic activityper-residue binding free energyreceptor affinityLipophilicityVoltage gated CaStereochemistry12+Calculated free energy of bindingRetinal ganglion03 medical and health sciencesσMolecular dynamics simulationChiral HPLCLipophilicityMolecular interactionsStructure affinity relationship030304 developmental biologyPharmacologyDU145 tumor cellinflux assayMolecular dynamics simulations010405 organic chemistryOrganic ChemistryDiastereomer0104 chemical sciencesChiral column chromatographyσ receptorsStructure affinity relationshipsEnantiomerEuropean Journal of Medicinal Chemistry
researchProduct

Separation of monoacylglycerols by reversed-phase high-performance liquid chromatography

1992

Abstract Reversed-phase high-performance liquid chromatography on a thermostated octadecylsilyl column was used to separate complex mixtures of monoacyglycerols formed by chemical deacylation of natural triacyclycerols. Acetonitrile-water mixtures were used for elution of the underivatized monoacylglycerols and a different refractometer was used for their detection. The order of elution of monoacylglycerols in complex mixtures varies as a function of the chain length, unsaturation, positional isomerism, analysis temperature and eluent water concentration. The peak areas were representative of the amounts of monoacylglycerols detected. The method can be applied to compositional analysis and …

Degree of unsaturationChromatographyElutionOrganic ChemistryAnalytical chemistryGeneral MedicineReversed-phase chromatographyMonoglycerideBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistryPhase (matter)DerivatizationJournal of Chromatography A
researchProduct