Search results for "capillary electrophoresis"

showing 10 items of 131 documents

Capillary electrophoretic and nuclear magnetic resonance studies of interactions between halophenols and ionic liquid or tetraalkylammonium cations.

2003

Aqueous capillary electrophoretic studies were performed to investigate interactions between halophenols and 1-ethyl-3-methylimidazolium tetrafluoroborate or tetraethylammonium tetrafluoroborate electrolytes. In both cases, increased halogen size correlated with increased affinity for the electrolyte cation. For isomers, the ortho substituted isomer exhibited higher affinity than the para isomer. Irreproducible CE results for analyte pairs in the presence of the ionic liquid stimulated investigations of the interactions between halophenols as well as with the cations of the electrolyte. These interactions were explored by proton and fluorine one-dimensional NMR. The NMR results indicated di…

TetraethylammoniumAqueous solutionChromatographyTetrafluoroborateMagnetic Resonance SpectroscopyChemistryOrganic ChemistryElectrophoresis CapillaryGeneral MedicineNuclear magnetic resonance spectroscopyElectrolyteBiochemistryAnalytical ChemistryHydrophobic effectQuaternary Ammonium Compoundschemistry.chemical_compoundCapillary electrophoresisHalogensPhenolsCationsIonic liquidJournal of chromatography. A
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Enantioseparation of nuarimol by affinity electrokinetic chromatography-partial filling technique using human serum albumin as chiral selector

2008

The present paper deals with the enantiomeric separation of nuarimol enantiomers by affinity EKC-partial filling technique using HSA as chiral selector. Firstly, a study of nuarimol interactions with HSA by CE-frontal analysis was performed. The binding parameters obtained for the first site of interaction were n(1) = 0.84; K(1) = 9.7 +/- 0.3x10(3 )M(-1) and the protein binding percentage of nuarimol at physiological concentration of HSA was 75.2 +/- 0.2%. Due to the moderate affinity of nuarimol towards HSA the possibility of using this protein as chiral selector for the separation of nuarimol using the partial filling technique was evaluated. A multivariate optimization approach of the mo…

TrisResolution (mass spectrometry)Analytical chemistryFiltration and SeparationChromatography AffinityAnalytical ChemistryChemometricschemistry.chemical_compoundCapillary electrophoresismedicineAnimalsHumansSerum AlbuminChromatographyMolecular StructureReproducibility of ResultsStereoisomerismHuman serum albuminbody regionsElectrophoresisPyrimidineschemistryFemaleEnantiomerQuantitative analysis (chemistry)Softwaremedicine.drugJournal of Separation Science
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Capillary Electrophoresis of Free Fatty Acids by Indirect Ultraviolet Detection: Application to the Classification of Vegetable Oils According to The…

2011

A method for the determination of fatty acids in vegetable oils by capillary electrophoresis with indirect UV–vis detection has been developed. The separation of fatty acids was optimized in terms of Brij surfactant nature and concentration and organic modifier (2-propanol) percentage. The optimal background electrolyte consisted of 10 mM p-hydroxybenzoate, 5 mM Tris at pH 8.8, 80 mM Brij 98, 40% acetonitrile, and 10% 2-propanol. Under these conditions, vegetable oils from five botanical origins (avocado, corn, extra virgin olive, hazelnut, and soybean) were analyzed and the fatty acid contents established. Linear discriminant analysis (LDA) models were constructed using fatty acid peak are…

Trischemistry.chemical_classificationChromatographyResolution (mass spectrometry)ChemistryElectrophoresis CapillaryFatty acidGeneral ChemistryFatty Acids Nonesterifiedmedicine.disease_causePolyethylene Glycols2-Propanolchemistry.chemical_compoundCapillary electrophoresisPulmonary surfactantmedicinePlant OilsGeneral Agricultural and Biological SciencesAcetonitrileUltravioletJournal of Agricultural and Food Chemistry
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Synthesis of spherical porous silicas in the micron and submicron size range: challenges and opportunities for miniaturized high-resolution chromatog…

2000

Classical silica technology has reached its limit with respect to an ultimate minimum particle size of about 2 microm in diameter. Here, a novel process is presented which allows one to synthesize porous silica beads and control their particle diameter in situ, within the range of 0.2-2.0 microm. As a result, no sizing is required and losses of silica are avoided. Furthermore, the process enables one to control in situ the pore structural parameters and the surface chemistry of the silica beads. Even though surface funtionalized silicas made according to this process can principally be applied in fast HPLC the column pressure drop will be high even for short columns. In addition, the column…

Van Deemter equationCapillary electrochromatographyChromatographySilica gelOrganic ChemistryAnalytical chemistryGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundElectrokinetic phenomenaCapillary electrophoresisElectrochromatographychemistryParticle sizeTheoretical plateParticle SizeChromatography LiquidChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Application of capillary electrophoresis-mass spectrometry for determining organic food contaminants and residues.

2008

Food contamination continues to be a serious problem around the world. Surveillance of chemical contaminants in foods is important not only for public health but also because of the negative economic impact of contamination. From the analytical perspective, analysis of contaminants in food is an extremely challenging area. There is a wide variety of questions, ranging from the quantification of extremely low levels of individual components to the detailed assessment and evaluation of the analytical technique possibilities. This review considers the applications of CE coupled to MS detection (CE-MS) for the analysis of organic contaminants in food. Analytical information on sample concentrat…

Waste managementPesticide residuebusiness.industryChemistryFood HandlingClinical BiochemistryAnalytical techniqueSolid Phase ExtractionPesticide ResiduesElectrophoresis CapillaryFood ContaminationPesticideContaminationBiochemistryCapillary electrophoresis–mass spectrometryDrug ResiduesMass SpectrometryAnalytical ChemistryEnvironmental chemistryChemical contaminantsFood processingOrganic ChemicalsbusinessWater Pollutants ChemicalFood contaminantElectrophoresis
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Determination of cow’s milk in non-bovine and mixed cheeses by capillary electrophoresis of whey proteins in acidic isoelectric buffers

2000

An improved method for the determination of cow's milk in non-bovine cheese is reported: electrophoresis of whey proteins in acidic, isoelectric buffers. Two background electrolytes (BGEs) have been tested: (i) 50 mM iminodiacetic acid (pH=isoelectric point=2.30 at 25 degrees C), 0.5% hydroxyethylcellulose, 0.1% Tween 20 and 6 M urea (apparent pH 3.1), E=300 V/cm, for the separation of alpha-lactalbumins (alpha-LAs); (ii) a BGE with the same composition, but supplemented with 10% Tween 20, E=450 V/cm, for the fractionation of beta-lactoglobulins (beta-LGs). Surfactants have a discriminating effect on the retention behaviour of the bovine alpha-LA and beta-LG proteins, owing to the different…

Whey proteinCheese ripeningFractionationBuffersSensitivity and SpecificityBiochemistryAnalytical ChemistryCapillary electrophoresisCheeseCaseinAnimalsFood scienceBeta-lactoglobulinSheepChromatographybiologyChemistryGoatsOrganic ChemistryElectrophoresis Capillaryfood and beveragesGeneral MedicineMilk ProteinsMilkWhey ProteinsIsoelectric pointbiology.proteinAlpha-lactalbuminCattleIsoelectric FocusingJournal of Chromatography A
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Enantiodifferentiation of N-benzyloxycarbonylaminophosphonic and phosphinic acids and their esters using cyclodextrins by means of capillary electrop…

2005

Capillary electrophoresis was successfully applied for separation of the enantiomers of N-benzyloxycarbonyl-alpha-aminophosphonic and alpha-aminophosphinic acids as well as their ethyl and phenyl monoesters with the use of a range of commercially available cyclodextrins (alpha, beta and hydroxypropyl-gamma-cyclodextrins) as chiral selectors. The dependence of effectiveness of separation on type and concentration of these chiral selectors as well as on pH of background electrolyte was examined in some detail.

aminophosphinatesaminophosphonatesOrganophosphonatescapillary electrophoresisElectrolyteBiochemistryAnalytical ChemistryInclusion compoundchemistry.chemical_compoundCapillary electrophoresisOrganic chemistrychemistry.chemical_classificationChromatographycyclodextrinsMolecular StructureCyclodextrinChemistryOrganic ChemistryenantiodiscriminationElectrophoresis CapillaryReproducibility of ResultsEstersStereoisomerismGeneral MedicineHydrogen-Ion ConcentrationPhosphinic AcidsPhosphinic AcidsPhase compositionEnantiomerJournal of Chromatography A
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Separation of aminoalkanephosphonic acid enantiomers by indirect UV detection capillary electrophoresis with application of cyclodextrins.

2003

Indirect UV detection capillary electrophoresis (CE) was used for the separation of aminoalkanephosphonic acid (AP) enantiomers by applying commercially available cyclodextrins as chiral discriminators. The results show that the separation of the enantiomers depends on pH of the background electrolyte, the molar ratio of cyclodextrin to aminophosphonic acid, and on the type of the applied chiral selector. Optimization of process conditions allowed enantiomeric baseline separation or partial separation of 12 out of 14 alpha-aminophosphonic acids studied. This type of CE might therefore be successfully used for routine determination of enantiomeric purity of aminophosphonic acids.

aminophosphonic acidsClinical Biochemistrycapillary electrophoresisOrganophosphonatesElectrolyteBiochemistryindirect UV detectionAnalytical ChemistryCapillary electrophoresisMolar ratiopolycyclic compoundsheterocyclic compoundsAmineschemistry.chemical_classificationCyclodextrinsChromatographyCyclodextrinorganic chemicalsElectrophoresis CapillaryStereoisomerismHydrogen-Ion ConcentrationProcess conditionschemistrycyclodextrinUv detectionEnantiomerenantiomer separationElectrophoresis
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Introduction to MIP synthesis, characteristics and analytical application

2019

Abstract One of the trends in analytical chemistry is associated with designing and developing new types of sample preparation techniques, which might significantly increase the efficiency and selectivity of the analytes isolation or/and preconcentration process. One of the most widely employed solutions is selective sorption materials, defined as molecularly imprinted polymers (MIPs), as well as the sorbents with the molecular fingerprint. Due to their simple preparation protocol, mechanical, thermal and chemical stability and selectivity, MIPs have found application as a stationary phase in separation techniques such as liquid chromatography or capillary electrophoresis, in electrochemica…

chemistry.chemical_classificationAnalyteMaterials scienceChromatographyCapillary electrophoresischemistryExtraction (chemistry)Molecularly imprinted polymerSorptionSample preparationChemical stabilityPolymer
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Speciation of the oxidation states of plutonium in aqueous solutions by UV/Vis spectroscopy, CE-ICP-MS and CE-RIMS

2007

For the speciation of the plutonium oxidation states in aqueous solutions, the online coupling of capillary electrophoresis (CE) with inductively coupled plasma mass spectrometry (ICP-MS) has been developed. Depending on the radius/electrical charge ratio, the oxidation states III, IV, V, and VI of plutonium are separated by CE, based on the different migration times through the capillary and are detected by ICP-MS. The detection limit is 20 ppb,i.e.109–1010atoms (10-12–10-13g) for one oxidation state with an uncertainty of the reproducibility of the migration times of ≤1% and ≤5% for the peak area. The redox kinetics of the different plutonium oxidation states in the presence of humic subs…

chemistry.chemical_classificationAqueous solutionInorganic chemistryAnalytical chemistrychemistry.chemical_elementMass spectrometryRedoxPlutoniumCapillary electrophoresischemistryOxidation stateHumic acidPhysical and Theoretical ChemistryInductively coupled plasma mass spectrometryRadiochimica Acta
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