Search results for "performance liquid chromatography"

showing 10 items of 649 documents

Detection of lactobacillic acid in low erucic rapeseed oil--A note of caution when quantifying cyclic fatty acid monomers in vegetable oils.

2010

International audience; The purpose of this work was to identify an unknown component which has been detected during the analysis of cyclic fatty acid monomers (CFAMs) in low erucic acid rapeseed oils (LEAR). A sample of crude LEAR was transformed into fatty acid methyl esters (FAMEs) and hydrogenated using PtO2. The hydrogenated sample was fractionated by reversed-phase high-performance liquid chromatography (RP-HPLC) and the fraction containing the CFAMs transformed into picolinyl esters. Analysing these picolinyl derivatives by gas-liquid chromatography coupled to mass spectrometry (GC-MS) showed that the unknown product observed in LEAR is the 11,12-methylene-octadecanoic acid. This cyc…

RapeseedFraction (chemistry)Mass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyGas Chromatography-Mass SpectrometryTHERMAL DEGRADATIONFatty Acids Monounsaturated03 medical and health scienceschemistry.chemical_compoundLOW ERUCIC ACID RAPESEED OIL[SDV.IDA]Life Sciences [q-bio]/Food engineering1112-METHYLENE-OCTADECANOIC ACIDOrganic chemistryPlant Oils[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringMolecular Biology030304 developmental biologychemistry.chemical_classification0303 health sciencesChromatographyChemistryCYCLIC FATTY ACID MONOMERS010401 analytical chemistryOrganic ChemistryFatty AcidsFatty acidMASS-SPECTROMETRYCell BiologySunflower0104 chemical sciencesErucic acidRapeseed OilQuantitative analysis (chemistry)Chemistry and physics of lipids
researchProduct

Efficient flow injection and sequential injection methods for spectrophotometric determination of oxybenzone in sunscreens based on reaction with Ni(…

2001

Spectrophotometric determination of a widely used UV-filter, such as oxybenzone, is proposed. The method is based on the complexation reaction between oxybenzone and Ni(II) in ammoniacal medium. The stoichiometry of the reaction, established by the Job method, was 1:1. Reaction conditions were studied and the experimental parameters were optimized, for both flow injection (FI) and sequential injection (SI) determinations, with comparative purposes. Sunscreen formulations containing oxybenzone were analyzed by the proposed methods and results compared with those obtained by HPLC. Data show that both FI and SI procedures provide accurate and precise results. The ruggedness, sensitivity and LO…

Reaction conditionsChromatographymedicine.diagnostic_testColor reactionAnalytical chemistryBiochemistryHigh-performance liquid chromatographySensitivity and Specificitychemistry.chemical_compoundSequential injectionBenzophenoneschemistryAmmoniaNickelSpectrophotometrySpectrophotometrymedicineIndicators and ReagentsOxybenzoneQuantitative analysis (chemistry)Sunscreening AgentsStoichiometryChromatography High Pressure LiquidFresenius' journal of analytical chemistry
researchProduct

Determination of acetazolamide in human urine samples by reversed-phase high-performance liquid chromatography in the presence of xanthines.

1992

A simple, rapid and selective high-performance liquid chromatographic assay for the determination of acetazolamide in urine samples is described. After extraction with ethyl acetate, the drug is chromatographed on an HP-Hypersil ODS-C18 column with a mobile phase of acetonitrile-phosphate buffer (pH 3) and ultraviolet detection at 275 nm. The efficiency of the extraction, the linearity and the reproducibility of the method permit the evaluation of acetazolamide urinary excretion a long time after its administration.

ReproducibilityChromatographyChemistryExtraction (chemistry)Ethyl acetateGeneral ChemistryReversed-phase chromatographyUrineHigh-performance liquid chromatographyAcetazolamidechemistry.chemical_compoundXanthinesmedicineHumansAcetazolamideDrug ContaminationQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography
researchProduct

Use of triacylglycerol profiles established by high performance liquid chromatography with ultraviolet–visible detection to predict the botanical ori…

2011

A method for the determination of triacylglycerols (TAGs) in vegetable oils from different botanical origins by HPLC with UV–vis detection has been developed. Using a core-shell particle packed column (C18, 2.6 micron), TAG separation was optimized in terms of mobile phase composition and column temperature. Using isocratic elution with acetonitrile/n-pentanol at 10 °C, excellent efficiency with good resolution between most of the TAG peak pairs, within a total analysis time of 15 min, was achieved. Using mass spectrometry detection, a total of 15 peaks, which were common to oils of six different botanical origins (corn, extra virgin olive, grapeseed, hazelnut, peanut and soybean) were iden…

Resolution (mass spectrometry)Analytical chemistrymedicine.disease_causeMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySpectrophotometrymedicinePlant OilsChromatography High Pressure LiquidTriglyceridesPacked bedBOTANICAL ORIGINIsocratic elutionChromatographymedicine.diagnostic_testChemistryOrganic ChemistryDiscriminant Analysisfood and beveragesGeneral MedicineTRIACYLGLYCEROLSLINEAR DISCRIMINANT ANALYSISPhase compositionSpectrophotometry UltravioletHPLCVEGETABLE OILSUltravioletJournal of Chromatography A
researchProduct

High pressure liquid chromatography resolution of racemic mixtures of chiral tricarbonyl arene chromium(0) and cyclopentadienyl-titanium(IV) complexes

1998

Abstract Enantiomers of chiral tricarbonyl arene chromium(0) and cyclopentadienyl-titanium(IV) complexes have been separated by high pressure liquid chromatography employing a Chiralcel OD (Daicel) column, eluting with hexane/2-propanol mixtures. The capacity factors ( k ) and selectivity factors ( α ) concerning the separation of these compounds have been determined. The resolution of tricarbonyl( η 6 -methyl o -acetylbenzoate)chromium ( IV ), was carried out on semipreparative scale: a comparison of the CD spectra of the enantiomers IVa and IVb with that reported in the literature for a similar complex allowed to establish the absolute configuration [( 1R )] for the most retained enantiom…

Resolution (mass spectrometry)ChemistryAbsolute configurationchemistry.chemical_elementMedicinal chemistryHigh-performance liquid chromatographyInorganic ChemistryHexanechemistry.chemical_compoundChromiumCyclopentadienyl complexMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryEnantiomerSelectivityInorganica Chimica Acta
researchProduct

Optimization of a LC method for the enantioseparation of a non-competitive glutamate receptor antagonist, by experimental design methodology

2006

Abstract The aim of this work was to obtain the direct optical resolution of a new glutamate receptor antagonist (( p -chloro)1-aryl-6,7,-dimethoxy-1,2,3,4-tetrahydroisoquinoline, PS3), by liquid chromatography on Chiralcel ® OD column. A response surface methodology (RSM) was employed to optimize the enantiomeric separation of the racemate with the lowest number of experiments; in particular, a face-centred design (FCD) was applied to evaluate the influence of critical parameters on the experimental response. Furthermore, in order to find the best compromise between several responses, a multicriteria decision-making approach, the Derringer's desirability function, was successful to simulta…

Resolution (mass spectrometry)Clinical BiochemistryAnalytical chemistryPharmaceutical ScienceChiral liquid chromatography Enantioresolution Chiralcel® OD Tetrahydroisoquinoline derivative Face-centred design Desirability functionHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundTetrahydroisoquinolinesDrug DiscoveryGlutamate receptor antagonistResponse surface methodologySpectroscopyChiral liquid chromatographyChromatographyMolecular StructureAntagonistChiralcel® ODStereoisomerismTetrahydroisoquinoline derivativeDesirability functionFace-centred designHexanechemistryModels ChemicalDesirability functionEnantiomerEnantioresolutionExcitatory Amino Acid AntagonistsChromatography Liquid
researchProduct

Characterization of the alcoholic fraction of vegetable oils by derivatization with diphenic anhydride followed by high-performance liquid chromatogr…

2008

Abstract Aliphatic and triterpene alcohols present in vegetable oils have been identified and determined by HPLC using UV–vis and MS detection after previous derivatization with diphenic anhydride. The alcoholic fraction was obtained by saponification, extraction and TLC (according to the European Union official procedure). Derivatization was performed in tetrahydrofuran in the presence of suspended grinded urea, which increases the reaction rate and yield. Derivatized extracts were chromatographed on a C8 column using gradient elution with acetonitrile/water mixtures containing 0.1% acetic acid, with UV–vis followed by negative-ion mode MS detection. Using linear discriminant analysis of t…

Resolution (mass spectrometry)Fraction (chemistry)Chemical FractionationSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryAcetic acidchemistry.chemical_compoundPlant Oilsmedia_common.cataloged_instanceEuropean unionDerivatizationChromatography High Pressure Liquidmedia_commonChromatographyEsterificationOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineModels ChemicalchemistryAlcoholsMultivariate AnalysisDibenzoxepinsSaponificationJournal of Chromatography A
researchProduct

Comparative modelling study on enantioresolution of structurally unrelated compounds with amylose-based chiral stationary phases in reversed phase li…

2020

[EN] Polysaccharide-based chiral stationary phases (CSPs) are the most used chiral selectors in HPLC. These CSPs can be used in normal, polar organic and aqueous-organic mobile phases. However, normal and polar organic mobile phases are not adequate for chiral separation of polar compounds, for the analysis of aqueous samples and for MS detection. In these situations, reversed phase conditions, without the usual non-volatile additives incompatible with MS detection, are preferable. Moreover, in most of the reported chiral chromatographic methods, retention is too large for routine work. In this paper, the chiral separation of 53 structurally unrelated compounds is studied using three commer…

Resolution (mass spectrometry)Reversed phase liquid hromatography010402 general chemistryMass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyAmylose-based chiral stationary phasesMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundAmylosePhase (matter)Least-Squares AnalysisAcetonitrileEnantioresolution modelling and descriptionChromatography High Pressure LiquidChromatography Reverse-PhaseAqueous solutionChromatography010401 analytical chemistryOrganic ChemistryDiscriminant partial least squaresStereoisomerismGeneral MedicineReversed-phase chromatography0104 chemical sciencesModels ChemicalchemistryFeature selectionRegression AnalysisAmyloseJournal of Chromatography A
researchProduct

Determination of liposoluble vitamins in cooked meals, milk and milk products by liquid chromatography

2002

A method for the simultaneous determination of liposoluble vitamins in cooked meals was established. Saponification was performed with 50% (w/v) KOH at 80 degrees C, and ascorbic acid was added as antioxidant. The subsequent extraction was carried out with diethyl ether. This was followed by a liquid chromatographic separation on a reversed-phase C18 column with methanol-water (94:6, v/v as the mobile phase. Retinyl acetate was used as the internal standard. The analytical parameters linearity, detection limit (0.19 and 8.33 microg/100 g for retinol and alpha-tocopherol, respectively), precision of the method (RSD=5.24 and 6.99% for retinol and alpha-tocopherol, respectively) and recovery a…

Retinyl acetateSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundAnimalsDetection limitChromatographyOrganic ChemistryExtraction (chemistry)RetinolReproducibility of Resultsfood and beveragesVitaminsGeneral MedicineAscorbic acidLipidsMilkSolubilitychemistrySpectrophotometry UltravioletDairy ProductsDiethyl etherSaponificationChromatography LiquidJournal of Chromatography A
researchProduct

Determination of total ribonucleotide pool in plant materials by high-pH anion-exchange high-performance liquid chromatography following extraction w…

2005

A new, improved method that only requires a potassium hydroxide extraction procedure is presented for the analysis of a full nucleotide pool in plant materials. Quantification was performed by high-pH anion-exchange chromatography (HPAEC) with UV detection after a potassium hydroxide extraction, and allowed the quantification of 13 linear ribonucleotides in a single run. The method has been validated by comparison of six extraction methods and also by measurement of the intracellular nucleotide levels of three plant species (cell cultures and leaves). The evolution of the nucleotide pool of Nicotiana tabacum cell culture during growth has also been measured, and showed an increase in the po…

RibonucleotidePotassium CompoundsNicotiana tabacumIon chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundSpecies SpecificityHydroxidesSample preparationAnion Exchange ResinsPotassium hydroxideChromatographybiologyIon exchangeOrganic ChemistryExtraction (chemistry)General MedicineHydrogen-Ion ConcentrationPlantsReference StandardsRibonucleotidesChromatography Ion Exchangebiology.organism_classificationchemistryJournal of Chromatography A
researchProduct