Search results for "liquid chromatography"

showing 10 items of 942 documents

Supported liquid membrane extraction with single hollow fiber for the analysis of fluoroquinolones from environmental surface water samples

2010

Abstract In this work, the simple analytical method for the determination of four fluoroquinolone antibiotics: ciprofloxacin, enrofloxacin, norfloxacin and danofloxacin, in environmental surface water samples is described. Sample pretreatment step was performed by the application of a technique based on supported liquid membrane extraction with the configuration of single hollow fiber (HF-SLM). The HPLC system with diode array detection was used for final analysis of studied analytes. Various parameters affecting the extraction efficiency during HF-SLM enrichment, such as type of membrane diluent, pH of donor (sample) and acceptor phases, as well as an enrichment time and salt content of sa…

DanofloxacinAnalytical chemistrySodium ChlorideBiochemistryHigh-performance liquid chromatographyDiluentSensitivity and SpecificityAnalytical ChemistryRiversmedicinehollow fiberenvironmental samplesSample preparationfluoroquinolonesChromatography High Pressure LiquidDetection limitChromatographysample preparationChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsMembranes ArtificialGeneral MedicineHydrogen-Ion ConcentrationAnti-Bacterial Agentssupported liquid membrane extractionWater treatmentHydrochloric AcidEnrichment factorWater Pollutants Chemicalmedicine.drugJournal of Chromatography A
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Recent advances on ionic liquid uses in separation techniques

2018

International audience; The molten organic salts with melting point below 100°C, commonly called ionic liquids (ILs) have found numerous uses in separation sciences due to their exceptional properties as non molecular solvents, namely, a negligible vapor pressure, a high thermal stability, and unique solvating properties due to polarity and their ionic character of molten salts. Other properties, such as viscosity, boiling point, water solubility, and electrochemical window, are adjustable playing with which anion is associated with which cation. This review focuses on recent development of the uses of ILs in separation techniques actualizing our 2008 article (same authors, J. Chromatogr. A…

Deep eutectic solventSpectrometry Mass Electrospray IonizationChromatography Gasgas chromatographydeep eutectic solventLiquid chromatographyIonic bonding02 engineering and technologyTrace anion detection01 natural sciencesBiochemistryAnalytical Chemistryionic liquidschemistry.chemical_compoundCountercurrent chromatographyCapillary electrophoresistrace anion detection[CHIM.ANAL]Chemical Sciences/Analytical chemistryliquid chromatographyCountercurrent DistributionGas chromatographyChromatographyViscosity010401 analytical chemistryOrganic ChemistryElectrophoresis CapillaryGeneral Medicine021001 nanoscience & nanotechnologyIonic liquids0104 chemical sciencesDeep eutectic solventBoiling pointchemistryIonic liquidSolventsMelting pointGases0210 nano-technologyChromatography LiquidElectrochemical windowJournal of Chromatography A
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Enantiomer separation by chiral-phase liquid chromatography of urethane derivatives of natural diacylglycerols previously fractionated by reversed-ph…

1991

Abstract Enantiomers of diacylglycerols such as 3,5-dinitrophenyl isocyanate (urethane) derivatives previously fractionated by reversed-phase high-performance liquid chromatography (HPLC) were separated by HPLC on a chiral phase column [N-( R )-1-(α-naphthyl)ethylamino-carbonyl-( S )-valine chemically bound to γ-aminopropylsilanized silica]. In addition to the separation of commercial monoacid-diacylglycerol isomers, separation of diacid-diacylglycerol isomers obtained from peanut oil and cottonseed oil triacylglycerols by chemical hydrolysis is reported. Hexane-ethylene dichloride-ethanol mixtures were used for elution of the diacylglycerol derivative isomers, which were detected by their …

Degree of unsaturationChromatographyChemistryElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryIsocyanateHigh-performance liquid chromatographyAnalytical ChemistryHydrolysischemistry.chemical_compoundOrganic chemistryRacemic mixtureEnantiomerJournal of Chromatography A
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Analysis and fractionation of natural source diacylglycerols as urethane derivatives by reversed-phase high-performance liquid chromatography

1991

Abstract Reversed-phase high-performance liquid chromatography on a thermostatted octadecylsilyl column was used to separate and fractionate mixtures of diacylglycerols after derivatization with 3,5-dinitrophenyl isocyanate (urethane derivatives). In addition to the separation of commercial diacylglycerol species, the separation of diacylglycerols obtained from peanut oil and cottonseed oil triacylglycerols by chemical hydrolysis is reported. Acetonitrile-acetone mixtures were used for elution of the diacylglycerol urethane derivatives. Unsaturated and saturated derivatives were detected by their refractive indices. They were then collected and their fatty acids analysed as methyl esters by…

Degree of unsaturationChromatographyElutionGlycerideOrganic ChemistryGeneral MedicineFractionationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrolysischemistry.chemical_compoundchemistryOrganic chemistrylipids (amino acids peptides and proteins)DerivatizationDiacylglycerol kinaseJournal of Chromatography A
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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
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Determination of molecular species of oil triacylglycerols by reversed-phase and chiral-phase high-performance liquid chromatography

1991

A method is described for the determination of molecular species of oil triacylglycerols. The method is based on the analytical separation of the enantiomericsn-1,2-andsn-2,3-diacylglycerols, derived from triacylglycerols, by high-performance liquid-chromatography (HPLC) on a chiral column containing N-(R)-1-(α-naphthyl)ethylaminocarbonyl-(S)-valinecarbonyl-(S)-valine as stationary phase. Model triacyl-glycerol molecules comprising three known fatty acids were isolated from peanut oil and cottonseed oil by a combination of argentation-TLC and reversed-phase HPLC and submitted to partial chemical deacylation. The derivedsn-1,2(2,3)-diacylglycerols were analyzed and fractionated as 3,5-dinitr…

Degree of unsaturationfood.ingredientChromatographyChemistryGeneral Chemical EngineeringOrganic ChemistryReversed-phase chromatographyHigh-performance liquid chromatographyfoodPhase (matter)Peanut oilMoleculeOrganic chemistryComposition (visual arts)EnantiomerJournal of the American Oil Chemists' Society
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Critical assessment of ionization patterns and applications of ambient desorption/ionization mass spectrometry using FAPA-MS

2016

Ambient desorption/ionization mass spectrometry (MS) has gained growing interest during the last decade due to its high analytical performance and yet simplicity. Here, one of the recently developed ambient desorption/ionization MS sources, the flowing atmospheric-pressure afterglow (FAPA) source, was investigated in detail regarding background ions and typical ionization patterns in the positive as well as the negative ion mode for a variety of compound classes, comprising alkanes, alcohols, aldehydes, ketones, carboxylic acids, organic peroxides and alkaloids. A broad range of signals for adducts and losses was found, besides the usually emphasized detection of quasimolecular ions, i.e. […

Desorption electrospray ionizationChemical ionizationChemistry010401 analytical chemistryAnalytical chemistryAtmospheric-pressure chemical ionization010402 general chemistryMass spectrometry01 natural sciencesIon source0104 chemical sciencesAtmospheric-pressure laser ionizationDirect electron ionization liquid chromatography–mass spectrometry interfaceSpectroscopyAmbient ionizationJournal of Mass Spectrometry
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A new interface to couple thin-layer chromatography with laser desorption/atmospheric pressure chemical ionization mass spectrometry for plate scanni…

2005

An interface to allow on-line qualitative and quantitative full-plate detection and analysis of compounds separated by thin-layer chromatography (TLC) is presented. A continuous wave diode laser is employed as a desorption source. Atmospheric pressure chemical ionization mass spectrometry ionizes and subsequently identifies the desorbed sample molecules. Besides direct laser desorption on untreated TLC plates, graphite particles were used as a matrix to couple in the laser power and improve the efficiency of desorption.

Desorption electrospray ionizationChromatographyMatrix-assisted laser desorption electrospray ionizationChemistryOrganic ChemistryAnalytical chemistryEquipment DesignMass spectrometryIon sourceSoft laser desorptionAnalytical ChemistryAtmospheric-pressure laser ionizationSpecimen HandlingEquipment Failure AnalysisSystems IntegrationAtmospheric PressureSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationDirect electron ionization liquid chromatography–mass spectrometry interfaceSpectroscopyAmbient ionizationRapid communications in mass spectrometry : RCM
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Determination of acrylamide in coffee and chocolate by pressurised fluid extraction and liquid chromatography-tandem mass spectrometry.

2007

A selective and sensitive procedure has been developed and validated for the determination of acrylamide in difficult matrices, such as coffee and chocolate. The proposed method includes pressurised fluid extraction (PFE) with acetonitrile, florisil clean-up purification inside the PFE extraction cell and detection by liquid chromatography (LC) coupled to atmospheric pressure ionisation in positive mode tandem mass spectrometry (APCI-MS-MS). Comparison of ionisation sources (atmospheric pressure chemical ionisation (APCI), atmospheric pressure photoionization (APPI) and the combined APCI/APPI) and clean-up procedures were carried out to improve the analytical signal. The main parameters aff…

Detection limitAcrylamideCacaoChromatographyAtmospheric pressureChemistryHealth Toxicology and MutagenesisExtraction (chemistry)Public Health Environmental and Occupational HealthAnalytical chemistryAtmospheric-pressure chemical ionizationGeneral ChemistryIsotope dilutionToxicologyMass spectrometryTandem mass spectrometryCoffeeChemistry (miscellaneous)Liquid chromatography–mass spectrometrySpainTandem Mass SpectrometryFood ScienceChromatography LiquidFood additives and contaminants
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Analysis of LSD in human body fluids and hair samples applying ImmunElute columns.

2000

Immunoaffinity extraction units (LSD ImmunElute) are commercially available for the analysis of lysergic acid diethylamide (LSD) in urine. The ImmunElute resin contains immobilized monoclonal antibodies to LSD. We applied the ImmunElute procedure to serum and also to human hair samples. For hair analysis the samples were first extracted with methanol under sonication. The extracts were then purified using the ImmunElute resin. LSD analysis was carried out with HPLC and fluorescence detection. The immunoaffinity extraction provides highly purified extracts for chromatographic analysis. The limit of detection (signal-to-noise ratio = 3) has been determined to be < 50 pg regardless of which sa…

Detection limitAdultMaleChromatographyAdolescentChemistryIllicit DrugsSonicationHair analysisExtraction (chemistry)UrineHigh-performance liquid chromatographyChromatography AffinityPathology and Forensic MedicineBody FluidsSubstance Abuse DetectionLysergic Acid DiethylamideAffinity chromatographyHumansGas chromatography–mass spectrometryLawChromatography High Pressure LiquidHairForensic science international
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