Search results for "Column chromatography"

showing 10 items of 143 documents

On-Line Derivatization into Precolumns for the Determination of Drugs by Liquid Chromatography and Column Switching:  Determination of Amphetamines i…

1996

A chromatographic system for the on-line derivatization of drugs using column switching is described. The system uses a 20 mm × 2.1 mm i.d. precolumn packed with a unmodified ODS stationary phase. This column is used for sample cleanup and enrichment of the analytes. Next, the trapped analytes are derivatized by injection of the derivatization reagent into the precolumn. Finally, the derivatives are transferred to the analytical column for their separation under reversed-phase conditions. The influence of several parameters such as the reaction time, the amount of derivatization reagent, or the system design has been studied using some amphetamines as model compounds and three derivatizatio…

AnalyteChromatographyAmphetaminesUrineChloroformateMethamphetamineAnalytical ChemistrySubstance Abuse Detectionchemistry.chemical_compoundColumn chromatographychemistryReagentIndicators and ReagentsColumn switchingDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidAnalytical Chemistry
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Procedure for automated background correction in flow systems with infrared spectroscopic detection and changing liquid-phase composition

2009

This paper describes a partial least squares (PLS) based automatic procedure to correct for changes in the spectral contribution of the solvent or solvent mixtures from solute spectra recorded in these solvents. The procedure was developed for successful on-line Fourier transform infrared (FT-IR) detection in gradient high-performance liquid chromatography (HPLC) separations. It requires a reference FT-IR data set containing all possible combinations of the expected variation in solvent composition. Furthermore, a spectral region ( A) in these spectra is required where the solvents show absorption but the analytes do not. This is the case for the system ACN:H2O, an often-applied solvent mi…

AnalyteChromatographyChemistryAnalytical chemistryInfrared spectroscopyMass spectrometryHigh-performance liquid chromatographyChemometricssymbols.namesakeFourier transformColumn chromatographysymbolsFourier transform infrared spectroscopyInstrumentationSpectroscopy
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Column-switching techniques for high-performance liquid chromatography of drugs in biological samples.

1993

In recent years, an increasing number of publications have demonstrated the potential of column-switching techniques for the chromatographic separation, determination and preparative isolation of analytes from biological matrices. Column-switching systems greatly facilitate drug analysis, by on-line sample clean-up and trace enrichment, or by improving the analytical separative process. In this paper, the main applications of column-switching techniques to drug analysis in biological samples, are reviewed.

AnalyteChromatographyChemistryGeneral ChemistryHigh-performance liquid chromatographyBiological materialsChromatographic separationColumn chromatographyPharmaceutical PreparationsAnimalsHumansColumn switchingDrug analysisQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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Comparison of the solid-phase extraction efficiency of a bounded and an included cyclodextrin-silica microporous composite for polycyclic aromatic hy…

2016

Solid-phase extraction is one of the most important techniques for sample purification and concentration. A wide variety of solid phases have been used for sample preparation over time. In this work, the efficiency of a new kind of solid-phase extraction adsorbent, which is a microporous material made from modified cyclodextrin bounded to a silica network, is evaluated through an analytical method which combines solid-phase extraction with high-performance liquid chromatography to determine polycyclic aromatic hydrocarbons in water samples. Several parameters that affected the analytes recovery, such as the amount of solid phase, the nature and volume of the eluent or the sample volume and …

Analytical chemistry010501 environmental sciences01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryAdsorptionColumn chromatographyLimit of DetectionPhase (matter)Sample preparationSolid phase extractionPolycyclic Aromatic HydrocarbonsChromatography High Pressure Liquid0105 earth and related environmental sciencesCyclodextrinsChromatographyChemistry010401 analytical chemistryExtraction (chemistry)Solid Phase ExtractionWaterMicroporous materialEquipment DesignSilicon Dioxide0104 chemical sciencesAdsorptionPorosityWater Pollutants ChemicalTalanta
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Ultra high performance liquid chromatography-time-of-flight high resolution mass spectrometry in the analysis of hexabromocyclododecane diastereomers…

2014

An efficient ultra high performance liquid chromatography (UHPLC)-time-of-flight high resolution mass spectrometry (TOF-HRMS) method was elaborated for the determination of hexabromocyclododecane (HBCD) diastereomers in fish samples and compared against UHPLC-Orbitrap-HRMS and UHPLC-triple quadrupole (QqQ) tandem MS (MS/MS) techniques. The TOF-HRMS analyzer was operated at high resolution (>10000 full width at half maximum (FWHM)) with scanning the m/z range from 600 to 700, to achieve picogram quantitation limits. The effects of various operational parameters on the instrumental response were systematically investigated. Evaluation of the influence of sample clean-up procedure steps on sig…

Analytical chemistryTandem mass spectrometryOrbitrapBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)Gel permeation chromatographychemistry.chemical_compoundColumn chromatographylawTandem Mass SpectrometryAnimalsMuscle SkeletalChromatography High Pressure LiquidHexabromocyclododecaneChromatographyEelsOrganic ChemistryFishesReproducibility of ResultsGeneral MedicineRepeatabilityTriple quadrupole mass spectrometerHydrocarbons BrominatedchemistryWater Pollutants ChemicalEnvironmental MonitoringJournal of chromatography. A
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Novel porous carbon packings in reversed-phase high-performance liquid chromatography

1980

Abstract Porous carbon packings of particle size 5–20 μm were prepared by calcination of purified active carbons and cokes having narrow size ranges. Highly efficient columns packed with 10-μm particles were obtained by means of the high-viscosity slurry technique, and exhibited about 3000 theoretical plates at 100 mm length and optimal eluent flow-rate. The loading of columns, θ0.1, was determined to be 25–50 μg of solute per gram of packing. Eluotropic series of solvents were found to be similar to those on pyrocarbon-modified carbons and silicas. The log k′ values for homologous compounds increased linearly with the hydrocarbonaceous surface area at constant eluent composition. Studies w…

Aqueous solutionChromatographyOrganic ChemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicineBiochemistryAnalytical Chemistrylaw.inventionColumn chromatographychemistrylawPolarizabilityPhase (matter)CalcinationParticle sizeTheoretical plateCarbonJournal of Chromatography A
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Micellar Liquid Chromatography: Fundamentals

2015

The reversed phase liquid chromatography (RPLC) mode with surfactant above the critical micellar concentration (CMC) has been called micellar liquid chromatography (MLC). In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and micellar pseudo-phase. Surfactant adsorption on the porous RPLC packing affects chromatographic retention, owing to the change of diverse surface properties of the stationary phase. In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and mice…

Aqueous solutionColumn chromatographyAqueous normal-phase chromatographyChemistryMicellar liquid chromatographyHydrophilic interaction chromatographytechnology industry and agricultureAnalytical chemistrylipids (amino acids peptides and proteins)macromolecular substancesReversed-phase chromatographyMicelleMicellar electrokinetic chromatography
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Determination of alkylamines in atmospheric aerosol particles: a comparison of gas chromatography–mass spectrometry and ion chromatography approaches

2014

Abstract. In recent years low molecular weight alkylamines have been recognized to play an important role in particle formation and growth in the lower atmosphere. However, major uncertainties are associated with their atmospheric processes, sources and sinks, mostly due to the lack of ambient measurements and the difficulties in accurate quantification of alkylamines at trace level. In this study, we present the evaluation and optimization of two analytical approaches, i.e., gas chromatography–mass spectrometry (GC-MS) and ion chromatography (IC), for the determination of alkylamines in aerosol particles. Alkylamines were converted to carbamates through derivatization with isobutyl chlorof…

Atmospheric ScienceIon chromatographyAnalytical chemistryMass spectrometrychemistryammoniachemistry.chemical_compoundColumn chromatographyaliphatic-aminesderivatizationlcsh:TA170-171phaseDerivatizationDetection limitChromatographyChemistrylcsh:TA715-787lcsh:Earthwork. Foundationsaromatic-aminesAerosollcsh:Environmental engineering13. Climate actionReagentnanoparticleschemical-compositionGas chromatography–mass spectrometryseasonal-variationsecondary organic aerosol
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Solution versus Fluorous versus Solid-Phase Synthesis of 2,5-Disubstituted 1,3-Azoles. Preliminary Antibacterial Activity Studies

2009

A small library of compounds with an oxa(thia)zole scaffold and structural diversity in both positions 2 and 5 has been synthesized. Double acylation of a protected glycine affords intermediate α-amido-β-ketoesters, which in turn can be dehydrated to afford 1,3-oxazoles or reacted with Lawesson’s reagent to furnish 1,3-thiazoles. This procedure was designed with its adaptation to fluorous techniques in mind. Thus, when a protected glycine with a fluorous tag in the ester moiety is used as a starting material, the synthesis can be easily completed without column chromatography purification of intermediate compounds with good to excellent yields, thus affording a suitable entry to the prepara…

AzolesStaphylococcus aureusANTIBACTERIAL ACTIVITYDrug Evaluation PreclinicalMicrobial Sensitivity TestsChemical synthesisSmall Molecule LibrariesAcylationchemistry.chemical_compoundSolid-phase synthesisColumn chromatographyAZOLESOrganic chemistryMoietyAntibacterial agentChemistryOrganic ChemistryCiencias QuímicasFLUOROUSCombinatorial chemistryAnti-Bacterial AgentsSolutionsQuímica OrgánicaMolecular ProbesSOLID-PHASELawesson's reagentAntibacterial activityCIENCIAS NATURALES Y EXACTAS
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4-hydroxy-ONN-azoxybenzene

2000

The oxidation of 4-hydroxy­azo­benzene provided a mixture of two azoxy compounds, which were separated by column chromatography. The isomer with the higher melting point appeared to belong to the α (ONN) series, as determined by X-ray diffraction. The mol­ecule, C12H10N2O2, is almost planar. The benzene rings are twisted by 11.7 (2) (substituted) and 4.1 (1)° (unsubstituted) with respect to the ONN plane. The mol­ecules are connected to one another by strong O—H⋯O hydrogen bonds forming chains extended along [001], which are bound by much weaker C—H⋯O hydrogen bonds forming layers in the bc plane.

AzoxyDiffractionPlane (geometry)Hydrogen bondStereochemistryGeneral MedicineCrystal structureGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographyColumn chromatographychemistryMelting pointBenzeneActa crystallographica. Section C, Crystal structure communications
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