Search results for "sample preparation"

showing 10 items of 343 documents

Solid-phase extraction of quaternary ammonium herbicides

2000

This paper highlights recent advances in the solid-phase extraction (SPE) of quaternary ammonium herbicides in water, soil, plant and biological samples. After a brief introduction summarizing the properties of quaternary ammonium herbicides and the difficulties involved in measuring them, attention is paid primarily to solid supports used for isolation and concentration, pre-treatments required for the different matrices, and eluents applied for quantitative desorption of these analytes. The determination techniques used after SPE and applications of the proposed SPE methodology are also briefly discussed.

ChromatographyEnvironmental analysisHerbicidesChemistryOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundAdsorptionDesorptionSample preparationTrace analysisAmmoniumSolid phase extractionChromatography LiquidJournal of Chromatography A
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Analysis of neuropeptide Y and its metabolites by high-performance liquid chromatography-electrospray ionization mass spectrometry and integrated sam…

2000

A novel restricted access cation exchanger with sulphonic acid groups at the internal surface was proven to be highly suitable in the sample clean up of peptides on-line coupled to HPLC-electrospray ionization (ESI)-MS. Neuropeptide Y (NPY) and several of its fragments in plasma were subjected to the sample clean-up procedure. The peptides were eluted by a step gradient from the restricted access column, applying 10 mM phosphate buffer pH 3.5 from 5 to 20% (v/v) of acetonitrile with 1 M NaCl and transferred to a Micra ODS II column (33x4.6 mm). The separation of the peptides and their fragments was performed by a linear gradient from 20 to 60% (v/v) acetonitrile in water with 0.1% formic ac…

ChromatographyFormic acidElectrospray ionizationOrganic ChemistryMolecular Sequence DataGeneral MedicineReversed-phase chromatographyMass spectrometryBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryTrifluoroacetic acidAnimalsSample preparationNeuropeptide YSolid phase extractionAmino Acid SequenceCation Exchange ResinsSulfonic AcidsChromatography High Pressure LiquidJournal of chromatography. A
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An automated on-line multidimensional HPLC system for protein and peptide mapping with integrated sample preparation.

2002

A comprehensive on-line two-dimensional 2D-HPLC system with integrated sample preparation was developed for the analysis of proteins and peptides with a molecular weight below 20 kDa. The system setup provided fast separations and high resolving power and is considered to be a complementary technique to 2D gel electrophoresis in proteomics. The on-line system reproducibly resolved approximately 1000 peaks within the total analysis time of 96 min and avoided sample losses by off-line sample handling. The low-molecular-weight target analytes were separated from the matrix using novel silica-based restricted access materials (RAM) with ion exchange functionalities. The size-selective sample fr…

ChromatographyIon exchangeChemistryIon chromatographyAnalytical chemistryProteinsUltrafiltrationFibroblastsMass spectrometryChromatography Ion ExchangeHigh-performance liquid chromatographyOnline SystemsPeptide MappingAnalytical ChemistryCell LineMatrix (chemical analysis)Matrix-assisted laser desorption/ionizationTwo-dimensional chromatographySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationHumansSample preparationElectrophoresis Polyacrylamide GelChromatography High Pressure LiquidAnalytical chemistry
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Sulphonic acid strong cation-exchange restricted access columns in sample cleanup for profiling of endogeneous peptides in multidimensional liquid ch…

2006

Abstract In this work, the pore structural parameters and size exclusion properties of LiChrospher strong cation-exchange and reverse phase restricted access materials (RAM) are analysed. The molecular weight size exclusion limit for polystyrenes was found to be about 17.7 kDa, while for standard proteins, the molecular weight size exclusion limit was higher, at approximately 25 kDa. The average pore diameter on a volume basis calculated from the pore network model changes from 8.5 nm (native LiChrospher) to 8.6 nm (diol derivative) to 8.2 nm (sulphonic acid derivative) to 6.9 nm ( n -octadecyl derivative). Additional characterisations were performed on restricted access materials with nitr…

ChromatographyIon exchangeChemistryOrganic ChemistrySize-exclusion chromatographyAnalytical chemistrySorptionGeneral MedicineBiochemistryAnalytical ChemistryGel permeation chromatographyAdsorptionMicroelectrophoresisSample preparationSolid phase extractionJournal of Chromatography A
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Determination of several aminoglycoside and macrolide antibiotics in animal tissues by liquid chromatography-electrospray ionization-tandem mass spec…

2008

ChromatographyLiquid chromatography electrospray ionization tandem mass spectrometryProtein mass spectrometryLiquid chromatography–mass spectrometrymedicine.drug_classChemistryAminoglycosidemedicineGeneral MedicineToxicologySample preparation in mass spectrometryMacrolide AntibioticsToxicology Letters
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Pesticides (New Generation) and Related Compounds, Analysis of

2017

Miscellaneous pesticides and related compounds comprise substances that can neither be included in the classical chemical category of pesticides nor classified by their mode of action. They are a heterogeneous group of substances, the most representative of which are macrocyclic lactones, chloronicotinyls, tetranortriterpenoids, ammonium quaternary salts, dinitroanilines, acetamides, oximes, triazoles, and pyridine-based molecules. The pesticides covered in this article have hardly changed in the last years. However, their analytical determination has undergone significant improvements. This article provides a well-defined and critical compilation of the sample treatment and clean-up proced…

ChromatographyLiquid chromatography–mass spectrometryChemistryOrganic chemistrySample preparationGas chromatographySolid phase extractionGas chromatography–mass spectrometryPesticideMass spectrometryHigh-performance liquid chromatography
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Comparison of microextraction procedures to determine pesticides in oranges by liquid chromatography-mass spectrometry.

2002

A liquid chromatographic-mass spectrometric method has been developed for the determination of bitertanol, carbendazim, fenthion, flusilazole, hexythiazox, imidacloprid, methidathion, methiocarb, pyriproxyfen and trichlorfon. Two procedures, based on stir bar sorptive extraction (SBSE) and matrix solid-phase dispersion (MSPD), have been evaluated for the extraction of these compounds in oranges. Their respective advantages and disadvantages are also discussed. The recoveries obtained by MSPD ranged from 47 to 96% and the relative standard deviations (RSDs) ranged from 1 to 15%, whereas with the SBSE method the recoveries were between 8 and 84% and the RSDs between 4 and 16%. Although, the l…

ChromatographyMethiocarbCarbendazimOrganic ChemistryEthyl acetateReproducibility of ResultsGeneral MedicineMethidathionBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometrySample preparationSolid phase extractionPesticidesChromatography LiquidCitrus sinensisJournal of chromatography. A
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Capillary electrophoresis for analyzing pesticides in fruits and vegetables using solid-phase extraction and stir-bar sorptive extraction.

2005

Two procedures based on solid-phase extraction (SPE) and stir-bar sorptive extraction (SBSE) in combination with micellar electrokinetic chromatography (MEKC)--diode array detection (DAD) were compared for the simultaneous extraction of acrinathrin, bitertanol, cyproconazole, fludioxonil, flutriafol, myclobutanil, pyriproxyfen, and tebuconazole in lettuce, tomato, grape, and strawberry. Selectivity and resolution of the MEKC procedure were studied changing the pH and the molarity of the buffer, the type and the concentration of surfactant, and the methanol content in the mobile phase. A buffer consisting of 6 mM sodium tetraborate decahydrate with 75 mM of cholic acid sodium solution (pH 9.…

ChromatographyMolar concentrationMyclobutanilSodiumOrganic Chemistrychemistry.chemical_elementElectrophoresis CapillaryGeneral MedicineBiochemistrySensitivity and SpecificityMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresischemistryFruitVegetablesSample preparationSolid phase extractionPesticidesQuantitative analysis (chemistry)Journal of chromatography. A
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Improving the solid-phase extraction of “quat” pesticides from water samples

1998

A novel strategy, based on the addition of a cationic surfactant, for preventing the interferences associated with a diminution in the efficacy of solid-phase extraction (SPE) with silica cartridges of diquat, paraquat and difenzoquat in water is developed. Conditions for extraction are optimised with respect to pH, cationic surfactant and its concentration. Humic acids, anionic surfactants, inorganic salts and other organic contaminants like pesticides, phenols, polycyclic aromatic hydrocarbons and polychlorinated biphenyls produce the studied interferences. The best performance is shown in the improvement of the "quats" recovery from waters with high levels of humic acids and anionic surf…

ChromatographyOrganic ChemistryCationic polymerizationGeneral MedicineBiochemistryDiquatAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantEnvironmental chemistrymedia_common.cataloged_instanceSample preparationPhenolsSolid phase extractionEuropean unionWater pollutionmedia_commonJournal of Chromatography A
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Critical study of and improvements in chromatographic methods for the analysis of type B trichothecenes

2001

Various analytical methods used in the analysis of type B trichothecenes (deoxynivalenol, nivalenol, 3- and 15-acetyldeoxynivalenol) in cereals were compared and optimised in this work. These methods use either GC-electron-capture detection (ECD) of trimethylsilyl, trifluoroacetyl and heptafluorobutyryl derivatives or HPLC with UV or photodiode array detection of analytes. A new HPLC procedure using fluorescence detection prior derivatisation with coumarin-3-carbonyl chloride has been also tested. Five extraction solvents and two solid-phase extraction cartridges (silica, Florisil) plus a especial clean-up column (MycoSep 225) were compared in order to obtain the best recovery of the mycoto…

ChromatographyOrganic ChemistryExtraction (chemistry)TrichotheceneGeneral MedicineSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryElectron capture detectorchemistry.chemical_compoundSpectrometry FluorescenceFusariumchemistryCalibrationSpectrophotometry UltravioletSample preparationSolid phase extractionGas chromatographyEdible GrainTrichothecenesDerivatizationChromatography High Pressure LiquidJournal of Chromatography A
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