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showing 10 items of 8586 documents

On-line preconcentration strategies for analyzing pesticides in fruits and vegetables by micellar electrokinetic chromatography.

2007

Five pesticides (fludioxonil, procymidone, pyriproxyfen, dinoseb and carbendazim) were separated in reversed migration micellar electrokinetic chromatography (RM-MEKC) using 20 mmol l(-1) phosphate buffer at pH 2.3, containing 25 mmol l(-1) sodium dodecylsulfate and 10% methanol. Three on-line concentration strategies, sweeping (SW), normal stacking with reversed migration and a water plug (SRW) and stacking with reverse migration and removal of sample matrix using polarity switching (SRMM), were compared. About 10-, 30- and 50-fold increases in detection sensitivity, compared with standard hydrodynamic injection (5 s at 0.5 psi), were observed with SW, SRW and SRMM, respectively. Limits of…

Detection limitChromatographyChemistryCarbendazimOrganic ChemistryAnalytic Sample Preparation MethodsElectrophoresis CapillaryGeneral MedicineBiochemistryOnline SystemsMicellar electrokinetic chromatographyAnalytical ChemistryFungicides Industrialchemistry.chemical_compoundElectrophoresisFruitDinosebVegetablesSample preparationSolid phase extractionProcymidonePesticidesFood AnalysisChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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On-line in-tube solid phase microextraction-capillary liquid chromatography method for monitoring degradation products of di-(2-ethylhexyl) phthalate…

2014

Abstract The main di-(2-ethylhexyl) phthalate (DEHP) degradation products, (2-ethylhexyl) phthalate (MEHP), diethyl phthalate (DEP) and dibutyl phthalate (DBP), have been tested. The proposed cost-effective method combines on-line, in-tube solid-phase micro extraction (IT-SPME) in in-valve configuration and capillary liquid chromatography with UV diode array detection (Cap-LC-DAD). Acidification of the samples at pH 3 improved markedly the estimation of MEHP. Aliquots of 4 mL of acidified water samples were directly processed. After sample loading, the analytes were desorbed with the mobile-phase and transferred to the monolithic capillary column. Satisfactory linearity and precision, absen…

Detection limitChromatographyChemistryDibutyl phthalateCapillary actionOrganic ChemistryExtraction (chemistry)Phthalic AcidsPhthalateGeneral MedicineSolid-phase microextractionDiethyl phthalateBiochemistryDibutyl PhthalateAnalytical Chemistrychemistry.chemical_compoundPlasticizersDiethylhexyl PhthalateSample preparationSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidJournal of Chromatography A
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Simultaneous determination of olanzapine, clozapine and demethylated metabolites in serum by on-line column-switching high-performance liquid chromat…

2001

An automated method for simultaneous routine quantification of the antipsychotic drugs clozapine, olanzapine and their demethylated metabolites is described. The method included adsorption on a cyanopropyl (CPS) coated clean-up column (10 microm; 10 x 2.0 mm I.D.), washing off interfering serum constituents to waste, and separation on C18 ODS Hypersil reversed phase material (5 microm; 250 x 4.6 mm I.D.) using acetonitrile-water-tetramethylethylenediamine (37:62.6:0.4, v/v/v) adjusted to pH 6.5 with concentrated acetic acid. UV-detection was performed at 254 nm. The limit of quantification was 10-20 ng/ml. Relative day to day standard variations ranged between 4.5 and 13.5%. The method is s…

Detection limitChromatographyChemistryMetaboliteReproducibility of ResultsGeneral ChemistryPirenzepineHigh-performance liquid chromatographySensitivity and SpecificityAcetic acidchemistry.chemical_compoundBenzodiazepinesAdsorptionPharmacokineticsOlanzapinemedicineHumansSpectrophotometry UltravioletQuantitative analysis (chemistry)ClozapineClozapineChromatography High Pressure Liquidmedicine.drugAntipsychotic AgentsJournal of chromatography. B, Biomedical sciences and applications
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Off-line solid-phase microextraction and capillary electrophoresis mass spectrometry to determine acidic pesticides in fruits.

2003

A method based on solid-phase microextraction (SPME) and capillary electrophoresis/mass spectrometry (CE/ MS) is described for determining simultaneously five acidic pesticides (o-phenylphenol, ioxynil, haloxyfop, acifluorfen, picloram) in fruits. The CE device is coupled to an electrospray interface by a commercial sheath-flow adapter. Emphasis is placed on fulfillment of the speed and sensitivity requirements. The best separation is achieved using 32 mM ammonium formate/acid formic buffer at pH 3.1, with a working voltage of 25 kV. The MS detection of the five pesticides was performed in negative ionization mode. Full-scan spectra with base peaks corresponding to [M-H]- were obtained exce…

Detection limitChromatographyChemistryPlant ExtractsAnalytical chemistryElectrophoresis CapillaryFood ContaminationAcifluorfenMass spectrometrySolid-phase microextractionCapillary electrophoresis–mass spectrometryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisFruitAmmonium formateSample preparationPesticidesAnalytical chemistry
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Identification of Leguminosae gums and evaluation of carob-guar mixtures by capillary zone electrophoresis of protein extracts.

2002

A procedure for the extraction and capillary zone electrophoresis (CZE) separation of proteins from carob, guar and tara gums in a background electrolyte (BGE) of pH 9 containing 0.1% polyvinyl alcohol is described. The CZE protein profiles exhibit characteristic peaks for each one of the Leguminosae gums, which can be used to construct models capable of identifying samples of carob, guar and tara gums, and predicting the guar content in binary carob-guar mixtures of different geographical origin and harvested in different years. The classification and prediction models are constructed by using linear discriminant analysis (LDA) and multiple linear regression (MLR), respectively. An excelle…

Detection limitChromatographyGuar gumResolution (mass spectrometry)ChemistryPlant ExtractsClinical BiochemistryExtraction (chemistry)GuarElectrophoresis CapillaryFabaceaeBiochemistryGalactansAnalytical ChemistryMannansCapillary electrophoresisModels ChemicalPolysaccharidesLinear regressionCalibrationPlant GumsElectrophoresis
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Determination of furosemide in urine samples by direct injection in a micellar liquid chromatographic system.

2002

A sensitive, selective and efficient micellar liquid chromatographic (MLC) procedure was developed for the determination of furosemide (4-chloro-N-furfuryl-5-sulfamoylanthranilic acid) in urine samples by direct injection and UV detection. The procedure makes use of a C18 reversed-phase column and a micellar mobile phase of 0.05 mol l(-1) sodium dodecyl sulfate-6% v/v propanol and phosphate buffer at pH 3 to resolve furosemide from its photochemical degradation products. The importance of protecting the standards and urine samples to be analysed from light in the assay of furosemide, avoiding its degradation, was verified. The limit of quantification was 0.15 microg ml(-1) and the relative …

Detection limitChromatographyMetabolitemedicine.medical_treatmentSodiumchemistry.chemical_elementFurosemideReversed-phase chromatographyUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryFurosemideElectrochemistrymedicineEnvironmental ChemistryHumansDiureticDiureticsQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure Liquidmedicine.drugChromatography Micellar Electrokinetic CapillaryThe Analyst
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In-tube solid-phase microextraction and liquid chromatography using a monolithic column for the selective determination of residual ethylenediamine i…

2009

The selective determination of the diamine ethylenediamine (EDA) in the presence of a higher amount of residual dimethylamine in cationic polymers has been developed. The strategy uses both a solution derivatization with a selective agent of primary amines such as o-phthaldialdehyde-N-acetyl-L-cysteine (OPA-NAC) and an in-tube solid-phase microextraction (IT-SPME) coupled to liquid chromatography (LC). A 70 cm long, 0.32 mm internal diameter, and 3 microm thick commercially available capillary column coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane was employed to replace the injection loop of a Rheodyne injection valve. A volume of 1 mL of derivatized sample was passed thro…

Detection limitChromatographyMonolithic HPLC columnPolydimethylsiloxaneCapillary actionPolymersCationic polymerizationSolid-phase microextractionEthylenediaminesAnalytical Chemistrychemistry.chemical_compoundchemistryChemical IndustryIndicators and ReagentsDerivatizationDimethylamineSolid Phase MicroextractionChromatography LiquidAnalytical chemistry
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Determination ofl-Ascorbic Acid and Total Ascorbic Acid in Vascular and Nonvascular Plants by Capillary Zone Electrophoresis

1998

A capillary zone electrophoresis (CZE) procedure for the determination of l-ascorbic acid (AA) and total ascorbic acid (TAA, as the sum of AA and dehydroascorbic acid) in vascular plants, lichens, bryophytes, and liverworts is described. The samples were frozen in liquid nitrogen and extracted with 2% metaphosphoric acid. To determine AA, an aliquot was directly injected in a fused-silica capillary. The determination of TAA was performed upon its reduction with dl-homocysteine at pH 7. The background electrolyte contained 60 mM sodium chloride, 60 mM sodium dihydrogen phosphate, 1 x 10(-4)% hexadimetrine bromide, and NaOH up to pH 7. The procedure was rapid and highly reproducible; the limi…

Detection limitChromatographySodiumBiophysicsElectrophoresis CapillaryReproducibility of Resultschemistry.chemical_elementAscorbic AcidCell BiologyElectrolytePlantsAscorbic acidSensitivity and SpecificityBiochemistryElectrophoresischemistry.chemical_compoundCapillary electrophoresischemistryBromideDehydroascorbic acidMolecular BiologyAnalytical Biochemistry
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Direct determination of oleic acid in soybean oil by capacitively coupled contactless conductivity detection capillary electrophoresis in an oil-misc…

2014

Este trabalho teve por objetivo desenvolver um método analítico direto e rápido para a determinação de ácido oleico em óleo de soja por eletroforese capilar com detecção condutométrica sem contato. O eletrólito de corrida empregado foi uma mistura metanol/1-propanol (1:6 v/v) contendo 4 × 10-2 mol L-1 de KOH e 10% (v/v) em etileno glicol. As amostras foram preparadas pela solubilização de 50 g L-1 de óleo de soja e 1,33 × 10-3 de ácido salicílico (padrão interno) no eletrólito de corrida. Os ensaios quantitativos foram realizados adicionando ácido oleico puro às amostras, na faixa entre 0,53 e 2,13 × 10-3 mol L-1. Sob polaridade negativa, os solutos aniônicos deslocaram-se mais rapidamente …

Detection limitChromatographyfood.ingredientcontactless capacitively coupled contactless conductivity detection (C4D)soybean oilGeneral ChemistryElectrolyteontactless capacitively coupled contactless conductivity detection (C4D)Soybean oilOleic acidchemistry.chemical_compound1-PropanolCapillary electrophoresisfoodchemistryoleic acidÓleo de sojanon-aqueous capillary electrophoresis (NACE)MethanolEletroforese capilarÁcido oléicoEthylene glycol
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Pressurised liquid extraction and capillary electrophoresis–mass spectrometry for the analysis of pesticide residues in fruits from Valencian markets…

2010

Abstract A procedure based in capillary electrophoresis–mass spectrometry (CE–MS) for the analysis of seven pesticides (flutolanil, simazine, haloxyfop, acifluorfen, dinoseb, picloram, and ioxynil) in four Mediterranean summer fruits with high water content (peaches, melon, watermelon, and apricot) is developed. Several conditions were studied for the optimisation of both, the separation and the electrospray (ESI) connection. The best results were obtained using 35 mM ammonium formiate (pH 9.7) as separation buffer, 20 °C as capillary temperature and 23 kV as applied voltage in an uncoated fused-silica capillary with 50 cm total length, 25 cm thermostated length, 25 cm at room temperature l…

Detection limitElectrosprayChromatographyPesticide residueChemistryFormic acidExtraction (chemistry)General MedicineMass spectrometryCapillary electrophoresis–mass spectrometryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisFood ScienceFood Chemistry
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