Search results for "Solid phase extraction"

showing 10 items of 297 documents

Analysis of thiabendazole and procymidone in fruits and vegetables by capillary electrophoresis–electrospray mass spectrometry

2002

Abstract A capillary electrophoresis–mass spectrometry method for determining procymidone and thiabendazole in apples, grapes, oranges, pears, strawberries and tomatoes is described. Separation is achieved using a buffer of formic acid–ammonium formate at pH 3.5 with 2% of methanol. Fungicide residues present in the sample are preconcentrated by both solid-phase extraction and injection of large sample volumes into the capillary by a stacking technique, to obtain lower detection limits. Ionization is performed at atmospheric pressure in an electrospray type source and detection is carried out using positive ionization and selected ion monitoring modes. The quantitation limits are 0.005 and …

Detection limitSpectrometry Mass Electrospray IonizationElectrosprayChromatographyOrganic ChemistryPesticide ResiduesElectrophoresis CapillaryGeneral MedicineMass spectrometrySensitivity and SpecificityBiochemistryFungicides IndustrialAnalytical ChemistryBridged Bicyclo Compoundschemistry.chemical_compoundCapillary electrophoresischemistryFruitThiabendazoleVegetablesSample preparationSelected ion monitoringSolid phase extractionProcymidoneJournal of Chromatography A
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Rugged Large Volume Injection for Sensitive Capillary LC-MS Environmental Monitoring

2017

A rugged and high throughput capillary column (cLC) LC-MS switching platform using large volume injection and on-line automatic filtration and filter back-flush (AFFL) solid phase extraction (SPE) for analysis of environmental water samples with minimal sample preparation is presented. Although narrow columns and on-line sample preparation are used in the platform, high ruggedness is achieved e.g. injection of 100 non-filtrated water samples would did not result in a pressure rise/clogging of the SPE/capillary columns (inner diameter 300 µm). In addition, satisfactory retention time stability and chromatographic resolution were also features of the system. The potential of the platform for …

Resolution (mass spectrometry)Capillary actionAnalytical chemistry02 engineering and technologycapillary LC01 natural scienceslaw.inventionlcsh:ChemistrylawLiquid chromatography–mass spectrometrySample preparationSolid phase extractionon-line solid phase extractionFiltrationOriginal ResearchDetection limitChromatographyChemistry010401 analytical chemistryGeneral ChemistryRepeatability021001 nanoscience & nanotechnology0104 chemical sciencespharmaceutical productsChemistrylcsh:QD1-999column switchinglarge volume injection0210 nano-technologyFrontiers in Chemistry
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Determination of type A and type B trichothecenes in paprika and chili pepper using LC-triple quadrupole-MS and GC-ECD.

2011

There is a need to develop sensitive and accurate analytical methods for determining deoxynivalenol (DON), HT-2 toxin and T-2 toxin in paprika to properly assess the relevant risk of human exposure. An optimized analytical method for determination of HT-2 toxin and T-2 toxin using capillary gas chromatography with electron capture detection and another method for determination of DON by liquid chromatography-mass spectrometry in paprika was developed. The method for determination of HT-2 toxin and T-2 toxin that gave the best recoveries involved extraction of the sample with acetonitrile-water (84:16, v/v), clean-up by solid-phase extraction on a cartridge made of different sorbent material…

Detection limitResidue (complex analysis)ChromatographyChromatography GasElutionChemistryExtraction (chemistry)Mass SpectrometryAnalytical ChemistryTriple quadrupole mass spectrometerT-2 ToxinHumansSample preparationGas chromatographySolid phase extractionCapsicumTrichothecenesChromatography LiquidTalanta
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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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Cloud point–dispersive μ-solid phase extraction of hydrophobic organic compounds onto highly hydrophobic core–shell Fe 2 O 3 @C magnetic nanoparticles

2012

Abstract A novel two-step extraction technique combining cloud point extraction (CPE) with dispersive micro-solid phase extraction (D-μ-SPE) is presented in this work for the first time. The method involves initial extraction of the target analytes by CPE in the micelles of a non-ionic surfactant medium; then highly hydrophobic polysiloxane-coated core–shell Fe 2 O 3 @C magnetic nanoparticles (MNPs) are used to retrieve the micellar phase. In that manner, the micellar phase containing the analytes is the target of the D-μ-SPE step rather than the analytes directly. MNPs are then collected by the application of an adscititious magnetic field overcoming the need for specific steps associated …

Cloud pointChromatographyChemistryOrganic ChemistryExtraction (chemistry)Analytical chemistryGeneral MedicineBiochemistryMicelleAnalytical ChemistryPulmonary surfactantPhase (matter)Magnetic nanoparticlesSolid phase extractionSolubilityJournal of Chromatography A
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Combination of supported liquid membrane and solid-phase extraction for sample pretreatment of triazine herbicides in juice prior to capillary electr…

2002

A possibility of a combination of supported liquid membrane (SLM) and solid-phase extraction (SPE) for the determination of atrazine at microgram level in different type of fruit juices is presented. In comparison to SPE extraction from juice samples, the application of SLM-SPE enrichment provides much cleaner extracts and the possibility of lowering the limit of detection as low as 30 microg/l. However, it was also shown that by appropriate manipulation of SLM extraction conditions mainly flow-rate of donor phase and volume ratio between donor and acceptor phase, the level of detection can be further decreased to 10 microg/l. The results suggest that the application of SLM extraction prior…

Biochemistryfruit juiceAnalytical ChemistryBeveragessupporter liquid membrane extractionchemistry.chemical_compoundCapillary electrophoresistriazinesSample preparationsolid-phase extractionSolid phase extractionAtrazineTriazineDetection limitChromatographyChemistryHerbicidesOrganic ChemistryElectrophoresis CapillaryMembranes ArtificialGeneral MedicinepesticidesMembraneCalibrationQuantitative analysis (chemistry)atrazineJournal of Chromatography A
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Sensitive determination of probenecid in urine samples by reversed-phase liquid chromatography and UV-visible detection using solid-phase extraction …

1993

This study describes a rapid method for the determination of probenecid in human urine by liquid chromatography with UV detection at 254 nm, after clean-up through a C8 solid-phase extraction column. Liquid chromatography was carried out on a C18-bonded phase using an acetonitrile-acetate buffer (pH=4) gradient elution. Ethacrynic acid was used as internal standard. The system has been applied to the determination of probenecid in the 0.10–100.0 μg/ml concentration range; the limit of detection was 5 ng/mL.

Detection limitChromatographyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyUrineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryProbenecidPhase (matter)medicineSolid phase extractionmedicine.drugChromatographia
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Evaluation by HPLC-UV of Polar Pesticides in Rice Fields

1999

ChromatographyChemical PhenomenaChemistry PhysicalHealth Toxicology and MutagenesisPesticide ResiduesOryzaGeneral MedicineHydrogen-Ion ConcentrationPesticideToxicologyPollutionHigh-performance liquid chromatographySurface-Active AgentsSpainEnvironmental sciencePaddy fieldPolarSpectrophotometry UltravioletTrace analysisSample preparationSolid phase extractionPesticidesChromatography High Pressure LiquidHalf-LifeBulletin of Environmental Contamination and Toxicology
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Determination of organic pollutants in Anguilla anguilla by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS)

2021

© 2021 The Authors.

ScienceClinical BiochemistryIllicit drugs010501 environmental sciencesQuechersTandem mass spectrometry01 natural sciences03 medical and health sciencesEmerging pollutantsLiquid chromatography–mass spectrometryPFASsPlaguicidesSolid phase extractionPesticides030304 developmental biology0105 earth and related environmental sciencesPollutant0303 health sciencesChromatographyChemistryExtraction (chemistry)QQuímicaQueChERsContaminationPesticideEMR-lipidMedical Laboratory TechnologyLiverPharmaceuticalsMuscleMethodsX
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Simultaneous determination of nine phytohormones in seaweed and algae extracts by HPLC-PDA.

2016

An RP-HPLC-PDA method for the simultaneous analysis of 9 compounds deriving from the phytohormones class was developed and optimized, namely indoleacetic acid (IAA), indolebutyric acid (IBA), phenyleacetic acid (PAA), naphtyleacetic acid (NAA), trans-zeatin (TZ), kinetin (KA), isopentenyladenine (IA), 6-benzylaminopurine (6-BA) and abscisic acid (ABA). Validation of the method was performed on the SFE-CO2 extract made out of the mixture of Baltic algae. The regression coefficients for plant hormones were in the range from 0.997 to 0.999. The LOD and LOQ were on the levels from 0.05–0.29 and 0.15–0.88 mg/L, respectively. Developed method was used for the separation and determination plant ho…

0106 biological sciencesSeaweed extractsClinical Biochemistry01 natural sciencesBiochemistryAnalytical ChemistrySFE-CO2 seaweed extractchemistry.chemical_compoundAlgaePlant Growth RegulatorsChlorophytaCladophora glomerataSpirulinaHplc pdaBiomassOrganic ChemicalsAbscisic acidChromatography High Pressure LiquidChromatography Reverse-PhaseChromatographybiology010401 analytical chemistryHormones levelsSolid Phase ExtractionSupercritical fluid extractionRP-HPLC-PDACell BiologyGeneral Medicinebiology.organism_classificationSeaweed0104 chemical sciencesPhytohormoneschemistryRegression AnalysisKinetinIndolebutyric Acid010606 plant biology & botanyJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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