Search results for "Sample preparation"

showing 10 items of 343 documents

Determination of Selected Phthalates by Gas Chromatography–Mass Spectrometry in Personal Perfumes

2015

A simple and fast method is proposed to analyze commercial personal perfumes. Our method includes measurement of phthalates, known to be major sources of endocrine disruptor chemicals (EDC), which originate from the less volatile fraction of perfumes. The quantification of phthalates were carried out directly with no sample preparation required on 30 samples of commercial products using gas chromatography and mass spectrometry (GC-MS) as a detector. The total concentrations of 15 investigated compounds ranged from 17 to 9650 mg/L with an average of 2643 mg/L. The highest total concentration was found in cologne. Diethyl phthalate (DEP), diisobutyl phthalate (DiBP), di(2-ethylhexyl) phthalat…

Gas-Chromatography–Mass SpectrometryPhthalates Gas-Chromatography–Mass Spectrometry Personal perfumesChromatographyHealth Toxicology and MutagenesisPhthalic AcidsPhthalateDiisobutyl phthalateEndocrine DisruptorsToxicologyDiethyl phthalateGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliPerfumePhthalic acidchemistry.chemical_compoundPhthalateschemistryEndocrine disruptorPersonal perfumesEnvironmental chemistrySettore CHIM/01 - Chimica AnaliticaSample preparationGas chromatographyGas chromatography–mass spectrometryEnvironmental MonitoringJournal of Toxicology and Environmental Health, Part A
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Determination of pharmaceuticals in soils and sediments by pressurized liquid extraction and liquid chromatography tandem mass spectrometry

2010

13 páginas, 4 figuras, 6 tablas.

Geologic SedimentsElectrosprayTandem mass spectrometryLiquid chromatographyChemical FractionationTandem mass spectrometrySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)SoilLiquid chromatography–mass spectrometryAntibioticsSoil PollutantsSample preparationSolid phase extractionEnvironmental analysisSolid-phase extractionChromatographyChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineMulti-residue methodPharmaceutical PreparationsLinear ModelsPharmaceuticalsSedimentChromatography Liquid
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Expanding the application of stir bar sorptive-dispersive microextraction approach to solid matrices: Determination of ultraviolet filters in coastal…

2018

This work describes a new method for the determination of organic compounds in solid samples based on the equilibrium desorption of the analytes in an aqueous phase followed by stir bar sorptive-dispersive microextraction (SBSDME). Sand samples, contaminated with UV filters due to bathing and recreational activities, were dispersed in an aqueous medium by using a coated stir bar with CoFe2O4@oleic acid magnetic nanoparticles. The UV filters were physically desorbed from the surface of the sand particles and rapidly adsorbed on the hydrophobic coating of the nanoparticles, which were retrieved by means of their magnetism after stopping the stirring. In this manner, both preconcentration of t…

Geologic SedimentsSorbent010501 environmental sciences01 natural sciencesBiochemistryBathing BeachesGas Chromatography-Mass SpectrometryAnalytical ChemistryAdsorptionDesorptionSample preparationOrganic ChemicalsSolid Phase Microextraction0105 earth and related environmental sciencesDetection limitChromatographyChemistryOsmolar Concentration010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Aqueous two-phase systemWaterGeneral Medicine0104 chemical sciencesStandard additionAdsorptionHydrophobic and Hydrophilic InteractionsSunscreening AgentsWater Pollutants ChemicalEnvironmental MonitoringJournal of Chromatography A
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Occurrence of glyphosate in beer from the Latvian market.

2018

A sensitive LC-MS/MS method for the determination of glyphosate in beer has been developed, validated, and applied to analyse 100 beer samples from 24 different producers and distributors in Latvia. The selected samples represented most beer brands and varieties sold in local supermarkets. Different procedures for sample preparation and chromatographic separation were compared. The final version of the method consisted of solid phase extraction, chromatographic separation on aminopropyl stationary phase, and detection using tandem mass spectrometry. The concentration of glyphosate in beer varied from below the LOD of 0.2 μg kg-1 up to 150 μg kg-1, higher than previously reported. Significan…

Health Toxicology and MutagenesiseducationGlycineFood Contamination010501 environmental sciencesToxicology01 natural scienceschemistry.chemical_compoundTandem Mass SpectrometryLc ms msSample preparationSolid phase extractionFood science0105 earth and related environmental sciencesMathematicsFinal versionMarketing010401 analytical chemistryPublic Health Environmental and Occupational Healthfood and beveragesBeerGeneral ChemistryGeneral MedicineLatvia0104 chemical sciencesChromatographic separationchemistryStationary phaseGlyphosateFood ScienceFood contaminantChromatography LiquidFood additivescontaminants. Part A, Chemistry, analysis, control, exposurerisk assessment
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Characterisation of disaccharide fragments from the enzymatic digestion of heparin by liquid secondary ion mass spectrometry

1988

Disaccharide fragments resulting from the enzymatic digestion of heparins with heparinase have been purified by gel filtration chromatography and directly analyzed by positive and negative ion liquid secondary ion mass spectrometry (LSIMS). Following the chromatographic purification from excess sodium salt, the mass spectra of di- and tetrasaccharide fragment mixtures enabled the identification of up to three covalently bound sulfate moieties per glycosaminoglycan-disaccharide unit, by means of their molecular ions, containing the corresponding alkali-counterions.

HeparinaseChromatographyChemistryClinical BiochemistrySize-exclusion chromatographyDisaccharideGeneral MedicineMass spectrometrySample preparation in mass spectrometryAnalytical ChemistrySecondary ion mass spectrometrychemistry.chemical_compoundMass spectrumTetrasaccharideGeneral Materials ScienceFresenius' Zeitschrift für analytische Chemie
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Current trends on the determination of organic UV filters in environmental water samples based on microextraction techniques – A review

2018

UV filters are a group of cosmetic ingredients commonly used in a wide variety of cosmetic products to protect users from UV solar radiation. They belong to different chemical families, such as benzophenones, p-aminobenzoates, salicylates, cinnamates, benzotriazoles, benzimidazoles, camphor derivatives, triazines, etc. These cosmetic ingredients are considered as emerging contaminants since they easily reach the aquatic environment, where they are accumulated causing harmful effects in the flora and fauna despite being present at the ng L-1 level. Therefore, the development of sensitive and selective analytical methods for their environmental surveillance monitoring is of high interest. In …

High interestLiquid Phase MicroextractionUltraviolet RaysChemistryEnvironmental surveillance010401 analytical chemistry02 engineering and technologyContamination021001 nanoscience & nanotechnology01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryEnvironmental waterAquatic environmentEnvironmental chemistryEnvironmental ChemistrySample preparationWater quality0210 nano-technologyWater pollutionSolid Phase MicroextractionWater Pollutants ChemicalSpectroscopyEnvironmental MonitoringAnalytica Chimica Acta
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Use of Nanomaterial-Based (Micro)Extraction Techniques for the Determination of Cosmetic-Related Compounds

2020

The high consumer demand for cosmetic products has caused the authorities and the industry to require rigorous analytical controls to assure their safety and efficacy. Thus, the determination of prohibited compounds that could be present at trace level due to unintended causes is increasingly important. Furthermore, some cosmetic ingredients can be percutaneously absorbed, further metabolized and eventually excreted or bioaccumulated. Either the parent compound and/or their metabolites can cause adverse health effects even at trace level. Moreover, due to the increasing use of cosmetics, some of their ingredients have reached the environment, where they are accumulated causing harmful effec…

High interestSkin Absorptionmedia_common.quotation_subjectPharmaceutical ScienceCosmeticsReview02 engineering and technologyChemical Fractionation01 natural sciencesCosmeticsAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryAdverse health effectDrug DiscoveryPhysical and Theoretical Chemistrycosmetic-related compoundsnanomaterialsmedia_commonmicroextraction techniquessample preparationConsumer demandEnvironmental surveillance010401 analytical chemistryOrganic ChemistryExtraction (chemistry)021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencesChemistry (miscellaneous)Percutaneous absorptionMolecular MedicineEnvironmental scienceBiochemical engineering0210 nano-technologyEnvironmental MonitoringMolecules
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Comparison of green sample preparation techniques in the analysis of pyrethrins and pyrethroids in baby food by liquid chromatography–tandem mass spe…

2017

A new selective and sensitive liquid chromatography triple quadrupole mass spectrometry method was developed for simultaneous analysis of natural pyrethrins and synthetic pyrethroids residues in baby food. In this study, two sample preparation methods based on ultrasound-assisted dispersive liquid–liquid microextraction (UA-DLLME) and salting-out assisted liquid–liquid extraction (SALLE) were optimized, and then, compared regarding the performance criteria. Appropriate linearity in solvent and matrix-based calibrations, and suitable recoveries (75–120%) and precision (RSD values ≤ 16%) were achieved for selected analytes by any of the sample preparation procedures. Both methods provided the…

InsecticidesAnalyteMaximum Residue LimitLiquid-Liquid ExtractionFood Contamination010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistryMatrix (chemical analysis)Baby foodchemistry.chemical_compoundLC–MS/MSTandem Mass SpectrometryLiquid chromatography–mass spectrometryEtofenproxNitrilesPyrethrinsAnimalsHumansSample preparationPesticidesFood contaminantsChromatographyChemistry010401 analytical chemistryOrganic ChemistryInfantGreen Chemistry TechnologyGeneral Medicine0104 chemical sciencesMilkUA-DLLMEGreen chemistryFruitSolventsInfant FoodEdible GrainEnrichment factorBaby foodsChromatography Liquid
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Confirmation of Fenthion Metabolites in Oranges by IT-MS and QqTOF-MS

2007

14 pages, 4 figures, 4 tables.-- PMID: 18020315 [PubMed].-- Printed version published Dec 15, 2007.

InsecticidesSulfoneElectrosprayFenoxon sulfoxideMass spectrometryMass SpectrometryAnalytical ChemistrySulfonechemistry.chemical_compoundSample preparationSulfonesPesticidesOrganophophorous pesticide fenthionChemical ionizationChromatographyFenthionHydrolysisSulfoxideFenoxon sulfoneSulfoxideFenthionchemistrySulfoxidesCholinesterase InhibitorsIon trapFood AnalysisCitrus sinensisAnalytical Chemistry
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Substitution–dilution method to correct the matrix effect in multi-element quantitative analysis by X-ray fluorescence

2001

Abstract A mathematical model based on the dilution–addition method (DAM) for multi-elemental analysis using an X-ray fluorescence technique is proposed. The conditions for sample preparation do not require both the unknown and standard samples to be similar in composition and mineralogy, and the unknown sample is replaced quantitatively by the standard sample, hence the denomination substitution–dilution method (SDM). This method makes it possible to correct the matrix effect in multi-elemental quantitative analysis by X-ray fluorescence for each analyte. The proposed model presents hyperbolic behaviour of the experimental data when the X-ray fluorescence intensities are represented versus…

Internal standardAnalyteChemistryHyperbolic functionAnalytical chemistryLinear modelDiluentAtomic and Molecular Physics and OpticsAnalytical ChemistryDilutionMatrix (chemical analysis)Sample preparationInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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