Search results for "sample preparation"

showing 10 items of 343 documents

Simultaneous determination of eight underivatised biogenic amines in fish by solid phase extraction and liquid chromatography-tandem mass spectrometr…

2010

Biogenic amines on fish tissue are formed as a result of bacterial contamination and spoilage during storage. A new method based on liquid chromatography (LC) and tandem mass spectrometry (MS/MS) using a triple quadrupole (QqQ) analyser was developed for the analysis of eight biogenic amines (cadaverine, histamine, phenylethylamine, putrescine, spermine, spermidine, tyramine and tryptamine) in fish tissues. Sample preparation was performed by extraction with trichloroacetic acid 5% and solid phase extraction clean up with STRATA X cartridge. The MS/MS method was validated and compared with a method based on the analysis of dansyl derivatives by LC and fluorescence detector (FD). MS/MS achie…

CadaverineBiogenic AminesChromatographyExtraction (chemistry)Solid Phase ExtractionFishesGeneral MedicineTandem mass spectrometryAnalytical ChemistryTriple quadrupole mass spectrometerchemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryPutrescineAnimalsSample preparationSolid phase extractionChromatography High Pressure LiquidFood ScienceChromatography LiquidFood chemistry
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In-situ suspended aggregate microextraction: A sample preparation approach for the enrichment of organic compounds in aqueous solutions.

2015

Abstract This work presents in-situ suspended aggregate microextraction (iSAME) as a new and expedient sample preparation method. This new concept capitalizes on the general principles of in-situ solvent formation microextraction, in the sense that extraction is carried out in a supramolecular aggregate phase, which is formed in-situ in the sample through one-step process involving ion-association between a cationic surfactant and a benzene sulfonic acid derivative. The suspended aggregate containing the analytes is then collected in the form of a thin-film on the surface of a common filter paper by suction filtration. The entrapped analytes are released by completely dissolving the thin-fi…

Calibration curveLiquid Phase MicroextractionAnalytical chemistryBiochemistryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)ElectrolyteslawSample preparationSolid phase extractionOrganic ChemicalsDissolutionFiltrationAqueous solutionChromatographyChemistryOrganic ChemistryExtraction (chemistry)Osmolar ConcentrationWaterGeneral MedicineHydrogen-Ion ConcentrationSolventsFiltrationWater Pollutants ChemicalJournal of chromatography. A
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An automated and self-cleaning nano liquid chromatography mass spectrometry platform featuring an open tubular multi-hole crystal fiber solid phase e…

2017

An open tubular (OT) sample preparation/separation platform was developed. A multi-channel polymer layer open tubular (mPLOT) solid phase extraction (SPE) column was prepared by wall-coating the 126 channels (8μm inner diameter (ID) each) of a crystal fiber capillary with an organic polymer, namely poly(styrene-co-octadecene-co-divinylbenzene) (PS-OD-DVB). The mPLOT SPE was coupled on-line with a 10μm×2m poly(styrene-co-divinylbenzene) (PS-DVB) OT liquid chromatography column with nanospray mass spectrometry (OTLC-MS). Compared to using monolithic/particle-packed SPEs, mPLOT-SPE-OTLC allowed both fast loading and sufficient refocusing on the OT analytical column of small model compounds (su…

Capillary actionAnalytical chemistry02 engineering and technologyMass spectrometry01 natural sciencesBiochemistryChemistry Techniques AnalyticalMass SpectrometryAnalytical Chemistrylaw.inventionCrystallawSample preparationFiberSolid phase extractionFiltrationchemistry.chemical_classificationChromatographyChemistrySolid Phase Extraction010401 analytical chemistryOrganic ChemistryGeneral MedicinePolymer021001 nanoscience & nanotechnologyESPECTROMETRIA DE MASSAS0104 chemical sciencesPolystyrenesPolyvinyls0210 nano-technologyChromatography Liquid
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Recent Advances in Sample Preparation for Pesticide Analysis

2012

Much progress has been made in pesticide analysis in the past decade. During this time, hyphenated techniques involving highly efficient separation with sensitive mass spectrometric detection have become the methods of choice. Even with such powerful instrumental techniques, a demanding task in pesticide residue analysis is the development of multiresidue methods for the determination of pesticides in air, water, soil, sediment, biota, and food. This chapter summarizes the analytical characteristics of the different methods of sample preparation for the determination of pesticide residues in a variety of food matrices, and surveys their recent applications in combination with gas chromatogr…

Capillary electrophoresisChromatographyPesticide residuebusiness.industryChemistryExtraction (chemistry)Molecularly imprinted polymerSupercritical fluid extractionSample preparationSolid phase extractionProcess engineeringbusinessSolid-phase microextraction
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Development and validation of a pressurized liquid extraction liquid chromatography–tandem mass spectrometry method for perfluorinated compounds dete…

2009

Abstract This paper describes the development and validation of an analytical methodology to determine eight perfluorinated compounds (PFCs) in edible fish using pressurized liquid extraction (PLE) with water and solid-phase extraction (SPE) with an ion-exchanger as extraction and pre-concentration procedures, followed by liquid chromatography–quadrupole-linear ion trap mass spectrometry (LC–QqLIT–MS). The rapidity and effectiveness of the proposed extraction procedure were compared with those most commonly used to isolate PFCs from fish (ion-pairing and alkaline digestion). The average recoveries of the different fish samples, spiked with the eight PFCs at three levels (the LOQ, 10 and 100…

Chemical Fractionation010501 environmental sciencesMass spectrometryTandem mass spectrometrySensitivity and Specificity01 natural sciencesBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundTandem Mass SpectrometryLiquid chromatography–mass spectrometryPressureAnimalsSample preparation14. Life underwaterSolid phase extractionMuscle Skeletal0105 earth and related environmental sciencesFluorocarbonsChromatography010401 analytical chemistryOrganic ChemistryExtraction (chemistry)FishesReproducibility of ResultsGeneral Medicine0104 chemical sciencesLiverchemistryLinear ModelsPerfluorooctanoic acidFood AnalysisChromatography LiquidJournal of Chromatography A
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Determination of carbosulfan and its metabolites in oranges by liquid chromatography ion-trap triple-stage mass spectrometry.

2005

Liquid chromatography ion-trap mass spectrometry LC-MSn has been successfully applied to identify and confirm carbosulfan and seven of its metabolites in oranges after pressurized liquid extraction (PLE) with dichloromethane. Mass spectra of carbosulfan and its metabolites were investigated using multiple stages of mass spectrometry. Although interpretation of the fragmentation pathways, based on mass spectra, enables structural elucidation and identification of these compounds, the proposed fragmentation pathways and ion structures need verification by exact mass measurements. The analytical method--PLE and LC-MS3 --was validated: limits of quantification (LOQ) ranged from 0.01 to 0.07 mg …

Chemical ionizationCitrusChromatographyChemistryOrganic ChemistryPesticide ResiduesReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical ChemistryMasschemistry.chemical_compoundMass spectrumCarbosulfanSample preparationIon trapCarbamatesChromatography LiquidJournal of chromatography. A
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Comparison of solid-phase microextraction and stir bar sorptive extraction for determining six organophosphorus insecticides in honey by liquid chrom…

2004

Abstract Two approaches based on sorptive extraction, solid-phase microextraction (SPME) and stir bar sorptive extraction (SBSE), in combination with liquid chromatography (LC)–atmospheric pressure chemical ionization mass spectrometry (MS) have been assayed for analyzing chlorpyriphos methyl, diazinon, fonofos, phenthoate, phosalone, and pirimiphos ethyl in honey. In both, SPME and SBSE, enrichment was performed using a poly(dimethylsiloxane) coating. Significant parameters affecting sorption process such as sample volume, sorption and desorption times, ionic strength, elution solvent, and dilution (water/honey) proportion were optimized and discussed. Performance of both methods has been …

Chemical ionizationInsecticidesChromatographyChemistryElutionOrganic ChemistryExtraction (chemistry)SorptionGeneral MedicineHoneyMass spectrometrySolid-phase microextractionBiochemistrySensitivity and SpecificityMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometrySample preparationChromatography LiquidJournal of chromatography. A
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Pesticide residue determination in fruit and vegetables by liquid chromatography–mass spectrometry

2000

An overview is given of pesticide residue determination in fruit and vegetables by liquid chromatography-mass spectrometry (LC-MS). Emphasis is placed on the thermospray, particle beam and atmospheric pressure ionization interfaces including advantages and drawbacks and typical detection limits. The capacity of each interface to provide useful data for identification/confirmation of analytes and the possibility of obtaining structural information for the identification of target and non-target compounds is discussed. Finally, sample preparation techniques are dealt with in relation to their influence on further LC-MS determination.

Chemical ionizationResidue (complex analysis)ElectrosprayChromatographyPesticide residueChemistryOrganic ChemistryPesticide ResiduesAnalytical chemistryThermosprayGeneral MedicineMass spectrometryBiochemistryMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryFruitVegetablesSample preparationChromatography LiquidJournal of Chromatography A
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Green Analytical Chemistry

2008

We discuss the origins and the fundamentals of Green Analytical Chemistry (GAC), based on the literature published about clean, environmentally-friendly or GAC methods. We pay special attention to the strategies and the tools available to make sample-pretreatment and analytical methods greener. We consider that the main principles are to replace toxic reagents, to miniaturize and to automate methods, making it possible to reduce dramatically the amounts of reagents consumed and wastes generated, so reducing or avoiding side effects of analytical methods. We also consider on-line decontamination or passivation of wastes to be of special interest in making analytical chemistry sustainable.

ChemistryAnalytical chemistrySample preparationAnalytical Chemistry (journal)Human decontaminationSpectroscopyAnalytical ChemistryTrAC Trends in Analytical Chemistry
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Current trends in affinity-based monoliths in microextraction approaches: A review

2019

Abstract This article reviews the research contributions along the past five years concerning to monolithic materials for the development of affinity-based sorbents in the field of microextraction techniques. The first part of this paper includes an introduction regarding monolithic affinity media and information of different binding agents (such as immunoglobulin-binding proteins, enzymes, lectins, antibodies, aptamers, dyes and immobilized metal ions and nanoparticles, among others) that can act as affinity ligands. Then, the preparation of monoliths and ligand immobilization strategies as well as the different available formats (syringes, pipette tips, spin columns, capillaries, disks an…

ChemistryAptamer010401 analytical chemistryMicrofluidicsNanoparticleNanotechnology02 engineering and technologyLigands021001 nanoscience & nanotechnology01 natural sciencesBiochemistryChromatography Affinity0104 chemical sciencesAnalytical ChemistryHumansEnvironmental ChemistrySample preparationAdsorption0210 nano-technologySolid Phase MicroextractionSpectroscopyAnalytica Chimica Acta
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