Search results for "Mass spectrometer"

showing 10 items of 75 documents

Optimization of LC–MS/MS using triple quadrupole mass analyzer for the simultaneous analysis of carbosulfan and its main metabolites in oranges

2006

This paper describes an analytical method involving a simple solvent extraction for the simultaneous liquid chromatography coupled to quadrupole tandem mass spectrometry (LC-MS/MS) determination of carbosulfan, its most toxic metabolite--carbofuran--, and its other main metabolites--3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenolcarbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran and dibutylamine--in oranges. Chromatography was performed on a Zorbax Bonus-RP (150 mm x 2.1 mm, 5 microm). The mobile phase was a ternary gradient water-methanol-acetonitrile with 1.0 mM ammonium acetate at flow rate of 0.2 ml min(-1). The LC separation and MS/MS optimization were studied to selec…

Detection limitChromatographyMetaboliteAnalytical chemistryTandem mass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerStandard curvechemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryEnvironmental ChemistrySample preparationCarbosulfanSpectroscopyAnalytica Chimica Acta
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Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry to identify contaminants in water: an insight on environment…

2013

Ultra-high pressure liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QqTOF-MS) acquiring full scan MS data for quantification, and automatic data dependent information product ion spectra (IDA-MS/MS) without any predefinition of the ions by the user was checked for identifying organic contaminants in water samples. The use of a database with more than 2000 compounds achieved high confidence results for a wide number of contaminants based upon retention time, accurate mass, isotopic pattern and MS/MS library searching. More than 20 contaminants, mostly pharmaceuticals, but also mycotoxins and polyphenols were unambiguously identified. Furthermore, the combination of s…

Detection limitChromatographyTime FactorsChemistryOrganic ChemistryAnalytical chemistryWaterGeneral MedicineContaminationMass spectrometryBiochemistryLibrary searchingAnalytical ChemistryTriple quadrupole mass spectrometerMolecular WeightRiversTandem Mass SpectrometryPrincipal component analysisQuadrupole time of flightUltra high performancePesticidesChromatography High Pressure LiquidWater Pollutants ChemicalJournal of chromatography. A
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Identification of unknown pesticides in fruits using ultra-performance liquid chromatography–quadrupole time-of-flight mass spectrometry

2007

Abstract Ultra-high-performance liquid chromatography–quadrupole time-of-flight mass spectrometry (UPLC-QqTOF-MS) is an emerging technique offering more rapid and efficient separation, as well as the possibility to obtain accurate mass measurement and tandem mass spectrometry (MS/MS). This paper deals with the use of UPLC-QqTOF-MS to identify the pesticide residues present in complex pear extracts. Carbendazim, imazalil, and ethoxyquin were successfully identified because of the accurate mass determination of their protonated molecule and their major fragments in the product ion mass spectra. A few plastic and latex additives were also found, most of them probably coming from the packaging …

Detection limitElectrosprayChromatographyCalibration curveChemistryOrganic ChemistryAnalytical chemistryGeneral MedicineTandem mass spectrometryMass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerLiquid chromatography–mass spectrometryMass spectrumJournal of Chromatography A
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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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Determination of trace elements by resonant ionization mass spectrometry (RIMS)

1988

A resonant ionization mass spectrometer has been developed as an analytical tool for the detection of trace elements, especially of plutonium and other radionuclides. The sample, deposited on a rhenium filament, is evaporated by electrical heating and the atoms of the element under investigation are selectively ionized by laser light delivered from three dye lasers pumped by a copper vapour laser. The resulting photoions are detected in a time-of-flight spectrometer with a channelplate detector. For plutonium a mass resolution of M/δM=1500 was obtained and an overall detection efficiency of 4×10−6 was determined for stepwise excitation and ionization via autoionizing states. With a laser li…

Dye laserSpectrometerPhysics::Instrumentation and DetectorsChemistryClinical BiochemistryAnalytical chemistryGeneral MedicineThermal ionization mass spectrometryMass spectrometryBiochemistryAnalytical ChemistryIonizationGeneral Materials SciencePhysics::Atomic PhysicsAtomic vapor laser isotope separationHyperfine structureHybrid mass spectrometerFresenius Zeitschrift f�r Analytische Chemie
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Analysis of fumonisins B1, B2 and B3 in corn-based baby food by pressurized liquid extraction and liquid chromatography/tandem mass spectrometry

2008

A sensitive and reliable method using pressurized liquid extraction (PLE) and liquid chromatography (LC)/electrospray ionization (ESI) tandem mass spectrometry with a triple quadrupole (QqQ) analyzer has been developed for the analysis of fumonisin B(1) (FB(1)), fumonisin B(2) (FB(2)) and fumonisin B(3) (FB(3)) in corn-based baby foods. Influence of several extraction parameters that affect PLE efficiency such as temperature, pressure, solvent extraction, number of cycles and dispersant/clean-up agents were studied. The selected PLE operating method was: 3g of sample was packed into 11 ml stainless-steel cell and fumonisins were extracted with methanol at 40 degrees C, 34 atm in one cycle o…

ElectrosprayChromatographyChemistryElectrospray ionizationOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineChemical FractionationFumonisinsZea maysBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryTriple quadrupole mass spectrometerTandem Mass SpectrometryLiquid chromatography–mass spectrometrymedia_common.cataloged_instanceInfant FoodSample preparationEuropean unionChromatography Liquidmedia_commonJournal of Chromatography A
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Distribution and fate of perfluoroalkyl substances in Mediterranean Spanish sewage treatment plants.

2014

The concentrations of 21 perfluoroalkyl substances (PFASs: C4-C14, C16, C18 carboxylates, C4, C6-C8 and C10 sulfonates and C8 sulfonamide) were determined in influent, effluent and sludge from 16 different sewage treatment plants (STPs) located in the Ebro (6), Guadalquivir (5), Jucar (2) and Llobregat (3) Rivers, in two consecutive years (2010 and 2011). The analytes were extracted by solid phase extraction (SPE) and determined by Liquid Chromatography triple Quadrupole Mass Spectrometer (LC-QqQ-MS). All samples, except two sludges from Guadalquivir River STPs, were contaminated with at least one PFAS. Perfluorobutanoate (PFBA), perfluoropentanoate (PFPeA) and perfluorooctane sulfonate (L-…

FluorocarbonsEnvironmental EngineeringSewageContaminationPollutionWaste Disposal FluidTriple quadrupole mass spectrometerPerfluorooctanechemistry.chemical_compoundDry weightchemistryWastewaterSpainEnvironmental chemistryEnvironmental ChemistrySewage treatmentSolid phase extractionWaste Management and DisposalEffluentWater Pollutants ChemicalEnvironmental MonitoringThe Science of the total environment
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Analysis of fumonisins in corn-based food by liquid chromatography with fluorescence and mass spectrometry detectors

2008

Abstract The presented procedure involves an extraction with methanol–water, centrifugation and cleanup with immunoaffinity columns. A comparison study between fluorescence detector, mass spectrometry, and tandem mass spectrometry with a triple quadrupole (QqQ) analyzer using an electrospray ionisation interface for the determination of fumonisin B1 and B2 in corn-based products has been performed. Limits of quantification obtained by the three detectors were lower than the maximum levels established by European Commission. Liquid chromatography coupled to tandem mass spectrometry provides higher sensitivity (12 μg kg−1for fumonisins B1 and B2) when compared to mass spectrometry (40 μg kg−1…

Fumonisin B2ElectrosprayFumonisin B1ChromatographyChemistryExtraction (chemistry)General MedicineTandem mass spectrometryMass spectrometryFluorescence spectroscopyAnalytical ChemistryTriple quadrupole mass spectrometerchemistry.chemical_compoundFood ScienceFood Chemistry
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Determination of mycotoxins in bee pollen by gas chromatography-tandem mass spectrometry.

2013

Bee pollen, promoted as a natural food supplement, is consumed increasingly by people to maintain a healthy diet. Depending on environmental conditions, pollen can also be an optimum medium for growth of molds such as Fusarium and Penicillium . A quick, easy, cheap, rapid, and safe (QuEChERS) extraction procedure followed by a gas chromatography-tandem mass spectrometry (GC-MS/MS) determination of eight selected Fusarium toxins in bee pollen was developed and optimized. Recovery studies at 20, 80, and 1000 μg/kg showed values between 73 and 95% with relative standard deviations (RSDs) of15% for all studied mycotoxins. Limits of quantitation (LOQ) ranged from 1 to 4 μg/kg. The proposed metho…

FusariumChromatographyGas Chromatography/Tandem Mass SpectrometrybiologyChemistryFood ContaminationGeneral ChemistryBeesMycotoxinsbiology.organism_classificationMass spectrometryQuechersmedicine.disease_causeGas Chromatography-Mass SpectrometryTriple quadrupole mass spectrometerchemistry.chemical_compoundFusariumBee pollenPollenDietary SupplementsmedicineAnimalsPollenGeneral Agricultural and Biological SciencesMycotoxinJournal of agricultural and food chemistry
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Emerging Fusarium mycotoxins in organic and conventional pasta collected in Spain

2012

Abstract One of the main sources of emerging Fusarium mycotoxins in human nutrition is the cereals and cereal products. In this study, an analytical method to determine enniatins A, A1, B and B1 (ENs), beauvericin (BEA) and fusaproliferin (FUS) based on Ultra-Turrax extraction followed by liquid chromatography coupled to triple quadrupole mass spectrometer detector (MS/MS QqQ), was applied for the analysis of pasta. For this purpose, 114 commercial samples of pasta were acquired from supermarkets located in Valencia. The results showed higher frequencies of contamination in organic pasta than in conventional pasta, while the concentration levels were variable for both types of pasta. In pos…

FusariumFood ContaminationToxicologychemistry.chemical_compoundFusariumTandem Mass SpectrometryLiquid chromatography–mass spectrometryDepsipeptidesHumansFood scienceMycotoxinOrganic AgriculturebiologyTerpenesDietary exposureReproducibility of ResultsGeneral MedicineMycotoxinsContaminationbiology.organism_classificationBeauvericinTriple quadrupole mass spectrometerHuman nutritionchemistrySpainPublic HealthEdible GrainChromatography LiquidFood ScienceFood and Chemical Toxicology
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