Search results for "Matrix"

showing 10 items of 3205 documents

Determination of dithiocarbamates and metabolites in plants by liquid chromatography–mass spectrometry

2004

Abstract A quantitative matrix solid-phase dispersion and liquid chromatography–atmospheric pressure chemical ionization mass spectrometry (LC–APCI–MS) method is outlined for the simultaneous analysis of dithiocarbamates (DTCs) and their degradation products in plants. Compounds analyzed are dazomet, disulfiram, thiram and the metabolites ethylenthiourea and propylenthiourea. The performance of two different sample preparation protocols, the proposed one and other based on solid-phase extraction, as well as, of both atmospheric pressure ionization sources, APCI and electrospray, were compared. The effect of several parameters on the extraction, separation and detection was studied. Dithioca…

Spectrometry Mass Electrospray IonizationChemical ionizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicinePlantsReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ThiocarbamatesLiquid chromatography–mass spectrometryFruitVegetablesIndicators and ReagentsSample preparationSolid phase extractionChromatography LiquidJournal of Chromatography A
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Routine application using single quadrupole liquid chromatography-mass spectrometry to pesticides analysis in citrus fruits.

2005

Abstract A rapid and sensitive liquid chromatography–electrospray ionization–mass spectrometry method has been developed for the routine analysis of buprofezin, bupirimate, hexaflumuron, tebufenpyrad, fluvalinate and pyriproxyfen in citrus fruits. Extracts were obtained by matrix solid-phase dispersion (MSPD) using C 18 as dispersant and dichloromethane-methanol (80:20, v/v) as eluent. Matrix effects were tested for all matrices by addition of standard to sample blank extracts (samples containing no detectable residues). Mean recoveries obtained at fortification levels between 0.01 and 5 mg kg −1 were 57–97% with relative standard deviations (RSDs) from 5 to 19%. The limits of quantificatio…

Spectrometry Mass Electrospray IonizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerMatrix (chemical analysis)Liquid chromatography–mass spectrometryFruitmedia_common.cataloged_instanceSample preparationSolid phase extractionEuropean unionPesticidesmedia_commonChromatography LiquidJournal of chromatography. A
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Characterization of heat-labile toxin-subunit B from Escherichia coli by liquid chromatography-electrospray ionization-mass spectrometry and matrix-a…

2012

The possibilities of characterizing the heat-labile enterotoxin (LT) of enterotoxigenic Escherichia coli (ETEC) by liquid chromatography electrospray mass spectrometry (LC/ESI-MS) and matrix-assisted laser desorption with time-of-flight mass spectrometry (MALDI-TOF-MS) were investigated. The B subunit from recombinant E. coli (expression in Pichia pastoris) can be detected by LC/ESI-MS expressed in P. pastoris and the charge envelope signals can be observed; LC/ESI-MS and MALDI-TOF-MS analysis allowed the acquisition of labile toxin subunit B (LTB) molecular weight and preliminary structural characterization of LTB toxin. MALDI-TOF analysis after reduction and alkylation of the protein evid…

Spectrometry Mass Electrospray IonizationElectrospray ionizationProtein subunitBacterial ToxinsMolecular Sequence DataToxicologyMass spectrometrymedicine.disease_causespettroemtria di massaPichiaPichia pastorisEnterotoxinsProtein sequencingEnterotoxigenic Escherichia colimedicineTrypsinAmino Acid SequenceDisulfidesPhosphorylationEscherichia colitossinaChromatographyMolecular massbiologyChemistryEscherichia coli ProteinsE. coliGeneral Medicinebiology.organism_classificationRecombinant ProteinsMolecular WeightProtein SubunitsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationFood ScienceChromatography LiquidFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association
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Mass spectrometric studies of benzoxazine resorcarenes

2002

Eleven differently substituted 3,4-dihydro-2H-1,3-benzoxazine resorcarenes were studied by electrospray ionisation (ESI) and matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry, using Fourier transform ion cyclotron resonance (FT-ICR) and time-of-flight (TOF) mass spectrometers, respectively. Under ESI conditions it was possible to transfer the intact resorcarenes from solution to the gas phase, yielding [M + H]+ and [M + 2H]+ ions as the main ions observed. Energy increase of the ions induced ready decomposition through successive eliminations of four CH2NR groups. Ion-molecule reactions showed that the ionising proton was situated somewhere inside the molecule and could …

Spectrometry Mass Electrospray IonizationElectrosprayChemistryOrganic ChemistryAnalytical chemistryResorcinolsMass spectrometryAlkali metalFourier transform ion cyclotron resonanceAnalytical ChemistryIonFragmentation (mass spectrometry)Spectrometry Mass Matrix-Assisted Laser Desorption-IonizationReagentOxazinesMoleculeSpectroscopyRapid Communications in Mass Spectrometry
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Liquid chromatography–electrospray quadrupole ion-trap mass spectrometry of nine pesticides in fruits

2004

A liquid chromatographic method, with electrospray ionization tandem mass spectrometry (LC-ESI-MS-MS), has been developed for determining acrinathrin, carbosulfan, cyproconazole, lambda-cyhalothrin, kresoxim methyl, pyrifenox, pyriproxyfen, propanil, and tebufenpyrad in fruits. The ions prominent in ESI spectra were [M + H]+ and [M + Na]+. In the mass analyzer, collision-induced dissociation fragmentation involved common pathways, for example, product ions of [M + H]+ resulted from the cleavage of the carbamic group or an oxygen bound. The utility of the method is demonstrated by the analysis of crude extracts obtained by matrix solid-phase dispersion (MSPD) using C18 as dispersant and dich…

Spectrometry Mass Electrospray IonizationElectrosprayChromatographyChemistryElectrospray ionizationOrganic ChemistryGeneral MedicineTandem mass spectrometryMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)FruitCalibrationSolid phase extractionIon trapPesticidesChromatography LiquidJournal of Chromatography A
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Development and Validation of a LC-ESI-MS/MS Method for the Determination of Alternaria Toxins Alternariol, Alternariol Methyl-Ether and Tentoxin in …

2016

Alternaria species are capable of producing several secondary toxic metabolites in infected plants and in agricultural commodities, which play important roles in food safety. Alternaria alternata turn out to be the most frequent fungal species invading tomatoes. Alternariol (AOH), alternariol monomethyl ether (AME), and tentoxin (TEN) are some of the main Alternaria mycotoxins that can be found as contaminants in food. In this work, an analytical method based on liquid chromatography (LC) tandem mass spectrometry (MS/MS) detection for the simultaneous quantification of AOH, AME, and TEN in tomato and tomato-based products was developed. Mycotoxin analysis was performed by dispersive liquid-…

Spectrometry Mass Electrospray IonizationHealth Toxicology and MutagenesisAlternariollcsh:MedicineFood ContaminationtomatoToxicologyTandem mass spectrometry01 natural sciencesAlternaria alternataPeptides CyclicArticleMatrix (chemical analysis)chemistry.chemical_compoundLactones0404 agricultural biotechnologySolanum lycopersicumTandem Mass SpectrometryLC-MS/MSdispersive liquid-liquid microextractionMycotoxinDetection limitChromatographybiology010401 analytical chemistrylcsh:RReproducibility of ResultsAlternaria04 agricultural and veterinary sciencesMycotoxinsAlternariabiology.organism_classification040401 food science0104 chemical scienceschemistryTentoxinChromatography Liquid<i>Alternaria</i>; LC-MS/MS; dispersive liquid-liquid microextraction; tomatoToxins; Volume 8; Issue 11; Pages: 328
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Structural analysis of the O-specific polysaccharide isolated from Plesiomonas shigelloides O51 lipopolysaccharide.

2009

Plesiomonasshigelloides strain CNCTC 110/92 (O51) was identified as a new example of plesiomonads synthesising lipopolysaccharides (LPSs) that show preference for a non-aqueous surrounding during phenol/water extraction. Chemical analyses combined with (1)H and (13)C NMR spectroscopy, MALDI-TOF and ESI mass spectrometry showed that the repeating units of the O-specific polysaccharides isolated from phenol and water phase LPSs of P. shigelloides O51 have the same structure: -->4)-beta-D-GlcpNAc3NRA-(1-->4)-alpha-L-FucpAm3OAc-(1-->3)-alpha-D-QuipNAc-(1-->, containing the rare sugar constituent 2,3-diamino-2,3-dideoxyglucuronic acid (GlcpNAc3NRA), and substituents such as D-3-hydroxybutyric ac…

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyStereochemistryMolecular Sequence DataAnalytical chemistryPolysaccharideBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhenolchemistry.chemical_classificationbiologyMolecular StructureOrganic ChemistryO AntigensGeneral MedicineNuclear magnetic resonance spectroscopyCarbon-13 NMRRare sugarbiology.organism_classificationNMR spectra databasechemistryCarbohydrate SequencePlesiomonas shigelloidesSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPlesiomonasBacteriaCarbohydrate research
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New perspectives on diastereoselective determination of hexabromocyclododecane traces in fish by ultra high performance liquid chromatography-high re…

2014

a b s t r a c t A new analytical method is presented for diastereoisomer-specific identification and quantitation of hexabromocyclododecanes (HBCD) in fish samples. The method is based on extraction of the target analytes from samples with a mixture of organic solvents, with further three-stage clean-up includ- ing destructive removal of matrix components with sulphuric acid and acid-impregnated silica gel, and Florisil adsorption column chromatography. Ultra high performance liquid chromatography (UPLC) cou- pled with high resolution (HR) Orbitrap mass spectrometry featuring heated electrospray ionization (HESI-II) interface operated in negative ion mode was employed for the identification…

Spectrometry Mass Electrospray IonizationSalmo salarAnalytical chemistrySilica GelMass spectrometryOrbitrapBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundColumn chromatographylawAnimalsChromatography High Pressure LiquidFlame RetardantsDetection limitHexabromocyclododecaneChromatographyChemistryOrganic ChemistryStereoisomerismGeneral MedicineRepeatabilityHydrocarbons BrominatedCalibrationWater Pollutants ChemicalJournal of chromatography. A
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Structural analysis of the lipid A isolated from Hafnia alvei 32 and PCM 1192 lipopolysaccharides[S]

2010

Hafnia alvei, a Gram-negative bacterium, is an opportunistic pathogen associated with mixed hospital infections, bacteremia, septicemia, and respiratory diseases. The majority of clinical symptoms of diseases caused by this bacterium have a lipopolysaccharide (LPS, endotoxin)-related origin. The lipid A structure affects the biological activity of endotoxins predominantly. Thus, the structure of H. alvei lipid A was analyzed for the first time. The major form, asymmetrically hexa-acylated lipid A built of beta-D-GlcpN4P-(1-->6)-alpha-D-GlcpN1P substituted with (R)-14:0(3-OH) at N-2 and O-3, 14:0(3-(R)-O-12:0) at N-2', and 14:0(3-(R)-O-14:0) at O-3', was identified by ESI-MS(n) and MALDI-tim…

Spectrometry Mass Electrospray IonizationendotoxinLipopolysaccharideAcylationOligosaccharidesQD415-436BiochemistryMicrobiologyLipid Achemistry.chemical_compoundOpportunistic pathogenEndocrinologyPalmitoylationEscherichiapalmitoylationmass spectrometryPolish Collection of MicroorganismsbiologyHafnia alveiBiological activityCell Biologybiology.organism_classificationOxygenHafnia alveiLipid AchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-Ionizationlipids (amino acids peptides and proteins)BacteriaResearch ArticleJournal of Lipid Research
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Isolated glyoxylic acid-water 1:1 complexes in low temperature argon matrices

2015

Abstract The 1:1 hydrogen bonded complexes between glyoxylic acid (GA) and water are studied in low temperature argon matrices. Four different complex structures were found in deposited matrices. The lowest energy conformer (T1) of GA was found to form complex, where the water molecule was attached to the opposite side of the intramolecular hydrogen bond in the molecule (T1B). Interestingly, this complex was estimated to be +8.0 kJ mol −1 higher in energy than the most stable structure (T1A), where the water is inserted into the internal hydrogen bond, and also found in solid argon but in smaller abundance. For the second-lowest energy conformer of GA (T2), the two lowest-energy complex str…

Spectrophotometry InfraredHydrogenMolecular Conformationconformerschemistry.chemical_elementVibrationkonformeeritAnalytical Chemistrychemistry.chemical_compoundIsomerismComputational chemistryglyoxylic acidMoleculematriisi isolaatioArgonvärähdysspektroskopiaInstrumentationConformational isomerismta116SpectroscopyGlyoxylic acidhydrogen bondArgonglyoksyylihappoHydrogen bondMatrix isolationGlyoxylatesWatermatrix isolationHydrogen Bondinglaskennallinen kemiacomputational chemistryAtomic and Molecular Physics and OpticsCold TemperatureCrystallographychemistryIntramolecular forcevetysidosSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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