Search results for "Electrospray Ionization"

showing 10 items of 275 documents

Laser preparation of bunched ion beams

1997

Abstract Laser ionization at ISOLDE is performed with high repetition laser beams in the ion source unit and for daughter elements with low repetition lasers synchronized with laser desorption from a secondary target. We are preparing an implementation of thermal adsorption followed by laser desorption and laser ionization in the target ion source unit of ISOLDE. The combination of resonance ionization with thermal bunching allows the preparation of bunched and chemically pure ion beams. Bunched ion beams of Mg or Ca are prepared for post-acceleration at REX-ISOLDE. In order to investigate the process of adsorption and pulsed laser desorption, experiments are performed with Ba vapour. In a …

Nuclear and High Energy PhysicsDye laserMatrix-assisted laser desorption electrospray ionizationChemistryAnalytical chemistryPhysics::OpticsLaserSoft laser desorptionIon sourcelaw.inventionAtmospheric-pressure laser ionizationX-ray laserlawIonizationPhysics::Atomic and Molecular ClustersPhysics::Accelerator PhysicsPhysics::Atomic PhysicsAtomic physicsInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Assessment of Human Exposure to Deoxynivalenol, Ochratoxin A, Zearalenone and Their Metabolites Biomarker in Urine Samples Using LC-ESI-qTOF.

2021

Human are exposed to a wide range of mycotoxins through dietary food intake, including processed food. Even most of the mycotoxin exposure assessment studies are based on analysis of foodstuffs, and evaluation of dietary intake through food consumption patterns and human biomonitoring methods are rising as a reliable alternative to approach the individual exposures, overcoming the limitations of the indirect dietary assessment. In this study, human urine samples were analyzed, seeking the presence of deoxynivalenol (DON), ochratoxin A (OTA), zearalenone (ZEA), and their metabolites. For this purpose, 40 urine samples from female and male adult residents in the city of Valencia (Spain) were …

Ochratoxin AAdultMaleSpectrometry Mass Electrospray IonizationAdolescentHealth Toxicology and MutagenesisUrineLC-ESI-qTOFToxicology01 natural sciencesArticleExcretionDietary Exposurechemistry.chemical_compoundYoung Adult0404 agricultural biotechnologymycotoxinsBiomonitoringHumansFood scienceMycotoxinZearalenonemetabolitesAgedChemistry010401 analytical chemistryRfood and beveragesbiomarkersrisk assessment04 agricultural and veterinary sciencesMiddle Aged040401 food scienceOchratoxinsurine0104 chemical sciencesHuman exposureBiomarker (medicine)MedicineZearalenoneFemaleTrichothecenesBiological MonitoringChromatography LiquidToxins
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Application of hybrid linear ion trap-high resolution mass spectrometry to the analysis of mycotoxins in beer

2011

This paper reports the application of liquid chromatography electrospray ionization ion trap-orbitrap mass spectrometry for the determination of 18 mycotoxins (aflatoxins, fumonisins, trichothecenes, ochratoxin A, sterogmatocystin, beauvaricin, zearalenone and zearalenol) in beer. The extraction procedure was carried out by solid phase extraction (SPE): SPE columns were conditioned with acetonitrile/methanol and water. Beer was loaded onto the column which was washed with water. In these conditions, the recoveries were more than 65% and the relative standard deviation (RSD) were below 18%. The lowest limits of quantification (LLOQ) ranged from 9 to 155 ng ml(-1). Matrix-matched calibration …

Ochratoxin AAflatoxinHealth Toxicology and MutagenesisElectrospray ionizationAnalytical chemistryToxicologyMass spectrometryMass Spectrometrychemistry.chemical_compoundLimit of DetectionLiquid chromatography–mass spectrometrymycotoxinsSolid phase extractionZearalenoneChromatography High Pressure LiquidChromatographyExtraction (chemistry)Public Health Environmental and Occupational HealthReproducibility of ResultsLC/MSGeneral ChemistryGeneral MedicineReference StandardschemistryCalibrationbeerFood Science
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Occurrence of Free and Conjugated Mycotoxins in Aromatic and Medicinal Plants and Dietary Exposure Assessment in the Moroccan Population.

2021

Aromatic and medicinal plants (AMPs), as herbal material, are subjected to contamination by various mycotoxin-producing fungi, either free and conjugated. Such a problem is associated with poor storage practices, and lack of adopting good agricultural practices and good harvesting practices. Nevertheless, AMPs are poorly investigated. The purpose of this study was to investigate the co-occurrence of 15 mycotoxins (four aflatoxins (AFB1, AFB2, AFG1, and AFG2), ochratoxin A (OTA), beauvericin (BEA), four enniatins (ENA, ENA1, ENB, and ENB1), zearalenone (ZEN), alternariol (AOH), tentoxin (TENT), T-2, and HT-2 toxins) in 40 samples of AMPs frequently consumed in Morocco by using liquid chromat…

Ochratoxin AAflatoxinSpectrometry Mass Electrospray IonizationHealth Toxicology and MutagenesisPopulationAlternariollcsh:MedicineToxicology01 natural sciencesRisk AssessmentArticleQ-TOF-LC/MSDietary Exposurechemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryTandem Mass Spectrometryco-occurrenceHumansFood scienceeducationMycotoxinZearalenoneeducation.field_of_studyPlants Medicinallcsh:R010401 analytical chemistry04 agricultural and veterinary sciencesMycotoxins040401 food scienceBeauvericin0104 chemical sciencesMoroccochemistryexposureFood MicrobiologyChromatography LiquidToxins
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Levels of ochratoxin A in wheat and maize bread from the central zone of Portugal.

2007

Ochratoxigenic fungi are natural contaminants of cereal and the produced toxins are harmful to humans and animals. Ochratoxin A (OTA) is among the most important mycotoxins, and the International Agency for Research on Cancer (IARC) classifies it as possibly carcinogenic to humans (group 2B). A total of 61 samples of bread from the central zone of Portugal were analysed for OTA by liquid chromatography (LC) with fluorescence detection (FD). For confirmation two procedures were applied, methyl ester derivatization with boron trifluoride-methanol and liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI/MS/MS). As far as we know, this is the first report where on-line…

Ochratoxin ATolerable daily intakeElectrospray ionizationFood ContaminationTandem mass spectrometryMicrobiologyZea mayschemistry.chemical_compoundHumansFood scienceMycotoxinDerivatizationOchratoxinTriticumDetection limitChromatographyPortugalIncidencefood and beveragesGeneral MedicineBreadOchratoxinschemistryConsumer Product SafetyFood MicrobiologyFood ScienceChromatography LiquidInternational journal of food microbiology
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Analytical utility of quadrupole time-of-flight mass spectrometry for the determination of pesticide residues in comparison with an optimized column …

2009

Abstract A multiresidue method for the analysis of 30 pesticides with different physicochemical properties in fruits and vegetables was developed. The method involves a rapid and small-scale extraction procedure based on matrix solid-phase dispersion using octadecylsilyl (C18) as the dispersant and dichloromethane as the eluent. The target pesticides were determined using column high-performance liquid chromatography/triple quadrupole-tandem mass spectrometry (LC/QqQ-MS/MS). The method was validated for sensitivity, linearity, reproducibility, and accuracy. A recovery study was conducted at 3 different levels, and the average ranged from 74 to 99 for all of the studied compounds, with relat…

PharmacologyDetection limitResidue (complex analysis)AnalyteSpectrometry Mass Electrospray IonizationChromatographyPesticide residueChemistryAnalytical chemistryPesticide ResiduesMass spectrometryTandem mass spectrometryHigh-performance liquid chromatographyAnalytical ChemistryColumn chromatographyTandem Mass SpectrometryEnvironmental ChemistryAgronomy and Crop ScienceChromatography High Pressure LiquidFood ScienceJournal of AOAC International
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Electrochemical and spectroscopic investigations of selected N -heteroalkylaminomethylenebisphosphonic acids with Pb(II) ions

2016

Abstract The coordination properties of aminomethylenebisphosphonic acids towards various metal ions have been exploited during the last decade. These compounds are good chelators for biologically important metal ions, such as Cu(II), Fe(II), Zn(II), Ca(II), and Mg(II), as well as a toxic ion (i.e., Cd(II)). In this study, the interactions of five aminomethylenebisphosphonates with N-substituted heteroalkyl moieties (L1, L2 and L3) and their N-pyridyl (L4) and N-benzylpiperazine (L5) derivatives with Pb(II) ions were investigated. A wide range of analytical methods were employed, including potentiometry, pulse polarography (DPP), nuclear magnetic resonance (NMR) spectroscopy and electrospra…

PolarographyChemical substance010405 organic chemistryChemistryLigandElectrospray ionizationMetal ions in aqueous solutionInorganic chemistryAnalytical chemistry010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryMaterials ChemistryPhysical and Theoretical ChemistrySpectroscopyCoordination Chemistry Reviews
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Interactions of N-heteroalkylaminomethylenebisphosphonic acids with Cd(II) ions: Electrochemical and spectroscopic investigations

2015

The aminomethylenebisphosphonates are known to be excellent chelators for many metal ions. In this work, the coordination properties of three different aminomethylenebisphosphonates with N-substituted heteroalkyl moieties (L1, L2 and L3) and their N-pyridyl derivative (L4) toward cadmium(II) ions are described. Due to their coordination abilities over a broad range of pH, the compounds of this group are good candidates for heavy metal detoxification. To determine the stability constants and the coordination mode of formed aminomethylenebisphosphonate-cadmium(II) complexes, four analytical methods were employed: potentiometry, pulse polarography (DPP), nuclear magnetic resonance spectroscopy…

PolarographyLigandMetal ions in aqueous solutionElectrospray ionizationInorganic chemistryNuclear magnetic resonance spectroscopyElectrochemistryInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryPhysical and Theoretical ChemistryStoichiometryDerivative (chemistry)Inorganica Chimica Acta
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The Formation of Glycerol Oligomers with Two New Types of End Groups in the Presence of a Homogeneous Alkaline Catalyst

2019

The purpose of this work was to synthesize and characterize oligoglycerols with the chains of more than four repeating units. Those oligoglycerols may have some interesting applications, among others, as polyoxyalkylation starters. The glycerol oligomerization process was carried out during 12 h, at 230 &deg

Polymers and PlasticscatalysisElectrospray ionizationmechanismGeneral ChemistryglycerolCarbon-13 NMRArticleCatalysisoligomerizationlcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryPolymer chemistryGlycerololigoglycerolCarboxylateFourier transform infrared spectroscopySodium carbonatepolyglycerolsBar (unit)Polymers
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PLA2-mediated catalytic activation of its inhibitor 25-acetyl-petrosaspongiolide M: serendipitous identification of a new PLA2 suicide inhibitor.

2004

Abstract25-Acetyl-petrosaspongiolide M (PMAc) (1), a mild non-covalent PLA2 inhibitor, unexpectedly recovers, after incubation with bvPLA2, the ability to covalently modify the enzyme target. This study demonstrates the catalytic effect of bvPLA2 in converting 1 in its deacetylated congener petrosaspongiolide M (PM) (2), a strong covalent PLA2 inhibitor whose molecular mechanism of inhibition has already been clarified. Moreover, our findings outline the potential role of PMAc as anti-inflammatory pro-drug, by virtue of its ability of delivering the active PM agent at the site of inflammation, functioning as a suicide inhibitor.

Protein ConformationMarine natural productLigandsBiochemistryMass SpectrometryProtein Structure SecondaryCIRCULAR-DICHROISMchemistry.chemical_compoundProtein structureStructural BiologyBINDINGEnzyme InhibitorsChromatography High Pressure Liquidchemistry.chemical_classificationbiologyMolecular StructureChemistryCircular DichroismHydrolysisTemperatureAcetylationHydrogen-Ion ConcentrationBEE VENOM PHOSPHOLIPASE-A2PoriferaPETROSASPONGIOLIDES M-RBiochemistryCovalent bondINACTIVATIONMANOALIDESpectrometry Mass Electrospray IonizationCYTOSOLIC PHOSPHOLIPASE A(2); BEE VENOM PHOSPHOLIPASE-A2; FLUORESCENCE DISPLACEMENT ASSAY; PETROSASPONGIOLIDES M-R; CIRCULAR-DICHROISM; NATURAL-PRODUCTS; INACTIVATION; MANOALIDE; POTENT; BINDINGStereochemistryBiophysicsGroup II Phospholipases A2CatalysisPhospholipases AAnti-inflammatory compoundManoalidePhospholipase A2NATURAL-PRODUCTSGeneticsTrifluoroacetic acidAnimalsBinding siteOleanolic AcidMolecular BiologyBinding SitesPOTENTCYTOSOLIC PHOSPHOLIPASE A(2)Cell BiologyMolecular WeightKineticsPhospholipases A2EnzymeAcetylationbiology.proteinFLUORESCENCE DISPLACEMENT ASSAYPhospholipase A2 inhibitionFEBS letters
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