Search results for "Carbamates"

showing 10 items of 94 documents

Determination of carbamate residues in fruits and vegetables by matrix solid-phase dispersion and liquid chromatography-mass spectrometry.

2000

Abstract Thirteen carbamates were analysed in orange, grape, onion and tomatoes by matrix solid-phase dispersion (MSPD) followed by liquid chromatography–mass spectrometry (LC–MS). Electrospray (ES) and atmospheric pressure chemical ionisation (APCI) were compared and both gave similar results in terms of sensitivity and structural information because at 20 V fragmentor voltages the fragmentation is minimal. The efficiency of different solid-phases (C18, C8, cyano, amine and phenyl) for the MSPD was compared. Mean recoveries using C8 varied from 64 to 106% with relative standard deviations of 5–15% in the concentration range of 0.01–10 mg kg−1. Matrix constituents did not interfere signific…

Detection limitChemical ionizationInsecticidesChromatographyChemistryOrganic ChemistryPesticide ResiduesAtmospheric-pressure chemical ionizationGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryFruitVegetablesmedia_common.cataloged_instanceSolid phase extractionCarbamatesEuropean unionChromatography High Pressure Liquidmedia_commonJournal of chromatography. A
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Carbosulfan, Carbofuran, 3-Hydroxycarbofuran, and Other Metabolites in …

2007

The potential of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QqTOF-MS) to identify and confirm carbosulfan and seven of its main metabolites (carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenol carbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran, dibutylamine) at trace levels from food is explored for the first time. The analytical method developed consists of pressurized liquid extraction (PLE) and LC-QqTOF-MS in positive ion mode, which attains unequivocal identification and quantification of the studied compounds in food, at levels well below of those of concern (0.05 mg/kg for the sum of carbosulfan, carbofuran, and 3-hydroxycarbofuran).…

Detection limitChromatographyMolecular StructureMetaboliteRepeatabilityButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryDibutylamineCarbofuranchemistry.chemical_compoundchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCarbosulfanCarbamatesQuantitative analysis (chemistry)CarbofuranFood AnalysisChromatography LiquidAnalytical Chemistry
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Pesticides in the Ebro River basin: Occurrence and risk assessment

2016

In this study, 50 pesticides were analyzed in the Ebro River basin in 2010 and 2011 to assess their impact in water, sediment and biota. A special emphasis was placed on the potential effects of both, individual pesticides and their mixtures, in three trophic levels (algae, daphnia and fish) using Risk Quotients (RQs) and Toxic Units (TUs) for water and sediments. Chlorpyrifos, diazinon and carbendazim were the most frequent in water (95, 95 and 70% of the samples, respectively). Imazalil (409.73 ng/L) and diuron (150 ng/L) were at the highest concentrations. Sediment and biota were less contaminated. Chlorpyrifos, diazinon and diclofenthion were the most frequent in sediments (82, 45 and 2…

Diazinon010504 meteorology & atmospheric sciencesLiquid chromatography – Mass spectrometryHealth Toxicology and MutagenesisDrainage basin010501 environmental sciencesEcotoxicologyToxicology01 natural sciencesDaphniachemistry.chemical_compoundWater Pollution ChemicalEbro basingeography.geographical_feature_categorybiologyFishesBiotaGeneral MedicineBiotaPollution6. Clean waterChlorpyrifosEnvironmental chemistryEnvironmental MonitoringMonitoringAlgaeRisk AssessmentToxic UnitsRiversAlgaeAnimalsPesticides0105 earth and related environmental sciencesMixture toxicitygeographyfungiPesticide ResiduesSedimentPesticidebiology.organism_classificationFishDaphniachemistrySpain13. Climate actionRisk quotientEnvironmental scienceBenzimidazolesCarbamatesWater Pollutants ChemicalEnvironmental Pollution
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Analysis of carbamate and phenylurea pesticide residues in fruit juices by solid-phase microextraction and liquid chromatography–mass spectrometry

2007

A new analysis method to detect carbamates and phenylurea pesticide residues in fruit juices was developed using solid-phase microextraction (SPME) coupled with liquid chromatography-single quadrupole mass spectrometry (LC/MS) and liquid chromatography-quadrupole ion trap mass spectrometry (LC/QIT-MS). The pesticide residues present in watery matrices as fruit juices were extracted using three types of fibers: 50-microm Carbowax/templated resin (CW/TPR), 60-mum poly(dimethylsiloxane)/divinylbenzene (PDMS/DVB) and 85-microm polyacrylate. The different extraction conditions were evaluated choosing as the best parameters 90 min (time), 20 degrees C (temperature) and 1 ml (volume). After extrac…

ElectrosprayChromatographyChemistryPhenylurea CompoundsElectrospray ionizationOrganic ChemistrySelected reaction monitoringPesticide ResiduesGeneral MedicineSolid-phase microextractionMass spectrometryBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryBeveragesLiquid chromatography–mass spectrometrySelected ion monitoringCarbamatesChromatography High Pressure LiquidJournal of Chromatography A
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Adverse events associated with encorafenib plus binimetinib in the COLUMBUS study: incidence, course and management.

2019

Abstract Background Dual inhibition of the mitogen-activated protein kinase pathway with BRAF/MEK inhibitor (BRAFi/MEKi) therapy is a standard treatment for BRAFV600-mutant metastatic melanoma and has historically been associated with grade III pyrexia or photosensitivity depending on the combination used. The objective of this study was to fully describe adverse events from the COLUMBUS study evaluating the most recent BRAF/MEK inhibitor combination encorafenib+binimetinib. Patients and methods Patients with locally advanced, unresectable or metastatic BRAFV600-mutant melanoma were randomised to receive encorafenib 450 mg once daily plus binimetinib 45 mg twice daily, encorafenib 300 mg on…

Encorafenib0301 basic medicineOncologyMaleCancer ResearchSkin NeoplasmsBinimetinib; Encorafenib; Melanoma; Safety; Vemurafenib;MedizinBinimetinibchemistry.chemical_compound0302 clinical medicineAntineoplastic Combined Chemotherapy Protocols1306 Cancer ResearchVemurafenibMelanomaFatigueeducation.field_of_studySulfonamidesMEK inhibitorMelanomaStandard treatmentIncidence10177 Dermatology ClinicBinimetinibNauseaMiddle AgedOncology030220 oncology & carcinogenesis2730 OncologyFemaleSafetyMitogen-Activated Protein Kinasesmedicine.drugProto-Oncogene Proteins B-rafmedicine.medical_specialtyVomitingPopulation610 Medicine & health03 medical and health sciencesInternal medicinemedicineHumanseducationAdverse effectProtein Kinase Inhibitorsbusiness.industrymedicine.diseaseDiscontinuation030104 developmental biologychemistryVemurafenibMutationBenzimidazolesCarbamatesbusinessEuropean journal of cancer (Oxford, England : 1990)
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Energy reserves mobilization in the yellow eel as herbicide exposure effect.

2015

Abstract Thiobencarb and propanil are two of the most extensive used herbicides worldwide in rice cultivation. Especially scanty is the available information regarding the effect of herbicides on fish energy resources. In the present study, the effect of sublethal exposure to these herbicides on the energy reserves of juvenile eel Anguilla anguilla was compared. Eels were exposed to 72 h to the herbicide thiobencarb (0.22 mg L −1 ) or Propanil (0.63 mg L −1 ), and allowed to recover in clean water (144 h). Caloric content was determined in liver and skeletal muscle. Fish exposed to thiobencarb rapidly mobilized energy. Reserves from liver were depleted (21%) compared to control values (2.50…

Environmental EngineeringHealth Toxicology and MutagenesisEnergy resourcesEnergy reservesFresh WaterBiologyPropanilchemistry.chemical_compoundRecovery periodAnimal scienceThiocarbamatesPropanilBotanymedicineEnvironmental ChemistryJuvenileAnimalsMuscle SkeletalMobilizationHerbicidesPublic Health Environmental and Occupational HealthClean waterSkeletal muscleGeneral MedicineGeneral ChemistryAnguillaPollutionmedicine.anatomical_structurechemistryLiverWater Pollutants ChemicalChemosphere
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Synthesis and evaluation of (S)-2-(2-[18F]fluoroethoxy)-4-([3-methyl-1-(2-piperidin-1-yl-phenyl)-butyl-carbamoyl]-methyl)-benzoic acid ([18F]repaglin…

2004

18F-labeled non-sulfonylurea hypoglycemic agent (S)-2-(2-[(18)F]fluoroethoxy)-4-((3-methyl-1-(2-piperidin-1-yl-phenyl)-butylcarbamoyl)-methyl)-benzoic acid ([(18)F]repaglinide), a derivative of the sulfonylurea-receptor (SUR) ligand repaglinide, was synthesized as a potential tracer for the non-invasive investigation of the sulfonylurea 1 receptor status of pancreatic beta-cells by positron emission tomography (PET) in the context of type 1 and type 2 diabetes. [(18)F]Repaglinide could be obtained in an overall radiochemical yield (RCY) of 20% after 135 min with a radiochemical purity higher than 98% applying the secondary labeling precursor 2-[(18)F]fluoroethyltosylate. Specific activity w…

Fluorine RadioisotopesCancer ResearchBiodistributionMetabolic Clearance RateReceptors DrugContext (language use)Sulfonylurea ReceptorsRats Sprague-DawleyIslets of Langerhanschemistry.chemical_compoundPiperidinesmedicineRadioligandAnimalsTissue DistributionRadiology Nuclear Medicine and imagingPotassium Channels Inwardly RectifyingBenzoic acidChemistryBiological activityLigand (biochemistry)RepaglinideRatsDissociation constantBiochemistryOrgan SpecificityRats Inbred LewIsotope LabelingPositron-Emission TomographyFeasibility StudiesMolecular MedicineATP-Binding Cassette TransportersCarbamatesMultidrug Resistance-Associated ProteinsRadiopharmaceuticalsNuclear chemistrymedicine.drugNuclear Medicine and Biology
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Comparative study of the toxicity of molinate for freshwater organisms.

2003

Food ChainHealth Toxicology and MutagenesisDaphnia magnaZoologyBranchiopodaBiologyToxicologyAlgaeChlorophytaThiocarbamatesNannochloris oculataEcotoxicologyAnimalsEcologyHerbicidesGeneral MedicineAzepinesFeeding BehaviorPesticidebiology.organism_classificationPollutionCladoceraDaphniaToxicityCarbamatesWater Pollutants ChemicalBulletin of environmental contamination and toxicology
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Genetic transfer of the mcd gene in soil.

2003

Aims: To investigate the role of horizontal gene transfer of mcd (methylcarbamate-degrading) gene in high genetic diversity of carbofuran-degrading bacteria. Methods and Results: The actuality of genetic transfer from degraders to an Agrobacterium tumefaciens strain was determined in liquid medium. The mcd gene was chosen for transfer experiments. Transconjugants were obtained irrespective of the type of the donor strain (Gram-positive or Gram-negative), size of the inoculum, or nature and concentration of the pesticide in the medium. Soil microcosms, inoculated with or without the donor and/or recipient strains were used. The size of the initial degrading population (treated or untreated s…

Gene Transfer HorizontalAgrobacteriumPopulationApplied Microbiology and BiotechnologyCARBOFURANEMicrobiologyCarbofuranPseudomonaseducation[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologySoil MicrobiologyElectrophoresis Agar Geleducation.field_of_studybiologyStrain (chemistry)Genetic transferPseudomonasGeneral MedicineAgrobacterium tumefaciensbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiodegradation EnvironmentalAgrobacterium tumefaciensGenes BacterialConjugation GeneticHorizontal gene transferCarbamatesBacteriaBiotechnologyJournal of applied microbiology
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Eel ATPase activity as biomarker of thiobencarb exposure

2003

Abstract European eels ( Anguilla anguilla ) were exposed to a sublethal thiobencarb concentration of 0.22 mg/L in a flow-through system for 96 h. Mg 2+ and Na + –K + adenosine triphosphatase (ATPase) activities were evaluated in gill and muscle tissues at 2, 12, 24, 48, 72, and 96 h of thiobencarb exposure. Gill ATPase activities were rapidly inhibited from 2 h of contact onward. Highest inhibition was registered for Na + , K + -ATPase (85%) from 2 to 12 h. Both Mg 2+ and total ATPase were inhibited (>73%) during the first hours of toxicant exposure. At the end of the exposure period (96 h) ATPase activities were still different from those of the controls (>50%). Significant inhibition was…

GillsMuscle tissueGillmedicine.medical_specialtyHealth Toxicology and MutagenesisATPasechemistry.chemical_compoundThiocarbamatesAnguillidaeInternal medicinemedicineAnimalsTissue DistributionMuscle SkeletalAdenosine Triphosphataseschemistry.chemical_classificationbiologyHerbicidesPublic Health Environmental and Occupational HealthEnvironmental ExposureGeneral MedicineAnguillabiology.organism_classificationPollutionmedicine.anatomical_structureEnzymeEndocrinologychemistryBiochemistryEnzyme inhibitorToxicitybiology.proteinBiomarkersWater Pollutants ChemicalToxicantEcotoxicology and Environmental Safety
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