Search results for "LIMIT"

showing 10 items of 2826 documents

Body size variability across habitats in the Brachionus plicatilis cryptic species complex

2020

AbstractThe body size response to temperature is one of the most recognizable but still poorly understood ecological phenomena. Other covarying environmental factors are frequently invoked as either affecting the strength of that response or even driving this pattern. We tested the body size response in five species representing the Brachionus plicatilis cryptic species complex, inhabiting 10 brackish ponds with different environmental characteristics. Principal Component Analysis selected salinity and oxygen concentration as the most important factors, while temperature and pH were less influential in explaining variation of limnological parameters. Path analysis showed a positive interclo…

Species complexMultidisciplinaryBrackish waterRotiferaTemperatureZoologyInterspecific competitionBody sizeBiologyBrachionusbiology.organism_classificationSalinityOxygenHabitatZoologiaAnimalsBody SizeLimiting oxygen concentrationEcosystem
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Rapid whole protein quantitation of staphylococcal enterotoxins A and B by liquid chromatography/mass spectrometry

2012

Abstract Staphylococcus aureus is an important pathogen and has been indicated as the fifth causative agent of food-borne human illness throughout the world. Staphylococcal enterotoxins (SEs) are toxic compounds excreted mainly by strains of S. aureus. Among these toxins, enterotoxins A (SEA) and B (SEB) are both of the most prevalent compounds in staphylococcal food poisoning. In this work, reverse phase liquid chromatography coupled to ESI mass spectrometry (LC–ESI/MS) has been applied for its rapid identification and quantification. Limit of detection (LOD) values were 0.5 and 0.2 ng for SEA and SEB, respectively and limit of quantification (LOQ) value was 1 ng for both enterotoxins. SEA…

Spectrometry Mass Electrospray IonizationComplete proteinEnterotoxinmedicine.disease_causeBiochemistryAnalytical ChemistryEnterotoxinsLimit of DetectionLiquid chromatography–mass spectrometrymedicineAnimalsPathogenDetection limitChromatography Reverse-PhaseChromatographyChemistryOrganic ChemistryReproducibility of ResultsGeneral MedicineReversed-phase chromatographyStaphylococcal Food PoisoningMilkStaphylococcus aureusFruitLinear ModelsCitrus sinensisJournal of Chromatography A
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Development of an improved method for trace analysis of quinolones in eggs of laying hens and wildlife species using molecularly imprinted polymers.

2012

A sensitive, selective, and efficient method was developed for simultaneous determination of 11 fluoroquinolones (FQs), ciprofloxacin, danofloxacin, difloxacin, enrofloxacin, flumequine, marbofloxacin, norfloxacin, ofloxacin, oxolinic acid, pipemidic acid, and sarafloxacin, in eggs by molecularly imprinted polymer (MIP) and column liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS). Samples were diluted with 50 mM sodium dihydrogen phosphate at pH 7.4, followed by purification with a commercial MIP (SupelMIP SPE-Fluoroquinolones). Recoveries for the 11 quinolones were in the range of 90-106% with intra- and interday relative standard deviation ranging from …

Spectrometry Mass Electrospray IonizationDanofloxacinPolymersanimal diseasesEggsImproved methodAnimals WildBiologyQuinolonesMolecular ImprintingLimit of DetectionmedicineEnrofloxacinAnimalsDifloxacinChromatographyMolecularly imprinted polymerGeneral Chemistrybiochemical phenomena metabolism and nutritionCiprofloxacinFlumequineTrace analysisFemaleGeneral Agricultural and Biological SciencesChickensmedicine.drugChromatography LiquidJournal of agricultural and food chemistry
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Estimation of alcohol consumption during >Fallas> festivity in the wastewater of Valencia city (Spain) using ethyl sulfate as a biomarker

2016

Alcohol consumption has been increasing in the last years and it has become a sociological problem due its derived health and safety problems. Ethyl sulfate is a secondary metabolite of the alcohol degradation that is excreted through the urine (0.010-0.016%) after alcohol ingestion and it is quite stable in water. In this study, a new methodology to determine ethyl sulfate by ion-pair liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed. Different ion-pairs and additives were tested directly in the sample extracts or in the mobile phase. The best ion-pair was set up adding 0.5M of tributylamine and 0.1% of formic acid to the sample. The limit of quantification was 0.3μgL…

Spectrometry Mass Electrospray IonizationEnvironmental EngineeringAlcohol DrinkingFormic acidPopulationUrine010501 environmental sciencesTributylamineSulfuric Acid EstersWastewaterLiquid chromatography–mass spectrometry01 natural sciencesEthyl sulfateSewage epidemiologychemistry.chemical_compoundLiquid chromatography–mass spectrometryTandem Mass SpectrometryEthanol biomarkerWater Pollution ChemicalEnvironmental ChemistryHumansAlcohol consumptioneducationWaste Management and DisposalEthyl sulfate0105 earth and related environmental sciencesHolidaysDetection limiteducation.field_of_studyChromatographyChemistry010401 analytical chemistryPollution0104 chemical sciencesWastewaterSpainBiomarkersWater Pollutants ChemicalChromatography Liquid
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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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Determination of acrylamide in foods by pressurized fluid extraction and liquid chromatography-tandem mass spectrometry used for a survey of Spanish …

2006

An automated and rapid method for the determination of acrylamide in different food products is presented. The method involves pressurized fluid extraction (PFE) of foods with acetonitrile and precipitation with Carrez reagents. The final extract is analysed by liquid chromatography coupled to electrospray ionization tandem mass spectrometry (ESI-MS-MS). The main parameters affecting the performance of ESI-MS-MS and PFE were optimized using a design of experiments approach. The limit of quantification of the method was 5 microg kg(-1), and recoveries from incurred samples ranged between 93 and 101%. The accuracy was evaluated using the reference test materials FAPAS T3002, T3005 and T3011. …

Spectrometry Mass Electrospray IonizationHealth Toxicology and MutagenesisElectrospray ionizationFood ContaminationToxicologyMass spectrometryTandem mass spectrometryCandychemistry.chemical_compoundLiquid chromatography–mass spectrometryPressuremedia_common.cataloged_instanceEuropean unionmedia_commonSolanum tuberosumDetection limitAcrylamideChromatographyExtraction (chemistry)Public Health Environmental and Occupational HealthReproducibility of ResultsGeneral ChemistryBreadchemistryChemistry (miscellaneous)SpainAcrylamideSolventsEdible GrainFood ScienceChromatography LiquidFood additives and contaminants
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Evaluation of enniatins A, A1, B, B1 and beauvericin in Portuguese cereal-based foods.

2012

Sixty-one samples of Portuguese cereal-based foods were analysed for the occurrence of emerging mycotoxins called enniatins (A, A1, B and B1) and beauvericin. Samples were extracted with a mixture of acetonitrile/water (85/15, v/v) using an Ultra-Turrax homogeniser, and mycotoxins were detected with liquid chromatography coupled to a mass spectrometer. This method was validated and adequate values of recovery (70-103%) and relative standard deviation (15%) were obtained. Signal suppression/enhancement was studied and matrix-matched calibration used to minimise this effect, but no additional clean-up step was necessary. The mass spectrometer was operated in selected reaction monitoring (SRM)…

Spectrometry Mass Electrospray IonizationHealth Toxicology and MutagenesisFood ContaminationToxicologyMass spectrometryTandem mass spectrometrychemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryDepsipeptidesHumansMycotoxinChromatography High Pressure LiquidTriticumDetection limitChromatographyPortugalSelected reaction monitoringPublic Health Environmental and Occupational HealthReproducibility of ResultsGeneral ChemistryGeneral MedicineContaminationMycotoxinsFood InspectionBeauvericinDietchemistrySeedsEdible GrainFood ScienceFood contaminantFood additivescontaminants. Part A, Chemistry, analysis, control, exposurerisk assessment
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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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Multi-site analytical evaluation of a chemiluminescent magnetic microparticle immunoassay (CMIA) for sirolimus on the Abbott ARCHITECT analyzer.

2009

Objective This study evaluated a new chemiluminescent magnetic microparticle immunoassay (CMIA) for sirolimus on the ARCHITECT analyzer. Design and methods Patient and laboratory proficiency samples were tested at three European sites and one site in the United States. Results The CMIA total %CV's were all < 8% and the Limit of Quantification (LOQ) was < 1.52 ng/mL across the four sites. It cross-reacts to sirolimus metabolites F4 and F5 and showed no hematocrit interference over a range of 25% to 55%. Patient specimen correlations to three LC/MS/MS methods gave R ≥ 0.91 at three sites and mean biases of 14%, 25% and 39%. CMIA patient specimen correlations to the Abbott IMx gave R ≥ 0.94 at…

Spectrum analyzerClinical BiochemistryHematocritSensitivity and Specificitylaw.inventionMagneticslawAntibody SpecificityTandem Mass SpectrometrymedicineHumansParticle SizeChemiluminescenceDetection limitImmunoassaySirolimusChromatographymedicine.diagnostic_testChemistryMulti siteGeneral MedicineImmunoassay methodImmunoassayLuminescent MeasurementsPositive biasImmunosuppressive AgentsChromatography LiquidClinical biochemistry
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Static and dynamic glass transitions in the 10-state Potts glass: What can Monte Carlo simulations contribute?

2002

The p-state Potts glass with infinite range Gaussian interactions can be solved exactly in the thermodynamic limit and exhibits an unconventional phase behavior if p >4: A dynamical transition from ergodic to non-ergodic behavior at a temperature T D is followed by a first order transition at T 0 < T D, where a glass order parameter appears discontinuously, although the latent heat is zero. If one assumes that a similar scenario occurs for the structural glass transition as well (though with the singular behavior at T D rounded off), the p-state Potts glass should be a good test case to develop methods to deal with finite size effects for the static as well as the dynamic transition, and to…

Spin glassGaussianMonte Carlo methodExtrapolationGeneral Physics and Astronomysymbols.namesakeHardware and ArchitectureThermodynamic limitsymbolsErgodic theoryStatistical physicsGlass transitionMathematicsPotts modelComputer Physics Communications
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