Search results for "libration"

showing 10 items of 901 documents

A mathematical model based on the limit dilution method to obtain linear calibration curves which eliminate the matrix effect in quantitative analysi…

1995

Abstract We propose a mathematical model from an analytical application viewpoint inspired in the limit dilution method. The theoretical development of the model and its results are given. The model shows that there is a linear relation between the inverse of fluorescence intensity and the inverse of the dilution factor; each analytic system (sample, diluent and analyte) is characterised by a general linear function which is easily obtained. The analytical applications arising from this linearity are of great importance in X-ray fluorescence analysis. The following immediate applications are proposed: direct procurement of the total correction factor Y/H, rapid calculation of the fluorescen…

AnalyteInternal standardSerial dilutionCalibration curveChemistryAnalytical chemistryLinearityAtomic and Molecular Physics and OpticsAnalytical ChemistryDilutionStandard curveMatrix (chemical analysis)InstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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Quantitative electron probe microanalysis of metallic oxide mixtures applying an empirical calibration technique

1997

Abstract An analytical procedure is proposed for the independent quantitative chemical analysis of each element in the presence of other elements in the matrix of a sample by Energy Dispersive Electron Probe Microanalysis. For this purpose, an empirical calibration technique (which we shall call here the JABO method), which studies the variation of the X-ray intensities in terms of the analyte concentration in a chemical system with a complex matrix, is established. The methodology consists of the modification of the unknown sample by addition of a diluent, an internal standard and the analyte itself (dilution-addition method). A mathematical model is proposed to calculate the K parameters …

AnalyteInternal standardZirconiumAnalytical chemistrychemistry.chemical_elementElectron microprobeAtomic and Molecular Physics and OpticsAnalytical ChemistryDilutionMatrix (chemical analysis)chemistryStandard additionCalibrationInstrumentationSpectroscopySpectrochimica Acta Part B: Atomic Spectroscopy
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Application of ultra-high pressure liquid chromatography linear ion-trap orbitrap to qualitative and quantitative assessment of pesticide residues

2014

Abstract The analysis of pesticides residues using a last generation high resolution and high mass accuracy hybrid linear ion trap-Orbitrap mass spectrometer (LTQ-Orbitrap-MS) was explored. Pesticides were extracted from fruits, fish, bees and sediments by QuEChERS and from water by solid-phase with Oasis HLB cartridges. Ultra-high pressure liquid chromatography (UHPLC)–LTQ-Orbitrap mass spectrometer acquired full scan MS data for quantification, and data dependent (dd) MS 2 and MS 3 product ion spectra for identification and/or confirmation. The regression coefficients ( r 2 ) for the calibration curves (two order of magnitude up to the lowest calibration level) in the study were ≥0.99. Th…

AnalyteMeatCalibration curveAnalytical chemistryOrbitrapQuechersMass spectrometryBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionlawAnimalsQuadrupole ion trapChromatography High Pressure LiquidChromatographyPesticide residueChemistryOrganic ChemistryFishesPesticide ResiduesGeneral MedicineBeesPesticideFruitEnvironmental PollutantsWater Pollutants ChemicalJournal of Chromatography A
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Multi-analyte method for the analysis of legacy and alternative brominated and chlorinated flame retardants in food products of animal origin using g…

2019

Abstract An analytical method was developed and validated for the analysis of 32 halogenated flame retardants (HFRs), including 13 polybrominated diphenyl ethers (PBDEs), 9 dechlorane-related compounds (DRCs) and 10 of the so-called alternative BFRs in food samples of animal origin. Gas chromatography (GC) coupled with magnetic sector high resolution mass spectrometry (HRMS) was used for the instrumental analysis. Intralaboratory validation of the developed method was performed in terms of recovery, repeatability, linear calibration ranges, instrumental and method limits of quantitation (i-LOQ and m-LOQ). Where possible, trueness was verified by the analysis of reference materials (RMs). Fo…

AnalyteMeatEnvironmental EngineeringEggsHealth Toxicology and Mutagenesis0208 environmental biotechnologyFood ContaminationPilot Projects02 engineering and technology010501 environmental sciences01 natural sciencesAnimal originGas Chromatography-Mass SpectrometryPolybrominated diphenyl ethersLimit of DetectionHalogenated Diphenyl EthersHydrocarbons ChlorinatedCalibrationAnimalsEnvironmental ChemistryFlame Retardants0105 earth and related environmental sciencesMulti analyteChromatographyPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryRepeatabilityPollution020801 environmental engineeringMilkFood productsEnvironmental scienceGas chromatographyChemosphere
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Science based calibration for the extraction of 'analyte-specific' HPLC-DAD chromatograms in environmental analysis

2010

Multivariate science based calibration (SBC) has been applied to the resolution of overlapped peaks in liquid chromatography with diode array detection (LC-DAD). Complex river water samples spiked with 11 pharmaceutical substances resulted in poorly resolved chromatograms containing additional peaks from interfering matrix compounds and a change in the background absorbance due to the mobile phase gradient. Applying the present multivariate approach it was possible to resolve all 11 analytes from overlapping peaks, obtaining linear calibration lines (R2 > 0.96). Recovery percentages on spiked samples ranged between 74.6 and 113.5%, which are quite satisfactory taking into account the low co…

AnalyteResolution (mass spectrometry)Adrenergic beta-AntagonistsStatistics as TopicAnalytical chemistryEnvironmentHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)AbsorbanceRiversSCIENCE BASED CALIBRATIONSample preparationLeast-Squares AnalysisElectrodesChromatography High Pressure LiquidAnalgesicsENVIRONMENTAL ANALYSISChromatographyChemistryOtras Ciencias QuímicasExtraction (chemistry)Ciencias QuímicasDrug ResiduesStandard curveHIGH PERFORMANCE LIQUID CHROMATOGRAPHY-DIODE ARRAY DETECTION (HPLC-DAD)CalibrationMultivariate AnalysisEnvironmental PollutantsCIENCIAS NATURALES Y EXACTAS
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Comparison between micellar liquid chromatography and capillary zone electrophoresis for the determination of hydrophobic basic drugs in pharmaceutic…

2007

[EN] The determination of highly hydrophobic basic compounds by means of conventional reversed-phase liquid chromatographic methods has several drawbacks. Owing to the characteristics of micellar liquid chromatography (MLC) and capillary electrophoresis (CE), these techniques could be advantageous alternatives to reversed-phase chromatographic methods for the determination of these kinds of compounds. The objective of this study was to develop and compare MLC and CE methods for the determination of antipsychotic basic drugs (amitryptiline, haloperidol, perphenazine and thioridazine) in pharmaceutical preparations. The chromatographic determination of the analytes was performed on a Kromasil…

AnalyteResolution (mass spectrometry)Capillary actionClinical BiochemistrySensitivity and SpecificityBiochemistryAnalytical ChemistryCapillary electrophoresischemistry.chemical_compoundCapillary electrophoresisBromideDrug DiscoveryQUIMICA ANALITICAAntipsychotic drugsMolecular BiologyPharmacologyDetection limitChromatographyElectrophoresis CapillaryReproducibility of ResultsGeneral MedicineHydrogen-Ion ConcentrationReference StandardsElectrophoresisPharmaceutical PreparationschemistryHydrophobic basic drugsMicellar liquid chromatographyCalibrationPharmaceutical analysisHydrophobic and Hydrophilic InteractionsCetyltrimethylammonium bromideMicellar liquid chromatographyAntipsychotic AgentsChromatography Liquid
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More about sampling and estimation of mercaptans in air samples

2013

[EN] Several strategies have been developed for sampling and determination of volatile thiols. The selectivity and sensitivity of the proposed methodologies are achieved by using a specific derivatizing reagent. The different procedures assayed are based on air sampling followed by derivatization of the analytes with OPA and isoleucine in alkaline solution. The derivatization products are separated and determined by liquid chromatography and fluorescence detection. To start, the derivatization conditions and stability of the derivates have been studied in order to establish the storage conditions. In general, the strategies studied consisted on trapping and detivatization the thiol compound…

AnalyteSorbentAir samplesAlkaliesHigh-performance liquid chromatographyAnalytical ChemistryCartridgeO-Phthalaldehydechemistry.chemical_compoundMercaptansQUIMICA ANALITICAHumansSulfhydryl CompoundsIsoleucineDerivatizationAir sampling systemFluorescent DyesAir PollutantsChromatographyAirSampling (statistics)DerivatizationSolutionsSpectrometry FluorescencechemistryReagentCalibrationHPLCo-PhthalaldehydeChromatography Liquid
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Determination of biochemical parameters in human serum by near-infrared spectroscopy

2014

NIR offers multiple advantages for serum analysis, permitting a fast and direct determination of several parameters simultaneously, with low sample handling and without the need for reagents during the measurement step. The aim of this paper was to provide an evaluation of this technique in a real world scale, for the simultaneous determination of several parameters and based on a considerable number of samples. Direct near infrared (NIR) absorbance measurements were used to determine the concentration of clinical parameters in human serum that are required in routine biochemical tests. Total protein, albumin, total cholesterol, high-density lipoprotein (HDL cholesterol), low-density lipopr…

AnalyteVery low-density lipoproteinChromatographyMean squared errorChemistryCholesterolGeneral Chemical EngineeringNear-infrared spectroscopyGeneral EngineeringAnalytical chemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundPartial least squares regressionCalibrationAnalytical Methods
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Immuno-SLM—a combined sample handling and analytical technique

2004

Immuno-supported liquid membrane (immuno-SLM) extraction is a new technique that makes use of antibody (Ab)-antigen interactions as the "extraction force" to drive the mass transfer in a selective way. In immuno-SLM, anti-analyte (Ag) Abs are introduced into the acceptor phase of the SLM unit to trap the Ag that passes from the flowing donor through the SLM into the stagnant acceptor. The amount of immuno-extracted analyte (AbAg) is quantified by connecting the immuno-SLM unit on-line with a non-competitive heterogeneous fluorescence flow immunoassay (FFIA) that makes use of a fluorescein-labeled analyte tracer that titrates the residual excess of Ab present in the acceptor. A restricted ac…

AnalytefluoresceinCalibration curveImmunologyAnalytical chemistryFresh WaterAntibodiesAntigen-Antibody ReactionsBeveragesMatrix (chemical analysis)Tap waterImmunology and AllergyImmunoassayDetection limitOrange juiceiImmuno extractionChromatographyrestricted accessHerbicidesChemistryElutiontap waterExtraction (chemistry)Membranes Artificialriver watersupported liquid membrane extractionorange juiceAtrazineWater Pollutants ChemicalJournal of Immunological Methods
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Headspace–mass spectrometry determination of benzene, toluene and the mixture of ethylbenzene and xylene isomers in soil samples using chemometrics

2007

A simple and fast method has been developed for the determination of benzene, toluene and the mixture of ethylbenzene and xylene isomers (BTEX) in soils. Samples were introduced in 10 mL standard glass vials of a headspace (HS) autosampler together with 150 microL of 2,6,10,14-tetramethylpentadecane, heated at 90 degrees C for 10 min and introduced in the mass spectrometer by using a transfer line heated at 250 degrees C as interface. The volatile fraction of samples was directly introduced into the source of the mass spectrometer which was scanned from m/z 75 to 110. A partial least squares (PLS) multivariate calibration approach based on a classical 3(3) calibration model was build with m…

Analytical chemistryBTEXXylenesMass spectrometryBiochemistryEthylbenzeneGas Chromatography-Mass SpectrometryMass SpectrometryAnalytical ChemistryChemometricsSoilchemistry.chemical_compoundIsomerismBenzene DerivativesEnvironmental ChemistryBenzeneSpectroscopyChromatographyChromatographyXyleneTemperatureBenzeneTolueneHydrocarbonsBiodegradation EnvironmentalModels ChemicalchemistryCalibrationGas chromatographyTolueneAnalytica Chimica Acta
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