Search results for "CHROMATOGRAPHY"

showing 10 items of 5037 documents

An investigation of the stability of free and glucuronidated 11-nor-delta9-tetrahydrocannabinol-9-carboxylic acid in authentic urine samples.

2004

Preanalytical stability of a drug and its major metabolites is an important consideration in pharmacokinetic studies or whenever the analyte pattern is used to estimate drug habits. Firstly, the stability of free and glucuronidated 11-nor-delta9-tetrahydrocannabinol-9-carboxylic acid (THCCOOH, THCCOOglu) in authentic urine samples was investigated. Random urine samples of cannabis users (n = 38) were stored at -20, 4, and 20 degrees C up to 15 days and up to 5 days at 40 degrees C, and alterations of the analyte pattern during storage were followed by liquid chromatography-tandem mass spectrometry. Secondly, the influence of pH (range 5.0-8.0) on the stability of the analytes was studied us…

AnalyteSubstance-Related DisordersHealth Toxicology and MutagenesisCarboxylic acidMetaboliteUrineToxicologyHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundGlucuronidesPharmacokineticsDrug StabilityEnvironmental ChemistryHumansDronabinolDiagnostic Errorschemistry.chemical_classificationChemical Health and SafetyChromatographyForensic MedicineHydrogen-Ion ConcentrationSubstance Abuse DetectionchemistryΔ9-tetrahydrocannabinolGlucuronideArtifactsJournal of analytical toxicology
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Observation of interaction forces by investigation of the influence of eluent additives on the retention behavior of aqueous nanoparticle dispersions…

2020

The investigation and subsequent understanding of the interactions of nanomaterials with components of their surrounding media is important to be able to evaluate both potential use cases as well as potential risks for human health and for the environment. To investigate such interactions, asymmetrical flow field-flow fractionation (AF4) is an interesting analytical tool. This statement grounds on the fact that interactions of the analyte with the membrane and with components of the eluent are crucial for the retention behavior of the analyte within the field-flow fractionation (FFF) channel. Therefore, the investigation of the retention behavior provides an insight in the nature of the int…

AnalyteTime FactorsHofmeister seriesSiloxanesHamaker constantStatic ElectricityElectrolyte010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrysymbols.namesakeDynamic light scatteringHumansComputer SimulationParticle SizeAqueous solutionChromatographyChemistryElution010401 analytical chemistryOrganic ChemistryOsmolar ConcentrationWaterGeneral MedicineDynamic Light ScatteringFractionation Field Flow0104 chemical sciencesChemical engineeringsymbolsNanoparticlesPolystyrenesvan der Waals forceJournal of chromatography. A
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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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Wide-range screening of banned veterinary drugs in urine by ultra high liquid chromatography coupled to high-resolution mass spectrometry

2012

In this work, an ultra high performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS) methodology is proposed for the multi-class multi-residue screening of banned and unauthorized veterinary drugs in bovine urine, using an Orbitrap Exactive™ analyzer working at a resolving power of 50,000 FWHM in full scan, both in positive and negative mode. The method currently covers 87 analytes belonging to different families such as steroid hormones, β-agonists, resorcylic acid lactones (RAL), stilbens, tranquillizers, nitroimidazoles, corticosteroids, NSAIDs, amphenicoles, thyreostatics and other substances such as dapsone. A database including the elemental composition, the po…

AnalyteVeterinary DrugsUrineQuechersOrbitrapSensitivity and SpecificityBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionlawAnimalsEuropean UnionAnimal HusbandryChromatography High Pressure LiquidElemental compositionChromatographyChemistryOrganic ChemistryReproducibility of ResultsVeterinary DrugsGeneral MedicineDrug ResiduesCattleUltra high performanceRetention timeJournal of Chromatography A
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Rapid assay of resveratrol in red wine by paper spray tandem mass spectrometry and isotope dilution.

2017

A rapid analytical approach for the assay of resveratrol in red wines, based on Paper Spray Mass Spectrometry (PS-MS) and Multiple Reaction Monitoring (MRM) is described. The assay involves the use of the stable isotope dilution method. The analytical parameters calculated analyzing fortified samples confirm the reliability of the proposed approach, with accuracy values about 100%, and LOD and LOQ values calculated at 0.5 and 0.8 μg/mL, respectively. Furthermore, both the recovery, which was quantitative for the analyte, and the reproducibility (RSD%), checked on different days on the same wine, always below 7%, highlighted the consistency of the methodology.

AnalyteWineFood chemistryIsotope dilution010402 general chemistryMass spectrometryTandem mass spectrometry01 natural sciencesQuantitative assayAnalytical ChemistryAmbient mass spectrometryIsotopesTandem Mass SpectrometryStilbenesWineReproducibilityChromatographyPaper sprayIsotopeChemistryMedicine (all)010401 analytical chemistrySelected reaction monitoringGeneral MedicineIsotope dilution0104 chemical sciencesResveratrolStilbeneFood ScienceFood chemistry
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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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Comparison of the solid-phase extraction efficiency of a bounded and an included cyclodextrin-silica microporous composite for polycyclic aromatic hy…

2016

Solid-phase extraction is one of the most important techniques for sample purification and concentration. A wide variety of solid phases have been used for sample preparation over time. In this work, the efficiency of a new kind of solid-phase extraction adsorbent, which is a microporous material made from modified cyclodextrin bounded to a silica network, is evaluated through an analytical method which combines solid-phase extraction with high-performance liquid chromatography to determine polycyclic aromatic hydrocarbons in water samples. Several parameters that affected the analytes recovery, such as the amount of solid phase, the nature and volume of the eluent or the sample volume and …

Analytical chemistry010501 environmental sciences01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryAdsorptionColumn chromatographyLimit of DetectionPhase (matter)Sample preparationSolid phase extractionPolycyclic Aromatic HydrocarbonsChromatography High Pressure Liquid0105 earth and related environmental sciencesCyclodextrinsChromatographyChemistry010401 analytical chemistryExtraction (chemistry)Solid Phase ExtractionWaterMicroporous materialEquipment DesignSilicon Dioxide0104 chemical sciencesAdsorptionPorosityWater Pollutants ChemicalTalanta
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Comprehensive analysis of airborne pesticides using hard cap espresso extraction-liquid chromatography-high-resolution mass spectrometry

2017

A hard cap espresso extraction procedure has been developed to recover airborne pesticides in particulate matter trapped in filters. This extraction step was made for 20s at 72°C and 19bar using 50mL of 20% (v/v) acetonitrile in water. After that, based on NaCl salting out, extracts were concentrated 22 times and analysed by ultra-high performance liquid chromatography - high resolution mass spectrometry. 35 pesticides were evaluated, as a proof of concept, being validated the whole methodology and compared the extraction method with that based on microwave assisted extraction for 20min. In short, the method avoids cross-contamination of samples, it is relatively fast and consumes only 10mL…

Analytical chemistry010501 environmental sciencesMass spectrometry01 natural sciencesBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundEspressoMicrowavesAcetonitrileSolvent extractionChromatography High Pressure Liquid0105 earth and related environmental sciencesAir PollutantsChromatographyPesticide residue010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Pesticide ResiduesGeneral MedicinePesticide0104 chemical scienceschemistrySalting outParticulate MatterJournal of Chromatography A
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Transmembrane electrochemistry of erythrocytes: Direct electrochemical test for detecting hemolysis in whole blood

2016

A rapid method for detecting hemolysis in whole blood based on a direct electrochemical assay either in venous blood and finger blood, respectively at glassy carbon and screen-printed graphite electrodes is described. The presence of hemolysis is detected from characteristic voltammetric signatures associated to Fe-heme units in healthy and hemolyzed erythrocytes. The voltammetric response of blood was also investigated using scanning electrochemical microscopy (SECM) and scanning tunneling microscopy (STM) and involved transmembrane electrochemistry of erythrocytes superimposed to molecular electrochemistry of heme-containing proteins and heme fragments in the plasma. Voltammetric testing …

Analytical chemistry02 engineering and technologyGlassy carbon010402 general chemistryElectrochemistry01 natural sciencesScanning electrochemical microscopyBlood plasmaMaterials ChemistrymedicineElectrochemistryElectrical and Electronic EngineeringInstrumentationWhole bloodHemolysis indexDetection limitChromatographyChemistryMetals and AlloysVenous blood021001 nanoscience & nanotechnologyCondensed Matter Physicsmedicine.diseaseHemolysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsVenous bloodFinger blood0210 nano-technology
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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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