Search results for "Reproducibility"

showing 10 items of 1976 documents

Optimisation of gradient elution with serially-coupled columns. Part I: single linear gradients.

2014

A mixture of compounds often cannot be resolved with a single chromatographic column, but the analysis can be successful using columns of different nature, serially combined through zero-dead volume junctions. In previous work (JCA 1281 (2013) 94), we developed an isocratic approach that optimised simultaneously the mobile phase composition, stationary phase nature and column length. In this work, we take the challenge of implementing optimal linear gradients for serial columns to decrease the analysis time for compounds covering a wide polarity range. For this purpose, five ACE columns of different selectivity (three C18 columns of different characteristics, a cyano and a phenyl column) we…

AnalyteChromatographySulfonamidesChromatographyAcetonitrilesResolution (mass spectrometry)LogarithmChemistryOrganic solventOrganic ChemistryAnalytical chemistryReproducibility of ResultsWaterGeneral MedicineModels TheoreticalBiochemistryAnalytical ChemistryColumn (typography)Gradient elutionRetention timeCyano columnAlgorithmsJournal of chromatography. A
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Control of propranolol intake by direct chromatographic detection of alpha-naphthoxylactic acid in urine.

2002

A rapid chromatographic procedure with a C18 column, a mobile phase of 0.15 M sodium dodecyl sulfate (SDS)-10% (v/v) 1-propanol at pH 3 (0.01 M phosphate buffer), and fluorimetric detection, is reported for the control of propranolol (PPL) intake in urine samples, which are injected directly without any other treatment than filtration. The peak of PPL was only observed in samples taken a few hours after ingestion of the drug due to its extensive conjugation and metabolisation. The detection of several unconjugated PPL metabolites was therefore considered: desisopropylpropranolol (DIP), propranolol glycol (PPG), alpha-naphthoxylactic acid (NLT) and alpha-naphthoxyacetic acid (NAC). NLT showe…

AnalyteClinical BiochemistryAdrenergic beta-AntagonistsUrinePropranololBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundOral administrationmedicineHumansSodium dodecyl sulfateDetection limitChromatographyElutionReproducibility of ResultsCell BiologyGeneral MedicinePropranololSpectrometry FluorescencechemistryMicellar liquid chromatographyLactatesmedicine.drugChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Application of solid-phase microextraction combined with derivatization to the enantiomeric determination of amphetamines.

2005

Abstract The utility of combining chiral derivatization and solid-phase microextraction (SPME) for the enantiomeric analysis of primary amphetamines by liquid chromatography has been investigated. Different derivatization/extraction strategies have been evaluated and compared using the chiral reagent o -phthaldialdehyde (OPA)– N -acetyl- l -cysteine (NAC) and fibres with a Carbowax-templated resin coating. Amphetamine, norephedrine and 3,4-methylenedioxyamphetamine (MDA) were used as model compounds. On the basis of the results obtained, a new method is presented based on the derivatization of the analytes in solution followed by SPME of the OPA–NAC derivatives formed. The proposed conditio…

AnalyteClinical BiochemistryPhenylpropanolaminePharmaceutical ScienceSolid-phase microextractionAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryHumansDerivatizationSpectroscopyChromatography High Pressure LiquidAqueous solutionChromatographyExtraction (chemistry)AmphetaminesReproducibility of ResultsStereoisomerismSolutionsSpectrometry FluorescencechemistryReagentCentral Nervous System StimulantsIndicators and ReagentsEnantiomerQuantitative analysis (chemistry)Journal of pharmaceutical and biomedical analysis
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Micellar liquid chromatography determination of rivaroxaban in plasma and urine. Validation and theoretical aspects.

2019

A Micellar Chromatographic method to determine rivaroxaban in plasma and urine has been developed. The samples were dissolved in the mobile phase (SDS 0.05 M – 1-propanol 12.5%, phosphate buffered at pH 7) and 20 μL directly injected, avoiding the extraction and purification steps. Using a C18 column and running under isocratic mode at 1 mL/min, analyte was eluted without interference from the matrix in <6.0 min. The detection absorbance wavelength was set to 250 nm. The procedure was validated by Food and Drug Administration guidelines in terms of: system suitability, calibration range (0.05–5 mg/L), linearity, sensitivity, robustness, carry-over effect, specificity, accuracy (−11.1 to 4.2…

AnalyteClinical Biochemistrypartition equilibriumUrine030226 pharmacology & pharmacy01 natural sciencesBiochemistryAnalytical Chemistrymicellar chromatographyMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineRivaroxabanLimit of Detectiondirect injectionHumansMicellesvalidationChromatographyElutionanticoagulant010401 analytical chemistryExtraction (chemistry)biological fluidReproducibility of ResultsCell BiologyGeneral MedicinePhosphate0104 chemical scienceschemistryMicellar liquid chromatographyPartition equilibriumLinear ModelsChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Determination of the herbicide benfuresate by its photo-induced chemiluminescence using flow multicommutation methodology.

2007

The present paper deals with an analytical strategy based on coupling photo-induced chemiluminescence in a multicommutation continuous-flow methodology for the determination of the herbicide benfuresate. The solenoid valve inserted as small segments of the analyte solution was sequentially alternated with segments of the NaOH solution for adjusting the medium for the photodegradation. Both flow rates (sample and medium) were adjusted to required time for photodegradation, 90 s; and then, the resulting solution was also sequentially inserted as segments alternated with segments of the oxidizing solution system, hexacyanoferrate (III) in alkaline medium. The calibration range from 1 microg L(…

AnalyteCorrelation coefficientAnalytical chemistryFresh WaterAlkaliesAnalytical Chemistrylaw.inventionlawOxidizing agentWater Pollution ChemicalHumansPhotodegradationChemiluminescenceBenzofuransDetection limitReproducibilityChromatographyPhotolysisMolecular StructureChemistryHerbicidesVolumetric flow rateFlow Injection AnalysisLuminescent MeasurementsMineral WatersSulfonic AcidsAcidsTalanta
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Determination of triamterene and its main metabolite hydroxytriamterene sulfate in human urine by capillary electrophoresis using ultraviolet absorba…

2002

Abstract Two capillary electrophoresis methods have been developed for the direct determination of triamterene and its main metabolite hydroxytriamterene sulfate in human urine. Analytes were detected using conventional UV detection as well as laser-induced fluorescence (LIF) detection with an HeCd-laser operating at a wavelength of 325 nm. The results of both detection techniques were compared. Indeed, the limit of quantification was eightfold lower using LIF detection (50 ng/ml) in comparison to UV detection (400 ng/ml). As no interference due to endogenous urine compounds was observed, direct urine analysis was feasible. Analysis was very simple and fast—one run could be performed within…

AnalyteMetaboliteClinical BiochemistryUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresismedicineHumansDiureticsLaser-induced fluorescenceDetection limitTriamtereneChromatographyChemistryLasersElectrophoresis CapillaryReproducibility of ResultsCell BiologyGeneral MedicineFluorescenceSpectrometry FluorescenceSpectrophotometry UltravioletTriamterenemedicine.drugJournal of Chromatography B
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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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Strategies for the enantiomeric determination of amphetamine and related compounds by liquid chromatography.

2002

This paper summarizes recent research on the stereospecific analysis of amphetamine, its analogs and metabolites, by liquid chromatography. The different methods proposed have been evaluated and compared in terms of resolution power, time of analysis, sensitivity, or potential for automation. Chiral derivatization, followed by separation of the diastereomers formed in achiral chromatographic systems, is still the method preferred for the analysis of amphetamines at trace levels, as derivatization also improves analyte detectability. This is the method of choice for the enantiomeric analysis of amphetamines at the low concentrations typically encountered in biological samples. In recent year…

AnalyteResolution (mass spectrometry)medicine.drug_classBiophysicsBiochemistrySensitivity and Specificitychemistry.chemical_compoundIsomerismmedicineHumansEphedrineDerivatizationAmphetamineChromatography High Pressure LiquidChromatographyStaining and LabelingIllicit DrugsAmphetaminesDiastereomerReproducibility of ResultsDesigner drugSubstance Abuse DetectionchemistryModels ChemicalEnantiomermedicine.drugChromatography LiquidJournal of biochemical and biophysical 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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