Search results for "analytical"

showing 10 items of 9586 documents

Determination of titratable acidity and ascorbic acid in fruit juices in continuous-flow systems

1993

Two continuous-flow systems for the determination of titratable acidity and ascrobic acid in fruit juice samples are described. The assemblies permit on-line dialysis of analytes prior to the reaction step, thus improving selectivity and performing sample dilution. Flow systems are built with a channel carrying the donor phase (sample in both determinations) and another channel carrying an acceptor phase, both of them entering the dialyser. The outcoming stream transporting the dialysed sample fills the valve loop, permitting its injection into a carrier stream which continuously passes through the spectrophotometric detector. For the titratable acidity, acceptor phase and carrier are disti…

AnalyteChromatographymedicine.diagnostic_testChemistryTitratable acidAscorbic acidBiochemistryAcceptorAnalytical Chemistrychemistry.chemical_compoundDistilled waterSpectrophotometryReagentBromothymol bluemedicineFresenius' Journal of Analytical Chemistry
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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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Materials and methods of signal enhancement for spectroscopic whole blood analysis: Novel research overview

2017

Abstract The early diagnosis of diseases is crucial for reducing morbidity and mortality and also for improving the quality of treatment process. Among various biological samples used to follow up the concentrations of disease markers, whole blood sensing can efficiently decrease analysis time by means of introducing methods with no pretreatment. In addition, the direct detection of markers in whole blood facilitates testing procedure and minimize the possibility of the loss of analytes in the process. Therefore, the assay of unprocessed whole blood is becoming increasingly important in clinical diagnostics and biomedical research. Incorporation of new advanced materials plays a major role …

AnalyteComputer science010401 analytical chemistryTreatment processNanotechnology02 engineering and technologyAdvanced materials021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistrySignal enhancementOptical sensingDisease markers0210 nano-technologySpectroscopyBiomedical engineeringPoint of careWhole bloodTrAC Trends in Analytical Chemistry
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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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Development of a Rapid Method for the Determination of Phenolic Antioxidants in Dark Chocolate Using Ultra Performance Liquid Chromatography Coupled …

2017

Development of a new comprehensive method based on one-step liquid-liquid extraction (LLE) combined with ultra-high-performance liquid chromatography-Orbitrap high resolution mass spectrometry (UHPLC-Orbitrap-HRMS) for the determination of eight phenolic compounds in dark chocolate is demonstrated. The study focuses on the optimization of sample preparation, chromatographic separation and Orbitrap-HRMS detection parameters to adjust selectivity and sensitivity of the method. The LLE mixture of formic acid-water-acetonitrile (2:58:40, v/v) and hexane at the component ratio of 1:1 (v/v) was applied for sample preparation. The inter-day and intra-day precision expressed from the relative stand…

AnalyteDark chocolateOrbitrapMass spectrometry01 natural sciencesAntioxidantsMass SpectrometryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundfoodPhenolsLimit of DetectionlawLiquid–liquid extractionSample preparationChocolateChromatography High Pressure LiquidChromatography010405 organic chemistryChemistry010401 analytical chemistryExtraction (chemistry)General Medicinefood.food0104 chemical sciencesHexaneJournal of Chromatographic Science
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Volatile dimethylsiloxanes in market seafood and freshwater fish from the Xúquer River, Spain

2016

Abstract Volatile dimethylsiloxanes are a family of synthetic organosilicon-compounds, which have received rising attention because of their widespread use and occurrence in the environment. In the present work, an analytical method based on ultrasound-assisted solid–liquid extraction (USAE) followed by gas chromatography coupled to tandem mass spectrometry (GC–MS/MS) has been optimized and applied to assess the presence of eight volatile dimethyl siloxanes (VMS) (hexamethylcyclotrisiloxane (D3), octamethylcyclotetra-siloxane (D4), decamethylcyclopentasiloxane (D5), dodecamethylcyclohexasiloxane (D6), octamethyltrisiloxane (MDM), decamethyltetrasiloxane (MD2M) and dodecamethylpentasiloxane …

AnalyteEnvironmental EngineeringDecamethylcyclopentasiloxaneFood ContaminationFresh Water010501 environmental sciences01 natural scienceschemistry.chemical_compoundAnimalsEnvironmental ChemistryDimethylpolysiloxanesWaste Management and Disposal0105 earth and related environmental sciencesChromatographybiologyGas Chromatography/Tandem Mass Spectrometry010401 analytical chemistryExtraction (chemistry)FishesContaminationbiology.organism_classificationPollution0104 chemical sciencesSeafoodchemistrySpainEnvironmental chemistryFreshwater fishGas chromatographyWater Pollutants ChemicalEnvironmental MonitoringFood contaminantScience of The Total Environment
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Selection and characterization of adsorbents for the analysis of an explosive-related molecule traces in the air

2013

International audience; This study is focused on the development of a 3D micro-preconcentrator for a sensitive analysis of an explosive-related compound: orthonitrotoluene (ONT). A set of potentially efficient adsorbents for the pre-concentration of ONT was investigated here. An in-depth characterization of their textural properties was carried out in order to better understand their adsorption behavior toward the target analyte. More particularly, this study allowed highlighting the interesting adsorption features of a hydrophobic zeolite and a porous activated carbon in relation to their preconcentration performances toward ONT at the ppb level. Moreover, we found a difference in the adso…

AnalyteExplosive material[ SPI.MAT ] Engineering Sciences [physics]/Materials[ PHYS.COND.CM-MS ] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]02 engineering and technology01 natural sciences[SPI.MAT]Engineering Sciences [physics]/MaterialsAdsorption[SPI.MECA.MEMA]Engineering Sciences [physics]/Mechanics [physics.med-ph]/Mechanics of materials [physics.class-ph]Materials ChemistrymedicineOrganic chemistryMoleculeElectrical and Electronic EngineeringZeolitePorosityInstrumentation[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Chemistry[ SPI.ACOU ] Engineering Sciences [physics]/Acoustics [physics.class-ph]010401 analytical chemistryMetals and Alloys[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics[ SPI.MECA.THER ] Engineering Sciences [physics]/Mechanics [physics.med-ph]/Thermics [physics.class-ph]0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)[ CHIM.POLY ] Chemical Sciences/Polymers[SPI.ELEC]Engineering Sciences [physics]/Electromagnetism[CHIM.POLY]Chemical Sciences/PolymersChemical engineering[ CHIM.MATE ] Chemical Sciences/Material chemistry[ SPI.MECA.MEMA ] Engineering Sciences [physics]/Mechanics [physics.med-ph]/Mechanics of materials [physics.class-ph][ SPI.ELEC ] Engineering Sciences [physics]/Electromagnetism[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci][SPI.MECA.THER]Engineering Sciences [physics]/Mechanics [physics.med-ph]/Thermics [physics.class-ph]0210 nano-technologyActivated carbonmedicine.drug
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First experimental proof of asymmetric charge transfer in ICP-MS/MS (ICP-QQQ-MS) through isotopically enriched oxygen as cell gas

2014

The quantification of a variety of elements in the field of ICP-MS is restricted by isobaric interferences. The recent development of ICP-MS/MS (“triple quadrupole” configuration) offers a new way to solve the problem of the detection of such elements affected by interferences because the signal caused by either the analyte or the isobaric interference can be shifted to another m/z through reactions with the cell gas (oxygen, ammonia or hydrogen). This system consists of two quadrupoles (Q1 and Q2) with a collision/reaction cell in between. When using the MS/MS mode of this configuration it becomes possible to restrict the ions entering the cell to a defined m/z and therefore get a better i…

AnalyteHydrogenAnalytical chemistrychemistry.chemical_elementOxygenAnalytical ChemistryTriple quadrupole mass spectrometerIonAmmoniachemistry.chemical_compoundchemistryIsobaric processInductively coupled plasma mass spectrometrySpectroscopyJournal of Analytical Atomic Spectrometry
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