Search results for "Matrix"

showing 10 items of 3205 documents

Measurement of nanoparticle mass distributions by laser desorption/ionization time-of-flight mass spectrometry.

2011

In this paper, access to the mass distribution analysis of nanoparticles is described based on laser desorption/ionization and time of flight mass spectrometry. Two examples are given, demonstrating the accurate mass distribution analysis of nanoparticles fabricated both ex situ and in situ during the laser-assisted desorption process. The potentials and the limitations of the method are discussed, with special emphasis on carbonaceous clusters and molecules.

Desorption electrospray ionizationStatic secondary-ion mass spectrometryMatrix-assisted laser desorption electrospray ionizationChemistryAnalytical chemistryGeneral Materials ScienceTime-of-flight mass spectrometryCondensed Matter PhysicsMass spectrometrySoft laser desorptionIon sourceAmbient ionizationJournal of physics. Condensed matter : an Institute of Physics journal
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Copper, iron and zinc determinations in human milk using FAAS with microwave digestion

2000

Abstract A method for determining copper, iron and zinc in human milk was optimized and validated. It includes microwave mineralization of the sample and measuring the elements by flame atomic absorption spectroscopy (FAAS). Only 2 ml of milk is needed, and the method is free of matrix interferences. The values obtained for the detection limits (0.07; 0.07; 0.11 μg/ml milk, for copper, iron and zinc) precision of the method, intra-assay (2.9; 5.2; 6.1%RSD for copper, iron and zinc) and accuracy, evaluated using recovery assays (98.8; 100.4; 95.9% for copper, iron and zinc) show that the method is useful for the purpose mentioned. Moreover, the method is rapid and simple, and the determinati…

Detection limitAccuracy and precisionChromatographyChemistryAnalytical chemistrychemistry.chemical_elementGeneral MedicineZincCopperAnalytical Chemistrylaw.inventionMatrix (chemical analysis)lawMicrowave digestionAtomic absorption spectroscopyAnalysis methodFood ScienceFood Chemistry
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Green determination of eight water-soluble B vitamins in cosmetic products by liquid chromatography with ultraviolet detection.

2021

Abstract B vitamins are a group of compounds with beneficious properties for dermatologic care, and therefore they are included in the cosmetic formulations as high added-value ingredients. In this paper, an analytical method for the simultaneous determination of eight water-soluble B vitamins in cosmetic products is reported for the first time. This method is based on liquid chromatography with ultraviolet detection (LC-UV) analysis after simple water leaching of the analytes from the cosmetic matrix. No organic solvents are required, beyond the ethanol used in the chromatographic mobile phase. The proposed method has been successfully validated showing good linearity, limits of detection …

Detection limitAnalyteChromatographyChemistryClinical BiochemistryPharmaceutical ScienceReproducibility of ResultsWaterRepeatabilityCosmeticsmedicine.disease_causeAnalytical ChemistryMatrix (chemical analysis)B vitaminsWater solubleLeaching (chemistry)Drug DiscoveryVitamin B ComplexmedicineSolventsSpectroscopyUltravioletChromatography High Pressure LiquidChromatography LiquidJournal of pharmaceutical and biomedical analysis
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New micromethod combining miniaturized matrix solid-phase dispersion and in-tube in-valve solid-phase microextraction for estimating polycyclic aroma…

2008

Abstract Miniaturized matrix solid-phase dispersion (MSPD) was developed for the extraction of common polycyclic aromatic hydrocarbons (PAHs) from bivalve samples (100 mg, dry weight). Additional clean-up and analyte enrichment was accomplished by in-tube solid-phase microextraction (SPME). For this purpose the extracts collected after MSPD were diluted with water and injected into a capillary column coated with the extractive phase. This capillary column was connected to the analytical column by means of a switching valve. Separation and quantification of the PAHs were carried out using a monolithic LC column and fluorescence detection. Since the in-tube SPME device allowed the processing …

Detection limitAnalyteChromatographyChemistryOrganic ChemistryExtraction (chemistry)Analytical chemistryReproducibility of ResultsGeneral MedicineReference StandardsSolid-phase microextractionBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryBivalviaMatrix (chemical analysis)AnimalsSample preparationSolid phase extractionPolycyclic Aromatic HydrocarbonsSolid Phase MicroextractionChromatography LiquidJournal of chromatography. A
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On-line trace enrichment for the determination of ethacrynic acid in urine by liquid chromatography and column-switching

1993

Abstract A chromatographic method based on liquid chromatography (LC) using column-switching for the determination of ethacrynic acid in urine samples, is described. The proposed system uses a Hypersil ODS-C18, 30 μm (20 mm × 2.1 mm i.d.) pre-column for the pre-concentration and separation of ethacrynic acid from the biological matrix. Polar urinary compounds are removed by flushing the pre-column with purified water, and the enriched analyte is then switched in back-flush mode onto an HP-LiChrospher RP C18, 5 μm (125 × 4 mm i.d.) analytical column, where it is chromatographed using an acetonitrile-acetate buffer gradient elution. The UV detector was set at 275 nm. The recovery of drug was …

Detection limitAnalyteChromatographyChemistrymedicine.medical_treatmentUrineBiochemistryPurified waterAnalytical ChemistryMatrix (chemical analysis)medicineEnvironmental ChemistryColumn switchingDiureticQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Simultaneous determination of oxybenzone and 2-ethylhexyl 4-methoxycinnamate in sunscreen formulations by flow injection-isodifferential derivative u…

2001

Abstract A flow injection procedure was developed for the simultaneous determination of two UV filters (oxybenzone and 2-ethylhexyl 4-methoxycinnamate) in sunscreen formulations, based on the isodifferential approach. The use of the second derivative spectra allowed a selective determination of the analytes free from matrix interferences and without pretreatment of samples. Standard solutions of the analytes were analyzed by the proposed procedure in order to select the appropriate wavelengths to solve the mixture. After this, the procedure was validated using commercial sunscreen formulations the concentrations of which were determined by an HPLC procedure. The two procedures gave comparab…

Detection limitAnalyteChromatographyInjection ProcedureAnalytical chemistryDerivativeStandard solutionBiochemistryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryEnvironmental ChemistryOxybenzoneSpectroscopySecond derivativeAnalytica Chimica Acta
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Spectrophotometric determination of phenols in water samples by the GHPSAM method

2001

Abstract The generalized H-point standard-additions method (GHPSAM) is proposed in order to obtain the phenol concentration in water samples when the matrix is completely unknown. The procedure involves solid-phase extraction in BondElut PPL cartridges and data handling of the UV-visible spectrophotometry measurements. The spectral regions where the unknown interferent behaviour can be considered as linear are found and the analyte concentration free from bias error is estimated. The percentages of recovery of phenols in spiked samples were similar to those obtained by HPLC. Cresols or chlorophenols can be also determined in real samples by this method. The concentration range tested was 0.…

Detection limitAnalyteChromatographymedicine.diagnostic_testChemistryHealth Toxicology and MutagenesisExtraction (chemistry)Public Health Environmental and Occupational HealthAnalytical chemistrySoil SciencePollutionHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundSpectrophotometrymedicineEnvironmental ChemistryPhenolSolid phase extractionWaste Management and DisposalWater Science and Technology
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Atomic absorption spectrometric determination of molybdenum in lubricating oils with use of emulsions

1985

Abstract Samples (0.1 g) containing molybdenum disulphide are digested with aqua regia or with a (1 + 1) hydrofluoric/nitric acid mixture, without complete destruction of the matrix, and the molybdenum is determined in an air/acetylene flame, after emulsification with a non-ionic surfactant (Nemol K-39). The detection limit is ca. 30 μg Mo g−1, and the r.s.d. is 2.9% for 6 analyses of a sample containing 6.5 mg Mo g−1.

Detection limitChemistryInorganic chemistrychemistry.chemical_elementBiochemistryAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundAcetylenePulmonary surfactantNitric acidMolybdenumlawEnvironmental ChemistryAqua regiaAtomic absorption spectroscopySpectroscopyAnalytica Chimica Acta
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Fishing for a drug: solid-phase microextraction for the assay of clozapine in human plasma

1999

Solid-phase microextraction (SPME) was investigated as a sample preparation method for assaying the neuroleptic drug clozapine in human plasma. A mixture of human plasma, water, loxapine (as internal standard) and aqueous NaOH was extracted with a 100-micron polydimethylsiloxane (PDMS) fiber (Supelco). Desorption of the fiber was performed in the injection port of a gas chromatograph at 260 degrees C (HP 5890; 30 m x 0.53 mm I.D., 1 micron film capillary; nitrogen-phosphorous selective detection). Fibers were used repeatedly in up to about 75 analyses. The recovery was found to be 3% for clozapine from plasma after 30 min of extraction. However, in spite of the low recovery, the analyte was…

Detection limitChromatography GasChromatographymedicine.diagnostic_testChemistryReproducibility of ResultsLoxapineGeneral ChemistryReference StandardsSolid-phase microextractionSensitivity and SpecificityHigh-performance liquid chromatographyMatrix (chemical analysis)Therapeutic drug monitoringmedicineHumansSample preparationSolid phase extractionGas chromatographyClozapineJournal of Chromatography B: Biomedical Sciences and Applications
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Determination of atranol and chloroatranol in perfumes using simultaneous derivatization and dispersive liquid-liquid microextraction followed by gas…

2013

Abstract A new analytical method based on simultaneous derivatization and dispersive liquid–liquid microextraction (DLLME) followed by gas chromatography–mass spectrometry (GC–MS), for the determination of the allergenic compounds atranol and chloroatranol in perfumes, is presented. Derivatization of the target analytes by means of acetylation with anhydride acetic in carbonate buffer was carried out. Thereby volatility and detectability were increased for improved GC–MS sensitivity. In addition, extractability by DLLME was also enhanced due to a less polar character of the solutes. A liquid–liquid extraction was performed before DLLME to clean up the sample and to obtain an aqueous sample …

Detection limitChromatographyAqueous solutionTime FactorsMolecular StructureLiquid Phase MicroextractionOsmolar ConcentrationHydrogen-Ion ConcentrationBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryPerfumeSolventMatrix (chemical analysis)chemistry.chemical_compoundchemistryReagentStandard additionBenzaldehydesSolventsEnvironmental ChemistryGas chromatography–mass spectrometryDerivatizationSpectroscopyAnalytica chimica acta
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