Search results for "Matrix"

showing 10 items of 3205 documents

Determination of ruthenium in photographic emulsions - Development and comparison of different sample treatments and mass spectrometric methods

1999

Different sample treatment procedures were combined with inductively coupled plasma mass spectrometry (ICP-MS) and negative thermal ionisation mass spectrometry (NTI-MS) for the determination of ruthenium traces in photographic emulsions. Dissolution of the samples in concentrated ammonia solution was used in connection with ICP-MS by external calibration, which has the advantage of a simple sample preparation technique but introduces high amounts of the silver matrix into the mass spectrometer. On the other hand, isotope dilution mass spectrometry (IDMS) with an enriched 99Ru spike solution was applied for ICP-MS and NTI-MS measurements, respectively, in connection with a significant reduc…

Detection limitChromatographyChemistryAnalytical chemistrychemistry.chemical_elementIsotope dilutionMass spectrometryBiochemistryRuthenium/dk/atira/pure/sustainabledevelopmentgoals/clean_water_and_sanitationMatrix (chemical analysis)Sample preparationPhotographic emulsionSDG 6 - Clean Water and SanitationInductively coupled plasma mass spectrometry
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A solid-phase extraction and size-exclusion liquid chromatographic method for polyethylene glycol 25 p-aminobenzoic acid determination in urine: Vali…

2007

No previous publications about percutaneous absorption of polyethylene glycol 25 p-aminobenzoic acid (PEG-25 PABA) have been found in the literature and the expected levels to be found in human urine after sunscreens use are unknown. The method proposed here is suitable to determine PEG-25 PABA in the urine of sunscreens users in order to carry out studies on body accumulation/excretion. It is based on solid-phase extraction (SPE) with size-exclusion liquid chromatography determination. Solid-phase extraction allows the analyte to be retained and subsequently eluted for a clean-up, using a silica-based cartridge. The size-exclusion liquid chromatography of the eluted allows the rest of matr…

Detection limitChromatographyChemistryElutionExtraction (chemistry)Fluorescence spectrometryReproducibility of ResultsUrineBiochemistryPolyethylene GlycolsAnalytical ChemistryMatrix (chemical analysis)ExcretionSpectrometry FluorescenceChromatography GelHumansEnvironmental ChemistrySolid phase extraction4-Aminobenzoic AcidSunscreening AgentsSpectroscopyAnalytica Chimica Acta
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Electrochemical detection of uric acid and ascorbic acid using r-GO/NPs based sensors

2021

Abstract A sensitive and selective electrochemical sensor, based on reduced graphene oxide and gold nanoparticles obtained by simple co-electrodeposition, was developed for the detection of uric acid and ascorbic acid. Because of the electrochemical oxidation of both uric and ascorbic acid depending on the pH, the sensor performances were studied at different pH values. Excellent results were obtained for uric acid detection in a linear range from 10 to 500 µmol dm−3 with a sensitivity of 0.31 µA cm−2 µM−1. A limit of detection and quantification of 3.6 µM and 10.95 µmol dm−3, respectively, was calculated. Sensors showed good selectivity toward different interfering species present in the m…

Detection limitChromatographyGeneral Chemical Engineering02 engineering and technologyUrineUric acid Food010402 general chemistry021001 nanoscience & nanotechnologyAscorbic acid01 natural sciences0104 chemical sciencesElectrochemical gas sensorMatrix (chemical analysis)chemistry.chemical_compoundBody fluidsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryLinear rangeElectrochemical sensorColloidal goldSettore ING-IND/17 - Impianti Industriali MeccaniciElectrochemistryUric acidAscorbic acid0210 nano-technology
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Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometry Analysis of Carbosulfan, Carbofuran, 3-Hydroxycarbofuran, and Other Metabolites in …

2007

The potential of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QqTOF-MS) to identify and confirm carbosulfan and seven of its main metabolites (carbofuran, 3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenol carbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran, dibutylamine) at trace levels from food is explored for the first time. The analytical method developed consists of pressurized liquid extraction (PLE) and LC-QqTOF-MS in positive ion mode, which attains unequivocal identification and quantification of the studied compounds in food, at levels well below of those of concern (0.05 mg/kg for the sum of carbosulfan, carbofuran, and 3-hydroxycarbofuran).…

Detection limitChromatographyMolecular StructureMetaboliteRepeatabilityButylaminesMass spectrometrySensitivity and SpecificityAnalytical ChemistryDibutylamineCarbofuranchemistry.chemical_compoundchemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationCarbosulfanCarbamatesQuantitative analysis (chemistry)CarbofuranFood AnalysisChromatography LiquidAnalytical Chemistry
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A cost-effective method for estimating di(2-ethylhexyl)phthalate in coastal sediments.

2013

This study describes the development of a new method for the analysis of di(2-ethylhexyl)phthalate (DEHP) using 0.1-0.3 g of sediment sample, based on matrix solid phase dispersion (MSPD) using C18 as dispersant phase (0.4 g) and acetonitrile-water as eluting solvent (3.4 mL 1:3.25, v/v). No evaporation step is required. 3 mL of extracts were processed on-line by in-tube solid phase microextraction (IT-SPME) coupled to capillary liquid chromatography (CapLC) and diode array detector (DAD). A short analytical column Zorbax SB C18 (35×0.5 mm, 5 μm) provided suitable results. FTIR-ATR was employed for characterizing sediment samples and MSPD procedure. The total analysis time was less than 20 …

Detection limitChromatographyOceans and SeasOrganic ChemistryAnalytical chemistryPhthalateEvaporationGeneral MedicineSolid-phase microextractionBiochemistryAnalytical ChemistryMatrix (chemical analysis)Solventchemistry.chemical_compoundchemistryChromatography detectorDiethylhexyl PhthalateSpectroscopy Fourier Transform InfraredSoil PollutantsLasers SemiconductorDispersion (chemistry)Solid Phase MicroextractionChromatography LiquidJournal of chromatography. A
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Rapid screening of organophosphorus pesticides in honey and bees by liquid chromatography—Mass spectrometry

2002

Twenty-two organophosphorus pesticide residues were simultaneously determined in honey and honeybee samples by extraction procedures based on solid-phase and liquid chromatography-atmospheric pressure chemical ionization-mass in positive and negative ionization modes. Pesticides in honeybee samples were extracted by matrix solid phase dispersion with C18 silica and subsequently eluted with a mixture of dichloromethane-methanol (85∶15, v/v). The average recoveries from spiked honeybees (0.5–10 μg g−1) ranged from 76% for coumaphos to 100% for omethoate, with relative standard deviations between 3 and 17%. Limits of detection were ≤0.13 μg g−1 and limits of quantification were ≤0.43 μg g−1. H…

Detection limitChromatographyOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryOmethoateSolid phase extractionChromatographia
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Improving detection limits for organotin compounds in several matrix water samples by derivatization-headspace-solid-phase microextraction and GC-MS.

2010

Triethyltin, tributyltin, diphenyltin and triphenyltin were selected as model compounds. The method is based on in situ ethylation and simultaneous headspace-solid-phase microextraction (HS-SPME) and gas chromatographic-mass spectrometry analysis (GC-MS). The extraction procedure was optimized studying some variables such as reaction time, salinity, sample volume and headspace volume. SPME-GC-MS and SPME-GC-FID techniques were compared; quality assurance parameters such as sensitivity, selectivity and precision were established. The proposed procedure showed limits of detection between 0.025 and 1 ng/L. The linearity was in the 0.025-5000 ng/L range. The precision expressed as relative stan…

Detection limitCromatografia de gasosChromatographyAnalytical chemistrySolid-phase microextractionAnalytical Chemistrylaw.inventionMatrix (chemical analysis)chemistry.chemical_compoundchemistrylawFlame ionization detectorSample preparationGas chromatographyCompostos organometàl·licsAigües residuals AnàlisiGas chromatography–mass spectrometryDerivatizationTalanta
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Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments.

2012

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Buchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also accepta…

Detection limitGeologic SedimentsExtraction (chemistry)SedimentGeneral MedicineRepeatabilityChemical FractionationManagement Monitoring Policy and LawPollutionGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Dry weightEnvironmental chemistryEnvironmental scienceEcotoxicologySeawaterSettore CHIM/01 - Chimica AnaliticaPolycyclic Aromatic HydrocarbonsGas chromatography–mass spectrometryAutomatic extraction .CRM . PAHs . Sediments . GC-MSSicilyWater Pollutants ChemicalEnvironmental MonitoringGeneral Environmental Science
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Antibody-Capped Mesoporous Nanoscopic Materials: Design of a Probe for the Selective Chromo-Fluorogenic Detection of Finasteride

2012

[EN] The synthesis of capped mesoporous silica nanoparticles (MSN) conjugated with an antibody (AB) as a gatekeeper has been carried out in order to obtain a delivery system able to release an entrapped cargo (dye) in the presence of a target molecule (antigen) to which the conjugated antibody binds selectively. In particular, MSN loaded with rhodamine B and functionalized on the external surface with a suitable derivative of N-(t-butyl)- 3-oxo-(5a,17b)-4-aza-androst-1-ene-17-carboxamide (finasteride) have been prepared (S1). The addition of polyclonal antibodies against finasteride induced capping of the pores due to the interaction with the anchored hapten-like finasteride derivative to g…

Detection limitINGENIERIA DE LA CONSTRUCCIONAqueous solutionChromatographyQUIMICA INORGANICANanotechnologyGeneral ChemistryMesoporous silicaFull PapersMCM-41finasterideMatrix (chemical analysis)chemistry.chemical_compoundQUIMICA ORGANICAchemistryQUIMICA ANALITICAhybrid materialsFinasterideRhodamine BantibodiesSelectivityMesoporous materialmolecular gatesChemistryOpen
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Optimization of Matrix Solid-Phase Dispersion method for simultaneous extraction of aflatoxins and OTA in cereals and its application to commercial s…

2010

Abstract A method based on Matrix Solid-Phase Dispersion (MSPD) has been developed for the determination of 5 mycotoxins (ochratoxin A and aflatoxins B and G) in different cereals. Several dispersants, eluents and ratios were tested during the optimization of the process in order to obtain the best results. Finally, samples were blended with C 18 and the mycotoxins were extracted with acetonitrile. Regarding to matrix effects, the results clearly demonstrated the necessity to use a matrix-matched calibration to validate the method. Analyses were performed by liquid chromatography–triple quadrupole-tandem mass spectrometry (LC–QqQ-MS/MS). The recoveries of the extraction process ranged from …

Detection limitOchratoxin AAflatoxinCereals analysisMatrix Solid-Phase DispersionChromatographyChemistryExtraction (chemistry)Ochratoxin ACoffeeOchratoxinsMass SpectrometryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundAflatoxinsLimit of Detectionmedia_common.cataloged_instanceSample preparationEuropean unionEdible GrainMycotoxinChromatography Liquidmedia_commonTalanta
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