Search results for "addition"

showing 10 items of 933 documents

Sequential-injection determination of traces of disodium phenyl dibenzimidazole tetrasulphonate in urine from users of sunscreens by on-line solid-ph…

2005

Abstract A sensitive and selective method to determine disodium phenyl dibenzimidazole tetrasulphonate (PDT) in the urine of sunscreen users, which is suitable for studies on body accumulation/excretion is proposed. On-line solid-phase extraction allows the analyte to be retained and subsequentely eluted, using a strong anion exchange (SAX) microcolumn. Standard addition calibration was carried out with only one standard. The wavelengths of excitation and emission were 330 and 454 nm, respectively. The method allows PDT to be determined in both, spiked and unspiked human urine samples, without any pre-treatment. Results obtained for spiked urine samples (40–200 ng ml −1 ) showed the accurac…

Detection limitAnalyteChromatographyChemistryElutionAdministration TopicalSkin AbsorptionClinical BiochemistryFluorescence spectrometryReproducibility of ResultsPharmaceutical ScienceUrineHydrogen-Ion ConcentrationAnalytical ChemistryExcretionSpectrometry FluorescenceStandard additionFlow Injection AnalysisDrug DiscoveryHumansBenzimidazolesSolid phase extractionSunscreening AgentsSpectroscopyJournal of Pharmaceutical and Biomedical Analysis
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A solid-phase extraction liquid chromatography-tandem mass spectrometry method for the percutaneous absorption assessment of 3-(4′-methylbenzylidene)…

2013

The UV filter 3-(4′-methylbenzylidene)camphor (MBC) is a common ingredient in sunscreen cosmetic products. However, different in vitro and in vivo studies suggest that MBC can cause endocrine disrupting effects. This report focuses on the development of an analytical method based on solid-phase extraction (SPE) prior to liquid chromatography tandem mass spectrometry (LC-MS/MS) for the determination of MBC and its main phase I metabolite, named 3-(4′-carboxybenzylidene)camphor (CBC), in urine from users of sunscreen cosmetic products containing MBC. The formation of phase II metabolites (i.e., glucuronide and sulphate conjugates) was also considered by carrying out an enzymatic hydrolysis of…

Detection limitAnalyteChromatographyGeneral Chemical EngineeringMetaboliteGeneral EngineeringAnalytical ChemistryCamphorchemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryStandard additionSolid phase extractionGlucuronideAnal. Methods
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Development of a fully automated sequential injection solid-phase extraction procedure coupled to liquid chromatography to determine free 2-hydroxy-4…

2010

Abstract 2-Hydroxy-4-methoxybenzophenone and 2-hydroxy-4-methoxybenzophenone-5-sulphonic acid, commonly known as benzophenone-3 (BZ3) and benzophenone-4 (BZ4), respectively, are substances widely used as UV filters in cosmetic products in order to absorb UV radiation and protect human skin from direct exposure to the deleterious wavelengths of sunlight. As with other UV filters, there is evidence of their percutaneous absorption. This work describes an analytical method developed to determine trace levels of free BZ3 and BZ4 in human urine. The methodology is based on a solid-phase extraction (SPE) procedure for clean-up and pre-concentration, followed by the monitoring of the UV filters by…

Detection limitAnalyteChromatographymedicine.diagnostic_testChemistryElutionSolid Phase ExtractionExtraction (chemistry)TemperatureHydrogen-Ion ConcentrationBiochemistryAnalytical ChemistryBenzophenonesSpectrophotometryStandard additionmedicineHumansEnvironmental ChemistrySpectrophotometry UltravioletSolid phase extractionSelectivitySunscreening AgentsChromatography High Pressure LiquidSpectroscopyAnalytica Chimica Acta
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Determination of aluminum at the parts per billion level by solvent extraction and flame atomic emission spectrometry

1991

A new method for the determination of aluminum at the parts per billion level, by N 2 O/ C 2 H 2 flame emission spectrometry with prior solvent extraction with acetylacetone or 8-hydroxyquinoline in 4-methylpentan-2-one, has been performed. The influence of extraction conditions and instrumental parameters on the sensitivity, precision, and dynamic range of the emission calibration curves have been studied. The limit of detection is between 5 and 10 ppb for both ligands, the variation coefficient being 0.2 and 3% at levels of 75 and 25 ppb, respectively. The method has been applied to the determination of Al in water and the results obtained are compared with those found by the standard add…

Detection limitCalibration curveAcetylacetoneExtraction (chemistry)Parts-per notationAnalytical chemistrychemistry.chemical_elementAnalytical Chemistrychemistry.chemical_compoundchemistryAluminiumLiquid–liquid extractionStandard additionSpectroscopyMicrochemical Journal
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Determination of chromium(III) and chromium(VI) in mineral water by bidirectional electrostacking and electrothermal atomic absorption spectrometry

2001

Abstract A feasibility investigation was carried out on the use of bidirectional electrostacking for simultaneous separation and pre-concentration of Cr(III) and Cr(VI) and their electrothermal atomic absorption spectrometry (ETAAS) determination. The bidirectional electrostacking manifold was improved, and the effects of sample tube cross-section and electrostacking time on the pre-concentration factor were investigated. Results indicate that the sample tube cross-section and electrostacking time are the main influence factors on the electrostacking pre-concentration, as well as the electric field strength and ionic mobility. The method developed was suitable for the simultaneous separatio…

Detection limitChemistryAnalytical chemistrychemistry.chemical_elementConductivityBiochemistryAnalytical Chemistrylaw.inventionChromiumCertified reference materialslawStandard additionCalibrationEnvironmental ChemistryAtomic absorption spectroscopyQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Multicommutation Fourier transform infrared determination of benzene in gasoline

2004

A fully mechanized method to determine benzene in motor gasolines has been developed based on the use of Fourier transform infrared spectroscopy (FT-IR) and multicommutation. The flow network comprised a set of three-way solenoid valves and was controlled by means of a microcomputer furnished with an electronic interface and running by a software written in QUICK BASIC 4.5. The flow network and control software were designed to implement the multicommutation approach providing facilities to handle sample and reagent solutions, so that, sample dilution, external calibration and standard addition could be easily performed on-line. The method permits the direct determination of benzene without…

Detection limitChemistryDirect methodAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformStandard additionsymbolsEnvironmental ChemistryGasolineFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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Direct determination of benzene in gasoline by flow-injection Fourier transform infrared spectrometry

1993

Abstract A Fourier transform infrared spectrometric procedure for the automated determination of benzene in gasoline was developed, based on the use of flow-injection analysis. The method permits the direct determination of benzene without any pretreatment of samples, with a limit of detection of 0.02% (v/v) and a relative standard deviation of ca. 1% [for five independent analyses of a diluted sample containing a 0.4% (v/v) of benzene]. Results found by direct analysis agreed with those obtained by off-line and on-line standard addition methods. A rapid quality control procedure was developed, based on the on-line injection of gasoline samples (diluted 1 + 9 in hexane) into a carrier strea…

Detection limitChromatographyAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryHexanechemistry.chemical_compoundsymbols.namesakeFourier transformchemistryStandard additionsymbolsEnvironmental ChemistryGas chromatographyGasolineBenzeneSpectroscopyAnalytica Chimica Acta
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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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Sensitive determination of free benzophenone-3 in human urine samples based on an ionic liquid as extractant phase in single-drop microextraction pri…

2007

Abstract Benzophenone-3 (BZ3), one of the compounds most commonly used as UV filter in cosmetic products, can be absorbed through the skin into the human body, since it can be found at trace levels in urine from users of cosmetic products that contain BZ3. Moreover, different undesirable effects have been attributed to this compound. Thus, sensitive analytical methods to monitor urinary excretion of this compound should be developed. This paper presents a selective and sensitive methodology for BZ3 determination at ultratrace levels in human urine samples. The methodology is based on a novel microextraction technique, known as single-drop microextraction (SDME). An ionic liquid (IL) has bee…

Detection limitChromatographyCentral composite designOrganic ChemistryAnalytical chemistryTemperatureIonic LiquidsGeneral MedicineBiochemistryHigh-performance liquid chromatographyChemistry Techniques AnalyticalAnalytical Chemistrychemistry.chemical_compoundBenzophenoneschemistryIonic strengthLiquid–liquid extractionStandard additionIonic liquidHumansSample preparationChromatography LiquidJournal of chromatography. A
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A rapid and sensitive gas chromatography-mass spectrometry method for the quality control of perfumes: simultaneous determination of phthalates

2013

A rapid and sensitive analytical gas chromatography-mass spectrometry (GC-MS) method for perfume analysis to determine the phthalates banned by the European Union Regulation on cosmetic samples is presented. This method has been tested in commercial alcoholic perfume samples for the determination of the following seven phthalates: dibutyl phthalate, bis(2-ethylhexyl) phthalate, bis(2-methoxyethyl) phthalate, n-pentyl-isopentylphthalate, di-n-pentyl phthalate, diisopentylphthalate and benzyl butyl phthalate. Sample evaporation and redissolution in ethanol is carried out before GC-MS analysis, with no dilution of the sample. External calibration and standard addition calibration are compared …

Detection limitChromatographyDibutyl phthalateGeneral Chemical EngineeringGeneral EngineeringPhthalateRepeatabilityAnalytical Chemistrychemistry.chemical_compoundchemistryBenzyl butyl phthalateStandard additionmedia_common.cataloged_instanceEuropean unionGas chromatography–mass spectrometrymedia_commonAnal. Methods
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