Search results for "performance"

showing 10 items of 4457 documents

A sequential-injection system for spectrophotometric determination of p -aminobenzoic acid in sunscreens.

2002

A sequential injection method is proposed for spectrophotometric determination of p-aminobenzoic acid (PABA) in cosmetic formulations. The method is based on diazotization of the analyte, coupling with 8-hydroxyquinoline, and the subsequent formation of a colored product. The experimental conditions used (coupling reagent, sandwich arrangement, volumes aspirated, propulsion flow rate, reaction coil length) were studied. Response of the sequential injection method were linearly dependent on concentrations up to 25 micro g mL(-1) and the detection limit was 2 micro g mL(-1). Throughput was 51 measurements per hour and a complete cycle, including three measurement per sample and a washing step…

Detection limitAnalyteChromatographymedicine.diagnostic_testSpectrum AnalysisColorReproducibility of ResultsSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrySpectrophotometrymedicine4-Aminobenzoic acidAminobenzoic acidSelectivity4-Aminobenzoic AcidAzo CompoundsSunscreening AgentsQuantitative analysis (chemistry)Analytical and Bioanalytical Chemistry
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Determination of phenolic antioxidants in vegetal and animal fats without previous extraction by dilution with n-propanol and micellar liquid chromat…

1999

Abstract A simple and rapid HPLC method for the determination of phenolic antioxidants (propyl and octyl gallates, tert -butylhydroquinone and 3- tert -butyl-4-hydroxyanisole) in sunflower, corn and olive oils, margarine, lard and butter oil is described. The samples are diluted with n -propanol, filtered and injected; solutions containing 30% (w/w) sample can be injected. The analytes are separated with a C18 column and a micellar mobile phase containing 0.1 M SDS, 2.5% n -propanol and 10 mM phosphate of pH 3, and detected at 290 nm. Calibration curves are linear ( r  > 0.9999) and the limits of detection range from 0.2 to 1.3 ng, which correspond to antioxidant concentrations well below t…

Detection limitAnimal fatChromatographyExtraction (chemistry)BiochemistryHigh-performance liquid chromatographyMicellar electrokinetic chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundchemistryMicellar liquid chromatographyEnvironmental ChemistryPhenolsSpectroscopyAnalytica Chimica Acta
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Urine polyamines determination using dansyl chloride derivatization in solid-phase extraction cartridges and HPLC

1999

The derivatization of biogenic amines such as putrescine, cadaverine, spermidine and spermine with dansyl chloride in solid phase extraction cartridges is described. Different types of filling materials were tested in order to have the highest retention of the different analytes. The best results were obtained by using C18 cartridges. The optimal conditions were: amine solution buffered at pH 12, 2 mM dansyl chloride (acetone-bicarbonate solution 20 mM (pH 9-9.5), 2 + 3 v/v) as reagent concentration, room temperature and 30 min reaction time. The developed procedure was applied to the determination of these polyamines in urine samples from healthy controls and cancer patients using HPLC wit…

Detection limitCadaverineChromatographyBiogenic PolyaminesDansyl chlorideBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNeoplasmsReagentBiomarkers TumorElectrochemistryPutrescineHumansEnvironmental ChemistrySolid phase extractionDerivatizationChromatography High Pressure LiquidSpectroscopyThe Analyst
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Study of passive sampling of polycyclic aromatic hydrocarbons in gas phase using Amberlite XAD resins as filling materials of semipermeable membranes

2013

Abstract In this work, a study was performed to evaluate the use of Amberlite XAD resins (XAD-2, XAD-4 and XAD-16), for the first time, as filling materials for low-density polyethylene membranes, which will be inserted as passive samplers for polycyclic aromatic hydrocarbons (PAHs) in gas phase. The use of samplers deployed for 48 h evidenced a relative capability to retain the compounds under study. A detailed study was performed to evaluate the recovery of analytes from the sampler through microwave-assisted extraction by using acetonitrile. A clean-up step using alumina-C18 cartridges was necessary before determination of the PAHs by high performance liquid chromatography with fluoresce…

Detection limitCartridgechemistry.chemical_compoundMembraneChromatographychemistryExtraction (chemistry)AmberlitePolyethyleneAcetonitrileHigh-performance liquid chromatographySpectroscopyAnalytical ChemistryMicrochemical Journal
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Fast Separation and Determination of Sterols in Vegetable Oils by Ultraperformance Liquid Chromatography with Atmospheric Pressure Chemical Ionizatio…

2010

A method for the determination of sterols in vegetable oils by ultraperformance liquid chromatography (UPLC) with atmospheric pressure chemical ionization mass spectrometry detection has been developed. The separation of sterols was optimized in terms of mobile phase composition, column temperature and flow rate. The optimal conditions were achieved using an Acquity UPLC BEH C18 column (50 x 2.1 mm, 1.7 microm) with a mobile phase consistent of acetonitrile/water (0.01% acetic acid) using a linear gradient, at a flow rate of 0.8 mL min(-1) and column temperature of 10 degrees C, giving a total analysis time below 5 min. The determination was performed in selective ion recording mode. The li…

Detection limitChemical ionizationChromatographyAtmospheric pressureChemistryAnalytical chemistryAtmospheric-pressure chemical ionizationGeneral ChemistryMass spectrometryHigh-performance liquid chromatographyMass SpectrometrySterolschemistry.chemical_compoundAtmospheric PressureVegetable oilPlant OilsGeneral Agricultural and Biological SciencesAcetonitrileChromatography LiquidJournal of Agricultural and Food Chemistry
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Comparison of gas and liquid chromatography coupled to mass spectrometry for the residue analysis of pesticides in organges

2001

Liquid chromatography-mass spectrometry (LC-MS) with atmospheric pressure chemical ionization (APCI), and gas chromatography-mass spectrometry (GC-MS) with electron impact ionization (EI), are compared for the determination of eight pesticides in oranges. Seven of the selected pesticides, chlorpyriphos, chlorpyriphos-methyl, imazalil, α and β-endosulfan, endosulfan sulphate and dicofol, are commonly determined by GC whereas one, thiabendazole, can only be directly determined by LC. Primary ions [M-H]− or [M-Cl+O]− are obtained using LC-APCI-MS in negative ionization (NI) mode. In contrast, a high degree of fragmentation is reported with GC-MS. Both techniques were applied to oranges, which …

Detection limitChemical ionizationChromatographyChemistryOrganic ChemistryClinical BiochemistryAnalytical chemistryAtmospheric-pressure chemical ionizationMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryIonizationGas chromatographyElectron ionizationChromatographia
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Determination of fungicide residues in fruits and vegetables by liquid chromatography–atmospheric pressure chemical ionization mass spectrometry

2002

Abstract A liquid chromatography (LC) method for the quantitative determination of five fungicide residues (dichloran, flutriafol, o -phenylphenol, prochloraz and tolclofos methyl) in oranges, lemons, bananas, peppers, chards and onions is described. The residues were extracted by matrix solid-phase dispersion (MSPD) using C 8 . Quantitative analysis was performed by isocratic LC coupled to quadrupole mass spectrometer using atmospheric pressure chemical ionization in the negative ionization mode. The limit of quantification was 0.01 mg kg −1 for flutriafol, o -phenylphenol and dichloran, and 0.1 mg kg −1 for prochloraz and tolclofos methyl. The MSPD method is also suitable for LC–UV analys…

Detection limitChemical ionizationChromatographyChemistryOrganic ChemistryReproducibility of ResultsAtmospheric-pressure chemical ionizationGeneral MedicineMass spectrometrySensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyMass SpectrometryFungicides IndustrialAnalytical ChemistryAtmospheric PressureFruitVegetablesSpectrophotometry UltravioletSample preparationSolid phase extractionQuadrupole mass analyzerChromatography LiquidJournal of Chromatography A
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Determination of carbamate residues in fruits and vegetables by matrix solid-phase dispersion and liquid chromatography-mass spectrometry.

2000

Abstract Thirteen carbamates were analysed in orange, grape, onion and tomatoes by matrix solid-phase dispersion (MSPD) followed by liquid chromatography–mass spectrometry (LC–MS). Electrospray (ES) and atmospheric pressure chemical ionisation (APCI) were compared and both gave similar results in terms of sensitivity and structural information because at 20 V fragmentor voltages the fragmentation is minimal. The efficiency of different solid-phases (C18, C8, cyano, amine and phenyl) for the MSPD was compared. Mean recoveries using C8 varied from 64 to 106% with relative standard deviations of 5–15% in the concentration range of 0.01–10 mg kg−1. Matrix constituents did not interfere signific…

Detection limitChemical ionizationInsecticidesChromatographyChemistryOrganic ChemistryPesticide ResiduesAtmospheric-pressure chemical ionizationGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryFruitVegetablesmedia_common.cataloged_instanceSolid phase extractionCarbamatesEuropean unionChromatography High Pressure Liquidmedia_commonJournal of chromatography. A
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Comparative evaluation of liquid chromatography versus gas chromatography using a β-cyclodextrin stationary phase for the determination of BTEX in oc…

2009

An HPLC method for the determination of benzene, toluene, ethylbenzene and o-xylene, m-xylene and p-xylene in occupational environments was developed and compared with a GC-MS method. Chromatographic analysis using a beta-cyclodextrin stationary phase was performed after active and passive air sampling by adsorption on activated charcoal and pressurized fluid extraction. The analytes were completely separated and quantified using both methods, although GC-MS provided better resolutions and lower detection limits than HPLC. The HPLC method was unsuccessfully applied to the determination of benzene in real samples because its sensitivity was too low. Both methods were applied to the analysis …

Detection limitChromatography GasChromatographybeta-CyclodextrinsAnalytical chemistryBenzeneBeta-CyclodextrinsBTEXXylenesHigh-performance liquid chromatographyEthylbenzeneAnalytical Chemistrychemistry.chemical_compoundCertified reference materialschemistryOccupational ExposureBenzene DerivativesGas chromatographyGas chromatography–mass spectrometryChromatography LiquidTolueneTalanta
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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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