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showing 10 items of 2426 documents

High-performance liquid chromatographic determination of tocopherols in infant formulas

2002

A method for the simultaneous determination of alpha-tocopherol acetate and alpha-, delta-, and gamma-tocopherols by normal-phase high-performance liquid chromatography (HPLC) with a fluorescent detector in infant formula is proposed. The values obtained in the determination of the analytical parameters: linearity, precision, limit of detection and accuracy (analysis of a standard reference material, SRM 1846), confirm the quality of the method. The proposed method is useful for the determination of alpha-, delta-, and gamma-tocopherols and alpha-tocopherol acetate in infant formulas at a low cost and in a total time of 2 h.

Detection limitChromatographyChemistryVitamine eOrganic ChemistryDetectorAnalytical chemistryInfantReproducibility of ResultsTocopherolsfood and beveragesLinearityGeneral MedicineSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySpectrometry FluorescenceHumansInfant FoodQuantitative analysis (chemistry)Chromatography High Pressure LiquidAnalysis methodJournal of Chromatography A
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Application of ACC method to synchronous luminiscence: determination of alpha-tocopherol and alpha-tocopheryl acetate in beverages.

2001

A new method based on the Q parameter, that permits the determination of the C(compound A)/C(compound B) ratio without preparing calibration graphs of the two compounds, is proposed. This method has been applied to signals obtained by synchronous luminiscence. Simultaneous determination of alpha-tocopherol and alpha-tocopheryl acetate in beverages using synchronous fluorescence has been carried out. To isolate the compounds from samples, liquid extraction with n-hexane as the organic phase was employed. The presence of interferences was tested using the apparent content curves (ACC) method and the C(alpha-tocopherol)/C(alpha-tocopheryl acetate) ratio was calculated using the Q parameter. Th…

Detection limitChromatographyExtraction (chemistry)Fluorescence spectrometryAnalytical chemistryReproducibility of ResultsAcetatesBiochemistrySensitivity and SpecificityBeverageschemistry.chemical_compoundSpectrometry FluorescencechemistryModels ChemicalLuminescent MeasurementsSolventsHexanesVitamin ETocopheryl acetateTocopherolalpha-TocopherolQuantitative analysis (chemistry)Vitamin E AcetateFresenius' journal of analytical chemistry
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High-performance liquid chromatography of lactose with evaporative light scattering detection, applied to determine fine particle dose of carrier in …

2005

A method for quantification of the fine particle dose of lactose is described, using a hydrophilic interaction chromatography (HILIC) method and evaporative light scattering detection. The HILIC method used an aminopropyl column and a mobile phase consisting of acetonitril/water (80/20, v/v) for isocratic elution. Sensitive chromatography was obtained using a low concentration of water in the extraction solvent. The detection limit (RSD10%) at an injection volume of 10 microL is 10 microg/mL. Linearity was obtained in the range of 10-80 microg/mL (R(2)0.99). A relative standard deviation (RSD) of 0.5% (N=6) demonstrated good precision of the optimized method.

Detection limitChromatographyLightChemistryHydrophilic interaction chromatographyOrganic ChemistryExtraction (chemistry)Analytical chemistryReproducibility of ResultsLactoseGeneral MedicineBiochemistryHigh-performance liquid chromatographyLight scatteringAnalytical ChemistrySolventChromatography detectorAdministration InhalationScattering RadiationParticlePowdersChromatography High Pressure LiquidJournal of Chromatography A
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Determination of amitraz and its transformation products in pears by ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.

2008

A method has been developed for identification and quantification of the acaricide amitraz and its transformation products, 2,4-dimethylaniline (DMA), 2,4-dimethylformamidine (DMF) and N-2,4-dimethylphenyl-N-methylformamidine (DMPF) in pears. The analytes were extracted using ethyl acetate and anhydrous sodium sulphate. Analysis was performed by liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using a triple quadrupole (QqQ) instrument. Two precursor-product ion transitions were monitored for each compound in the selected reaction monitoring (SRM) mode. The method was validated with pears taken from the orchard before the amitraz treatment …

Detection limitChromatographyMaximum Residue LimitAniline CompoundsToluidinesSulfatesOrganic ChemistrySelected reaction monitoringEthyl acetatePesticide ResiduesReproducibility of ResultsGeneral MedicineAcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerPyruschemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryAmitrazChromatography LiquidJournal of chromatography. A
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Determination ofl-Ascorbic Acid and Total Ascorbic Acid in Vascular and Nonvascular Plants by Capillary Zone Electrophoresis

1998

A capillary zone electrophoresis (CZE) procedure for the determination of l-ascorbic acid (AA) and total ascorbic acid (TAA, as the sum of AA and dehydroascorbic acid) in vascular plants, lichens, bryophytes, and liverworts is described. The samples were frozen in liquid nitrogen and extracted with 2% metaphosphoric acid. To determine AA, an aliquot was directly injected in a fused-silica capillary. The determination of TAA was performed upon its reduction with dl-homocysteine at pH 7. The background electrolyte contained 60 mM sodium chloride, 60 mM sodium dihydrogen phosphate, 1 x 10(-4)% hexadimetrine bromide, and NaOH up to pH 7. The procedure was rapid and highly reproducible; the limi…

Detection limitChromatographySodiumBiophysicsElectrophoresis CapillaryReproducibility of Resultschemistry.chemical_elementAscorbic AcidCell BiologyElectrolytePlantsAscorbic acidSensitivity and SpecificityBiochemistryElectrophoresischemistry.chemical_compoundCapillary electrophoresischemistryBromideDehydroascorbic acidMolecular BiologyAnalytical Biochemistry
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Amphetamine and methamphetamine determination in urine by reversed-phase high-performance liquid chromatography with sodium 1,2-napthoquinone 4-sulfo…

1995

A rapid method is described for the identification and determination of amphetamine and methamphetamine in human urine samples by liquid chromatography with UV-Vis detection. The samples were transferred onto a C18 solid-phase extraction column and chromatographed on a Hypersil ODS RP C18, 5 microns (250 x 4 mm I.D.) with an acetonitrile-water elution gradient containing propylamine. Under these conditions, the amines are eluted with a short retention time. The procedure has been applied to the determination of amphetamine and methamphetamine in the range 0.3-4.0 micrograms/ml in spiked urine samples. The detection limits at 280 nm were 4 and 2 ng/ml for amphetamine and methamphetamine, res…

Detection limitChromatographySpectrophotometry InfraredElutionChemistryExtraction (chemistry)Reproducibility of ResultsPropylamineGeneral ChemistryMethamphetamineHigh-performance liquid chromatographyMethamphetamineAmphetaminechemistry.chemical_compoundmedicineHumansIndicators and ReagentsSolid phase extractionQuantitative analysis (chemistry)Chromatography High Pressure LiquidNaphthoquinonesmedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
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A rapid and reliable size-exclusion chromatographic method for determination of kojic dipalmitate in skin-whitening cosmetic products

2007

A size-exclusion chromatographic method has been developed to determine the relatively novel skin-whitening agent called kojic dipalmitate (KDP) in skin-whitening cosmetic products. Preliminary experiments were carried out in order to select the solvent for standard and sample solution, and also for mobile phase composition. A PLGel Mixed-D (polystyrene/divinylbenzene co-polymer) column and isocratic mobile phase of pure tetrahydrofuran (at 1.5 mL min(-1) flow rate) were used. Detection was carried out by means of an UV/vis spectrometry detector set at 248 nm. A study of interferences reveals that KDP can be determined without interferences coming from cosmetic matrices. Most other cosmetic…

Detection limitChromatographymedicine.diagnostic_testSize-exclusion chromatographyReproducibility of ResultsSkin PigmentationSkin whiteningCosmeticsDivinylbenzeneSensitivity and SpecificityAnalytical ChemistrySolventGel permeation chromatographychemistry.chemical_compoundchemistryPyronesSpectrophotometryChromatography GelmedicineSpectrophotometry UltravioletCosmetic industryTalanta
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Zwitterionic Sulfonates as m/z Shift Reagents for 5-Methylcytosine Detection in Deoxyribonucleic Acids (DNA) Using Flow Injection Analysis and Electr…

2015

5-Methylcytosine (5-MC) is an important epigenetic modification of DNA. Abnormally high concentrations of this substance appear because of the hypermethylation of cytosine. Therefore, the measurement of the quantity of this compound in mammals is of great importance. Recently, we reported that several imidazolium-based zwitterionic sulfonates form complexes with 5-MC in solution, which can be studied by electrospray ionisation mass spectrometry (ESI-MS). It is shown in this paper that such an association can be utilised for the detection of 5-MC in a DNA sample using high-throughput a flow injection analysis ESI-MS method. A variety of the sulfonate zwitterions have been tested as m/ z shi…

Detection limitFlow injection analysisSpectrometry Mass Electrospray IonizationElectrosprayChromatographyChemistryElectrospray ionizationAnalytical chemistryReproducibility of ResultsDNAGeneral MedicineDNA MethylationTandem mass spectrometryMass spectrometryAtomic and Molecular Physics and OpticsSample preparation in mass spectrometryFlow Injection Analysis5-MethylcytosineAnimalsCattleA-DNASulfonic AcidsSpectroscopyEuropean Journal of Mass Spectrometry
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Validated, non-destructive and environmentally friendly determination of cocaine in euro bank notes.

2005

A non-destructive, fast and environmentally friendly procedure has been developed for cocaine determination in euro bank notes. Cocaine was extracted with 15 ml methanol by vortex agitation during 5 min. The extract was evaporated and reconstituted in 0.5 ml methanol. GC-MS-MS analysis was performed using as precursor ion m/z 182.2, with an excitation energy voltage of 1.60 eV, being the product ions measured m/z 150.2 and 82.0. A limit of detection of 0.15 ng per note and a repeatability of 6%, established from the relative standard deviation, of a 1 ng ml(-1) level, were achieved. Recoveries of 101+/-2 and 98+/-3% were obtained for samples spiked with 100 and 10 microg respectively. Resul…

Detection limitPaperChromatographyOrganic ChemistryForensic SciencesAnalytical chemistryReproducibility of ResultsGeneral MedicineRepeatabilityBiochemistryEnvironmentally friendlySensitivity and SpecificityGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryCocaineSample preparationMethanolGas chromatographyGas chromatography–mass spectrometryQuantitative analysis (chemistry)Journal of chromatography. A
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Determination of abamectin in citrus fruits by liquid chromatography-electrospray ionization mass spectrometry.

2000

Liquid chromatography coupled to electrospray mass spectrometry (LC-ES-MS) with positive ion detection was used to determine abamectin in oranges. MS conditions were optimized to achieve maximum sensitivity. The main ion for abamectin was [M+Na]+ at a fragmentor voltage of 180 V. Abundant structural information can be obtained at different fragmentor voltages. The detection limit for the standard solution was 12 pg injected, and good linearity and reproducibility were observed. Abamectin residues were extracted using matrix solid-phase dispersion. Orange samples were homogenized with C18 bonded silica placed onto a glass column and eluted with dichloromethane. Recoveries of the abamectin fr…

Detection limitQuality ControlElectrosprayCitrusInsecticidesChromatographyIvermectinElutionElectrospray ionizationOrganic ChemistryReproducibility of ResultsGeneral MedicineMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryAbamectinSolid phase extractionChromatography High Pressure LiquidJournal of chromatography. A
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