Search results for "LIMIT"

showing 10 items of 2826 documents

A reliable and environmentally-friendly liquid-chromatographic method for multi-class determination of fat-soluble UV filters in cosmetic products.

2013

An environmentally-friendly analytical method for the simultaneous determination of 15 fat-soluble ultraviolet (UV) filters currently authorized by the European Union regulation on cosmetic products has been developed. The determination was performed by liquid chromatography with UV spectrophotometric detection. Different parameters, such as type of column, oven temperature, mobile phase composition and flow rate were studied. The best chromatographic separation was obtained under the following conditions: C18 column set at 60°C and gradient ethanol:water (containing 1% formic acid and 20mM of 2-hydroxypropyl-β-cyclodextrin) as mobile phase pumped at 1mL min(-1). 2-Hydroxypropyl-β-cyclodext…

Detection limitChromatographyFormic acidmedia_common.quotation_subjectAnalytical chemistrymedicine.disease_causeBiochemistryCosmeticsEnvironmentally friendlyAnalytical Chemistrychemistry.chemical_compoundchemistryPhase (matter)Phase compositionmedicineEnvironmental Chemistrymedia_common.cataloged_instanceEuropean unionSpectroscopyUltravioletmedia_commonAnalytica 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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Identification of Leguminosae gums and evaluation of carob-guar mixtures by capillary zone electrophoresis of protein extracts.

2002

A procedure for the extraction and capillary zone electrophoresis (CZE) separation of proteins from carob, guar and tara gums in a background electrolyte (BGE) of pH 9 containing 0.1% polyvinyl alcohol is described. The CZE protein profiles exhibit characteristic peaks for each one of the Leguminosae gums, which can be used to construct models capable of identifying samples of carob, guar and tara gums, and predicting the guar content in binary carob-guar mixtures of different geographical origin and harvested in different years. The classification and prediction models are constructed by using linear discriminant analysis (LDA) and multiple linear regression (MLR), respectively. An excelle…

Detection limitChromatographyGuar gumResolution (mass spectrometry)ChemistryPlant ExtractsClinical BiochemistryExtraction (chemistry)GuarElectrophoresis CapillaryFabaceaeBiochemistryGalactansAnalytical ChemistryMannansCapillary electrophoresisModels ChemicalPolysaccharidesLinear regressionCalibrationPlant GumsElectrophoresis
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Fast extraction methodologies for the determination of toxic arsenic in meat

2017

Summary A nonchromatographic analytical procedure has been developed for the determination of arsenic in meat samples including the major toxic arsenic species arsenite, arsenate, monomethylarsonic acid (MMA) and dimetylarsinic acid (DMA). The method is based on the extraction of arsenic species in mild conditions, selective trivalent hydride formation and final determination by hydride generation atomic fluorescence spectroscopy (HG-AFS). Different extractant agents and two different procedures, microwave-assisted extraction (MAE) and ultrasound assisted extraction at room temperature, were evaluated for As species extraction. The method provided a limit of detection of 0.013 ng mL−1 and a…

Detection limitChromatographyHydride010401 analytical chemistryExtraction (chemistry)Relative standard deviationArsenatechemistry.chemical_elementMonomethylarsonic acid010501 environmental sciences01 natural sciencesIndustrial and Manufacturing Engineering0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental chemistryArsenic0105 earth and related environmental sciencesFood ScienceArseniteInternational Journal of Food Science & Technology
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Hydride generation atomic fluorescence spectrometric determination of ultratraces of selenium and tellurium in cow milk

2003

Abstract A sensitive procedure has been developed for selenium and tellurium determination in milk by hydride generation atomic fluorescence spectrometry (HG-AFS) after microwave-assisted sample digestion. The method provides sensitivity values of 1591 and 997 fluorescence units ng−1 ml−1 with detection limits of 0.005 and 0.015 ng ml−1 for Se and Te, respectively. The application of the developed methodology to the analysis of cow milk samples of the Spanish market evidenced the presence of concentration ranges from 11.1 to 26.0 ng ml−1 for Se, and from 1.04 to 9.7 ng ml−1 for Te having found a good comparability with data obtained after dry-ashing of samples.

Detection limitChromatographyHydrideMicrowave ovenchemistry.chemical_elementBiochemistryAtomic fluorescence spectrometryFluorescenceAnalytical ChemistryCow milkchemistryEnvironmental ChemistryTelluriumSpectroscopySeleniumAnalytica Chimica Acta
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A chemiluminescence flow-based procedure for determination of carbaryl in natural waters exploiting multicommutation and enzymatic reaction

2007

A chemiluminescence procedure for the determination of carbaryl in natural waters using acetylcholinesterase and choline oxidase is described. The flow system designed to implement multicommutation approach controlled by microcomputer comprised five solenoid valves, two columns with immobilized enzymes on controlled pore glass beads and chemiluminometric flow cell. In the best experimental conditions a linear response ranging from 25 to 700 µg L-1 carbaryl was obtained. Water samples were spiked with carbaryl in order to access the accuracy and recoveries between 95 and 101% were obtained for a concentration level ranging from 25 to 100 µg L-1 carbaryl. Detection limit and variation coeffic…

Detection limitChromatographyImmobilized enzymeChemistryPotassiumchemistry.chemical_elementGeneral ChemistryCholine oxidasechemiluminescenceLuminollaw.inventionpesticide carbarylchemistry.chemical_compoundmulticommutationlawReagentCarbarylflow analysisChemiluminescenceenzymatic reaction
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A headspace solid-phase microextraction method of use in monitoring hexanal and pentane during storage: Application to liquid infant foods and powder…

2006

The determination of two secondary lipid oxidation compounds (hexanal and pentane) in liquid infant foods using a headspace solid-phase microextraction gas chromatographic (HS-SPME-GC) method has been developed and validated. The HS-SPME analytical conditions (fibre position, equilibration and sampling times) were selected. The analytical parameters of the method (linearity: hexanal from 2.48 to 84.78 ng/g, pentane from 6.21 to 79.55 ng/g; precision: hexanal 2.87%, pentane 2.343.46%; recovery: hexanal 106.60%, pentane 95.39%; detection limit: hexanal 3.63 ng and pentane 4.2 ng) demonstrate the usefulness of the method. Once optimized, the method was applied to liquid infant foods based on m…

Detection limitChromatographyInfants AlimentacióFood storageGeneral MedicineSolid-phase microextractionHexanalAnalytical ChemistryPentanechemistry.chemical_compoundchemistryLipid oxidationSolid phase extractionFood Science
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Direct vapor generation Fourier transform infrared spectrometric determination of ethanol in blood

1996

Abstract A new procedure is proposed for a direct determination of ethanol in plasma and whole blood. The method is based on the injection of a discrete sample volume of 10 μl into an electrically heated Pyrex glass reactor in which, at a temperature of 90 °C, the ethanol is volatilized and introduced by means of a N 2 carrier flow inside a long-path infrared gas cell and the corresponding flow analysis recording registered as a function of time. The measurement of the area of the flow injection recording, obtained from the absorbance of the transient signal in the range 1150−950 cm −1 , allows the direct quantification of ethanol upto 2 g l −1 , with a limit of detection of 0.020 g l −1 an…

Detection limitChromatographyInfraredChemistryCoefficient of variationDrop (liquid)Analytical chemistryInfrared spectroscopyPlasmaBiochemistryAnalytical ChemistryAbsorbancesymbols.namesakeFourier transformsymbolsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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Mid- and near-infrared determination of metribuzin in agrochemicals

2008

Abstract Two infrared-based methodologies were developed for metribuzin determination in pesticide formulations after extraction with acetonitrile. Fourier transform mid infrared (MIR) procedure was based on peak area measurements between 1692 and 1670 cm −1 corrected with a baseline fixed at 1877 cm −1 . Fourier transform near infrared (NIR) determination was made by measuring the peak area between 6498 and 6332 cm −1 corrected using a two points baseline defined between 6570 and 6212 cm −1 . Repeatability, as relative standard deviation, of 5 independent measurements at mg g −1 concentration level was 0.3% and 0.03% for MIR and NIR, respectively, and limit of detection values of 9 and 17 …

Detection limitChromatographyInfraredChemistryNear-infrared spectroscopyExtraction (chemistry)Analytical chemistryRepeatabilitychemistry.chemical_compoundsymbols.namesakeFourier transformMetribuzinsymbolsAcetonitrileSpectroscopyVibrational Spectroscopy
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Novel approach for the determination of azithromycin in pharmaceutical formulations by Fourier transform infrared spectroscopy in film-through transm…

2013

Abstract This work reports the development of a new method for the determination of azithromycin in pharmaceutical formulations employing Fourier transform infrared (FTIR) technique. The measurements were performed using a novel approach based on a film-through transmission mode. Several variables that could influence the analytical performance of the method were evaluated (solvent, nominal resolution, number of scans, mode of measurement and spectral region selected for measurement). Acetonitrile was the best solvent for the determination of azithromycin, employing the absorption band of the C O group at 1729 cm− 1. The extraction of azithromycin from the formulations was made by mechanica…

Detection limitChromatographyInfraredChemistryResolution (electron density)Analytical chemistryAnalytical ChemistrySolventsymbols.namesakechemistry.chemical_compoundFourier transformAbsorption bandsymbolsFourier transform infrared spectroscopyAcetonitrileSpectroscopyMicrochemical Journal
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