Search results for "STANDARD"

showing 10 items of 3299 documents

Selective determination of clenbuterol residues in urine by molecular imprinted polymer—Ion mobility spectrometry

2017

Abstract Clenbuterol is banned for sports use and strictly regulated in livestock industry. In this study, a procedure for the determination of clenbuterol residues in water and urine has been developed using selective supports combined with ion mobility spectrometry (IMS) determination. A molecular imprinted polymer (MIP) was used for efficient clean-up and preconcentration of clenbuterol followed to a dispersive liquid-liquid microextraction (DLLME) in order to improve selectivity and sensitivity of IMS determinations. Quantitative recoveries from 81 to 99% were obtained for water and spiked urine samples using MIP-DLLME-IMS method. A precision of 4.5%, established as the relative standar…

Detection limitChromatographyChemistryIon-mobility spectrometry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymer02 engineering and technologyUrine021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryLiquid chromatography–mass spectrometryClenbuterolmedicine0210 nano-technologySpectroscopymedicine.drugMicrochemical Journal
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Solid-Phase Microextraction Liquid Chromatography/Tandem Mass Spectrometry To Determine Postharvest Fungicides in Fruits

2003

A method to determine five postharvest fungicides (dichloran, flutriafol, o-phenylphenol, prochloraz, tolclofos methyl) in fruits (cherries, lemons, oranges, peaches) has been developed using solid-phase microextraction (SPME) coupled to liquid chromatography (LC) with photodiode array (DAD), mass spectrometry (MS), or tandem mass spectrometry (MS/MS) with ion trap detection. Extraction involved sample homogenization with an acetone/water solution (5:1), filtration, and acetone evaporation prior to fiber extraction. The pesticides were isolated with a fused-silica fiber coated with 50-microm Carbowax/template resin. The effects of pH, ion strength, sample volume, and extraction time were in…

Detection limitChromatographyChemistryPesticide ResiduesReference StandardsSolid-phase microextractionMass spectrometryTandem mass spectrometryMass SpectrometryFungicides IndustrialAnalytical ChemistryLiquid chromatography–mass spectrometryFruitDesorptionCalibrationIndicators and ReagentsSpectrophotometry UltravioletSample preparationIon trapChromatography LiquidAnalytical Chemistry
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Solid-phase extraction on C18 in the trace determination of selected polychlorinated biphenyls in milk.

1995

The utility of solid-phase extraction with octadecylsilica for determining fifteen polychlorinated biphenyl (PCB) congeners from milk samples was examined. Recoveries higher than 80% and relative standard deviations better than 10% were obtained for PCBs from different kinds of milk (whole, skimmed, 2%, powdered, breast and evaporated). A comparison with other procedures was made. The described method provides better detection limits than those attainable with the liquid-liquid extractions currently used as standard methods, when capillary gas-liquid chromatography is used for the final determination. A study of the separation was also performed using six different fused-silica capillary co…

Detection limitChromatographyChromatography GasMilk HumanOrganic ChemistryExtraction (chemistry)food and beveragesPolychlorinated biphenylGeneral MedicineStandard methodsBiochemistryPolychlorinated BiphenylsAnalytical Chemistrychemistry.chemical_compoundMilkchemistryAnimalsSolid phase extractionJournal 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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Improved detection limit for ammonium/ammonia achieved by Berthelot's reaction by use of solid-phase extraction coupled to diffuse reflectance spectr…

2005

Abstract The proposed procedure is based on the extraction of the indothylmol blue into C 18 solid-phase extraction (SPE) membranes and direct quantification on the membrane surface by diffuse reflectance spectroscopy. The analytical performance of the proposed method has been evaluated for standard solutions of ammonium using reflectance values, R , as well as the Kubelka–Munk function, F ( R ). The results have been compared with those obtained by the conventional method, which uses UV–vis absorption spectroscopy with a sensor-based method. The described methodology provided satisfactory linearity and reproducibility within the ammonium concentration intervals 25–250 μg L −1 and 25–500 μg…

Detection limitChromatographyDiffuse reflectance infrared fourier transformExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationAmmoniumSolid phase extractionSpectroscopyAnalytica Chimica Acta
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Die direkte quantitative auswertung von dünnschichtchromatogrammen durch remissions- und fluoreszenzmessungen

1971

Abstract Direct quantitative evaluation of thin-layer chromatograms by remission- and fluorescence measurements. Part 6. Determination of adrenaline, noradrenaline and dopamine from urine Adrenaline, noradrenalineand dopamine were separated from urine on aluminium oxide columns; after elution they were converted into ther O 3 ,O 4 ,N-triacetyl derivatives and separated using thin-layer chromatography. The triacetyl derivatives were in situ converted to fluorescing compounds using ethylene diamine and quantitatively estimated using the Chromatogram-Spectrophotometer (Carl Zeiss, Oberkochen). The advantage of this method over the conventional fluorometric determination of catecholamines in so…

Detection limitChromatographyEthylene diamineChemistryElutionOrganic ChemistryRelative standard deviationThin layerGeneral MedicineBiochemistryAnalytical ChemistryJournal of Chromatography A
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Enhanced flow-injection–chemiluminometric determination of sulphonamides by on-line photochemical reaction

2003

Abstract The viability of the tandem photochemical reaction-chemiluminescence detection has been studied for an heterogeneous group of sulphonamides (sulphamethoxazole, sulphadiazine, sulphamerazine, sulphamethoxypyridazine, sulphacetamide, sulphadimidine, sulphanilamide, sulphathiazole and sulphaguanidine) using sulphamethoxazole (whose chemiluminescent behaviour has not been previously reported) as a test substance. The ‘on-line’ photochemical-reaction of sulphonamides provides an enhancing influence on the chemiluminometric response of the drugs during their oxidation by potassium permanganate in sulphuric acid medium (sulphamethoxazole, sulphacetamide, sulphadimidine and sulphanilamide …

Detection limitChromatographyFluorescence spectrometryPhotochemistryBiochemistryOrders of magnitude (mass)Analytical Chemistrylaw.inventionStandard curvePotassium permanganatechemistry.chemical_compoundchemistrylawSulphaguanidineEnvironmental ChemistryPhotodegradationSpectroscopyChemiluminescenceAnalytica Chimica Acta
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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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Bromide/bromate speciation by NTI-IDMS and ICP-MS coupled with ion exchange chromatography

1997

Two different mass spectrometric methods, negative thermal ionization isotope dilution mass spectrometry (NTI-IDMS) and inductively coupled plasma mass spectrometry (ICP-MS), off-line and on-line coupled with anion exchange chromatography, have been developed for simultaneous bromide and bromate determinations in water samples. The detection limits of these methods are in the range of 0.03–0.09 μg/L using a 50 mL sample.The results are independent of the content of other anions, which could be demonstrated by the analyses of six mineral waters containing chloride and sulfate of up to 160 mg/L and 1500 mg/L, respectively. Bromide has been analyzed by the NTI-IDMS method in the range of 10–50…

Detection limitChromatographyIon chromatographyIsotope dilutionBromateBiochemistrychemistry.chemical_compoundchemistryBromideStandard additionmedia_common.cataloged_instanceEuropean unionInductively coupled plasma mass spectrometrymedia_commonFresenius' Journal of Analytical Chemistry
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Uptake and translocation monitoring of imidacloprid to chili and tomato plants by molecularly imprinting extraction - ion mobility spectrometry

2019

Abstract The degradation of imidacloprid in soil and its uptake and translocation to chili and tomato plants was evaluated, as a proof of concept, of the possibilities of the combination of molecularly imprinted polymers (MIPs) and ion mobility spectrometry (IMS) for a fast and sensitive bioprocesses monitoring tool. To do it, a method based on the selective extraction of imidacloprid from soil and plant materials was developed. In the selected conditions, the MIP-IMS procedure provided a recovery of imidacloprid in soil and plant samples from 102 to 114%, for spiked concentration levels from 0.2 to 2.0 μg g−1. Precision of the methodology, expressed as the relative standard deviation (RSD)…

Detection limitChromatographyIon-mobility spectrometryChemistry010401 analytical chemistryRelative standard deviationMolecularly imprinted polymerChromosomal translocation02 engineering and technologyPesticideStandard solution021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundImidacloprid0210 nano-technologySpectroscopyMicrochemical Journal
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