Search results for "RESOLUTION"

showing 10 items of 1928 documents

Sensitive determination of parabens in human urine and serum using methacrylate monoliths and reversed-phase capillary liquid chromatography-mass spe…

2014

A method for the determination of parabens in human urine and serum by capillary liquid chromatography (cLC) with UV-Vis and mass spectrometry (MS) detection using methacrylate ester-based monolithic columns has been developed. The influence of composition of polymerization mixture was studied. The optimum monolith was obtained with butyl methacrylate monomer at 60/40% (wt/wt) butyl methacrylate/ethylene dimethacrylate ratio and 50wt% porogens (composed of 36wt% of 1,4-butanediol, 54wt% 1-propanol and 10wt% water). Baseline resolution of analytes was achieved through a mobile phase of acetonitrile/water in gradient elution mode. Additionally, dispersive liquid-liquid microextraction (DLLME)…

Detection limitAnalytegeographyChromatography Reverse-PhaseChromatographygeography.geographical_feature_categoryResolution (mass spectrometry)ChemistryOrganic ChemistryParabensGeneral MedicineUrineUrinalysisMethacrylateMass spectrometryBiochemistryMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometryLimit of DetectionHumansMethacrylatesMonolithBlood Chemical AnalysisJournal of chromatography. A
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Fourier transform infrared determination of Fluometuron in pesticide formulations

2003

Abstract A single method has been developed for Fourier transform infrared (FTIR) determination of Fluometuron in pesticide formulations. Samples were ultrasonically shaken with CHCl3 for 5 min and the FTIR spectra of sample extracts and standards were obtained at a nominal resolution of 4 cm−1 from 4000 to 900 cm−1 accumulating 25 scans. Fluometuron determination is based on the measure of peak area from 1342 to 1321 cm−1 corrected using a baseline defined from 1352 to 1294 cm−1. This procedure provided a limit of detection of 6.5 μg g−1, a sensitivity of 0.852 a.u. g mg−1 for a pathlength of 0.11 mm, a relative standard deviation of 1.6% for three analysis of a sample containing 50.4% (w/…

Detection limitChromatographyChloroformFluometuronResolution (mass spectrometry)Analytical chemistryHigh-performance liquid chromatographychemistry.chemical_compoundsymbols.namesakeFourier transformchemistryLinear regressionsymbolsFourier transform infrared spectroscopySpectroscopyVibrational Spectroscopy
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In situ derivatization for double confirmation of 2C–C in oral fluids by ion mobility spectrometry

2017

Ion mobility spectrometry (IMS) is a powerful tool to carry out quick and sensitive detection of illicit activities and has been employed for the determination of the psychedelic drug 2,5-dimethoxy-4 chlorophenethylamine (2C–C) in oral fluid samples. Saliva samples were extracted with chloroform and analysed by IMS reaching a limit of detection (LOD) of 14 μg L−1. Nevertheless, IMS has a scarce resolution and selectivity of the method can be often compromised by the presence of potential interferents with similar molecular weights and drift times. Thus, a rapid and in situ derivatization with acetone, to form the corresponding imine, has been proposed in the present study to confirm the pre…

Detection limitChromatographyChloroformResolution (mass spectrometry)Ion-mobility spectrometryGeneral Chemical Engineering010401 analytical chemistryGeneral EngineeringAmfepramoneNaphazolineDerivative010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineDerivatizationmedicine.drugAnalytical Methods
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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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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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Fourier transform infrared determination of imidacloprid in pesticide formulations

2004

A simple method has been developed for Fourier Transform Infrared (FTIR) determination of Imidacloprid in pesticide formulations. Samples were diluted with CHCl3 and the FTIR spectra of samples and standards were obtained at a nominal resolution of 4 cm-1 from 4000 to 900 cm-1 accumulating 25 scans. Imidacloprid determination was based on the measure of either peak area from 1577 to 1567 cm-1 or peak height at 1572 cm-1, both corrected using a horizontal baseline defined at 1900 cm-1. The limits of detection achieved, of the order of 9 µg g-1, were appropriate for the determination of Imidacloprid in commercially available formulations. FTIR results were statistically comparable to those fo…

Detection limitChromatographyMaterials scienceHPLC-UVResolution (mass spectrometry)InfraredImidaclopridGeneral ChemistryHigh-performance liquid chromatographylcsh:Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformchemistrylcsh:QD1-999FTIRImidaclopridsymbolsSample preparationFourier transform infrared spectroscopypesticide formulations
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Development of a simple and low cost device for vapour phase Fourier Transform Infrared spectrometry determination of ethanol in mouthwashes

2006

Abstract A new vapour phase manifold coupled with Fourier Transform Infrared (FTIR) spectroscopy was developed for ethanol determination in mouthwashes. Two microliters of samples were injected, without any previous pre-treatment into a reactor heated at 70 °C, and the vapour phase generated transported to the FTIR spectrometer using a carrier nitrogen flow of 6 ml min−1. FTIR spectra were continuously recorded, as a function of time, by accumulating two scans and employing 8 cm−1 nominal resolution. Analytical measurements for ethanol were made in the range from 1130 to 992 cm−1 with a baseline defined between 1158 and 957 cm−1. After ethanol measurement the carrier flow was increased to 3…

Detection limitChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformPhase (matter)symbolsEnvironmental ChemistryGas chromatographyFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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FT–Raman spectrometry determination of Malathion in pesticide formulations

2003

Abstract A fast and environmentally friendly method has been developed for Fourier transform–Raman (FT–Raman) spectrometry determination of Malathion in pesticide emulsifiable concentrate formulations. The method is based on the measurement of intensity peak height values at 1737 cm −1 Raman shift corrected using a baseline defined at 1900 cm −1 . Samples were diluted with CHCl 3 and the FT–Raman spectra collected in back-scattering mode over 3.3 min at a nominal resolution of 4 cm −1 accumulating 50 scans per spectra and using a laser power of 1250 mW. The developed procedure provided a limit of detection of 1.8% w/w in the original sample. Results found by FT–Raman spectrometry were stati…

Detection limitChromatographyResolution (mass spectrometry)ChemistryAnalytical chemistryInfrared spectroscopyMass spectrometryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformsymbolsGas chromatographyRaman spectroscopyTalanta
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An Infrared Method, with Reduced Solvent Consumption, for the Determination of Chlorsulfuron in Pesticide Formulations

2003

A simple method has been developed for the determination of Chlorsulfuron in pesticide formulations by Fourier Transform Infrared (FTIR). Samples were diluted with CHCl3− , and the FTIR spectra of the samples and standards were obtained at a nominal resolution of 4 cm− 1 from 4000 to 900 cm− 1 with the accumulation of 25 scans. Chlorsulfuron determination was based on the measurement of peak area values from 1373 to 1363 cm− 1 which were corrected by use of a two points baseline defined from 1401 to 1302 cm− 1. The limit of detection achieved, which was of the order of 6 µg g− 1, was appropriate for the determination of Chlorsulfuron in commercially available formulations. FTIR results were…

Detection limitChromatographyResolution (mass spectrometry)ChemistryInfraredAnalytical chemistryPesticideHigh-performance liquid chromatographyAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventsymbols.namesakeFourier transformsymbolsFourier transform infrared spectroscopySpectroscopySpectroscopy Letters
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Supercritical fluid chromatography in drug analysis: A literature survey

1996

The applications of supercritical fluid chromatography to the analysis of drugs have been carefully revised from the literature compiled in the Analytical Abstracts until March 1994. Easy-to-read tables provide useful information about the state-of-the-art and possibilities offered by SFC in pharmaceutical analysis. The tables comprise extensive data about samples analyzed, pharmaceutical principles determined, solvents used and sample quantity injected, supercritical fluids and modifiers employed, injection system, instrumentation, experimental conditions for chromatographic separations (density, pressure, flow, temperature), characteristics of columns employed (type, support, length, diam…

Detection limitChromatographyResolution (mass spectrometry)ChemistryInstrumentationSupercritical fluid chromatographyAnalytical chemistryParticleLiterature surveyBiochemistryQuantitative analysis (chemistry)Supercritical fluidAnalytical Chemistry
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