Search results for "Spectroscopy"

showing 10 items of 10293 documents

High-pressure flow-injection assembly. Indirect determination of glycine by atomic absorption spectrometry.

1991

A procedure for the determination of glycine is described. The method is based on the reaction of the analyte with finely powdered, solid copper(II) carbonate in a continuous-flow assembly. The optimum experimental conditions of pH, temperature, sample volume, flow-rate, column length and internal diameter, and the linear range of calibration, were studied. Interference from foreign substances that accompany this amino acid in pharmaceutical formulations was studied, and the method was applied to the determination of glycine.

AnalyteAnalytical chemistryGlycinechemistry.chemical_elementBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawElectrochemistryCalibrationEnvironmental ChemistrySpectroscopychemistry.chemical_classificationChromatographyChemistrySpectrophotometry AtomicTemperatureHydrogen-Ion ConcentrationCopperAmino acidLinear rangeGlycineCarbonic AcidCarbonateIndicators and ReagentsAtomic absorption spectroscopyThe Analyst
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Mepanipyrim haptens and antibodies with nanomolar affinity

2013

Mepanipyrim is an anilinopyrimidine fungicide used worldwide for crop protection. With the aim of developing useful immunoreagents for mepanipyrim immunoanalysis, two new functionalized derivatives were prepared and antibodies were generated. Affinity and specificity were assessed by direct and indirect competitive ELISA using homologous and heterologous conjugates. Although all antibodies were selective for the target analyte, the immunizing hapten structure was revealed as a determinant for high-affinity antibody production (IC50 = 3 nM). © 2013 The Royal Society of Chemistry.

AnalyteAntibody AffinityHeterologousBiochemistryAntibodiesAnalytical ChemistryElectrochemistryAnimalsEnvironmental ChemistryMepanipyrimIC50SpectroscopyA determinantImmunoassayChromatographybiologyChemistryAntibody productionPyrimidinesBiochemistrybiology.proteinFemaleRabbitsAntibodyHaptensHaptenConjugateThe Analyst
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Tuning the selectivity of molecularly imprinted polymer extraction of arylcyclohexylamines: From class-selective to specific

2020

Abstract A molecularly imprinted polymer (MIP) has been prepared in presence of 3-hydroxy phencyclidine (3-OH PCP) as template by bulk polymerization using N,N-dimethylformamide, as porogenic solvent, for the selective solid-phase extraction (SPE) of arylcyclohexylamines from oral fluids. Experimental variables of the extraction procedure have been studied in order to increase both, extraction recovery of 3-OH PCP, used as model analyte, and imprinting factor. By modifying the composition of the washing solvent, the selectivity of the MIP extraction procedure can be tuned, moving from an arylcyclohexylamine selective method to a 3-OH PCP specific method. The applicability of the synthesized…

AnalyteArylcyclohexylamineBulk polymerizationSurface PropertiesIon-mobility spectrometry02 engineering and technology01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecularly Imprinted PolymersIon Mobility SpectrometrymedicineEnvironmental ChemistryParticle SizeSpectroscopyDetection limitCyclohexylaminesChromatographyMolecular StructureChemistry010401 analytical chemistryMolecularly imprinted polymer021001 nanoscience & nanotechnology0104 chemical sciencesSolvent0210 nano-technologySelectivitymedicine.drugAnalytica Chimica Acta
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Synergistic combination of polyamide-coated paper-based sorptive phase for the extraction of antibiotics in saliva.

2021

Abstract The development of analytical methods that allow the simultaneous determination of a wide range of analytes with different properties is one of the focuses of attention in Analytical Chemistry. This work describes a proof-of-concept of the synergistic extraction of a planar paper-based sorptive phase modified with a polyamide such as nylon. This as-prepared sorptive phase enables the extraction of six penicillin-derived antibiotics of different polarity from human saliva samples in the same analysis, since the analytes either interact with the paper or with the nylon. The synthesis of the sorptive phase is simple as it only requires dipping the paper into an organic solution of the…

AnalyteBioanalysisFormic acid02 engineering and technology01 natural sciencesBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionDesorptionPhase (matter)Environmental ChemistryHumansSalivaSpectroscopyDetection limitCoated paperChromatographyChemistry010401 analytical chemistryExtraction (chemistry)021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsNylons0210 nano-technologyChromatography LiquidAnalytica chimica acta
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Amphetamine-type stimulants analysis in oral fluid based on molecularly imprinting extraction

2018

Abstract A methamphetamine-based molecularly imprinted polymer (MIP) has been prepared by bulk polymerization to recognize new psychoactive substances (NPS) of the amphetamine, cathinones and 2C families in oral fluid samples, being the first precedent of a synthetized MIP for the extraction and preconcentration 32 NPS including amphetamine type substances and synthetic cathinones from oral fluids. Pre-polymerization complex and resulting materials were appropriately characterized by infrared spectroscopy, scanning electron microscopy, and nitrogen adsorption-desorption isotherms. Appropriateness of the material for the specific recognition of the target analytes was also evaluated through …

AnalyteCathinoneIon-mobility spectrometryInfrared spectroscopy02 engineering and technologyChemical FractionationMass spectrometry01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecular ImprintingmedicineHumansEnvironmental ChemistrySolid phase extractionSpectroscopyDetection limitChromatographyChemistrySolid Phase Extraction010401 analytical chemistryMolecularly imprinted polymerGreen Chemistry Technology021001 nanoscience & nanotechnologyBody Fluids0104 chemical sciencesAmphetamineCentral Nervous System StimulantsAdsorption0210 nano-technologymedicine.drugAnalytica Chimica Acta
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Isotope dilution mass spectrometry as a calibration method for the analysis of trace elements in powder samples by LA-ICP-MS

2003

The applicability of the isotope dilution (ID) technique for trace element determinations in powdered solid samples by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is demonstrated. LA-ICP-IDMS combines the advantage of the isotope dilution technique as a definitive method with the powerful capability of LA-ICP-MS for a fast and direct multi-element analysis of solid samples. LA-ICP-IDMS therefore allows matrix-matched quantification of element concentrations without any external standard, which is not possible by other calibration strategies used in LA-ICP-MS, up to now. The sample preparation effort is kept minimal and consists of an addition of the corresponding…

AnalyteCertified reference materialsChromatographyIsotopeChemistrySample (material)Trace elementCalibrationAnalytical chemistrySample preparationIsotope dilutionSpectroscopyAnalytical ChemistryJ. Anal. At. Spectrom.
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Spectrophotometric determination of promazine with an oxidative column in FIA manifolds

1992

Abstract A simple flow-injection spectrophotometric method for the determination of promazine is described. The two proposed procedures are based on the oxidation of analyte with a manganese dioxide column. Concentrations of promazine in the ranges 2–20 and 1–6 are determined with a relative standard deviation of 1.0%. The injection rates are 62 and 80 samples h −1 , respectively. The influence of foreign species and the determination of promazine in a pharmaceutical formulation are also reported.

AnalyteChemistry PharmaceuticalClinical BiochemistryRelative standard deviationPharmaceutical Sciencechemistry.chemical_elementManganesePharmaceutical formulationRedoxDosage formAnalytical ChemistryDrug DiscoverymedicinePromazineSpectroscopyPromazineFlow injection analysisManganeseChromatographyChemistryOxidesHydrogen-Ion ConcentrationManganese CompoundsCalibrationFlow Injection AnalysisSpectrophotometry UltravioletOxidation-Reductionmedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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Quantification of minerals from ATR-FTIR spectra with spectral interferences using the MRC method.

2017

A method for quantifying the individual components of mineral samples based on attenuated total reflectance - Fourier transform infrared spectroscopy (ATR-FTIR) is described, extending the constant ratio (CR) method to analytes absorbing in a common range of wavenumbers. Absorbance values in the spectral region where the analytes absorb relative to the absorbance of an internal standard absorbing at a wavenumber where the analytes do not absorb, permits the quantification of N analytes using measurements at N fixed wavenumbers. The method was tested for mixtures of albite, orthoclase, kaolin and quartz.

AnalyteChemistryAnalytical chemistry02 engineering and technology010501 environmental sciencesengineering.material021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and OpticsAnalytical ChemistryFtir spectraAbsorbanceOrthoclaseAlbiteAttenuated total reflectionengineeringFourier transform infrared spectroscopy0210 nano-technologyInstrumentationQuartzSpectroscopy0105 earth and related environmental sciencesSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Nutritional parameters of commercially available milk samples by FTIR and chemometric techniques

2004

Abstract A chemometric study on the prediction of the main nutritional aspects of milk has been carried out by using fourier transform infrared spectroscopy (FTIR) attenuated total reflectance (ATR) measurements of commercially available milk samples of different types. Whole, semi and skimmed milks, enriched or not with calcium, vitamins or modified by alteration of lipid or sugar composition were considered. After evaluating different strategies for data acquisition and ATR cleaning between samples, hierarchical cluster analysis (HCA) was carried out for classification of samples in order to choose the calibration set. The prediction capabilities of partial least squares (PLS) data treatm…

AnalyteChemistryAnalytical chemistryInfrared spectroscopyBiochemistryStandard deviationFourier transform spectroscopyAnalytical ChemistryChemometricsAttenuated total reflectionPartial least squares regressionEnvironmental ChemistryFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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Evaluation and elimination of the “blank bias error” using the H-point standard addition method

1992

Abstract The basis of the H-point standard addition method in the cases where the analyte determination requires the use of an absorbent reagent is considered. The method evaluates and eliminates the blank bias error present in such procedures by using the absorbance increment at two selected wavelengths as the analytical signal of the calibration graphs. Three different determinations were tested: the determination of proteins with the biuret method, thorium with thoron and of magnesium with Titan Yellow. These procedures are better described by the proposed method than by the traditional approach using absorbance values against reagent blank.

AnalyteChemistryAnalytical chemistryTitan yellowBiochemistryBlankBiuret testAnalytical ChemistryAbsorbancechemistry.chemical_compoundReagentStandard additionCalibrationEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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