Search results for "Analyte"

showing 10 items of 303 documents

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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Plasma-to-Blood Ratios of Congener Analytes

2005

AnalyteChemical Health and SafetyChromatographyCongenerChemistryHealth Toxicology and MutagenesisEnvironmental ChemistryToxicologyAnalytical ChemistryJournal of Analytical Toxicology
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Direct gravimetric sensing of GBL by a molecular recognition process in organic cage compounds.

2013

Organic cages were identified as highly potent affinity materials for the tracing of γ-butyrolactone. The selectivity over ethanol and water is based on the interior functional groups which allow preferential hydrogen bonding to the target analyte.

AnalyteChemical substanceEthanolChemistryHydrogen bondMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundMolecular recognitionMaterials ChemistryCeramics and CompositesGravimetric analysisOrganic chemistrySelectivityScience technology and societyChemical communications (Cambridge, England)
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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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Semi-physiologic model validation and bioequivalence trials simulation to select the best analyte for acetylsalicylic acid

2015

Abstract The objective of this paper is to apply a previously developed semi-physiologic pharmacokinetic model implemented in NONMEM to simulate bioequivalence trials (BE) of acetyl salicylic acid (ASA) in order to validate the model performance against ASA human experimental data. ASA is a drug with first-pass hepatic and intestinal metabolism following Michaelis–Menten kinetics that leads to the formation of two main metabolites in two generations (first and second generation metabolites). The first aim was to adapt the semi-physiological model for ASA in NOMMEN using ASA pharmacokinetic parameters from literature, showing its sequential metabolism. The second aim was to validate this mod…

AnalyteChemistry PharmaceuticalMetaboliteCmaxPharmaceutical ScienceBioequivalencePharmacologyModels BiologicalBiomarkers PharmacologicalFirst pass effectchemistry.chemical_compoundPharmacokineticsIn vivoHumansMedicineComputer SimulationTissue DistributionBiotransformationChromatographyAspirinDose-Response Relationship Drugbusiness.industryHippuratesAnti-Inflammatory Agents Non-SteroidalNONMEMDrug LiberationTherapeutic EquivalencychemistryPharmacology ClinicalSalicylic AcidbusinessAlgorithmsSoftwareEuropean Journal of Pharmaceutical Sciences
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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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Determination of Bisulfites in Wines with an Electronic Tongue Based on Pulse Voltammetry

2009

Electronic tongues were developed some ten years ago. These systems consist of an array of nonspecific sensors and a signal processing unit. The sensor signals are processed by pattern recognition methods which makes possible the extraction of specific properties from the sample. Depending on the calibration, attributes such as quality or taste can be determined. These systems also detect changes in the sample that they are not calibrated for which makes possible the detection of anomalous occurrences. Such sensor systems are suitable for process control and surveillance. Important factors are the sensitivity and stability, specifically the sensor's ability to respond to small changes and t…

AnalyteChemistryElectronic tongueSample (material)ElectrodeElectrochemistryCalibrationAnalytical chemistryPolishingBiological systemAscorbic acidElectrical conductivity meterAnalytical ChemistryElectroanalysis
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