Search results for "Detection limit"

showing 10 items of 810 documents

Fluorometric determination of chemically available lysine: adaptation, validation and application to different milk products.

2004

A spectrophotometric method based on the reaction between available lysine and ortho-phthaldialdehyde (OPA) was adapted and validated for fluorometric determination of the chemically available lysine contents in milk matrices (UHT and conventional in-bottle sterilized cow milk, milk-based infant formulas and infant formula ingredients). The values of the analytical parameters show its usefulness as a routine method (linearity, r = 0.9992; detection limit, 0.0066 mg/mL assay; accuracy, 99-108%; precision, intra-day 2.1-5.9% and inter-day 3.5 10.2%). No statistically significant differences (p < 0.05) were found between the values obtained with the adapted method and those obtained applying t…

Food HandlingLysineFluorescence spectrometryPasteurizationBiological AvailabilitySensitivity and Specificitylaw.inventionCow milkMilk productslawAnimalsHumansFluorometryFood scienceDetection limitChromatographyChemistryLysineSterilized milkInfant Newbornfood and beveragesInfantReproducibility of ResultsMilkInfant formulaCalibrationInfant FoodFood ScienceDie Nahrung
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The consequences of physical post-treatments (microwave and electron-beam) on food/packaging interactions: A physicochemical and toxicological approa…

2016

IF 4.052; The safety of microwave and electron-beam treatments has been demonstrated, in regards to the formation of reaction products that could endanger human health. An integrated approach was used combining the potential toxicity of all the substances likely to migrate to their chemical characterizations. This approach was applied to polypropylene (PP) films prepared with a selection of additives. Components were identified by liquid and gas chromatography using a mass selective detector system. Their potential toxicity was assessed using three in vitro short-term bioassays and their migrations were carried out using a standards-based approach. After the electron-beam treatment some add…

Food packaging;Food safety;By-product componentsElectrons02 engineering and technology[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainPolypropylenes01 natural sciencesBioassaysAnalytical ChemistryFood safetychemistry.chemical_compoundFood packagingBioassayHumansMicrowavesMigrationDetection limitPolypropyleneChromatographyChemistry010401 analytical chemistryGeneral MedicineElectron-beamIntegrated approach021001 nanoscience & nanotechnology0104 chemical sciencesPolyolefinFood packagingBy-product componentsGas chromatography0210 nano-technologyMicrowaveMicrowaveFood Science
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Scaling the Analytical Information Given by Several Types of Colorimetric and Spectroscopic Instruments Including Smartphones: Rules for Their Use an…

2021

The analytical information given by different types of instruments was scaled in order to establish suitably the figures of merit of a given methodology based on color measurements. Different lab and portable instruments, including smartphones with and without a miniaturized spectrophotometer accessory, have been tested. In order to obtain broad information and using objective criteria, these instruments have been compared from (1) the analytical point of view, considering mainly the detection limit (limits of detection [LODs]), selectivity, accuracy and intra- and interday precision, size, components, and costs; and (2) the environmental point of view, based on their footprint as kilograms…

FootprintDetection limitComputer engineeringChemistryInstrumentation010401 analytical chemistryFigure of meritRGB color model010402 general chemistry01 natural sciencesScaling0104 chemical sciencesAnalytical ChemistryAnalytical chemistry
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Comparison of extraction and clean-up procedures for analysis of zearalenone in corn, rice and wheat grains by high-performance liquid chromatography…

2002

The aim of this work was the optimization of some procedures usually used in the analysis of zearalenone (ZEA) in corn and other cereals by high-performance liquid chromatography (HPLC) with photodiode array and/or fluorescence detection. The comparison of five extraction solvents is presented. Three solid-phase extraction cartridges (C-18, silica, Florisil) and immuno-affinity columns were also compared to obtain the best recovery of the mycotoxin with the minimal presence of co-extractives in the chromatograms. Mixtures of methanol-1% aqueous NaCl (80.20 or 60:40 v/v) were the best extraction solvents. Florisil provided higher recovery of ZEA than C-18, and silica proved unsuitable. The i…

FusariumHealth Toxicology and MutagenesisFood ContaminationToxicologyHigh-performance liquid chromatographyZea mayschemistry.chemical_compoundHumansEstrogens Non-SteroidalMycotoxinZearalenoneChromatography High Pressure LiquidTriticumDetection limitChromatographybiologyChemistryExtraction (chemistry)Public Health Environmental and Occupational HealthOryzaGeneral Chemistrybiology.organism_classificationSeparation processChemistry (miscellaneous)ZearalenoneEdible GrainQuantitative analysis (chemistry)Food AnalysisFood ScienceFood additives and contaminants
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Fumonisin production in rice cultures of Fusarium verticillioides under different incubation conditions using an optimized analytical method.

2004

Fumonisin B1 (FB1) and fumonisin B2 (FB2) are the main members of a family of mycotoxins produced by various fungal species belonging to the Gibberella fujikuroi complex. The present work shows the results of a comparative study of various clean-up and derivatization procedures for analysis of fumonisins in rice cultures. Fumonisins were extracted from rice with acetonitrile/water (50/50, v/v). For clean-up, three solid-phase extraction procedures were assayed (C18 cartridge, SAX cartridge, and a combination of both). Two reagents (o-phthaldialdehyde and 4-fluoro-7-nitro-benzofurazan) were studied comparatively for formation of fluorescent derivatives. The separation was carried out by LC u…

FusariumWater activityFood ContaminationBiologyMicrobiologyFumonisinsSensitivity and SpecificityFluorescencechemistry.chemical_compoundFusariumFumonisinBotanyFood scienceDerivatizationMycotoxinDetection limitFumonisin B2Fumonisin B1TemperatureWaterOryzabiology.organism_classificationchemistryConsumer Product SafetyFood ScienceChromatography LiquidFood microbiology
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Photochemical sample treatment: a greener approach to chlorobenzene determination in sediments.

2014

Abstract Due to worker׳s exposure, solvent and stationary phases׳ consumption, sample purification is one of the most polluting steps in analytical procedures for determination of organic pollutants in real samples. The use of photochemical sample treatment represents a valid alternative methodology for extracts clean up allowing for a reduction of the used amount of organic solvents. In this paper we report the first application on the photolytic destruction of organic substances to eliminate some of the interferences in the analysis of Chlorobenzenes in sediment samples. The method׳s efficiency and robustness were compared with classic silica column purification process currently used in …

Geologic SedimentsPhotochemistryPhotochemistryChlorobenzenesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliGas Chromatography-Mass SpectrometryAnalytical ChemistrySpecimen Handlingchemistry.chemical_compoundLimit of DetectionSediment analysiClean upSoil PollutantsSettore CHIM/01 - Chimica Analiticasample treatmentPollutantDetection limitReproducibilityChromatographyChromatographySediment AnalysisPhotochemicalUV irradiationTemperatureReproducibility of ResultsWaterGreen Chemistry TechnologySettore CHIM/06 - Chimica OrganicaReplicateClean-upchemistryChlorobenzeneEnvironmental chemistrySolventsSediment analysisAnalytical proceduresChlorobenzeneTalanta
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Expanding the application of stir bar sorptive-dispersive microextraction approach to solid matrices: Determination of ultraviolet filters in coastal…

2018

This work describes a new method for the determination of organic compounds in solid samples based on the equilibrium desorption of the analytes in an aqueous phase followed by stir bar sorptive-dispersive microextraction (SBSDME). Sand samples, contaminated with UV filters due to bathing and recreational activities, were dispersed in an aqueous medium by using a coated stir bar with CoFe2O4@oleic acid magnetic nanoparticles. The UV filters were physically desorbed from the surface of the sand particles and rapidly adsorbed on the hydrophobic coating of the nanoparticles, which were retrieved by means of their magnetism after stopping the stirring. In this manner, both preconcentration of t…

Geologic SedimentsSorbent010501 environmental sciences01 natural sciencesBiochemistryBathing BeachesGas Chromatography-Mass SpectrometryAnalytical ChemistryAdsorptionDesorptionSample preparationOrganic ChemicalsSolid Phase Microextraction0105 earth and related environmental sciencesDetection limitChromatographyChemistryOsmolar Concentration010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Aqueous two-phase systemWaterGeneral Medicine0104 chemical sciencesStandard additionAdsorptionHydrophobic and Hydrophilic InteractionsSunscreening AgentsWater Pollutants ChemicalEnvironmental MonitoringJournal of Chromatography A
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Determination of 3-MCPD by GC-MS/MS with PTV-LV injector used for a survey of Spanish foodstuffs

2007

3-Monochloropropane-1,2-diol (3-MCPD) is the most common chemical contaminant of the group of chloropropanols. It can occur in foods and food ingredients at low levels as a result of processing, migration from packaging materials during storage and domestic cooking. A sensitive method for determination of 3-MCPD in foodstuffs using programmable temperature vaporization (PTV) with large-volume injection (LVI) gas chromatography (GC) with tandem mass spectrometry detection (MS/MS) has been developed and optimized. The optimization of the injection and detection parameters was carried out using statistical experimental design. A Plackett-Burman design was used to estimate the influence of reso…

GlycerolQuality ControlTolerable daily intakeDetection limitChromatographyChemistryTemperatureAnalytical chemistryAlpha-Chlorohydrinalpha-ChlorohydrinFood ContaminationMass spectrometryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundSpain3-MCPDmedia_common.cataloged_instanceMaximum Allowable ConcentrationGas chromatographyVolatilizationEuropean unionGas chromatography–mass spectrometrymedia_commonTalanta
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In syringe hybrid monoliths modified with gold nanoparticles for selective extraction of glutathione in biological fluids prior to its determination …

2020

Abstract In this work, a simple device for extraction glutathione (GSH) in biological fluids using a hybrid monolithic material within a polypropylene syringe is developed. For this purpose, glycidyl methacrylate-based monolith was firstly prepared within this housing material, and the polymer was modified with different ligands (ammonia, cysteamine and cystamine). The resulting materials (containing amine or thiol groups, respectively) were then functionalized with gold nanoparticles (AuNPs). The hybrid material that gave the largest AuNPs coverage was selected as solid-phase (SPE) sorbent and several variables affecting the extraction recovery of this compound were investigated. Under opt…

Glycidyl methacrylateMetal Nanoparticles02 engineering and technology01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionHumansSolid phase extractionMonolithDerivatizationSalivaChromatography High Pressure LiquidDetection limitgeographygeography.geographical_feature_categoryChromatographySyringes010401 analytical chemistryExtraction (chemistry)Solid Phase ExtractionReproducibility of Results021001 nanoscience & nanotechnologyGlutathione0104 chemical scienceschemistryColloidal goldEpoxy CompoundsMethacrylatesGold0210 nano-technologyHybrid materialTalanta
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Extraction of β-blockers from urine with a polymeric monolith modified with 1-allyl-3-methylimidazolium chloride in spin column format

2020

Abstract A glycidyl methacrylate-based monolith was modified with imidazolium-based ionic liquid (IL) to be used as stationary phase for solid-phase extraction (SPE). The host monolithic support was prepared by in-situ UV polymerization in spin column format. Two approaches were developed to incorporate the IL into the polymeric monolithic matrix: generation of IL onto the surface monolith, and copolymerization by addition of the IL to the polymerization mixture, which gave the best results. The resulting sorbent materials were morphologically characterized and used for the isolation of five β-blockers from human urine samples. All SPE steps were accomplished by centrifugation, which reduce…

Glycidyl methacrylatePolymersSurface PropertiesAdrenergic beta-Antagonists02 engineering and technology01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundSpin column-based nucleic acid purificationHumansSolid phase extractionParticle SizeMonolithDetection limitgeographygeography.geographical_feature_categoryChromatographyChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)Imidazoles021001 nanoscience & nanotechnology0104 chemical sciencesAllyl CompoundsEpoxy CompoundsMethacrylates0210 nano-technologyTalanta
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