Search results for "Detection limit"

showing 10 items of 810 documents

Hapten Synthesis and Polyclonal Antibody-Based Immunoassay Development for the Analysis of Forchlorfenuron in Kiwifruit

2010

High-affinity polyclonal antibodies directed against the synthetic cytokinin forchlorfenuron (CPPU) were produced from three immunizing haptens with equivalent spacer arms located at different positions. A competitive immunoassay was developed with a limit of detection in buffer of 12.42 +/- 3.06 ng/L. In addition, the ability of the produced antibodies to recognize a set of synthetic CPPU analogues was studied. It was evidenced that the linker position had a strong impact on the specificity of the generated polyclonals, which were more sensitive to changes at moieties of the target analyte located furthest from the derivatization site of the immunogen. Finally, matrix effects of gold and g…

ImmunoassayDetection limitAnalyteImmunogenChromatographymedicine.diagnostic_testbiologyPyridinesPhenylurea CompoundsActinidiaGeneral ChemistryForchlorfenuronAntibodieschemistry.chemical_compoundPlant Growth RegulatorschemistryLimit of DetectionPolyclonal antibodiesImmunoassaymedicinebiology.proteinGeneral Agricultural and Biological SciencesDerivatizationHaptensHaptenJournal of Agricultural and Food Chemistry
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Carbonyl metallo immuno assay: a new application for Fourier transform infrared spectroscopy

2000

Abstract We describe here the development of a new, non-isotopic immunological assay termed CMIA (carbonyl metallo immunoassay) that uses metal carbonyl complexes as tracers and Fourier transform infrared spectroscopy (FT-IR) as the detection method. This assay is based on the particular spectral features of these complexes, which show very strong absorption bands in the 1800–2200 cm −1 spectral range where proteins and organic molecules do not absorb. In Section 1 , the optimisation of the quantitative detection of these tracers is detailed. In Section 2 , the implementation of mono-CMIA is described, including the CMIA assays of three antiepileptic drugs (carbamazepine, phenobarbital, phe…

ImmunoassayDetection limitChromatographymedicine.diagnostic_testChemistryClinical BiochemistryPharmaceutical ScienceInfrared spectroscopyMetal carbonylCombinatorial chemistryAnalytical Chemistrysymbols.namesakeFourier transformImmunoassaySpectroscopy Fourier Transform InfraredDrug DiscoverymedicinesymbolsAnticonvulsantsFourier transform infrared spectroscopyAbsorption (electromagnetic radiation)Quantitative analysis (chemistry)SpectroscopyJournal of Pharmaceutical and Biomedical Analysis
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Hapten synthesis, monoclonal antibody generation, and development of competitive immunoassays for the analysis of picoxystrobin in beer.

2010

Abstract This paper describes the original synthesis of a functionalized derivative of the fungicide picoxystrobin and the generation of the first reported monoclonal antibodies against this strobilurin pesticide. The synthetic hapten was prepared by total synthesis from commercial chemicals and incorporating the spacer arm through a carbon–carbon single bond. Also, to obtain the immunogen, an uncommon hapten activation strategy based on N,N′-disuccinimidyl carbonate was employed, affording high activation yields and clean and reproducible coupling results. With these immunoreagents, two enzyme-linked immunosorbent assays (ELISAs) were developed: a competitive one-step assay using the antib…

Immunogenmedicine.drug_classPyridinesEnzyme-Linked Immunosorbent AssayMonoclonal antibodyBiochemistryChemical synthesisAnalytical ChemistryCell LineMiceLimit of DetectionmedicineEnvironmental ChemistryAnimalsSpectroscopyDetection limitChromatographyChemistryFungiTotal synthesisAntibodies MonoclonalBeerHigh activationStrobilurinsFungicides IndustrialAcrylatesStrobilurinHaptenHaptensAnalytica chimica acta
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Designing solid optical sensors for in situ passive discrimination of volatile amines based on a new one-step hydrophilic PDMS preparation

2016

Abstract We reported an optimal material for embedding chemoresponsive dyes based on modified commercial PDMS. A new approach to impart hydrophilicity to H-PDMS in an unique step was developed by addition of tetraethyl orthosilicate (TEOS) and in absence of basic or acid aqueous mixtures or hydroxyl-compounds during the PDMS coating process. This incorporation significantly enhances the performance of PDMS-based devices for sensing applications. New colorimetric sensors for passive detection and in situ discrimination of volatile amines have been obtained. The limit of detection achieved was 1.5 mg m −3 for both, dimethylamine and methylamine, suitable to control real working atmospheres. T…

In situMaterials scienceOne-Step02 engineering and technologyengineering.material010402 general chemistry01 natural scienceschemistry.chemical_compoundCoatingMaterials ChemistryOrganic chemistryElectrical and Electronic EngineeringInstrumentationDimethylamineDetection limitAqueous solutionMethylamineMetals and Alloys021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsTetraethyl orthosilicatechemistryChemical engineeringengineering0210 nano-technologySensors and Actuators B: Chemical
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Diels-Alder Reactions ofin situ generated N-benzoylindolo-2,3-quinodimethane with carbodienophiles

1993

The indolo-2,3-quinodimethane (5), generated from 2,3-bis(bromomethyl)indole (4), was trapped with unsymmetrical carbodienophiles or N, N′-p-phenylenedimaleimide to furnish the 1,2,3,4-tetrahydrocarbazoles (6–9). [4 + 2]-Cycloaddition of 5 with tetracyanoethylene gave rise to the tetracyanocarbazole (10) and a subsequent product 11a or 11b. The Diels-Alder reaction of 5 with divinyl sulfone was regiospecific within the detection limits of HPLC analysis. Similarly, the reaction of 5 with N, N′-p-phenylenedimaleimide yielded solely the stereoisomer 9.

Indole testIn situDetection limitHplc analysischemistry.chemical_compoundchemistryDiels alderOrganic chemistryTetracyanoethyleneDivinyl sulfoneJournal f�r Praktische Chemie/Chemiker-Zeitung
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Sequential injection analysis (SIA)-chemiluminescence determination of indomethacin using tris[(2,2'-bipyridyl)]ruthenium(III) as reagent and its app…

2006

Abstract Automated sequential injection (SIA) method for chemiluminescence (CL) determination of nonsteroidal anti-inflammatory drug indomethacin ( I ) was devised. The CL radiation was emitted in the reaction of I (dissolved in aqueous 50% v/v ethanol) with intermediate reagent tris(2,2′-bipyridyl)ruthenium(III) (Ru(bipy) 3 3+ ) in the presence of acetate. The Ru(bipy) 3 3+ was generated on-line in the SIA system by the oxidation of 0.5 mM tris(2,2′-bipyridyl)ruthenium(II) (Ru(bipy) 3 2+ ) with Ce(IV) ammonium sulphate in diluted sulphuric acid. The optimum sequence, concentrations, and aspirated volumes of reactant zones were: 15 mM Ce(IV) in 50 mM sulphuric acid 41 μL, 0.5 mM Ru(bipy) 3 …

IndomethacinAnalytical chemistrychemistry.chemical_elementBiochemistryDosage formAnalytical Chemistrylaw.inventionlawSpectrophotometrymedicineOrganometallic CompoundsEnvironmental ChemistrySpectroscopyChemiluminescenceDetection limitDosage FormsAqueous solutionmedicine.diagnostic_testMolecular StructureReproducibility of ResultsRutheniumStandard curvechemistryReagentCalibrationFlow Injection AnalysisLuminescent MeasurementsSolventsNuclear chemistryAnalytica chimica acta
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Determination of phenolic antioxidants additives in industrial wastewater from polypropylene production using solid phase extraction with high-perfor…

2019

Abstract This paper describes a new method for the effective extraction of the residues of five synthetic phenolic antioxidants (AOs): Ditertbutylphenol (DTF), Irganox 1010, Irganox 1076, Ethanox 330 and Cyanox 1790, from industrial water produced during the polypropylene (PP) deodorization process. In the deordorization process, PP is stored in a column for an average time of four hours and exposed to nitrogen and water vapor to remove inflammable compounds which may generate atypical odors in the PP. The samples of interest were taken in the desorber, followed by cleansing and pre-concentration using modified styrene divinylbenzene polymer cartridges. Liquid chromatography was performed w…

Industrial WasteWastewater010402 general chemistryPolypropylenes01 natural sciencesBiochemistryHigh-performance liquid chromatographyAntioxidantsAnalytical ChemistryStyreneIndustrial wastewater treatmentchemistry.chemical_compoundPhenolsLimit of DetectionSolid phase extractionChromatography High Pressure LiquidDetection limitChromatographyChemistry010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Solid Phase ExtractionReproducibility of ResultsGeneral MedicineContaminationDivinylbenzene0104 chemical sciencesCalibrationWater Pollutants ChemicalJournal of chromatography. A
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Determination of urea-derived pesticides in fruits and vegetables by solid-phase preconcentration and capillary electrophoresis

2001

A multiresidue analytical method based on solid-phase extraction (SPE) enrichment combined with capillary electrophoresis (CE), using micellar electrokinetic capillary chromatography (MEKC), was developed to determine ten substituted urea pesticides in orange and tomato samples. Several factors such as pH, composition and concentration of the buffer, concentration of surfactant, addition of organic solvent, and working voltage were optimized to obtain the best compound separation in the shortest time. Separation can be achieved in 7 min using a micellar aqueous pH 9 buffer composed of 4 mM borate and 35 mM sodium dodecyl sulfate. After an SPE procedure, which provided a 10-fold enrichment, …

InsecticidesClinical BiochemistryFood ContaminationBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresisVegetablesUreamedia_common.cataloged_instanceSolid phase extractionPesticidesSodium dodecyl sulfateEuropean unionMicellesmedia_commonDetection limitChromatographyAqueous solutionHerbicidesMethanolElectrophoresis CapillarySodium Dodecyl SulfatechemistryFruitEnrichment factorELECTROPHORESIS
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Dispersive magnetic immunoaffinity extraction. Anatoxin-a determination.

2017

Specific monoclonal antibodies were coupled with magnetic Sepharose-based beads and used, for the first time. The methodology was applied to preconcentrate anatoxin-a from water and the later determination by ion mobility spectrometry (IMS). Dispersive magnetic immunoaffinity (d-MagIA) extraction methodology provided a limit of detection of 0.02μgL-1 and a satisfactory precision with a relative standard deviation lower than 15%. Recoveries were evaluated at 0.5, 1.0 and 5.0μgL-1 anatoxin-a with quantitative values from 91 to 115%. Additionally, isobaric interferences with phenylalanine were completely avoided by the use of the developed d-MagIA extraction coupled to IMS determinations.

Ion-mobility spectrometryRelative standard deviationAnalytical chemistry02 engineering and technology01 natural sciencesBiochemistryAnalytical ChemistryAnatoxin-aSepharosechemistry.chemical_compoundMagneticsLimit of DetectionIon Mobility SpectrometryDetection limitChromatographyCyanobacteria ToxinsSepharose010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Antibodies MonoclonalWaterGeneral Medicine021001 nanoscience & nanotechnology0104 chemical scienceschemistryIsobaric process0210 nano-technologyWater Pollutants ChemicalEnvironmental MonitoringTropanesJournal of chromatography. A
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Comparison between sodium dodecylsulphate and cetyltrimethylammonium bromide as mobile phases in the micellar liquid chromatography determination of …

2004

The retention behaviour of non-steroidal anti-inflammatory drugs (NSAIDs) using micellar mobile phases of sodium dodecylsulphate (SDS) is studied and compared with that observed with micellar mobile phases of cetyltrimethylammonium bromide (CTAB). A liquid chromatographic procedure for the determination of acemetacin, diclofenac, indomethacin, ketoprofen, naproxen and tolmetin in pharmaceutical preparations is described. The proposed system uses a Kromasil C18 analytical column and a solution of 0.15 M SDS at pH 3 with 10% 1-propanol as mobile phase. Under these conditions, the studied NSAIDs elute between 6 and 10 min at a 1 mL min(-1) flow rate. Limits of detection (LOD) are lower than 0.…

KetoprofenNaproxenSodiumClinical BiochemistryAcemetacinPharmaceutical Sciencechemistry.chemical_elementAnalytical Chemistrychemistry.chemical_compoundBromideDrug DiscoverymedicineSpectroscopyChromatography Micellar Electrokinetic CapillaryDetection limitChromatographyElutionCetrimoniumAnti-Inflammatory Agents Non-SteroidalSodium Dodecyl SulfateReference StandardsSolutionschemistryMicellar liquid chromatographyCalibrationCetrimonium CompoundsIndicators and ReagentsSpectrophotometry Ultravioletmedicine.drugJournal of pharmaceutical and biomedical analysis
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