Search results for "Detection limit"

showing 10 items of 810 documents

Highly sensitive monoclonal antibody-based immunoassays for the analysis of fluopyram in food samples

2019

Monoclonal antibody-based techniques have become a useful analytical technology in the agro-food sector. Nowadays, residues of the recently registered fungicide fluopyram are increasingly being found in quality control programs. In the present study, novel chemical derivatives of this pesticide were prepared and specific and high-affinity monoclonal antibodies to fluopyram were raised for the first time. Moreover, immunoassays to fluopyram were developed in two alternative enzyme-linked immunosorbent assay formats, using homologous and heterologous assay conjugates, with limits of detection below 0.05 µg L−1. The optimized immunoassays were applied to the analysis of fluopyram in fortified …

GrapesPyridinesmedicine.drug_classMustWineMonoclonal antibody01 natural sciencesAnalytical ChemistryFood safetychemistry.chemical_compound0404 agricultural biotechnologyLimit of DetectionStone fruitsmedicineImmunoassayDetection limitChromatographyFluopyrammedicine.diagnostic_test010401 analytical chemistryAntibodies Monoclonal04 agricultural and veterinary sciencesGeneral Medicine040401 food science0104 chemical sciencesHighly sensitiveSuccinate DehydrogenaseHaptenchemistryImmunoassayBenzamidesELISAFluopyramFood Science
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Determination of Mercury in Milk by Cold Vapor Atomic Fluorescence: A Green Analytical Chemistry Laboratory Experiment

2011

Green analytical chemistry principles were introduced to undergraduate students in a laboratory experiment focused on determining the mercury concentration in cow and goat milk. In addition to traditional goals, such as accuracy, precision, sensitivity, and limits of detection in method selection and development, attention was paid to the evaluation of green parameters of the analytical methods. Milk samples were evaluated by cold vapor atomic fluorescence spectrometry (CV-AFS) and the wastes were minimized by co-precipitation with Fe(III).

Green chemistryDetection limitChemistryAnalytical chemistryfood and beverageschemistry.chemical_elementGeneral ChemistryAtomic spectroscopyFluorescence spectroscopyEducationMercury (element)Cold vaporLaboratory experimentSpectroscopyJournal of Chemical Education
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Fast simultaneous determination of prominent polyphenols in vegetables and fruits by reversed phase liquid chromatography using a fused-core column

2015

A reversed-phase high-performance liquid chromatography method with photodiode array detection has been developed enabling the joint determination of 17 prominent flavonoids and phenolic acids in vegetables and fruits. A multi-segmented gradient program using a fused-core column for the separation of several phenolic classes (phenolic acids and flavonoids) has been optimised. The influence of extraction conditions (sample freeze-drying, ultrasound extraction, solvent composition and extraction time) has been also optimised using response surface methodology with tomato samples as a model. Complete recoveries (76-108%) were obtained for the phenolic compounds present in tomato. The developed…

HPLC-DADAnalytical ChemistryFused corePhenolsResponse surface methodologyLimit of DetectionVegetablesResponse surface methodologyChromatography High Pressure LiquidFlavonoidsDetection limitChromatography Reverse-PhaseChromatographyChemistryExtraction (chemistry)Polyphenolsfood and beveragesGeneral MedicineReversed-phase chromatographyRepeatabilityGENETICAFunctional qualityPolyphenolFoodFruitUltrasound-assisted extractionResponse Surface MethodologyColumn (botany)Food Science
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Quantitative determination of trichothecenes in breadsticks by gas chromatography-triple quadrupole tandem mass spectrometry.

2014

Breadsticks are pencil-sized sticks of dry bread widely consumed as a pre-meal appetiser. They are basically wheat-based snacks, which makes them a good matrix to evaluate mycotoxin contamination, since wheat is very susceptible to fungal attack. In this sense, the fast, selective and sensitive gas chromatography-triple quadrupole tandem mass spectrometry (GCQqQ- MS/MS) method proposed here allows simultaneous determination of deoxynivalenol (DON), 3-acetyldeoxynivalenol, fusarenon-X, diacetoxyscirpenol, nivalenol, neosolaniol, HT-2 and T-2 toxin in breadsticks after QuEChERS extraction and clean-up. The performance of the method was assessed with respect to European Commission Regulations …

Health Toxicology and MutagenesisAnalytical chemistryFood ContaminationToxicologyTandem mass spectrometryQuechersDiacetoxyscirpenolGas Chromatography-Mass SpectrometryMatrix (chemical analysis)chemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryToxicologiaMycotoxinDetection limitChromatographyChemistryPublic Health Environmental and Occupational Healthfood and beveragesAliments ToxicologiaGeneral ChemistryGeneral MedicineBreadEnvironmental ExposureTriple quadrupole mass spectrometerGas chromatographyTrichothecenesFood ScienceFood additivescontaminants. Part A, Chemistry, analysis, control, exposurerisk assessment
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Speciation of methylmercury in market seafood by thermal degradation, amalgamation and atomic absorption spectroscopy

2014

Sample thermal decomposition followed by mercury amalgamation and atomic absorption has been employed for the determination of methylmercury (MeHg) in fish. The method involves HBr leaching of MeHg, extraction into toluene, and back-extraction into an aqueous l-cysteine solution. Preliminary studies were focused on the extraction efficiency, losses, contaminations, and species interconversion prevention. The limit of detection was 0.018µgg(-1) (dry weight). The intraday precision for three replicate analysis at a concentration of 4.2µgg(-1) (dry weight) was 3.5 percent, similar to the interday precision according to analysis of variance (ANOVA). The accuracy was guaranteed by the use of for…

Health Toxicology and Mutagenesischemistry.chemical_elementlaw.inventionchemistry.chemical_compoundDry weightlawAnimalsCysteineMethylmercuryDetection limitChemistrySpectrophotometry AtomicFishesPublic Health Environmental and Occupational HealthGreen Chemistry TechnologyMercuryGeneral MedicineReplicateMethylmercury CompoundsPollutionMercury (element)Certified reference materialsSeafoodEnvironmental chemistryLeaching (metallurgy)Atomic absorption spectroscopyEnvironmental MonitoringEcotoxicology and Environmental Safety
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Application of accelerated solvent extraction followed by gel performance chromatography and high-performance liquid chromatography for the determina…

2005

Accelerated solvent extraction (ASE) has been evaluated as a fast alternative to methanolic saponification for the extraction of 12 polycyclic aromatic hydrocarbons (PAHs) from mussel tissue. Several solvent systems and different operating conditions were investigated. The mixture dichloromethane-acetone (1:1, v/v) gave the best recoveries at 125 degrees C and 1500 psi, in a total time of 10 min. No yield difference was found between freeze-drying (Fd) or drying the wet mussel with diatomaceous earth (Ded) prior to extraction. The ASE method was validated using the standard reference material SRM 2977, a freeze-dried mussel tissue with naturally present organic contaminants. The performance…

Hot TemperatureTime FactorsHealth Toxicology and MutagenesisFood ContaminationToxicologyHigh-performance liquid chromatographymedia_common.cataloged_instanceAnimalsEuropean unionOrganic ChemicalsPolycyclic Aromatic HydrocarbonsChromatography High Pressure Liquidmedia_commonchemistry.chemical_classificationDetection limitChromatographyTissue ExtractsExtraction (chemistry)Public Health Environmental and Occupational HealthGeneral ChemistryMusselContaminationBivalviaHydrocarbonFreeze DryingchemistryChemistry (miscellaneous)Chromatography GelSolventsEnvironmental PollutantsSaponificationFood ScienceFood additives and contaminants
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A gated material as immunosensor for in-tissue detection of IDH1-R132H mutation in gliomas

2021

[EN] A nanodevice consisted on nanoporous anodic alumina (NAA) supports functionalized with specific and selective antibody-based gatekeepers for the detection of IDH1-R132H mutant enzyme is here reported. Molecular profile and tissue mutations of the tumours (such as IDH1/IDH2 mutations in gliomas) are a great source of information that already make a difference in terms of prognosis and prediction of response to combined therapy. However, standardized methodologies to determine this mutation are time-consuming and cannot provide information before or during surgical intervention, which significantly limits their utility in terms of intraoperative decisionmaking. To solve this limitation, …

IDH1MutantIDH1 R132Hmedicine.disease_causeIDH2QUIMICA ORGANICAGated materialFluorometerMaterials ChemistrymedicineElectrical and Electronic EngineeringInstrumentationAntibodyDetection limitMutationChemistryQUIMICA INORGANICAMetals and AlloysCondensed Matter PhysicsMolecular biologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIDH1Nanoporous anodic aluminaGlioblastomaBiosensor
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Fluorogenic Sensing of Carcinogenic Bisphenol A using Aptamer-Capped Mesoporous Silica Nanoparticles

2017

[EN] Mesoporous silica nanoparticles loaded with rhodamine B and capped with a bisphenol A aptamer were used for the selective and sensitive detection of this lethal chemical. The pores of the nanoparticles are selectively opened in the presence of bisphenol A (through its selective coordination with the aptamer) with subsequent rhodamine B delivery. With this capped material a limit of detection as low as 3.5 mu m of bisphenol A was measured.

INGENIERIA DE LA CONSTRUCCIONendocrine systemBisphenol AAptamerMesoporous silica nanoparticlesAptamerNanoparticle02 engineering and technology010402 general chemistryElectron Microscopy Service of the UPV01 natural sciencesCatalysischemistry.chemical_compoundQUIMICA ORGANICAQUIMICA ANALITICARhodamine BOrganic chemistryreproductive and urinary physiologyCarcinogenDetection limiturogenital systemGated nanomaterialsQUIMICA INORGANICAOrganic ChemistryGeneral ChemistryMesoporous silica021001 nanoscience & nanotechnology0104 chemical sciencesBisphenol aFluorogenic sensingchemistry0210 nano-technologyhormones hormone substitutes and hormone antagonistsNuclear chemistryChemistry - A European Journal
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Multi‐residue extraction to determine organic pollutants in mussel hemolymph

2021

This study assesses the extraction of eleven pharmaceuticals, five pesticides, five perfluoroalkyl substances, and two illicit drugs in hemolymph from (Mytilus Galloprovincialis). Four extraction procedures using Phree™ Phospholipid Removal cartridges were tested using different volumes of methanol (400 and 600 μL) and acetonitrile (300 and 450 μL). The pollutants were determined by high-performance liquid chromatography–tandem mass spectrometry. The use of methanol gave several problems during the extraction procedure, such as longer times and sample loss. Three methods (acetonitrile 300 and 450 μL; and methanol 600 μL) were validated. Recoveries at three concentration levels (5, 50, and 1…

Illicit drugsFiltration and Separation010501 environmental sciencesMass spectrometry01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundHemolymphHemolymphAnimalsSolid phase extractionPesticidesAcetonitrile0105 earth and related environmental sciencesDetection limitSolid-phase extractionFluorocarbonsChromatographyIllicit Drugs010401 analytical chemistryExtraction (chemistry)Pesticide0104 chemical sciencesPerfluoroalkyl substanceschemistryPharmaceuticalsEnvironmental PollutantsMethanolJournal of Separation Science
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Automated Determination of Paroxetine and Its Main Metabolite by Column Switching and On-Line High-Performance Liquid Chromatography

1994

An automated column-switching method coupled to isocratic high-performance liquid chromatography has been developed for simultaneous determination of blood levels of paroxetine and its nonconjugated main metabolite BRL 36610. The lower limits of detection were 9-15 nmol/L (3-5 ng/ml) and linearity between drug concentration and detector response was found for 0-1,500 nmol/L (0-500 ng/ml). The method could be applied to the analysis of serum samples obtained from depressed patients who were treated with daily oral doses of 20 or 40 mg of paroxetine. After the 20-mg dose, the mean blood level of paroxetine was 69 nM (23 ng/ml), whereas the metabolite BRL 36610 was detectable in only one of 5 …

ImipramineMetaboliteSensitivity and SpecificityHigh-performance liquid chromatographyImipramineMixed Function Oxygenaseschemistry.chemical_compoundCytochrome P-450 Enzyme SystemPiperidinesOral administrationDesipraminemedicineHumansDrug InteractionsPharmacology (medical)Chromatography High Pressure LiquidPharmacologyDetection limitChromatographyParoxetineParoxetineCytochrome P-450 CYP2D6chemistryFemaleQuantitative analysis (chemistry)medicine.drugTherapeutic Drug Monitoring
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