Search results for "LIMIT"

showing 10 items of 2826 documents

Determination of ochratoxin A in beer marketed in Spain by liquid chromatography with fluorescence detection using lead hydroxyacetate as a clean-up …

2005

Abstract A new sample treatment for liquid chromatographic analysis of ochratoxin A (OTA) in beer is proposed. Degassed beer is mixed with lead hydroxyacetate, which precipitates some bulk components but does not remove OTA. The precipitate is separated and the acidified liquid is extracted with chloroform. The solvent is evaporated and the residue is dissolved in mobile phase (acetonitrile–water, 40:60, v/v; acidified at pH 3.0 with phosphoric acid) and separated by liquid chromatography using fluorescence detection. The limit of detection was 0.005 ng/ml. The average recovery rate and the average RSD of recovery in the spiking level range 0.01–0.5 ng/ml were 95.5% and about 5%, respective…

Ochratoxin ADetection limitChromatographyOrganic ChemistryBeerFood ContaminationGeneral MedicineReversed-phase chromatographyAcetatesOchratoxinsBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySolventchemistry.chemical_compoundSpectrometry FluorescenceLeadchemistrySpainChemical PrecipitationSample preparationOchratoxinPhosphoric acidChromatography LiquidJournal of Chromatography A
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New method for determination of ochratoxin A in beer using zinc acetate and solid-phase extraction silica cartridges

2006

Abstract A new method for the determination of ochratoxin A (OTA) in beer has been developed. The new method has been compared with a reference method currently accepted as AOAC official first action. The limits of detection and quantification of the proposed method were 0.0008 and 0.0025 ng/ml, respectively, while they were 0.0025 and 0.0075 ng/ml, respectively, in the AOAC method used as reference. The recovery levels in the 0.025–0.40 ng OTA/ml spiking range for the proposed and the reference methods were 80.6–87.6% and 78.2–83.8%, respectively. The relative standard deviations of recoveries were 2.6–7.5% for the proposed method and 0.7–6.1% for the reference method. Passing and Bablok r…

Ochratoxin ADetection limitChromatographyOrganic ChemistryZinc AcetateAnalytical chemistryBeerGeneral MedicineReversed-phase chromatographyReference StandardsSilicon DioxideOchratoxinsBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistrymedia_common.cataloged_instanceSample preparationSolid phase extractionEuropean unionOchratoxinChromatography Liquidmedia_commonJournal of Chromatography A
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Rapid determination of ochratoxin A in cereals and cereal products by liquid chromatography.

2004

A new method based on extraction with octylsilica (C8) followed by liquid chromatography coupled with fluorescence detection (LC-FLD) was studied to determine ochratoxin A (OTA) from cereals and cereal products. Optimization of different parameters, such as type and amount of solid phase, type and volume of eluent and amount of sample were carried out. Recovery of OTA from rice samples spiked at 10 ng/g level was of 86% with relative standard deviation of 5%. The limits of detection and quantification of the proposed method were 0.25 and 0.75 ng/g, respectively. Furthermore, LC-FLD after of OTA methylation and liquid chromatography coupled to mass spectrometry with an electrospray interface…

Ochratoxin ADetection limitElectrosprayChromatographyOrganic ChemistryExtraction (chemistry)food and beveragesGeneral MedicineMass spectrometryBiochemistryOchratoxinsSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundColumn chromatographySpectrometry FluorescencechemistryMycotoxinEdible GrainOchratoxinChromatography LiquidJournal of chromatography. A
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Determination of ochratoxin A in organic and non-organic cereals and cereal products from Spain and Portugal

2008

The objective of this work was to know the occurrence of OTA in organic and non-organic cereals and cereal products from Spain and Portugal. A method based on extraction with matrix solid phase dispersion (MSPD) using octylsilica (C8) followed by liquid chromatography coupled with fluorescence detection (LC-FD) was used to determine OTA from the selected samples. Recoveries of OTA from the studied samples spiked at 10 ng/g level ranged from 78% to 89% with a standard deviation of 3.66. The limits of detection and quantification of this method were 0.05 and 0.19 ng/g, respectively. Furthermore, LC-FD after OTA methylation was used to confirm the identity of OTA in all positive samples. This …

Ochratoxin ADetection limitOrganicPortugalExtraction (chemistry)Ochratoxin AGeneral MedicineContaminationNon-organicAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundchemistryBotanyEuropean commissionFood scienceMycotoxinOchratoxinFood ScienceFood Chemistry
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Improved sensitivity of ochratoxin A analysis in coffee using high-performance liquid chromatography with hybrid triple quadrupole-linear ion trap ma…

2016

A novel and sensitive method utilising high-performance liquid chromatography coupled to triple quadrupole-linear ion trap mass spectrometry (LC-QqQLIT-MS/MS) was developed in order to analyse the content of ochratoxin A (OTA) in coffee samples. The introduction of the triple-stage MS scanning mode (MS(3)) has been shown to increase greatly sensitivity and selectivity by eliminating the high chromatographic baseline caused by interference of complex coffee matrices. The analysis included the sample preparation procedure involving extraction of OTA using a methanol-water mixture and clean-up by immunoaffinity columns and detection using the MS(3) scanning mode of LC-QqQLIT-MS/MS. The propose…

Ochratoxin AHealth Toxicology and MutagenesisAnalytical chemistryToxicologyTandem mass spectrometryQuechersMass spectrometryCoffee01 natural sciencesHigh-performance liquid chromatographychemistry.chemical_compound0404 agricultural biotechnologyLimit of DetectionTandem Mass Spectrometrymedia_common.cataloged_instanceEuropean unionChromatography High Pressure Liquidmedia_commonDetection limitChromatography010401 analytical chemistryPublic Health Environmental and Occupational Health04 agricultural and veterinary sciencesGeneral ChemistryGeneral MedicineOchratoxins040401 food science0104 chemical sciencesTriple quadrupole mass spectrometerchemistryFood ScienceFood Additives & Contaminants: Part A
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Immunoanalytical methods for ochratoxin A monitoring in wine and must based on innovative immunoreagents.

2020

Immunochemical methods are highly deployed in analytical laboratories worldwide for monitoring the incidence of mycotoxins in the food chain. Nevertheless, most conventional immunoassays for ochratoxin A (OTA), including commercial kits, show limitations to robustly determine this mycotoxin in grape-derived products below regulated levels (2 ng/mL). Herein, two rapid tests for sensitive OTA determination in wine and must were developed capitalizing on a collection of bioconjugates from innovative synthetic haptens and monoclonal antibodies with subnanomolar affinity. The ELISA (LOD = 8 pg/mL) showed excellent performance in recovery studies, and it was applied to survey commercial wines and…

Ochratoxin AMonoclonal antibodyFood ContaminationWine01 natural sciencesAnalytical ChemistryFood safetychemistry.chemical_compound0404 agricultural biotechnologyLimit of DetectionScreening methodDipstickMycotoxinWineImmunoassayMycotoxinChromatographybusiness.industry010401 analytical chemistryfood and beverages04 agricultural and veterinary sciencesGeneral MedicineDipstickContaminationFood safety040401 food scienceOchratoxins0104 chemical sciencesHaptenchemistryCompetitive immunoassayCompetitive immunoassayEnvironmental scienceIndicators and ReagentsbusinessFood AnalysisFood ScienceFood chemistry
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Analytical, thermodynamical and kinetic characteristics of photoluminescence immunosensor for the determination of Ochratoxin A

2017

Ochratoxin A (OTA) is one of the most widespread and dangerous food contaminants. Therefore, rapid, label-free and precise detection of low OTA concentrations requires novel sensing elements with advanced bio-analytical properties. In the present paper we report photoluminescence (PL) based immunosensor for the detection of OTA. During the development of immunosensor photoluminescent ZnO nanorods (ZnO-NRs) were deposited on glass substrate. Then the ZnO-NRs were silanized and covalently modified by Protein-A (Glass/ZnO-NRs/Protein-A). The latest structure was modified by antibodies against OTA (Anti-OTA) in order to form OTA-selective layer (Glass/ZnO-NRs/Protein-A/Anti-OTA). In order to im…

Ochratoxin AOptical fiberMaterials sciencePhotoluminescenceBiomedical EngineeringBiophysicsAnalytical chemistryFood ContaminationBiosensing Techniques02 engineering and technology01 natural sciencesAntibodieslaw.inventionsymbols.namesakechemistry.chemical_compoundLimit of DetectionlawElectrochemistryHumansDetection limitNanotubesChromatography010401 analytical chemistrySubstrate (chemistry)General Medicine021001 nanoscience & nanotechnologyOchratoxins0104 chemical sciencesGibbs free energychemistrysymbolsNanorodGoldZinc Oxide0210 nano-technologySelectivityFood AnalysisBiotechnologyBiosensors and Bioelectronics
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Levels of ochratoxin A in wheat and maize bread from the central zone of Portugal.

2007

Ochratoxigenic fungi are natural contaminants of cereal and the produced toxins are harmful to humans and animals. Ochratoxin A (OTA) is among the most important mycotoxins, and the International Agency for Research on Cancer (IARC) classifies it as possibly carcinogenic to humans (group 2B). A total of 61 samples of bread from the central zone of Portugal were analysed for OTA by liquid chromatography (LC) with fluorescence detection (FD). For confirmation two procedures were applied, methyl ester derivatization with boron trifluoride-methanol and liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI/MS/MS). As far as we know, this is the first report where on-line…

Ochratoxin ATolerable daily intakeElectrospray ionizationFood ContaminationTandem mass spectrometryMicrobiologyZea mayschemistry.chemical_compoundHumansFood scienceMycotoxinDerivatizationOchratoxinTriticumDetection limitChromatographyPortugalIncidencefood and beveragesGeneral MedicineBreadOchratoxinschemistryConsumer Product SafetyFood MicrobiologyFood ScienceChromatography LiquidInternational journal of food microbiology
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Direct Analysis of Psilocin and Muscimol in Urine Samples Using Single Drop Microextraction Technique In-Line with Capillary Electrophoresis

2020

The fully automated system of single drop microextraction coupled with capillary electrophoresis (SDME-CE) was developed for in-line preconcentration and determination of muscimol (MUS) and psilocin (PSC) from urine samples. Those two analytes are characteristic active metabolites of Amanita and Psilocybe mushrooms, evoking visual and auditory hallucinations. Study analytes were selectively extracted from the donor phase (urine samples, pH 4) into the organic phase (a drop of octanol layer), and re-extracted to the acidic acceptor (background electrolyte, BGE), consisting of 25 mM phosphate buffer (pH 3). The optimized conditions for the extraction procedure of a 200 &micro

OctanolAnalyteLiquid Phase MicroextractionCalibration curveAmanitacapillary electrophoresisPharmaceutical ScienceElectrolyteUrinesingle drop microextraction01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicineCapillary electrophoresislcsh:Organic chemistryLimit of DetectionDrug DiscoverymedicineHumans030216 legal & forensic medicinePhysical and Theoretical ChemistrypsilocinChromatographyChemistrygreen chemistry010401 analytical chemistryOrganic ChemistryElectrophoresis CapillaryHydrogen-Ion ConcentrationmuscimolurinePsilocybin0104 chemical sciencesDilutionChemistry (miscellaneous)PsilocinCalibrationHallucinogensSolventsMolecular MedicinePsilocybemedicine.drugMolecules
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A passive sampling-based analytical strategy for the determination of volatile organic compounds in the air of working areas.

2010

Abstract An analytical methodology based on the use of a polyethylene layflat tube filled with activated carbon and Florisil (ACFL-VERAM) was employed for the passive sampling of volatile organic compounds (VOCs) in the air of working areas of packing industries. VOCs amount in the ACFL-VERAM sampler was directly determined through head-space-gas chromatography–mass spectrometry (HS-GC–MS) allowing a direct determination in only 20 min without the need of any previous treatment. Uptake parameters, like sampling rate ( R S ) and sampler–air partition coefficient ( K SA ), were determined for every studied VOC from adsorption isotherm data. Additionally, experimental equations have been propo…

OctanolAnalytical chemistryAir Pollutants OccupationalMass spectrometryBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionmedicineEnvironmental ChemistryIndustryVolatile organic compoundSpectroscopychemistry.chemical_classificationVolatile Organic CompoundsChromatographyDirect methodAirPolyethylenePartition coefficientchemistryGas chromatographyAdsorptionVolatilizationActivated carbonmedicine.drugEnvironmental MonitoringAnalytica chimica acta
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