Search results for "LIMIT"

showing 10 items of 2826 documents

Evaluation of a Real-Time PCR Assay for the Detection and Quantification of Group Spores in Food

2010

A procedure based on quantitative real-time PCR was evaluated for the detection and quantification of Bacillus cereus spores. Several methods for DNA isolation, such as various heat treatments and germination solutions, were evaluated on spore suspensions of representative strains of the B. cereus group. Overall, the commercially available DNeasy tissue kit yielded the maximum amount of DNA. The procedure also was used to construct calibration curves for different food matrices, with a wide spore quantification range of 5 log units using serial dilutions of spore suspensions of B. cereus CECT 148T. The detection limit for B. cereus in artificially contaminated liquid egg and reconstituted i…

Detection limitChromatographySerial dilutionfungiBacillus cereusBiologybiology.organism_classificationMicrobiologyEndosporeDNA extractionMicrobiologySporeCereusGerminationFood ScienceJournal of Food Protection
researchProduct

Determination of hydroxylated benzophenone UV filters in sea water samples by dispersive liquid-liquid microextraction followed by gas chromatography…

2010

A new analytical method for the determination of four hydroxylated benzophenone UV filters (i.e. 2-hydroxy-4-methoxybenzophenone (HMB), 2,4-dihydroxybenzophenone (DHB), 2,2'-dihydroxy-4-methoxybenzophenone (DHMB) and 2,3,4-trihydroxybenzophenone (THB)) in sea water samples is presented. The method is based on dispersive liquid-liquid microextraction (DLLME) followed by gas chromatography-mass spectrometry (GC-MS) determination. The variables involved in the DLLME process were studied. Under optimized conditions, 1000 microL of acetone (disperser solvent) containing 60 microL of chloroform (extraction solvent) were injected into 5 mL of aqueous sample adjusted to pH 4 and containing 10% NaCl…

Detection limitChromatographySilylationOrganic ChemistryGeneral MedicineBSTFAChemical FractionationBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundBenzophenoneschemistryStandard additionSample preparationSeawaterGas chromatographyGas chromatography–mass spectrometryDerivatizationWater Pollutants ChemicalJournal of chromatography. A
researchProduct

Determination ofl-Ascorbic Acid and Total Ascorbic Acid in Vascular and Nonvascular Plants by Capillary Zone Electrophoresis

1998

A capillary zone electrophoresis (CZE) procedure for the determination of l-ascorbic acid (AA) and total ascorbic acid (TAA, as the sum of AA and dehydroascorbic acid) in vascular plants, lichens, bryophytes, and liverworts is described. The samples were frozen in liquid nitrogen and extracted with 2% metaphosphoric acid. To determine AA, an aliquot was directly injected in a fused-silica capillary. The determination of TAA was performed upon its reduction with dl-homocysteine at pH 7. The background electrolyte contained 60 mM sodium chloride, 60 mM sodium dihydrogen phosphate, 1 x 10(-4)% hexadimetrine bromide, and NaOH up to pH 7. The procedure was rapid and highly reproducible; the limi…

Detection limitChromatographySodiumBiophysicsElectrophoresis CapillaryReproducibility of Resultschemistry.chemical_elementAscorbic AcidCell BiologyElectrolytePlantsAscorbic acidSensitivity and SpecificityBiochemistryElectrophoresischemistry.chemical_compoundCapillary electrophoresischemistryBromideDehydroascorbic acidMolecular BiologyAnalytical Biochemistry
researchProduct

Micellar modified spectrophotometric determination of nitrobenzenes based upon reduction with tin(II), diazotisation and coupling with the Bratton–Ma…

1997

Abstract Nitrobenzenes, such as the antibiotic chloramphenicol, the vasodilator nicardipine, and the herbicides dinitramin, dinobuton, fenitrothion, methylparathion, oxyfluorfen, parathion, pendimethalin, quintozene, and trifluralin, were determined by using a spectrophotometric method in the visible region (540 nm). The method was based on the reduction of the nitrobenzenes to arylamines with tin(II) chloride, diazotisation of the arylamines and coupling of the diazonium ions with the Bratton–Marshall reagent. The two latter reactions were performed in a micellar medium of sodium dodecyl sulphate. The linear calibration range was 2×10 −6 to 7×10 −5 M ( r >0.999), with limits of detection i…

Detection limitChromatographySodiumTrifluralinchemistry.chemical_elementChlorideAnalytical ChemistryNitrobenzenechemistry.chemical_compoundParathionchemistryReagentmedicineTinmedicine.drugTalanta
researchProduct

Determination of pesticides in soil samples by solid phase extraction disks

1993

A systematic study comparing the methodology and analytical results obtained in an investigation of seven pesticide residues (Molinate, Atrazine, Carbofuran, Pirimicarb, Prometryn, Malathion and Tetrachlorvinphos) in soil samples is reported. Solid-phase extraction (SPE) using glass columns and 47 mm disks of octyl and octadecyl-bonded silica was used in the pesticide analysis. The best extraction efficiency and clearest extracts are obtained with C8 disks. The analyses were carried out by capillary gas chromatography with nitrogen and phosphorus detection. Recovery experiments were performed at ppb levels in spiked soil samples. The average recoveries of the compounds were 53–77%. Detectio…

Detection limitChromatographySoil testPesticide residueOrganic ChemistryClinical BiochemistryExtraction (chemistry)BiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryEnvironmental chemistrySolid phase extractionGas chromatographyAtrazineCarbofuranChromatographia
researchProduct

Implementing the contamination prevention programs in the pesticide industry by infrared spectroscopy.

2014

Abstract An infrared spectroscopy based methodology has been successfully developed to implement contamination prevention programs in the pesticide industry. Sensitivity of the IR procedure, traditionally considered the Achilles Hell of the technique, has been improved by using a transmission cell with an open upper side, an internal volume of 35 µL and an optical pathlength of 0.5 mm, providing detection limits of 32 mg L−1 for folpet and 48 mg L−1 for cymoxanil. The manufacturing of folpet and cymoxanil was employed as an example and the IR methodology was validated for the implementation of contamination prevention programs in the pesticide industry. The swab test and rinsate method were…

Detection limitChromatographySpectrophotometry InfraredChemistryChlorpyrifos-methylAnalytical chemistryInfrared spectroscopyContaminationPesticideOptical pathlengthGas Chromatography-Mass SpectrometryAnalytical ChemistryLimit of DetectionChemical IndustryEnvironmental PollutantsPesticidesTalanta
researchProduct

Amphetamine and methamphetamine determination in urine by reversed-phase high-performance liquid chromatography with sodium 1,2-napthoquinone 4-sulfo…

1995

A rapid method is described for the identification and determination of amphetamine and methamphetamine in human urine samples by liquid chromatography with UV-Vis detection. The samples were transferred onto a C18 solid-phase extraction column and chromatographed on a Hypersil ODS RP C18, 5 microns (250 x 4 mm I.D.) with an acetonitrile-water elution gradient containing propylamine. Under these conditions, the amines are eluted with a short retention time. The procedure has been applied to the determination of amphetamine and methamphetamine in the range 0.3-4.0 micrograms/ml in spiked urine samples. The detection limits at 280 nm were 4 and 2 ng/ml for amphetamine and methamphetamine, res…

Detection limitChromatographySpectrophotometry InfraredElutionChemistryExtraction (chemistry)Reproducibility of ResultsPropylamineGeneral ChemistryMethamphetamineHigh-performance liquid chromatographyMethamphetamineAmphetaminechemistry.chemical_compoundmedicineHumansIndicators and ReagentsSolid phase extractionQuantitative analysis (chemistry)Chromatography High Pressure LiquidNaphthoquinonesmedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
researchProduct

Determination of caffeine in tea samples by Fourier transform infrared spectrometry

2002

A sustainable and environmentally friendly procedure has been developed for the FTIR determination of caffeine in tea leaf samples. The method is based on the extraction with ammonia and CHCl3 and direct determination of caffeine on the chloroform extracts using peak height absorbance measurements at 1658.5 cm(-1) and external calibration. The method provides a sensitivity of 0.2142 absorbance units mg(-1) mL and a limit of detection of 1 mg L(-1), corresponding to 0.002% m/m caffeine in tea leaves. As compared with a reference procedure, based on UV absorbance measurement at 276 nm after low pressure column chromatography, the developed procedure reduces the consume of CHCl3 by a factor of…

Detection limitChromatographyTeaChemistryExtraction (chemistry)Infrared spectroscopyBiochemistryAnalytical ChemistryPlant LeavesAbsorbancechemistry.chemical_compoundColumn chromatographyCaffeineSpectroscopy Fourier Transform InfraredFourier transform infrared spectroscopyDiethyl etherCaffeineAnalytical and Bioanalytical Chemistry
researchProduct

Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry to identify contaminants in water: an insight on environment…

2013

Ultra-high pressure liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QqTOF-MS) acquiring full scan MS data for quantification, and automatic data dependent information product ion spectra (IDA-MS/MS) without any predefinition of the ions by the user was checked for identifying organic contaminants in water samples. The use of a database with more than 2000 compounds achieved high confidence results for a wide number of contaminants based upon retention time, accurate mass, isotopic pattern and MS/MS library searching. More than 20 contaminants, mostly pharmaceuticals, but also mycotoxins and polyphenols were unambiguously identified. Furthermore, the combination of s…

Detection limitChromatographyTime FactorsChemistryOrganic ChemistryAnalytical chemistryWaterGeneral MedicineContaminationMass spectrometryBiochemistryLibrary searchingAnalytical ChemistryTriple quadrupole mass spectrometerMolecular WeightRiversTandem Mass SpectrometryPrincipal component analysisQuadrupole time of flightUltra high performancePesticidesChromatography High Pressure LiquidWater Pollutants ChemicalJournal of chromatography. A
researchProduct

Analysis of T-2 toxin by HPLC and GC in samples of corn and oats

1984

HPLC is the only physico-chemical method for the analysis of trichothecenes for which no derivatization is necessary. Hence a combination of different methods can be performed. For exclusion of any faulty interpretation of data and in order to decrease the detection limit HPLC should be followed by GC.

Detection limitChromatographyToxinClinical BiochemistryTrichotheceneGeneral Medicinemedicine.disease_causeHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineGeneral Materials ScienceGas chromatographyDerivatizationMycotoxinFresenius' Zeitschrift für analytische Chemie
researchProduct