Search results for "SAMPLE"

showing 10 items of 2270 documents

Zwitterionic Sulfonates as m/z Shift Reagents for 5-Methylcytosine Detection in Deoxyribonucleic Acids (DNA) Using Flow Injection Analysis and Electr…

2015

5-Methylcytosine (5-MC) is an important epigenetic modification of DNA. Abnormally high concentrations of this substance appear because of the hypermethylation of cytosine. Therefore, the measurement of the quantity of this compound in mammals is of great importance. Recently, we reported that several imidazolium-based zwitterionic sulfonates form complexes with 5-MC in solution, which can be studied by electrospray ionisation mass spectrometry (ESI-MS). It is shown in this paper that such an association can be utilised for the detection of 5-MC in a DNA sample using high-throughput a flow injection analysis ESI-MS method. A variety of the sulfonate zwitterions have been tested as m/ z shi…

Detection limitFlow injection analysisSpectrometry Mass Electrospray IonizationElectrosprayChromatographyChemistryElectrospray ionizationAnalytical chemistryReproducibility of ResultsDNAGeneral MedicineDNA MethylationTandem mass spectrometryMass spectrometryAtomic and Molecular Physics and OpticsSample preparation in mass spectrometryFlow Injection Analysis5-MethylcytosineAnimalsCattleA-DNASulfonic AcidsSpectroscopyEuropean Journal of Mass Spectrometry
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Liquid chromatographic determination of trimethylamine in water.

2004

A method for the selective determination of trimethylamine (TMA) in aqueous matrices by liquid chromatography is reported. The proposed procedure is based on the derivatization of the analyte with 9-fluorenylmethyl chloroformate (FMOC) in a precolumn (Hypersil C18, 30 microm, 20 mm x 2.1 mm i.d.) connected on-line to the analytical column (LiChrosphere 100 RP18, 5 microm, 125 mm x 4 mm i.d.). Gradient elution was performed with a mixture of acetonitrile-water-0.05 M borate buffer (pH 9.0). The method has been applied to the direct determination of TMA in water within the 0.25-10.0 microg/ml concentration interval, and can also be adapted to the determination of TMA over the range 0.05-1.0 m…

Detection limitFluorenesChromatographyTertiary amineChemistryOrganic ChemistryWaterTrimethylamineGeneral MedicineReversed-phase chromatographyChloroformateSensitivity and SpecificityBiochemistryAnalytical ChemistryMethylamineschemistry.chemical_compoundSample preparationSolid phase extractionDerivatization
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Improvement of the electrophoretic protein profiles of Leguminosae gums extracts using gamanase and application to the evaluation of carob–guar mixtu…

2004

Abstract A quantitative assay for guar gum in carob gum, based on the extraction of proteins in acetonitrile–water (7:3), separation by capillary electrophoresis and multiple linear regression (MLR) using the areas of nine selected peaks as predictors, was improved by performing the extraction in the presence of gamanase. In the absence of the enzyme, peak migration times and areas depended on the guar content, which complicated peak identification and evaluation. Manual correction of the migration times by comparison with standard electropherograms obtained with pure carob and carob–guar mixtures was required; however, when the proteins were extracted under sonication at 60 °C for 30 min i…

Detection limitGuar gumChromatographyChemistrySonicationExtraction (chemistry)GuarBiochemistryAnalytical ChemistryElectrophoresisCapillary electrophoresisEnvironmental ChemistrySample preparationSpectroscopyAnalytica Chimica Acta
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Determination of organophosphorus pesticides in honeybees after solid-phase microextraction.

2001

A method based on solid-phase microextraction (SPME) followed by gas chromatography with nitrogen-phosphorus detection was developed for the purpose of determining 18 organophosphorus pesticide residues in honeybee samples (Apis mellifera). The extraction capacities of polyacrylate and poly(dimethylsiloxane) fibers were compared. The main factors affecting the SPME process, such as the absorption time profile, salt, and temperature, were optimized. The method involved honeybee sample homogenization, elution with an acetone:water solution (1:1) and dilution in water prior to fiber extraction. Moreover, the matrix effect on the extraction was evaluated. In samples spiked at the 0.2 mg kg(-1) …

Detection limitInsecticidesChromatographyChemistryElutionOrganic ChemistryExtraction (chemistry)Osmolar ConcentrationTemperatureGeneral MedicineBeesSolid-phase microextractionBiochemistrySensitivity and SpecificityAnalytical ChemistryDilutionOrganophosphorus CompoundsSolventsAnimalsSample preparationSaltsSolid phase extractionGas chromatographyJournal of chromatography. A
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Optimization of sample preparation conditions for detecting trace amounts of β-tegafur in α- and β-tegafur mixture.

2012

We report a semiquantitative method for determining trace amounts (<1%) of thermodynamically stable forms in polymorphic mixtures, focusing on sample preparation ef- fects on solid phase transitions. Tegafur (5-fluoro-1-(oxolan-2-yl)-1,2,3,4-tetrahydropyrimidine- 2,4-dione) was used as a model material in this study. The amounts of the thermodynamically stable $ tegafur were increased to levels detectable by powder X-ray diffractometry by grind- ing the samples in a ball mill in the presence of water. The limit of detection for this method was as low as 0.0005% of $ tegafur in " and $ tegafur mixtures. The amount of $ tegafur after sample preparation was found to be proportional to the init…

Detection limitLangmuirAntimetabolites AntineoplasticTrace AmountsChemistryAnalytical chemistryPharmaceutical ScienceTegafurPhase TransitionPolymorphism (materials science)IsomerismX-Ray DiffractionLimit of DetectionmedicineThermodynamicsSample preparationBall millMass fractionPowder Diffractionmedicine.drugTegafurJournal of pharmaceutical sciences
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Multi-element trace determinations in pure alkaline earth fluoride powders by high-resolution ICP-MS using wet-chemical sample preparation and laser …

2003

Four alternative analytical procedures for the determination of ten important trace impurities (Mg, Cr, Fe, Cu, Zn, Sr, Zr, Cd, Ba, and Pb) in pure alkaline earth fluoride powders were applied using high-resolution inductively coupled plasma mass spectrometry (ICP-MS). Two procedures are based on a wet-chemical microwave digestion with boric acid and quantification by the standard addition technique and isotope dilution mass spectrometry (IDMS), respectively. In addition, analyses are also performed by laser ablation as a direct solid sampling technique applying matrix-matched external calibration as well as isotope dilution of the powdered sample. For most elements good agreement between t…

Detection limitLaser ablationChemistryStandard additionAnalytical chemistryAnalytical proceduresSample preparationIsotope dilutionMicrowave digestionBiochemistryInductively coupled plasma mass spectrometryAnalytical ChemistryAnalytical and bioanalytical chemistry
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Flow injection flame atomic spectrometric determination of iron, calcium, magnesium, sodium and potassium in ceramic materials by using a variable-vo…

1993

A series of different ceramic materials, such as porcelain, feldspar, kaolin, varnish, clay and stoneware have been analyzed. Iron, calcium and magnesium have been determined in these materials by flame atomic absorption and sodium and potassium by flame emission. The use of a variable-volume injector enables one to carry out these analyses in a flow system (after fusion of samples with lithium metaborate) and does not require different dilutions for the determination of each type of sample considered, nor the use of different flow injection manifolds. The developed procedure provides a limit of detection of 100 μg/l for Na, 70 μg/l for Ca, 50 μg/l for both Fe and K and 8 μg/l for Mg. The c…

Detection limitMagnesiumPotassiumSodiumAnalytical chemistrychemistry.chemical_elementCeramic materialsBiochemistrylaw.inventionLithium metaborateAbsorbancechemistry.chemical_compoundchemistrylawSample preparationAtomic absorption spectroscopyFresenius' Journal of Analytical Chemistry
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Optimization of clean-up procedure for patulin determination in apple juice and apple purees by liquid chromatography

2009

Patulin (PAT) is a mycotoxin produced in fruits, mainly in apples, by several fungal species that can be carried into industrial apple juice by-products during factory processing. An analytical method for determination of PAT in apple juice and another one for determination of this compound in apple purees and apple compotes by liquid chromatography are proposed in the present paper. These methods have better precision and sensitivity than previously reported methods and focus mainly on extraction and clean-up. To accomplish analytical methods with higher accuracy, lower limits of detection and simpler procedures for application in quality control of the goods, different extraction and clea…

Detection limitMalusChromatographybiologyExtraction (chemistry)Food ContaminationHydrogen-Ion Concentrationbiology.organism_classificationAnalytical ChemistryBeveragesPatulinchemistry.chemical_compoundPatulinchemistryFruitMalusBy-productSpectrophotometry UltravioletSample preparationFood scienceFood qualityMycotoxinChromatography LiquidTalanta
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Calibration of LA-ICP-MS via standard addition using dried picoliter droplets

2020

A novel microanalytical calibration approach for quantitative spatially resolved analysis of thin layered materials with laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) is presented. This method relies on standard addition via the generation of dried pL-droplet residues. Therefore, a drop on demand dosing device based on a modified commercial ink cartridge and a dosing interface, both accessible via a self-constructed microcontroller, were developed. This dosing device enables the precise deposition of pL-droplets onto solid samples for the generation of residues with dimensions in the low μm-range. The LA-ICP-MS analysis of such residues allows calibration over at l…

Detection limitMaterials scienceThin sectionSample (material)010401 analytical chemistryAnalytical chemistry02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometryLaser01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionCartridgelawStandard addition0210 nano-technologySpectroscopyJournal of Analytical Atomic Spectrometry
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GFAAS determination of selenium in infant formulas using a microwave digestion method.

1994

A method for determining the selenium content of infant formulas is proposed. It includes wet digestion with nitric acid and hydrogen peroxide in medium pressure teflon bombs in a microwave oven and determination by graphite furnace atomic absorption spectrometry (GFAAS). The absence of interferences is checked. Values obtained for the limit of detection (19.4 ng/g), precision (RSD = 2.2%) and accuracy by analysis of a reference material show that the method is reliable.

Detection limitMicrowave ovenSpectrophotometry AtomicAnalytical chemistrychemistry.chemical_elementInfantHydrogen PeroxideNitric Acidlaw.inventionchemistry.chemical_compoundSeleniumchemistrylawNitric acidHumansSample preparationInfant FoodMagnesiumMicrowave digestionGraphite furnace atomic absorptionAtomic absorption spectroscopyMicrowavesSeleniumPalladiumFood ScienceDie Nahrung
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