Search results for "Quantitative analysis."

showing 10 items of 304 documents

High-performance liquid chromatographic determination of furfural compounds in infant formulas

2002

Furfural contents in adapted and follow-up infant formulas were measured by RP-HPLC. The evolution of furfural compound contents during storage (a year at 20 and 37 °C) was studied. 2-Furylmethylketone and 5-methyl-2-furaldehyde were not detectable in analysed samples. The differences in the furfural compounds at point zero between both infant formulas has to be ascribed to the differences in protein and iron contents. An increase in free 5-hydroxymethyl-2-furfuraldehyde (HMF), 2-furaldehyde (F) and HMF+F contents was observed in all samples, although the differences were not statistically significant. The storage temperature affected the total HMF content and the storage time affected the …

ChromatographyChemistryOrganic ChemistryPasteurizationGeneral MedicineReversed-phase chromatographyFurfuralBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionMaillard reactionsymbols.namesakechemistry.chemical_compoundInfant formulalawBrowningsymbolsQuantitative analysis (chemistry)Journal of Chromatography A
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Quantification of low levels of amorphous content in maltitol

2004

A method for the quantification of low levels of amorphous content of maltitol with hyper-DSC (high speed DSC) was developed. The method is based on the fact that the change of specific heat ( � Cp) at the glass transition is linearly proportional to the amorphous content. Twelve synthetic mixtures with various degrees of crystalline and amorphous maltitol were prepared. � Cp was determined at both fictive and

Materials scienceSpecific heatAnalytical chemistryCondensed Matter PhysicsAmorphous solidchemistry.chemical_compoundDifferential scanning calorimetrychemistryContent (measure theory)MaltitolPhysical and Theoretical ChemistryGlass transitionThermal analysisInstrumentationQuantitative analysis (chemistry)Thermochimica Acta
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Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

1999

A rapid, sensitive and reproducible high-performance liquid chromatographic assay for busulfan in human plasma was developed. After extraction of plasma samples with acetonitrile and methylene chloride, busulfan and the internal standard [1,5-bis(methanesulfonyloxy)pentane] were derivatized with 8-mercaptoquinoline to yield fluorescent compounds which were detected with a fluorescence detector equipped with filters of 360 nm (excitation) and 425 nm (emission). Calibration graphs showed a linear correlation (r>0.9990) over the concentration range of 20-2000 ng/ml. The recovery of busulfan from plasma standards was 70+/-5%. The detection and quantification limits for busulfan in plasma sample…

ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral ChemistryReference StandardsHigh-performance liquid chromatographyFluorescenceSensitivity and SpecificityFluorescence spectroscopyPentanechemistry.chemical_compoundSpectrometry FluorescenceCalibrationmedicineHumansDerivatizationQuantitative analysis (chemistry)Antineoplastic Agents AlkylatingBusulfanBusulfanChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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Election Campaigning Online

2005

This article presents an integrated quantitative analysis of the functional, formal and content-related aspects of German political party websites during the 2002 National Elections. The analysis is guided by the normalization hypothesis of cyberspace, which infers a transfer of ‘real-world’ features of politics to the Internet. Results provide empirical evidence of a limited normalization in German e-campaigning: indeed, German party websites primarily serve information functions while neglecting interactive features. Yet, no overall gap in professionalism is found between major and minor parties analysed. Finally, online campaigning is dominated by a high level of self-referentiality but…

business.industryCommunication05 social sciences050801 communication & media studiesPublic relationsLanguage and Linguisticslanguage.human_language0506 political sciencePersonalizationGermanPolitics0508 media and communicationsQuantitative analysis (finance)Content analysisPolitical science050602 political science & public administrationlanguagebusinessEuropean Journal of Communication
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Qualitative and quantitative analysis of the phenazepam tablets 12 years after manufacturing

2007

StatisticsPhenazepammedicinePharmaceutical ScienceQuantitative analysis (chemistry)Mathematicsmedicine.drugEuropean Journal of Pharmaceutical Sciences
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Flow injection-FTIR determination of dithiocarbamate pesticides

2000

A flow injection Fourier transform infrared spectrometric procedure has been developed for the determination the dithiocarbamate pesticides Ziram and Thiram in solid samples. All the operations involved, such as extraction, filtration and measurement, were integrated in the experimental set-up in order to avoid excessive manipulation of samples and standards. Ultrasonic assisted and mechanical extraction were evaluated for the solubilization of the analytes and, additionally, the effect of carrier flow rate, sample loop volume and the ratio between sample mass and volume of solvent employed were studied. Quantitative extractions with chloroform were obtained for both Ziram and Thiram, after…

Flow injection analysisDetection limitZiramThiramChromatographyChemistryExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAbsorbancechemistry.chemical_compoundElectrochemistryEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyThe Analyst
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Determination of organic and inorganic anions in insect haemolymph and midgut contents by ion chromatography

1997

A simple and rapid ion-exchange chromatographic method with conductimetric detection for the determination of carboxylic acids (succinic, malic and citric) and inorganic anions (chloride, phosphate and sulphate) in haemolymph and midgut content of Lepidoptera larvae is provided. The mobile phase is 0.975 mM phthalic acid at pH 4.1. The procedure of sample extractions was simple. Comparison of the results with whose reported in the bibliography showed that the values were similar. The ion-exchange chromatographic–conductimetric detection method permits the analysis of various organic and inorganic anions in small biological samples.

ChromatographyConductometrybiologyfungiOrganic ChemistryIon chromatographyGeneral MedicinePhosphateBiochemistryChlorideAnalytical ChemistryPhthalic acidchemistry.chemical_compoundchemistrymedicinebiology.proteinCarboxylateQuantitative analysis (chemistry)medicine.drugOrganic anionJournal of Chromatography A
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Comparison of extraction and clean-up procedures for analysis of zearalenone in corn, rice and wheat grains by high-performance liquid chromatography…

2002

The aim of this work was the optimization of some procedures usually used in the analysis of zearalenone (ZEA) in corn and other cereals by high-performance liquid chromatography (HPLC) with photodiode array and/or fluorescence detection. The comparison of five extraction solvents is presented. Three solid-phase extraction cartridges (C-18, silica, Florisil) and immuno-affinity columns were also compared to obtain the best recovery of the mycotoxin with the minimal presence of co-extractives in the chromatograms. Mixtures of methanol-1% aqueous NaCl (80.20 or 60:40 v/v) were the best extraction solvents. Florisil provided higher recovery of ZEA than C-18, and silica proved unsuitable. The i…

FusariumHealth Toxicology and MutagenesisFood ContaminationToxicologyHigh-performance liquid chromatographyZea mayschemistry.chemical_compoundHumansEstrogens Non-SteroidalMycotoxinZearalenoneChromatography High Pressure LiquidTriticumDetection limitChromatographybiologyChemistryExtraction (chemistry)Public Health Environmental and Occupational HealthOryzaGeneral Chemistrybiology.organism_classificationSeparation processChemistry (miscellaneous)ZearalenoneEdible GrainQuantitative analysis (chemistry)Food AnalysisFood ScienceFood additives and contaminants
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Determination of α-Tocopherol in Plasma by High Performance Liquid Chromatography with Fluorescence Detection and Stability of α-Tocopherol under Dif…

2011

In order to study the clinical effects of the antioxidant alpha-tocopherol (tocofersolan, CAS 30999-06-5) a simple, robust, sensitive and reliable high performance liquid chromatography (HPLC) method using fluorescence detection for the daily measurement of alpha-tocopherol concentration in plasma is described. Several methods of HPLC analysis using fluorescence techniques are published, however, investigations of the stability of alpha-tocopherol during sample preparation under different conditions are relevant in the routine measurements and have to date not been reported. Therefore a modified method, both sensitive and robust, qualified for the day-by-day measurement of alpha-tocopherol …

ChromatographyChemistryalpha-TocopherolAnalytical chemistryReproducibility of Resultsfood and beveragesLiquid nitrogenHigh-performance liquid chromatographyFluorescenceFluorescence spectroscopyTocofersolanSpecimen Handlingchemistry.chemical_compoundSpectrometry FluorescenceDrug DiscoveryHumansSample preparationTocopherolQuantitative analysis (chemistry)Chromatography High Pressure LiquidArzneimittelforschung
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On-line solvent recycling: a tool for the development of clean analytical chemistry in flow injection Fourier transform infrared spectrometry. Determ…

1998

Abstract A flow injection strategy has been developed for the direct determination of ketoprofen in pharmaceuticals by Fourier transform infrared spectrometry also incorporating a distillation unit which allows the carbon tetrachloride employed to dissolve samples and standards and used as a carrier to be recovered on-line. The system developed permits a drastic reduction of reagent consumption and easy and fast sampling and cleaning of the measurement cell. For the quantification of ketoprofen in pharmaceuticals the carbonyl bands at 1712 and 1666 cm −1 were employed and the developed method provided a 3 σ limit of detection of 0.04 mg ml −1 , a dynamic range up to 10 mg ml −1 and typical …

Detection limitChromatographyDynamic rangeChemistryAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical Chemistrylaw.inventionSolventsymbols.namesakeFourier transformlawReagentsymbolsEnvironmental ChemistryQuantitative analysis (chemistry)DistillationSpectroscopyAnalytica Chimica Acta
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