Search results for "Quantitative"

showing 10 items of 2409 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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Indirect Quantitative Determination of Organolithium Compounds by Gas Chromatography

1976

ChromatographyChemistryOrganolithium compoundsGeneral MedicineGas chromatographyQuantitative determinationAnalytical ChemistryJournal of Chromatographic Science
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Chromatographic determination of caffeine in pharmaceutical formulations using micellar mobile phases

1996

An HPLC procedure is described for the determination of caffeine in pharmaceutical preparations. A Spherisorb octadecylsilane ODS-2 C18 analytical column and spectrophotometric detection at 273 nm were used. The chromatographic behaviour of caffeine with different micellar eluents containing sodium dodecyl sulphate (SDS) is described. The determination of caffeine in pharmaceutical preparations was performed by use of a mobile phase containing 0.05 M sodium dodecylsulphate (SDS) and 1.5% propanol at pH7. At a 6.0 μg mL−1 concentration level the peak area and peak height repeatability were 2.6 and 2.4%, respectively. The application of the proposed method to the analysis of five pharmaceutic…

ChromatographyChemistrySodiumOrganic ChemistryClinical Biochemistrychemistry.chemical_elementRepeatabilityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundMicellar liquid chromatographySpherisorb octadecylsilaneCaffeineQuantitative analysis (chemistry)
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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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Extractive Spectrophotometric Determination of Ondansetron by Ion-Pair Formation with Bromocresol Green

1996

Abstract An empirical spectrophotometric procedure for the determination of the antiemetic ondansetron is carried out. The method is based on the formation of a 1:1 ion pair with bromocresol green in the pH range over 3.2 – 4.4, extraction into chloroform layer and spectrophotometric measurement at 420.8 nm. The calibration graph is linear over the range 0.1 – 20 μg ml−1 ondansetron, with a relative standard deviation of 2.7%; the influence of foreign substances is also studied. The method is applied to ondansetron determination in human urine.

ChromatographyChloroformBromocresol greenmedicine.diagnostic_testCalibration curveBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Ion pairsBiochemistryAnalytical ChemistryOndansetronchemistry.chemical_compoundchemistrySpectrophotometryElectrochemistrymedicineQuantitative analysis (chemistry)Spectroscopymedicine.drugAnalytical Letters
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Improved sample preparation for the testosterone hydroxylation assay using disposable extraction columns

1992

The preparation of samples for injection into a high-performance liquid chromatograph from assay mixtures for the determination of cytochrome P-450-dependent testosterone hydroxylation has been substantially facilitated. By replacing the multiple cumbersome extraction steps of the conventional method with a single column extraction the time for sample preparation was reduced from hours to minutes. The new procedure also yields better recoveries for most of the testosterone metabolites than the original protocol. The use of extraction columns for sample preparation allows the simultaneous treatment of a large number of samples or even the automation of the whole assay procedure. The modified…

ChromatographyChromatography10050 Institute of Pharmacology and Toxicology610 Medicine & health1600 General ChemistryGeneral ChemistryHydroxylationHigh-performance liquid chromatographyHydroxylationchemistry.chemical_compoundchemistry570 Life sciences; biologySample preparationTestosteroneQuantitative analysis (chemistry)
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Determination of Lobenzarit Disodium in Human Plasma by High-Performance Liquid Chromatography

1998

Abstract A reversed-phase high performance liquid chromatographic procedure was developed for determination of lobenzarit disodium in human plasma over the range 0.5−17.5 μg/mL with diphenylamine as internal standard. Plasma samples were extracted with acetonitrile and an aliquot was injected onto a Lichrospher 100 RP-18 column with ultraviolet absorbance detection at 308 nm. Composition of the mobile phase was acetonitrile-water-glacial acetic acid (50:50:0.2 v/v/v).

ChromatographyClinical BiochemistryDiphenylaminePharmaceutical ScienceReversed-phase chromatographyLobenzaritBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryAcetic acidchemistry.chemical_compoundchemistrymedicineCarboxylateAcetonitrileQuantitative analysis (chemistry)medicine.drugJournal of Liquid Chromatography & Related Technologies
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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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Extraktionschromatographische trennung der freien uroporphyrinisomere i und iii und deren simultane quantitative bestimmung

1968

Abstract Separation and simultaneous quantitative determination of the free uroporphyrin isomers I and III by means of extraction chromatography Separation and quantitative determination of the uroporphyrin isomers I and III in the acid from can be performed simultaneously in the partition system tri-n-butylphosphate/I N hydrochloric acid using columns with a large number of theoretical plates (N) = 300-450). The eluent is passed through a flow cuvette and the transmission is recorded continuously. The transmission peaks of the isomers are digitized and transformed into extinction values. By integrating the extinction peaks, the amount of the uroporphyrins can be evaluated from the correspo…

ChromatographyElutionOrganic ChemistryAnalytical chemistryHydrochloric acidGeneral MedicineUroporphyrinsBiochemistryQuantitative determinationAnalytical ChemistryCuvettechemistry.chemical_compoundColumn chromatographychemistryPartition (number theory)Theoretical plateJournal of Chromatography A
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Determination of sialic acid and gangliosides in biological samples and dairy products: A review

2009

Gangliosides are sphingolipids containing one or more moieties of sialic acid in their structure. Both gangliosides and sialic acid are bioactive compounds related to animal physiology. Due to their biological relevance, analytical methods adapted to each type of matrix have been developed over time. The present study reviews the main methods applied to the analysis of sialic acid and gangliosides in biological samples and dairy products.

ChromatographyGangliosideChromatographySpectrum AnalysisClinical BiochemistryPharmaceutical ScienceSphingolipidN-Acetylneuraminic AcidAnalytical ChemistrySialic acidcarbohydrates (lipids)chemistry.chemical_compoundGlycolipidBiochemistrychemistryMilk productsGangliosidesDrug DiscoveryAnimalsDairy ProductsQuantitative analysis (chemistry)SpectroscopyJournal of Pharmaceutical and Biomedical Analysis
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