Search results for "CHROMATOGRAPHY"

showing 10 items of 5037 documents

A preliminary study on the stability of benzodiazepines in blood and plasma stored at 4 degrees C.

1997

An approach to determine the stability of benzodiazepines and some of their metabolites (n = 13) by means of a routinely applied gas chromatographic method using electron capture detection was made in this preliminary study. Validation data of the method are given. Spiked blood and plasma samples were stored at 4 degrees C and analysed at selected times up to 240 days. The concentrations of all analytes had decreased to at least 60% of the original levels at the end of the observation period. A clear pattern of breakdown could not be established. The data obtained suggest that results from long-term stored samples should be interpreted cautiously. Further investigations concerning the stabi…

AnalyteChromatographyChromatography GasPlasma samplesChemistryObservation periodForensic toxicologyPlasmaForensic MedicinePathology and Forensic MedicineSpecimen HandlingSubstance Abuse DetectionBenzodiazepinesPlasmaBloodReference ValuesRefrigerationReference valuesLinear ModelsHumansGas chromatographyInternational journal of legal medicine
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Development and validation of a fast and sensitive chromatographic assay for all-trans-retinol and tocopherols in human serum and plasma using liquid…

2002

A sensitive HPLC assay for all-trans-retinol, alpha-tocopherol, and gamma-tocopherols in human serum and plasma is reported. Sample preparation is performed in one step and involves precipitation of proteins and extraction of lipids with two volumes of an ethanol-chloroform mixture (3:1, v/v) without I.S. addition. After removal of the precipitated protein, 20 microl aliquots of the supernatant (equivalent to 6.7 microl of serum or plasma) were injected into the HPLC system and analyzed using fluorometric detection. RP-HPLC was performed using a C(18) S3 ODS2 column with a methanol-water step gradient (97:3 to 100) at 1.0 ml/min. The quantification limit expressed as nanograms of analyte pe…

AnalyteChromatographyClinical BiochemistryExtraction (chemistry)RetinolReproducibility of ResultsTocopherolsLiterCell BiologyGeneral MedicineBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundSpectrometry FluorescencechemistryLiquid–liquid extractionHumansSample preparationAll trans retinolVitamin AChromatography High Pressure LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Determination of tannic acid by direct chemiluminescence in a FIA assembly

2002

The determination of tannic acid is performed in a FIA assembly on the basis of the analytical output obtained by oxidation of the acid. The analyte solution was daily prepared in a mixture of quinine as sensitiser and perchloric acid and it was injected into a pure water stream acting as a carrier. This solution merges with the mixture potassium permanganate in perchloric medium and the resulting chemiluminescence is monitored. The method was applied over the range 0.5-20 mg l(-1) of tannic acid with a LOD 100 mug l(-1). The reproducibility was 2.1% and the sample throughput 54 h(-1). The influence of foreign substances was studied and the new method is applied to the determination of tann…

AnalyteChromatographyDosage formAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistrylawTannic acidPhenolsPerchloric acidQuantitative analysis (chemistry)ChemiluminescenceTalanta
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Determination of aliphatic amines in water by liquid chromatography using solid-phase extraction cartridges for preconcentration and derivatization

2001

Bond Elut C18 solid-phase extraction cartridges were used for preconcentration and pre-column derivatization with 3,5-dinitrobenzoyl chloride (DNB) of aliphatic amines in water. Conditions for analyte preconcentration and derivatization (including the volume of sample, concentration of reagent, time of reaction and pH) were investigated, using ethylamine, isopropylamine and dimethylamine as model compounds. On the basis of these studies, a rapid and sensitive method for the determination of aliphatic amines in water is presented. The analytes are retained and purified on the cartridges and then derivatized and desorbed by drawing in succession the DNB solution and acetonitrile. The collecte…

AnalyteChromatographyElutionReproducibility of ResultsBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryElectrochemistryHumansEnvironmental ChemistrySolid phase extractionIsopropylamineAminesEthylamineDerivatizationAliphatic compoundDimethylamineWater Pollutants ChemicalSpectroscopyChromatography LiquidThe Analyst
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Analytical potential of mid-infrared detection in capillary electrophoresis and liquid chromatography: a review.

2010

Literature published in the last decade concerning the use of mid-infrared spectrometry as a detection system in separation techniques employing a liquid mobile phase is reviewed. In addition to the continued use of isocratic liquid chromatographic (LC) techniques, advances in chemometric data evaluation techniques now allow the use of gradient techniques on a routine basis, thus significantly broadening the range of possible applications of LC-IR. The general trend towards miniaturized separation systems was also followed for mid-IR detection where two key developments are of special importance. Firstly, concerning on-line detection the advent of micro-fabricated flow-cells with inner volu…

AnalyteChromatographyEnvironmental analysisChemistryCapillary actionMicrofluidicsBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistryChemometricsCapillary electrophoresisAttenuated total reflectionEnvironmental ChemistrySpectroscopyAnalytica chimica acta
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Determination of the Herbicide Fluometuron by Photo‐induced Chemiluminescence in a Continuous‐flow Multicommutation Assembly

2007

Abstract This study was dealing with the chemiluminometric determination of the selective herbicide Fluometuron or 1,1‐dimethyl‐3‐(α,α,α‐trifluoro‐m‐tolyl)urea, (C10H11F3N2O) with a molecular weight 232.29 belongs to the phenyl urea herbicides family. The analytical strategy is based on the continuous‐flow manifold, multicommutation and the analyte pre‐treatment, the photo‐degradation. The optimization of chemical (pH, medium, temperature, and organized media) and hydrodynamic parameters (volume of reagents and flow rate) was performed by univariant and multiparametric simplex procedure respectively. Analytical figures of merit and the effect of foreign substances were studied. The method r…

AnalyteChromatographyFluometuronContinuous flowBiochemistry (medical)Clinical BiochemistryBiochemistryAnalytical ChemistryVolumetric flow ratelaw.inventionchemistry.chemical_compoundchemistrylawReagentElectrochemistryUreaAnalytical strategySpectroscopyChemiluminescenceAnalytical Letters
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Enhancement of retention predictions in reversed-phase liquid chromatography using reference compounds

2004

Abstract The use of reference compounds to correct errors associated with the preparation of mobile phase is studied, in order to enhance modelling of retention for optimisation purposes in reversed-phase liquid chromatography. The method fits individual retention models for a set of reference compounds, which are present in all injections. In second step, mobile-phase composition is corrected for each chromatogram, according to the fitted models of the reference compounds. The enhanced precision provided by the large number of replicates for the reference compounds is partially propagated to the retention models of the analytes. The approach is assayed in the separation of amino acids, aft…

AnalyteChromatographyIsoindolesChemistryAnalytical chemistryReversed-phase chromatographyBiochemistryAnalytical Chemistrychemistry.chemical_compoundReagentPhase (matter)Environmental ChemistryDerivatizationAcetonitrileSpectroscopyPhthalaldehydeAnalytica Chimica Acta
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Capillary electrophoretic and extraction conditions for the analysis of Catha edulis FORKS active principles

2013

A capillary electrophoretic method, which allowed the detection and separation of the active principles of Catha edulis, i.e. cathinone, cathine and phenylpropanolamine, was developed. A suitable internal standard (nicotinamide), which permitted the quantification of the analytes reducing the variability of the migration times due to EOF changes, was identified. The analytical method was validated, assessing linearity, sensitivity and repeatability, showing optimal features for the analysis of the vegetable material. Moreover extraction conditions were investigated to achieve the exhaustion of the plant material in the fastest and most efficient way to meet the requirements of the Court.

AnalyteChromatographyMolecular StructureCathinonePlant ExtractsChemistryCapillary actionPhenylpropanolamineExtraction (chemistry)Vegetable materialElectrophoresis CapillaryReproducibility of ResultsCathaRepeatabilityPathology and Forensic MedicineElectrophoresisAlkaloidsSettore MED/43 - Medicina LegaleCathinone Cathine PhenylpropanolaminemedicineLawCathinemedicine.drug
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A new 8-oxo-7,8-2 ' deoxyguanosine nanoporous anodic alumina aptasensor for colorectal cancer diagnosis in blood and urine

2021

Many important human diseases, and especially cancer, have been related to the overproduction of 8-oxo-7,8-dihydro-2 '-deoxyguanosine (8-oxo-dG). This molecule is a product of oxidative stress processes over nucleophilic bases in DNA. In this work, an aptasensor for the rapid, selective and accurate detection of this oncomarker is presented. The aptasensor consists of a nanoporous anodic alumina material loaded with a dye and is functionalized with an aptamer-based "molecular gate". In the presence of target 8-oxo-dG, the capping aptamer displaces from the surface due to the high affinity of the analyte with the capping aptamer, thus inducing delivery of the preloaded fluorescent dye. In co…

AnalyteChromatographyNanoporousColorectal cancerChemistryAptamerDeoxyguanosineCancerUrinemedicine.diseaseFluorescenceNanoporeschemistry.chemical_compound8-Hydroxy-2'-DeoxyguanosineAluminum OxidemedicineHumansDeoxyguanosineGeneral Materials ScienceColorectal Neoplasms
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Determination of trimethoprim by the linear absorbances method

1995

The determination of trimethoprim in the presence of dyphylline, proxyphylline, theophylline and caffeine by the linear absorbances method is described. Collinear couples of wavelengths, for the interfering dyphylline-proxyphylline-theophylline-caffeine system (in H2SO4, 0.05 mol/L), are provided in order to allow the determination of the analyte in the presence of these interfering substances.

AnalyteChromatographyProxyphyllineAnalytical chemistryBiochemistryTrimethoprimAnalytical ChemistryDyphyllinechemistry.chemical_compoundchemistrymedicineTrace analysisTheophyllineAnalysis methodmedicine.drugFresenius' Journal of Analytical Chemistry
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