Search results for "liquid"

showing 10 items of 4351 documents

A new ionic liquid dimethyldinonylammonium bromide as a flow modifier for the simultaneous determination of eight carboxylates by capillary electroph…

2005

Two new methods of capillary zone electrophoresis based on aqueous phosphate running buffers with UV spectrophotometric detection were developed and optimized for the determination of eight carboxylates as copper complexes. Metalcomplexes are negatively charged, so measurements were made as anion analyses with flow reversal in the capillary. Two flow modifiers were used: a common tetradecyltrimethylammonium bromide (TTAB) and a new ionic liquid dimethyldinonylammonium bromide (DMDNAB). The methods were compared to each other. Better separation was achieved with DMDNAB as the flow modifier. Method development was done using a fused silica capillary (61 cm x 50 microm i.d.). Optimization was …

ChromatographyAqueous solutionmedicine.diagnostic_testCapillary actionOrganic ChemistryAnalytical chemistryCarboxylic Acidschemistry.chemical_elementElectrophoresis CapillaryGeneral MedicineBiochemistryCopperTrimethyl Ammonium CompoundsAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundElectrophoresisCapillary electrophoresischemistrySpectrophotometryIonic liquidmedicineSpectrophotometry UltravioletCarboxylateWater Pollutants ChemicalJournal of chromatography. A
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Determination of Caffeine in Analgesic Formulations Using the Apparent Content Curves Method

1994

Abstract The determination of caffeine by UV spectroscopy in pharmaceutical samples, containing different compounds which provide spectral interferences as aspirin, paracetamol, chlorfeniramine or propylphenazone, is carried out. The proposed procedure is based on the apparent content curves method in order to resolve binary, ternary and multicomponent mixtures. Results obtained are, in all cases, in agreement with contents found by a HPLC procedure used as reference method.

ChromatographyBiochemistry (medical)Clinical BiochemistryAnalgesicAnalytical chemistryBiochemistryHigh-performance liquid chromatographyDosage formAnalytical Chemistrychemistry.chemical_compoundUltraviolet visible spectroscopychemistryContent (measure theory)ElectrochemistryTernary operationCaffeineQuantitative analysis (chemistry)SpectroscopyAnalytical Letters
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Influence of the addition of modifiers on solute-micelle interaction in hybrid micellar liquid chromatography

1998

In reversed-phase micellar liquid chromatography (MLC) organic modifiers are usually added to the mobile phase to modify the eluent strength and to increase the efficiency of the chromatographic peaks. The effect of the modifiers methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, acetonitrile and tetrahydrofuran on the critical micelle concentration (cmc) of the anionic surfactant sodium dodecylsulphate (SDS) has been studied to enable understanding of the interactions between solute, micelles and bulk liquid in such hybrid eluents. Methanol, acetonitrile and tetrahydrofuran increased thecmc, whereas the other alcohols reduced its value. For butanol and pentanol, which partition into the…

ChromatographyButanolOrganic ChemistryClinical BiochemistryThermodynamics of micellizationAlcoholBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationChromatographia
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Simple high-performance liquid chromatographic assay for polyamines and their monoacetyl derivatives.

1993

A rapid reversed-phase high-performance liquid chromatographic method, using pre-column derivatization with benzoyl chloride and ultraviolet detection at 254 nm, was developed for the simultaneous measurement of polyamines and their monoacetyl derivatives. Calibration curves were linear for concentrations from 1.25 to 25 nmol/ml. The method was employed to assay these compounds in chick embryo retina explants using organic solvent extraction and 1,7-diaminoheptane as an internal standard. This simple and sensitive method can be applied to routine determinations of these compounds in various biological samples.

ChromatographyCalibration curveOrganic solventExtraction (chemistry)Reproducibility of ResultsAcetylationGeneral ChemistryChick EmbryoDiaminesHigh-performance liquid chromatographyRetinachemistry.chemical_compoundBenzoyl chloridechemistryPolyaminesAnimalsSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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Gas-liquid chromatographic analyses

1985

ChromatographyCapillary actionChemistryOrganic ChemistryOrganic chemistryGeneral MedicineBiochemistryGas liquid chromatographicAnalytical ChemistryJournal of Chromatography A
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Synchronized gradient elution in capillary liquid chromatography

2013

Abstract The synchronization of injection valve operation and gradient elution in capillary liquid chromatography (cHPLC) is studied. Focus is placed on the cHPLC systems which rely on the splitting of a primary flow to provide the much smaller secondary flow required at the injection device and analytical column. Owing to the tiny secondary flow rates, synchronization is necessary to achieve proper optimization of gradient elution methods. Otherwise, there is a risk of having the analytes totally or partially eluted in the initial isocratic conditions, and there is no control on the actual gradient profile reaching the column. Synchronization is first achieved by switching back the valve t…

ChromatographyCapillary actionElutionChemistryOrganic ChemistryMixing (process engineering)Analytical chemistryBenzeneGeneral MedicineInjectorSecondary flowBiochemistryAnalytical Chemistrylaw.inventionSynchronization (alternating current)Volume (thermodynamics)lawSpark plugChromatography High Pressure LiquidJournal of Chromatography A
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Gas—liquid chromatographic analyses

1984

Abstract The gas choromatographic retention behaviour of veratrole and all nine chlorinated veratroles was studied on SE-30 and OV-351 capillary columns. Temperature programming from 100°C at 6°C min−1 and isothermal operation at 140, 160, 180 and 200°C were used. The complete separation of a mixture was obtained on SE-30, the isomers being eluted in order of their degree of chlorination. On OV-351, however, the 3,4,5-trichloro and tetrachloro isomers overlap with temperature programming, being separated at 140, 160 and 200°C. Retention indices and increments of retention indices for each position of substitution are examined and the effect of increasing temperature on retention is discusse…

ChromatographyCapillary columnCapillary actionElutionChemistryOrganic ChemistryKovats retention indexGeneral MedicineGas chromatographyBiochemistryGas liquid chromatographicIsothermal processAnalytical ChemistryJournal of Chromatography A
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Validation of a high-performance chromatographic method for determination of cefotaxime in biological samples

1999

An analytical method for detecting and quantifying cefotaxime in plasma and several tissues is described. The method was developed and validated using plasma and tissues of rats. The samples were analyzed by reversed phase liquid chromatography (HPLC) with UV detection (254 nm). Calibration graphs showed a linear correlation (r > 0.999) over the concentration ranges of 0.5–200 μg/mL and 1.25–25 μg/g for plasma and tissues, respectively. The recovery of cefotaxime from plasma standards prepared at the concentrations of 25 μg/mL and 100 μg/mL was 98.5 ± 3.5% and 101.8 ± 2.2%, respectively. The recovery of cefotaxime from tissue standards of liver, fat and muscle, prepared at the concentration…

ChromatographyCefotaximePharmacokineticsChemistryCoefficient of variationBlood plasmamedicineReversed-phase chromatographyBiochemistryQuantitative analysis (chemistry)High-performance liquid chromatographyAntibacterial agentmedicine.drugFresenius' Journal of Analytical Chemistry
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Evaluation by HPLC-UV of Polar Pesticides in Rice Fields

1999

ChromatographyChemical PhenomenaChemistry PhysicalHealth Toxicology and MutagenesisPesticide ResiduesOryzaGeneral MedicineHydrogen-Ion ConcentrationPesticideToxicologyPollutionHigh-performance liquid chromatographySurface-Active AgentsSpainEnvironmental sciencePaddy fieldPolarSpectrophotometry UltravioletTrace analysisSample preparationSolid phase extractionPesticidesChromatography High Pressure LiquidHalf-LifeBulletin of Environmental Contamination and Toxicology
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Ultra-high-pressure liquid chromatography tandem mass spectrometry method for the determination of 9 organophosphate flame retardants in water samples

2016

Few methods are available for comprehensive organophosphate flame retardants (PFRs) detection in water and wastewater. Gas chromatography has been employed previously, but this approach is less selective, not amenable for use with deuterated standards and can suffer unfavorable fragmentation. Ultra-high-pressure liquid chromatography tandem mass spectrometry (UHPLC-QqQ-MS/MS) has become the most promising platform, already applied successfully for analysis of selected PFRs in some environmental matrices like water and wastewater. However, the presence of some interferences from the dissolvent, the equipment and the used materials should be taken into account. The procedure involves: The fir…

ChromatographyChemistry010401 analytical chemistryClinical BiochemistryAnalytical chemistryAnalysis of organophosphate flame retardants in water by SPE and UHPLC–MS/MS using a trap column.solid phase extractionWater010501 environmental sciences01 natural sciencesTrap column0104 chemical sciencesOrganophosphate flame retardantsMedical Laboratory TechnologyWastewaterLC–MS/MSLiquid chromatography–mass spectrometryInterferencesLc ms msEnvironmental ScienceGas chromatographyUltra high pressureSolid phase extraction0105 earth and related environmental sciencesComputingMethodologies_COMPUTERGRAPHICSMethodsX
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