Search results for "Micellar"

showing 10 items of 185 documents

Determination of barbiturates in urine by micellar liquid chromatography and direct injection of sample.

2000

Abstract A liquid chromatographic procedure for the determination of six barbiturates (barbital, diallyl barbituric acid, phenobarbital, butabarbital, amobarbital and pentobarbital) in urine samples is described. The proposed system uses a Spherisorb octadecyl-silane ODS-2 C 18 analytical column and a guard column of similar characteristics. The UV detector was set at 240 nm. A study to select adequate composition of the micellar mobile phase for the separation of these compounds in urine samples is performed. Maximum resolution was achieved with a 0.07 M sodium dodecylsulphate-0.3% propanol at pH 7.4 eluent. Limits of detection at 240 nm were ranged between 0.13 μg ml −1 for diallyl barbit…

AmobarbitalClinical BiochemistryPharmaceutical Science1-PropanolBarbitalAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyDrug DiscoverymedicineHumansSample preparationPentobarbitalSpectroscopyDetection limitBarbituric acidChromatographyButabarbitalHydrogen-Ion ConcentrationchemistryAlkanesulfonic AcidsMicellar liquid chromatographyBarbitalPhenobarbitalBarbituratesCalibrationAmobarbitalmedicine.drugChromatography LiquidJournal of pharmaceutical and biomedical analysis
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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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Control of propranolol intake by direct chromatographic detection of alpha-naphthoxylactic acid in urine.

2002

A rapid chromatographic procedure with a C18 column, a mobile phase of 0.15 M sodium dodecyl sulfate (SDS)-10% (v/v) 1-propanol at pH 3 (0.01 M phosphate buffer), and fluorimetric detection, is reported for the control of propranolol (PPL) intake in urine samples, which are injected directly without any other treatment than filtration. The peak of PPL was only observed in samples taken a few hours after ingestion of the drug due to its extensive conjugation and metabolisation. The detection of several unconjugated PPL metabolites was therefore considered: desisopropylpropranolol (DIP), propranolol glycol (PPG), alpha-naphthoxylactic acid (NLT) and alpha-naphthoxyacetic acid (NAC). NLT showe…

AnalyteClinical BiochemistryAdrenergic beta-AntagonistsUrinePropranololBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundOral administrationmedicineHumansSodium dodecyl sulfateDetection limitChromatographyElutionReproducibility of ResultsCell BiologyGeneral MedicinePropranololSpectrometry FluorescencechemistryMicellar liquid chromatographyLactatesmedicine.drugChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Micellar liquid chromatography determination of rivaroxaban in plasma and urine. Validation and theoretical aspects.

2019

A Micellar Chromatographic method to determine rivaroxaban in plasma and urine has been developed. The samples were dissolved in the mobile phase (SDS 0.05 M – 1-propanol 12.5%, phosphate buffered at pH 7) and 20 μL directly injected, avoiding the extraction and purification steps. Using a C18 column and running under isocratic mode at 1 mL/min, analyte was eluted without interference from the matrix in <6.0 min. The detection absorbance wavelength was set to 250 nm. The procedure was validated by Food and Drug Administration guidelines in terms of: system suitability, calibration range (0.05–5 mg/L), linearity, sensitivity, robustness, carry-over effect, specificity, accuracy (−11.1 to 4.2…

AnalyteClinical Biochemistrypartition equilibriumUrine030226 pharmacology & pharmacy01 natural sciencesBiochemistryAnalytical Chemistrymicellar chromatographyMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineRivaroxabanLimit of Detectiondirect injectionHumansMicellesvalidationChromatographyElutionanticoagulant010401 analytical chemistryExtraction (chemistry)biological fluidReproducibility of ResultsCell BiologyGeneral MedicinePhosphate0104 chemical scienceschemistryMicellar liquid chromatographyPartition equilibriumLinear ModelsChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Comparison between micellar liquid chromatography and capillary zone electrophoresis for the determination of hydrophobic basic drugs in pharmaceutic…

2007

[EN] The determination of highly hydrophobic basic compounds by means of conventional reversed-phase liquid chromatographic methods has several drawbacks. Owing to the characteristics of micellar liquid chromatography (MLC) and capillary electrophoresis (CE), these techniques could be advantageous alternatives to reversed-phase chromatographic methods for the determination of these kinds of compounds. The objective of this study was to develop and compare MLC and CE methods for the determination of antipsychotic basic drugs (amitryptiline, haloperidol, perphenazine and thioridazine) in pharmaceutical preparations. The chromatographic determination of the analytes was performed on a Kromasil…

AnalyteResolution (mass spectrometry)Capillary actionClinical BiochemistrySensitivity and SpecificityBiochemistryAnalytical ChemistryCapillary electrophoresischemistry.chemical_compoundCapillary electrophoresisBromideDrug DiscoveryQUIMICA ANALITICAAntipsychotic drugsMolecular BiologyPharmacologyDetection limitChromatographyElectrophoresis CapillaryReproducibility of ResultsGeneral MedicineHydrogen-Ion ConcentrationReference StandardsElectrophoresisPharmaceutical PreparationschemistryHydrophobic basic drugsMicellar liquid chromatographyCalibrationPharmaceutical analysisHydrophobic and Hydrophilic InteractionsCetyltrimethylammonium bromideMicellar liquid chromatographyAntipsychotic AgentsChromatography Liquid
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Characterization of poly(4-vinylpyridine 1-oxide) by free-solution capillary electrophoresis and micellar electrokinetic chromatography

2008

The migration characteristics of poly(4-vinylpyridine 1-oxide) (PVP-NO) in phosphate buffers of acidic pH (20 mM H 3 PO 4 or NaH 2 PO 4 ) have been studied using both free-solution capillary electrophoresis (FSCE) and MEKC. To inhibit adsorption, 250 mM o-phosphoethanolamine (2-aminoethyl dihydrogen phosphate) was used. In FSCE, PVP-NO showed a narrow peak and a broader band, both having anionic behavior. These peak and band were attributed to the free and aggregated or micellized PVP-NO forms, respectively. According to surface tension measurements, the CMC of SDS in the BGE was 1.8 and 0.48 mM in the absence and in the presence of 1000 μpg/mL PVP-NO, respectively, and the association of t…

AnionsDetergentsClinical BiochemistryOxidemacromolecular substancesBuffersBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical ChemistrySurface tensionchemistry.chemical_compoundCapillary electrophoresisAdsorptionSurface TensionMicellesLaunderingchemistry.chemical_classificationChromatographyChromatographytechnology industry and agricultureElectrophoresis CapillaryWaterPolymerPhosphateOrganophosphatesSolutionschemistryPolyvinylpyridine N-OxideELECTROPHORESIS
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Development and validation of a procedure for estimating the hydrophobicity of structurally unrelated compounds by micellar liquid chromatography

1999

Reversed-phase liquid chromatography has been used most often to estimate values of log P, but despite years of study, there is no universally accepted method of performing these estimations. The main problem has to do with the fact that the hydrophobic parameter, log k w , depends on the hydrogen bond acceptor-donor character of the compounds. The use of micellar mobile phases to perform these estimations is evaluated here, and the influence of the nature of the surfactant (anionic, cationic, and nonionic) on the log k-log P relationships is studied. The use of a nonionic surfactant, such as Brij35, to prepare the mobile phases provided adequate results regardeless of the hydrogen bond acc…

AnthraceneChromatographyHydrogen bondAnalytical chemistryCationic polymerizationGeneral MedicineMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographyPyrene
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Volumes, heat capacities and solubilities of amyl compounds in decyltrimethylammonium bromide aqueous solutions

1989

Apparent molar heat capacities and volumes of amylamine (PentNH2) 0.02m, capronitrile (PentCN) 0.02m and nitropentane (PentNO2) 0.009m in decyltrimethylammonium bromide (DeTAB) micellar solutions, in water and in octane were measured at 25°C. By assuming that their concentration approaches the standard infinite dilution state, heat capacities and volumes were rationalized by means of previously reported equations following which the distribution constant between the aqueous and the micellar phase and heat capacity and volume of the additives in both phases are simultaneously derived. The present results are compared to those we have previously obtained for pentanol (PentOH). The thermodynam…

Aqueous solutionChemistryDistribution constantBiophysicsThermodynamicsBiochemistryHeat capacityDilutionchemistry.chemical_compoundMolar volumeMicellar solutionsOrganic chemistryPhysical and Theoretical ChemistrySolubilityMolecular BiologyOctaneJournal of Solution Chemistry
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Enthalpies of mixing of some nitriles aqueous solutions with dodecylsurfactants micellar solutions

1988

The enthalpies of mixing of some n-nitriles (from acetonitrile to valeronitrile) aqueous solutions with dodecyltzimethylammonium bromide, sodium dodecylsulfate and dodecyltzimethylammonium oxide micellar solutions were determined. The measurements were performed by systematically changing the surfactant concentration at a given solute concentration. The experimental enthalpies were rationalized in terms of the standard enthalpy of transfer of solute from the aqueous to the micellar phase and of the distribution constant between the two phase. Information on the effect of the nature of the surfactant on the standard thermodynamic quantities of transfer(ΔG t o , ΔH t o , TΔS t o ) is reported…

Aqueous solutionChemistryDistribution constantEnthalpyInorganic chemistryBiophysicsEntropy of mixingBiochemistryMicelleStandard enthalpy of formationPhase (matter)Micellar solutionsPhysical chemistryPhysical and Theoretical ChemistryMolecular BiologyJournal of Solution Chemistry
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Micellar Liquid Chromatography: Fundamentals

2015

The reversed phase liquid chromatography (RPLC) mode with surfactant above the critical micellar concentration (CMC) has been called micellar liquid chromatography (MLC). In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and micellar pseudo-phase. Surfactant adsorption on the porous RPLC packing affects chromatographic retention, owing to the change of diverse surface properties of the stationary phase. In pure micellar systems, the retention behavior is explained by considering three phases or environments: surfactant-modified stationary phase, bulk aqueous solvent, and mice…

Aqueous solutionColumn chromatographyAqueous normal-phase chromatographyChemistryMicellar liquid chromatographyHydrophilic interaction chromatographytechnology industry and agricultureAnalytical chemistrylipids (amino acids peptides and proteins)macromolecular substancesReversed-phase chromatographyMicelleMicellar electrokinetic chromatography
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