Search results for "solution"

showing 10 items of 5638 documents

Solution Properties of Polyelectrolytes. VI. Secondary Effects in Aqueous Size-Exclusion Chromatography

1990

Abstract An independent analysis of different operational variables in aqueous size exclusion chromatography of poly electrolytes has been carried out using a silica-based support. The effect of polyion concentration, pH and ionic strength on sodium polystyrenesulfonate calibration plots has been investigated. Finally, a novel semi-empirical model has been developed from thermodynamic considerations which relates the support effective pore volume to the polyelectrolyte molecular weight and qualitatively describes secondary effects.

ChromatographyAqueous solutionVolume (thermodynamics)Ionic strengthChemistrySodiumSize-exclusion chromatographyMolecular Medicinechemistry.chemical_elementElectrolytePolyelectrolyteJournal of Liquid Chromatography
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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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Chromatographic Efficiency in Micellar Liquid Chromatography: Should it Be Still a Topic of Concern?

2013

Micellar liquid chromatography (MLC) was first proposed as an attractive alternative to avoid the use of organic solvents. It was soon apparent that pure micellar solutions yield poor efficiencies. This problem was remediated by the addition of a small amount of an organic solvent. However, the general opinion of the poor peak shape has prevailed as a handicap for MLC, in spite of the fact that the hybrid mode often offers similar or even improved efficiencies (for basic compounds) relative to that attained in the hydro-organic mode. Only the efficiencies for apolar non-ionizable compounds are still clearly inferior. This work describes the type of interactions and polarity changes with org…

ChromatographyChemistryHydrophilic interaction chromatographyAnalytical chemistryFiltration and SeparationSilanol effect suppressionAnalytical ChemistryAdsorptionHybrid mobile phasesPulmonary surfactantMicellar liquid chromatographyYield (chemistry)Mass transferBand broadeningMicellar solutionsMass transferenceWettingMicellar liquid chromatographyStationary phase architecture and wettingSeparation & Purification Reviews
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2020

In this study, the potential for correlation between disintegration and dissolution performance of enteric-coated (EC) dosage forms was investigated. Different enteric hard shell capsule formulations containing caffeine as model drug were tested for disintegration (in a compendial disintegration tester) and for dissolution in both USP type I (basket) and type II (paddle) apparatuses using different media. Overall, good correlations were obtained. This was observed for both the basket and the paddle apparatus, indicating that the use of disintegration testing as a surrogate for dissolution testing (allowed by International Conference on Harmonization (ICH) for immediate release dosage forms …

ChromatographyChemistryPharmaceutical ScienceCapsule02 engineering and technology021001 nanoscience & nanotechnologyPositive correlation030226 pharmacology & pharmacySmall intestineDosage formIn vitro03 medical and health sciences0302 clinical medicinemedicine.anatomical_structuremedicineDissolution testingImmediate release0210 nano-technologyDissolutionPharmaceutics
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Determination of Anticonvulsant Drugs in Pharmaceutical Preparations by Micellar Liquid Chromatography

2004

A micellar liquid chromatographic method for quality control of pharmaceutical preparations (capsules, pills, tablets, injections, drops, and suppositories) containing the anticonvulsant drugs acetazolamide, carbamacepine, chlordiazepoxide, diazepam, ethosuximide, phenytoin, phenobarbital, and zopiclone has been developed. This methodology involves the use of micellar solutions of cetyltrimethylammonium bromide (CTAB) as mobile phases and UV detection. The proposed approach is rapid and reproducible. Sample preparation only requires dissolution with micellar solvent and adequate dilution with the mobile phase before injection into the chromatographic system.

ChromatographyChemistrymedicine.medical_treatmentClinical Biochemistrytechnology industry and agriculturePharmaceutical ScienceBiochemistryDosage formAnalytical ChemistryChlordiazepoxideSolventEthosuximideAnticonvulsantMicellar liquid chromatographyMicellar solutionsmedicinelipids (amino acids peptides and proteins)Sample preparationmedicine.drugJournal of Liquid Chromatography & Related Technologies
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Peak deconvolution in one-dimensional chromatography using a two-way data approach.

2002

A deconvolution methodology for overlapped chromatographic signals is proposed. Several single-wavelength chromatograms of binary mixtures, obtained in different runs at diverse concentration ratios of the individual components, were simultaneously processed (multi-batch approach), after being arranged as two-way data. The chromatograms were modelled as linear combinations of forced peak profiles according to a polynomially modified Gaussian equation. The fitting was performed with a previously reported hybrid genetic algorithm with local search, leaving all model parameters free. The approach yielded more accurate solutions than those found when each experimental chromatogram was fitted in…

ChromatographyChromatographyResolution (mass spectrometry)Matching (graph theory)Chemistrybusiness.industryOrganic ChemistryBinary numberGeneral MedicineBiochemistryAnalytical Chemistrysymbols.namesakeData Interpretation StatisticalGaussian functionsymbolsFigure of meritLocal search (optimization)DeconvolutionbusinessLinear combinationJournal of chromatography. A
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A theoretical plate model accounting for slow kinetics in chromatographic elution.

2011

The chromatographic elution has been studied from different perspectives. However, in spite of the simplicity and evident deficiencies of the plate model proposed by Martin and Synge, it has served as a basis for the characterization of columns up-to-date. This approach envisions the chromatographic column as an arbitrary number of theoretical plates, each of them consisting of identical repeating portions of mobile phase and stationary phase. Solutes partition between both phases, reaching the equilibrium. Mobile phase transference between the theoretical plates is assumed to be infinitesimally stepwise (or continuous), giving rise to the mixing of the solutions in adjacent plates. This yi…

ChromatographyComputer simulationElutionChemistryOrganic ChemistryKineticsGeneral MedicineModels TheoreticalKinetic energyBiochemistryAnalytical ChemistryVolumetric flow rateSolutionsKineticsPharmaceutical PreparationsMass transferPartition (number theory)Theoretical plateChromatography High Pressure LiquidJournal of chromatography. A
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Prediction of peak shape as a function of retention in reversed-phase liquid chromatography

2004

Optimisation of the resolution of multicomponent samples in HPLC is usually carried out by changing the elution conditions and considering the variation in retention of the analytes, to which a standard peak shape is assigned. However, the change in peak shape with the composition of the mobile phase can ruin the optimisation process, yielding unexpected overlaps in the experimental chromatograms for the predicted optimum, especially for complex mixtures. The possibility of modelling peak shape, in addition to peak position, is therefore attractive. A simple modified-Gaussian model with a parabolic variance, which is a function of conventional experimental parameters: retention time (tR), p…

ChromatographyElutionChemistryOrganic ChemistryResolution (electron density)Analytical chemistryGeneral MedicineReversed-phase chromatographyFunction (mathematics)Models TheoreticalBiochemistryHigh-performance liquid chromatographyStandard deviationAnalytical ChemistryApproximation errorPhase (matter)Chromatography LiquidJournal of Chromatography A
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Levels in the interpretive optimisation of selectivity in high-performance liquid chromatography: a magical mystery tour.

2006

Interpretive approaches for selectivity optimisation, which are those supported by retention models, are able to exploit efficiently the capabilities of the chromatographic system. The resolution of a mixture is usually faced in a first trial by looking for a unique experimental condition, able to resolve all compounds in the sample. If this is not possible, the problem can be outlined with less ambitious aims, focusing on only some compounds. In an extreme case, a single analyte can be individually optimised. Current strategies that give answer to the different goals pursued in the analysis, which are classified as total, partial and specific, are reviewed. Optimisation oriented to deconvo…

ChromatographyExploitChemistryComputer aidOrganic ChemistryAdrenergic beta-AntagonistsReproducibility of ResultsSample (statistics)General MedicineResolution (logic)Models TheoreticalBiochemistryHydrocarbons AromaticAnalytical ChemistryMultivariate AnalysisGradient elutionDeconvolutionAmino AcidsChromatography High Pressure LiquidJournal of chromatography. A
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Alkaline haematin D-575, a new tool for the determination of haemoglobin as an alternative to the cyanhaemiglobin method. I. description of the method

1984

A new method for the rapid and accurate measurement of haemoglobin has been developed as an alternative to the conventional cyanhaemiglobin method. This method is based on the conversion of all haeme, haemoglobin, and haemiglobin species into a stable end product by an alkaline solution of a non-ionic detergent ('AHD reagent'). The reaction product, designated as alkaline haematin D-575, is extremely stable and shows a characteristic absorption peak at 575 nm. As compared to the cyanhaemiglobin method, the determination of haemoglobin by alkaline haematin D-575 offers several advantages such as (1) extreme stability of the AHD reagent and the conversion product, (2) decreased conversion tim…

ChromatographyHemeproteinOctoxynolChemistryStereochemistrySmokingBiochemistry (medical)Clinical BiochemistryHemeGeneral MedicineHydrogen-Ion ConcentrationBiochemistryHaematinPolyethylene GlycolsReaction productPhotometryHemoglobinschemistry.chemical_compoundBasic solutionReagentHeminHumansHemoglobinClinica Chimica Acta
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