Search results for "cellar"

showing 10 items of 230 documents

Quality control of pharmaceuticals containing non-steroidal anti-inflammatory drugs by micellar liquid chromatography

2002

A liquid chromatographic procedure is described for the determination of acemetacin, diclofenac, indomethacin, ketoprofen, nabumetone, naproxen, piketoprofen, and tolmentin in pharmaceutical preparations. The compounds were separated on a Kromasil C18 analytical column, with a guard column of similar characteristics; the mobile phase was 0.06 M cetyltrimethylammonium bromide, at pH 7, containing 10% 1-butanol. At a flow rate of 1 mL min−1 the elution time of the most retained compound was 23 min. Limits of detection were between 0.01 μ g mL−1 for diclofenac and 0.2 μ g mL−1 for naproxen. The proposed method enables the determination of non-steroidal anti-inflammatory drugs in pharmaceutical…

KetoprofenNaproxenChromatographyElutionChemistryOrganic ChemistryClinical BiochemistryAcemetacinReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMicellar liquid chromatographymedicinePiketoprofenmedicine.drugChromatographia
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Comparison between sodium dodecylsulphate and cetyltrimethylammonium bromide as mobile phases in the micellar liquid chromatography determination of …

2004

The retention behaviour of non-steroidal anti-inflammatory drugs (NSAIDs) using micellar mobile phases of sodium dodecylsulphate (SDS) is studied and compared with that observed with micellar mobile phases of cetyltrimethylammonium bromide (CTAB). A liquid chromatographic procedure for the determination of acemetacin, diclofenac, indomethacin, ketoprofen, naproxen and tolmetin in pharmaceutical preparations is described. The proposed system uses a Kromasil C18 analytical column and a solution of 0.15 M SDS at pH 3 with 10% 1-propanol as mobile phase. Under these conditions, the studied NSAIDs elute between 6 and 10 min at a 1 mL min(-1) flow rate. Limits of detection (LOD) are lower than 0.…

KetoprofenNaproxenSodiumClinical BiochemistryAcemetacinPharmaceutical Sciencechemistry.chemical_elementAnalytical Chemistrychemistry.chemical_compoundBromideDrug DiscoverymedicineSpectroscopyChromatography Micellar Electrokinetic CapillaryDetection limitChromatographyElutionCetrimoniumAnti-Inflammatory Agents Non-SteroidalSodium Dodecyl SulfateReference StandardsSolutionschemistryMicellar liquid chromatographyCalibrationCetrimonium CompoundsIndicators and ReagentsSpectrophotometry Ultravioletmedicine.drugJournal of pharmaceutical and biomedical analysis
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On the Retention of Diuretics in Micellar Liquid Chromatography and Their Site of Action Within the Nephron

1993

Abstract The therapeutical action of diuretics has been attributed to their hydrophobic character, among other properties. Therapeutical and physiological classifications of diuretics are correlated. The site of action of high efficacay diuretics is the loop of Henle, that of intermediate efficacy diuretics is the distal tubule and that of low efficacy diuretics is the proximal and distal tubules, and the collecting duct. Partition coefficients between water and micelles offer a scale for hydrophobicity, which leads to a further correlation between retention in Micellar Liquid Chromatography (MLC), with a sodium dodecyl sulphate mobile phase and an ODS-C18 column, and the sites of action wi…

KidneyChromatographyChemistrymedicine.medical_treatmentSodiumBiochemistry (medical)Clinical Biochemistrychemistry.chemical_elementNephronBiochemistryAnalytical Chemistrymedicine.anatomical_structureMicellar liquid chromatographyElectrochemistrymedicineLoop of HenleDiureticAcetazolamideSite of actionSpectroscopymedicine.drugAnalytical Letters
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Description of the retention behaviour of solutes in micellar liquid chromatography with organic modifiers: Comparison of two methods

1995

Two methods for the description of the retention behaviour of solutes in micellar liquid chromatography are compared. One of them divides the parameter space into triangular subspaces, fitting a different equation in each subspace. The second method makes use of a unique equation, valid in the whole parameter space. In both cases, equations of the type log k=f (μ, ϕ), and 1/k=f (μ, ϕ), (μ and ϕ are the concentration of surfactant and alcohol, respectively), were used to describe the retention. The use of the hyperbolic function, 1/k=c0+c1μ+c3μϕ, to describe the whole parameter space yielded the best prediction. When a small portion of the parameter space was modelled, a simpler hyperbolic f…

LogarithmChemistryOrganic ChemistryClinical BiochemistryHyperbolic functionAnalytical chemistryThermodynamicsType (model theory)Parameter spaceBiochemistryLinear subspaceAnalytical ChemistryMicellar liquid chromatographyPhase compositionSubspace topologyChromatographia
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New Insights and Recent Developments in Micellar Liquid Chromatography

2009

Abstract: Micellar liquid chromatography (MLC) is an efficient alternative to conventional reversed–phase liquid chromatography with hydro‐organic mobile phases. Almost three decades of experience have resulted in an increasing production of analytical applications. Current concern about the environment also reveals MLC as an interesting technique for “green” chemistry because it uses mobile phases containing 90% or more water. These micellar mobile phases have a low toxicity and are not producing hazardous wastes. After a rapid overview of the two first decades of the technique, this review focuses on the recent advances on fundamental aspects and analytical applications. Traditional and n…

Low toxicityMicellar liquid chromatographyChemistryCritical micelle concentrationPhase (matter)Hydrophilic interaction chromatographyOrganic chemistryFiltration and SeparationNanotechnologyMicelleAnalytical ChemistrySeparation & Purification Reviews
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Temperature and concentration effects on supramolecular aggregation and phase behavior for poly(propylene oxide)–b-poly(ethylene oxide) –b-poly(propy…

2011

The micro- and mesoscopic structure of reverse Pluronic 25R4 in aqueous mixtures has been studied by SANS, SAXS and shear rheology. These techniques have been able to give a deep insight into the complex structure of the system phase diagram, that includes an isotropic water-rich liquid phase L(1), and liquid crystalline phases with hexagonal, E, or lamellar order, D. Particular attention has been paid to the isotropic water-rich phase L(1), which has a large stability region in the temperature-composition phase diagram. This region is crossed by a large "cloudy zone". Below it, namely at low temperature and composition, SANS data show the presence of polymer unimers in a gaussian coil conf…

Macromolecular SubstancesSurface PropertiesTemperatureWaternanoaggregateReverse Pluronic Lyotropic Phases Micellar Aggregates Defects Packed Vesciclesphase diagramPolyethylene GlycolsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsColloid and Surface Chemistryco-block polymerPropylene GlycolsSettore CHIM/02 - Chimica Fisica
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A three-factor optimisation strategy for micellar liquid chromatography

2000

An interpretive optimisation methodology for micellar liquid chromatography (MLC) is shown, taking into account pH, surfactant (sodium dodecyl sulphate) and organic modifier (propanol) concentration. Two objectives are considered: to develop a highly practical straightforward three-factor optimisation for practical MLC, and, in order to avoid unecessary experiments, to link two and three-factor optimisations through a step-wise construction of the experimental design at different pH levels. The whole pH range for an ODS column (from 3 to 7) is covered. The proposed strategy was thoroughly evaluated using the chromatographic data from 81 experimental mobile phases, applied to the separation …

Mean squared errorChemistryOrganic ChemistryClinical BiochemistryAnalytical chemistryBiochemistryHigh-performance liquid chromatographyMicellar electrokinetic chromatographyAnalytical ChemistrySet (abstract data type)ChemometricsPropanolchemistry.chemical_compoundMicellar liquid chromatographyTest setBiological systemChromatographia
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Secondary chemical equilibria in reversed-phase liquid chromatography

2017

Abstract The addition of reagents to a reversed-phase liquid chromatography (RPLC) mobile phase enables the separation of ionizable compounds, inorganic anions, and metal ions, using conventional instrumentation, silica-based materials, and hydro-organic mixtures, thanks to a variety of secondary equilibria. This gives rise to several chromatographic modes, the main features of which are outlined in this chapter. The effect of the mobile phase pH on the retention of ionizable compounds is described, together with the recommended experimental practice. The mechanism of adsorption of amphiphilic anions or cations on the stationary phase to attract analytes with opposite charge, or suppress th…

Metal ions in aqueous solution010401 analytical chemistryInorganic chemistryReversed-phase chromatography010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundSilanolAdsorptionchemistryMicellar liquid chromatographyCritical micelle concentrationIonic liquidMicroemulsion
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Quantitation of antihistamines in pharmaceutical preparations by liquid chromatography with a micellar mobile phase of sodium dodecyl sulfate and pen…

2002

Abstract A reversed-phase liquid chromatographic procedure with a micellar mobile phase of sodium dodecyl sulfate (SDS), containing a small amount of pentanol, was developed for the control of 7 antihistamines of diverse action in pharmaceutical preparations (tablets, capsules, powders, solutions, and syrups): azatadine, carbinoxamine, cyclizine, cyproheptadine, diphenhydramine, doxylamine, and tripelennamine. The retention times of the drugs were <9 min with a mobile phase of 0.15M SDS–6% (v/v) pentanol. The recoveries with respect to the declared compositions were in the range of 93–110%, and the intra- and interday repeatabilities and interday reproducibility were <1.2%. Th…

MicelleDosage formAnalytical Chemistrychemistry.chemical_compoundPentanolsmedicineCyclizineHumansEnvironmental ChemistrySodium dodecyl sulfateMicellesDosage FormsPharmacologyChromatographyChemistrySodium Dodecyl SulfatePharmaceutical PreparationsDoxylamineMicellar solutionsHistamine H1 AntagonistsCarbinoxamineAzatadineAgronomy and Crop ScienceChromatography LiquidFood Sciencemedicine.drug
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Dal Micro al Macro

2018

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Micro Macro Didattica Modello Particellare
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