Search results for "Micellar liquid chromatography"

showing 10 items of 108 documents

Analysis of Urine Samples Containing Cardiovascular Drugs by Micellar Liquid Chromatography with Fluorimetric Detection

1999

A simple direct injection chromatographic procedure with fluorimetric detection is successfully applied to the determination of mixtures of 4 diuretics (amiloride, bendroflumethiazide, piretanide, and triamterene) and 6 beta-blockers (acebutolol, atenolol, labetalol, metoprolol, nadolol, and propranolol), which are usually administered in combinations for the treatment of hypertension, in urine samples. The procedure makes use of C18 columns and micellar mobile phases of sodium dodecyl sulphate (SDS), propanol, and phosphate buffer at pH 3. The adequate resolution of most drugs is obtained with a chemometrics approach where the retention is modeled as a first step using the retention factor…

Quality Controlmedicine.medical_treatmentAdrenergic beta-AntagonistsMicellar electrokinetic chromatographyAnalytical ChemistryPropanolSurface-Active Agentschemistry.chemical_compoundmedicineHumansFluorometryBendroflumethiazideDiureticsAntihypertensive AgentsMicellesTriamtereneChromatographyChemistryElutionPiretanideGeneral MedicineHydrogen-Ion ConcentrationMicellar liquid chromatographyIndicators and ReagentsDiureticMathematicsChromatography Liquidmedicine.drugJournal of Chromatographic Science
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Biopartitioning micellar chromatoraphy to predict blood to lung, blood to liver, blood to fat and blood to skin partition coefficients of drugs

2009

[EN] Biopartitioning micellar chromatography (BMC), a mode of micellar liquid chromatography that uses micellar mobile phases of Brij35 in adequate experimental conditions, has demonstrated to be useful in mimicking the drug partitioning process into biological systems. In this paper, the usefulness of BMC for predicting the partition coefficients from blood to lung, blood to liver. blood to fat and blood to skin is demonstrated. PLS2 and multiple linear regression (MLR) models based on BMC retention data are proposed and compared with other ones reported in bibliography. The proposed models present better or similar descriptive and predictive capability. (C) 2008 Elsevier B.V. All rights r…

Quantitative structure–activity relationshipBlood to skinQuantitative Structure-Activity RelationshipPredictive capabilityPartition coefficientsBiochemistryAnalytical ChemistryPharmacokineticsBlood to lungLinear regressionQUIMICA ANALITICAmedicineAnimalsHumansEnvironmental ChemistryPharmacokineticsTissue DistributionLungMicellesSpectroscopySkinLungChromatographyChemistryComputational BiologyChromatography liquidBiopartitioning micellar chromatographyRatsPartition coefficientmedicine.anatomical_structureAdipose TissueLiverPharmaceutical PreparationsMicellar liquid chromatographyLinear ModelsBlood to fatRabbitsChromatography LiquidBlood to liver
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Reliability of the capacity factor at zero micellar concentration and the solute-micelle association constant estimates by micellar liquid chromatogr…

1997

In micellar liquid chromatography, MLC, the hydrophobicity of a compound is the predominant effect on its retention and interaction with micelles. The capacity factors at zero micellar concentration, k(m), and the solute-micelle association constants, KAM- have recently been used as the hydrophobicity index of compounds and are important in QSAR studies. These parameters could be estimated (by regression) from the (k,[M]) data, where k is the capacity factor and [M] the surfactant concentration minus the critical micelle concentration. km and KAM are usually obtained from the intercept and slope, respectively, of the plot 1/k vs. [M]. In spite of the general use of this equation, the reliab…

Quantitative structure–activity relationshipChromatographyChemistrySurface PropertiesOrganic ChemistryOsmolar ConcentrationLinear modelAnalytical chemistryRegression analysisGeneral MedicineBiochemistryMicelleCapacity factorAnalytical ChemistryOsmolar ConcentrationModels ChemicalMicellar liquid chromatographyCritical micelle concentrationRegression AnalysisComputer SimulationDiureticsMicellesChromatography LiquidJournal of chromatography. A
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Development of predictive retention-activity relationship models of tricyclic antidepressants by micellar liquid chromatography.

1999

The distribution of tricyclic antidepressants from plasma to brain, where these drugs exert their main clinical action, and other organs is related to transport events across the cell membranes of the different tissues. It could be expected that all the molecular features that condition the transport processes (mainly hydrophobicity and molar total charge) also control the pharmacokinetic and biochemical behavior. Micellar liquid chromatography (MLC) has been proposed to emulate in vitro the partitioning process in the biomembranes. The use of micellar solutions of Brij35 as mobile phases in reversed-phase liquid chromatography has proven to be valid to predict the biological activities of …

SerotoninAntidepressive Agents TricyclicModels BiologicalMicellar electrokinetic chromatographyNorepinephrineStructure-Activity RelationshipPharmacokineticsReceptors Adrenergic alpha-1Drug DiscoveryDistribution (pharmacology)AnimalsEnzyme InhibitorsAdrenergic alpha-AntagonistsMicelleschemistry.chemical_classificationChromatographyChemistryCapacity factorRatsMembraneMicellar liquid chromatographyMicellar solutionsAdenylyl Cyclase InhibitorsHistamine H1 AntagonistsMolecular MedicineSelective Serotonin Reuptake InhibitorsTricyclicChromatography LiquidJournal of medicinal chemistry
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Reversed-phase liquid chromatography with mixed micellar mobile phases of Brij-35 and sodium dodecyl sulphate: a method for the analysis of basic com…

2015

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode, which uses a surfactant as a modifier, with significant changes in retention and selectivity with regard to the classical RPLC mode that employs mixtures of water and organic solvent. The anionic sodium dodecyl sulphate (SDS) is the most usual surfactant in MLC, but it also requires the addition of an organic solvent to decrease the retention times and increase the efficiency. In particular, positively charged basic compounds are strongly retained by the stationary phase modified by adsorption of SDS monomers and require the addition of a strong solvent, such as propanol or pentanol. The non-ionic s…

SolventPropanolchemistry.chemical_compoundAdsorptionChromatographyPulmonary surfactantChemistryMicellar liquid chromatographyChemical polarityEnvironmental ChemistryReversed-phase chromatographySelectivityPollutionGreen Chemistry
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Retention-structure relationship studies for some steroidal hormones in micellar liquid chromatography

2000

The retention behavior in a C18 column of fourteen steroidal hormones (clostebol acetate, dehydrotestosterone, dydrogesterone, medroxyprogesterone, medroxyprogesterone acetate, methandienone, methyltestosterone, nandrolone, nandrolone decanoate, progesterone, testosterone, testosterone enanthate, testosterone propionate and, stanozolol) with pure micellar mobile phases prepared from sodium dodecyl sulfate (SDS), and hybrid mobile phases comprising SDS-acetonitrile and SDS-pentanol, was correlated with their octanol-water partition coefficients. Similar correlations were found with retention data obtained by other authors in gas chromatography, conventional reversed-phase liquid chromatograp…

Testosterone propionateChromatographyChemistrymedicine.medical_treatmentMedroxyprogesteroneOrganic ChemistryClinical BiochemistryBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistrySteroidchemistry.chemical_compoundMicellar liquid chromatographyNandroloneCLOSTEBOL ACETATEmedicineMethyltestosteronemedicine.drug
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DETERMINATION OF STEROIDAL HORMONES IN URINE SAMPLES BY MICELLAR LIQUID CHROMATOGRAPHY FOLLOWING SOLID-PHASE EXTRACTION

2001

Steroidal hormones were determined in spiked urine samples using micellar mobile phases of sodium dodecyl sulphate (SDS)-pentanol, solid-phase extraction (SPE), and detection in the UV region. In the optimized procedure, a 10 mL aliquot of urine sample is loaded into a C18 cartridge and washed with 2 mL of 50:50 (v/v) methanol-water, followed by 200 μL of 70:30 (v/v) methanol-water. The retained steroids are eluted with 2 mL of methanol and the eluate evaporated to dryness under nitrogen at 50°C. The residue is redissolved with 200 μL of the micellar mobile phase used in the chromatographic separation and injected into the chromatograph. The performance of the procedure was checked for 13 s…

Testosterone propionateChromatographyElutionMedroxyprogesteroneClinical BiochemistryPharmaceutical ScienceBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNandroloneMicellar liquid chromatographymedicineSolid phase extractionMethyltestosteronemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Screening of some banned aromatic amines in textile products from Indian bandhani and gamthi fabric and in human sweat using micellar liquid chromato…

2021

Certain dyes in textile products, which are capable of reductively splitting into carcinogenic aromatic amines, are strictly controlled in many countries. A simple, rapid, sensitive and green chromatographic method has been developed and validated for the simultaneous determination of 4-aminophenol (4-AMP), p-phenylenediamine (p-PPD) and benzidine (BNZ), banned aromatic amines in dyeing clothes and human sweat. The separation was achieved using a micellar mobile phase of 0.1 M SDS, 4% 1- butanol (v/v) buffered to pH 7 with sodium dihydrogen phosphate, flowing under isocratic mode at 1 mL/min through a C18 column. Photodiode array detector was set at 210 nm. Using the above chromatographic c…

TextileCalibration curve02 engineering and technologydyes01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundSpectroscopyvalidationChromatographytextilebusiness.industryChemistryElutionButanol010401 analytical chemistry021001 nanoscience & nanotechnologyBenzidine0104 chemical sciencessweatMicellar liquid chromatographychromatographyDyeing0210 nano-technologySelectivitybusinesscarcinogenicMicrochemical Journal
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Micellar liquid chromatography in doping control.

2010

The issue of doping control in sport involves the development of reliable analytical procedures and efficient strategies to process a large number of samples in a short period of time. Reversed-phase LC techniques with aqueous–organic mobile phases and MS or diode-array detection yield satisfactory results for the identification of prohibited substances in sport. However, time-consuming sample pretreatment steps are required, which reduces sample throughput. Micellar LC (MLC) that uses hybrid mobile phases of surfactant above its critical micellar concentration and organic solvent has been revealed as an interesting alternative. The surfactant sodium dodecyl sulfate solubilizes the protein…

Time FactorsClinical BiochemistryAnalytical chemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundSurface-Active AgentsPulmonary surfactantHumansGeneral Pharmacology Toxicology and PharmaceuticsSodium dodecyl sulfateDiureticsMicellesDoping in SportsChromatographyChemistryProteinsReproducibility of ResultsSodium Dodecyl SulfateWaterGeneral MedicineDilutionMedical Laboratory TechnologySolubilityMicellar liquid chromatographyCritical micelle concentrationYield (chemistry)SolventsAnalytical proceduresSelectivityChromatography LiquidBioanalysis
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Chromatographic determination of diuretics in urine samples using hybrid micellar mobile phases with fluorimetric detection

1998

Abstract A rapid and simple chromatographic procedure, that uses hybrid micellar mobile phases of sodium dodecyl sulphate (SDS), propanol and phosphate buffer at pH 3, and fluorimetric detection ( λ exc =270 nm, λ em =430 nm), is reported for the determination of mixtures of seven diuretics of diverse efficacy (amiloride, bendroflumethiazide, bumetanide, furosemide, hydroflumethiazide, piretanide and triamterene), in urine samples. The application of a sequential optimization procedure for the resolution of the mixtures of the diuretics was problematic. However, their separation was achieved through the use of an interpretive optimization procedure based on the accurate description of the r…

TriamtereneDetection limitHydroflumethiazideChromatographyChemistrymedicine.medical_treatmentPiretanideBiochemistryAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographymedicineEnvironmental ChemistryBendroflumethiazideDiureticSpectroscopyBumetanidemedicine.drugAnalytica Chimica Acta
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