0000000000006246

AUTHOR

Samuel Carda-broch

showing 50 related works from this author

Retention mechanisms for basic drugs in the submicellar and micellar reversed-phase liquid chromatographic modes.

2008

The reversed-phase liquid chromatographic (RPLC) behavior (retention, elution strength, selectivity, efficiency, and peak asymmetry) for a group of basic drugs (beta-blockers), with mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) and acetonitrile, revealed different separation environments, depending on the concentrations of both modifiers: hydro-organic, submicellar at low surfactant concentration and high concentration of organic solvent, micellar, and submicellar at high concentration of both surfactant and organic solvent. In the surfactant-mediated modes, the anionic surfactant layer adsorbed on the stationary phase interacts strongly with the positively ch…

ChromatographyAcetonitrilesElutionSodium Dodecyl SulfateReversed-phase chromatographyMicelleAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantchemistryPharmaceutical PreparationsPhase (matter)SolventsSolubilitySodium dodecyl sulfateAcetonitrileMicellesChromatography LiquidAnalytical chemistry
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Analytical Techniques for Furosemide Determination

2006

Abstract Due to the clinical importance of furosemide, a large number of analytical procedures to detect the presence of this drug in pharmaceutical and physiological samples has been developed. In this manuscript, a review of the most frequent analytical techniques described to determine furosemide is presented. Special attention has been paid to spectrophotometric and chromatographic techniques, but also to relevant methods using capillary electrophoresis or flow‐injection analysis, as well as the detection modes coupled to these techniques. The review also focuses on the different degradation pathways of the drug and cautions to prevent it, otherwise rarely or confusedly mentioned in the…

ChromatographyCapillary electrophoresisChemistrymedicineFurosemideFiltration and SeparationAnalytical proceduresBiochemical engineeringAnalytical Chemistrymedicine.drugSeparation & Purification Reviews
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On the use of ionic liquids as mobile phase additives in high-performance liquid chromatography. A review.

2015

The popularity of ionic liquids (ILs) has grown during the last decades in several analytical separation techniques. Consequently, the number of reports devoted to the applications of ILs is still increasing. This review is focused on the use of ILs (mainly imidazolium-based associated to chloride and tetrafluoroborate) as mobile phase additives in high-performance liquid chromatography (HPLC). In this approach, ILs just function as salts, but keep several kinds of intermolecular interactions, which are useful for chromatographic separations. Both cation and anion can be adsorbed on the stationary phase, creating a bilayer. This gives rise to hydrophobic, electrostatic and other specific in…

TetrafluoroborateHETEROCYCLIC AROMATIC-AMINESBiochemistryHigh-performance liquid chromatographyChlorideAnalytical Chemistrychemistry.chemical_compoundSilanol suppressionAdsorptionSOLUBILIZING ABILITIES[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhase (matter)medicineEnvironmental ChemistryOrganic chemistryOptimisationSpectroscopyHALF-WIDTH PLOTSMechanisms of retentionOVERLOADED BAND PROFILESANALYTICAL-CHEMISTRYSILANOL-SUPPRESSING POTENCYHYDROCARBONACEOUS STATIONARY PHASESIntermolecular forceAdditivesHigh-performance liquid chromatographyIonic liquidsSilanolROOM-TEMPERATURERETENTION MECHANISMChemical engineeringchemistryRP-HPLCIonic liquidmedicine.drugAnalytica chimica acta
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Ionic Liquid Based Headspace Solid-Phase Microextraction-Gas Chromatography for the Determination of Volatile Polar Organic Compounds

2010

Solid-phase microextraction (SPME) with an ionic liquid (IL) coating was developed for headspace extraction of a group of low molecular weight alcohols (ethanol, n-propanol, butanol, and isopropyl alcohol), acetone, ethyl acetate, and acetonitrile. A first SPME fiber was simply coated with a dedicated IL whose synthesis is described. A second SPME fiber was prepared by gluing silica (Si) particles on which the synthesized IL was chemically bonded. The analytes SPME extraction was optimized for time, temperature, and NaCl salting out content. The headspace extracted analytes were determined by simple temperature desorption into the hot injection port of a gas chromatograph. The coated-IL fib…

ChromatographyProcess Chemistry and TechnologyGeneral Chemical EngineeringExtraction (chemistry)Ethyl acetateFiltration and SeparationIsopropyl alcoholGeneral ChemistrySolid-phase microextractionchemistry.chemical_compoundchemistryIonic liquidSalting outFiberGas chromatographySeparation Science and Technology
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Use of a three-factor interpretive optimisation strategy in the development of an isocratic chromatographic procedure for the screening of diuretics …

2000

Screening of diuretics in urine is feasible through direct injection of the samples into the chromatographic system and isocratic reversed-phase liquid chromatography (RPLC) with micellar-organic mobile phases of sodium dodecyl sulfate (SDS) and 1-propanol. The surfactant coverage of the chromatographic column makes the addition of organic competing amines less necessary than in conventional aqueous-organic RPLC to achieve well-shaped peaks. Also, the range of elution strengths of micellar mobile phases required to elute mixtures of hydrophobic and hydrophilic diuretics is smaller. This allows the isocratic separation of the diuretics within adequate analysis times. An interpretive methodol…

medicine.medical_treatmentBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundmedicineHumansDiureticsMicellesTriamtereneChromatographyChemistryElutionOrganic ChemistryPiretanideGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationMicellar liquid chromatographyCalibrationSpectrophotometry UltravioletXipamideBenzthiazideDiureticmedicine.drugChromatography LiquidJournal of chromatography. A
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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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Micellar versus hydro-organic mobile phases for retention-hydrophobicity relationship studies with ionizable diuretics and an anionic surfactant

2004

Abstract Logarithm of retention factors (log  k ) of a group of 14 ionizable diuretics were correlated with the molecular (log  P o/w ) and apparent (log  P app ) octanol–water partition coefficients. The compounds were chromatographed using aqueous–organic (reversed-phase liquid chromatography, RPLC) and micellar–organic mobile phases (micellar liquid chromatography, MLC) with the anionic surfactant sodium dodecyl sulfate (SDS), in the pH range 3–7, and a conventional octadecylsilane column. Acetonitrile was used as the organic modifier in both modes. The quality of the correlations obtained for log  P app at varying ionization degree confirms that this correction is required in the aqueou…

OctanolsChromatographyStatic ElectricityOrganic ChemistryAnalytical chemistryWaterGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPartition coefficientHydrophobic effectSurface-Active Agentschemistry.chemical_compoundchemistryPulmonary surfactantMicellar liquid chromatographySpectrophotometry UltravioletSodium dodecyl sulfateDiureticsAcetonitrileChromatography High Pressure LiquidMicellesJournal of Chromatography A
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Retention mechanisms in micellar liquid chromatography.

2008

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode with mobile phases containing a surfactant (ionic or non-ionic) above its critical micellar concentration (CMC). In these conditions, the stationary phase is modified with an approximately constant amount of surfactant monomers, and the solubilising capability of the mobile phase is altered by the presence of micelles, giving rise to diverse interactions (hydrophobic, ionic and steric) with major implications in retention and selectivity. From its beginnings in 1980, the technique has evolved up to becoming a real alternative in some instances (and a complement in others) to classical RPLC with hydro…

ChromatographyChemistryOrganic ChemistrySolvationIonic bondingGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryMicelleAnalytical ChemistrySilanolchemistry.chemical_compoundSurface-Active AgentsModels ChemicalSolubilityMicellar liquid chromatographyPhase (matter)Critical micelle concentrationSolventsAdsorptionHydrophobic and Hydrophilic InteractionsAlgorithmsMicellesChromatography LiquidJournal of chromatography. A
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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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Micellar Liquid Chromatography: Method Development and Applications

2015

ChromatographyMicellar liquid chromatographyChemistryReversed-phase chromatographyMethod development
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Hydrophobicity of ionisable compounds studied by countercurrent chromatography

2011

Countercurrent chromatography (CCC) is a liquid chromatography technique in which the stationary phase is also a liquid. The main chemical process involved in solute separation is partitioning between the two immiscible liquid phases: the mobile phase and the support-free liquid stationary phase. The octanol-water partition coefficients (P(o/w)) is the accepted parameter measuring the hydrophobicity of molecules. It is considered to estimate active principle partitioning over a biomembrane. It was related to the substance biological activity. CCC is able to work with an octanol stationary phase and an aqueous mobile phase. In this configuration, CCC is a useful and easy alternative to measu…

OctanolAdrenergic beta-AntagonistsHydrophobicityAnalytical chemistryIonic bonding01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCountercurrent chromatographyPhase (matter)MoleculeDiureticsCountercurrent DistributionAqueous solutionChromatography010405 organic chemistryHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryOctanol–water partition coefficientsGeneral Medicine0104 chemical sciencesPartition coefficientPharmaceutical PreparationschemistryCountercurrent chromatographyIonisable compoundsHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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Submicellar and micellar reversed-phase liquid chromatographic modes applied to the separation of beta-blockers.

2009

The behaviour of a reversed-phase liquid chromatographic (RPLC) system (i.e. elution order, resolution and analysis time), used in the analysis of β-blockers with acetonitrile-water mobile phases, changes drastically upon addition of an anionic surfactant (sodium dodecyl sulphate, SDS). Surfactant monomers cover the alkyl-bonded phase in different extent depending on the concentration of both modifiers, in the ranges 1 × 10-3-0.15 M SDS and 5-50% acetonitrile. Meanwhile, the surfactant is dissolved in the mobile phase as free monomers, associated in small clusters or forming micelles. Four characteristic RPLC modes are yielded, with transition regions between them: hydro-organic, micellar, …

AcetonitrilesAdrenergic beta-AntagonistsAnalytical chemistryBiochemistryMicelleSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantSurfactant-mediated chromatographic systemsPhase (matter)Sodium dodecyl sulphateSelectivityAcetonitrileAcetonitrileMicellesChromatographyElutionChemistryOrganic ChemistryCationic polymerizationAnalysis timeSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyDirect transfer mechanismModels ChemicalCritical micelle concentrationSolventsβ-BlockersAlgorithmsChromatography LiquidJournal of chromatography. A
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High Submicellar Liquid Chromatography

2013

Surfactant addition above the critical micellar concentration (CMC), in reversed-phase liquid chromatography (RPLC), was proposed as a way to modify the selectivity and analysis time, giving rise to a chromatographic mode called micellar liquid chromatography (MLC). However, solutions containing only surfactant are too weak and yield poor peak shape. This was remediated by the addition of a small amount of organic solvent. To preserve the existence of micelles, in MLC high contents of organic solvent are avoided. Nevertheless, there is no reason to neglect the potentiality of mobile phases containing a surfactant above its CMC in water and a high organic solvent content (without micelles). …

Chromatographycolumn interactionsElutionChemistryHydrophilic interaction chromatographyAnalytical chemistryFiltration and Separationmacromolecular substancesReversed-phase chromatographyMicelleAnalytical Chemistryreversed-phase liquid chromatographyCountercurrent chromatographyPulmonary surfactantMicellar liquid chromatographyCritical micelle concentrationchromatographic performancesubmicellar liquid chromatographySeparation & Purification Reviews
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Are analysts doing method validation in liquid chromatography?

2014

International audience; Method validation is being applied in the reported analytical methods for decades. Even before this protocol was defined, authors already somehow validated their methods without full awareness. They wished to assure the quality of their work. Validation is an applied approach to verify that a method is suitable and rugged enough to function as a quality control tool in different locations and times. The performance parameters and statistical protocols followed throughout a validation study vary with the source of guidelines. Before single laboratory validation, an analytical method should be fully developed and optimized. The purpose of the validation is to confirm p…

Quality ControlValidation studyDIODE-ARRAY DETECTIONMethod validationmedia_common.quotation_subjectLiquid chromatographyValidation Studies as TopicGuidelinesBiochemistryField (computer science)Analytical Chemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistrySIMPLE HPLC METHODHumansQuality (business)HUMAN PLASMATANDEM MASS-SPECTROMETRYRAT PLASMAFunction (engineering)SurveyRP-LC METHODmedia_commonProtocol (science)AnalystsChromatographyPoint (typography)ChemistryData CollectionOrganic ChemistryGeneral MedicineEvaluated validation parametersMethod developmentFully developedSOLID-PHASE EXTRACTIONESI-MS/MS METHODPHARMACEUTICAL DOSAGE FORMChromatography LiquidTHIN-LAYER-CHROMATOGRAPHY
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Effect of buffer nature and concentration on the chromatographic performance of basic compounds in the absence and presence of 1-hexyl-3-methylimidaz…

2019

Abstract In reversed-phase liquid chromatography, the performance for basic compounds is affected by the interaction of the protonated (cationic) species with the anionic free silanols on the alkyl-bonded stationary phases. Using aqueous-organic mobile phases in the absence of additives, the retention may be too high, and the peaks be broad and asymmetric. The performance is improved by addition to the mobile phase of ionic liquids, from which 1-hexyl-3-methylimidazolium chloride ([C6MIm][Cl]) has especially good characteristics. A recent report has also revealed that the use of the phosphate system as buffer, at varying concentration and pH, may have a significant role in the chromatograph…

buffer systemsAcetonitrilesAdrenergic beta-AntagonistsIonic LiquidsProtonationBuffers010402 general chemistry01 natural sciencesBiochemistryChlorideAnalytical Chemistryionic liquidschemistry.chemical_compoundreversed-phase liquid chromatographyBoratesmedicineFormateβ-Adrenoceptor antagonistsChromatography High Pressure LiquidChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryCationic polymerizationImidazolesWatersilanol effectGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationPhosphate0104 chemical sciencesSilanolchemistryIonic liquidSolventsmedicine.drug
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Oil-In-Water Microemulsion Liquid Chromatography

2018

Oil-in-water microemulsions (O/W MEs) are obtained spontaneously by mixing two immiscible liquids (water and oil) in the presence of a surfactant. A co-surfactant is also often needed for ME stabil...

animal structuresChromatographyChemistry010401 analytical chemistryMixing (process engineering)Filtration and Separation02 engineering and technology021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical ChemistryOil in waterPulmonary surfactantMicroemulsion0210 nano-technologySeparation & Purification Reviews
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Micellar-organic versus aqueous-organic mobile phases for the screening of β-blockers

2002

A comparative study of the performance of reversed-phase liquid chromatography with micellar-organic (MLC) and aqueous-organic (RPLC) mobile phases is reported for the separation of 16 -blockers (acebutolol, alprenolol, atenolol, bisoprolol, carteolol, celiprolol, esmolol, labetalol, metoprolol, nadolol, oxprenolol, pindolol, practolol, propranolol, sotalol, and timolol). MLC with hybrid mobile phases of sodium dodecyl sulfate (SDS) and propanol is revealed as a very competitive technique for the screening of these drugs. Using a conventional Spherisorb C18 column, the theoretical plates ( N) and asymmetry factors (B/A) for the optimal mobile phase compositions were in the ranges N = 2200–4…

ChromatographyElutionAnalytical chemistryReversed-phase chromatographyAtenololBiochemistryAcebutololAnalytical ChemistryPropanolchemistry.chemical_compoundchemistryOxprenololmedicineEnvironmental ChemistrySodium dodecyl sulfateTriethylamineSpectroscopymedicine.drugAnalytica Chimica Acta
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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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Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
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Procedure for the Screening of Eggs and Egg Products to Detect Oxolonic Acid, Ciprofloxacin, Enrofloxacin, and Sarafloxacin Using Micellar Liquid Chr…

2019

A method based on micellar liquid chromatography was developed to determine oxolinic acid, ciprofloxacin, enrofloxacin, and sarafloxacin in eggs and egg products. The antimicrobial drugs were obtained in a micellar solution which was directly injected. The analytes were resolved using a C18 column and a mobile phase of 0.05 M sodium dodecyl sulfate—7.5% 1-propanol—0.5% triethylamine, buffered at pH 3 with phosphate salt, running under the isocratic mode. The signal was monitored by fluorescence. Validation was successfully performed according to the EU Commission Decision 2002/657/EC in terms of specificity, calibration range (LOQ to 1 mg/kg), linearity (R2 &gt

Microbiology (medical)Analytelaying hen01 natural sciencesBiochemistryMicrobiologyArticlechemistry.chemical_compoundSarafloxacinOxolinic acidEnrofloxacinmedicinePharmacology (medical)General Pharmacology Toxicology and PharmaceuticsTriethylamineDetection limitvalidationResidue (complex analysis)Chromatography010405 organic chemistryChemistry010401 analytical chemistrylcsh:RM1-950solid-to-liquid extraction0104 chemical sciencesfood safetyInfectious Diseaseslcsh:Therapeutics. PharmacologyMicellar liquid chromatographyfluorescenceoptimizationmedicine.drugAntibiotics
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Effect of short-chain alcohols on surfactant-mediated reversed-phase liquid chromatographic systems.

2010

The behaviour of β-blockers in a reversed-phase liquid chromatographic (RPLC) column with mobile phases containing a short-chain alcohol (methanol, ethanol or 1-propanol), with and without the surfactant sodium dodecyl sulphate (SDS), was explored. Two surfactant-mediated RPLC modes were studied, where the mobile phases contained either micelles or only surfactant monomers at high concentration. Acetonitrile was also considered for comparison purposes. A correlation was found between the effects of the organic solvent on micelle formation (monitored by the drop weight procedure) and on the nature of the chromatographic system (as revealed by the retention, elution strength and peak shape of…

AcetonitrilesAdrenergic beta-Antagonists1-PropanolBiochemistryMicelleAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundSurface-Active AgentsPulmonary surfactantPhase (matter)AcetonitrileMicellesChromatography Reverse-PhaseChromatographyEthanolElutionChemistryMethanolOrganic ChemistryCationic polymerizationSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyAlcoholsData Interpretation StatisticalJournal of chromatography. A
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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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Evaluation of several global resolution functions for liquid chromatography

1999

Abstract An interpretative approach, that makes use of the overlapped fraction of each chromatographic peak as elementary resolution criterion, was applied to the separation of mixtures of compounds. The elementary resolution measurements for all peaks in the chromatogram were reduced to a single numerical value using several functions: normalised by the mean resolution product, unnormalised product, geometrical mean of the unnormalised product, and worst elementary resolution value. The descriptive capability of these reduction functions was evaluated through the observation of global resolution diagrams and the change in the shape of the chromatograms in the selected factor space. michrom…

ChromatographyResolution (mass spectrometry)ElutionChemistryFraction (chemistry)BiochemistryAnalytical ChemistryReduction (complexity)Product (mathematics)Phase compositionmedicineEnvironmental ChemistryGeometric meanSpectroscopyThiazidemedicine.drugAnalytica Chimica Acta
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Improvement of peak shape and separation performance of beta-blockers in conventional reversed-phase columns using solvent modifiers.

2003

A comparative study of peak shape, elution behavior, and resolution of 16 beta-blockers (acebutolol, alprenolol, atenolol, bisoprolol, carteolol, celiprolol, esmolol, labetalol, metoprolol, nadolol, oxprenolol, pindolol, practolol, propranolol, sotalol, and timolol) chromatographed with hybrid mobile phases of triethylamine (TEA)-acetonitrile and sodium dodecyl sulfate (SDS)-propanol is performed using conventional reversed-phase columns and isocratic elution. Both solvent modifiers (TEA and SDS) prevent the interaction of the basic drugs with the alkyl-bonded phase. However, the protection mechanisms of silanols on the packing are different. Whereas TEA associates with the silanol sites (b…

ChromatographyElutionAdrenergic beta-AntagonistsAnalytical chemistryGeneral MedicineReversed-phase chromatographyHigh-performance liquid chromatographyAnalytical ChemistrySolventchemistry.chemical_compoundSilanolchemistryOxprenololmedicineSolventsSpectrophotometry UltravioletSodium dodecyl sulfateTriethylamineChromatography High Pressure Liquidmedicine.drugJournal of chromatographic science
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Quantitative structure-retention and retention-activity relationships of beta-blocking agents by micellar liquid chromatography.

2001

Abstract Sixteen β-blocking agents (acebutolol, alprenolol, atenolol, bisoprolol, carteolol, celiprolol, esmolol, labetalol, metoprolol, nadolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) showing a large range of hydrophobicity (octanol–water partition coefficients, log P between −0.026 and 2.81) were subjected to micellar liquid chromatography with sodium dodecyl sulfate as micelle forming agent, and n-propanol as organic modifier. The correlation between log P and the retention factor extrapolated to a mobile phase free of micelles and organic modifier was investigated. The use of an interpolated retention factor or the retention factor for specific individual exp…

ChromatographyChemistryOrganic ChemistryAdrenergic beta-AntagonistsQuantitative Structure-Activity RelationshipGeneral MedicineBiochemistryMicelleAcebutololMicellar electrokinetic chromatographyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundMicellar liquid chromatographyOxprenololmedicineAlprenololSodium dodecyl sulfateMicellescirculatory and respiratory physiologymedicine.drugChromatography LiquidJournal of chromatography. A
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COMPARISON OF THE COURSE SYLLABUS OF THE THEORY SUBJECT "CHEMISTRY" IN CHEMISTRY GRADE AND IN ENGINEERING STUDIES

2016

Comunicació presentada a INTED2016, 10th International Technology, Education and Development Conference. (March 7-9, 2016, Valencia, Spain). The aim of the chemistry-related subjects, taught in the first academic year of several grades at the University Jaume I, is to provide a broad overview about general chemistry. However, these defined subjects are adapted to the structure, objectives and curricula of each grade. In this paper, a comparison of the course syllabus of the Chemistry subjects taught in the "Chemistry grade" and in several "Engineering grades" (Agricultural, Mechanical, Electrical, Industrial Technology and Chemical) is detailed. The differences and similarities of the subje…

Engineering studiesSyllabusChemistryComputer scienceengineeringMathematics educationSubject (documents)Chemistry (relationship)course syllabuschemistrycomparisionsubjectINTED2016 Proceedings
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MICELLAR LIQUID CHROMATOGRAPHIC DETERMINATION OF ANTI-CONVULSANT DRUGS IN PILLS AND CAPSULES

2000

A simple chromatographic procedure is reported for the determination of several anti-convulsant drugs in pharmaceuticals: carbamazepine, and the benzodiazepines bentazepam, halazepam, oxazepam, pinazepam, and tetrazepam. The procedure utilizes a C18 column, a hybrid micellar mobile phase of 0.1 M SDS-3% butanol-0.1% triethylamine-0.01 M phosphate buffer (pH 3), and UV detection (230 nm). The drugs eluted in less than 13 min, in accordance to their relative polarities, as indicated by their octanol-water partition coefficients. The limits of detection (μg/mL), and intra and inter-day repeatabilities (%), for 4 μg/mL were: carbamazepine (0.03, 1.0, 4.1), bentazepam (0.05, 1.3, 1.6), halazepam…

Detection limitChromatographyPinazepamChemistryClinical BiochemistryPharmaceutical ScienceBiochemistryBentazepamHalazepamDosage formMicellar electrokinetic chromatographyAnalytical ChemistryOxazepamTetrazepammedicinemedicine.drugJournal of Liquid Chromatography & Related Technologies
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Use of micellar mobile phases for the chromatographic determination of clorazepate, diazepam, and diltiazem in pharmaceuticals

2001

An ODS-2 column, a micellar mobile phase of high elution strength containing 0.1M sodium dodecyl sulfate and 3% (v/v) butanol, and ultraviolet detection at 230 nm are used for the determination of either of two benzodiazepines (clorazepate and diazepam) and a benzothiazepine (diltiazem) in pharmaceuticals. The procedure is shown to be competitive against conventional chromatography with methanol-water mobile phases, especially for diltiazem. The composition of the micellar mobile phase is selected using a predictive strategy based on an accurate retention model and assisted by computer simulation. Calibration graphs are linear at least in the 2.5 to 20 microg/mL, 4 to 20 microg/mL, and 5 to…

Detection limitChromatographyDiazepamChemistrymedicine.drug_classElutionGeneral MedicineHigh-performance liquid chromatographyDosage formAnalytical ChemistryHypnoticDiltiazemPharmaceutical PreparationsCalibrationmedicineClorazepateSpectrophotometry UltravioletDiltiazemDiazepamClorazepate DipotassiumMicellesmedicine.drugChromatography Liquid
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Peak half-width plots to study the effect of organic solvents on the peak performance of basic drugs in micellar liquid chromatography.

2009

The addition of the anionic surfactant sodium dodecyl sulphate (SDS) to hydro-organic mixtures of methanol, ethanol, propanol or acetonitrile with water yielded enhanced peak shape (i.e. increased efficiencies and symmetrical peaks) for a group of basic drugs (β-blockers) chromatographed with a Kromasil C18 column. The effect can be explained by the thin layer of surfactant associated to the hydrocarbon chain on the stationary phase in the presence of the organic solvents, which covers the free silanols on the siliceous support avoiding their interaction with the cationic basic drugs. These instead interact with the anionic head of the surfactant increasing their retention and allowing a mo…

AcetonitrilesInorganic chemistryAdrenergic beta-AntagonistsBiochemistryMicelleAnalytical ChemistryPropanolchemistry.chemical_compoundPulmonary surfactantBasic compoundsSodium dodecyl sulphatePeak performanceSodium dodecyl sulfateAcetonitrileMicelleschemistry.chemical_classificationChromatographyOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineOrganic solventsHydrocarbonchemistryMicellar liquid chromatographyAlcoholsLinear Modelsβ-BlockersMethanolMicellar liquid chromatographyPeak half-widthsChromatography LiquidJournal of chromatography. A
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Ionic liquids in separation techniques.

2007

The growing interest in ionic liquids (ILs) has resulted in an exponentially increasing production of analytical applications. The potential of ILs in chemistry is related to their unique properties as non-molecular solvents: a negligible vapor pressure associated to a high thermal stability. ILs found uses in different sub-disciplines of analytical chemistry. After drawing a rapid picture of the physicochemical properties of selected ILs, this review focuses on their use in separation techniques: gas chromatography (GC), liquid chromatography (LC) and electrophoretic methods (CE). In LC and CE, ILs are not used as pure solvents, but rather diluted in aqueous solutions. In this situation IL…

ChromatographyChromatography GasOrganic ChemistryElectrophoresis CapillaryIonic LiquidsGeneral MedicineReversed-phase chromatographyBiochemistryMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundChaotropic agentCapillary electrophoresisCountercurrent chromatographychemistryLyotropicIonic liquidSolventsGas chromatographyCountercurrent DistributionChromatography LiquidChromatography Micellar Electrokinetic CapillaryJournal of chromatography. A
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Effect of ionization and the nature of the mobile phase in quantitative structure-retention relationship studies.

2005

Abstract The octanol–water distribution constant, commonly called partition coefficient, Po/w, is a parameter often retained as a measure of the hydrophobicity of a molecule. log Po/w, for a given molecule, can be conveniently evaluated constructing correlation lines between standard retention factor logarithms (log k) in reversed-phase liquid chromatography (RPLC) and standard log Po/w values. Many compounds of pharmaceutical interest can be quite hydrophobic and have, simultaneously, basic nitrogen atoms or acidic sulfur containing groups in their structure. This renders them ionizable. The hydrophobicity of the molecular drug form (Po/w value) is completely different from its ionic form …

IonsChromatographyChemistryElutionOrganic ChemistryDistribution constantAnalytical chemistryGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectPartition coefficientStructure-Activity RelationshipMicellar liquid chromatographyLipophilicityChromatography LiquidJournal of chromatography. A
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HYDRO-ORGANIC AND MICELLAR-ORGANIC REVERSED-PHASE LIQUID CHROMATOGRAPHIC PROCEDURES FOR THE EVALUATION OF SULPHONAMIDES IN PHARMACEUTICALS

2001

Two reversed-phase liquid chromatographic procedures were developed for the analysis of ten pharmaceutical formulations used in medicine and veterinary, which contained one of the following sulphonamides: sulphacetamide, sulphadiazine, sulphaguanidine, sulphamethazine, sulphamethizole, sulphamethoxazole, or sulphathiazole. In both chromatographic modes, the same C18 column was utilized and the mobile phase contained a low amount of acetonitrile and citric buffer at pH 3.0. In one of the procedures, the surfactant sodium dodecyl sul phate was added to the mobile phase. The presence of micelles allowed a decrease in the amount of organic solvent from 11% to 6%, and facilitated sample dissolut…

ChromatographyAqueous solutionElutionChemistryBiochemistry (medical)Clinical BiochemistryReversed-phase chromatographyBiochemistryMicelleDosage formAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantElectrochemistryAcetonitrileDissolutionSpectroscopyAnalytical Letters
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Recent advances on ionic liquid uses in separation techniques

2018

International audience; The molten organic salts with melting point below 100°C, commonly called ionic liquids (ILs) have found numerous uses in separation sciences due to their exceptional properties as non molecular solvents, namely, a negligible vapor pressure, a high thermal stability, and unique solvating properties due to polarity and their ionic character of molten salts. Other properties, such as viscosity, boiling point, water solubility, and electrochemical window, are adjustable playing with which anion is associated with which cation. This review focuses on recent development of the uses of ILs in separation techniques actualizing our 2008 article (same authors, J. Chromatogr. A…

Deep eutectic solventSpectrometry Mass Electrospray IonizationChromatography Gasgas chromatographydeep eutectic solventLiquid chromatographyIonic bonding02 engineering and technologyTrace anion detection01 natural sciencesBiochemistryAnalytical Chemistryionic liquidschemistry.chemical_compoundCountercurrent chromatographyCapillary electrophoresistrace anion detection[CHIM.ANAL]Chemical Sciences/Analytical chemistryliquid chromatographyCountercurrent DistributionGas chromatographyChromatographyViscosity010401 analytical chemistryOrganic ChemistryElectrophoresis CapillaryGeneral Medicine021001 nanoscience & nanotechnologyIonic liquids0104 chemical sciencesDeep eutectic solventBoiling pointchemistryIonic liquidSolventsMelting pointGases0210 nano-technologyChromatography LiquidElectrochemical windowJournal of Chromatography A
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Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulations

2017

Abstract Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary phases, which is translated in poor peak shape and high consumption of organic solvent to get appropriate retention times. Micellar mobile phases containing surfactants give rise to modified stationary phases, where silanols are masked, improving the peak shape. However, mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) require a small amount of organic solvent to conveniently decrease the retention of cationic analytes. An alternative is…

AnalyteMethod validation01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPulmonary surfactantlawmedicineSample preparationSodium dodecyl sulfateBrij-35β-Adrenoceptor antagonistsSodium dodecyl sulfateSpectroscopyFiltrationChromatography010405 organic chemistryChemistry010401 analytical chemistryCationic polymerizationEnvironmentally friendly0104 chemical sciencesOxprenololPharmaceutical formulationsmedicine.drug
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CHROMATOGRAPHIC DETECTION OF SESQUITERPENE LACTONES IN PARTHENIUM PLANTS FROM NORTHWEST ARGENTINA

1999

Several chloroformic extracts containing some sesquiterpene lactones from autochtonous plants of Parthenium hysterophorus, collected in the province of Salta (Argentina), were separated and identified by high performance reversed-phase liquid chromatography with C18 column and propanol-water mobile phases, using gradient elution and concentrations of propanol larger than 10% (v/v). Lactones previously purified and characterized by H1 RMN, C13 RMN, IR, and mass spectrometry, were used as standards. The objective of the study was to check if the nature of the lactones was modified according to the altitude of the region where the plants were grown. Among the lactones, five were already descri…

chemistry.chemical_classificationChromatographybiologyClinical BiochemistryPharmaceutical ScienceParthenium hysterophorusPharmacognosySesquiterpenebiology.organism_classificationBiochemistryHigh-performance liquid chromatographyTerpenoidAnalytical ChemistryPropanolPartheniumchemistry.chemical_compoundchemistryLactoneJournal of Liquid Chromatography & Related Technologies
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Countercurrent chromatography: People and applications

2009

The scientific literature was scanned for the published research articles dealing with countercurrent chromatography (CCC) over the time period 1980-May 2008. The search returned 1638 articles that were analyzed focussing on people and applications. Concerning the people, it was found that the geographical location of the CCC authors was relatively well balanced between USA, Asia with mainly China and Japan and Europe. Yoichiro Ito, the inventor of the technique, is by far the most productive author in the field with 331 articles or more than one over five CCC articles published in the time period. Without surprise, English is the dominant language with more than 82% of the articles. A sign…

PublishingBiological ProductsSubject HeadingsChromatographyImpact factorChemistryNatural compoundOrganic ChemistryGeneral MedicineScientific literatureBibliometricsBiochemistryAuthorshipAnalytical ChemistryImpact indexCountercurrent chromatographyBibliometricsJournal Impact FactorPeriodicals as TopicCountercurrent distributionCountercurrent DistributionJournal of Chromatography A
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Determination of furosemide in urine samples by direct injection in a micellar liquid chromatographic system.

2002

A sensitive, selective and efficient micellar liquid chromatographic (MLC) procedure was developed for the determination of furosemide (4-chloro-N-furfuryl-5-sulfamoylanthranilic acid) in urine samples by direct injection and UV detection. The procedure makes use of a C18 reversed-phase column and a micellar mobile phase of 0.05 mol l(-1) sodium dodecyl sulfate-6% v/v propanol and phosphate buffer at pH 3 to resolve furosemide from its photochemical degradation products. The importance of protecting the standards and urine samples to be analysed from light in the assay of furosemide, avoiding its degradation, was verified. The limit of quantification was 0.15 microg ml(-1) and the relative …

Detection limitChromatographyMetabolitemedicine.medical_treatmentSodiumchemistry.chemical_elementFurosemideReversed-phase chromatographyUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryFurosemideElectrochemistrymedicineEnvironmental ChemistryHumansDiureticDiureticsQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure Liquidmedicine.drugChromatography Micellar Electrokinetic CapillaryThe Analyst
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Half-width plots, a simple tool to predict peak shape, reveal column kinetics and characterise chromatographic columns in liquid chromatography: Stat…

2013

Peak profiles in chromatography are characterised by their height, position, width and asymmetry; the two latter depend on the values of the left and right peak half-widths. Simple correlations have been found between the peak half-widths and the retention times. The representation of such correlations has been called half-width plots. For isocratic elution, the plots are parabolic, although often, the parabolas can be approximated to straight-lines. The plots can be obtained with the half-widths/retention time data for a set of solutes experiencing the same kinetics, eluted with a mobile phase at fixed or varying composition. When the analysed solutes experience different resistance to mas…

Peak profiles in chromatography are characterised by their height position width and asymmetry; the two latter depend on the values of the left and right peak half-widths. Simple correlations have been found between the peak half-widths and the retention times. The representation of such correlations has been called half-width plots. For isocratic elution the plots are parabolic although often the parabolas can be approximated to straight-lines. The plots can be obtained with the half-widths/retention time data for a set of solutes experiencing the same kinetics eluted with a mobile phase at fixed or varying composition. When the analysed solutes experience different resistance to mass transfer the plots will be solute dependent and should be obtained with the data for each solute eluted with mobile phases at varying composition. The half-width plots approach is a simple tool that facilitates the prediction of peak shape (width and asymmetry) with optimisation purposes reveal the interaction kinetics of solutes in different columns and characterise chromatographic columns. This work shows half-width plots for different situations in isocratic elution including the use of different flows the effect of temperature the modification of the stationary phase surface by an additive the existence of specific interactions within the column and the comparison of columns. The adaptation to gradient elution is also described. Previous knowledge on half-width plots is structured and analysed to which new results are added.Work (thermodynamics)Column characterisationmedia_common.quotation_subjectKineticsLiquid chromatographyAnalytical chemistryHalf-widthsInteraction kineticsBiochemistryAsymmetryAnalytical ChemistryPeak shapeColumn (typography)Position (vector)Mass transferPhase (matter)media_commonChromatographyElutionChemistryOrganic ChemistryGeneral MedicineModels TheoreticalKineticsPredictionChromatography LiquidJournal of Chromatography A
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Determination of isoniazid and pyridoxine in plasma sample of tuberculosis patients by micellar liquid chromatography

2021

It is no doubt Isoniazid is a powerful tuberculosis drug, but it might give rise to Vitamin B6 (Pyridoxine) deficiency. In this case, a usual treatment is the combined administration of Isoniazid and Pyridoxine. An easy-to-conduct procedure based on Micellar Liquid Chromatography has been developed to quantify Isoniazid and Pyridoxine in plasma from Tuberculosis patients. The sample was diluted in mobile phase, filtered and directly injected, thus avoiding extraction or purification steps. Both drugs were adequately resolved from the matrix and endogenous compounds using a mobile phase made up of 0.15 M sodium dodecyl sulfate – 8%(v/v) 1-butanol – 0.01 M phosphate buffer at pH 3, running at…

DrugBioanalysismedia_common.quotation_subjectmicellar02 engineering and technology01 natural sciencespatientsAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundmedicineantituberculosisSodium dodecyl sulfateSpectroscopyplasmamedia_commonChromatographyChemistry010401 analytical chemistryExtraction (chemistry)Isoniaziddrug021001 nanoscience & nanotechnologyPyridoxine0104 chemical sciencesMicellar liquid chromatography0210 nano-technologyoptimizationmedicine.drug
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Extent of the influence of phosphate buffer and ionic liquids on the reduction of the silanol effect in a C18 stationary phase

2017

The presence of anionic free silanols in the silica-based stationary phases gives rise to broad and asymmetrical peaks when cationic basic compounds are chromatographed using hydro-organic mobile phases. The addition to the mobile phase of a reagent with ionic character prevents the access of analytes to the free silanols, improving the peak shape. The silanol activity can be affected by the buffer concentration and mobile phase pH, factors that are not always considered sufficiently in the literature. In this work, the chromatographic behaviour of three basic β-adrenoceptor antagonists (acebutolol, nadolol and timolol), using mobile phases containing acetonitrile, was examined at different…

Static ElectricityInorganic chemistryIonic LiquidsIonic bonding02 engineering and technologyBuffers01 natural sciencesBiochemistryPhosphatesAnalytical Chemistrychemistry.chemical_compoundPhase (matter)Alkylchemistry.chemical_classificationChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryCationic polymerizationGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationSilanes021001 nanoscience & nanotechnologyPhosphate0104 chemical sciencesSilanolchemistryIonic liquid0210 nano-technologyJournal of Chromatography A
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LC of high to moderately polar basic drugs in urine with water and detergent, and direct injection

2016

Background: Micellar LC was first proposed as a ‘green’ mode using mobile phases of water and surfactant. However, in most procedures a small amount of organic solvent is required to decrease the retention to convenient values. Results & methodology: Mixed micellar mobile phases prepared with both cationic (sodium dodecyl sulphate) and nonionic surfactant (Brij-35) modulate the retention of high to moderately polar basic drugs to practical times, eliminating the need of organic solvent. While the mobile phase is continuously recycled through the system, the stationary phase performance is maintained after repetitive injection of the samples. Discussion & conclusion: Through an exte…

SodiumClinical Biochemistrychemistry.chemical_elementUrine010402 general chemistry01 natural sciencesPolyethylene GlycolsAnalytical ChemistrySurface-Active AgentsPulmonary surfactantLimit of DetectionPhase (matter)HumansGeneral Pharmacology Toxicology and PharmaceuticsMicellesChromatographyChemistryOrganic solvent010401 analytical chemistryCationic polymerizationSodium Dodecyl SulfateWaterGeneral Medicine0104 chemical sciencesMedical Laboratory TechnologyPharmaceutical PreparationsStationary phaseFlow Injection AnalysisPolarChromatography LiquidBioanalysis
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Determination of albendazole and ivermectin residues in cattle and poultry-derived samples from India by micellar liquid chromatography

2021

We have developed a method, based on micellar liquid chromatography, to determine albendazole and ivermectin in dairy products and biological waste from bovine, as well as edible tissues from poultry. Anthelmitics were resolved in less than 10 min using a C18 column and a mobile phase of 0.15 mol/L sodium dodecyl sulfate – 6% 1-pentanol at buffered at pH 7 with a 0.01 M phosphate salt, running under isocratic mode at 1 mL/min. Detection was by absorbance at 292 nm. Method was successfully validated following official validation guidelines, in terms of: selectivity, sensitivity, calibration range (0.0125−0.5 mg/kg to 25−50 mg/kg), linearity (r2 > 9990), trueness (86.3–105.6%), precision (<12…

chemistry.chemical_classificationbiological wasteChromatographyanthelminticmicellar liquid chromatographydairy productsfood analysisalbendazoledrug residueSalt (chemistry)PhosphateAlbendazoleivermectinAbsorbancechemistry.chemical_compoundIvermectinchemistryMicellar liquid chromatographyfood compositionmedicineAnthelminticSodium dodecyl sulfateedible tissuesFood Sciencemedicine.drugJournal of Food Composition and Analysis
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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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Modulation of retention and selectivity in oil-in-water microemulsion liquid chromatography: A review

2019

Microemulsions (MEs) are stable, isotropically clear solutions consisting of an oil and water stabilized by a surfactant and a co-surfactant. Oil-in-water microemuslion liquid chromatography (MELC) is a relatively new chromatographic mode, which uses an O/W ME as mobile phase. Retention, selectivity and efficiency can be modified by changing the concentration of the ME components and the ratio between the aqueous and oil phases. This work makes a critical survey on the information found in the literature about the mobile phase compositions that lead to the creation of successful O/W ME mobile phases, as well as the effect of pH for ionizable compounds and temperature. The viability of perfo…

Work (thermodynamics)modulation of selectivity010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistrySurface-Active AgentsPulmonary surfactantPhase (matter)Microemulsionmicroemulsion liquid chromatographyChromatographyAqueous solutionChemistry010401 analytical chemistryOrganic ChemistryWaterGeneral Medicineoil-in-water microemulsionsexperimental factors0104 chemical sciencesoptimization of resolutionReagentYield (chemistry)SelectivityOilsChromatography LiquidJournal of Chromatography A
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Furosemide assay in pharmaceuticals by Micellar liquid chromatography: study of the stability of the drug.

2000

A simplified high-performance liquid chromatographic procedure is described for the determination of furosemide (4-chloro-N-furfuryl-5-sulphamoylanthranillic acid), which makes use of UV detection, a C18, reversed-phase column, and micellar mobile phases of sodium dodecyl sulphate (SDS) and 1-propanol at pH 3 buffered with phosphate system. The most adequate experimental conditions to handle furosemide solutions in the analytical laboratory are studied. The mixture of furosemide and its degradation products which are formed upon light exposition was resolved with a mobile phase of 0.04 M SDS-2% propanol. Separation of furosemide from its common impurities and the hydrolytic product, 4-chlor…

Clinical BiochemistryPharmaceutical ScienceDosage formMicellar electrokinetic chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundDrug StabilityFurosemideDrug DiscoverymedicineSodium dodecyl sulfateDiureticsSpectroscopyChromatography High Pressure LiquidMicellesChromatographyPhotolysisElutionHydrolysisFurosemideSodium Dodecyl SulfateHydrogen-Ion ConcentrationSolutionschemistryMicellar liquid chromatographyCalibrationIndicators and ReagentsSpectrophotometry UltravioletQuantitative analysis (chemistry)medicine.drugTabletsJournal of pharmaceutical and biomedical analysis
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Optimised procedures for the reversed-phase liquid chromatographic analysis of formulations containing tricyclic antidepressants.

2003

The chromatographic behaviour (retention, selectivity, peak shape and resolution) of seven tricyclic antidepressants (TCAs), amitryptiline, clomipramine, doxepin, imipramine, maprotiline, nortryptiline and trimipramine, was examined. Conventional unendcapped Cs and C18 columns and an endcapped XTerra MS C18 column recommended for the analysis of basic compounds were used together with acetonitrile-water and micellar sodium dodecylsulfate (SDS)-pentanol mobile phases. The two best combinations were XTerra C18/acetonitrile, which yielded the largest efficiencies and resolution, and C8/SDS-pentanol, which eliminated the peak tails that were still observed with the XTerra C18 column. Both the s…

AcetonitrilesResolution (mass spectrometry)Clinical BiochemistryPharmaceutical ScienceCapsulesAntidepressive Agents TricyclicSensitivity and SpecificityDosage formAnalytical Chemistrychemistry.chemical_compoundDrug DiscoverymedicineAcetonitrileSpectroscopyChromatography High Pressure LiquidChromatographyExtraction (chemistry)Reproducibility of ResultsReversed-phase chromatographyDoxepinTrimipraminechemistry1-PentanolSolventsmedicine.drugTabletsJournal of pharmaceutical and biomedical analysis
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Performance of short-chain alcohols versus acetonitrile in the surfactant-mediated reversed-phase liquid chromatographic separation of β-blockers

2010

Organic solvents are traditionally added to micellar mobile phases to achieve adequate retention times and peak profiles, in a chromatographic mode which has been called micellar liquid chromatography (MLC). The organic solvent content is limited to preserve the formation of micelles. However, at increasing organic solvent contents, the transition to a situation where micelles do not exist is gradual. Also, there is no reason to neglect the potentiality of mobile phases containing only surfactant monomers instead of micelles (high submicellar chromatography, HSC). This is demonstrated here for the analysis of β-blockers. The performance of four organic solvents (methanol, ethanol, 1-propano…

Chromatography Reverse-PhaseAcetonitrilesChromatographyElutionAdrenergic beta-AntagonistsOrganic ChemistrySodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyMicelleAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundModels ChemicalchemistryPulmonary surfactantMicellar liquid chromatographyAlcoholsData Interpretation StatisticalMethanolAcetonitrileAlgorithmsMicellesJournal of Chromatography A
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Micellar liquid Chromatographic determination of diuretics by diazotization and coupling with the Bratton-Marshall reagent

1997

Abstract A Chromatographic procedure that uses micellar mobile phases of sodium dodecyl sulphate (SDS) and propanol at pH 3 is reported for the determination, in urine samples, of thiazide diuretics (althiazide, bendroflumethiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide, and trichloromethiazide), and other diuretics having a sulphonamide substituent in the benzene ring. Precolumn derivatization with sodium nitrite and N -(1-naphthyl)ethylenediamine, to form the coloured azo dyes of the hydrolyzed diuretics, decreased the polarity of the compounds and, consequently, their retention in the micellar eluents, and permitted detection in the visible region, eliminating thus the …

HydroflumethiazideChromatographySodiumchemistry.chemical_elementBiochemistryAnalytical ChemistryMatrix (chemical analysis)HydrochlorothiazidechemistryMicellar liquid chromatographyReagentmedicineEnvironmental ChemistryBendroflumethiazideSpectroscopyThiazidemedicine.drugAnalytica Chimica Acta
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Simultaneous detection of hazardous skin whitening agents in Indian cosmetic products using a green chromatographic technique

2021

The present work mainly highlights the simultaneous detection of four skin whitening agents i.e. hydroquinone (HQ), resorcinol (RS), catechol (CC) and 3,3′-dichlorobenzidine (DCB) in facial creams and body lotion. Among these, the first three are positional isomers of dihydroxybenzene so simultaneous separation is difficult with the conventional reverse-phase high-performance liquid chromatographic technique (RP-HPLC). The selected skin whitening agents were detected in facial cream and body lotion using micellar liquid chromatography coupled to a photodiode array detector (MLC-PDA). In the present study, optimization of the method was accomplished using response surface methodology (RSM) w…

Detection limitChromatographyQD71-142Correlation coefficientCentral composite designmicellar liquid chromatographycosmeticsResorcinolCosmeticsresponse surface methodologychemistry.chemical_compoundSkin whitening agentsskin whitening agentschemistryPulmonary surfactantResponse surface methodologyMicellar liquid chromatographyLotionResponse surface methodologyAnalytical chemistryMicellar liquid chromatographyJournal of Chromatography Open
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