Search results for "liquid"

showing 10 items of 4351 documents

Comparison of two partial least squares infrared spectrometric methods for the quality control of pediculosis lotions.

2006

Two vibrational spectroscopy procedures have been developed and compared for the direct and simultaneous determination of piperonyl butoxide and tetramethrin, the active ingredients of alcoholic capillary lotions, for hair pediculosis diseases. Nine lotions, purchased from the Spanish market, were analyzed using both, attenuated total reflectance (ATR) and transmission FT-IR measurements, and based on the use of partial least squares (PLS) multivariate calibration. A reduced set of 15 matched standards (11 for calibration and 4 for validation) was employed using both measurement modes. The spectral wave number ranges between 1757 and 1712 cm(-1) was selected to determine tetramethrin by bot…

Quality ControlPiperonyl butoxideChromatographyChemistryPiperonyl ButoxideAdministration TopicalAnalytical chemistryInfrared spectroscopyLice InfestationsBiochemistryHigh-performance liquid chromatographyFourier transform spectroscopyAnalytical Chemistrychemistry.chemical_compoundAttenuated total reflectionPartial least squares regressionPhthirapteraPyrethrinsSpectroscopy Fourier Transform InfraredCalibrationEnvironmental ChemistryAnimalsLeast-Squares AnalysisTetramethrinSpectroscopyAnalytica chimica acta
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Detection of batch effects in liquid chromatography-mass spectrometry metabolomic data using guided principal component analysis.

2014

Metabolomics based on liquid chromatography-mass spectrometry (LC-MS) is a powerful tool for studying dynamic responses of biological systems to different physiological or pathological conditions. Differences in the instrumental response within and between batches introduce unwanted and uncontrolled data variation that should be removed to extract useful information. This work exploits a recently developed method for the identification of batch effects in high throughput genomic data based on the calculation of a delta statistic through principal component analysis (PCA) and guided PCA. Its applicability to LC-MS metabolomic data was tested on two real examples. The first example involved t…

Quality ControlPrincipal Component AnalysisChromatographyChemistryGenomic dataGuided principal component analysisMass spectrometryBatch effectMass SpectrometryAnalytical ChemistryData setPlasmaMetabolomicsLiquid chromatography–mass spectrometryPeak intensityPrincipal component analysisCalibrationLiquid chromatography-mass spectrometry (LC-MS)HumansMetabolomicsBiological systemStatisticChromatography LiquidTalanta
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High-performance micellar liquid chromatography determination of sulphonamides in pharmaceuticals after azodye precolumn derivatization

1995

Abstract A chromatographic procedure with precolumn derivatization to form the N-(1-naphthyl)ethylenediamine dihydrochloride azodyes is proposed for the analysis of several sulphonamides (sodium sulphacetamide, sulphadiazine, sulphaguanidine, sulphamerazine, sulphamethizole, sulphamethoxazole, sulphanilamide and sulphathiazole) in pharmaceutical preparations (tablets, pills, capsules, suspensions and drops). The separation is performed with a 0.05 M sodium dodecyl sulphate/2.4% pentanol eluent at pH 7. The precolumn derivatization improved the resolution in the chromatograms and increased the selectivity in the determination of mixtures of sulphonamides and in preparations where other drugs…

Quality ControlSulfonamidesChromatographyChemistrySodiumClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementHydrogen-Ion ConcentrationHigh-performance liquid chromatographyDosage formAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyMicellar liquid chromatographyDrug DiscoveryIndicators and ReagentsSpectrophotometry UltravioletDerivatizationAzo CompoundsQuantitative analysis (chemistry)Chromatography High Pressure LiquidMicellesSpectroscopyAntibacterial agentJournal of Pharmaceutical and Biomedical Analysis
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Plasma pharmacokinetics and tissue distribution study of cajaninstilbene acid in rats by liquid chromatography with tandem mass spectrometry

2010

Cajaninstilbene acid (CSA; 3-hydroxy-4-prenyl-5-methoxystilbene-2-carboxylic acid) is a major active constituent of pigeonpea leaves, has been proven to be effective in clinical treatment of diabetes, hepatitis, measles and dysentery. A rapid and sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of CSA in rat plasma and various tissues (brain, heart, lung, liver, spleen, small intestine and kidney) of rat for the first time. Rat plasma and tissue distribution pre-treated by protein precipitation with acetoacetate was analyzed using LC-MS/MS with an electrospray ionization (ESI) interface, and isoliquiritigenin was us…

Quality ControlTime FactorsMetabolic Clearance RateFormic acidElectrospray ionizationClinical BiochemistryCarboxylic AcidsPharmaceutical ScienceTandem mass spectrometrySensitivity and SpecificityHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundCajanusDrug StabilityPharmacokineticsTandem Mass SpectrometryLiquid chromatography–mass spectrometryFreezingStilbenesDrug DiscoveryAnimalsProtein precipitationTissue DistributionSpectroscopyChromatographyMolecular StructureTemperatureReproducibility of ResultsHalf-lifeRats Inbred StrainsReference StandardsSalicylatesRatschemistryArea Under CurveCalibrationFemaleChromatography LiquidHalf-LifeJournal of Pharmaceutical and Biomedical Analysis
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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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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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Determination of the relative quantum yields of the conformational species of autoassociating polypeptide gramicidin A in organic solvent using combi…

1987

Abstract A simple, novel method is proposed for the accurate determination of the relative quantum yields of each of the interconverting conformational species of the autoassociating polypeptide gramicidin A in organic solution. The method is based on fitting the experimental results obtained independently from fluorescence emission spectroscopy and high performance liquid chromatography. The fluorescence parameters obtained are discussed in terms of the structural features of the individual conformational species. The advantages of this approach and its possible application to other different organic solvents or to other autoassociating polypeptides are also considered.

Quantitative Biology::BiomoleculesChromatographyAqueous solutionChemistryComputational chemistryGeneral EngineeringQuantum yieldMoleculeEmission spectrumSolvent effectsFluorescenceHigh-performance liquid chromatographyFluorescence spectroscopySpectrochimica Acta Part A: Molecular Spectroscopy
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Conformational Changes of a Single Semiflexible Macromolecule Near an Adsorbing Surface: A Monte Carlo Simulation

2009

The properties of a single semiflexible chain tethered to a planar surface with a long-ranged attractive potential are studied by means of Monte Carlo simulations. We employ the bond fluctuation lattice model and the Wang-Landau sampling technique. We present the diagram of states for semiflexible chains consisting of N = 64 and 128 monomer units as a function of temperature T and strength of the adsorption potential, epsilon(w), and also compare this with the diagram of states for flexible chains of these two lengths. The diagram of states consists of the regions of a coil, liquid globule, solid isotropic globule, adsorbed coil, and quasi-two-dimensional solid globule with nematic bond ord…

Quantitative Biology::BiomoleculesLattice model (finance)Condensed matter physicsMacromolecular SubstancesSurface PropertiesChemistryIsotropyMonte Carlo methodDiagramMolecular ConformationTemperatureBond orderSurfaces Coatings and FilmsCondensed Matter::Soft Condensed MatterCrystalModels ChemicalLiquid crystalChemical physicsPhase (matter)Materials ChemistryComputer SimulationAdsorptionPhysical and Theoretical ChemistryMonte Carlo MethodThe Journal of Physical Chemistry B
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Ferrochirality: a simple theoretical model of interacting, dynamically invertible, helical polymers, 2. Molecular field approach: supports and the de…

1995

Using a molecular field approach, the effect of interaction between reversibly invertible, helical polymers is investigated theoretically. The helices are modelled by nearest-neighbour statistical thermodynamics. If the interaction energy between two helices of common handedness is lower than that of oppositely handed ones, a critical temperature Tc exists, below which the system spontaneously must leave the racemic state, though there is no contact to any chiral centre or force. This is analogous to the second-order phase transition of ferromagnets. The critical point increases with molecular weight and optical persistence of the helices. At the critical point the system is highly sensitiv…

Quantitative Biology::BiomoleculesPhase transitionPolymers and PlasticsStereochemistryChemistryOrganic ChemistrySupramolecular chemistryInteraction energyCondensed Matter PhysicsInorganic ChemistryCritical point (thermodynamics)Chemical physicsLiquid crystalHelixMaterials ChemistryOptical rotationPhase diagramMacromolecular Theory and Simulations
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PREDICTION OF THERMODYNAMIC INSTABILITIES OF PROTEIN SOLUTIONS FROM SIMPLE PROTEIN-PROTEIN INTERACTIONS

2013

Statistical thermodynamics of protein solutions is often studied in terms of simple, microscopic models of particles interacting via pairwise potentials. Such modelling can reproduce the short range structure of protein solutions at equilibrium and predict thermodynamics instabilities of these systems. We introduce a square well model of effective protein-protein interaction that embeds the solvent's action. We modify an existing model [45] by considering a well depth having an explicit dependence on temperature, i.e. an explicit free energy character, thus encompassing the statistically relevant configurations of solvent molecules around proteins. We choose protein solutions exhibiting dem…

Quantitative Biology::BiomoleculesSpinodalRange (particle radiation)Liquid–liquid demixingSpinodal lineChemistrySolvent mediated protein-protein interactionEnthalpyProtein solutionGeneral Physics and AstronomyThermodynamicsEntropy driven phase transitionLiquid-liquid demixingAction (physics)Settore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Solvent mediated protein–protein interactionProtein–protein interactionSpinodal lines SW potential free energy parametrizationPhysics and Astronomy (all)Mean field theoryFinite potential wellMoleculePhysical and Theoretical ChemistrySquare well potential
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