Search results for "Liquid Chromatography"

showing 10 items of 942 documents

Matrix solid-phase dispersion microextraction and determination by high-performance liquid chromatography with UV detection of pesticide residues in …

1999

A multiresidue method based on matrix solid-phase dispersion (MSPD) microextraction was studied to determine the carbamate, benfuracarb, and urea insecticides, diflubenzuron, flufenoxuron hexaflumuron and hexythiazox, used in control of citrus pests. Optimisation of different parameters, such as the type of solid support for matrix dispersion, elution solvents and the clean-up step were carried out. The method used 0.5 g of orange sample, C8 bonded silica as MSPD sorbent and dichloromethane as eluting solvent. Recoveries, at spiked concentrations below the maximum residue levels established by Spanish Government, were between 74 and 84% with relative standard deviations ranging from 2 to 4%…

Quality ControlCarbamateInsecticidesmedicine.medical_treatmentBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistrymedicineSample preparationSolid phase extractionChromatography High Pressure LiquidBenzofuransChromatographyPesticide residueChemistryElutionPhenylurea CompoundsOrganic ChemistryPesticide ResiduesGeneral MedicineReversed-phase chromatographySolventFruitBenzamidesbeta-AlanineIndicators and ReagentsDiflubenzuronJournal of chromatography. A
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Complementary mobile-phase optimisation for resolution enhancement in high-performance liquid chromatography.

2000

An optimisation methodology in high-performance liquid chromatography (HPLC) is presented for the selection of two or more mobile phases having an optimal complementary resolution. The complementary mobile phases (CMPs) are selected in such a way that each one resolves optimally only some compounds in the mixture, while the remainder, resolved by the other mobile phase(s), can overlap among them. The methodology is based on the computation of a peak purity measurement for each solute, using an asymmetrical peak model for peak simulation. Two global resolution criteria (product of elementary resolutions and worst elementary resolution) and two methods for solving the problem (a systematic ex…

Quality ControlChromatographyChemistryComputationOrganic ChemistryResolution (electron density)Phase (waves)General MedicineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryChemometricsModels ChemicalPhase compositionRemainderAlgorithmsChromatography High Pressure LiquidSoftwareJournal of chromatography. A
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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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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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