Search results for "performance liquid chromatography"

showing 10 items of 649 documents

Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera and determination by HPLC

2000

Supercritical fluid extraction of resveratrol from grape skin of Vitis vinifera was studied. Extraction variables such pressure, modifier concentration (ethanol), and extraction time were optimised. Final extraction conditions were: 40 degrees C, 150 bar, 7.5% ethanol and extraction time 15 min. Extraction recovery and precision (variation coefficient between 0.2 and 1.0%) were calculated. The resveratrol content in the ethanolic extract was determined by HPLC with UV detection at 306 nm. Acetic acid-methanol-water was used as the mobile phase, and C-18 and C-8 columns were tested, instrumental parameters were optimised, and analytical parameters were calculated (lineal interval 0-75 mg l(-…

Detection limitWinechemistry.chemical_compoundChromatographychemistryCoefficient of variationExtraction (chemistry)Supercritical fluid extractionResveratrolHigh-performance liquid chromatographyQuantitative analysis (chemistry)Analytical ChemistryTalanta
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Determination of glyphosate and aminomethylphosphonic acid in natural water using the capillary electrophoresis combined with enrichment step

2005

A previously elaborated capillary electrophoresis (CE) method used for the determination of glyphosate and aminomethylphosphonic acid (AMPA) was slightly modified in order to improve the sensitivity. However, detection limits attained (5 μg mL−1 for glyphosate and 4 μg mL−1 for AMPA) were still not satisfactory for analytical purposes, thus the addition of a preconcentration step before the CE analysis was proposed. AMBERLITE®IRA-900, a strong anion-exchange resin, was used to preconcentrate both analytes in environmental aqueous samples. The experimental conditions optimised in a previous work were readapted, by decreasing the eluent concentration due to CE limitations. Satisfactory result…

Detection limitaminomethylphosphonic acid (AMPA)Chromatographyanion-exchange resinsChemistrycapillary electrophoresisBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundColumn chromatographyCapillary electrophoresisglyphosateGlyphosateenvironmental analysisUltrapure waterEnvironmental ChemistryAminomethylphosphonic acidSample preparationHPLCSpectroscopyAnalytica Chimica Acta
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Determination of the UV filters worldwide authorised in sunscreens by high-performance liquid chromatography

2001

Simultaneous determination of organic UV filters worldwide authorised in sunscreen formulations was performed by HPLC with UV spectrophotometric detection. The filters determined were: benzophenone-4, benzophenone-3, butyl methoxydibenzoylmethane, octyl dimethyl PABA, octyl methoxycinnamate, homosalate and octyl salicylate. A C18 stationary phase and an isocratic mobile phase of ethanol-water-acetic acid (70:29.5:0.5) containing 65.4 mM of hydroxypropyl-beta-cyclodextrin, were used with a flow-rate of 0.6 ml/min. UV measurements were carried out at 313 nm. The time required for the analysis was 20 min and the limits of detection were between 1.5 and 2.3 mg/l. The procedure proposed provides…

Detection limitchemistry.chemical_classificationChromatographyCyclodextrinOrganic ChemistryOctyl methoxycinnamateGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHomosalatechemistry.chemical_compoundchemistrymedicineOctyl salicylateQuantitative analysis (chemistry)medicine.drugJournal of Chromatography A
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Direct injection analysis of fatty and resin acids in papermaking process waters by HPLC/MS

2011

A novel HPLC-atmospheric pressure chemical ionization/MS (HPLC-APCI/MS) method was developed for the rapid analysis of selected fatty and resin acids typically present in papermaking process waters. A mixture of palmitic, stearic, oleic, linolenic, and dehydroabietic acids was separated by a commercial HPLC column (a modified stationary C(18) phase) using gradient elution with methanol/0.15% formic acid (pH 2.5) as a mobile phase. The internal standard (myristic acid) method was used to calculate the correlation coefficients and in the quantitation of the results. In the thorough quality parameters measurement, a mixture of these model acids in aqueous media as well as in six different pape…

Detection limitchemistry.chemical_compoundChemical ionizationChromatographychemistryFormic acidPhase (matter)Myristic acidFiltration and SeparationMethanolSelectivityHigh-performance liquid chromatographyAnalytical ChemistryJournal of Separation Science
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Determination of arsenic compounds in beverages by high-performance liquid chromatography-inductively coupled plasma mass spectrometry.

2005

Arsenic compounds including arsenous acid (As(III)), arsenic acid (As(V)), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) were separated by high-performance liquid chromatography (HPLC) and detected by inductively coupled plasma mass spectrometry (ICP-MS). A Hamilton PRX-100 anionic-exchange column and a pH 8.5 K(2)HPO(4)/KH(2)PO(4) 5.0x10(-3)molL(-1) mobile phase were used to achieve arsenic speciation. The separation of arsenic species provided peaks of As(III) at 2.75min, DMA at 3.33min, MMA at 5.17min and As(V) at 12.5min. The detection limits, defined as three times the standard deviation of the lowest standard measurements, were found to be 0.2, 0.2, 0.3 and 0.5ngmL(-1) f…

Detection limitchemistry.chemical_compoundChromatographyCertified reference materialsChemistryArsenous acidchemistry.chemical_elementArsenic CompoundHigh-performance liquid chromatographyArsenic acidInductively coupled plasma mass spectrometryArsenicAnalytical ChemistryTalanta
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Determination of sertraline in rat plasma by HPLC and fluorescence detection and its application toin vivopharmacokinetic studies

2012

A simple, rapid, and sensitive HPLC method based on 9H-fluoren-9-ylmethyl chloroformate derivatization for the quantification of sertraline in rat plasma has been developed, requiring a plasma sample of only 0.1 mL, which was deproteinized and derivatized for 5 min in two single steps. The obtained derivative was stable at room temperature and was determined by HPLC using a fluorescence detector. The analytical column was a C(18) column and the mobile phase was acetonitrile and water (80:20, v/v). Calibration curves were linear in the range of 10-500 ng/mL. The limit of detection was approximately 3 ng/mL, and the lower limit of quantification was established at 10 ng/mL. The bias of the me…

Detection limitchemistry.chemical_compoundChromatographyPharmacokineticsChemistryCalibration curveFiltration and SeparationDerivativeChloroformateDerivatizationHigh-performance liquid chromatographyFluorescence spectroscopyAnalytical ChemistryJournal of Separation Science
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A validated and fast procedure for FTIR determination of Cypermethrin and Chlorpyrifos.

2005

Abstract A FTIR methodology has been developed for the simultaneous determination of Cypermethrin and Chlorpyrifos in pesticide commercially available formulations. The method involves the extraction of both active principles with CHCl3 and direct measurement of the peak area values between 1747 and 1737 cm−1 corrected with a baseline defined at 2000 cm−1 for Cypermethrin and peak height values established at 1549 cm−1 corrected using a baseline situated at 1650 cm−1 for Chlorpyrifos. The limits of detection achieved were of the order of 0.7 and 0.4% (w/w), and the relative standard deviation 0.4 and 0.2% for Cypermethrin and Chlorpyrifos, respectively. The developed procedure provided stat…

Detection limitchemistry.chemical_compoundChromatographychemistryChlorpyrifosExtraction (chemistry)Analytical chemistrySample preparationHigh-performance liquid chromatographyFourier transform spectroscopyStandard deviationAnalytical ChemistryCypermethrinTalanta
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A bioluminescence technique for quantitative and structure-associated imaging of pyruvate

2006

A novel bioluminescence assay has been developed for measuring pyruvate within sections of snap-frozen tissue in a quantitative manner as well as with a spatial resolution on a microscopical level. The assay was verified via HPLC and two independent photometric tests. The novel assay makes it possible to determine pyruvate concentrations in cryosections in the range of 0-5.0 micromol/g tissue (dry weight). Based on the analysis of samples of given pyruvate concentrations, the assay exhibits a recovery with a deviationor =15%. The minimal detectable amount was 0.02 pmol based on a 20 microm thick tissue section with an area of 1 cm(2). Combination of the already established imaging biolumine…

Diagnostic ImagingMetaboliteBiologyHigh-performance liquid chromatographyPathology and Forensic Medicinechemistry.chemical_compoundMuscular DiseasesPyruvic AcidBiomarkers TumorFrozen SectionsHumansBioluminescenceGlycolysisLactic AcidNeoplasms Squamous CellRadiosensitivityMolecular BiologyChromatography High Pressure LiquidMusclesCell BiologyLactic acidLuminescent ProteinschemistryBiochemistryHead and Neck NeoplasmsLuminescent MeasurementsCancer cellBiological AssayGlycolysisOxidation-ReductionQuantitative analysis (chemistry)Laboratory Investigation
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The pyrrole moiety as a template for COX-1/COX-2 inhibitors

2000

Aroyl- and thiophene-substituted pyrrole derivatives have been synthesized as a new class of COX-1/COX-2 inhibitors. The inhibition of COX-1 was evaluated in a biological system using bovine PMNLs as the enzyme source, whereas LPS-stimulated human monocytes served as the enzyme source for inducible COX-2. The determination of the concentration of arachidonic acid metabolites was performed by HPLC for COX-1 and RIA for COX-2. Variation of the substitution pattern led to a series of active compounds which showed inhibition for COX-1 and COX-2. Structural requirements for the development of COX-1/COX-2 inhibitors are discussed.

DiclofenacNeutrophilsStereochemistryIndomethacinThiophenesHigh-performance liquid chromatographyMonocytesPyrrole derivativeschemistry.chemical_compoundDrug DiscoveryAnimalsHumansStructure–activity relationshipMoietyCyclooxygenase InhibitorsPyrrolesSulfonesPyrrolePharmacologychemistry.chemical_classificationArachidonic AcidCyclooxygenase 2 InhibitorsMolecular StructureAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryMembrane ProteinsGeneral MedicineIsoenzymesEnzymechemistryMembrane proteinBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesCyclooxygenase 1Leukocytes MononuclearCattleArachidonic acidEuropean Journal of Medicinal Chemistry
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Sensitive determination of aliphatic amines in water by high-performance liquid chromatography with chemiluminescence detection.

2004

A sensitive method has been developed for liquid chromatographic determination of short aliphatic amines in water samples. Analytes are preconcentrated and dansylated on solid sorbents (C18 solid-phase extraction cartridges). The dansyl derivatives are chromatographed and post-column mixed with peroxyoxalate (TCPO) and H2O2 in order to perform chemiluminescence detection. Optimal results have been obtained using a sample volume of 5 ml. The method has been applied to the quantification or screening of several aliphatic amines: methylamine, ethylamine, butylamine, diethylamine, pentylamine and hexylamine. The screening procedure has been developed including also polyamines (putrescine, cadav…

DiethylamineDetection limitChromatographyOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyPeroxyoxalateSensitivity and SpecificityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSpectrometry FluorescencechemistrylawHexylamineLuminescent MeasurementsSpectrophotometry UltravioletEthylaminePentylamineAminesChromatography High Pressure LiquidChemiluminescenceJournal of chromatography. A
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