Search results for "high-performance liquid chromatography"

showing 10 items of 629 documents

Characterization of methyl orange and its photocatalytic degradation products by HPLC/UV–VIS diode array and atmospheric pressure ionization quadrupo…

2002

Abstract HPLC/UV–VIS diode array and HPLC/MS techniques were successfully applied to the analysis of sulfonated molecules present in samples coming from the photocatalytic degradation of the azo dye indicator, methyl orange. The substrate was chosen as a simple model for the study of reactions involving the more complex commercial products used for the dyeing of textile fibers. Unexpected MS fragmentation path was observed, due to the very stable methyl orange molecular structure. The chromatographic information were combined with the obtained MS, MS/MS data and the UV–VIS diode array spectra and allowed to rationalize the molecular structures attributable to the various degradation product…

Atmospheric pressureChemistryAnalytical chemistrySubstrate (chemistry)Condensed Matter PhysicsMass spectrometryHigh-performance liquid chromatographychemistry.chemical_compoundIonizationMethyl orangePhysical and Theoretical ChemistryQuadrupole ion trapDyeingInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Authentication of phacelia honeys (Phacelia tanacetifolia) based on a combination of HPLC and HPTLC analyses as well as spectrophotometric measuremen…

2019

Abstract The growing interest in the quality of honey affects customer preferences and consumption trends. Generally, monofloral honeys are more expensive than multifloral honeys, and the price strictly depends on its botanical origin. The increasing popularity of a variety of monofloral brands has led to the increasing number of adulterations and therefore for the need to develop new analytical methods for assessing honey authenticity. The purpose of the present study was to develop a method for the authentication of phacelia honeys on the basis of HPLC and HPTLC analyses and spectrophotometry. The results obtained by spectrophotometric analysis indicated significant differences only betwe…

Authentication of monofloral honeysbiologyHigh-performance thin-layer chromatographyPhacelia honeyContext (language use)biology.organism_classificationmedicine.disease_causeHigh-performance liquid chromatographyHoney samplesPhenolic compoundsHigh-performance liquid chromatographyPhacelia tanacetifoliaPhaceliaPollenmedicineFood scienceFood ScienceMathematicsLWT
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Analysis of pesticides in fruits by pressurized liquid extraction and liquid chromatography-ion trap-triple stage mass spectrometry.

2005

A multi-residue method using pressurized liquid extraction (PLE) and liquid chromatography-quadrupole ion trap-triple stage mass spectrometry (LC-IT-MS(3)) has been developed for determining trace levels of pesticides in fruits. The selected pesticides can be distinguished in: benzimidazoles and azoles, organophosphorus, carbamates, neonicotinoids, and acaricides. PLE has been optimized to extract these pesticide residues from oranges and peaches by studying the effect of experimental variables on PLE efficiency. Samples were extracted at high temperature and pressure (75 degrees C and 1500psi) using ethyl acetate as extraction solvent and acidic alumina as drying agent. The recoveries obta…

AzolesEthyl acetateAcetatesMass spectrometryBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnabasineMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundOrganophosphorus Compoundsmedia_common.cataloged_instanceEuropean unionPesticidesmedia_commonResidue (complex analysis)ChromatographyPesticide residueChemistryOrganic ChemistryExtraction (chemistry)Pesticide ResiduesTemperatureReproducibility of ResultsGeneral MedicineFruitBenzimidazolesIon trapCarbamatesChromatography LiquidJournal of chromatography. A
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Determination of phenytoin in plasma by molecularly imprinted solid-phase extraction.

2001

Abstract A molecularly imprinted polymer (MIP) using phenytoin as template and methacrylamide as the functional monomer was prepared. The selectivity was measured by comparing capacity factors of phenytoin and other structurally related compounds. The polymer was evaluated as a selective sorbent in molecularly imprinted solid-phase extraction (MISPE). Several washing solvents were tested to study their ability to disrupt the non-specific interactions occurring between the sample and the polymer matrix and the role of water in the recognition process was also investigated. It was shown that the key step of successful sample extraction is the right choice of the washing solvent. Plasma sample…

BioanalysisChromatographyChemistryPolymersOrganic ChemistryExtraction (chemistry)Molecularly imprinted polymerReproducibility of ResultsGeneral MedicineReference StandardsBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)PhenytoinCalibrationHumansSample preparationAnticonvulsantsSolid phase extractionMolecular imprintingJournal of chromatography. A
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Application of a low transition temperature mixture for the dispersive liquid–liquid microextraction of illicit drugs from urine samples

2021

© 2021 by the authors.

BioanalysisLiquid Phase MicroextractionProductes biològicsIllicit drugsDispersive liquid–liquid mi-croextractionPharmaceutical ScienceOrganic chemistryUrineUrineHigh-performance liquid chromatographyBiological samples; Deep eutectic solvents; Dispersive liquid–liquid mi-croextraction; Drugs; High performance liquid chromatography; Illicit drugs; Low transition temperature mixtures; UrineArticleLow transition temperature mixturesAnalytical Chemistrychemistry.chemical_compoundBiological samplesQD241-441Limit of DetectionDrug DiscoveryHumansTransition TemperatureSample preparationPhysical and Theoretical ChemistryChromatographyChemistryExtraction (chemistry)Deep eutectic solventsDrugsSolventCold TemperatureChemistry (miscellaneous)Dispersive liquid–liquid microextractionMolecular MedicineDroguesGlass transitionCholine chlorideHigh performance liquid chromatography
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An Optimized and Rapid DNA Extraction Method From Leaves of Grapevine Suitable for PCR-DGGE Based Analysis

2010

Molecular techniques and genetic studies require a fair amount of DNA of high quality in order to produce reliable and clear results (Li et al., 2007). In grapevine, the yield and quality of DNA can be significantly affected by secondary metabolites such as polyphenols, polysaccharides and tannins, that may be consistently abundant during the different stages of leaf development (Iandolino et al., 2004). The development of a simple, rapid and reliable method for the extraction of genomic DNA from grape leaves collected at several stages during development, as well as from healthy grape leaves and leaves infected by pathogenic microorganisms, was the main objective of this study. The protoco…

BioengineeringBiologyApplied Microbiology and BiotechnologyHigh-performance liquid chromatographyAnisodaminelaw.inventionchemistry.chemical_compoundLaboratory flaskErlenmeyer flasklawBioreactorDNA extractionPCR-DGGEChromatographyInoculationSettore AGR/12 - Patologia VegetaleCTABGeneral MedicinepolyphenolchemistryPolyphenolpolysaccharideVitis viniferaAerationSettore AGR/16 - Microbiologia AgrariaBiotechnologyJournal of Biotechnology
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UDP-glucosyltransferase activity toward exogenous substrates in Drosophila melanogaster.

1991

To investigate the capacity of Drosophila extracts to glucosylate exogenous substrates we have developed a fast and sensitive method for the detection of UDP-glucosyltransferase activity using 4-nitrophenol, 1-naphthol, or 2-naphthol as substrates. High-performance liquid chromatography was used to separate and quantitate the reaction products, allowing detection of activities that produced as little as 1 pmol of 2-naphthol glucoside (fluorescence detection) or 16 pmol of 4-nitrophenol glucoside (absorbance detection). Optimal activity was found at 43 degrees C and alkaline pH. The affinity of the Drosophila enzyme was 250-fold higher for 1-naphthol or 2-naphthol (Km approximately 4 microM)…

BiophysicsNaphtholsBiochemistryHigh-performance liquid chromatographyUridine DiphosphateSubstrate SpecificityAbsorbanceNitrophenolschemistry.chemical_compoundGlucosideDrosophilidaeAnimalsMolecular BiologyChromatography High Pressure Liquidchemistry.chemical_classificationChromatographybiologySubstrate (chemistry)Cell BiologyHydrogen-Ion Concentrationbiology.organism_classificationFluorescenceEnzymeDrosophila melanogasterchemistryBiochemistryGlucosyltransferasesDrosophila melanogasterAnalytical biochemistry
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Determination of Phenolic Endocrine Disruptors in Cosmetics by High-Performance Liquid Chromatography Mass Spectrometry

2017

An analytical method for the simultaneous determination of bisphenol A, 4-t-octylphenol, 4-n-octylphenol, and 4-n-nonylphenol in cosmetic samples has been developed. These compounds have toxic effe...

Bisphenol AChromatographyChemistrymedia_common.quotation_subject010401 analytical chemistryBiochemistry (medical)Clinical Biochemistry010501 environmental sciencesMass spectrometry01 natural sciencesBiochemistryHigh-performance liquid chromatographyCosmetics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundEnvironmental chemistryElectrochemistrySpectroscopy0105 earth and related environmental sciencesmedia_commonAnalytical Letters
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Cyclooxygenase-1/2 (COX-1/COX-2) and 5-lipoxygenase (5-LOX) inhibitors of the 6,7-diaryl-2,3-1H-dihydropyrrolizine type

2003

A series of 6,7-diaryl-2,3-1H-dihydropyrrolizines was prepared as COX-1/COX-2 and 5-LOX inhibitors. The inhibition of COX-1 was evaluated using intact bovine platelets as the enzyme source, whereas LPS-stimulated human monocytes served as the enzyme source for inducible COX-2. The determination of arachidonic metabolites was performed by HPLC for COX-1 and RIA for COX-2. The balance between COX-1/COX-2 and 5-LOX inhibition can be shifted by modifying the substitution pattern of the phenyl moiety at the 6- and 7-position of the pyrrolizine nucleus. Structure-activity relationships are discussed.

Blood PlateletsRadioimmunoassayHigh-performance liquid chromatographyIsozymeMonocytesDrug DiscoverymedicineCox 1 cox 2AnimalsHumansMoietyStructure–activity relationshipPyrrolesPlateletLipoxygenase InhibitorsEnzyme InhibitorsChromatography High Pressure LiquidPharmacologychemistry.chemical_classificationbiologyChemistryOrganic ChemistryMembrane ProteinsGeneral MedicineIn vitroIsoenzymesmedicine.anatomical_structureEnzymeBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesEnzyme inhibitorDrug DesignArachidonate 5-lipoxygenaseCyclooxygenase 1biology.proteinCattleCyclooxygenaseNucleusEuropean Journal of Medicinal Chemistry
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In-vitro test system for the evaluation of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) inhibitors based on a single HPLC run with UV detect…

2001

Objective and Design: The aim of this study was to develop a new, whole-cell test system which is easy to handle and requires a standard equipment for the parallel screening of COX-1 and COX-2 inhibitors.¶Materials: Bovine aortic endothelial cells (BAECs).¶Treatment and methods: Unstimulated bovine aortic coronary endothelial cells (BAECs) were used as a source of COX-1 and BAECs pretreated with ASA (100 μM) and activated with phorbol myristate acetate (PMA) were used as a source of COX-2. The time- and concentration-dependent induction of COX-2 expression in the BAECs was evaluated by a kinetic profile (HPLC analysis) and detected by Western-Blot analysis using polyclonal antibodies agains…

Blotting WesternImmunologyDrug Evaluation PreclinicalAorta ThoracicIn Vitro TechniquesHigh-performance liquid chromatographyLipoxygenaseDiclofenacmedicineAnimalsCyclooxygenase InhibitorsLipoxygenase InhibitorsIC50Chromatography High Pressure LiquidPharmacologyCyclooxygenase 2 InhibitorsbiologyChemistryMolecular biologyIsoenzymesKineticsMeloxicamBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesPolyclonal antibodiesCyclooxygenase 1biology.proteinTetradecanoylphorbol AcetateAceclofenacCattleSpectrophotometry UltravioletEndothelium VascularCyclooxygenasemedicine.drugInflammation Research
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