Search results for "liquid chromatography"

showing 10 items of 942 documents

Automated synthesis and purification of [18F]fluoro-[di-deutero]methyl tosylate

2013

Automated synthetic procedures of [ 18 F]fluoro-[di-deutero]methyl tosylate on a GE TRACERlab FX F-N module and a non-commercial synthesis module have been developed. The syntheses included azeotropic drying of the [ 18 F]fluoride, nucleophilic 18 F-fluorination of bis(tosyloxy)-[di-deutero]methane, HPLC purification and subsequent formulation of the synthesized [ 18 F]fluoro-[di-deutero]methyl tosylate (d2-[ 18 F]FMT) in organic solvents. Automation shortened the total synthesis time to 50min, resulting in an average radiochemical yield of about 50% and high radiochemical purity (>98%). The possible application of this procedure to commercially available synthesis modules might be of signi…

Methyl tosylateOrganic ChemistryTotal synthesisBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryNucleophileYield (chemistry)Drug DiscoveryOrganic chemistryRadiology Nuclear Medicine and imagingFluorideSpectroscopyJournal of Labelled Compounds and Radiopharmaceuticals
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Determination of mycotoxins produced by Fusarium isolates from banana fruits by capillary gas chromatography and high-performance liquid chromatograp…

1997

A method of analysis for trichothecenes (nivalenol, deoxynivalenol, 3- and 15-acetyldeoxynivalenol, diacetoxyscirpenol, neosolaniol, T-2 tetraol, T-2 and HT-2 toxins), zearalenone and zearalenols, and another method for determination of fumonisin B1 are described and applied to cultures of Fusarium isolated from bananas. Both methods were adapted from different techniques of extraction, clean-up and determination of these mycotoxins. The first method involves extraction with methanol-1% aqueous sodium chloride, clean-up of extracts by partition with hexane and dichloromethane, additional solid reversed-phase clean-up and analysis of two eluates by both high-performance liquid chromatography…

Microbiological TechniquesChromatography GasTrichotheceneCarboxylic AcidsBiochemistryHigh-performance liquid chromatographyFumonisinsZea maysDiacetoxyscirpenolAnalytical Chemistrychemistry.chemical_compoundFusariumFumonisinSolid phase extractionZearalenoneChromatography High Pressure LiquidFumonisin B1ChromatographyChemistryOrganic Chemistryfood and beveragesElectrophoresis CapillaryOryzaGeneral MedicineMycotoxinsFruitZearalenoneZeranolSpectrophotometry UltravioletGas chromatographyTrichothecenesJournal of chromatography. A
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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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Use of Micellar Liquid Chromatography to Determine Mebendazole in Dairy Products and Breeding Waste from Bovine Animals

2020

Mebendazole is an anthelmintic drug used in cattle production. However, residues may occur in produced food and in excretions, jeopardizing population health. A method based on micellar liquid chromatography (MLC) was developed to determine mebendazole in dairy products (milk, cheese, butter, and curd) and nitrogenous waste (urine and dung) from bovine animals. Sample treatment was expedited to simple dilution or solid-to-liquid extraction, followed by filtration and direct injection of the obtained solution. The analyte was resolved from matrix compounds in less than 8 min, using a C18 column and a mobile phase made up of 0.15 M sodium dodecyl sulfate (SDS)&ndash

Microbiology (medical)Analytemicellar01 natural sciencesBiochemistryMicrobiologyArticleMatrix (chemical analysis)chemistry.chemical_compoundmedicinePharmacology (medical)AnthelminticGeneral Pharmacology Toxicology and PharmaceuticsSodium dodecyl sulfateDetection limitvalidationmilkChromatographyanthelmintic010405 organic chemistryfood010401 analytical chemistryExtraction (chemistry)lcsh:RM1-950food and beveragesurine0104 chemical sciencesDilutionInfectious Diseaseslcsh:Therapeutics. PharmacologychemistryMicellar liquid chromatographymedicine.drugAntibiotics
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Characterization of isomeric 1,2,4-oxadiazolyl-N-methylpyridinium salts by electrospray ionization tandem mass spectrometry.

2007

The mass spectrometric behavior of 1,2,4-oxadiazolyl- N-methylpyridinium salts has been investigated. These substances are of current interest as perspective ionic liquids, compounds used as green solvents for synthesis, and for their catalytic properties. The studies have been developed through electrospray ionization tandem mass spectrometry (ESI-MS/MS) experiments. The obtained results demonstrate a ready distinction between the two isomeric classes, 3- N-methylpyridinium- and 5- N-methylpyridinium-1,2,4-oxadiazoles, is possible through ESI-MS/MS experiments. A deeper investigation on the principal fragmentation pathways of characteristic ions has been also developed.

Models MolecularSpectrometry Mass Electrospray IonizationProtein mass spectrometry020209 energyElectrospray ionizationIonic Liquids02 engineering and technologyTandem mass spectrometrySample preparation in mass spectrometrychemistry.chemical_compoundIsomerismESI-MS ionic kiquids oxadiazolylpyridiniumComputational chemistry0202 electrical engineering electronic engineering information engineeringDirect electron ionization liquid chromatography–mass spectrometry interfaceSpectroscopyChromatographySelected reaction monitoringExtractive electrospray ionizationGeneral MedicineAtomic and Molecular Physics and OpticschemistryModels ChemicalSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIonic liquidSaltsEuropean journal of mass spectrometry (Chichester, England)
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Modelling the enantioresolution capability of cellulose tris(3,5-dichlorophenylcarbamate) stationary phase in reversed phase conditions for neutral a…

2018

[EN] To the best of our knowledge, the prediction of the enantioresolution ability of polysaccharides-based stationary phases in liquid chromatography for structurally unrelated compounds has not been previously reported. In this study, structural information of neutral and basic compounds is used to model their enantioresolution levels obtained from an immobilised cellulose tris(3,5-dichlorophenylcarbamate) stationary phase in reversed phase conditions. Thirty-four structurally unrelated chiral drugs and pesticides, from seven families, are studied. Categorical enantioresolution levels (RsC, 0 = no baseline enantioresolution and 1 = baseline enantioresolution) are established from the expe…

Models MolecularTrisPhenylcarbamatesEnantioresolution modelling01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundMolecular descriptorPhase (matter)Tris(35-dichlorophenylcarbamate)MoleculeLeast-Squares AnalysisPesticidesCelluloseCelluloseChromatography High Pressure LiquidReversed phase liquid chromatographyEnantioseparationsChromatography Reverse-PhasePrincipal Component AnalysisChromatography010405 organic chemistry010401 analytical chemistryOrganic ChemistryDiscriminant partial least squaresDiscriminant AnalysisStereoisomerismGeneral MedicineReversed-phase chromatography0104 chemical scienceschemistryStationary phaseAsymmetric carbonStationary phaseJournal of Chromatography A
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Assay for O6-alkylguanine-DNA-alkyltransferase using oligonucleotides containing O6-methylguanine in a BamHI recognition site as substrate

1992

Abstract Double-stranded oligonucleotides, 40 bases in length containing an O 6 -methylguanine in a Bam HI restriction site, were developed as substrates for the determination of human O 6 -alkylguanine-DNA-alkyltransferase (AGT). The assay proved highly sensitive and quantitative. After incubation of the 5′-end-labeled oligonucleotides with cell homogenates of peripheral blood lymphocytes, the DNA was digested with Bam HI. Cleavage with this restriction enzyme did not occur in the O 6 -methylguanine-containing oligonucleotide unless the fragment was repaired. The cleaved oligonucleotide was separated from the intact parent oligonucleotide by reverse-phase high-performance liquid chromatogr…

Molecular Sequence DataOligonucleotidesBiophysicsBiologyCleavage (embryo)Sensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyO(6)-Methylguanine-DNA Methyltransferasechemistry.chemical_compoundHumansLymphocytesMolecular BiologyChromatography High Pressure LiquidBase SequenceOligonucleotideSubstrate (chemistry)MethyltransferasesCell BiologyMolecular biologyPeptide FragmentsRestriction siteRestriction enzymeBiochemistrychemistryBamHIPhosphorus RadioisotopesDNAAnalytical Biochemistry
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Monolithic silica columns of various format in automated sample clean-up/multidimensional liquid chromatography/mass spectrometry for peptidomics.

2007

The following particulate and monolithic silica columns were implemented in a fully automated and flexible multidimensional LC/MS system with integrated sample clean-up, to perform the analysis of endogeneous peptides from filtered urine and plasma samples: restricted access sulphonic acid strong cation-exchanger (RAM-SCX) for sample clean-up, RP 18 Chromolith guard columns as trap columns and 100 microm I.D. monolithic RP 18 fused silica capillary columns as last LC dimension. The results show sufficient overall system reproducibility and repeatability. Implementation of monolithic silica columns added an additional flexibility with respect to flow rate variation and adjustment due to the …

Monolithic HPLC columnChromatographyChemistryOrganic ChemistryAnalytical chemistryReproducibility of ResultsGeneral MedicineRepeatabilityReversed-phase chromatographyMass spectrometrySilicon DioxideBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical ChemistryLiquid chromatography–mass spectrometrySample preparationSolid phase extractionPeptidesChromatography LiquidJournal of chromatography. A
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Preparation of organic monolithic columns in polytetrafluoroethylene tubes for reversed-phase liquid chromatography

2017

[EN] In this work, a method for the preparation and anchoring of polymeric monoliths in a polytetrafluoroethylene (PTFE) tubing as a column housing for microbore HPLC is described. In order to assure a covalent attachment of the monolith to the inner wall of the PTFE tube, a two-step procedure was developed. Two surface etching reagents, a commercial sodium naphthalene solution (Fluoroetch®), or mixtures of H2O2 and H2SO4, were tried and compared. Then, the obtained hydroxyl groups on the PTFE surface were modified by methacryloylation. Attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy and scanning electron microscopy (SEM) confirmed the successful modification…

Monolithic HPLC columnMicrobore column02 engineering and technology01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundSurface modificationQUIMICA ANALITICAEnvironmental ChemistryMonolith attachmentMonolithReversed-phase liquid chromatographyPolytetrafluoroethyleneSpectroscopychemistry.chemical_classificationChromatography Reverse-PhasegeographyChromatographygeography.geographical_feature_categoryPolytetrafluoroethyleneChemistry010401 analytical chemistryPolymer monolithEquipment DesignPolymer021001 nanoscience & nanotechnology0104 chemical sciencesChemical engineeringPolymerizationAttenuated total reflectionSurface modificationAlkylbenzenes0210 nano-technologyAnalytica Chimica Acta
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Photografted fluoropolymers as novel chromatographic supports for polymeric monolithic stationary phases

2018

[EN] In this study, porous polymer monoliths were in situ synthesized in fluoropolymers tubing to prepare microbore HPLC columns. To ensure the formation of robust homogeneous polymer monoliths in these housing supports, the inner surface of fluoropolymer tubing was modified in a two-step photografting process. Raman spectroscopy and scanning electron microscopy (SEM) confirmed the successful modification of the inner poly(ethylene-co-tetrafluoroethylene) (ETFE) wall and the subsequent attachment of a monolith onto the wall. Poly(glycidyl methacrylate-co-divinylbenzene), poly(butyl methacrylate-co-ethyleneglycol dimethacrylate) and poly(styrene-co-divinylbenzene) monoliths were in situ synt…

Monolithic columnMonolithic HPLC columnFluoropolymer02 engineering and technology01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundETFEPhotograftingQUIMICA ANALITICAMonolithReversed-phase liquid chromatographyAlkylchemistry.chemical_classificationgeographyEthylene-tetrafluoroethylenegeography.geographical_feature_categoryChromatography010401 analytical chemistryPolymer021001 nanoscience & nanotechnology0104 chemical scienceschemistryPolymerizationPhotograftingFluoropolymer0210 nano-technology
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