Search results for "liquid"

showing 10 items of 4351 documents

Last trends in pesticide residue determination by liquid chromatography–mass spectrometry

2014

Liquid chromatography–mass spectrometry (LC–MS) is as an excellent analytical tool in the determination of pesticides. Multiresidue analysis of these compounds at trace levels is one of the oldest analytical schemes within environmental and food safety. However, the issue of “pesticide residue determination” is still a hot topic for the analytical community. This review discusses current approaches and recent advances in using LC–MS for pesticide identification and quantification. We outline how MS has influenced the sample preparation process. We critically assess and compare various mass spectrometers, highlighting their strengths and limitations. We, then, review the main applications of…

ChromatographyPesticide residueLiquid chromatography–mass spectrometryChemistryEnvironmental chemistryPesticide identificationEnvironmental ChemistrySample preparationPesticideMass spectrometryAnalytical ChemistryTrends in Environmental Analytical Chemistry
researchProduct

1-Naphthyl Acetate-Dependent Medium Acidification by Zea mays L. Coleoptile Segments

1991

Zea mays L. cv INRA 5a coleoptile segments ecidify the incubation medium on the addition of 1-naphthyl acetate (1-NA). The buffering capacity of the bathing solution increases during 1-NA stimulated medium acidification. The solution bathing the 1-NA treated coleoptile segment was analyzed by high performance liquid chromatography. A considerable amount of acetic acid was detected in the bathing solution used to measure 1-NA-dependent medium acidification. For the first time, the data demonstrate directly the release of acetic acid from 1-NA. The extent of medium acidification was proportional to 1-NA concentration. Simultaneous measurement of medium acidification and acetate content upon a…

ChromatographyPhysiologyChemistryPlant ScienceMetabolismEsteraseHigh-performance liquid chromatographyHydrolysisAcetic acidchemistry.chemical_compoundColeoptileBiochemistryDevelopment and Growth RegulationGeneticsExtracellularIncubationPlant Physiology
researchProduct

Infrared biospectroscopy for a fast qualitative evaluation of sample preparation in metabolomics.

2014

Liquid chromatography-mass spectrometry (LC-MS) has been increasingly used in biomedicine to study the dynamic metabolomic responses of biological systems under different physiological or pathological conditions. To obtain an integrated snapshot of the system, metabolomic methods in biomedicine typically analyze biofluids (e.g. plasma) that require clean-up before being injected into LC-MS systems. However, high resolution LC-MS is costly in terms of resources required for sample and data analysis and care must be taken to prevent chemical (e.g. ion suppression) or statistical artifacts. Because of that, the effect of sample preparation on the metabolomic profile during metabolomic method d…

ChromatographyPlasma samplesChemistryPlasma compositionIon suppression in liquid chromatography–mass spectrometryBlood ProteinsMass spectrometryMethod developmentMass SpectrometryAnalytical ChemistryMice Inbred C57BLExploratory data analysisMetabolomicsSpectroscopy Fourier Transform InfraredAnimalsMetabolomicsSample preparationFemaleChromatography LiquidTalanta
researchProduct

MALDI-TOF characterization of macromonomers

1996

Methacryloyl endfunctionalized oligostyrene macromonomers were characterized by matrix assisted laser desorption ionization/time of flight (MALDI-TOF) spectroscopy and by isocratic and gradient high performance liquid chromatography (HPLC). The molar mass distribution derived by the different techniques coincide for the investigated oligomers. Mixing experiments revealed that the MALDI-TOF peak areas do not necessarily represent the mixing ratio of the components. Combination of gradient HPLC and MALDI-TOF has resolved the chemical composition of the coupling products formed by reaction of the living anion with oxygen.

ChromatographyPolymers and PlasticsChemistryOrganic ChemistryMatrix isolationAnalytical chemistryMass spectrometryMacromonomerHigh-performance liquid chromatographyTime of flightMatrix-assisted laser desorption/ionizationMaterials ChemistryMolar mass distributionSpectroscopyMacromolecular Rapid Communications
researchProduct

Pressurized liquid extraction of organic contaminants in environmental and food samples

2015

Pressurized liquid extraction (PLE) is an automated technique that uses elevated temperature and pressure to achieve exhaustive extraction from solid matrices, so reducing solvent consumption and enhancing sample throughput when compared with traditional procedures. Hence, it can be considered an environment-friendly technique, generating small volumes of waste and reducing costs and time. This review focuses on application of this green technique to the analysis of organic contaminants in food and environmental matrices for monitoring purposes. We examine fundamentals and key aspects of the development of a PLE method, including pressurized hot-water extraction, together with some relevant…

ChromatographyPressurized fluid extractionChemistrybusiness.industryAssisted solvent extractionExtraction (chemistry)Supercritical fluid extractionContaminationEnvironmentAutomated techniqueSupercritical fluid extractionAnalytical ChemistryPressurized hot-water extractionIn-cell clean-upTemperature and pressureSoxhlet extractionFoodPressurized liquid extractionMicrowave-assisted extractionSolid phase extractionProcess engineeringbusinessSpectroscopyTrAC - Trends in Analytical Chemistry 71: 55-64 (2015)
researchProduct

Target analysis of primary aromatic amines combined with a comprehensive screening of migrating substances in kitchen utensils by liquid chromatograp…

2015

An analytical strategy including both the quantitative target analysis of 8 regulated primary aromatic amines (PAAs), as well as a comprehensive post-run target screening of 77 migrating substances, was developed for nylon utensils, using liquid chromatography-orbitrap-high resolution mass spectrometry (LC-HRMS) operating in full scan mode. The accurate mass data were acquired with a resolving power of 50,000 FWHM (scan speed, 2 Hz), and by alternating two acquisition events, ESI+ with and without fragmentation. The target method was validated after statistical optimization of the main ionization and fragmentation parameters. The quantitative method presented appropriate performance to be u…

ChromatographyPrimary (chemistry)Food contactChemistryRelative standard deviationAnalytical chemistryTarget analysisFood ContaminationOrbitrapCooking and Eating UtensilsAnalytical Chemistrylaw.inventionMassNylonsKitchen utensilslawTandem Mass SpectrometryAnalytical strategyHumansAminesOrganic ChemicalsChromatography LiquidTalanta
researchProduct

Ionic Liquid Based Headspace Solid-Phase Microextraction-Gas Chromatography for the Determination of Volatile Polar Organic Compounds

2010

Solid-phase microextraction (SPME) with an ionic liquid (IL) coating was developed for headspace extraction of a group of low molecular weight alcohols (ethanol, n-propanol, butanol, and isopropyl alcohol), acetone, ethyl acetate, and acetonitrile. A first SPME fiber was simply coated with a dedicated IL whose synthesis is described. A second SPME fiber was prepared by gluing silica (Si) particles on which the synthesized IL was chemically bonded. The analytes SPME extraction was optimized for time, temperature, and NaCl salting out content. The headspace extracted analytes were determined by simple temperature desorption into the hot injection port of a gas chromatograph. The coated-IL fib…

ChromatographyProcess Chemistry and TechnologyGeneral Chemical EngineeringExtraction (chemistry)Ethyl acetateFiltration and SeparationIsopropyl alcoholGeneral ChemistrySolid-phase microextractionchemistry.chemical_compoundchemistryIonic liquidSalting outFiberGas chromatographySeparation Science and Technology
researchProduct

Quick determination of Glyphosate and AMPA at sub µg/L in drinking water by direct injection into LC-MS/MS

2021

Abstract A sensitive, simple and quick method for the determination of glyphosate (Gly) and its degradation product, Aminomethyl phosphonic acid (AMPA), in water through ion chromatography coupled to quadrupole-linear ion trap mass spectrometry has been developed. Sample treatment was based on direct injection and acquisition was implemented in both MS2 and MS3 modes. The LoQs of the method were 0.03 µ/L for both Gly-and AMPA. The recoveries were between 91 and 118% and RSD was lower than 15%. The developed methodology was applied on 436 water samples.

ChromatographyQD71-142ChemistryMass spectrometry 4Ion chromatographyLiquid chromatography 3Water 2AMPA receptorGlyphosate 1chemistry.chemical_compoundGlyphosateLc ms msAnalytical chemistryIon trap mass spectrometryTalanta Open
researchProduct

Study of conformational effects of recombinant interferon gamma adsorbed on a non-porous reversed-phase silica support.

1995

Abstract Reversed-phase chromatography is a powerful method for separating recombinant interferon γ and one of its analogues differing only by a single amino acid residue. Structural differences of the proteins explain this separation ability as demonstrated from adsorption studies on a non-porous reversed-phase support. To reveal the structural differences occurring in the adsorbed state, two different and independent methods were employed. The variation of the retention with the slope of the linear gradient gave information about the molecular contact area of the protein with the support. For different experimental conditions, these data were correlated with the adsorbent capacities measu…

ChromatographyRecombinant interferonChemistryProtein ConformationTemperatureGeneral ChemistrySilicon DioxideRecombinant Proteinslaw.inventionResidue (chemistry)Interferon-gammaAdsorptionlawPhase (matter)Recombinant DNAmedicineHumansInterferon gammaAdsorptionContact areaPorosityChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical applications
researchProduct

Resolution assessment and performance of several organic modifiers in hybrid micellar liquid chromatography

2001

The performance of four criteria that measure the elementary resolution (modified selectivity, modified RS, peak purity, and orthogonal valley-to-peak ratio) was critically assessed using as global resolution function, the product of elementary measurements. The peak purities and valley-to-peak criteria yielded the best description of the overall separation according to the shape of the resolution surfaces compared to the peak arrangements in the chromatograms, the capability of defining unambiguously the composition regions of complete resolution, and the resolution achieved in the predicted optimums. Peak purities were used to compare the effect of five organic modifiers (1-propanol, 1-bu…

ChromatographyResolution (mass spectrometry)Analytical chemistryPrimary alcoholBiochemistryMicellar electrokinetic chromatographyAnalytical ChemistrySolventchemistry.chemical_compoundchemistryMicellar liquid chromatographyEnvironmental ChemistryAcetonitrileSelectivitySpectroscopyTetrahydrofuranAnalytica Chimica Acta
researchProduct