Search results for "PRESSURE"

showing 10 items of 4493 documents

Target analysis and retrospective screening of mycotoxins and pharmacologically active substances in milk using an ultra-high-performance liquid chro…

2020

Milk is a nutritious food suitable for infants and adults, and it plays an important role in the human diet. However, it may also be a vehicle for food contaminants. In this report, we developed a method using ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-Q-Exactive Orbitrap HRMS; Thermo Fisher Scientific, Waltham, MA) for simultaneous identification of target pharmacologically active substances and mycotoxins in milk. We also used the Q-Orbitrap operating in full scan mode to identify other possible drugs and microbial metabolites that occurred in samples. Fifty-six commercially available milk samples from the Italian market were analyze…

AnalyteQuEChERSTarget analysisFood ContaminationOrbitrapMass spectrometryQuechersretrospective analysiMass Spectrometrylaw.inventionmycotoxin03 medical and health scienceschemistry.chemical_compoundlawGeneticsAnimalsMycotoxinChromatography High Pressure Liquid030304 developmental biologyRetrospective Studies0303 health sciencesChromatographyultra-high-performance liquid chromatography/high-resolution mass spectrometry (UHPLC-Q-Orbitrap HRMS)pharmacologically active substanceChemistry0402 animal and dairy science04 agricultural and veterinary sciencesContaminationMycotoxins040201 dairy & animal scienceMilkItalyAnimal Science and ZoologyFood ScienceFood contaminantJournal of dairy science
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Science based calibration for the extraction of 'analyte-specific' HPLC-DAD chromatograms in environmental analysis

2010

Multivariate science based calibration (SBC) has been applied to the resolution of overlapped peaks in liquid chromatography with diode array detection (LC-DAD). Complex river water samples spiked with 11 pharmaceutical substances resulted in poorly resolved chromatograms containing additional peaks from interfering matrix compounds and a change in the background absorbance due to the mobile phase gradient. Applying the present multivariate approach it was possible to resolve all 11 analytes from overlapping peaks, obtaining linear calibration lines (R2 > 0.96). Recovery percentages on spiked samples ranged between 74.6 and 113.5%, which are quite satisfactory taking into account the low co…

AnalyteResolution (mass spectrometry)Adrenergic beta-AntagonistsStatistics as TopicAnalytical chemistryEnvironmentHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)AbsorbanceRiversSCIENCE BASED CALIBRATIONSample preparationLeast-Squares AnalysisElectrodesChromatography High Pressure LiquidAnalgesicsENVIRONMENTAL ANALYSISChromatographyChemistryOtras Ciencias QuímicasExtraction (chemistry)Ciencias QuímicasDrug ResiduesStandard curveHIGH PERFORMANCE LIQUID CHROMATOGRAPHY-DIODE ARRAY DETECTION (HPLC-DAD)CalibrationMultivariate AnalysisEnvironmental PollutantsCIENCIAS NATURALES Y EXACTAS
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Strategies for the enantiomeric determination of amphetamine and related compounds by liquid chromatography.

2002

This paper summarizes recent research on the stereospecific analysis of amphetamine, its analogs and metabolites, by liquid chromatography. The different methods proposed have been evaluated and compared in terms of resolution power, time of analysis, sensitivity, or potential for automation. Chiral derivatization, followed by separation of the diastereomers formed in achiral chromatographic systems, is still the method preferred for the analysis of amphetamines at trace levels, as derivatization also improves analyte detectability. This is the method of choice for the enantiomeric analysis of amphetamines at the low concentrations typically encountered in biological samples. In recent year…

AnalyteResolution (mass spectrometry)medicine.drug_classBiophysicsBiochemistrySensitivity and Specificitychemistry.chemical_compoundIsomerismmedicineHumansEphedrineDerivatizationAmphetamineChromatography High Pressure LiquidChromatographyStaining and LabelingIllicit DrugsAmphetaminesDiastereomerReproducibility of ResultsDesigner drugSubstance Abuse DetectionchemistryModels ChemicalEnantiomermedicine.drugChromatography LiquidJournal of biochemical and biophysical methods
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Wide-range screening of banned veterinary drugs in urine by ultra high liquid chromatography coupled to high-resolution mass spectrometry

2012

In this work, an ultra high performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS) methodology is proposed for the multi-class multi-residue screening of banned and unauthorized veterinary drugs in bovine urine, using an Orbitrap Exactive™ analyzer working at a resolving power of 50,000 FWHM in full scan, both in positive and negative mode. The method currently covers 87 analytes belonging to different families such as steroid hormones, β-agonists, resorcylic acid lactones (RAL), stilbens, tranquillizers, nitroimidazoles, corticosteroids, NSAIDs, amphenicoles, thyreostatics and other substances such as dapsone. A database including the elemental composition, the po…

AnalyteVeterinary DrugsUrineQuechersOrbitrapSensitivity and SpecificityBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionlawAnimalsEuropean UnionAnimal HusbandryChromatography High Pressure LiquidElemental compositionChromatographyChemistryOrganic ChemistryReproducibility of ResultsVeterinary DrugsGeneral MedicineDrug ResiduesCattleUltra high performanceRetention timeJournal of Chromatography A
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Comparison of the solid-phase extraction efficiency of a bounded and an included cyclodextrin-silica microporous composite for polycyclic aromatic hy…

2016

Solid-phase extraction is one of the most important techniques for sample purification and concentration. A wide variety of solid phases have been used for sample preparation over time. In this work, the efficiency of a new kind of solid-phase extraction adsorbent, which is a microporous material made from modified cyclodextrin bounded to a silica network, is evaluated through an analytical method which combines solid-phase extraction with high-performance liquid chromatography to determine polycyclic aromatic hydrocarbons in water samples. Several parameters that affected the analytes recovery, such as the amount of solid phase, the nature and volume of the eluent or the sample volume and …

Analytical chemistry010501 environmental sciences01 natural sciencesHigh-performance liquid chromatographyAnalytical ChemistryAdsorptionColumn chromatographyLimit of DetectionPhase (matter)Sample preparationSolid phase extractionPolycyclic Aromatic HydrocarbonsChromatography High Pressure Liquid0105 earth and related environmental sciencesCyclodextrinsChromatographyChemistry010401 analytical chemistryExtraction (chemistry)Solid Phase ExtractionWaterMicroporous materialEquipment DesignSilicon Dioxide0104 chemical sciencesAdsorptionPorosityWater Pollutants ChemicalTalanta
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Comprehensive analysis of airborne pesticides using hard cap espresso extraction-liquid chromatography-high-resolution mass spectrometry

2017

A hard cap espresso extraction procedure has been developed to recover airborne pesticides in particulate matter trapped in filters. This extraction step was made for 20s at 72°C and 19bar using 50mL of 20% (v/v) acetonitrile in water. After that, based on NaCl salting out, extracts were concentrated 22 times and analysed by ultra-high performance liquid chromatography - high resolution mass spectrometry. 35 pesticides were evaluated, as a proof of concept, being validated the whole methodology and compared the extraction method with that based on microwave assisted extraction for 20min. In short, the method avoids cross-contamination of samples, it is relatively fast and consumes only 10mL…

Analytical chemistry010501 environmental sciencesMass spectrometry01 natural sciencesBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundEspressoMicrowavesAcetonitrileSolvent extractionChromatography High Pressure Liquid0105 earth and related environmental sciencesAir PollutantsChromatographyPesticide residue010401 analytical chemistryOrganic ChemistryExtraction (chemistry)Pesticide ResiduesGeneral MedicinePesticide0104 chemical scienceschemistrySalting outParticulate MatterJournal of Chromatography A
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Pressure-induced magnetic switching and linkage isomerism in K0.4Fe4[Cr(CN)6]2.8 x 16 H2O: X-ray absorption and magnetic circular dichroism studies.

2008

The effect of applied pressure on the magnetic properties of the Prussian blue analogue K0.4Fe4[Cr(CN)6]2.8 x 16 H2O (1) has been analyzed by dc and ac magnetic susceptibility measurements. Under ambient conditions, 1 orders ferromagnetically at a critical temperature (T(C)) of 18.5 K. Under application of pressure in the 0-1200 MPa range, the magnetization of the material decreases and its critical temperature shifts to lower temperatures, reaching T(C) = 7.5 K at 1200 MPa. Pressure-dependent Raman and Mossbauer spectroscopy measurements show that this striking behavior is due to the isomerization of some Cr(III)-C[triple bond]N-Fe(II) linkages to the Cr(III)-N[triple bond]C-Fe(II) form. A…

Analytical chemistryBiochemistryCatalysisMagnetizationsymbols.namesakeMagneticsColloid and Surface ChemistryIsomerismX-Ray DiffractionChromium CompoundsMössbauer spectroscopyTavernePressureLinkage isomerismCyanidesMagnetic circular dichroismChemistrySpectrum AnalysisX-RaysTemperatureWaterGeneral ChemistryMagnetic susceptibilityX-ray magnetic circular dichroismsymbolsDiamagnetismRaman spectroscopyCrystallizationIron CompoundsJournal of the American Chemical Society
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New insights in the formation of silanol defects in silicalite-1 by water intrusion under high pressure.

2010

International audience; The "water-silicalite-1" system is known to act as a molecular spring. The successive intrusion-extrusion cycles of liquid water in small crystallites (6 × 3 × 0.5 μm(3)) of hydrophobic silicalite-1 were studied by volumetric and calorimetric techniques. The experiments displayed a decrease of the intrusion pressure between the first intrusion-extrusion cycle and the consecutive ones, whereas the extrusion pressures remained unchanged. However, neither XRD studies nor SEM observations revealed any structural and morphological modifications of silicalite-1 at the long-range order. Such a shift in the value of the intrusion pressure after the first water intrusion-extr…

Analytical chemistryGeneral Physics and AstronomyInfrared spectroscopy02 engineering and technologyCalorimetry010402 general chemistryMolecular sieve01 natural scienceschemistry.chemical_compoundX-Ray DiffractionSpectroscopy Fourier Transform InfraredPressure[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistryFourier transform infrared spectroscopyZeoliteSilicatesWaterSilanes021001 nanoscience & nanotechnology0104 chemical sciencesSilanolchemistryChemical engineeringSiloxaneX-ray crystallographyZeolitesCrystallite0210 nano-technologyCrystallizationPhysical chemistry chemical physics : PCCP
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Applicability of hybrid linear ion trap-high resolution mass spectrometry and quadrupole-linear ion trap-mass spectrometry for mycotoxin analysis in …

2012

Abstract Recent developments in mass spectrometers have created a paradoxical situation; different mass spectrometers are available, each of them with their specific strengths and drawbacks. Hybrid instruments try to unify several advantages in one instrument. In this study two of wide-used hybrid instruments were compared: hybrid quadrupole-linear ion trap-mass spectrometry (QTRAP ® ) and the hybrid linear ion trap-high resolution mass spectrometry (LTQ-Orbitrap ® ). Both instruments were applied to detect the presence of 18 selected mycotoxins in baby food. Analytical parameters were validated according to 2002/657/CE. Limits of quantification (LOQs) obtained by QTRAP ® instrument ranged …

Analytical chemistryMass spectrometryOrbitrapBiochemistryMass SpectrometryAnalytical ChemistryIonlaw.inventionBaby foodchemistry.chemical_compoundlawLimit of DetectionMSPDHumansQuadrupole ion trapMycotoxinQTRAPChromatography High Pressure LiquidChromatographyBaby foodOrganic ChemistryInfantGeneral MedicineMycotoxinsOrbitrapchemistryQuadrupoleInfant FoodJournal of chromatography. A
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Identification of fish species by reversed-phase high-performance liquid chromatography with photodiode-array detection

1998

A method for the separation of sarcoplasmic fish proteins by RP-HPLC is described. The procedure revealed significant differences useful for reliable identification of fish species. Sixteen of the most common Finnish freshwater fish species were differentiated by species-specific HPLC chromatograms obtained using photodiode-array detection (PAD) at 200-350 nm. The analytical column was a Hi-Pore RP-304 reversed-phase column. The separation was performed by a linear gradient of acetonitrile and water with a small amount of trifluoracetic acid (TFA). Star-symbol plots were constructed from the chromatograms to visualize the data. Clearly different HPLC protein profiles for most fish species w…

Analytical chemistryMuscle ProteinsFresh WaterFish ProteinsHigh-performance liquid chromatographyfoodSpecies SpecificityCoregonus lavaretusPhase (matter)SpectrophotometrymedicineAnimalsChromatography High Pressure LiquidFinlandChromatographybiologymedicine.diagnostic_testfood.dishChemistryFishesReproducibility of ResultsGeneral ChemistryReversed-phase chromatographybiology.organism_classificationSarcoplasmic ReticulumFreshwater fishSpectrophotometry UltravioletSpecific identificationJournal of Chromatography B: Biomedical Sciences and Applications
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