Search results for "ROMA"

showing 10 items of 13919 documents

One-Pot Analysis: a New Integrated Methodology for Determination of TAG and FA Determination through LC/MS and in-silico Saponification

2017

Vegetable oils differ significantly for their lipid profile and are mainly constituted by triacylglycerols (TAGs). These are esters formed bonding glycerol to three fatty acids (FAs). To the best of our knowledge, FA and TAG profiles in oils and fats are obtained using at least two different experimental techniques. In particular, FA determination requires elaborated procedures for sample preparation and analyte derivatization. In this work, we propose a one-pot analysis able to determine both TAG and FA contents of edible oils, using experimental data obtained from a simple liquid chromatography/mass spectrometry determination of TAGs. This experimental procedure is followed by an in silic…

AnalyteMass spectrometryTriacylglycerol01 natural sciencesApplied Microbiology and BiotechnologyAnalytical Chemistrychemistry.chemical_compound0404 agricultural biotechnologyLiquid chromatography–mass spectrometryGlycerolSample preparationFood scienceSafety Risk Reliability and QualityDerivatizationChromatography010401 analytical chemistry04 agricultural and veterinary sciencesFatty acid040401 food scienceFAME0104 chemical sciencesLipid profileVegetable oilBlood chemistrychemistryIn silico saponificationSafety ResearchSaponificationFood ScienceFood Analytical Methods
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Experimental Study of the Oriented Immobilization of Antibodies on Photonic Sensing Structures by Using Protein A as an Intermediate Layer

2018

[EN] A proper antibody immobilization on a biosensor is a crucial step in order to obtain a high sensitivity to be able to detect low target analyte concentrations. In this paper, we present an experimental study of the immobilization process of antibodies as bioreceptors on a photonic ring resonator sensor. A protein A intermediate layer was created on the sensor surface in order to obtain an oriented immobilization of the antibodies, which enhances the interaction with the target antigens to be detected. The anti-bovine serum albumin (antiBSA)-bovine serum albumin (BSA) pair was used as a model for our study. An opto-fluidic setup was developed in order to flow the different reagents and,…

AnalyteMaterials scienceIntegrated photonicsSerum albuminBiosensing TechniquesRing resonator02 engineering and technologylcsh:Chemical technologyBiotecnologia01 natural sciencesBiochemistryAntibodiesArticleAnalytical Chemistry010309 opticsResonatorring resonatorsensorQUIMICA ANALITICATEORIA DE LA SEÑAL Y COMUNICACIONES0103 physical scienceslcsh:TP1-1185Electrical and Electronic EngineeringStaphylococcal Protein AInstrumentationIntegrated photonics; ring resonator; sensor; biosensingSensorDetection limitPhotonsChromatographybiologyBiosensingbusiness.industrySerum Albumin BovineRepeatabilityÒptica021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Opticsbiology.proteinbiosensingPhotonics0210 nano-technologybusinessProtein ABiosensorSensors
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Highly Sensitive Detection of Naphthalene in Solvent Vapor Using a Functionalized PBG Refractive Index Sensor

2012

We report an optical refractive index sensor system based on a planar Bragg grating which is functionalized by substituted γ-cyclodextrin to determine low concentrations of naphthalene in solvent vapor. The sensor system exhibits a quasi-instantaneous shift of the Bragg wavelength and is therefore capable for online detection. The overall shift of the Bragg wavelength reveals a linear relationship to the analyte concentration with a gradient of 12.5 ± 1.5 pm/ppm. Due to the spectral resolution and repeatability of the interrogation system, this corresponds to acquisition steps of 80 ppb. Taking into account the experimentally detected signal noise a minimum detection limit of 0.48 ± 0.05 pp…

AnalyteMaterials sciencegas detection; optical sensor; Bragg grating; cyclodextrin; aromatic hydrocarbonsTransducersaromatic hydrocarbonsAnalytical chemistryPhysics::OpticsNaphthaleneslcsh:Chemical technologyBiochemistryNoise (electronics)gas detectionArticleAnalytical ChemistryFiber Bragg gratinglcsh:TP1-1185Electrical and Electronic Engineeringoptical sensorInstrumentationDetection limitCyclodextrinsEquipment DesignAtomic and Molecular Physics and OpticsEquipment Failure AnalysisRefractometryWavelengthTransducercyclodextrinSolventsBragg gratingGasesRefractometryRefractive indexSensors
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Application of ultra-high pressure liquid chromatography linear ion-trap orbitrap to qualitative and quantitative assessment of pesticide residues

2014

Abstract The analysis of pesticides residues using a last generation high resolution and high mass accuracy hybrid linear ion trap-Orbitrap mass spectrometer (LTQ-Orbitrap-MS) was explored. Pesticides were extracted from fruits, fish, bees and sediments by QuEChERS and from water by solid-phase with Oasis HLB cartridges. Ultra-high pressure liquid chromatography (UHPLC)–LTQ-Orbitrap mass spectrometer acquired full scan MS data for quantification, and data dependent (dd) MS 2 and MS 3 product ion spectra for identification and/or confirmation. The regression coefficients ( r 2 ) for the calibration curves (two order of magnitude up to the lowest calibration level) in the study were ≥0.99. Th…

AnalyteMeatCalibration curveAnalytical chemistryOrbitrapQuechersMass spectrometryBiochemistryMass SpectrometryAnalytical Chemistrylaw.inventionlawAnimalsQuadrupole ion trapChromatography High Pressure LiquidChromatographyPesticide residueChemistryOrganic ChemistryFishesPesticide ResiduesGeneral MedicineBeesPesticideFruitEnvironmental PollutantsWater Pollutants ChemicalJournal of Chromatography A
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Multi-analyte method for the analysis of legacy and alternative brominated and chlorinated flame retardants in food products of animal origin using g…

2019

Abstract An analytical method was developed and validated for the analysis of 32 halogenated flame retardants (HFRs), including 13 polybrominated diphenyl ethers (PBDEs), 9 dechlorane-related compounds (DRCs) and 10 of the so-called alternative BFRs in food samples of animal origin. Gas chromatography (GC) coupled with magnetic sector high resolution mass spectrometry (HRMS) was used for the instrumental analysis. Intralaboratory validation of the developed method was performed in terms of recovery, repeatability, linear calibration ranges, instrumental and method limits of quantitation (i-LOQ and m-LOQ). Where possible, trueness was verified by the analysis of reference materials (RMs). Fo…

AnalyteMeatEnvironmental EngineeringEggsHealth Toxicology and Mutagenesis0208 environmental biotechnologyFood ContaminationPilot Projects02 engineering and technology010501 environmental sciences01 natural sciencesAnimal originGas Chromatography-Mass SpectrometryPolybrominated diphenyl ethersLimit of DetectionHalogenated Diphenyl EthersHydrocarbons ChlorinatedCalibrationAnimalsEnvironmental ChemistryFlame Retardants0105 earth and related environmental sciencesMulti analyteChromatographyPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryRepeatabilityPollution020801 environmental engineeringMilkFood productsEnvironmental scienceGas chromatographyChemosphere
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Determination of triamterene and its main metabolite hydroxytriamterene sulfate in human urine by capillary electrophoresis using ultraviolet absorba…

2002

Abstract Two capillary electrophoresis methods have been developed for the direct determination of triamterene and its main metabolite hydroxytriamterene sulfate in human urine. Analytes were detected using conventional UV detection as well as laser-induced fluorescence (LIF) detection with an HeCd-laser operating at a wavelength of 325 nm. The results of both detection techniques were compared. Indeed, the limit of quantification was eightfold lower using LIF detection (50 ng/ml) in comparison to UV detection (400 ng/ml). As no interference due to endogenous urine compounds was observed, direct urine analysis was feasible. Analysis was very simple and fast—one run could be performed within…

AnalyteMetaboliteClinical BiochemistryUrineBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary electrophoresismedicineHumansDiureticsLaser-induced fluorescenceDetection limitTriamtereneChromatographyChemistryLasersElectrophoresis CapillaryReproducibility of ResultsCell BiologyGeneral MedicineFluorescenceSpectrometry FluorescenceSpectrophotometry UltravioletTriamterenemedicine.drugJournal of Chromatography B
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Analysis of basic drugs by liquid chromatography with environmentally friendly mobile phases in pharmaceutical formulations

2017

Abstract Basic drugs are positively charged in the usual working pH (2–8) in reversed-phase liquid chromatography. This gives rise to a strong association with the residual ionized silanols in conventional silica-based stationary phases, which is translated in poor peak shape and high consumption of organic solvent to get appropriate retention times. Micellar mobile phases containing surfactants give rise to modified stationary phases, where silanols are masked, improving the peak shape. However, mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) require a small amount of organic solvent to conveniently decrease the retention of cationic analytes. An alternative is…

AnalyteMethod validation01 natural sciencesAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPulmonary surfactantlawmedicineSample preparationSodium dodecyl sulfateBrij-35β-Adrenoceptor antagonistsSodium dodecyl sulfateSpectroscopyFiltrationChromatography010405 organic chemistryChemistry010401 analytical chemistryCationic polymerizationEnvironmentally friendly0104 chemical sciencesOxprenololPharmaceutical formulationsmedicine.drug
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Optimisation of chromatographic resolution using objective functions including both time and spectral information.

2014

The optimisation of the resolution in high-performance liquid chromatography is traditionally performed attending only to the time information. However, even in the optimal conditions, some peak pairs may remain unresolved. Such incomplete resolution can be still accomplished by deconvolution, which can be carried out with more guarantees of success by including spectral information. In this work, two-way chromatographic objective functions (COFs) that incorporate both time and spectral information were tested, based on the peak purity (analyte peak fraction free of overlapping) and the multivariate selectivity (figure of merit derived from the net analyte signal) concepts. These COFs are s…

AnalyteMultivariate statisticsChromatographyChromatographyAcetonitrilesTime FactorsResolution (mass spectrometry)ChemistryOrganic ChemistryOrthographic projectionWaterGeneral MedicineBiochemistrySignalChemistry Techniques AnalyticalAnalytical ChemistryPhenolsAlternating least squaresFigure of meritDeconvolutionJournal of chromatography. A
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Determination of amphetamines in hair by integrating sample disruption, clean-up and solid phase derivatization

2016

The utility of matrix solid phase dispersion (MSPD) for the direct analysis of amphetamines in hair samples has been evaluated, using liquid chromatography (LC) with fluorescence detection and precolumn derivatization. The proposed approach is based on the employment of MSPD for matrix disruption and clean-up, followed by the derivatization of the analytes onto the dispersant-sample blend. The fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) has been used for derivatization. Different conditions for MSPD, analyte purification and solid phase derivatization have been tested, using amphetamine (AMP), methamphetamine (MET), ephedrine (EPE) and 3,4-methylenedioxymethamphetamine (MDMA)…

AnalyteN-Methyl-34-methylenedioxyamphetamine02 engineering and technologyChloroformate01 natural sciencesBiochemistryMethamphetamineAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundmedicineHumansEphedrineDerivatizationFluorescent DyesEphedrineDetection limitFluorenesChromatographyAmphetamines010401 analytical chemistryOrganic ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesClean-upAmphetaminechemistryReagent0210 nano-technologyChromatography LiquidHairmedicine.drugJournal of Chromatography A
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Stir bar sorptive-dispersive microextraction mediated by magnetic nanoparticles-metal organic framework composite: Determination of N-nitrosamines in…

2019

Abstract A new analytical method based on the recently proposed stir bar sorptive-dispersive microextraction (SBSDME) technique has been developed to determine eight hazardous N-nitrosamines in cosmetic products. As previous step, a simple clean-up is carried out with hexane to remove those highly lipophilic compounds that disturb the SBSDME step. Subsequently, SBSDME is performed by using magnetic nanoparticles–metal organic framework composite, CoFe2O4/MIL-101(Fe), as sorbent to entrap the target analytes, which are later chemically desorbed and measured by liquid chromatography–tandem mass spectrometry (LC–MS/MS). The experimental variables related to the SBSDME procedure were studied to…

AnalyteNitrosaminesSorbentLiquid Phase MicroextractionCosmetics010402 general chemistryMass spectrometry01 natural sciencesBiochemistryChemistry Techniques AnalyticalAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryLiquid chromatography–mass spectrometryMagnetite NanoparticlesMetal-Organic FrameworksDetection limitChromatography010401 analytical chemistryOrganic ChemistryGeneral MedicineRepeatability0104 chemical sciencesHexanechemistryMagnetic nanoparticlesHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of Chromatography A
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