Search results for "Fluorescence spectroscopy"

showing 10 items of 188 documents

Chemosensors displaying pH controlled multistage fluorescence emission

1999

A large number of systems displaying pH controlled multistages of fluorescence emission intensity, have not been recognized from this point of view. In this work we present two paradigmatic cases: (i) polyamine receptors linked to a fluorophore unit, in which the signal is modulated by an intra-molecular pH dependent electron transfer process, (ii) phenols presenting adiabatic excited state proton transfer. In the first example the chemosensors are constituted by a receptor unit containing a polyaza moiety suitable for binding protons (but also metal ions or anions). The receptor is linked to a benzene or naphthalene unit that acts as a fluorophore. The fluorescence signal is dependent on t…

FluorophoreChemistryGeneral Chemical EngineeringGeneral Physics and AstronomyProtonationGeneral ChemistryPhotochemistryFluorescenceFluorescence spectroscopychemistry.chemical_compoundElectron transferExcited stateMoietyCyclophaneJournal of Photochemistry and Photobiology A: Chemistry
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Spectroscopic Methods for the Determination of Protein Interactions

2005

This unit provides guidelines on how to use steady-state fluorescence spectroscopy for the quantification of protein-protein interactions. The fluorescence of a protein is characterized by its excitation and emission spectra, quantum yield, and anisotropy. These parameters can change upon interaction with another protein and can be used to measure the extent of complex formation. The source of fluorescence can be an intrinsic fluorophore, such as tryptophan or tyrosine; a covalently attached fluorescent dye; or a fluorescent binding partner, such as a nucleotide or cofactor, that interacts specifically with the complex. Protocols are provided in this unit for determining affinity constants …

FluorophoreChemistryProteinsfood and beveragesQuantum yieldFluorescence in the life sciencesBiochemistryFluorescenceFluorescence spectroscopyProtein–protein interactionchemistry.chemical_compoundBimolecular fluorescence complementationCrystallographySpectrometry FluorescenceStructural BiologyBiophysicsTitrationProtein BindingCurrent Protocols in Protein Science
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Analysis of fumonisins in corn-based food by liquid chromatography with fluorescence and mass spectrometry detectors

2008

Abstract The presented procedure involves an extraction with methanol–water, centrifugation and cleanup with immunoaffinity columns. A comparison study between fluorescence detector, mass spectrometry, and tandem mass spectrometry with a triple quadrupole (QqQ) analyzer using an electrospray ionisation interface for the determination of fumonisin B1 and B2 in corn-based products has been performed. Limits of quantification obtained by the three detectors were lower than the maximum levels established by European Commission. Liquid chromatography coupled to tandem mass spectrometry provides higher sensitivity (12 μg kg−1for fumonisins B1 and B2) when compared to mass spectrometry (40 μg kg−1…

Fumonisin B2ElectrosprayFumonisin B1ChromatographyChemistryExtraction (chemistry)General MedicineTandem mass spectrometryMass spectrometryFluorescence spectroscopyAnalytical ChemistryTriple quadrupole mass spectrometerchemistry.chemical_compoundFood ScienceFood Chemistry
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Occurrence of Fusarium mycotoxins in Italian cereal and cereal products from organic farming.

2013

In the present study, the occurrence of eighteen mycotoxins, nine trichothecenes (deoxynivalenol, 3-acetyl-deoxynivalenol, 15-acetyl-deoxynivalenol, nivalenol, neosolaniol, diacetoxyscirpenol, fusarenon-X, T-2 toxin and HT-2 toxin), three zearalenones (zearalenone, α-zearalenol and β-zearalenol), and six emergent mycotoxins, beauvericin and five enniatins (A, A1, B, B1 and B4), was monitored in different Italian organic cereals and cereal products by using a liquid chromatography coupled to triple quadrupole mass spectrometry method. A total of 93 organic cereal samples (wheat, barley, rye and oat) were collected from Italy. Limits of quantification ranged from 5 to 15 μg/kg. 80% of analyze…

Fusariumorganic foodFood SafetyFood ContaminationMass spectrometrymedicine.disease_causeDiacetoxyscirpenolAnalytical Chemistrymycotoxin03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyFusariumGastric cancer Gastrokine-1 Pichia pastoris Recombinant synthesis Mass spectrometry Circular dichroism Fluorescence spectroscopy Limited proteolysis Cell proliferation.medicineFood scienceMycotoxinZearalenone030304 developmental biology2. Zero hunger0303 health sciencesOrganic AgriculturebiologyToxin04 agricultural and veterinary sciencesGeneral MedicineMycotoxinsbiology.organism_classification040401 food scienceBeauvericinchemistryAgronomyItalyEnniatinEdible GrainFood ScienceFood chemistry
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Investigating different skin and gastrointestinal tract (GIT) pathologies ex vivo by autofluorescence spectroscopy and optical imaging

2017

The skin neoplasias are on a second place in the world statistics of cancer incidence, and gastrointestinal tract (GIT) tumours are also in the “top ten” list. For the most of cutaneous and gastrointestinal tumours could be obtained better prognoses for patients, if an earlier and precise diagnostics procedure is applied. One of the most promising approaches for development of improved diagnostic techniques, is based on optical detection, and analysis of the signatures of biological tissues for detecting the presence of pathological alterations in the investigated objects. It is important to develop and combine novel diagnostic techniques for an accurate early stage diagnosis to improve the…

Gastrointestinal tractPathologymedicine.medical_specialtygastrointestinal tract tumourHigh resolutionBiologycutaneous tumourFluorescence spectraoptical imagingOptical imagingCancer incidencemedicineAutofluorescence spectroscopyautofluorescence spectroscopyStage (cooking)Ex vivoSPIE Proceedings
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Fluorescence of soil humic acids and their fractions obtained by tandem size exclusion chromatography-polyacrylamide gel electrophoresis

2002

Humic acids (HAs) extracted from soils of different origin (chernozem, ferralsol and ranker) and their fractions (A, B and C+D) obtained by tandem size exclusion chromatography–polyacrylamide gel electrophoresis were investigated by steady-state fluorescence spectroscopy in the emission mode. Independently of HA source, high molecular size fractions A and B are shown to be weakly fluorescent. The main fluorophores, especially those emitting at long wavelength (around 500–510 nm), are contained in the polar and low molecular size fractions C+D. As indicated by the observed pH effect, aromatic structures bearing carboxylate and OH substituents may be involved in these longer wavelength emissi…

Gel electrophoresis[SDE] Environmental SciencesChromatographyChemistry[SDV]Life Sciences [q-bio]Size-exclusion chromatographyMineralogyFluorescenceFluorescence spectroscopy[SDV] Life Sciences [q-bio]Electrophoresischemistry.chemical_compoundGeochemistry and Petrology[SDE]Environmental SciencesCarboxylatePolyacrylamide gel electrophoresisChernozem
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Determination of Mercury in Milk by Cold Vapor Atomic Fluorescence: A Green Analytical Chemistry Laboratory Experiment

2011

Green analytical chemistry principles were introduced to undergraduate students in a laboratory experiment focused on determining the mercury concentration in cow and goat milk. In addition to traditional goals, such as accuracy, precision, sensitivity, and limits of detection in method selection and development, attention was paid to the evaluation of green parameters of the analytical methods. Milk samples were evaluated by cold vapor atomic fluorescence spectrometry (CV-AFS) and the wastes were minimized by co-precipitation with Fe(III).

Green chemistryDetection limitChemistryAnalytical chemistryfood and beverageschemistry.chemical_elementGeneral ChemistryAtomic spectroscopyFluorescence spectroscopyEducationMercury (element)Cold vaporLaboratory experimentSpectroscopyJournal of Chemical Education
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The solubilisation behaviour of some dichloroalkanes in aqueous solutions of PEO-PPO-PEO triblock copolymers: a dynamic light scattering, fluorescenc…

2006

The aggregation behaviour of PEO-PPO-PEO triblock copolymers in water and in water + chlorinated additive mixtures was studied by means of fluorescence spectroscopy, dynamic light scattering (DLS), and small-angle neutron scattering (SANS). The copolymers were chosen such as to investigate the effects of molecular architecture (L35 and 10R5) and molecular weight by keeping constant the hydrophilic/hydrophobic balance (F88 and F108). 1,2-Dichloroethane was used as a prototype of water basins contaminants. The hydrodynamic radius of the block copolymer aggregates (R(h,M)) and the intensity ratio of pyrene of the first and the third vibrational band (I(1)/I(3)) were determined as a function of…

Hydrodynamic radiusAnalytical chemistryGeneral Physics and AstronomyMICELLIZATIONNeutron scatteringPHASE-BEHAVIORFluorescence spectroscopyPolyethylene GlycolsDynamic light scattering:OSCILLATORY SHEAR MEASUREMENTSBLOCK-COPOLYMERAlkanesCopolymerOrganic chemistryMOLAR VOLUMESSURFACTANTSPhysical and Theoretical ChemistrySolubilityTEMPERATUREAqueous solutionChemistryWaterSmall-angle neutron scatteringSolutionsMICELLAR STRUCTURENeutron DiffractionRefractometrySpectrometry FluorescenceSolubilityWATER-OIL SYSTEMSPropylene GlycolsTHERMODYNAMIC PROPERTIESChlorinePhysical chemistry chemical physics : PCCP
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A Highly Luminescent Nitrogen-Doped Nanographene as an Acid- and Metal-Sensitive Fluorophore for Optical Imaging.

2021

Dibenzo[hi,st]ovalene (DBOV) has excellent photophysical properties, including strong fluorescence and high ambient stability. Moreover, the optical blinking properties of DBOV have enabled optical super-resolution single-molecule localization microscopy with an imaging resolution beyond the diffraction limit. Various organic and inorganic fluorescent probes have been developed for super-resolution imaging, but those sensitive to pH and/or metal ions have remained elusive. Here, we report a diaza-derivative of DBOV (N-DBOV), synthesized in eight steps with a total yield of 15%. Nitrogen (N)-bearing zigzag edges were formed through oxidative cyclization of amino groups in the last step. UV-v…

IONSFluorophoreNitrogenMetal ions in aqueous solutionIronOvalenePhotochemistryOXIDATIONBiochemistryCatalysisFluorescence spectroscopyArticlechemistry.chemical_compoundColloid and Surface ChemistryMicroscopyFLUORESCENCEFluorescent DyesCONSTRUCTIONMolecular StructureChemistryDERIVATIVESWARPED NANOGRAPHENEGeneral ChemistryFluorescenceNanostructuresLuminescent MeasurementsCHEMOSENSORGraphiteN-HETEROCYCLESCyclic voltammetryAQUEOUS-MEDIUMLuminescenceSYSTEMCopperJournal of the American Chemical Society
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Self-Organization Pathways and Spatial Heterogeneity in Insulin Amyloid Fibril Formation

2009

At high temperature and low pH, the protein hormone insulin is highly prone to form amyloid fibrils, and for this reason it is widely used as a model system to study fibril formation mechanisms. In this work, we focused on insulin aggregation mechanisms occurring in HCl solutions (pH 1.6) at 60 degrees C. By means of in situ Thioflavin T (ThT) staining, the kinetics profiles were characterized as a function of the protein concentration, and two concurrent aggregation pathways were pointed out, being concentration dependent. In correspondence to these pathways, different morphologies of self-assembled protein molecules were detected by atomic force microscopy images also evidencing the prese…

In situAmyloidHot Temperaturemedicine.medical_treatmentKineticsNucleationMicroscopy Atomic ForceFibrilchemistry.chemical_compoundMicroscopyMaterials ChemistrymedicineAnimalsInsulinBenzothiazolesPhysical and Theoretical ChemistryInsulin Amyloid Fibrils Secondary Nucleation Thioflavin T (ThT) Scanning Force Microscopy (SFM) Spatial HeterogeneityChemistryInsulinfluorescence spectroscopyFluorescenceSurfaces Coatings and FilmsThiazolesBiochemistryBiophysicsCattleThioflavinHydrochloric AcidProtein aggregation
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