Search results for "Dye"

showing 10 items of 577 documents

Warm white LED light by frequency down-conversion of mixed yellow and red Lumogen®

2013

This work reports on the benefits and promising opportunities offered by white LED hybrid technology, based on a mixing perylene-based dyes in order to obtain a warm white light for frequency-down conversion. In a standard Ce:YAG-based white LED, the white light appears cold due to the weakness of red wavelength components in the emission spectrum. In order to obtain a warmer white, one possible solution is to add a red phosphor to the yellow one to move the chromatic coordinates properly, though the luminous efficiency drastically decreases due to the increased light absorption of the coating layer. It is generally believed that the low efficiency of warm white LEDs is the main issue today…

Warm white LEDs hybrid LEDs perylene-based dyes Lumogen® LED optical characterization dip coatingMaterials sciencebusiness.industryPhosphorColor temperatureSettore ING-INF/01 - Elettronicalaw.inventionLuminous fluxColor rendering indexLED lampchemistry.chemical_compoundchemistrylawOptoelectronicsbusinessLuminous efficacyPeryleneLight-emitting diode
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White LED light obtained by frequency down-conversion of perylene-based dyes

2012

White LED Perylene dyes Frequency down-conversionSettore ING-INF/01 - Elettronica
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Cytofluorometric detection of wine lactic acid bacteria: application of malolactic fermentation to the monitoring

2012

Abstract In this study we report for the first time a rapid, efficient and cost-effective method for the enumeration of lactic acid bacteria (LAB) in wine. Indeed, up to now, detection of LAB in wine, especially red wine, was not possible. Wines contain debris that cannot be separated from bacteria using flow cytometry (FCM). Furthermore, the dyes tested in previous reports did not allow an efficient staining of bacteria. Using FCM and a combination of BOX/PI dyes, we were able to count bacteria in wines. The study was performed in wine inoculated with Oenococcus oeni (106 CFU ml−1) stained with either FDA or BOX/PI and analyzed by FCM during the malolactic fermentation (MLF). The analysis …

WineBioengineeringSaccharomyces cerevisiaeApplied Microbiology and Biotechnologychemistry.chemical_compoundMalolactic fermentationLactic AcidFood scienceOenococcusFluorescent DyesOenococcus oeniWinemakingWinebiologydigestive oral and skin physiologyfood and beveragesFlow CytometryFluoresceinsThiobarbituratesbiology.organism_classificationYeastLactic acidBiochemistrychemistryWhite WineFermentationFermentationPropidiumBiotechnologyJournal of Industrial Microbiology and Biotechnology
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Synthesis, stability and spectral behavior of fluorogenic sulfone-pyronin and sulfone-rosamine dyes

2018

International audience; The first synthesis of sulfone-pyronin and sulfone-rosamine dyes bearing optically tunable primary amino groups (acting as fluorogenic centers) is presented. Sulfone analogs of xanthene-based fluorophores have recently been highlighted as a new class of near-infrared (NIR) fluorescent dyes (Liu et al. ACS Appl Mater Interfaces 2016; 8(35):22953-62), and the availability of fluorogenic derivatives is essential for the rapid construction of “turn-on” reactive probes for chemoselective bioimaging. However, these fluorescent anilines have been found to be unstable in aqueous physiological conditions due to the marked electrophilicity of their meso-position and hence its …

XantheneAqueous solutionPrimary (chemistry)NIR dye010405 organic chemistryHetero-xanthene dye[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringFluorogenic enzyme substrateRosamine010402 general chemistry01 natural sciencesFluorescenceCombinatorial chemistry0104 chemical sciencesSulfonechemistry.chemical_compoundNucleophilechemistryElectrophileMoleculePyronin
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Synthesis of new asymmetric xanthene dyes via catalyst-free SNAr with sulfur nucleophiles

2014

Addition of a single functional handle to the tricyclic moiety of fluorescein results in asymmetric xanthene dyes. Our synthesis of a new class of asymmetric xanthenes proceeds via an unusual SNAr with sulfur nucleophiles on electron rich aromatic xanthenes scaffolds in the absence of a metal catalyst. The resulting 3'-thioethers exhibit high photostability and are conveniently converted into reactive dyes for macromolecule labelling.

XantheneAzidesOrganic Chemistrychemistry.chemical_elementElectronsHydrogen-Ion ConcentrationSulfidesPhotochemistryBiochemistrySulfurCombinatorial chemistryCatalysisCatalysischemistry.chemical_compoundSpectrometry FluorescenceXantheneschemistryNucleophileNucleophilic aromatic substitutionMoietyPhysical and Theoretical ChemistrySulfurFluorescent DyesMacromoleculeOrganic & Biomolecular Chemistry
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Straightforward access to water-soluble unsymmetrical sulfoxanthene dyes: application to the preparation of far-red fluorescent dyes with large stoke…

2014

An efficient synthesis of water-soluble unsymmetrical sulforhodamine/sulforhodol fluorophores containing a single julolidine fragment is presented. Owing to their valuable spectral properties in aqueous buffers, these dyes, especially those bearing a free aniline or phenol moiety, are valuable components of fluorogenic probes for a variety of biosensing applications. A further extension of this synthetic methodology to unusual phenols, namely 7-N,N-dialkylamino-4-hydroxy coumarins has enabled us to provide a new family water-soluble dyes of large Stokes’ shift with far-red spectral features.

[CHIM.THER]Chemical Sciences/Medicinal ChemistryBiosensing Techniques010402 general chemistryPhotochemistry01 natural sciencesCatalysisRhodaminessymbols.namesakechemistry.chemical_compoundAniline[CHIM.ANAL]Chemical Sciences/Analytical chemistryCoumarinsStokes shiftMoietyJulolidineComputingMilieux_MISCELLANEOUSFluorescent DyesAqueous solution010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryRhodaminesOrganic ChemistryWaterGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisHydrogen-Ion ConcentrationFluorescence0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrySpectrometry FluorescenceXanthenessymbolsSolventsBiosensor[CHIM.CHEM]Chemical Sciences/CheminformaticsChemistry (Weinheim an der Bergstrasse, Germany)
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Analysis of fluorescent MRI contrast agent behavior in the liver and thoracic aorta of mice.

2004

To characterize the behavior of magnetofluorescent products injected in mice intravenously.The magnetic resonance imaging (MRI) products were labelled with fluorescent molecules to examine the biodistribution process in vivo and observe them at the cellular level by means of confocal microscopy. Three-dimensional (3D) sequences of images were obtained by spectral analysis of sample preparations in a multiphoton confocal microscope and analyzed by the factor analysis of medical image sequence algorithm, which provides factor curves. Factor images are the result of image-processing methods that utilize information from emission spectra. Preparations are also screened in the counting mode to p…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingContrast MediaAorta ThoracicMiceMESH : Image CytometryMESH: Microscopy ConfocalMESH : FemaleMESH : Fluorescent DyesMESH: AnimalsMESH : Algorithms[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/Imaginghealth care economics and organizationsImage CytometryMice Inbred BALB CMicroscopy ConfocalMESH: Fluorescent DyesMESH: Staining and LabelingLiverMESH : MeglumineFemaleMESH : Organometallic CompoundsAlgorithmsMESH: Aorta ThoraciceducationMESH: Mice Inbred BALB CMESH: AlgorithmsMESH: MeglumineMESH : Staining and LabelingMeglumineMESH: Contrast MediaMESH : MiceOrganometallic CompoundsAnimalsMESH : Microscopy ConfocalMESH: MiceMESH : Mice Inbred BALB CFluorescent DyesMESH : Aorta ThoracicMESH : Contrast MediaStaining and LabelingMESH : LiverMESH: Organometallic CompoundsMESH : Xanthenes[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingXanthenesMESH: XanthenesMESH : AnimalsMESH: FemaleMESH: Image CytometryMESH: Liver
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Modular Assembly of Multimodal Imaging Agents through an Inverse Electron Demand Diels–Alder Reaction

2019

International audience; The combination of two imaging probes on a same biomolecule gives access to targeted bimodal imaging agents that can provide more accurate diagnosis, complementary information, or that may be used in different applications, such as PET imaging and fluorescence imagingassisted surgery. In this study, we demonstrate that dichlorotetrazine, a small, commercially available compound, can be used as a modular platform to easily assemble various imaging probes. Doubly-labeled tetrazines can then be conjugated to a protein through a biorthogonal IEDDA reaction. A series of difunctionalized tetrazine compounds containing various chelating agents and fluorescent dyes was synth…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingTetrazineBiomedical EngineeringContrast MediaPharmaceutical SciencebimodalBioengineeringNanotechnology02 engineering and technology[CHIM.THER]Chemical Sciences/Medicinal ChemistryMultimodal ImagingProof of Concept Study01 natural sciencesMiceAnimalsHumansInverse electron-demand Diels–Alder reactionFluorescent DyesPharmacologyMultimodal imagingchemistry.chemical_classificationCycloaddition Reaction010405 organic chemistryChemistrybusiness.industryBiomoleculeOrganic ChemistryModular design021001 nanoscience & nanotechnology0104 chemical sciencestrastuzumabProof of conceptSPECT-CTSite-specificfluorescence0210 nano-technologybusinessBiotechnology
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Long-Term Potentiation in the Neonatal Rat Barrel Cortex In Vivo

2012

Long-term potentiation (LTP) is important for the activity-dependent formation of early cortical circuits. In the neonatal rodent barrel cortex, LTP has been studied only in vitro . We combined voltage-sensitive dye imaging with extracellular multielectrode recordings to study whisker stimulation-induced LTP in the whisker-to-barrel cortex pathway of the neonatal rat barrel cortex in vivo . Single whisker stimulation at 2 Hz for 10 min induced an age-dependent expression of LTP in postnatal day (P) 0 to P14 rats, with the strongest expression of LTP at P3–P5. The magnitude of LTP was largest in the activated barrel-related column, smaller in the surrounding septal region, and no LTP could b…

animal structuresPatch-Clamp TechniquesLong-Term PotentiationBiophysicsStimulationBiologyIn Vitro TechniquesStatistics NonparametricIn vivoCortex (anatomy)Evoked Potentials SomatosensoryExtracellularmedicineAnimalsNeuronsSerotonin Plasma Membrane Transport ProteinsCortical circuitsNeonatal ratAfferent PathwaysGeneral Neurosciencemusculoskeletal neural and ocular physiologyAge FactorsLong-term potentiationSomatosensory CortexBarrel cortexElectric StimulationVoltage-Sensitive Dye ImagingRatsmedicine.anatomical_structurenervous systemAnimals NewbornVibrissaeBiophysicsBrief CommunicationsNeuroscience
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Polycationic Monomeric and Homodimeric Asymmetric Monomethine Cyanine Dyes with Hydroxypropyl Functionality—Strong Affinity Nucleic Acids Binders

2021

New analogs of the commercial asymmetric monomethine cyanine dyes thiazole orange (TO) and thiazole orange homodimer (TOTO) with hydroxypropyl functionality were synthesized and their properties in the presence of different nucleic acids were studied. The novel compounds showed strong, micromolar and submicromolar affinities to all examined DNA ds-polynucleotides and poly rA–poly rU. The compounds studied showed selectivity towards GC-DNA base pairs over AT-DNA, which included both binding affinity and a strong fluorescence response. CD titrations showed aggregation along the polynucleotide with well-defined supramolecular chirality. The single dipyridinium-bridged dimer showed intercalatio…

antiproliferative activityCircular dichroismSupramolecular chiralityDimerIntercalation (chemistry)cyanine dye010402 general chemistry01 natural sciencesBiochemistryMicrobiologyArticlechemistry.chemical_compoundCell Line TumorHumansCyanineDNA bindingColoring AgentsBiologyMolecular BiologyBinding Sites010405 organic chemistrycyanine dye ; DNA binding ; RNA binding ; fluorescence ; circular dichroism ; antiproliferative activityDNARNA bindingCombinatorial chemistryQR1-502Intercalating Agents3. Good health0104 chemical sciencescircular dichroismchemistryPolynucleotideNucleic acidcyanine dye; DNA binding; RNA binding; fluorescence; circular dichroism; antiproliferative activityfluorescenceDNA
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