Search results for "Microscopy"

showing 10 items of 3390 documents

Monolayer-to-mesoscale modulation of the optical properties in 2D CrI3 mapped by hyperspectral microscopy

2023

Magnetic 2D materials hold promise to change the miniaturization paradigm of unidirectional photonic components. However, the integration of these materials in devices hinges on the accurate determination of the optical properties down to the monolayer limit, which is still missing. By using hyperspectral wide-field imaging at room temperature, we reveal a nonmonotonic thickness dependence of the complex optical dielectric function in the archetypal magnetic 2D material CrI3 extending across different length scales: onsetting at the mesoscale, peaking at the nanoscale, and decreasing again down to the single layer. These results portray a modification of the electronic properties of the mat…

Magnetic 2D materialsCrI3Condensed Matter - Mesoscale and Nanoscale PhysicsOptical propertiesMesoscaleHyperspectral microscopyMesoscale and Nanoscale Physics (cond-mat.mes-hall)MonolayerFOS: Physical sciences
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Effects of different cellulose derivatives on drug release mechanism studied at a preformulation stage

2003

As a matter of fact, in vitro dissolution is well known to be the method of choice for the pharmaceutical industry to develop effective medicines. However, many experiments must be performed all along a new product life and they represent an overcharge of work for researchers. The purpose of this paper was to assess the relevance of new parameters obtained during preformulation stage by Nuclear Magnetic Resonance (NMR) experiments to better understand drug release mechanism. This study was carried out with three cellulose derivatives currently used as carrier matrices (Microcrystalline cellulose (MCC), Hydroxypropylmethyl cellulose (HPMC) and Ethyl cellulose (EC)). Granules and tablets were…

Magnetic Resonance SpectroscopyChemistry PharmaceuticalPharmaceutical ScienceMethylcelluloseDosage formExcipientschemistry.chemical_compoundHypromellose DerivativesTheophyllineEthyl celluloseOrganic chemistrySolubilityCelluloseCelluloseDrug CarriersNuclear magnetic resonance spectroscopyHypromellose DerivativesMicrocrystalline cellulosePharmaceutical PreparationsSolubilitychemistryChemical engineeringMicroscopy Electron ScanningPowdersDrug carrierAlgorithmsTabletsJournal of Controlled Release
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Design, synthesis and stimuli responsive gelation of novel stigmasterol-amino acid conjugates.

2020

Abstract An efficient synthesis of three novel stigmasterol-amino acid (glycine, l -leucine and l -phenylalanine) conjugates as stimuli responsive gelators is reported. The gelation properties of the prepared compounds were investigated in a variety of organic as well as aqueous solvents. The most striking finding of our investigation was that the hydrochloride salts of the prepared conjugates acted as gelators, whereas the neutral conjugates were either non-gelators or formed only a weak gel in anisole. The hydrochloride salts of stigmasteryl glycinate and l -leucinate form gels in n-alcohols (n = 4–10) and in ethane-1,2-diol, and that of stigmasteryl l -phenylalaninate forms gels in aroma…

Magnetic Resonance SpectroscopyHydrochloridePhenylalanineGlycineStigmasterolPhenylalaninePhase TransitionBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryLeucineSpectroscopy Fourier Transform InfraredOrganic chemistrychemistry.chemical_classificationBiological ProductsAqueous solutionChemistryWaterHydrogen BondingHydrogen-Ion ConcentrationAnisoleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidDelayed-Action PreparationsGlycineSelf-healing hydrogelsMicroscopy Electron ScanningSolventsHydrochloric AcidLeucineGelsJournal of colloid and interface science
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NEW SELF-ASSEMBLING POLYASPARTYLHYDRAZIDE COPOLYMER MICELLES FOR ANTICANCER DRUG DELIVERY.

2010

A new amphiphilic copolymer have been synthesized starting from the hydrosoluble polyaspartylhydrazide (PAHy) polymer, by grafting both hydrophilic PEG(2000) chains and hydrophobic palmitic acid (C(16)) moieties on polymer backbone, and the structure of obtained PAHy-PEG(2000)-C(16) copolymer have been characterized by 2D (1)H/(13)C NMR experiments. PAHy-PEG(2000)-C(16) copolymer showed the ability of self-assembling in aqueous media giving a core-shell structure and resulted potentially useful for encapsulating and dissolving hydrophobic drug. The formation of micellar core-shell structure has been investigated by 2D (1)H NMR NOESY experiments. The presence of cross-peaks for protons of C(…

Magnetic Resonance SpectroscopyLightCell SurvivalPolymersChemistry PharmaceuticalDrug CompoundingPalmitic AcidPharmaceutical ScienceAntineoplastic AgentsBreast NeoplasmsDRUG DELIVERY SELF ASSEMBLING POLYASPARTYLHYDRAZIDE MICELLES.MicelleFluorescencePolyethylene GlycolsDynamic light scatteringMicroscopy Electron TransmissionCell Line TumorAmphiphilePolymer chemistryCopolymerOrganic chemistryHumansNanotechnologyScattering RadiationTechnology PharmaceuticalSolubilityParticle SizeMicellesDrug CarriersDose-Response Relationship DrugChemistrytechnology industry and agricultureNuclear magnetic resonance spectroscopyHydrophobeTamoxifenSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoFemaleDrug carrierPeptidesHydrophobic and Hydrophilic Interactions
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Pegylated nanoparticles based on a polyaspartamide. Preparation, physico-chemical characterization and intracellular uptake

2006

Nanoparticles with different surface PEGylation degree were prepared by using as starting material alpha,beta-poly(N-2-hydroxyethyl)-d,l-aspartamide (PHEA). PHEA was functionalized with a PEG amino-derivative for obtaining PHEA-PEG(2000) copolymer. Both PHEA and PHEA-PEG(2000) were derivatized with methacrylic anhydride (MA) for obtaining poly(hydroxyethylaspartamide methacrylated) (PHM) and poly(hydroxyethylaspartamide methacrylated)-PEGylated (PHM-PEG(2000)), respectively. Nanoparticles were obtained by UV irradiation of an inverse microemulsion, using as internal phase an aqueous solution of PHM alone or of the PHM/PHM-PEG(2000) mixture at different weight ratio and as external phase a m…

Magnetic Resonance SpectroscopyPolymers and PlasticsUltraviolet RaysNanoparticleMethacrylic anhydrideBioengineeringPolyethylene GlycolsBiomaterialschemistry.chemical_compoundMicroscopy Electron TransmissionPEG ratioPolymer chemistrySpectroscopy Fourier Transform InfraredMaterials ChemistryZeta potentialHumansMicroemulsionParticle SizeNanoparticlesalphabeta-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA)methacrylic anhydride.Aqueous solutionchemistryPropylene carbonatePEGylationMethacrylatesNanoparticlesK562 CellsPeptidesNuclear chemistry
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SELF-ASSEMBLED AMPHIPHILIC HYALURONIC ACID GRAFT COPOLYMERS FOR TARGETED RELEASE OF ANTITUMORAL DRUG

2009

Polymeric micelles obtained by self-assembling of amphiphilic hyaluronic acid (HA) graft copolymers have been prepared and characterized. In particular, hyaluronic acid (HA) has been grafted to polylactic acid (PLA) and polyethylenglycol chains (PEG), then the copolymers able to form micelles in aqueous medium have been chosen to entrap the antitumoral drug Doxorubicin. The critical aggregation concentration of HA-g-PLA or HA-g-PLA-g-PEG micelles has been determined by using pyrene as a fluorescent probe, whereas their shape and size have been evaluated by light scattering measurements, scanning and transmission electron microscopies. The selective cytotoxicity of drug loaded micelles towar…

Magnetic Resonance SpectroscopySELF ASSEMBLING HYALURONIC ACID DRUG RELEASEPolymersMolecular Sequence DataPharmaceutical ScienceAntineoplastic Agentsmacromolecular substancesMicelleCell Linechemistry.chemical_compoundMiceDrug Delivery SystemsPolylactic acidCell Line TumorHyaluronic acidPEG ratioAmphiphileCopolymerOrganic chemistryAnimalsHumansHyaluronic AcidMicellesDrug CarriersChemistrytechnology industry and agricultureMicroscopy ElectronCarbohydrate SequenceMicroscopy FluorescenceSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiophysicsPyreneDrug carrier
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Spectral and microscopic study of self-assembly of novel cationic spermine amides of betulinic acid

2016

Supramolecular characteristics of two spermine amides of betulinic acid (1 and 2) were studied by measuring and evaluating their UV-VIS-NIR spectra in aqueous acetonitrile and DOSY-NMR spectra in tetradeuteromethanol, accompanied by atomic force microscopy (AFM) images, scanning electron microscopy (SEM) micrographs, and transmission electron microscopy (TEM) micrographs. Fibrous supramolecular self-assembly of 1 and 2 was observed by AFM images, as well as by the SEM and TEM micrographs. Bathochromic shifts of the absorbance maximum at 870nm to 1015-970nm in the UV-VIS-NIR spectra were observed with increasing water content in the acetonitrile/water systems, indicating formation of fibrous…

Magnetic Resonance SpectroscopyScanning electron microscopeClinical BiochemistrySupramolecular chemistrymacromolecular substancesDOSY-NMRMicroscopy Atomic Force010402 general chemistry01 natural sciencesBiochemistryAbsorbancechemistry.chemical_compoundEndocrinologyMicroscopy Electron TransmissionBathochromic shiftBetulinic AcidAcetonitrileta116Molecular BiologyPharmacologyAqueous solutionMolecular Structure010405 organic chemistryChemistryOrganic Chemistryta1182technology industry and agricultureAmidesTriterpenes0104 chemical sciencesCrystallographyTransmission electron microscopySEMTEMSpermineMicroscopy Electrochemical ScanningAFMPentacyclic TriterpenesChirality (chemistry)Steroids
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A top-down synthesis route to ultrasmall multifunctional Gd-based Silica nanoparticles for theranostic applications

2013

International audience; New, ultrasmall nanoparticles with sizes below 5 nm have been obtained. These small rigid platforms (SRP) are composed of a polysiloxane matrix with DOTAGA (1,4,7,10-tetraazacyclododecane-1-glutaric anhydride-4,7,10-triacetic acid)-Gd3+ chelates on their surface. They have been synthesised by an original top-down process: 1) formation of a gadolinium oxide Gd2O3 core, 2) encapsulation in a polysiloxane shell grafted with DOTAGA ligands, 3) dissolution of the gadolinium oxide core due to chelation of Gd3+ by DOTAGA ligands and 4) polysiloxane fragmentation. These nanoparticles have been fully characterised using photon correlation spectroscopy (PCS), transmission elec…

Magnetic Resonance SpectroscopySiloxanesGadoliniumtheranosticAnalytical chemistryContrast Mediachemistry.chemical_elementNanoparticle02 engineering and technologySubstance P010402 general chemistry01 natural sciencesCatalysisFluorescence spectroscopylaw.inventionHeterocyclic Compounds 1-RingMicroscopy Electron TransmissionDynamic light scatteringlawcancer[CHIM]Chemical SciencesChelationSpectroscopyElectron paramagnetic resonanceOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopySilicon Dioxide021001 nanoscience & nanotechnologyMagnetic Resonance Imaging0104 chemical sciencesSpectrometry Fluorescencechemistrysilicananoparticlesgadolinium0210 nano-technologyRadiotherapy Image-GuidedNuclear chemistry
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Self-assembling and auto-crosslinkable hyaluronic acid hydrogels with a fibrillar structure

2008

Abstract A hyaluronic acid derivative bearing pendant l -benzoyl-cysteine portions (with a derivatization degree equal to 10 mol.%) was synthesized by linking N,N′-dibenzoyl- l -cystine to the polysaccharide and then reducing its disulfide bridge to thiol groups. The formation of π–π stacking interactions between the benzoyl moieties was studied by fluorescence spectroscopy as a function of polymer concentration and oxidation time. The efficiency of oxidation of thiol groups to disulfide bridges occurring in phosphate buffer pH 7.4, was determined by colorimetric assays. The hydrogel formed by means of oxidative crosslinking has shown the presence of fibrillar aggregates as detected by ligh…

Magnetic Resonance SpectroscopyTime FactorsMaterials scienceCell SurvivalPolymersBiomedical EngineeringCystineStackingBiochemistryFluorescence spectroscopyPhosphatesBiomaterialschemistry.chemical_compoundMaterials TestingSpectroscopy Fourier Transform InfraredPolymer chemistryHyaluronic acidHumansDisulfidesHyaluronic AcidDerivatizationMolecular BiologyCell Proliferationchemistry.chemical_classificationHydrogelsGeneral MedicinePolymerFibroblastsHydrogen-Ion ConcentrationOxygenCross-Linking ReagentschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsMicroscopy Electron ScanningThiolCystineself assembling tissue engineering hyaluronic acid cell entrapmentBiotechnology
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Self-assembly and alterable relaxivity of an organic cation-encapsulated gadolinium-containing polyoxometalate

2012

A new amphiphilic molecule bearing poly(ethylene oxide) (PEO) and quaternary ammonium group, was designed and synthesized to encapsulate paramagnetic Gd(III)-containing polyoxometalate (Gd-POM) through electrostatic interaction for obtaining a water-soluble organic-inorganic hybrid building block based on POM. The yielding organic cation-encapsulated Gd-POM (OCEP-Gd) complex exhibited water-solubility and amphiphility, leading to the spontaneous self-assembly into a regular vesicular structure with PEO chains towards water phase and POM units locating at the middle. The vesicular aggregate which has a regular monolayer structure, was further studied by means of dynamic light scattering, tra…

Magnetic Resonance Spectroscopyanimal structuresAqueous solutionMaterials scienceEthylene oxideStatic ElectricityContrast MediaWaterGadoliniumNanotechnologyTungsten CompoundsInorganic Chemistrychemistry.chemical_compoundX-Ray DiffractionChemical engineeringchemistryDynamic light scatteringCoordination ComplexesTransmission electron microscopyCationsPhase (matter)MonolayerPolyoxometalatesense organsSelf-assemblyDalton Transactions
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