Search results for "CYCLODEXTRINS"

showing 10 items of 108 documents

On Complex Formation between 5-Fluorouracil and β-Cyclodextrin in Solution and in the Solid State: IR Markers and Detection of Short-Lived Complexes …

2020

In this work, the nuclear magnetic resonance (NMR) and IR spectroscopic markers of the complexation between 5-fluorouracil (5-FU) and &beta

Magnetic Resonance SpectroscopyDiffusionPopulationPharmaceutical ScienceAntineoplastic Agents010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441DiffusionDrug Delivery Systemslcsh:Organic chemistryDrug DiscoveryMolecule5-FUPhysical and Theoretical Chemistryeducationchemistry.chemical_classificationeducation.field_of_studyAqueous solutionCyclodextrin010405 organic chemistrymolecular modelingβ-CDOrganic Chemistrybeta-CyclodextrinsNuclear magnetic resonance spectroscopyequipment and suppliesNMR0104 chemical sciencesNMR spectra databasechemistrySolubilityChemistry (miscellaneous)Attenuated total reflectionIRMolecular MedicinePhysical chemistryFluorouracilhuman activitiesinclusion complexMolecules
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Impact of 7-Ketocholesterol and Very Long Chain Fatty Acids on Oligodendrocyte Lipid Membrane Organization: Evaluation Via LAURDAN and FAMIS Spectral…

2011

International audience; In the context of multiple sclerosis and X-linked adrenoleukodystrophy, 7-ketocholesterol (7KC) and very long chain fatty acids (C24:0, C26:0) are supposed to induce side effects respectively on oligodendrocytes which are myelin (which is a lipoproteic complex) synthesizing cells. The effects of 7KC (25, 50 mu M), C24:0 and C26:0 (10, 20 mu M) on cell viability and lipid membrane organization were investigated on 158N murine oligodendrocytes. Concerning 7KC and fatty acids (at 20 mu M only):1) cell growth was strongly inhibited; 2) marked induction of cell death was revealed with propidium iodide (PI); 3) no apoptotic cells were found with C24:0 and C26:0 (absence of…

MaleMYELINlaw.inventionchemistry.chemical_compoundMice0302 clinical medicinelawFAMIS2-Naphthylamine[SDV.IDA]Life Sciences [q-bio]/Food engineeringEnzyme InhibitorsLipid bilayerKetocholesterols0303 health sciencesMicroscopy ConfocalOXYSTEROLSFatty AcidsMULTIPLE-SCLEROSISvery long chain fatty acidsCell biologyPEROXISOMAL DISORDERSAPOPTOSISOligodendrogliaX-LINKED ADRENOLEUKODYSTROPHYmedicine.anatomical_structureMembraneCHOLESTEROL OXIDESlipids (amino acids peptides and proteins)Laurdanalpha-CyclodextrinsHistologyContext (language use)BiologyMETABOLISMPathology and Forensic Medicine158N oligodendrocytes03 medical and health sciencesMembrane LipidsConfocal microscopymedicineAnimals[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringViability assayPropidium iodideLAURDAN7-ketocholesterol030304 developmental biologyFluorescent DyesCell MembraneCENTRAL-NERVOUS-SYSTEMCell BiologyOligodendrocytechemistryCELLSmono-photon confocal microscopy030217 neurology & neurosurgeryLaurates
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Hyaluronic acid and beta cyclodextrins films for the release of corneal epithelial cells and dexamethasone

2016

In this work we prepared hydrogels based on hyaluronic acid and β-cyclodextrins to sustain the release of both corneal epithelial cells and dexamethasone. This steroid is administered as eye drops several times per day to reduce the risk of rejection in the post operative period after the cornea transplantation and cell release techniques. Hydrogels were produced by crosslinking an amino derivative of hyaluronic acid, with the divinyl sulfone derivative of β-cyclodextrins, this last employed as a crosslinker and solubilizing agent. Drug release studies revealed that dexamethasone containing samples are able to extend the release of this drug for at least five days. Biological studies, condu…

Materials Chemistry2506 Metals and AlloysPolymers and Plasticsmedicine.medical_treatmentCellBeta-CyclodextrinsCell release systemmacromolecular substances02 engineering and technologyPharmacology010402 general chemistry01 natural sciencesDexamethasoneSteroidCorneachemistry.chemical_compoundCorneaHyaluronic acidMaterials ChemistrymedicineCorneal woundHumansHyaluronic acid hydrogelHyaluronic AcidDexamethasoneCells CulturedDrug CarriersPolymers and Plasticbeta-CyclodextrinsOrganic Chemistrytechnology industry and agricultureEpithelial CellsHydrogelsAnatomy021001 nanoscience & nanotechnologyeye diseases0104 chemical sciencesTransplantationDrug Liberationmedicine.anatomical_structurechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelssense organs0210 nano-technologymedicine.drug
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Copolymer−Cyclodextrin Inclusion Complexes in Water and in the Solid State. A Physico-Chemical Study

2008

The formation of inclusion complexes (ICs) composed of cyclodextrins (CDs) and poly(ethylene oxides)-poly(propylene oxides)-poly(ethylene oxides) (PEO-PPO-PEO) was studied. To this purpose, native and hydroxypropyl cyclodextrins with different cavity size were chosen. The PEO-PPO-PEO copolymers were selected to study the role of the molecular weight, keeping constant the hydrophilic/hydrophobic ratio, and the hydrophilicity. The volumetric studies at 25 degrees C allowed to determine the equilibrium constant and the volume change for the IC formation in water as well as the IC stoichiometry. Surface tension experiments evidenced that the copolymer and the CD interfacial behavior is controll…

Materials scienceChemical PhenomenaPolymersPolypropylenesPolyethylene GlycolsSurface tensionDifferential scanning calorimetryPhase (matter)Copolymer Cyclodextrin calorimetrySpectroscopy Fourier Transform InfraredMaterials ChemistryCopolymerSurface TensionOrganic chemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyEquilibrium constantchemistry.chemical_classificationCyclodextrinsCyclodextrinChemistry Physicaltechnology industry and agricultureWaterSurfaces Coatings and FilmsChemical engineeringchemistrySolventsThermodynamicsStoichiometry
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Detecting ni(ii) in aqueous solution by 3-(2-pyridyl)-[1,2,3]triazolo[1,5-a]pyridine and dimethyl-beta-cyclodextrin

2013

Abstract A new supramolecular sensitizer for nickel(II) ion in aqueous solution based on a pyridyltriazolopyridine-cyclodextrin inclusion complex is proposed. The inclusion complexation behavior, characterization and binding ability of pyridyltriazolopyridine (PTP) with dimethyl-β-cyclodextrin (DMβCD) has been investigated both in solution and solid state by means of absorption, fluorescence, 1H NMR, DSC, and molecular modeling methods. The stoichiometry of the inclusion complex is 1:1, and the thermodynamic studies indicate that the inclusion of PTP is mainly an entropic driven process. The 2D NMR studies revealed that the pyridyl-triazolopyridine is included by both sides of cyclodextrin …

Models MolecularPolymers and PlasticsPyridinesSupramolecular chemistryAnalytical chemistryMolecular ConformationDivalentchemistry.chemical_compoundNickelPyridineMaterials Chemistrychemistry.chemical_classificationAqueous solutionCyclodextrinChemistryOrganic Chemistrybeta-CyclodextrinsWaterTriazolesSolutionsProton NMRPhysical chemistrySelectivityTwo-dimensional nuclear magnetic resonance spectroscopyWater Pollutants ChemicalEnvironmental Monitoring
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Spectroscopic studies of the interaction of 3-(2-thienyl)-[1,2,3]triazolo[1,5-a]pyridine with 2,6-dimethyl-β-cyclodextrin and ctDNA

2016

The inclusion complexation behavior of 3-(2-thienyl)-[1,2,3]triazolo[1,5-a] pyridine (TTP) with native β-cyclodextrin and derivatized cyclodextrins was investigated. Stability constants for complexes with 1 : 1 molar ratios were calculated from phase solubility diagrams. The solubilizing efficiency of the TTP inclusion complex is enhanced in the order of DMβCD > HPβCD > βCD. The TTP-DMβCD inclusion complex was further characterized in solution by means of absorption, fluorescence, 2D NMR and molecular modeling methods. The thermodynamic studies indicate that the inclusion of TTP into the cyclodextrin cavity is mainly an enthalpy-driven process. The 2D NMR studies revealed that the thienyl m…

Models MolecularPyridinesStereochemistryIntercalation (chemistry)Antineoplastic Agents010402 general chemistry01 natural sciencesBiochemistryHydrophobic effectchemistry.chemical_compoundPyridineCarbohydrate ConformationAnimalsMoietyPhysical and Theoretical ChemistrySolubilitychemistry.chemical_classificationCyclodextrin010405 organic chemistrySpectrum Analysisbeta-CyclodextrinsOrganic ChemistryDNATriazoles0104 chemical sciencesCrystallographychemistryDocking (molecular)CattleTwo-dimensional nuclear magnetic resonance spectroscopyOrganic & Biomolecular Chemistry
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Structural and physicochemical characterization of the inclusion complexes of cyclomaltooligosaccharides (cyclodextrins) with melatonin

2002

The stoichiometry, geometry, stability, and solubility of the inclusion complexes of melatonin (MLT) with native cyclomaltooligosaccharides (α-, β- or γ-cyclodextrins, CDs) are determined experimentally by high-resolution NMR spectroscopy, calorimetric and solubility measurements, and mass spectrometry. The observed differences are discussed in terms of molecular recognition expression of the host-guest (h-g) interactions within the hydrophobic CDs cavities of different size. The 1:1 h-g stoichiometry in water solution prevails at low CD concentrations; the trend to form higher order associations is observed at increasing CD concentrations. The stability order β-CD>γ-CD>α-CD for the c…

Models MolecularSpectrometry Mass Electrospray IonizationElectrospray ionizationProtonationCalorimetryCalorimetryMass spectrometryBiochemistryInclusion complexeAnalytical ChemistryExcipientsMolecular recognitionCyclodextrinSolubilityNuclear Magnetic Resonance BiomolecularMelatoninCyclodextrinsMass spectrometryChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopyNMRCrystallographySolubilityThermodynamicsStoichiometry
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Cyclodextrin and Adamantane Host-Guest Interactions of Modified Hyperbranched Poly(ethylene imine) as Mimetics for Biological Membranes

2011

Models MolecularSurface PropertiesAdamantaneImineBeta-CyclodextrinsAdamantaneCatalysischemistry.chemical_compoundBiomimeticsPolymer chemistryMoleculeParticle SizeFluorescent Dyeschemistry.chemical_classificationCyclodextrinMolecular StructureChemistryCell Membranebeta-CyclodextrinsBiological membraneGeneral ChemistryGeneral MedicineFluoresceinsMembraneSelf-assemblyIminesPolyethylenesAngewandte Chemie
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PROPERTIES AND APPLICATIONS OF POLYAMINOCYCLODEXTRIN DERIVATIVES

Nel presente lavoro sono state prese in esame le potenziali applicazioni delle poliamminociclodestrine. In particolare, diversi derivati poliamminociclodestrinici (amCD) sono stati ottenuti utilizzando un approccio sintetico diretto, tramite reazione di sostituzione nucleofila tra la heptakis-(6-deossi)-(6-bromo)-βCD (BrβCD) e poliammine lineari. Una volta effettuata l’opportuna caratterizzazione NMR, ESI-MS e potenziometrica, sono state investigate diverse possibili utilizzazioni di tali materiali. Anzitutto, sono state valutate le capacità di dare complessi di inclusione host-guest con diversi derivati organici sia delle amCD libere che di materiali costituiti da nanospugne a base di amCD…

NanospongesPhotoreductionCyclodextrinsNitroarene reductionLangmuir-Hinshelwood modelSettore CHIM/06 - Chimica OrganicaSolid-state NMRPalladium NanoparticlesCatalysisSupramolecular ChemistryPolarimetryPolyaminesGold NanoparticlesGene deliveryAntibacterial activityEnzyme activitySilver Nanoparticles
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Nanoassemblies Based on Supramolecular Complexes of Nonionic Amphiphilic Cyclodextrin and Sorafenib as Effective Weapons to Kill Human HCC Cells

2015

Sorafenib (Sor), an effective chemiotherapeutic drug utilized against hepatocellular carcinoma (HOC), robustly interacts with nonionic amphiphilic cyclodextrin (aCD, SC6OH), forming, in aqueous solution, supramolecular complexes that behave as building blocks of highly water-dispersible colloidal nanoassemblies. SC6OH/Sor complex has been characterized by complementary spectroscopic techniques, such as UV-vis, steady-state fluorescence and anisotropy, resonance light scattering and H-1 NMR. The spectroscopic evidences and experiments carried out in the presence of an adamantane derivative, which competes with drug for CD cavity, agree with the entrapment of Sor in aCD, pointing out the role…

NiacinamideErythrocytesPolymers and PlasticsCell SurvivalAdamantaneDrug CompoundingSupramolecular chemistryBioengineeringNanotechnologyAdamantaneAntineoplastic AgentsBinding CompetitiveHemolysisAmphiphilic Cyclodextrins; Nanoparticles; Sorafenib; HCC cellsHCC cellsBiomaterialschemistry.chemical_compoundSurface-Active AgentsIn vivoCell Line TumorAmphiphileMaterials ChemistryHumanschemistry.chemical_classificationCyclodextrinsAqueous solutionCyclodextrinPhenylurea CompoundsSorafenibFluorescenceCombinatorial chemistrydigestive system diseasesNanostructuresBINDING INTERACTION THERAPY PHARMACOKINETICS BIOAVAILABILITY NANOPARTICLESDrug LiberationKineticsnanoassembliecyclodextrinchemistryDelayed-Action PreparationsProton NMRHepatocytes
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