Search results for "Cyclodextrin"

showing 10 items of 266 documents

Temperature-controlled poly(propylene) glycol hydrophobicity on the formation of inclusion complexes with modified cyclodextrins. A DSC and ITC study.

2011

The study highlighted the main forces driving the formation of hydroxypropyl-cyclodextrins (HP-CDs) + poly(propylene) glycol 725 g mol(-1) inclusion complexes. The temperature parameter was chosen as the variable to modulate the hydrophobicity of the polymer, and consequently ITC experiments as functions of temperature as well as DSC measurements were done in a systematic way. The polymer is not included into HP-α-CD, it is strongly bound to HP-β-CD and it is floating in HP-γ-CD. The stability of the inclusion complexes is entropy controlled. The gain of the entropy is a unique result compared to the opposite literature findings for inclusion complexes based on polymers and CDs. This peculi…

PolymersEnthalpyGeneral Physics and AstronomyCalorimetrychemistry.chemical_compoundsymbols.namesakeDifferential scanning calorimetryOrganic chemistryPropylene oxidePhysical and Theoretical ChemistrySolubilitySettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationBinodalCyclodextrinsTemperatureWaterPolymerchemistrySolubilityPropylene GlycolssymbolsPhysical chemistryThermodynamicsvan der Waals forceCalorimetry polymer Cyclodextrins supramoleculesEthylene glycolHydrophobic and Hydrophilic InteractionsPhysical chemistry chemical physics : PCCP
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Pore formation by Vibrio cholerae cytolysin requires cholesterol in both monolayers of the target membrane

2007

Vibrio cholerae cytolysin (VCC) forms oligomeric transmembrane pores in cholesterol-rich membranes. To better understand this process, we used planar bilayer membranes. In symmetric membranes, the rate of the channel formation by VCC has a superlinear dependency on the cholesterol membrane fraction. Thus, more than one cholesterol molecule can facilitate VCC-pore formation. In asymmetric membranes, the rate of pore formation is limited by the leaflet with the lower cholesterol content. Methyl-beta-cyclodextrin, which removes cholesterol from membranes, rapidly inhibits VCC pore formation, even when it is added to the side opposite that of VCC addition. The results suggest that cholesterol i…

Pore Forming Cytotoxic Proteinsgenetic structuresLipid BilayersBiologymedicine.disease_causeBiochemistrychemistry.chemical_compoundMonolayermedicineAnimalsMoleculeVibrio choleraePore-forming toxinMembrane GlycoproteinsPerforinCholesterolbeta-CyclodextrinsGeneral Medicineeye diseasesTransmembrane proteinCholesterolMembraneBiochemistrychemistryVibrio choleraeBiophysicsCattlelipids (amino acids peptides and proteins)sense organsCytolysinBiochimie
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Water Dynamics at the Solid-Liquid Interface to Unveil the Textural Features of Synthetic Nanosponges.

2020

A Fast-Field-Cycling NMR investigation was carried out on a set of polyurethane cyclodextrin nanosponges, in order to gain information on their textural properties, which have been proven to be quite difficult to assess by means of ordinary porosimetric techniques. Experiments were performed on both dry and wet samples, in order to evaluate the behavior of the “non-exchangeable” C-bound 1H nuclei, as well as the one of the mobile protons belonging to the skeletal hydroxyl groups and the water molecules. The results acquired for the wet samples accounted for the molecular mobility of water molecules within the channels of the nanosponge network, leading back to the possible pore size distrib…

Pore sizeNanospongesMaterials scienceFFC-NMR RelaxometrySettore AGR/13 - Chimica AgrariaOligosaccharides010402 general chemistry01 natural sciencesArticleAbsorptionWater dynamicsNanosponges0103 physical sciencesMaterials ChemistryQuantitative assessmentMoleculePhysical and Theoretical ChemistryMaterialsSolid liquidSettore CHIM/02 - Chimica FisicaConnectivityCyclodextrins010304 chemical physicsPorosimetrySettore CHIM/06 - Chimica Organica0104 chemical sciencesSurfaces Coatings and FilmsChemical engineeringMacrocyclic compoundsThe journal of physical chemistry. B
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Synthesis and characterization of new polyamino-cyclodextrin materials.

2011

With the aim of the synthesis of chemically modified cyclodextrins bearing polyamine pendant groups, potentially useful as capping agents for the preparation of nanosized metal systems or as auxiliaries for gene transfection, the reaction between the heptakis-(6-iodo)-(6-deoxy)-b-cyclodextrin and various polyamines has been explored. This synthetic approach allows obtaining materials constituted by mixtures of cyclodextrins, having different degrees of substitution, which were satisfactorily characterized by means of various complementary techniques (ESI-MS, NMR, potentiometric titration). The products obtained were successfully subjected to preliminary tests for their binding abilities tow…

Potentiometric titrationSilverPotentiometric titrationMetal NanoparticlesChemistry Techniques SyntheticBiochemistrySilver nanoparticleAnalytical ChemistryMetalchemistry.chemical_compoundPolarimetryOrganic chemistryAmineschemistry.chemical_classificationCyclodextrinsAniline CompoundsCyclodextrinModified cyclodextrinOrganic ChemistrySettore CHIM/06 - Chimica OrganicaGeneral MedicineGene transfectionESI-MS mass spectrometryCharacterization (materials science)chemistryvisual_artvisual_art.visual_art_mediumSilver nanoparticlesPolyamineCarbohydrate research
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Silver nanoparticles stabilized by a polyaminocyclodextrin as catalysts for the reduction of nitroaromatic compounds

2015

Abstract Silver nanoparticles stabilized by means of poly -(6- N , N -dimethyl-propylenediamino)-(6-deoxy)-β-cyclodextrin were synthesized, characterized by different techniques (UV–vis spectroscopy, Dynamic Light Scattering, High Resolution Transmission Electron Microscopy, Fourier-transform IR Spectroscopy) and used as catalysts for the reduction of various nitrobenzene derivatives with sodium borohydride. The nanocomposites obtained appear to have an organized structure, with a metal core surrounded by a layer-structured coating shell. Kinetic data, rationalized in terms of a modified Langmuir–Hinshelwood model, evidenced a non-linear dependence of the reaction rate on the concentration …

Process Chemistry and TechnologyInduction periodInorganic chemistryInfrared spectroscopySettore CHIM/06 - Chimica OrganicaCatalysisSilver nanoparticleCatalysisReaction rateSodium borohydridechemistry.chemical_compoundDynamic light scatteringchemistryPolyaminocyclodextrin Nitroarene reduction Silver nanocompositePhysical and Theoretical ChemistryHigh-resolution transmission electron microscopyJournal of Molecular Catalysis A: Chemical
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ESR, electrochemical and cyclodextrin-inclusion studies of triazolopyridyl pyridyl ketones and dipyridyl ketones derivatives.

2008

Abstract The electron spin resonance (ESR) spectra of free radicals obtained by electrolytic reduction of triazolopyridyl pyridyl ketones and dipyridyl ketones derivatives were measured in dimethylsulfoxide (DMSO). The hyperfine patterns indicate that the spin density delocalization is dependent of the rings presented in the molecule. The electrochemistry of these compounds was characterized using cyclic voltammetry, in DMSO as solvent. When one carbonyl is present in the molecule one step in the reduction mechanism was observed while two carbonyl are present two steps were detected. The first wave was assigned to the generation of the correspondent free radical species, and the second wave…

PyridinesRadicalElectrochemistryPhotochemistryAnalytical Chemistrylaw.inventionDelocalized electronlawElectrochemistryMoleculePhysics::Chemical PhysicsElectron paramagnetic resonanceInstrumentationHyperfine structureSpectroscopychemistry.chemical_classificationCyclodextrinsCyclodextrinMolecular StructureChemistryElectron Spin Resonance SpectroscopyKetonesAtomic and Molecular Physics and OpticsSolubilityPhysical chemistryCyclic voltammetryAzo CompoundsSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Enantiomeric quality control of antihistamines in pharmaceuticals by affinity electrokinetic chromatography with human serum albumin as chiral select…

2007

The present paper deals with the enantiomeric separation of six antihistaminic enantiomers by affinity electrokinetic chromatography (AEKC)-partial filling technique using human serum albumin (HSA) as chiral selector. A multivariate optimization approach of the most critical experimental variables in enantioresolution, running pH, HSA concentration and HSA plug length (SPL) was carried out since there are interactions between variables that could not be considered in an univariate optimization. The estimated and experimental resolution values obtained for antihistaminic enantiomers varied from 1.13 (for orphenadrine) to 2.15 (for brompheniramine). The optimum experimental conditions for ena…

Quality ControlSerum albuminElectronsBeta-CyclodextrinsBiochemistryChromatography AffinityAnalytical ChemistryChlorcyclizineAffinity chromatographyOrphenadrinemedicineHumansEnvironmental ChemistrySerum AlbuminSpectroscopyChromatographybiologyChemistrybeta-CyclodextrinsStereoisomerismBrompheniramineHuman serum albuminSolutionsbody regionsKineticsPharmaceutical PreparationsCalibrationembryonic structuresHistamine H1 Antagonistsbiology.proteinEnantiomermedicine.drugAnalytica Chimica Acta
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Modeling the chiral resolution ability of highly sulfated β-cyclodextrin for basic compounds in electrokinetic chromatography

2013

Abstract Despite the fact that extensive research in the field of enantioseparations by capillary electrophoresis has been carried out, it is difficult to predict whether a concrete chiral selector would be useful for the separation of a racemic compound. Hence, several experimental effort is necessary to test the abilities of individual chiral selectors, usually by trial and error procedures. Thus, the enantioseparation of a new racemate becomes a time- and money-consuming task. In this work, the ability of highly sulfated β-cyclodextrin (HS-β-CD) as chiral selector in electrokinetic chromatography (EKC) is modeled for the first time, using exclusively directly-available structural data of…

Quantitative structure–activity relationshipQuantitative Structure-Activity RelationshipBiochemistryAnalytical ChemistryPolar surface areaElectrokinetic phenomenaCapillary electrophoresisPartial least squares regressionLeast-Squares AnalysisChromatography Micellar Electrokinetic Capillarychemistry.chemical_classificationPrincipal Component AnalysisChromatographyCyclodextrinSulfatesChemistrybeta-CyclodextrinsOrganic ChemistryTemperatureStereoisomerismGeneral MedicineHydrogen-Ion ConcentrationBupivacaineChiral resolutionPartition coefficientModels ChemicalPharmaceutical PreparationsJournal of Chromatography A
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Liposomes as nonspecific nanocarriers for 5-Fluorouracil in the presence of cyclodextrins

2021

Abstract 5-Fluorouracil (5-FU) is one of anticancer drugs with broad activity. Due to its severe side effects, recent studies concentrate on new ways of directed 5-FU delivery and its release in ill tissue. One of selective carriers could be cyclodextrins and liposomes. The combination of novel methods, leading to formation of inclusion complexes (IC) between host molecule of β-cyclodextrin (β-CD) or 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) and 5-FU guest and its subsequent encapsulation in dipalmitoylphosphatidylcholine (DPPC) liposomes is studied experimentally in the present work. Several methods are applied to proof the encapsulation of the analysed drug and its release over time at 37 …

Release mechanismLiposomeCyclodextrins5-Fluorouraciltechnology industry and agricultureCondensed Matter PhysicsCombinatorial chemistryAtomic and Molecular Physics and OpticsFluorescence spectroscopyElectronic Optical and Magnetic MaterialsNMR spectra databasechemistry.chemical_compoundDifferential scanning calorimetrychemistryDipalmitoylphosphatidylcholineLiposomesMaterials ChemistryProton NMRMoleculelipids (amino acids peptides and proteins)Physical and Theoretical ChemistryNanocarriersSpectroscopyControlled drug deliveryJournal of Molecular Liquids
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Enantioresolution in electrokinetic chromatography-complete filling technique using sulfated gamma-cyclodextrin. Software-free topological anticipati…

2016

Few papers have tried to predict the resolution ability of chiral selectors in capillary electrophoresis for the separation of the enantiomers of chiral compounds. In a previous work, we have used molecular information available on-line to establish enantioresolution levels of basic compounds using highly sulfated β-CD (HS-β-CD) as chiral selector in electrokinetic chromatography-complete filling technique (EKC-CFT). The present study is a continuation of this previous work, introducing some novelties. In this work, the ability of sulfated γ-cyclodextrin (S-γ-CD) as chiral selector in EKC-CFT is modelled for the first time. Thirty-three structurally unrelated cationic and neutral compounds …

Resolution (mass spectrometry)02 engineering and technologyTopology01 natural sciencesBiochemistryAnalytical ChemistryElectrokinetic phenomenaCapillary electrophoresisCationsMoleculeLeast-Squares AnalysisPesticidesTopology (chemistry)Chromatography Micellar Electrokinetic CapillaryChromatographyChemistry010401 analytical chemistryOrganic ChemistryCationic polymerizationDiscriminant AnalysisStereoisomerismGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesPharmaceutical PreparationsAsymmetric carbonIndicators and ReagentsEnantiomer0210 nano-technologySoftwaregamma-CyclodextrinsJournal of Chromatography A
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