Search results for "dextrin"

showing 10 items of 297 documents

Host-guest interactions for extracting antibiotics with a γ-cyclodextrin poly(glycidyl-co-ethylene dimethacrylate) hybrid sorbent

2021

Abstract A procedure for the solid-phase extraction of antibiotics (enoxacin, ofloxacin, norfloxacin, ciprofloxacin, and sparfloxacin) in water has been developed. The sorbent used is based on a poly(glycidyl-co-ethylene dimethacrylate) network, whose previously modified surface has been functionalized with γ-cyclodextrin through a click-chemistry reaction. The architecture of the material has been characterized by thermogravimetric analysis, N2 adsorption-desorption, Raman spectroscopy, confocal microscopy, and scanning electron microscopy, showing good capability to be used as a filler for extraction cartridges. The optimization of the extraction methodology shows good intra-day and inter…

chemistry.chemical_classificationDetection limitThermogravimetric analysisAqueous solutionSorbentCyclodextrinChemistrySolid Phase Extraction010401 analytical chemistryExtraction (chemistry)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesAnti-Bacterial Agents0104 chemical sciencesAnalytical Chemistrysymbols.namesakesymbolsMethacrylatesSurface modificationAdsorption0210 nano-technologyRaman spectroscopygamma-CyclodextrinsNuclear chemistryTalanta
researchProduct

A spectrofluorimetric study of binary fluorophore-cyclodextrin complexes used as chiral selectors

2005

Abstract Six binary complexes between three fluorophores (pyrene, xanthone and anthraquinone) and β-cyclodextrin (β-CD) or heptakis-(6-amino)-(6-deoxy)-β-cyclodextrin (am-β-CD) were tested at two pH values (8.0 and 9.0) as chiral selectors for three α-amino acids chosen as model. The conditional constant (β2T) values for ternary complexes (fluorophore-CD-amino acid), determined by means of fluorescence spectroscopy, showed that the binary complexes are suitable receptors for chiral recognition. The effect of α-amino acids on stability and stoichiometric ratio of the binary complexes has also been studied. The binary complexes were in most cases stabilized by adding the ternary agent. The tr…

chemistry.chemical_classificationFluorophoreCyclodextrinChemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaBiochemistryFluorescenceAnthraquinoneFluorescence spectroscopychemistry.chemical_compoundDrug DiscoveryXanthonePhysical chemistryPyreneOrganic chemistrycyclodextrin binding abilityTernary operation
researchProduct

Stability and stoichiometry of some binary fluorophore-cyclodextrin complexes

2004

The stability and stoichiometric ratio of binary complexes among five fluorophores and β-cyclodextrin (β-CD) or heptakis-(6-amino-6-deoxy)-β-cyclodextrin (am-β-CD) were determined by means of fluorescence measurements in borate buffer at pH=8.0 and 9.0. Structure of both host and guest affected the characteristics of the binary complexes. Pyrene and anthraquinone formed a 1:2 (fluorophore: cyclodextrin) complex with both cyclodextrins. Xanthone formed 1:1 complex with β-CD and 1:2 complex with am-β-CD. A more defined behaviour was observed for crysene. In fact, both stoichiometric different complexes were detected with both hosts. Only 1:1 complexes were observed for antracene. The complex …

chemistry.chemical_classificationFluorophoreCyclodextrinOrganic ChemistryBinary numbercyclodextrin fluorophoreBiochemistryFluorescenceAnthraquinonechemistry.chemical_compoundCrystallographychemistryDrug DiscoveryXanthonePyreneOrganic chemistryStoichiometry
researchProduct

Cyclodextrin-[60]fullerene conjugates: synthesis, characterization, and electrochemical behavior

2006

Three different functionalized β-cyclodextrins (β-CDs) bearing the C60 moiety linked covalently have been prepared in good yields by reaction between the parent β-CD and [60]fullerene via 1,3-dipolar cycloaddition. These compounds have been fully spectroscopically characterized and their electrochemical behavior has been investigated. Surprisingly, the electrochemical properties of the C60 cage remain unaltered even after chemical functionalization, making these systems very appealing as supramolecular hosts for electron-transfer processes.

chemistry.chemical_classificationFullereneCyclodextrinOrganic ChemistrySupramolecular chemistrySettore CHIM/06 - Chimica OrganicaElectrochemistrycyclodextrin fullereneBiochemistryCombinatorial chemistryCycloadditionchemistryCovalent bondDrug Discovery13-Dipolar cycloadditionOrganic chemistryMoiety
researchProduct

Cyclodextrin-assisted Glycan Chain Extension on a Protected Glycosyl Amino Acid

2000

By the use of cyclodextrins, we have enhanced the solubility of the protected amino acid glycan Fmoc-Thr(GalNAcα1)-OtBu (1b) up to 100-fold. This improvement enabled us to carry out an enzymatic glycosylation employing a β-galactosidase in combination with an α2,3-sialyltransferase without the aid of organic cosolvents. After optimization of the one-pot reaction, the sialylated core 1 structure Fmoc-Thr[Neu5Ac(α2-3)Gal(β1-3)GalNAcα1]-OtBu (3b) could be obtained with 50% yield.

chemistry.chemical_classificationGlycanGlycosylationbiologyCyclodextrinStereochemistryOrganic ChemistryBiochemistryAmino acidcarbohydrates (lipids)chemistry.chemical_compoundchemistryBiosynthesisYield (chemistry)Drug Discoverybiology.proteinOrganic chemistryGlycosylSolubilityTetrahedron
researchProduct

A Hybrid Cavitand Made by Capping Permethylated α-Cyclodextrin with Cyclotriveratrylene

2012

A hybrid C 3 -symmetric cavitand 1, in which permethylated α-cyclodextrin (PM α-CDX) is capped with cyclotriveratrylene (CTV), has been prepared in 8 % yield by intramolecular cyclization of a vanillyl alcohol derivative attached to the primary rim of the CDX platform. The reaction proceeds diastereoselectively (dr ≈ 6:1), the chirality of the α-glucopyranosyl units controlling the chirality of the CTV component. Interestingly, in polar solvents, 1 shows self-complexation properties as the primary methoxy groups of the CDX component are directed towards the CTV cavity.

chemistry.chemical_classificationIntramolecular reactionCyclodextrinChemistryStereochemistryOrganic ChemistryCavitandCyclotriveratryleneInclusion compoundchemistry.chemical_compoundVanillyl alcoholPhysical and Theoretical ChemistryChirality (chemistry)CyclophaneEuropean Journal of Organic Chemistry
researchProduct

Effect of?-cyclodextrin complexation on the photohaemolitic activity induced by Ketoprofen and Naproxen sensitization

1993

Red blood cell lysis photosensitized by two non-steroidal anti-inflammatory drugs Naproxen (NAP) and Ketoprofen (KPF) was investigated in the presence of β-cyclodextrin (β-Cyd). The photohaemolysis was inhibited by the addition of β-Cyd both for NAP and, to a lesser extent, for KPF. The protective action was found only in a restricted range of concentration of β-Cyd. Higher amounts of β-Cyd interfered with the resistance of the cell to the osmotic shock induced by the photosensitization process. The complexing action of β-Cyd was ascertained through UV-vis absorption spectroscopy, induced circular dichroism and emission spectroscopy. The isolated complexes Naproxen-β-Cyd (NAP-β-Cyd) and Ket…

chemistry.chemical_classificationKetoprofenNaproxenCircular dichroismLysisCyclodextrinOsmotic shockStereochemistryGeneral ChemistryCondensed Matter PhysicsNapchemistryBiophysicsmedicinePhototoxicityFood Sciencemedicine.drugJournal of Inclusion Phenomena and Molecular Recognition in Chemistry
researchProduct

Kinetics of Molecule Transfer between Lipid Vesicles and β-Cyclodextrins

1996

Abstract We propose a calorimetric method based on the van't Hoff model of depression of the freezing temperature to investigate slow kinetics involving lipid vesicles (liposomes) and drug–β-cyclodextrin (Cyd) complexes. Some nonsteroidal antiinflammatory drugs (NSAIDs) were examined and standard phospholipid liposomes were used in our experiments. Three different kinetic processes were investigated: (a)9Transfer of drugs from water-soluble Cyd-complexes to void liposomes. (b)9Uptake of drugs from the surface of liposomes by free Cyd dissolved in the aqueous phase. (c)9Exchange of drugs from loaded to void vesicles, and the effect of free Cyd in enhancing such a transfer. Most experiments w…

chemistry.chemical_classificationLiposomeChromatographyCyclodextrinChemistryVesicleBilayerKineticsPhospholipidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInclusion compoundBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryDifferential scanning calorimetryBiophysicsJournal of Colloid and Interface Science
researchProduct

Heads or Tails? Sandwich-Type Metallo Complexes of Hexakis(2,3-di-O-methyl)-α-cyclodextrin

2020

Native and synthetically modified cyclodextrins (CDs) are useful building blocks in the construction of large coordination complexes and porous materials with various applications. Sandwich-type co...

chemistry.chemical_classificationMaterials scienceCyclodextrin010405 organic chemistryGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences3. Good health0104 chemical sciencesSandwich typeCrystallographychemistryX-ray crystallographyGeneral Materials SciencePorous mediumCrystal Growth & Design
researchProduct

Interaction of 5‐fluorouracil with β‐cyclodextrin: A density functional theory study with dispersion correction

2020

Detailed studies on the stability, interaction, and microstructure of host‐guest complexes in the vacuum of 5‐fluorouracil (5FU) with β‐cyclodextrin (βCD) were performed using B3LYP with the inclusion of Grimme's dispersion correction GD3 term and 6‐31+G(d,p) basis set. Among several studied 1:1 5FU‐βCD complexes, the one placing the keto tautomer of 5FU vertically in the host cavity and forming N‐H···OCD and CO···HOCD hydrogen bonds with hydroxyl groups of the smaller rim of βCD has the highest stability (Eint = −195 kJ/mol). Interestingly, there are no interactions with the inner hydrophobic part of the βCD host cavity. The strength of the intermolecular H‐bonds to the smaller rim of βC…

chemistry.chemical_classificationMaterials scienceCyclodextrinInteraction energyCondensed Matter Physics5‐fluorouracil (5FU)Atomic and Molecular Physics and OpticsDFT‐D3β‐cyclodextrin (βCD)chemistryChemical physicsDispersion (optics)Density functional theoryPhysical and Theoretical Chemistryinclusion complexinteraction energyInternational Journal of Quantum Chemistry
researchProduct