Search results for "Colloid"

showing 10 items of 1288 documents

An approach to rheological and electrokinetic behaviour of lipidic vesicles covered with chitosan biopolymer

2008

The rheological and electrokinetic properties of soybean lecithin vesicles prepared from concentrated soy lecithin dispersions (250 g/L) obtained by slow swelling under shear conditions and mixed with chitosan biopolymer solutions were studied. The rheological behaviour of lecithin-chitosan vesicles was determined by shear stress against shear rate measurements, as well as by the variation on the hysteresis loop area. The results were compared with the rheopectic behaviour of soy lecithin dispersions without chitosan. An important change on the rheological properties of the complex dispersion was observed, depicting in a thixotropic behaviour with a plastic character in the presence of chit…

ThixotropyMaterials scienceChromatographyVesicleREOLOGÍAengineering.materialPOLÍMEROSChitosanShear ratechemistry.chemical_compoundElectrokinetic phenomenaColloid and Surface ChemistrychemistryRheologyChemical engineeringRHEOLOGYengineeringmedicineSOY LECITHINBiopolymerQUITOSANOSwellingmedicine.symptomPOLYMERS
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Gold Nanoparticles Supported on Nanoparticulate Ceria as a Powerful Agent against Intracellular Oxidative Stress

2012

Ceria-supported gold nanoparticles are prepared exhibiting peroxidase activity and acting as radical traps. Au/CeO2 shows a remarkable biocompatibility as demonstrated by measuring cellular viability, proliferation, and lack of apoptosis for two human cell lines (Hep3B and HeLa). The antioxidant activity of Au/CeO2 against reactive oxygen species (ROS) is demonstrated by studying the cellular behavior of Hep3B and HeLa in a model of cellular oxidative stress. It is determined that Au/CeO2 exhibits higher antioxidant activity than glutathione, the main cytosolic antioxidant compound, and its CeO2 carrier. Overall the result presented here shows the potential of implementing well-established …

Time FactorsAntioxidantMaterials scienceBiocompatibilityCell SurvivalPolymersPeroxidase activitymedicine.medical_treatmentMetal NanoparticlesApoptosisBiocompatible MaterialsIntracellular oxidative stressmedicine.disease_causeAntioxidantsCatalysisCell LineBiomaterialsHeLachemistry.chemical_compoundCeriaQUIMICA ORGANICAmedicineHumansNanotechnologyGold nanoparticlesGeneral Materials ScienceCell Proliferationchemistry.chemical_classificationReactive oxygen speciesbiologyGeneral ChemistryGlutathionebiology.organism_classificationOxidative StressNanomedicinePeroxidasesBiochemistrychemistryColloidal goldNanoparticlesGoldReactive Oxygen SpeciesIntracellularOxidative stressHeLa CellsBiotechnologySmall
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Detoxifying antitumoral drugs via nanoconjugation: the case of gold nanoparticles and cisplatin

2021

Nanoparticles (NPs) have emerged as a potential tool to improve cancer treatment. Among the proposed uses in imaging and therapy, their use as a drug delivery scaffold has been extensively highlighted. However, there are still some controversial points which need a deeper understanding before clinical application can occur. Here the use of gold nanoparticles (AuNPs) to detoxify the antitumoral agent cisplatin, linked to a nanoparticle via a pH-sensitive coordination bond for endosomal release, is presented. The NP conjugate design has important effects on pharmacokinetics, conjugate evolution and biodistribution and results in an absence of observed toxicity. Besides, AuNPs present unique o…

Time FactorsCancer TreatmentMetal Nanoparticleslcsh:MedicinePharmacologyMiceNanotechnologyTissue Distributionlcsh:Sciencemedia_commonDrug DistributionDrug CarriersMultidisciplinaryChemistryDNA NeoplasmOrgan SizeHydrogen-Ion ConcentrationEndocytosisOncologyColloidal goldDrug deliveryInactivation MetabolicMedicinemedicine.drugResearch ArticleBiotechnologyDrugBiodistributionDrugs and Devicesmedia_common.quotation_subjectMaterials ScienceAntineoplastic AgentsMaterial by AttributePharmacokineticsCell Line TumormedicineAnimalsHumansPharmacokineticsBiologyNanomaterialsCisplatinUnited States Food and Drug Administrationlcsh:RChemotherapy and Drug TreatmentUnited StatesBionanotechnologylcsh:QGoldNanocarriersCisplatinConjugate
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Real-Time Nuclear Magnetic Resonance Detection of Fumarase Activity Using Parahydrogen-Hyperpolarized [1- 13 C]Fumarate

2019

Hyperpolarized fumarate can be used as a probe of real-time metabolism in vivo, using carbon-13 magnetic resonance imaging. Dissolution dynamic nuclear polarization is commonly used to produce hyperpolarized fumarate, but a cheaper and faster alternative is to produce hyperpolarized fumarate via PHIP (parahydrogen-induced polarization). In this work, we trans-hydrogenate [1-13C]acetylene dicarboxylate with para-enriched hydrogen using a commercially available Ru catalyst in water to produce hyperpolarized [1-13C]fumarate. We show that fumarate is produced in 89% yield, with succinate as a side product in 11% yield. The proton polarization is converted into 13C magnetization using a constant…

Time FactorsHydrogenNuclear Magnetic Resonancechemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesBiochemistryCatalysisFumarate HydrataseCatalysisMagnetizationchemistry.chemical_compoundColloid and Surface ChemistryFumaratesMoleculeCarbon IsotopesMolecular StructureFumarase activityCarbon Isotopes; Fumarate Hydratase; Fumarates; Molecular Structure; Time Factors; Nuclear Magnetic Resonance BiomolecularGeneral Chemistry0104 chemical sciencesAcetylenechemistryFumaraseBiomolecularJournal of the American Chemical Society
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Influence of Remote Substituents on the Equatorial/Axial Selectivity in the Monooxygenation of Methylene C−H Bonds of Substituted Cyclohexanes

2001

The reactivity of individual C--H bonds in the methyl(trifluoromethyl)dioxirane TFDO oxygenation of stereogenic methylene groups in conformationally homogeneous monosubstituted cyclohexanes (2) has been determined. The unexpectedly high occurrence of O-atom insertion into C--H(ax) bonds suggests an in plane trajectory attack in the oxygenation while the diastereoselectivity of the reaction is qualitatively interpreted on the basis of the distinct hyperconjugative stabilization by the substituent of diastereomeric transition states due to long-range through bond interactions.

TrifluoromethylStereochemistrySubstituentGeneral ChemistryBiochemistryCatalysisTransition stateStereocenterchemistry.chemical_compoundColloid and Surface ChemistrychemistryDioxiraneCyclohexanesReactivity (chemistry)MethyleneJournal of the American Chemical Society
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Darstellung einiger oligomerer Cyclo{oligo[(2-hydroxy-1,3-phenylen)methylen]}e. Spektroskopische Untersuchung ihrer Pseudorotation

1978

Es wird die Darstellung von Cyclo{tris[(2-hydroxy-5-methyl-1,3-phenylen)methylen]-(2-hydroxy-5-tert-butyl-1,3-phenylen)methylen} (4a), Cyclo{bis[(2-hydroxy-5-methyl-1,3-phenylen)methylen]-bis[(2-hydroxy-5-tert-butyl-1,3-phenylen)methylen]}(4b) und Cyclo-{pentakis[(2-hydroxy-5-methyl-1,3-phenylen)methylen]} (4c) beschrieben. Die IR-Spektren zeigen, das die phenolischen Hydroxygruppen der Vierringverbindungen 4a und 4b intramolekulare, vom Losungs(CCl4)- oder Zerteilungsmittel (KBr) weitgehend unabhangige Wasserstoffbrucken bilden, die bei der pentameren Ringverbindung 4c schwacher sind. Anhand der 1H-NMR-Spektren last sich bei diesen Verbindungen eine Pseudorotation nachweisen. Die Massenspe…

TrisPolymers and PlasticsHydrogen bondStereochemistryPentamerInfrared spectroscopyMedicinal chemistrychemistry.chemical_compoundColloid and Surface ChemistrychemistryIntramolecular forcePolymer chemistryMaterials ChemistryMoleculePseudorotationPhysical and Theoretical ChemistryMethyleneDie Makromolekulare Chemie
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When Does Gold Behave as a Halogen? Predicted Uranium Tetraauride and Other MAu4 Tetrahedral Species, (M = Ti, Zr, Hf, Th)

2003

Quantum chemical calculations suggest that a series of molecules with the general formula MAu4 are stable, where M = U, Th, and a group-4 atom. They correspond to Au in the formal valence state -1 and indicate that gold can act as a ligand similar to the halogen series. Of the MAu4 species studied, UAu4, the first predicted mixed gold uranium compound, has a short M-Au bond distance, 2.71 A, which would locate Au between Br and I from the bond length point of view in the U-tetrahalide series. Energetically, the U-Au bond is weaker than the corresponding U-Br and U-I bonds.

Valence (chemistry)LigandStereochemistrychemistry.chemical_elementGeneral MedicineGeneral ChemistryElectronic structureUraniumBiochemistryCatalysisBond lengthCrystallographyColloid and Surface ChemistrychemistryGold CompoundsMolecular vibrationAtomHalogenddc:540TetrahedronMolecule
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A New Valence Tautomerism Example in an Electroactive Ferrocene Substituted Triphenylmethyl Radical

2003

A new molecular system combining an open-shell organic radical that acts as an acceptor group, different from an o-quinone moiety, covalently linked to a ferrocene moiety, acting as the donor group, is shown to exhibit valence tautomerism.

Valence (chemistry)StereochemistryGeneral ChemistryBiochemistryAcceptorTautomerCatalysisTriphenylmethyl radicalchemistry.chemical_compoundColloid and Surface ChemistryFerrocenechemistryCovalent bondPolymer chemistryMoietyMoleculeJournal of the American Chemical Society
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Viscoelastic properties of concentrated dispersions in water of soy lecithin

2003

Abstract Viscoelastic properties of soy lecithin dispersions at 60, 120, 180 and 240 g l−1 in water have been studied as a function of ionic strength (NaCl concentrations in the range 10−5–10−2 mol l−1) and of preparation method (sonication, freezing–unfreezing). Viscosity measurements of sonicated dispersions in a rotatory viscometer show Newtonian and plastic (Bingham) behavior, whereas the frozen–unfrozen dispersions show a spectacular change in their viscoelastic properties, that is, a non-Newtonian behavior with pseudoplastic characteristics and rheopexy. These properties have been related to electrokinetic characteristics of the segregated vesicles in each case. A decrease in ζ-potent…

ViscosityElectrokinetic phenomenaColloid and Surface ChemistryShear thinningChromatographyMaterials scienceChemical engineeringIonic strengthSonicationNewtonian fluidViscometerViscoelasticityColloids and Surfaces A: Physicochemical and Engineering Aspects
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Controlled assembly of single colloidal crystals using electro-osmotic micro-pumps.

2017

We assemble charged colloidal spheres at deliberately chosen locations on a charged unstructured glass substrate utilizing ion exchange based electro-osmotic micro-pumps. Using microscopy, a simple scaling theory and Brownian Dynamics simulations, we systematically explore the control parameters of crystal assembly and the mechanisms through which they depend on the experimental boundary conditions. We demonstrate that crystal quality depends crucially on the assembly distance of the colloids. This is understood as resulting from the competition between inward transport by the electro-osmotic pump flow and the electro-phoretic outward motion of the colloids. Optimized conditions include sub…

Void (astronomy)Materials scienceIon exchangedigestive oral and skin physiologyGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyColloidal crystalCondensed Matter - Soft Condensed Matter010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencescomplex mixtures0104 chemical sciencesCrystalCondensed Matter::Soft Condensed MatterColloidChemical physicsBrownian dynamicsSoft Condensed Matter (cond-mat.soft)SPHERESPhysical and Theoretical ChemistrySingle domain0210 nano-technologyPhysical chemistry chemical physics : PCCP
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