Search results for "oxides"

showing 10 items of 547 documents

Kinetics of the lipoperoxyl radical-scavenging activity of indicaxanthin in solution and unilamellar liposomes

2007

Abstract The reaction of the phytochemical indicaxanthin with lipoperoxyl radicals generated in methyl linoleate methanol solution by 2,20-azobis(2,4-dimethylvaleronitrile), and in aqueous soybean phosphatidylcholine unilamellar liposomes by 2,20-azobis(2- amidinopropane)hydrochloride, was studied. The molecule acts as a chain-terminating lipoperoxyl radical scavenger in solution, with a calculated inhibition constant of 3.63 £ 105M21 s21, and a stoichiometric factor approaching 2. Indicaxanthin incorporated in liposomes prevented lipid oxidation, inducing clear-cut lag periods and decrease of the propagation rate. Both effects were concentration-dependent, but not linearly related to the p…

Indicaxanthin membranes radical scavenger liposomesLipid PeroxidesAntioxidant12-DipalmitoylphosphatidylcholinePyridinesmedicine.medical_treatmentRadicalLipid Bilayersalpha-TocopherolAmidinesContext (language use)In Vitro TechniquesBiochemistryAntioxidantsLipid peroxidationchemistry.chemical_compoundLipid oxidationSuspensionsPhosphatidylcholineNitrilesmedicineOrganic chemistryLiposomeDose-Response Relationship DrugMolecular StructureMethanolDrug SynergismGeneral MedicineFree Radical ScavengersBetaxanthinsSolutionsKineticschemistryLinoleic AcidsLiposomesPhosphatidylcholinesSolventsLipid PeroxidationIndicaxanthinAzo CompoundsOxidation-ReductionNuclear chemistry
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Di-n-butyltin(IV)-catalyzed dimethyl carbonate synthesis from carbon dioxide and methanol: An in situ high pressure 119Sn{1H} NMR spectroscopic study

2011

The reactivity of five di-n-butyltin(IV) complexes, n-Bu2Sn(OR)(2) (1), n-Bu2SnO (3), [n-Bu2Sn(OR)](2)O (4), (n-Bu2SnO)(2)(CO2) (6) and (n-Bu2SnO)(6)[(n-Bu2SnOR)(2)(CO3)](2) (7) (R = CH3), with CO2, suggested as possible catalyst precursors and key-intermediates for the direct synthesis of dimethyl carbonate from carbon dioxide and methanol, has been investigated using high-pressure Sn-119{H-1} NMR (HP-NMR) spectroscopy. Four of the five precursors studied, i.e. 3, 4, 6 and 7 give rise to an identical Sn-119{H-1} NMR pattern which can be explicitly attributed to the fingerprint of the dimeric form of the 1-methoxy-3-methylcarbonatotetrabutyldistannoxane {5}(2). However, with 1, a new pair o…

Inorganic chemistryOxideAlkoxidesBiochemistryMedicinal chemistryCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistrySpectroscopyOrganic carbonatesReactivityOrganic ChemistryOxideChemistryCarbon dioxidechemistryCarbon dioxideProton NMRMethanolDimethyl carbonateOrganooxotin ClusterCarbon dioxide utilizationHigh-pressure NMR spectroscopyRelevantDiorganotin(IV)Journal of Organometallic Chemistry
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Confirmation of Fenthion Metabolites in Oranges by IT-MS and QqTOF-MS

2007

14 pages, 4 figures, 4 tables.-- PMID: 18020315 [PubMed].-- Printed version published Dec 15, 2007.

InsecticidesSulfoneElectrosprayFenoxon sulfoxideMass spectrometryMass SpectrometryAnalytical ChemistrySulfonechemistry.chemical_compoundSample preparationSulfonesPesticidesOrganophophorous pesticide fenthionChemical ionizationChromatographyFenthionHydrolysisSulfoxideFenoxon sulfoneSulfoxideFenthionchemistrySulfoxidesCholinesterase InhibitorsIon trapFood AnalysisCitrus sinensisAnalytical Chemistry
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Interaction of antibodies to proteinase 3 (classic anti-neutrophil cytoplasmic antibody) with human renal tubular epithelial cells: impact on signali…

2002

Abstract Among the anti-neutrophil cytoplasmic Abs (ANCA), those targeting proteinase 3 (PR3) have a high sensitivity and specificity for Wegener’s granulomatosis (WG). A pathogenetic role for these autoantibodies has been proposed due to their capacity of activating neutrophils in vitro. Recently, PR3 was also detected in human renal tubular epithelial cells (TEC). In the present study, the effect of murine monoclonal anti-PR3 Abs (anti-PR3) and purified c-ANCA targeting PR3 from WG serum on isolated human renal tubular cell signaling and inflammatory mediator release was characterized. Priming of TEC with TNF-α resulted in surface expression of PR3, as quantified in immunofluorescence stu…

Intracellular Fluidmedicine.medical_specialtyMyeloblastinImmunologyImmunofluorescencePhosphatidylinositolsAutoantigensDinoprostoneFlow cytometryAntibodies Antineutrophil CytoplasmicAntigen-Antibody ReactionsThromboxane A2Proteinase 3SuperoxidesInternal medicinemedicineCyclic AMPImmunology and AllergyHumanscardiovascular diseasesCells CulturedArachidonic Acidmedicine.diagnostic_testbiologyHydrolysisImmune SeraCell MembraneSerine EndopeptidasesAntibodies MonoclonalEpithelial CellsLipid signalingIn vitroCell biologyEndocrinologyKidney Tubulesbiology.proteinCyclooxygenaseSignal transductionInflammation MediatorsIntracellularSignal TransductionJournal of immunology (Baltimore, Md. : 1950)
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Intercalation of [M(ox)3]3− (M=Cr, Rh) complexes into NiIIFeIII-LDH

2010

Abstract Layered Double Hydroxides (LDH) containing paramagnetic NiII and FeIII ions in the hydroxide layers and chromium or rhodium oxalate complexes at the interlayer space were prepared by ion exchange from a NiFe-LDH precursor with sebacate anions between the hydroxide layers. The precursor was synthesized by coprecipitation at controlled pH in order to avoid the formation of solid phases different from LDH. Magnetic studies demonstrated that both LDHs, NiFe–Cr(ox)3 and NiFe–Rh(ox)3, exhibited a behaviour similar to the precursor. Nevertheless, the substitution of intercalated sebacate anions with oxalate complexes compresses the LDH basal spacing, increasing the intensity of dipolar in…

Ion exchangeCoprecipitationIntercalation (chemistry)Inorganic chemistryLayered double hydroxidesGeologyengineering.materialOxalatechemistry.chemical_compoundParamagnetismchemistryGeochemistry and PetrologyengineeringHydroxideHybrid materialApplied Clay Science
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Evaluation of changes in ion release and biological properties of NeoMTA‐Plus and Endocem‐MTA exposed to an acidic environment

2018

AIM To analyse in vitro changes in ion release and biological properties of Endocem-MTA (Maruchi, Wonju, Korea) and NeoMTA-Plus (Avalon Biomed Inc, Bradenton, FL, USA) exposed to acidic or neutral environment on human dental periodontal ligament stem cells (hPDLSCs). METHODOLOGY Cell viability and wound healing assays were performed using eluates of each material. Cell death and changes in phenotype induced by the set endodontic sealer eluates were evaluated through flow cytometry. To evaluate cell attachment to the different materials, hPDLSCs were directly seeded onto the material surfaces and analysed by scanning electron microscopy. The chemical composition of the materials was determin…

IonsProgrammed cell deathmedicine.diagnostic_testPeriodontal ligament stem cellsSilicatesOxidesPemetrexedCalcium CompoundsFlow cytometryRoot Canal Filling MaterialsButyric acidDrug Combinationschemistry.chemical_compoundchemistryApoptosisMaterials TestingRepublic of KoreamedicineHumansMTT assayViability assayAluminum CompoundsCytotoxicityGeneral DentistryNuclear chemistryInternational Endodontic Journal
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Dinitrosyl-iron triggers apoptosis in Jurkat cells despite overexpression of Bcl-2

2004

Cells expressing the cytokine-inducible NO synthase are known to trigger apoptosis in neighboring cells. Paramagnetic dinitrosyl nonheme iron complexes (DNIC) were found in tumor tissue about 40 years ago; however, the role of these NO(+)-bearing species is not completely understood. In the human Jurkat leukemia cell line, the application of the model complex DNIC-thiosulfate (50-200 microM) induced apoptosis (defined by phosphatidylserine externalization) in a concentration- and time-dependent manner. In Jurkat cells, the pan-caspase inhibitor, zVADfmk (50 microM), and/or stable transfection of antiapoptotic protein, Bcl-2, was unable to afford protection against DNIC-induced apoptosis. Th…

IronNitrosationCellApoptosisBiochemistryJurkat cellsMetal ChelatorNitric oxideJurkat Cellschemistry.chemical_compoundPhysiology (medical)medicineExtracellularPiHumansElectron Spin Resonance SpectroscopyGlutathioneCaspase InhibitorsCell biologymedicine.anatomical_structureGene Expression RegulationProto-Oncogene Proteins c-bcl-2chemistryApoptosisCaspasesNitrogen OxidesFree Radical Biology and Medicine
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Photocatalytic Degradation of 4-Nitrophenol in Aqueous Suspension by Using Polycrystalline TiO2 Impregnated with Lanthanide Double-Decker Phthalocyan…

2007

The photocatalytic activity of polycrystalline TiO2 samples impregnated with rare-earth-metal diphthalocyanines was investigated. The 4-nitrophenol (4-NP) photocatalytic degradation in aqueous suspension was used as a probe reaction. Commercial anatase TiO2 was impregnated with home-prepared double-decker phthalocyanine complexes of the lanthanide metals, such as Ce, Pr, Nd, Sm, Ho, and Gd. In particular, the impregnation with Ho, Sm, and Nd complexes, acting as sensitizers, proved beneficial for the photoactivity of the studied systems. Significant improvements of the TiO2-based catalytic system appeared possible in terms of lower impregnation loading, enhanced photoreactivity under solar …

LanthanideAnataseMaterials scienceInorganic chemistryPhthalocyanineOxides4-NitrophenolDecompositionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundGeneral EnergychemistryPhotocatalystsMineralsIrradiationPhotocatalysisPhthalocyanineCrystallitePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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Lanthanide molecular oxohydroxides: Synthesis and characterisation of [Y4(μ4-O)(μ-OEt)2(μ,η2-AAA)2(η2-AAA)3]2(μ3-OH)4(μ3-OEt)2 (HAAA = allylacetatoac…

2007

International audience; The reaction between Y5O(OPri)13 and allylacetatoacetate or 2-(methacryloyloxy)ethyl acetatoacetate in 1:5 stoichiometry afforded octanuclear oxohydroxo species. Structural characterization was achieved for the allylacetatoacetate derivative homo and copolymerisation reactions with styrene were evaluated for doping of polystyrene. Hydoxo species, Y4(OH)2(AAA)10, where also obtained by reacting Y[N(SiMe3)]3 and HAAA.

LanthanideInorganic chemistrychemistry.chemical_element02 engineering and technologyAlkoxides010402 general chemistry01 natural sciences"Polymerizable ligands"StyreneInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryYttriumPhysical and Theoretical ChemistryPolymerizable ligands"Alkoxides"Doping"X-ray structure"Yttrium[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnology[SDE.ES]Environmental Sciences/Environmental and Society0104 chemical scienceschemistryPolystyreneX-ray structure0210 nano-technology"Yttrium"Derivative (chemistry)Stoichiometry
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Photoelectrochemical Synthesis of Conducting Polymers Layers on Large Band Gap Nb2O5 and Ta2O5 Anodic Oxides Films

2008

Large band gap oxides
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