Search results for "HYDROGEN"

showing 10 items of 4254 documents

A French prospective pilot study for identifying dihydropyrimidine dehydrogenase (DPD) deficiency in breast cancer patients (pts) receiving capecitab…

2013

e13519 Background: For fluoropyrimidines, and especially cap, Health Authorities point out that DPD deficiency confers a significant risk of major toxicity (tox). Identification of at-risk pts is thus relevant. This multicentric prospective study of the French GPCO group (Groupe de Pharmacologie Clinique Oncologique, Unicancer) evaluated the sensitivity, specificity and predictive values of DPD phenotyping and genotyping for predicting severe cap-related tox in metastatic breast cancer pts. Methods: 303 pts were included (15 institutions), 88% received cap as monotherapy, 28% were treated as first line (mean dose at 1st cycle 1957 mg/m2/d). Pre-treatment dihydrouracil (UH2) and uracil (U) …

Cancer Researchmedicine.medical_specialtymacromolecular substances030226 pharmacology & pharmacyGastroenterology[SPI.AUTO]Engineering Sciences [physics]/AutomaticCapecitabine03 medical and health scienceschemistry.chemical_compound0302 clinical medicineBreast cancerInternal medicine[ SPI.AUTO ] Engineering Sciences [physics]/AutomaticmedicineDihydropyrimidine dehydrogenaseProspective cohort studybusiness.industryDihydrouracilmedicine.diseaseMetastatic breast cancer3. Good healthSurgery[SPI.AUTO] Engineering Sciences [physics]/AutomaticOncologychemistry030220 oncology & carcinogenesisRelative riskToxicitybacteriaPublished in Journal of Clinical Oncology vol. 31 : 2013 (Suppl ;abstr e13519)businessmedicine.drug
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The oxygen radicals involved in the toxicity induced by parthenolide in MDA-MB-231 cells

2014

It has been shown that the sesquiterpene lactone parthenolide lowers the viability of MDA-MB-231 breast cancer cells, in correlation with oxidative stress. The present report examined the different radical species produced during parthenolide treatment and their possible role in the toxicity caused by the drug. Time course experiments showed that in the first phase of treatment (0-8 h), and in particular in the first 3 h, parthenolide induced dichlorofluorescein (DCF) signal in a large percentage of cells, while dihydroethidium (DHE) signal was not stimulated. Since the effect on DCF signal was suppressed by apocynin and diphenyleneiodonium (DPI), two inhibitors of NADPH oxidase (NOX), we s…

Cancer Researchparthenolide oxygen radicals NADPH oxidase breast cancer cellsCell SurvivalBreast NeoplasmsSuperoxide dismutasechemistry.chemical_compoundSuperoxide Dismutase-1DichlorofluoresceinSuperoxidesCell Line TumorSettore BIO/10 - BiochimicaHumansParthenolidechemistry.chemical_classificationReactive oxygen speciesNADPH oxidasebiologySuperoxideSuperoxide DismutaseAnti-Inflammatory Agents Non-SteroidalNADPH OxidasesGeneral MedicineHydrogen PeroxideMolecular biologyMitochondriaOncologychemistryApocyninbiology.proteinFemaleSesquiterpenesPeroxynitrite
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Monitoring the chemical changes in Pd induced by hydrogen absorption using microcantilevers.

2003

Abstract The reactivity of the palladium shaped as a microcantilever is investigated as a function of the hydrogen stoichiometry. A small cell holding the microcantilever is designed to monitor the deflection and the flexural resonance response from high vacuum to a hydrogen gas pressure of several bars. The measurements show that the Young's modulus is accurate if the cantilever is thick enough to be described by a continuum mechanics approach. The orientation distribution function of the palladium grains determined by X-ray diffraction enables to correlate Young's modulus measured using microcantilevers with the elastic constant tensor issued from the literature. The surface stress induce…

CantileverHydrogenHydrideSurface stressUltra-high vacuumAnalytical chemistrychemistry.chemical_elementYoung's modulusAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialssymbols.namesakechemistrysymbolsInstrumentationStoichiometryPalladiumUltramicroscopy
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Cavitation of electron bubbles in liquid parahydrogen

2011

Within a finite-temperature density functional approach, we have investigated the structure of electron bubbles in liquid parahydrogen below the saturated vapour pressure, determining the critical pressure at which electron bubbles explode as a function of temperature. The electron-parahydrogen interaction has been modelled by a Hartree-type local potential fitted to the experimental value of the conduction band-edge for a delocalized electron in pH(2). We have found that the pressure for bubble explosion is, in absolute value, about a factor of two smaller than that of the homogeneous cavitation pressure in the liquid. Comparison with the results obtained within the capillary model shows t…

Capillary actionChemistryVapor pressureBubbleBiophysicselectron bubblesElectronCondensed Matter PhysicsSpin isomers of hydrogenThermal conductionMolecular physicsPhysics::Fluid Dynamicscapillary approximationNuclear magnetic resonanceCavitationliquid parahydrogenPhysics::Atomic and Molecular ClustersDensity functional theoryPhysical and Theoretical ChemistryMolecular Biologydensity functional theoryMolecular Physics
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Thermodynamic analysis of binding between drugs and glycosaminoglycans by isothermal titration calorimetry and fluorescence spectroscopy

2007

The thermodynamics of the interaction of positively charged drug molecules with negatively charged glycosaminoglycans (GAGs) is investigated by isothermal titration calorimetry (ITC) and fluorescence spectroscopy. The drugs considered are propranolol hydrochloride, tacrine, and aminacrine, and the polymers used as model GAGs are dextran sulfate, chondroitin sulfate, and hyaluronic acid. The ITC results show that the interaction between drugs and GAGs is via direct binding and that GAGs bind to drugs at one set of sites. Large negative values of heat capacity change (DeltaC(p)) are observed upon binding of GAGs to drugs. Such negative DeltaC(p) is not expected for purely electrostatic intera…

CarbohydratesFluorescence spectrometryPharmaceutical ScienceCalorimetryCalorimetryFluorescence spectroscopychemistry.chemical_compoundChondroitin sulfateHyaluronic AcidFluorescent DyesGlycosaminoglycansLiaisonChemistryChondroitin SulfatesTemperatureProteinsMembranes ArtificialIsothermal titration calorimetryHydrogen-Ion ConcentrationPropranololAminacrineSpectrometry FluorescenceMembranePharmaceutical PreparationsBiochemistryDrug deliveryTacrineBiophysicsThermodynamicsIndicators and ReagentsEuropean Journal of Pharmaceutical Sciences
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1H, 13C and 15N NMR spectral characterization of twenty-seven 1,2-diaryl-(4E)-arylidene-2-imidazolin-5-ones.

2006

1H, 13C and 15N NMR chemical shifts and couplings nJ(H,C) in DMSO-d6 at 30 °C have been determined for 1,2-diaryl-(4E)-arylidene-2-imidazolin-5-one derivatives 1–27. Their chemical shift assignments are based on PFG DQF 1H,1H COSY, PFG 1H,13C HMQC as well as PFG 1H,13C and 1H,15N HMBC experiments. For compounds 1–10 including aryl fluorine substituent(s) also the couplings nJ(F,C) (n = 1 − 4) are reported. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopyMolecular StructureNitrogen IsotopesStereochemistryArylChemical shiftSubstituentchemistry.chemical_elementGeneral ChemistryCarbon-13 NMRchemistry.chemical_compoundchemistryProton NMRFluorineGeneral Materials ScienceImidazolinesHydrogenMagnetic resonance in chemistry : MRC
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Complete 1H and 13C NMR assignments of clerodane diterpenoids of Salvia splendens.

2006

Unambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes, four of them isolated from Salvia splendens (salviarin, splendidin and splenolides A and B) and one obtained by acetylation of splenolide A, are presented. The assignments are based on 2D shift-correlated [1H,1H–COSY, 1H,13C-gHSQC–1J(C,H) and 1H,13C-gHMBC-nJ(C,H) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(H,H) values and NOE results. Copyright © 2006 John Wiley & Sons, Ltd.

Carbon IsotopesMagnetic Resonance SpectroscopybiologyStereochemistryChemistryChemical shiftAcetylationGeneral ChemistryNuclear Overhauser effectCarbon-13 NMRSalviabiology.organism_classificationDiterpenes ClerodaneUnambiguous and complete assignments of 1H and 13C NMR chemical shifts for five clerodane diterpenes four of them isolated from Salvia splendens (salviarin splendidin and splenolides A and B) and one obtained by acetylation of splenolide A are presented. The assignments are based on 2D shiftcorrelated [1H1H–COSY 1H13C-gHSQC–1J(CH) and 1H13C-gHMBC-nJ(CH) (n = 2 and 3)] and nuclear Overhauser effect (NOE) experiments. The conformation of the rings of these compounds is supported by the 3J(HH) values and NOE results. Copyright  2006 John Wiley & Sons LtdClerodane DiterpenesProton NMRGeneral Materials ScienceSalviaHydrogenMagnetic resonance in chemistry : MRC
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Origin and significance of the production of carbon dioxide during the ozonization of 13C-labeled D-glucose at different pH values.

2001

Abstract [1- 13 C], [2- 13 C] and [6- 13 C] d -glucose were, respectively, ozonized in a semi-batch reactor in acidic and basic conditions. The composition of the gas phase was evaluated by on-line mass spectrometry measurements. The quantitative and isotopic analyses of the carbon dioxide formed during ozonization are presented and discussed. The data, correlated with previous literature results, clearly show that at pH 2.5 the production of carbon dioxide from C-6 and C-1 carbon atoms is nearly equivalent. Conversely, at higher pH values, CO 2 is released with a greater selectivity from the reducing end. The importance of the decarboxylation reaction in the formation of by-products with f…

Carbon IsotopesOzoneDecarboxylationOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral MedicineCarbon DioxideHydrogen-Ion ConcentrationBiochemistryMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundGlucoseOzonechemistryTotal inorganic carbonD-GlucoseCarbon dioxideOrganic chemistrySelectivityCarbonElectrochemical reduction of carbon dioxideCarbohydrate research
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DFT calculation of 1J(119Sn,13C) and 2J(119Sn,1H) coupling constants in di- and trimethyltin(IV) compounds

2008

We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data has been found with several hybrid functionals and a double-zeta basis set for a set of molecules comprising tetra-, penta-, and hexa-coordinated tin(IV). Then, some of the protocols have been applied to the calculation of the 2J(119Sn, 1H) of the aquodimethyltin(IV) ion and dimethyltin(IV) complex with D-ribonic acid and to the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) of the dimethyltin(IV)-glycylglycin…

Carbon Isotopes; Dipeptides; Glycylglycine; Hydrogen; Organotin Compounds; Solvents; Tin; Trimethyltin Compounds; Water; Quantum Theorychemistry.chemical_elementInorganic ChemistryOrganotin(IV) DFT NMR relativistic effects tin couplingsComputational chemistryOrganotin CompoundsMoleculePhysical and Theoretical ChemistryBasis setCoupling constantCarbon IsotopesNMR tin derivatives coupling constantsTrimethyltin CompoundsbiologyGlycylglycineWaterDipeptidesbiology.organism_classificationHybrid functionalSolventchemistryTinSolventsQuantum TheoryTetraSolvent effectsTinHydrogen
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Assessment for the mean value total dressing method: Comparison with coupled cluster including triples methods for BF, NO+, CN+, C2, BeO, NH3, CH2, H…

1997

Limited previous experience with the mean value total dressing (MVTD) method had shown that MVTD energies for closed shell systems are generally better than CCSD(T) ones compared to FCI. The method, previously published as total dressing 2′(td-2′), is based on the single reference intermediate Hamiltonian theory. It is not a CC method but deals in a great part with the same physical effects that CC methods that incorporate amplitudes of triples such as CCSDT or its CCSDT-1n approaches. A number of test calculations comparing to diverse CC methods, as well as FCI and experiment when available, have been performed. The tests concern equilibrium energies in NH3 and CH2, equilibrium energies an…

Carbon compoundsGeneral Physics and AstronomyBoron compounds ; Nitrogen compounds ; Water ; Ammonia ; Ozone ; Organic compounds ; Carbon compounds ; Beryllium compounds ; Hydrogen compounds ; Silicon compounds ; Lithium ; Lithium compounds ; Carbon ; Neon compounds ; Coupled cluster calculations ; Dissociation ; Dissociation energies ; Positive ionsLithiumDissociation (chemistry)Nitrogen compoundsIonDissociation energiesOzoneCoupled cluster calculationsAmmoniaBeryllium compoundsOrganic compoundsMoleculeSilicon compoundsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Open shellChemistryNeon compoundsMean valueWaterLithium compoundsHydrogen compoundsDiatomic moleculeCarbonUNESCO::FÍSICA::Química físicaCoupled clusterAmplitudeBoron compoundsPositive ionsAtomic physicsDissociation
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