Search results for "ExAC"

showing 10 items of 1440 documents

Histological evaluation of bone repair using beta-Tricalcium Phosphate

2010

Objectives: The aim of the present study was to evaluate bone repair in defects induced in the cranium of Wistar rats using ?-tricalcium phosphate. Study Design: In this research, we used 30 rats, randomly distributed in three groups of 10 animals (G1, G2 and G3), corresponding respectively to time of histological evaluation (7, 15 and 30 days). This was a paired study, a defect being induced in the parietal bone on either side of the median sagittal suture of the animals, being the left-hand side the experimental subgroup (filled by biomaterial) and the right control. The histological evaluation was performed by means of light microscopy. The collected data were submitted to the Fisher Exa…

Calcium PhosphatesMaleBone RegenerationBiocompatible MaterialsBone healingsymbols.namesakeMcNemar's testmedicineAnimalsRats WistarBone regenerationGeneral DentistryFisher's exact testβ tricalcium phosphatebusiness.industryAnatomy:CIENCIAS MÉDICAS [UNESCO]RatsSagittal suturemedicine.anatomical_structureOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASsymbolsSurgerybusinessNuclear medicineParietal bone
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Geochemical evidence for arsenic cycling in living microbialites of a High Altitude Andean Lake (Laguna Diamante, Argentina)

2020

Arsenic is best known as an environmental toxin, but this element could also serve as a metabolic energy source to certain microorganisms. Moreover, As cycling may have driven microbial life on early Earth prior to oxygenation of the atmosphere. Still, little is known about the arsenic cycling processes occurring in the presence of microorganisms and the possible traces that could be preserved in the rock record. To advance our understanding of this we studied the geochemical proxies of microbial As metabolism in living microbialites from Laguna Diamante, a likely Precambrian ecosystem analogue (Catamarca, Argentina). In this study, we show that the coexistence of As(III) and As(V) strongly…

Carbonate010504 meteorology & atmospheric sciencesSynchrotron-based X-ray imagingchemistry.chemical_element010502 geochemistry & geophysicsGeologic record01 natural sciencesEarly lifechemistry.chemical_compoundPrecambrian[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryANDES LAKESGeochemistry and PetrologyExtremophileEcosystemArsenic cyclingArsenic0105 earth and related environmental sciencesEXTREMOPHILEEcologyMicrobialitesOtras Ciencias Naturales y ExactasGeologyARCHEAEEarly Earthchemistry13. Climate actionCarbonateCalciumARSENICCyclingCIENCIAS NATURALES Y EXACTASGeologyChemical Geology
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Photoactivation of Anticancer Ru Complexes in Deep Tissue: How Deep Can We Go?

2017

Activation of anticancer therapeutics such as ruthenium (Ru) complexes is currently a topic of intense investigation. The success of phototherapy relies on photoactivation of therapeutics after the light passes through skin and tissue. In this paper, the photoactivation of anticancer Ru complexes with 671-nm red light through tissue of different thicknesses was studied. Four photoactivatable Ru complexes with different absorption wavelengths were synthesized. Two of them (Ru3 and Ru4) were responsive to wavelengths in the “therapeutic window” (650–900 nm) and could be activated using 671-nm red light after passing through tissue up to 16-mm-thick. The other two (Ru1 and Ru2) could not be ac…

Cell SurvivalInfrared Rayschemistry.chemical_elementAntineoplastic Agents02 engineering and technologyAbsorption (skin)010402 general chemistryPhotochemistry01 natural sciencesCatalysisRutheniumMETALLODRUGDeep tissueCoordination ComplexesHumansRed lightPHOTOTHERAPYTherapeutic windowChemistryPHOTOCHEMISTRYOtras Ciencias QuímicasOrganic ChemistryLight activatedCiencias QuímicasGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesRutheniumRU COMPLEXSpectrophotometryCancer cellANTICANCER0210 nano-technologyCIENCIAS NATURALES Y EXACTASHeLa Cells
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Overview of the JET results

2015

Since the installation of an ITER-like wall, the JET programme has focused on the consolidation of ITER design choices and the preparation for ITER operation, with a specific emphasis given to the bulk tungsten melt experiment, which has been crucial for the final decision on the material choice for the day-one tungsten divertor in ITER. Integrated scenarios have been progressed with the re-establishment of long-pulse, high-confinement H-modes by optimizing the magnetic configuration and the use of ICRH to avoid tungsten impurity accumulation. Stationary discharges with detached divertor conditions and small edge localized modes have been demonstrated by nitrogen seeding. The differences in…

Chemical analysiMagnetic confinementEdge localized modeTokamak:Física [Ciências exactas e naturais]Nuclear engineeringplasma-facing componentsTungsten7. Clean energyiter-like walllaw.inventionheat loadsAlcator C-ModlawPlasma-facing componentalcator C-MODQCPhysicsJet (fluid)Thermally activatedDivertormagnetic confinementMagnetic confinement fusionTokamak deviceerosionCondensed Matter PhysicsChemical erosionPost mortem analysiCondensed Matter Physics; Nuclear and High Energy PhysicsBerylliumAtomic physicstokamaksTokamaksNuclear and High Energy Physicschemistry.chemical_elementImpurity accumulationCondensed Matter PhysicNuclear and High Energy Physics; Condensed Matter PhysicsTungstenFísica Física:Physical sciences [Natural sciences]divertorNuclear fusionNuclear and High Energy PhysicPhysics Physical sciencesGas fuel analysifuel retentionSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)operationOrders of magnitudechemistryJETtransportMagnetic configuration
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Spatially limited diffusion coupled with ohmic potential drop and/or slow interfacial exchange: a new method to determine the diffusion time constant…

2004

Abstract We have analyzed chronoamperometric curves, I ( t ), after small-amplitude potential steps Δ E (PITT technique) for the model of linear diffusion of a species inside an electroactive film, taking into account ohmic effects in the external media (solution and electrode) as well as a finite rate of the interfacial exchange. For its short-time interval, t ≪ τ d ( τ d is the diffusion time constant, corresponding to unlimited diffusion from the interface), three approximate analytical expressions have been proposed. One of these represents an interpolation formula between the value of the current at the start of the diffusion process, I (0)=Δ E / R ext (after the end of the EDL chargin…

ChemistryGeneral Chemical EngineeringMathematical analysisTime constantAnalytical chemistryChronoamperometryAnalytical ChemistrySolution of Schrödinger equation for a step potentialExact solutions in general relativityDiffusion processElectrochemistryLimit (mathematics)Diffusion (business)Cottrell equationJournal of Electroanalytical Chemistry
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Structural Characterization and Magnetic Properties of the First 2,2‘-Bipyrimidine-Containing Iron(III) Complexes

1998

Two new iron(III) complexes of the formulas [Fe(bpm)Cl3(H2O)]·H2O (1) and [Fe2(bpm)Cl6(H2O)2]·2H2O (2) (bpm = 2,2‘-bipyrimidine) have been synthesized and their crystal structures determined by single-crystal X-ray diffraction. 1 and 2 crystallize in the monoclinic system, space group P21/n, with a = 8.593(2) A, b = 17.669(4) A, c = 8.928(2) A, β = 102.36(2)°, and Z = 4 for 1 and a = 6.422(3) A, b = 11.999(4) A, c = 12.297(6) A, β = 93.82(4)°, and Z = 2 for 2. The structure of complex 1 is made up of neutral [Fe(bpm)Cl3(H2O)] mononuclear units and water molecules of crystallization. The monuclear units are linked through hydrogen bonds involving the coordinated water molecule and one of the…

ChemistryHydrogen bondHexacoordinateCrystal structurelaw.inventionInorganic ChemistryMetalCrystallographyOctahedronlawvisual_artvisual_art.visual_art_mediumMoleculePhysical and Theoretical ChemistryCrystallizationMonoclinic crystal systemInorganic Chemistry
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Rational design of covalently bridged [FeIII2MIIO] clusters

2010

We are reporting the first supramolecular dimeric units of basic carboxylates. The neutral [FeIII 2MIIO] motif for different 3d M metals is covalently bound through 2,2′-bipyrimidine. We have structurally characterized the hexanuclear clusters and the related trinuclear building blocks. Their magnetic properties have been fully analyzed and DFT calculations have been performed as a supplementary tool. All results evidence a weak antiferromagnetic interaction through the bpym bridge between isolated spin ground states (in some examples) arising from intra-Fe 2MO core exchange couplings. Fil: Alborés, Pablo. Johannes Gutenberg Universitat Mainz; Alemania. Consejo Nacional de Investigaciones C…

ChemistryOtras Ciencias Químicasbasic carboxylateCiencias QuímicasRational designSupramolecular chemistrybipyrimidineInorganic Chemistrycovalently linkComputational chemistryCovalent bondAntiferromagnetismmagnetic propertiesSpin (physics)CIENCIAS NATURALES Y EXACTASDalton Transactions
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Organotin(IV) chloride complexes with phosphocholine and dimyristoyl-L-?-phosphatidylcholine

2000

Several complexes of R n SnCl 4-n (R = Me, Ph, n = 1-3; R = nBu, n = 2, 3) with phosphocholine and dimyristoyl-L-α-phosphatidylcholine (phospholipid) have been synthesized and characterized by means of Mossbauer spectroscopy and NMR. Triorganotin chlorides form complexes of (R 3 SnCl) 2 .L stoichiometry with a trigonal bipyramidal pentacoordinate tin environment, while the others form 1:1 complexes with an octahedral hexacoordinate tin environment, with the ligands coordinating through anionic phosphodiester moieties in all cases.

ChemistryStereochemistryHexacoordinatechemistry.chemical_elementGeneral ChemistryMedicinal chemistryChemical synthesisInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundOctahedronMössbauer spectroscopyPhosphodiester bondTinPhosphocholineApplied Organometallic Chemistry
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Tin(IV) complexes with O-ethyl(N-ethyl-N,N-dimethylammoniomethyl)phosphonate

1999

Abstract O,O-Diethyl-(N,N-dimethylaminomethyl)phosphonate undergoes ethyl migration leading to O-ethyl-(N-ethyl-N,N-dimethylammoniomethyl)phosphonate (L). Several new complexes of tin(IV) and organotin(IV) chlorides with the title ligand have been synthesized. The stoichiometry of the obtained complexes is as follows: (R3SnCl)2 · L (R=Me, Bu, Ph), R2SnCl2 · L (R=Me, Bu, Ph), RSnCl3 L (R=Me, Ph) and SnCl4 · L. All the complexes have been studied in solution by means of 1H-, 13C-, 31P- and 119Sn-NMR spectroscopy. Their solid state structures have been investigated by means of Mossbauer spectroscopy and the molecular structure of the complex (Ph3SnCl)2 · L has been determined by X-ray crystall…

ChemistryStereochemistryLigandOrganic ChemistryHexacoordinatechemistry.chemical_elementBridging ligandBiochemistryMedicinal chemistryPhosphonateInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometryOctahedronMaterials ChemistryMoleculePhysical and Theoretical ChemistryTin
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HCHs and DDTs in sediment-dwelling animals from the Yangtze Estuary, China

2005

HCHs and DDTs in sediment-dwelling animals including mollusks and crabs from the Yangtze Estuary were deter- mined by GC-ECD. Levels of t-HCH were in the range of 1.2-5.5 ng g � 1 and averaged 3.5 ng g � 1 in mollusks, while t-DDT concentrations ranged from 26.0 to 68.8 ng g � 1 , with a mean of 34.5 ng g � 1 . In crabs t-HCH concentrations var- ied from 2.0 to 25.7 ng g � 1 and averaged 13.8 ng g � 1 , whereas the concentrations of t-DDT were in the range of 1.5- 24.8 ng g � 1 with a mean value of 5.9 ng g � 1 . The HCHs and DDTs levels depend on geographical position and sources, showing the high levels at fresh water area in the estuary, such as XP, CM and LHK sites, and lower at brackis…

ChinaGeologic SedimentsEnvironmental EngineeringBrachyuraHealth Toxicology and MutagenesisDDTChineAnimalsEnvironmental ChemistryPersistent organic pollutantgeographygeography.geographical_feature_categorybiologyBrackish waterDecapodaEcologyPublic Health Environmental and Occupational HealthSedimentBiotaEstuaryGeneral MedicineGeneral Chemistrybiology.organism_classificationPollutionCrustaceanMolluscaEnvironmental chemistryHexachlorocyclohexaneWater Pollutants ChemicalEnvironmental MonitoringChemosphere
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