Linking the physical and chemical characteristics of Qdots to their toxicity
Linking the physical and chemical characteristics of Qdots to their toxicity
批准号:
8332607
负责人:
Terrance J Kavanagh
金额:
$6.6万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-24 至 2012-04-30
关键词:
A/J MouseAirApoptosisArsenicBenignBioinformaticsBiologicalBiological MarkersBiologyBreathingCadmiumCarbonCarbon NanotubesCell Culture SystemCell LineCell SurvivalCell modelCellsCharacteristicsChargeChemicalsChromosome MappingComplementary DNAComputer softwareConceptusCustomDataDevelopmentDoseElementsEmbryoEndothelial CellsEngineeringEnvironmentEnvironmental ExposureEpigenetic ProcessEpithelialEpithelial CellsEpitheliumExcretory functionExposure toFemaleFluorescent DyesGene ExpressionGenetic PolymorphismGenomicsGoalsGoldHealthHeartHeavy MetalsHepatocyteHistopathologyHumanHydrophobicityHypersensitivityIn VitroInbred MouseInbred Strains MiceInflammatoryKidneyLeadLinkLiquid substanceLiverLungMapsMaterials TestingMeasuresMercuryMetabolismMethodsMitochondriaModelingMusNanosphereNanotubesNational Institute of Environmental Health SciencesNatureNecrosisOccupationalOxidation-ReductionOxidative StressPathway AnalysisPathway interactionsPhasePoisonProteinsQuantum DotsRequest for ApplicationsResearchRiskRisk AssessmentSeleniumSemiconductorsShapesSignal PathwaySignal TransductionSilverSiteSmall Interfering RNASpleenSplenocyteSports EquipmentStressStructureSunscreening AgentsSurfaceSurface PropertiesSystemTechniquesTelluriumTestingTestis BrainThymus GlandTissuesToxic effectToxicologyTransfectionTubular formationVascular Endothelial CellWound Healingabsorptionaerosolizedbasecell typeceric oxidechemical propertycytokinecytotoxicitydesignepigenomicsgenetic technologyhuman tissueimaging modalityin vivoin vivo Modelinsightinterestiron oxidekidney epithelial celllymph nodesmacrophagemalemembermetal oxidenanoGoldnanocrystalnanofibernanomaterialsnanoparticlenanoparticulatenanorodnanosilveroptical imagingparticlephysical propertypredictive modelingpregnantprogramsresistant strainresponsesertoli celltitanium dioxideuptake
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Engineered nanomaterials are being used or are being proposed for use in a large number of commercial products. Because of their highly diverse physical and chemical characteristics, and their small size, concerns have been raised regarding their potential to cause harm to human health or the environment. One important class of ENMs are quantum dots (Qdots) which are luminescent semiconductor nanocrystals composed of heavy metal cores (e.g. CdSe, CdTe, HgTe) with cap and coating structures that vary greatly, depending upon the characteristics required for various applications. Certain characteristics are known to be determinants for the interaction of nanoparticles with cells and tissues, including shape, size, hydrophobicity, and surface charge. Because of the highly variable nature of these and other engineered nanomaterials, it will be nonetheless difficult to predict their toxicity. Modern advances in genomics, epigenetics and bioinformatics, and the availability of multiple strains of inbred mice with well characterized polymorphisms and regulatory sequences have made it possible to map and predict toxicity pathways for many toxic substances including nanomaterials. The research proposed herein will utilize in vitro and in vivo models of airway exposure to aerosolized quantum dot nanoparticles to 1) define the physical and chemical characteristics that govern their absorption, distribution, metabolism, excretion and toxicity; 2) using multiple inbred strains of mice, map toxicity pathways associated with these characteristics; and 3) incorporate the information that is obtained from these in vitro and in vivo models into a risk assessment paradigm that will be used to predict nanomaterial toxicity to humans. Such information will not only define which physical and chemical characteristics are important for the adverse biological effects of quantum dots, but will also simultaneously advance the fields of nanomaterial toxicology and functional epigenomics. These advances can then be used in safe design and manufacturing of nanomaterials so as to maximize their utility for many applications.
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Pilot Project Program
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批准号:8830359
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项目类别:
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资助金额:$20.27万
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依托单位:
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依托单位:
Core 2: Administration Core
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批准号:8274473
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资助金额:$6.86万
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依托单位:
Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8464705
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项目类别:
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财政年份:2010
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负责人:Terrance J Kavanagh
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依托单位:
Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8675245
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项目类别:
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资助金额:$104.74万
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Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8258515
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项目类别:
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资助金额:$3.01万
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财政年份:2010
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负责人:Terrance J Kavanagh
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依托单位:
Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8016872
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项目类别:
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负责人:Terrance J Kavanagh
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依托单位:
Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8274474
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项目类别:
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资助金额:$109.01万
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财政年份:2010
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依托单位:
Core 2: Administration Core
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批准号:8066922
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项目类别:
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资助金额:$3.5万
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财政年份:2010
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负责人:Terrance J Kavanagh
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依托单位:
Project 2: In vivo Studies: Characterize absorption, distribution, metabolism, el
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批准号:8066918
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Linking the physical and chemical characteristics of Qdots to their toxicity
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批准号:8147704
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财政年份:2007
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依托单位:
Modulation of Qdot nanoparticle toxicity by glutathione in GCL transgenic mice
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批准号:7626716
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项目类别:
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资助金额:$47.15万
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财政年份:2007
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依托单位:
Modulation of Qdot nanoparticle toxicity by glutathione in GCL transgenic mice
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批准号:7497474
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资助金额:$45.83万
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财政年份:2007
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依托单位:
CORE--Analytical Cytology Laboratory
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批准号:6880487
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项目类别:
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资助金额:$9.66万
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财政年份:2005
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依托单位:
CORE--RESEARCH DEVELOPMENT
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批准号:6948125
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项目类别:
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资助金额:$7.08万
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财政年份:2005
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依托单位:
CORE--TRAINING
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批准号:6613360
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资助金额:$22.2万
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财政年份:2002
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依托单位:
CORE--TRAINING
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资助金额:$22.2万
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财政年份:2002
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Glutamate-L-cysteine ligase expression and liver injury
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依托单位:
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