Multifunctional Nanoassemblies for Ligand-directed Imaging and Therapy of Endocri
Multifunctional Nanoassemblies for Ligand-directed Imaging and Therapy of Endocri
批准号:
7983100
负责人:
WADIH ARAP
金额:
$30.65万
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:
2010-09-01 至 2015-07-31
关键词:
AddressAdenocarcinomaAdhesionsArchivesAreaBacteriophagesBlood VesselsCancer BiologyChemicalsClinicalCollaborationsComputer SimulationDetectionDevelopmentDiseaseDrug CarriersEarly DiagnosisEndocrineEngineeringGenerationsGoldHeatingHomingHumanImageImmunohistochemistryInfrared RaysIslet Cell TumorLigandsLiposomesMalignant NeoplasmsMalignant neoplasm of ovaryMethodsModalityMolecularNanotechnologyOutputOvarianPancreasPeptide LibraryPhage DisplayPharmacologic SubstancePropertyRaman Spectrum AnalysisRelative (related person)SamplingScienceScreening procedureServicesShapesSignal TransductionSiliconSpecificityStreptozocinSurfaceSurface PropertiesSystemTherapeuticTherapeutic AgentsTherapeutic EffectThermal Ablation TherapyTissuesTracerTransgenic MiceTranslatingVascular EndotheliumX-Ray Computed Tomographyangiogenesisbasebiomathematicschemotherapycombinatorialdensitydesignhormone therapyhuman diseaseimaging probein vivomathematical modelmolecular imagingmouse modelnanonanoassemblynanoengineeringnanoparticlenoveloncologyovarian neoplasmpancreatic neoplasmparticlephysical propertyreceptorreceptor expressionresponsescaffoldselective expressionsimulationtargeted deliverytooltool developmenttumorvascular bed
中文摘要
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英文摘要
PROJECT TITLE: Multifunctional Nanoassemblies for Ligand-Directed Imaging and Therapy of Endocrine Pancreatic Tumors
PROJECT SUMMARY: The development of tools for the targeted delivery of Imaging-probes and therapeufic agents has become the focus of intense efforts in the context of many human diseases. The in vivo screening method in which phage can be selected from engineered combinatorial peptide libraries for their ability to target specific vascular beds has uncovered a vascular address system that allows specific angiogenesis-related targeting to blood vessels in cancer. This phage display-based targeting Is expanded by the direct-assembly of gold and nanoporous silicon nanoparticles onto phage for nanomedical applications. Through exploiting the nanodimensions of the phage particle as a molecular network we generated biologically active nanoassemblies (NAs) with concomitant unique and tunable chemical and physical properties. These properties include near-infrared (NIR) radiation conversion to heat, enhancement of fluorescent signals, NIR surface enhanced Raman scattering (SERS) and the ability to conjugate and incorporate therapies or imaging-tracers. This tuning capability combined with the programmable tissue targefing affords the Integrafion of multiple funcfionalities into a single NA and serves as a complementary and non-mutually exclusive tool among different applicafions, including chemotherapy targeting and molecular imaging. Project 4 aims to develop the ligand-directed Si particles- phage- Au particles NAs as novel systems for targeted imaging and therapy in endocrine pancreatic tumors. These efforts will be
translated into wide-ranging clinical applicafions
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