Phosphane Functionalized Diblock Copolymers for Targeted siRNA Delivery
Phosphane Functionalized Diblock Copolymers for Targeted siRNA Delivery
批准号:
7326230
负责人:
Patrick E Guire
金额:
$9.99万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-25 至 2009-09-24
关键词:
AdsorptionAnimal ModelCaliberCancer ModelCellsChargeComplexConditionDoseDown-RegulationElectrostaticsEpoxy CompoundsEvaluationFolic AcidGene ExpressionGene SilencingGoalsGovernmentLaboratoriesLengthLigandsLigationMalignant neoplasm of ovaryMammalian CellMethodologyMolecular WeightPersonsPharmaceutical PreparationsPhasePolymersPurposeRNARNA InterferenceReagentResearchSafetySmall Business Funding MechanismsSmall Business Innovation Research GrantSmall Interfering RNASurfaceSystemTechniquesTechnologyTherapeuticToxic effectViralWorkbasecytotoxicitydesigndesiredi-block copolymerdrug discoveryfunctional genomicsfunctional groupinnovationnanoparticlenovelphosphinepolycationpolymerizationsurvivintrafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This SBIR project is designed to develop a new non-viral carrier for target-specific delivery of small interfering RNA (siRNA). One of the major challenges in transforming siRNA from laboratory reagents to therapeutics is developing a target-specific delivery system to introduce siRNAs into target cells. Maximal therapeutic benefit with decrease in the required drug dose and avoidance of nonspecific silencing and toxicity in nontarget cells could thereby be achieved. This proposal describes a new diblock copolymer with a positively charged block to complex with siRNA, a poly(ethyleneoxide) block for protection against non-specific adsorption, and a phosphane group on the PEG end for targeting ligand conjugation through Staudinger ligation. The Phase II work is expected to investigate the safety and efficacy of this novel siRNA delivery system in an animal model for therapeutic application. Specific aims of this Phase I proposal include: 1) optimize the synthesis of special diblock copolymers; 2) conjugate targeting ligands to diblock copolymers; 3) develop the methodology for preparing siRNA/polymer nanoparticles; 4) evaluate cytotoxicity of the new siRNA delivery system; 5) demonstrate inhibition of gene expression; and 6) investigate intracellular trafficking.
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