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filingDate 2012-09-05^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fde624ff192bc9618bacf4c180af883
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f4cf891e2888cc368f0b990d11516d0
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publicationDate 2013-03-14^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2013036532-A1
titleOfInvention Amphipathic co-oligomers for the delivery of sirna
abstract Co-oligomer compounds, complexes of the same with polyanions, such as siRNAs, and methods for using the same are provided. the delivery of polynucleotides, into a cell. The subject co-oligomers include at least a liphopilic monomer and at least a hydrophilic monomer (e.g., a guanidinium containing monomer). In some embodiments, the co-oligomer compounds are capable of complexing a siRNA of interest, thereby increasing the cell permeability of the siRNA, prior to release of the siRNA into the cell. In some embodiments, the subject method is a method of delivery a siRNA into a cell. In some embodiments, the subject method is a method of reducing expression of a protein target of a siRNA of interest. The subject co-oligomer / siRNA complexes may be formulated and administered to a subject to treat a condition resulting from expression of a protein target of the siRNA of interest.
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