Amphipathic Co-Oligomers for the Delivery of SIRNA
AssigneeThe Board of Trustees of the Leland Stanford Junio University
InventorsChristina Barnes Cooley, Erika Geihe Stanzl, Robert M. Waymouth, Paul Wender
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AssigneeThe Board of Trustees of the Leland Stanford Junio University
InventorsChristina Barnes Cooley, Erika Geihe Stanzl, Robert M. Waymouth, Paul Wender
Estimating the term…
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.
A composition comprising:
A method for intracellular delivery of a siRNA to a cell, the method comprising:
Dependencies are inferred from the claim text.