IP Library Granted Patent US 7,601,367
Granted Patent B2
US 7,601,367 · App. 10/845,968 · Granted Oct 13, 2009

Compositions and processes using siRNA, amphipathic compounds and polycations

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,601,367
App. No.
10/845,968
Granted
Oct 13, 2009
Kind
B2
Abstract

Described is a deliverable composition with low toxicity comprising an amphipathic compound, a polycation, and a siRNA. The composition may be used in the process of delivering a siRNA to an animal cell or more particularly, a mammal cell.

Claims (10)

1. A composition for delivery of siRNA to a mammalian cell comprising: said siRNA, a first amphipathic compound that is a cationic lipid, a second amphipathic compound that is a cationic lipid and a polycation, wherein the polycation is not a DNA-binding protein and is selected from the group consisting of: polyvinylamine, polyallylamine, polyethylenimine and ethoxylated polyethylenimine wherein said second amphipathic compound consists of an amphipathic compound having the structure:

wherein R1 and R2 are selected from the group consisting of a C6 to C24 alkane, C6-C24 alkene, mono-substituted alkyl silane, di-substituted alkyl silane, tri-substituted alkyl silane, cycloalkyl, sterol, steroid, substituted lipid, acyl segment of a fatty acid, hydrophobic hormone, and hydrophobic hormone analog.

2. The composition of claim 1 wherein said second amphipathic compound consists of an amphipathic compound having the structure:

3. A composition for delivery of siRNA to a mammalian cell comprising: said siRNA, a first amphipathic compound that is a cationic lipid, a second amphipathic compound that is a cationic lipid and a polycation, wherein the polycation is not a DNA-binding protein and is selected from the group consisting of: polyvinylamine, polyallylamine, polyethylenimine and ethoxylated polyethylenimine wherein said first amphipathic compound consists of an amphipathic compound having the structure:

and said second amphipathic compound consists of an amphipathic compound having the structure:

4. A kit for siRNA transfection comprising: a container containing a preparation comprising: a first amphipathic compound that is a cationic lipid, a second amphipathic compound that is a cationic lipid and a polycation wherein the polycation is not a DNA-binding protein and is selected from the group consisting of: polyvinylamine, polyallylamine, polyethylenimine and ethoxylated polyethylenimine, and instructions for an amount of the preparation and an amount of the siRNA to be admixed wherein said second amphipathic compound consists of an amphipathic compound having the structure:

wherein R1 and R2 are selected from the group consisting of a C6 to C24 alkane, C6-C24 alkene, mono-substituted alkyl silane, di-substituted alkyl silane, tri-substitued alkyl silane, cycloalkyl, sterol, steroid, substituted lipid, acyl segment of a fatty acid, hydrophobic hormone, and hydrophobic hormone analog.

5. The kit of claim 4 wherein said second amphipathic compound consists of an amphipathic compound having the structure:

6. A kit for siRNA transfection comprising: a container containing a preparation comprising: a first amphipathic compound that is a cationic lipid, a second amphipathic compound that is a cationic lipid and a polycation wherein the polycation is not a DNA-binding protein and is selected from the group consisting of: polyvinylamine, polyallylamine, polyethylenimine and ethoxylated polyethylenimine, and instructions for an amount of the preparation and an amount of the siRNA to be admixed wherein said first amphipathic compound consists of an amphipathic compound having the structure:

and said second amphipathic compound consists of an amphipathic compound having the structure: