IP Library Granted Patent US 9,526,693
Granted Patent B2
US 9,526,693 · App. 13/049,825 · Granted Dec 27, 2016

Delivery of agents using interfering nanoparticles

Inventor: Tariq M. Rana (San Diego, CA)
Assignee: Sanford-Burnham Medical Research Inslilute
A61K9/0019A61K47/48038A61K47/48092A61K47/48323C12N15/87C12N2810/10
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Quick Facts
Patent No.
US 9,526,693
App. No.
13/049,825
Granted
Dec 27, 2016
Kind
B2
Abstract

Provided are compositions and methods for delivery of therapeutic agents, such as chemically stabilized antisense oligonucleotides useful in RNA silencing. The compositions include interfering nanoparticles (iNOPs) associated with one or more agents. Several functional iNOP derivatives are provided which allow for targeted delivery of agents to specific cell types as well as exhibiting reduced cellular toxicity.

Claims (14)

1. A composition comprising a nanotransporter interfering nanoparticle-7 (iNOP-7) having a polylysine dendrimer generation 4 (LDG4) core conjugated to a lipid functional group having the following structure:

wherein the iNOP-7 is functionalized with any of functional surface groups A-I by being conjugated to iNOP-7 through an amide bond formed via an NH 2 group of the iNOP7:

wherein A forms iNOP-7E; B foul's iNOP-7LE; C foul's iNOP-7DS; D forms iNOP-7His; E-forms iNOP-7Bio; F forms iNOP-7AD; G forms iNOP-7PEG; H forms iNOP-7A; and I forms iNOP-7Lac.

2. The composition of claim 1 , wherein the iNOP-7 is associated with a nucleic acid molecule or pharmaceutical agent.

3. The composition of claim 2 , wherein the iNOP-7 is associated with a nucleic acid molecule.

4. The composition of claim 3 , wherein the nucleic acid molecule is an antisense oligonucleotide.

5. The composition of claim 4 , wherein the antisense oligonucleotide is RNA.

6. The composition of claim 5 , wherein the RNA is chemically modified.

7. The composition of claim 6 , wherein the chemical modification comprises a 2′-O—F, 2′-Ome, 2′MOE, 2′-H, 2′-amino, 4-thioU or 6-thioG modification of one or more nucleotides, introduction of one or more phosphorothioate linkages, introduction of one or more locked nucleotides, or a combination thereof.

8. The composition of claim 5 , wherein the RNA is selected from the group consisting of microRNA mimic, anti-microRNA, dsRNA, siRNA, stRNA, or shRNA.

9. The composition of claim 8 , wherein the RNA is anti-microRNA, microRNA mimic, dsRNA or siRNA.

10. The composition of claim 9 , wherein an antisense strand, a sense strand, or both, of the RNA is chemically modified.

11. The composition of claim 10 , wherein the chemical modification comprises a 2′-O—F, 2′-Ome, 2′MOE, 2′-H, 2′-amino, 4-thioU or 6-thioG modification of one or more nucleotides, introduction of one or more phosphorothioate linkages, introduction of one or more locked nucleotides, or a combination thereof.

12. The composition of claim 5 , wherein the antisense oligonucleotide is about 7-36 nucleotides in length.

Assignments (2)
CHANGE OF NAME Recorded Jan 8, 2020
From: SANFORD-BURNHAM MEDICAL RESEARCH INSTITUTE
To: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
Reel/Frame 051514/0969 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2011
From: RANA, TARIQ M.
To: SANFORD-BURNHAM MEDICAL RESEARCH INSTITUTE
Reel/Frame 026335/0552 →
Continuity (2)
Provisional Application 61314500 · Mar 16, 2010
Related Publication 20110263514A1 · Oct 27, 2011