IP Library › Granted Patent US 9,433,681
Granted Patent B2
US 9,433,681 · App. 14/178,538 · Granted Sep 6, 2016

Lipids and compositions for intracellular delivery of biologically active compounds

Inventors: Rainer Constien (Kulmbach, DE); Anke Geick (Bayreuth, DE); Philipp Hadwiger (Kulmbach, DE); Torsten Haneke (Kulmbach, DE); Ludger Markus Ickenstein (Kulmbach, DE); Carla Alexandra Hernandez Prata (Kulmbach, DE); Andrea Schuster (Bayreuth, DE); Timo Weide (Kulmbach, DE)
Assignee: AXOLABS GMBH
A61K47/18A61K9/1271A61K9/145A61K31/575A61K31/70A61K31/7088A61K31/713A61K38/02A61K39/00A61K47/22B82Y5/00C07C211/11C07C211/13C07C211/14C07C211/22C07C217/08C07C217/28C07C217/42C07D241/04C07D295/30
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Quick Facts
Patent No.
US 9,433,681
App. No.
14/178,538
Granted
Sep 6, 2016
Kind
B2
Abstract

The present invention provides novel amino-lipids, compositions comprising such amino-lipids and methods of producing them. In addition, lipid nanoparticles comprising the novel amino-lipids and a biologically active compound are provided, as well as methods of production and their use for intracellular drug delivery.

Claims (21)

1. A cyclic amino-lipid of the formula:

2. A lipid nanoparticle comprising a cyclic amino-lipid of claim 1 .

3. The lipid nanoparticle of claim 2 , further comprising an additional lipid selected from the group consisting of: cationic lipid, helper lipid, and PEG-lipid.

4. The lipid nanoparticle of claim 2 , further comprising a hydrophobic small molecule.

5. The lipid nanoparticle of claim 2 , further comprising a biologically active compound.

6. The lipid nanoparticle of claim 5 , wherein the biologically active compound is selected from the group consisting of: a small molecule, a peptide, a protein, a carbohydrate, a nucleic acid; and a lipid.

7. The lipid nanoparticle of claim 3 , wherein the cationic lipid is a lipid comprising a quaternary amine with a nitrogen atom having four organic substituents.

8. The lipid nanoparticle of claim 3 , wherein the helper lipid is a neutral zwitterionic lipid.

9. The lipid nanoparticle of claim 4 , wherein the hydrophobic small molecule is selected from the group consisting of a sterol and a hydrophobic vitamin.

10. The lipid nanoparticle of claim 9 , wherein the hydrophobic small molecule is cholesterol.

11. The lipid nanoparticle of claim 7 , wherein the protein is selected from the group consisting of a nucleoprotein, a mucoprotein, a lipoprotein, a synthetic polypeptide, a small molecule linked to a protein, and a glycoprotein.

12. The lipid nanoparticle of claim 6 , wherein the nucleic acid is in the form of a single stranded or partially double stranded oligomer or a polymer composed of ribonucleotides.

13. The lipid nanoparticle of claim 6 , wherein the nucleic acid is selected from the group consisting of an miRNA, an antisense oligonucleotide, an siRNA, an immune-stimulatory oligonucleotide, an aptamer, a ribozyme, and a plasmid encoding a specific gene or siRNA.

14. A pharmaceutical composition comprising a cyclic amino-lipid according to claim 1 .

15. A pharmaceutical composition comprising a lipid nanoparticle according to claim 2 .

16. The pharmaceutical composition of claim 15 , further comprising a biologically active compound.

17. The pharmaceutical composition of claim 16 , wherein the biologically active compound is a nucleic acid.

18. The pharmaceutical composition of claim 17 , wherein the nucleic acid is in the form of a single stranded or partially double stranded oligomer or a polymer composed of ribonucleotides.

19. A method of treating a disease that is caused by the over-expression of one or several proteins in a subject, said method comprising the administration of a lipid nanoparticle according to claim 5 to the subject, wherein the biologically active compound is a nucleic acid, and wherein treatment refers to alleviation of symptoms, decreasing the rate of disease progression, amelioration or palliation of the disease state, remission or improved prognosis, or slowing the progression of the disease.

20. A method of treating a disease that is caused by a reduced, suppressed or missing expression of one or several proteins in a subject, said method comprising administration of a lipid nanoparticle according to claim 5 to the subject, wherein the biologically active compound is a nucleic acid, and wherein treatment refers to alleviation of symptoms, decreasing the rate of disease progression, amelioration or palliation of the disease state, remission or improved prognosis, or slowing the progression of the disease.

21. A method for generating an immune response in a subject, said method comprising the administration of a lipid nanoparticle according to claim 5 to the subject, wherein the biologically active compound is an immune-stimulatory nucleic acid.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2014
From: CONSTIEN, RAINER; GEICK, ANKE; HADWIGER, PHILIPP; HANEKE, TORSTEN; ICKENSTEIN, LUDGER MARKUS; HERNANDEZ PRATA, CARLA ALEXANDRA; SCHUSTER, ANDREA; WEIDE, TIMO
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 032902/0113 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2014
From: F. HOFFMANN-LA ROCHE LTD
To: ARROWHEAD RESEARCH CORPORATION
Reel/Frame 032902/0188 →
CERTIFICATE Recorded May 15, 2014
From: F. HOFFMANN-LA ROCHE AG
To: F. HOFFMANN-LA ROCHE LTD
Reel/Frame 032902/0227 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2014
From: ARROWHEAD RESEARCH CORPORATION
To: AXOLABS GMBH
Reel/Frame 032902/0291 →
Priority Claims (1)
EP 11166353 · May 17, 2011 · regional
Continuity (2)
Division 13466640 · May 8, 2012
Related Publication 20140162962A1 · Jun 12, 2014