In vivo polynucleotide delivery conjugates having enzyme sensitive linkages
View Patent ↗The present invention is directed compositions for delivery of RNA interference (RNAi) polynucleotides to cells in vivo. The compositions comprise amphipathic membrane active polyamines reversibly modified with enzyme cleavable dipeptide-amidobenzyl-carbonate masking agents. Modification masks membrane activity of the polymer while reversibility provides physiological responsiveness. The reversibly modified polyamines (dynamic polyconjugate or DPC) are further covalently linked to an RNAi polynucleotide or co-administered with a targeted RNAi polynucleotide-targeting molecule conjugate.
1. A compound for reversibly modifying an amphipathic membrane active polyamine comprising: a targeting ligand covalently linked to a dipeptide-amidobenzyl-carbonate having the structure represented by:
wherein
X is —NH—,
Y is —NH—,
R1 is —CH 3 ,
R2 is —(CH 2 ) 3 —NH—C(o)—NH 2 ,
R4 is uncharged and comprises a targeting ligand,
R5 is at position 2, 4, or 6 and is —CH 2 —O—C(O)—Z wherein Z is
and
R6 is hydrogen.
2. The compound of claim 1 wherein the targeting ligand comprises an asialoglycoprotein receptor (ASGPr) ligand.
3. The compound of claim 2 wherein the ASGPr ligand is selected from the list consisting of: lactose, galactose, N-acetylgalactosamine, galactosamine, N-formylgalactosamine, N-propionylgalactosamine, N-n-butanoylgalactosamine, and N-iso-butanoyl-galactosamine.
4. The compound of claim 1 wherein Z is
5. A delivery polymer for delivering an RNA interference (RNAi) polynucleotide to a cell in vivo comprising:
M 1 y -P-M 2 z
wherein:
P is an amphipathic membrane active polyamine,
M 1 is a targeting ligand linked to P via a dipeptide-amidobenzyl-carbamate linkage,
M 2 is a steric stabilizer linked to P via a dipeptide-amidobenzyl-carbamate linkage,
y and z are each integers greater than or equal to zero,
y+z has a value greater than 50% of the primary amines on polyamine P as determined by the quantity of amines on P in the absence of any masking agents, and
the dipeptide-amidobenzyl-carbamate linkage has the structure represented by:
wherein
X is —NH—, —O—, or —CH 2 —
Y is —NH— or —O—
R1 is —CH 2 — phenyl, —CH—(CH 3 ) 2 , —CH 2 —CH—(CH 3 ) 2 , —CH(CH 3 )—CH 2 —CH 3 , —CH 3 ,
R2 is hydrogen, —(CH 2 ) 3 —NH—C(O)—NH 2 , —(CH 2 ) 4 —N—(CH 3 ) 2 , or —CH 2 —C(O)—NH 2 ,
R4 comprises the targeting ligand of M 1 or the steric stabilizer of M 2 , and polyamine is the amphipathic membrane active polyamine.
6. The delivery polymer of claim 5 wherein the steric stabilizer is a polyethylene glycol (PEG).
7. The delivery polymer of 5 wherein the targeting ligand comprises an ASGPr ligand.
8. The delivery polymer of claim 7 wherein the ASGPr ligand is selected from the list consisting of: lactose, galactose, N-acetylgalactosamine, galactosamine, N-formylgalactosamine, N-propionylgalactosamine, N-n-butanoylgalactosamine, and N-iso-butanoyl-galactosamine.
9. The delivery polymer of claim 5 wherein the amphipathic membrane active polyamine is selected from the list consisting of: random, block, or alternating synthetic polymer.
10. The delivery polymer of claim 5 wherein the amphipathic membrane active polyamine is a melittin peptide.
11. The delivery polymer of claim 5 wherein the amphipathic membrane active polyamine is further covalently linked to the RNAi polynucleotide.
12. A method for delivering an RNAi polynucleotide to a cell in a mammal in vivo comprising: co-administering the RNAi polynucleotide with the delivery polymer of claim 5 to the mammal.
13. The method of claim 12 wherein the RNAi-polynucleotide is covalently linked to the delivery polymer.
14. The method of claim 12 wherein the cell is a hepatocyte or a hepatic cancer cell.