Aminoalcohol lipidoids and uses thereof
Aminoalcohol lipidoids are prepared by reacting an amine with an epoxide-terminated compound are described. Methods of preparing aminoalcohol lipidoids from commercially available starting materials are also provided. Aminoalcohol lipidoids may be prepared from racemic or stereochemically pure epoxides. Aminoalcohol lipidoids or salts forms thereof are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the amino moiety of these aminoalcohol lipidoid compounds, they are particularly suited for the delivery of polynucleotides. Complexes, micelles, liposomes or particles containing the inventive lipidoids and polynucleotide have been prepared. The inventive lipidoids may also be used in preparing microparticles for drug delivery. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings.
1. A compound of formula:
wherein:
each occurrence of R A is independently unsubstituted, cyclic or acyclic, branched or unbranched C 1-20 aliphatic; substituted or unsubstituted, cyclic or acyclic, branched or unbranched C 1-20 heteroaliphatic; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl;
wherein at least one R A is
each occurrence of R 5 is independently unsubstituted, cyclic or acyclic, branched or unbranched C 8-16 aliphatic; substituted or unsubstituted aryl; or substituted or unsubstituted heteroaryl;
each occurrence of x is an integer between 1 and 10, inclusive;
each occurrence of y is an integer between 1 and 10, inclusive;
or a pharmaceutically acceptable salt thereof.
2. A pharmaceutical composition comprising a compound of claim 1 ; and a pharmaceutical agent.
3. The pharmaceutical composition of claim 2 , wherein the pharmaceutical agent is selected from the groups consisting of polynucleotides, proteins, peptides, and small molecule drugs.
4. The compound of claim 1 , wherein each
5. The compound of claim 1 , wherein each
6. The compound of claim 1 , wherein each occurrence of R A is independently
7. The compound of claim 1 , wherein each occurrence of R 5 is C 8 -C 16 alkyl.
8. The compound of claim 1 , wherein each occurrence of x is 1.
9. The compound of claim 1 , wherein each occurrence of x is 2.
10. The compound of claim 1 , wherein y is 1.
11. The compound of claim 1 , wherein y is 2.
12. The compound of claim 1 , wherein at least one R A is selected from the group consisting of unsubstituted, cyclic and acyclic, branched and unbranched C 1-20 alkenyl; unsubstituted, cyclic and acyclic, branched and unbranched C 1-20 alkynyl; and substituted and unsubstituted, cyclic and acyclic, branched and unbranched C 1-20 heteroaliphatic.
13. The compound of claim 1 , wherein two R A variables are the same.
14. The compound of claim 1 , wherein each R A variable is different from the other.
15. The pharmaceutical composition of claim 3 , wherein the pharmaceutical agent is a polynucleotide.
16. The pharmaceutical composition of claim 15 , wherein the polynucleotide is DNA.
17. The pharmaceutical composition of claim 15 , wherein the polynucleotide is RNA.
18. The pharmaceutical composition of claim 15 , wherein the polynucleotide is dsRNA, siRNA, shRNA, miRNA, or antisense RNA.
19. The pharmaceutical composition of claim 15 , wherein the polynucleotide encodes a protein or peptide.