Amphoteric liposomes
View Patent ↗A serum-stable mixture of lipids capable of encapsulating an active agent to form a liposome, said mixture comprising phosphatidylcholine and phosphatidylethanolamine in a ratio in the range of about 0.5 to about 8. The mixture may also include pH sensitive anionic and cationic amphiphiles, such that the mixture is amphoteric, being negatively charged or neutral at pH 7.4 and positively charged at pH 4. Amphoteric liposomes comprising such a mixture may be used for encapsulating nucleic acid therapeutics, such as oligonucleotides and DNA plasmids. The drug/lipid ratio may be adjusted to target the liposomes to particular organs or other sites in the body.
1. An amphoteric liposome comprising POPC, DOPE, MoChol, and CHEMS, wherein MoChol and CHEMS combined comprise 50 to 80 mol % of the amphoteric liposome, wherein POPC and DOPE combined comprise 20 to 50 mol % of the amphoteric liposome, wherein POPC, DOPE, MoChol, and CHEMS combined comprise substantially 100 mol % of the amphoteric liposome, wherein the ratio of DOPE to POPC is from 0.5 to 8, and wherein the MoChol is in excess over the CHEMS.
2. The amphoteric liposome of claim 1 , wherein the ratio of CHEMS to MoChol is from 0.3 to 0.75.
3. The amphoteric liposome of claim 1 , wherein the amphoteric liposome consists of formulation POPC/DOPE/MoChol/CHEMS 6:24:47:23 (mol. %).
4. The amphoteric liposome of claim 1 , wherein the amphoteric liposome consists of formulation POPC/DOPE/MoChol/CHEMS 6:24:53:17 (mol. %).
5. The amphoteric liposome of claim 1 , wherein the amphoteric liposome has a size of from 50 to 500 nm.
6. The amphoteric liposome of claim 1 , wherein the amphoteric liposome encapsulates at least one active agent.
7. The amphoteric liposome of claim 6 , wherein the active agent comprises a nucleic acid.
8. The amphoteric liposome of claim 6 , wherein the active agent is a circular DNA plasmid, a linear DNA construct, an antisense oligonucleotide, a decoy oligonucleotide, an agent influencing transcription, an agent influencing splicing, a ribozyme, a DNAzyme, or an aptamer.
9. The amphoteric liposome of claim 6 , wherein the active agent is a decoy oligonucleotide.
10. The amphoteric liposome of claim 6 , wherein the active agent is an RNA, an siRNA, an mRNA, an shRNA, or an miRNA.
11. The amphoteric liposome of claim 6 , wherein the active agent comprises one or more modified nucleosides selected from locked nucleic acids (LNA), peptide nucleic acids (PNA), 2′O-methyl RNA (2′Ome), or 2′O-methoxyethyl RNA (2′MOE) in their phosphate or phosphothioate forms.
12. The amphoteric liposome of claim 6 , wherein the active agent modulates expression of CD40 in mammalian cells.
13. A pharmaceutical composition comprising an effective amount of the active agent-loaded amphoteric liposome of claim 6 .
14. A method for treating an inflammatory, immune, or autoimmune disorder in a human in need thereof, the method comprising administering to the human a pharmaceutical composition according to claim 13 .
15. The method of claim 14 , wherein the pharmaceutical composition is administered systemically, topically or locally.