Liposome composition for improved intracellular delivery of a therapeutic agent
A liposomal composition and a method of using the same for achieving intracellular delivery of a liposome-entrapped agent is described. The liposomes are composed of a pH sensitive lipid and include a targeting ligand to direct the liposomes to a target cell. The liposomes also include a stabilizing component, such a polymer-derivatized lipid, where the polymer is attached to the lipid by a releasable linkage. Administration of the liposomes results in cellular internalization and destabilization of the liposome for intracellular delivery of the entrapped agent.
1. A liposome composition for intracellular delivery of a therapeutic agent, comprising
liposomes consisting essentially of (i) a pH-sensitive lipid; (ii) between 1–20 mole percent of a lipid derivatized with a hydrophilic polymer, said polymer attached to said lipid by a bond effective to release the hydrophilic polymer in response to an existing or an induced physiologic condition; (iii) a targeting ligand; and (iv) an entrapped therapeutic agent;
wherein said composition is adapted to bind to a target cell and to release said entrapped agent to achieve at least a two-fold increase in intracellular concentration of the agent, when compared to intracellular concentration of the agent delivered by similar liposomes lacking said releasable bond and/or said targeting ligand wherein, said releasable bond is a dithiobenzyl bond.
2. The composition of claim 1 , wherein said pH-sensitive lipid is dioleoylphosphatidylethanolmaine (DOPE).
3. The composition of claim 1 , wherein said liposomes further include a stabilizing component.
4. The composition of claim 3 , wherein said stabilizing component is cholesteryl hemisuccinate (CHEMS).
5. The composition of claim 1 , wherein said lipid derivatized polymer is phosphatidylethanolamine derivatized with polyethyleneglycol.
6. The composition of claim 1 , wherein said targeting ligand an antibody or an antibody fragment.
7. The composition of claim 6 , wherein said antibody fragment is selected from the group consisting of anti-CD19, anti-CD20, anti-CD22.
8. A method for increasing intracellular cytotoxicity of a liposome-entrapped agent, comprising
providing liposomes consisting essentially of (i) a pH-sensitive lipid; (ii) between 1–20 mole percent of a lipid derivatized with a hydrophilic polymer, said polymer attached to said lipid by a bond effective to release the hydrophilic polymer in response to an existing or an induced physiologic condition; (iii) a targeting ligand; and (iv) an entrapped therapeutic agent;
administering said liposomes to achieve (i) cleavage of the releasable bond, thereby releasing said hydrophilic polymer chain; (ii) binding of said ligand to a target cell, where said binding occurs prior to or subsequent to said cleavage; and (iii) internalization of said liposome by said target cell;
whereby said administering is effective to achieve at least a two-fold higher intracellular cytotoxicity of said agent, relative to intracellular concentration of the agent delivered by similar liposomes lacking said releasable bond and/or said targeting ligand wherein, said releasable bond is a dithiobenzyl bond.
9. The method of claim 8 , wherein cleavage of said releasable bond after said administering is achieved by naturally-occurring blood components.
10. The method of claim 8 , wherein said pH-sensitive lipid is dioleoylphosphatidylethanolmaine (DOPE).
11. The method of claim 8 , wherein said liposomes further include a stabilizing component.
12. The method of claim 11 , wherein said stabilizing component is cholesteryl hemisuccinate (CHEMS).
13. The method of claim 8 , wherein said lipid derivatized polymer is phosphatidylethanolamine derivatized with polyethyleneglycol.
14. The method of claim 8 , wherein said targeting ligand an antibody or an antibody fragment.
15. The method of claim 14 , wherein said antibody fragment is selected from the group consisting of anti-CD19, anti-CD20, anti-CD22.
16. A method for increasing accumulation of a therapeutic agent into cellular nuclei, comprising
providing liposomes consisting essentially of (i) a pH-sensitive lipid; (ii) between 1–20 mole percent of a lipid derivatized with a hydrophilic polymer, said polymer attached to said lipid by a bond effective to release the hydrophilic polymer in response to an existing or an induced physiologic condition; (iii) a targeting ligand; and (iv) an entrapped therapeutic agent;
administering said liposomes to achieve (i) cleavage of the releasable bond, thereby releasing said hydrophilic polymer chain; (ii) binding of said ligand to a target cell, where said binding occurs prior to or subsequent to said cleavage; and (iii) internalization of said liposome by said target cell;
whereby said administering is effective to achieve at least a two-fold higher accumulation of said agent in the nucleus of the target cell, when compared to intracellular concentration of the agent delivered by similar liposomes lacking said releasable bond and/or said targeting ligand wherein, said bond is a dithiobenzyl bond.
17. The method of claim 16 , wherein cleavage of said releasable bond after said administering is achieved by naturally-occurring blood components.
18. The method of claim 16 , wherein said pH-sensitive lipid is dioleoylphosphatidylethanolmaine (DOPE).
19. The method of claim 16 , wherein said liposomes further include a stabilizing component.
20. The method of claim 19 , wherein said stabilizing component is cholesteryl hemisuccinate (CHEMS).
21. The method of claim 16 , wherein said lipid derivatized polymer is phosphatidylethanolamine derivatized with polyethyleneglycol.
22. The method of claim 16 , wherein said targeting ligand an antibody or an antibody fragment.
23. The method of claim 22 , wherein said antibody fragment is selected from the group consisting of anti-CD19, anti-CD20, anti-CD22.