Liposomal formulations comprising dihydrosphingomyelin and methods of use thereof
View Patent ↗The present invention includes novel liposomes comprising dihydrosphingomyelin. The invention also includes compositions comprising these liposomes and a therapeutic agent, in addition to methods and kits for delivering a therapeutic agent or treating a disease, e.g., a cancer, using these compositions.
1. A liposomal composition comprising a liposome, wherein said liposome comprises phospholipid and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid/cholesterol to 25/75 (mol/mol) total phospholipid/cholesterol, wherein said at least 20% (molar basis) of total phospholipid present in said liposome is dihydrosphingomyelin (DHSM), wherein the interior of said liposome comprises MnSO 4 or MgSO 4 , and wherein said liposome comprises a therapeutic agent.
2. The liposomal composition of claim 1 , wherein said DHSM constitutes at least 50% (molar basis) of total phospholipid present in said liposome.
3. The liposomal composition of claim 1 , wherein the N-acyl chain of said DHSM consists of 12 to 24 carbon atoms.
4. The liposomal composition of claim 1 , wherein the DHSM is selected from the group consisting of: N-palmitylsphinganyl-1-O-phosphorylcholine; N-stearylsphinganyl-1-O-phosphorylcholine; N-myristylsphinganyl-1-O-phosphorylcholine; and N-arachidylsphinganyl-1-O-phosphorylcholine.
5. The liposomal composition of claim 1 , wherein the DHSM N-acyl and dihydrosphingosine chains comprise carbon chains that are not different in length by more than four carbon atoms.
6. The liposomal composition of claim 1 , wherein the therapeutic agent is an antineoplastic agent.
7. The liposomal composition of claim 6 , wherein the antineoplastic agent is selected from the group consisting of: vinca alkaloids, camptothecins, etoposide, and taxanes.
8. The liposome composition of claim 1 , further comprising empty liposomes.
9. A method of delivering a therapeutic agent to a patient, comprising administering to the patient a pharmaceutical composition comprising a liposome-encapsulated therapeutic agent, wherein said liposome comprises phospholipid and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid/cholesterol to 25/75 (mol/mol) total phospholipid/cholesterol, wherein at least 50% (molar basis) of total phospholipid present in said liposome is dihydrosphingomyelin (DHSM), and wherein the interior of said liposome comprises MnSO 4 or MgSO 4 .
10. The method of claim 9 , wherein the therapeutic agent is an antineoplastic agent.
11. The method of claim 10 , wherein the antineoplastic agent is selected from the group consisting of: vinca alkaloids, camptothecins, etoposide, and taxanes.
12. A method of treating a cancer in a mammal, comprising administering to the mammal a pharmaceutical composition comprising a liposome-encapsulated therapeutic agent, wherein said liposome comprises phospholipid and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid:cholesterol to 25/75 (mol/mol) total phospholipid:cholesterol, wherein at least 50% of total phospholipids present in said liposome is dihydrosphingomyelin (DHSM), and wherein the interior of said liposome comprises MnSO 4 or MgSO 4 .
13. The method of claim 12 , wherein the cancer is a leukemia or lymphoma.
14. The method of claim 12 , wherein the cancer is a solid tumor.
15. A method of producing a pharmaceutical composition, comprising loading a liposome comprising phospholipid id and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid:cholesterol to 25/75 mol/mol total phospholipid:cholesterol with a therapeutic agent, wherein at least 50% of the total phospholipids present in said liposome is dihydrosphingomyelin (DHSM), and wherein the interior of said liposome comprises MnSO 4 or MgSO 4 .
16. The method of claim 15 , wherein said liposome comprises a buffer containing MnSO 4 at a concentration equal to or greater than 300 mM, wherein said loading is performed at a temperature equal to or greater than 60° C. and in the presence of an ionophore.
17. A method of loading a therapeutic agent into a liposome comprising: incubating a liposome comprising phospholipid and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid:cholesterol to 25/75 (mol/mol) total phospholipid:cholesterol and having an encapsulated medium comprising MnSO 4 or MgSO 4 , wherein at least 50% of the total phospholipid of the liposome is dihydrosphingomyelin (DHSM), with an external solution comprising said therapeutic agent and an ionophore at a temperature greater than 60° C. to form a therapeutic agent-loaded liposome.
18. A kit comprising:
(a) a liposome comprising phospholipid and cholesterol at a molar ratio from 75/25 (mol/mol) total phospholipid:cholesterol to 25/75 (mol/mol) total phospholipid:cholesterol, wherein said at least 50% of total phospholipid present in said liposome is dihydrosphingomyelin (DHSM), and wherein the interior of said liposome comprises MnSO 4 or MgSO 4 , and
(b) a therapeutic agent.