IP Library Granted Patent US 8,992,970
Granted Patent B2
US 8,992,970 · App. 14/175,365 · Granted Mar 31, 2015

Liposomes useful for drug delivery

Inventors: Keelung Hong (San Francisco, CA); Daryl C. Drummond (Pacifica, CA); Dmitri Kirpotin (San Francisco, CA)
Assignee: Merrimack Pharmaceuticals, Inc.
A61K9/127A61K9/0019A61K9/1271A61K31/4745A61K31/475A61K31/704A61K31/337C07H13/12
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Quick Facts
Patent No.
US 8,992,970
App. No.
14/175,365
Granted
Mar 31, 2015
Kind
B2
Abstract

The present invention provides liposome compositions containing substituted ammonium and/or polyanion, and optionally with a desired therapeutic or imaging entity. The present invention also provides methods of making the liposome compositions provided by the present invention.

Claims (14)

1. A liposomal composition comprising liposomes in an aqueous medium, the liposomes having an interior aqueous space separated from the aqueous medium by a membrane comprising 1,2-distearoyl-SN-phosphatidylcholine, cholesterol and N-(omega-methoxy-poly(ethylene glycol)-oxycarbonyl)-1,2-distearoylphosphatidyl ethanolamine, and entrapped inside the liposomes are either: 1) irinotecan and sucrose octasulfate, or 2) irinotecan, sucrose octasulfate and a substituted ammonium compound; wherein, the irinotecan entrapped inside the liposomes is at a concentration that exceeds the concentration of the irinotecan in the aqueous medium.

2. The liposomal composition of claim 1 , where irinotecan, sucrose octasulfate, and substituted ammonium compound are entrapped inside the liposomes and wherein the substituted ammonium compound has a formula: R 1 —(R 2 —)N + (—R 3 )—R 4 , wherein N is a an ammonium nitrogen atom, each of R 1 , R 2 , R 3 , and R 4 is independently a hydrogen atom or an organic group having each independently not more than 8 carbon atoms, and in totality not more than 18 carbon atoms inclusive, wherein at least one of R 1 , R 2 , R 3 , and R 4 is an organic group; wherein the organic group is independently alkyl, alkylidene, heterocyclic alkyl, cycloalkyl, aryl, alkenyl, cycloalkenyl, or a hydroxy-substituted derivative thereof, optionally including S, O, or N atoms forming an ether, ester, thioether, amine, or amide bond; and wherein at least three of R 1 , R 2 , R 3 , and R 4 are the organic groups; or at least one of the organic groups has a secondary or tertiary carbon atom directly linked to the ammonium nitrogen atom.

3. The liposomal composition of claim 2 , wherein the substituted ammonium compound is selected from the group consisting of isopropylethylammonium, isopropylmethylammonium, diisopropylammonium, tert-butylethylammonium, dicyclo-hexylammonium, morpholinium, pyridinium, piperidinium, pyrrolidinium, piperazinium, tert-butylammonium, 2-ammonio-2-methyl-propanol-1,2-ammonio-2-methyl-propandiol-1,3, tris-(hydroxyethyl)-ammoniomethane, N,N′-diethyl-ethanolammonium, N,N′,N″-tris-(2-hydroxyethyl)ammonium, N,N′-bis-(2-hydroxyethyl)ethylammonium, trimethyl-ammonium, triethylammonium, diethylmethyl-ammonium, diisopropylethylammonium, triisopropylammonium, N-methyl-morpholinium, 1-(2-hydroxyethyl)piperidinium, 1-methylpyrrolidinium, 1,4-dimethyl-piperazinium, tetramethylammonium, tetraethyl-ammonium, and tetrabutylammonium.

4. The liposomal composition of claim 2 , wherein the substituted ammonium compound is triethylammonium.

5. The liposomal composition of claim 2 , wherein the substituted ammonium compound is diethylammonium.

6. The liposomal composition of claim 1 , wherein the membrane comprises about 59.8 mol. % of the 1,2-distearoyl-SN-phosphatidylcholine; about 39.9 mol. % of the cholesterol and about 0.3 mol. % of the N-(omega-methoxy-poly(ethylene glycol)-oxycarbonyl)-1,2-distearoylphosphatidyl ethanolamine.

7. The liposomal composition of claim 6 , wherein the poly(ethylene glycol) in the N-(omega-methoxy-poly(ethylene glycol)-oxycarbonyl)-1,2-distearoylphosphatidyl ethanolamine has a molecular weight of about 2,000.

8. The liposomal composition of claim 1 , wherein the composition is a fluid pharmaceutical formulation for parenteral administration.

9. The liposomal composition of claim 1 , wherein molar ratio of the irinotecan to the totality of the lipids is at least 1.0.

10. The liposomal composition of claim 1 , wherein the relative amounts of the irinotecan and the sucrose octasulfate are near the point of stoichiometric equivalency.

11. The liposomal composition of claim 1 , wherein the relative amounts of the irinotecan and the sucrose octasulfate are at the point of stoichiometric equivalency.

12. The liposomal composition of claim 1 , wherein the irinotecan and the sucrose octasulfate are comprised in the form of a salt.

13. The liposomal composition of claim 1 , wherein the aqueous medium comprises hydroxyethylpiperazine-ethylsulfonate (HEPES) and NaCl.

14. The liposomal composition of claim 1 , wherein the irinotecan has been partially or substantially removed from the aqueous medium.

Assignments (6)
CHANGE OF ADDRESS OF ASSIGNEE Recorded May 17, 2017
From: MERRIMACK PHARMACEUTICALS, INC.
To: IPSEN BIOPHARM LTD.
Reel/Frame 042522/0334 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2017
From: MERRIMACK PHARMACEUTICALS, INC.
To: IPSEN BIOPHARM LTD.
Reel/Frame 042377/0696 →
RELEASE OF SECURITY INTEREST Recorded Apr 14, 2017
From: U.S. BANK NATIONAL ASSOCIATION
To: MERRIMACK PHARMACEUTICALS, INC.
Reel/Frame 042254/0349 →
SECURITY INTEREST Recorded Dec 28, 2015
From: MERRIMACK PHARMACEUTICALS, INC.
To: U.S. BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 037394/0285 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2014
From: HONG, KEELUNG; DRUMMOND, DARYL C.; KIRPOTIN, DMITRI
To: HERMES BIOSCIENCES, INC.
Reel/Frame 033623/0932 →
MERGER Recorded Aug 27, 2014
From: HERMES BIOSCIENCES, INC.
To: MERRIMACK PHARMACEUTICALS, INC.
Reel/Frame 033623/0992 →
Continuity (5)
Continuation 13654373 · Oct 17, 2012
Continuation 13416204 · Mar 9, 2012
Continuation 11121294 · May 2, 2005
Provisional Application 60567921 · May 3, 2004
Related Publication 20140154298A1 · Jun 5, 2014