IP Library Granted Patent US 9,259,471
Granted Patent B2
US 9,259,471 · App. 14/150,474 · Granted Feb 16, 2016

Diketopiperazine salts for drug delivery and related methods

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Quick Facts
Patent No.
US 9,259,471
App. No.
14/150,474
Granted
Feb 16, 2016
Kind
B2
Abstract

Drug delivery systems have been developed based on the formation of diketopiperazine carboxylate salts and microparticles containing the same. The systems may further comprise a bioactive agent. Related methods for making and using the biologically active agent delivery compositions are also provided. In certain embodiments, the pharmaceutically acceptable salts described can be formed by removal of solvent by methods including distillation, evaporation, spray drying or lyophilization.

Claims (24)

1. A microparticulate system for drug delivery comprising a composition comprising:

microparticles of a pharmaceutically acceptable anion of a diketopiperazine compound comprising a carboxylate group, a divalent cation, and a biologically active agent,

wherein the diketopiperazine compound is represented by the following general formula:

wherein E 1 and E 2 are NH, and R 1 and R 2 are independently selected from succinate-4-aminobutyl, glutarate-4-aminobutyl, maleate-4-aminobutyl, citraconate-4-aminobutyl, malonate-4-aminobutyl, oxalate-4-aminobutyl, and fumarate-4-aminobutyl.

2. The microparticulate system of claim 1 wherein said biologically active agent is a hormone, an anticoagulant, an immunomodulating agent, a cytotoxic agent, an antibiotic, an antiviral, an antisense, an antigen, an antibody or an active fragment or an analog thereof.

3. The microparticulate system of claim 1 wherein said biologically active agent is insulin, a cannabinoid, heparin, calcitonin, felbamate, parathyroid hormone or a fragment thereof, growth hormone, erythropoietin, glucagon-like peptide-1, somatotrophin-releasing hormone, follicle stimulating hormone, cromolyn, adiponectin, RNAse, ghrelin, zidovudine, didanosine, tetrahydrocannabinol, atropine, granulocyte colony stimulating factor, lamotrigine, chorionic gonadotropin releasing factor, luteinizing releasing hormone, β-galactosidase, or Argatroban.

4. The microparticulate system of claim 3 wherein said biologically active agent is insulin.

5. The microparticulate system of claim 3 wherein said biologically active agent is glucagon-like peptide-1.

6. The microparticulate system of claim 1 wherein said anion comprises 3,6-di(succinate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(maleate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(citraconate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(glutarate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(malonate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(oxalate-4-aminobutyl)-2,5-diketopiperazine, or 3,6-di(fumarate-4-aminobutyl)-2,5-diketopiperazine.

7. The microparticulate system of claim 6 wherein said anion is 3,6-di(fumarate-4-aminobutyl)-2,5-diketopiperazine.

8. The microparticulate system of claim 1 wherein said microparticles have a diameter between about 0.5 microns and about ten microns.

9. The microparticulate system of claim 1 wherein said composition comprises a suspension for drug delivery.

10. The microparticulate system of claim 9 , wherein said suspension is administered orally.

11. The microparticulate system of claim 3 wherein said anion is 3,6-di(succinate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(maleate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(citraconate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(glutarate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(malonate-4-aminobutyl)-2,5-diketopiperazine, 3,6-di(oxalate-4-aminobutyl)-2,5-diketopiperazine, or 3,6-di(fumarate-4-aminobutyl)-2,5-diketopiperazine.

12. The microparticulate system of claim 11 , wherein said biologically active agent is glucagon-like peptide-1.

13. The microparticulate system of claim 11 , wherein said biologically active agent is insulin.

14. The microparticulate system of claim 13 wherein said anion is 3,6-di(fumarate-4-aminobutyl)-2,5-diketopiperazine.

15. The microparticulate system of claim 3 , wherein said microparticles have a diameter between about 0.5 microns and about ten microns.

16. The microparticulate system of claim 6 , wherein the divalent cation comprises Mg++ or Ca++.

17. The microparticulate system of claim 16 wherein said cation comprises Mg++.

18. The microparticulate system of claim 17 , wherein said biologically active agent is glucagon-like peptide-1.

19. The microparticulate system of claim 17 , wherein said biologically active agent is insulin.

20. The microparticulate system of claim 16 , wherein said microparticles are suitable for pulmonary administration.

21. The microparticulate system of claim 1 , wherein said divalent cation is calcium or magnesium.

Assignments (5)
PATENT SECURITY AGREEMENT Recorded Aug 12, 2025
From: MANNKIND CORPORATION
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 072444/0525 →
RELEASE OF SECURITY INTEREST Recorded Apr 5, 2024
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: MANNKIND CORPORATION; MANNKIND LLC
Reel/Frame 067024/0082 →
RELEASE OF SECURITY INTEREST Recorded Aug 13, 2019
From: DEERFIELD PRIVATE DESIGN FUND II, L.P.; DEERFIELD PRIVATE DESIGN INTERNATIONAL II, L.P.; HORIZON SANTE FLML SARL
To: MANNKIND CORPORATION
Reel/Frame 050044/0138 →
SECURITY INTEREST Recorded Aug 13, 2019
From: MANNKIND CORPORATION; MANNKIND LLC
To: MIDCAP FINANCIAL TRUST, AS AGENT
Reel/Frame 050044/0181 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2014
From: LEONE-BAY, ANDREA; MOYE-SHERMAN, DESTARDI; WILSON, BRYAN R.
To: MANNKIND CORPORATION
Reel/Frame 032624/0638 →