Compositions comprising SIA for the treatment of diabetes

• US 8,426,362 B2
• Filed: 04/07/2009
• Issued: 04/23/2013
• Est. Priority Date: 04/07/2008
• Status: Active Grant

• Current Assignee: Extended Delivery Pharmaceuticals
• Original Assignee: National Institute Of Immunology (Government of India), Indian Institute of Science
• Inventors: Surolia, Avadhesha, Gupta, Sarika, Singh, Mahendra Pal, Chattopadhyay, Tandrika
• Primary Examiner(s): Chandra, Gyan
• Application Number:
  US12/419,669
• Publication Number:
  US 20090258818A1
• Time in Patent Office: 1,477 Days
• Field of Search: None
• US Class Current: 514/5.9
• CPC Class Codes: A61K 38/23 Calcitonins
• CPC Class Codes: A61K 38/28 Insulins
• CPC Class Codes: A61K 9/0002 Galenical forms characterised by the drug release technique; Application systems commanded by energy
• CPC Class Codes: A61P 19/02 for joint disorders, e.g. arthritis, arthrosis
• CPC Class Codes: A61P 19/10 for osteoporosis
• CPC Class Codes: A61P 25/02 for peripheral neuropathies
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: A61P 3/10 for hyperglycaemia, e.g. antidiabetics
• CPC Class Codes: A61P 31/04 Antibacterial agents
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: A61P 37/00 Drugs for immunological or allergic disorders
• CPC Class Codes: A61P 37/08 Antiallergic agents antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61P 5/48 of the pancreatic hormones

Abstract

A supramolecular insulin assembly and supramolecular exendin-4 assembly, which is useful as a protein therapeutic agent for the treatment of metabolic disorders particularly diabetes. The supramolecular assemblies disclosed in the present invention consists of insoluble and aggregated oligomers the protein. The invention also provides pharmaceutical compositions comprising the supramolecular assembly.

Claims

1. An isolated and stable supramolecular insulin assembly (SIA) useful as a protein therapeutic for the treatment of metabolic disorders selected from the group consisting of type 1, type 2 diabetes mellitus and complications thereof, wherein said assembly comprises insoluble and aggregated oligomeric form of insulin and wherein said assembly is protease resistant, exhibits no binding to Congo Red, has both α

-helical and β

-sheet components, and releases biologically active insulin monomers in vitro or in vivo.

2. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly shows a sharp peak at 1647-1645 cm⁻

1 in Fourier Transform infrared spectroscopy (FTIR).

3. The supramolecular assembly (SIA) of claim 1, wherein said insulin is recombinant human insulin, bovine insulin, pig insulin, or a therapeutically-active mutant or analog of insulin.

4. The supramolecular assembly (SIA) of claim 1, wherein said assembly releases insulin at a rate ranging from 0.1 to 5.4 ng/ml for about 7 to 180 days, in vivo.

5. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly releases insulin at a rate ranging from 4-5.4 ng/ml for at least 7-10 days.

6. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly releases insulin at a rate ranging from 0.5-1.8 ng/ml for at least 160 days.

7. A pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1, type 2 diabetes mellitus and complications thereof, said composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) of claim 6 further comprising pharmaceutically acceptable carriers, additives or diluents.

8. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly releases insulin at a rate ranging from 0.1-0.7 ng/ml for at least 180 days.

9. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly upon administration to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for at least 160 days in said subject.

10. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly in the range of 0.125 to 3.75 mg/kg body weight to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for at least 7 to 180 days in said subject.

11. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly in the range of 0.75 to 1.25 mg/kg body weight to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for at least 160 days in said subject.

12. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for 30 days in said subject.

13. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for more than 20-25 weeks in said subject.

14. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for at least 7 to 180 days in said subject, wherein concentration of the assembly in the dose is in the range of 25 to 750 μ

g.

15. The supramolecular insulin assembly (SIA) of claim 1, wherein a single dose of said assembly to a diabetic subject maintains near-normoglycemic level (120±

30 mg/dl) for at least 160 days in said subject, wherein concentration of the assembly in the dose is in the range of 150 to 250 μ

g.

16. The supramolecular insulin assembly (SIA) of claim 1, wherein said SIA comprises a non cytotoxic, non immunogenic, non-apoptotic and non-mitogenic prodrug.

17. The supramolecular insulin assembly (SIA) of claim 1 wherein said assembly achieves a tightly regulated glycemic control without fasting hypoglycemia in a diabetic subject.

18. The supramolecular insulin assembly (SIA) of claim 1 wherein said assembly demonstrates fluorescence intensity in the range of 7-9% of the total thioflavin-T (Th-T) fluorescence observed in fully formed amyloid fibers.

19. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly comprises linear association of elongated clusters of insulin monomers and said clusters comprise a height of 12±

2 nm.

20. The supramolecular insulin assembly (SIA) of claim 1, wherein said assembly is prepared at a pH ranging from 6.8-7.8.

21. A pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1, type 2 diabetes mellitus and complications thereof, said composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) of claim 1.

22. The pharmaceutical composition of claim 21 further comprising pharmaceutically acceptable carriers, additives or diluents.

23. The pharmaceutical composition of claim 21 in a form suitable for administration intramuscularly, intradermally or subcutaneously.

24. The composition of claim 21, wherein said SIA releases insulin at a rate ranging from 0.1 to 5.4 ng/ml for about 7 to 180 days, in vivo.

25. A process of preparation of supramolecular insulin assembly (SIA) of claim 1, said process comprising;

a) dissolving insulin at a temperature of about 25 to 60°

C. in a solution having a pH in the range of about 4 to 7.8; and

b) incubating the above for a period of about 2 to 48 hours with constant shaking to obtain Supramolecular Insulin Assembly (SIA), wherein SIA comprises insoluble and aggregated oligomeric form of insulin.

26. The process of claim 25, wherein said process further comprises

a) washing said SIA with PBS;

and

b) re-suspending said SIA in PBS.

27. The process of claim 25, wherein said period is about 6 to 12 hours.

28. The process of claim 25, wherein the solution is selected from phosphate buffer (PBS) having pH 6 to 7.5, and citrate buffer having pH in the range of about 4 to 6.

29. The process of claim 25, wherein said temperature is 37°

C.

30. The process of claim 25, wherein pH of said solution is 6.8 to 7.8.

31. The process of claim 25, wherein said period is about 6 to 48 hours.

32. The process of claim 25, wherein pH of said solution is 6.8-7.8 and said period is about 6 to 48 hours.

33. The process of claim 25 wherein supramolecular insulin assembly formation is monitored by acquisition of thioflavin-T (Th-T) fluorescence.

34. A process of preparation of supramolecular insulin assembly (SIA) of claim 1, said process comprising;

a) dissolving insulin at a temperature of about 37°

C. in a solution having a pH in the range of about 6.8 to 7.8; and

b) incubating the above for a period of about 6 to 48 hours with constant shaking to obtain Supramolecular Insulin Assembly (SIA), wherein SIA comprises insoluble and aggregated oligomeric form of insulin.