Process for Preparation of Sevelamer Carbonate

• US 20100331516A1
• Filed: 04/06/2009
• Published: 12/30/2010
• Est. Priority Date: 04/08/2008
• Status: Abandoned Application

• Current Assignee: Usv Limited (USV Private Limited)
• Original Assignee: Usv Limited (USV Private Limited)
• Inventors: Sathe, Govind Dhananjay, Patil, Samadhan Daulat, Mondkar, Harish Kashinath, Jadhav, Tanaji Shamrao
• Application Number:
  US12/525,863
• Publication Number:
  US 20100331516A1
• Time in Patent Office: Days
• US Class Current: 528/393
• CPC Class Codes: A61K 31/785 Polymers containing nitrogen
• CPC Class Codes: C08F 126/06 by a heterocyclic ring containing nitrogen
• CPC Class Codes: C08F 26/02 by a single or double bond to nitrogen
• CPC Class Codes: C08F 2810/20 leading to a crosslinking, either explicitly or inherently
• CPC Class Codes: C08F 8/00 Chemical modification by after-treatment graft polymers, block polymers, crosslinking with unsaturated monomers or with polymers C08F251/00 - C08F299/00; of conjugated diene rubbers C08C
• CPC Class Codes: C08F 8/18 Introducing halogen atoms or halogen-containing groups

Abstract

The present invention discloses simple process for preparation of salt of polyallylamine polymer.

Claims

1. A process for preparation of carbonate salt of amine polymers comprising interacting allylamine compound with suitable carbonate source.

2. A process for preparation of carbonate salt of amine polymers as claimed in claim 1 comprising interacting allylamine compound with about 0.5-5 w/w of suitable carbonate source with respect to allylamine compound.

3. A process for preparation of carbonate salt of amine polymers as claimed in claim 2 comprising interacting allylamine compound with about 2.5 w/w of suitable carbonate source with respect to allylamine compound.

4. A process for preparation of carbonate salt of amine polymers as claimed in claim 3 comprising interacting allylamine compound with about 1.5 w/w of suitable carbonate source with respect to allylamine compound.

5. A process for preparation of carbonate salt of amine polymers as claimed in claim 4 comprising interacting allylamine compound with equimolar amount of suitable carbonate source with respect to allylamine compound.

6. The process as claimed in claim 1 wherein said allylamine compound comprises allylamine, polyallylamine, Sevelamer and Sevelamer hydrochloride.

7. The process as claimed in claim 1 wherein said salt of amine polymers is Sevelamer carbonate.

8. The process as claimed in claim 1 wherein said interaction is carried out in 24 hours.

9. The process as claimed in claim 8 wherein said interaction is performed under atmospheric pressure.

10. The process as claimed in claim 9 wherein said interaction is performed at temperature in the range of 0-100°

C.

11. The process as claimed in claim 10 wherein said reaction is performed preferably at 25-35°

C.

12. The process as claimed in claim 10 wherein said reaction is performed more preferably at 60-65°

C.

16. The process as claimed in claim 7 wherein said Sevelamer carbonate is dried at 80-100°

C. under atmospheric pressure in air tray dryer (ATD).

17. The process as claimed in claim 7 wherein said Sevelamer carbonate is dried at 50-100°

C. in vacuum tray dryer (VTD).

18. The process as claimed in claim 7 wherein said Sevelamer carbonate is dried at 80-110°

C. in Fluidized Bed Dryer (FBD).

19. The process as claimed in claim 7 wherein said Sevelamer carbonate is dried at 50-100°

C. in rotary evaporator.

45. The process as claimed in any of the preceding claims wherein said carbonate source is selected from carbon dioxide gas, carbonic acid prepared in situ by dissolving carbon dioxide gas in water or dry ice, carbonate salts of alkali metal or alkaline earth metal salts.

46. The process as claimed in any of the preceding claims wherein said base is alkali metal or alkaline earth metal salts comprising sodium carbonate, potassium carbonate, calcium carbonate, sodium bicarbonate and sodium hydroxide in solid or solution form.

47. Sevelamer carbonate as claimed in claim any of the preceding claims wherein the drying and packing of material is done in such way to control the Loss on drying below 10%.

13. A process for drying carbonate salt of amine polymers.

14. The process as claimed in claim 13 said drying is performed in air tray dryer (ATD) or vacuum tray dryer (VTD) or Fluidized Bed Dryer (FBD) or rotary evaporator to maintain loss on drying content less than about 10% and not less than about 5%.

15. The process as claimed in claim 14 wherein said drying is carried out at elevated temperature for 1 to 48 hours.

20. A process for preparation of Sevelamer carbonate comprising

a) making polyallylamine from polyallylamine hydrochloride using suitable base

b) treating polyallylamine with suitable carbonate source to get polyallylamine carbonate

c) subjecting to crosslinking the obtained polyallylamine carbonate with suitable crosslinking agent optionally in presence of emulsifier and/or surfactant to get Sevelamer carbonate

21. The process as claimed in claim 20 wherein polyallylamine base is treated with carbon dioxide gas in water at 25-65°

C.

22. The process as claimed in claim 20 wherein polyallylamine base is treated with sodium carbonate at 25-75°

C.

23. The process as claimed in claim 20 wherein polyallylamine base is treated with sodium bicarbonate at 25-75°

C.

24. The process as claimed in claim 20 step b) further comprises isolating polyallylamine carbonate from suitable solvent and partially neutralizing with suitable base.

25. The process as claimed in claim 24 wherein said partial neutralization comprises adding 65-70 mole % of base to the solution of polyallylamine carbonate in suitable solvent.

26. The process as claimed in claim 25 wherein said solvent is selected from benzene, toluene, xylenes, chlorobenzenes, nitrobenzenes and said aliphatic hydrocarbons are selected from chlorinated methylene chloride and ethylene chloride, water or mixtures thereof.

27. The process as claimed in claim 20 wherein said emulsifier is sorbtian trioleate and said surfactant is sodium dodecyl sulfate and like.

28. The process as claimed in claim 20(c) wherein said crosslinking is carried out at elevated temperature.

29. Carbonate salt of amine polymer having carbonate content from about 3 to about 7 meq/gm, Phosphate Binding Capacity of about 3 to about 7 mmol/gm and chloride content not more than 0.05%, residue on ignition not more than 0.1% and loss on drying not more than 10%.

30. Sevelamer carbonate having less than 0.05% chloride content.

31. The process for preparation of Sevelamer carbonate comprising

a) treating allylamine with suitable carbonate source to get allylamine carbonate;

b) converting the obtained allylamine carbonate into polyallylamine carbonate;

c) crosslinking obtained polyallylamine carbonate with crosslinking agent optionally in presence of emulsifier/surfactant;

d) isolating Sevelamer carbonate

32. The process as claimed in claim 31 wherein step b) further comprises isolating polypallylamine carbonate from organic solvent.

33. The process as claimed in claim 31 further comprises partially neutralizing polyallylamine carbonate using base.

34. The process as claimed in claim 31 wherein said emulsifier/surfactant used is selected from trioleate surfactants and sorbitane trioleate.

35. A process for preparation of Sevelamer carbonate comprising contacting Sevelamer hydrochloride with suitable carbonate source.

36. The process as claimed in claim 35 wherein said treatment of carbonate source is performed at 25-75°

C.

37. The process as claimed in claim 35 wherein Sevelamer hydrochloride is treated with sodium carbonate.

38. The process as claimed in claim 37 wherein said sodium carbonate is used in an amount of 0.5 to 5 w/w of Sevelamer hydrochloride.

39. The process as claimed in claim 35 wherein Sevelamer hydrochloride is treated with sodium bicarbonate.

40. The process as claimed in claim 39 wherein said sodium bicarbonate is used in an amount in the range of 0.5 to 5 w/w of Sevelamer hydrochloride.

41. The process as claimed in claim 40 wherein said sodium bicarbonate is used in 1:

1 ratio.

42. The process as claimed in claim 35 wherein optionally Sevelamer hydrochloride is further treated with sodium bicarbonate to get Sevelamer carbonate with chloride content below 0.05%

43. The process as claimed in claim 35 wherein Sevelamer hydrochloride is treated with carbon dioxide at pressure in the range of about 1 to 15 Kg/cm².

44. A process for preparation of Sevelamer carbonate comprising contacting Sevelamer hydrochloride with suitable base to get Sevelamer base and treating obtained Sevelamer base with suitable carbonate source to get Sevelamer carbonate.