IP Library Granted Patent US 8,420,857
Granted Patent B2
US 8,420,857 · App. 12/675,130 · Granted Apr 16, 2013

Removal of silica from water soluble compounds by nanofiltration and reverse phase chromatography

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Quick Facts
Patent No.
US 8,420,857
App. No.
12/675,130
Granted
Apr 16, 2013
Kind
B2
Abstract

A process for separating soluble silica species such as monomeric silicic acid (or monosilicic acid) and low molecular weight soluble polymeric silica from impure water soluble compounds by membrane nanofiltration is provided. A process for separating soluble silica species and colloidal silica from impure water soluble compounds by reverse phase liquid chromatography is also provided.

Claims (49)

1. A process for purifying a product solution comprising a product compound and a silica species selected from at least one of soluble mono silicic acid, soluble polymeric silica and colloidal silica, the process comprising:

processing the product solution in a nanofiltration membrane apparatus to separate the product solution into a permeate stream comprising silica species having a molecular weight below the molecular weight cut-off of the membrane and a retentate stream comprising the product compound and silica species having a molecular weight above the molecular weight cut-off of the membrane; and,

loading the retentate stream on a chromatographic apparatus containing a stationary phase and separating the product compound from the silica species having a molecular weight above the molecular weight cut-off of the membrane to form a chromatographic product compound stream and a chromatographic silica stream containing the silica species having a molecular weight above the molecular weight cut-off of the membrane.

2. The process of claim 1 wherein the silica species comprises mono silicic acid and soluble polymeric silica.

3. The process of claim 2 wherein the silica species further comprises colloidal silica.

4. The process of claim 1 wherein the permeate stream and retentate stream are processed in continuous or discontinuous diafiltration.

5. The process of claim 4 wherein the number of diafiltrations is from 3 to 15.

6. The process of claim 1 further comprising isolating the product compound from the chromatographic product compound stream, wherein the final silica content of the product compound is less than about 0.1 percent by weight.

7. The process of claim 6 wherein the final silica content of the product compound is less than about 0.01 percent by weight.

8. The process of claim 7 wherein the final silica content of the product compound is less than about 0.005 percent by weight.

9. The process of claim 1 wherein the product compound is an x-ray contrast agent.

10. The process of claim 9 wherein the x-ray contrast agent is selected from iopamidol, iomeprol, iohexyl, iopentol, iopromide, iosimide, ioversol, iotrolan, iotasul, iodixanol, iodecimol, ioglucamide, ioglunide, iogulamide, iosarcol, ioxilan, iopamiron, metrizamide, iobitridol and iosimenol.

11. The process of claim 1 wherein the product compound is a magnetic resonance imaging contrast agent.

12. The process of claim 11 wherein the magnetic resonance imaging contrast agent is selected from gadofosveset trisodium, gadoxdetate, gadomelitol, gadobenate dimeglumine, and the corresponding ligands thereof.

13. The process of claim 1 wherein the chromatographic apparatus is a reverse phase chromatographic apparatus.

14. The process of claim 13 wherein the stationary phase is silica based.

15. The process of claim 13 wherein the silica species having a molecular weight above the molecular weight cutoff of the membrane contained in the chromatographic silica stream is concentrated with reference to the chromatographic product compound stream and the product compound contained in the chromatographic product compound stream is concentrated with reference to the chromatographic silica stream.

16. The process of claim 13 wherein the weight ratio of the silica contained in the chromatographic silica stream to the silica contained in the chromatographic product compound stream is at least 2:1.

17. The process of claim 13 wherein the retentate is concentrated or dried prior to being loaded on the chromatographic apparatus.

18. A process for purifying a product solution comprising a product compound and polymeric silica, the process comprising loading the product solution on a reverse phase chromatographic apparatus containing a silica-based stationary phase and eluting one or more pre-fraction streams and one or more purified product fraction streams, wherein

the polymeric silica contained in the sum of the pre-fraction streams is concentrated with reference to the sum of the purified product fraction streams;

and the purified product compound contained in the sum of the purified product fraction streams is concentrated with reference to the sum of the pre-fraction streams.

19. The process of claim 18 wherein the polymeric silica comprises colloidal silica.

20. The process of claim 18 wherein the weight ratio of the silica contained in the sum of the pre-fraction streams to the silica contained in the sum of the purified product fraction streams is at least 2:1.

21. The process of claim 18 wherein the one or more purified product fraction streams further comprises monosilicic acid, and the one or more purified product fraction streams are further processed in a selective nanofiltration membrane apparatus to separate the purified product fraction streams into a permeate stream comprising the soluble silica species having a molecular weight below the molecular weight cut-off of the membrane and a retentate stream comprising the product compound and the soluble silica species having a molecular weight above the molecular weight cutoff of the membrane.

22. The process of claim 21 wherein the permeate stream and retentate stream are processed in continuous or discontinuous diafiltration.

23. The process of claim 22 wherein the number of diafiltrations is from 3 to 15.

24. The process of claim 21 further comprising isolating the product compound from the retentate stream, wherein the final silica content of the product compound is less than about 0.1 percent by weight.

25. The process of claim 24 wherein the final silica content of the product compound is less than about 0.01 percent by weight.

26. The process of claim 25 wherein the final silica content of the product compound is less than about 0.005 percent by weight.

27. The process of claim 18 wherein the product compound is an x-ray contrast agent.

28. The process of claim 27 wherein the x-ray contrast agent is selected from iopamidol, iomeprol, iohexyl, iopentol, iopromide, iosimide, ioversol, iotrolan, iotasul, iodixanol, iodecimol, ioglucamide, loglunide, iogulamide, iosarcol, ioxilan, iopamiron, metrizamide, iobitridol and iosimenol.

29. The process of claim 18 wherein the product compound is a magnetic resonance imaging contrast agent.

30. The process of claim 29 wherein the magnetic resonance imaging contrast agent is selected from gadofosveset trisodium, gadoxdetate, gadomelitol, gadobenate dimeglumine, and the corresponding ligands thereof.

31. A process for purifying a product solution comprising a product compound and polymeric silica, the process comprising loading the product solution on a reverse phase chromatographic apparatus containing a stationary phase and forming by separation a product compound stream comprising the product compound and a polymeric silica stream comprising the polymeric silica.

32. The process of claim 31 wherein the stationary phase is silica based.

33. The process of claim 31 wherein the polymeric silica contained in polymeric silica stream is concentrated with reference to the product compound stream and the product compound contained in the product compound stream is concentrated with reference to the polymeric silica stream.

34. The process of claim 31 wherein the polymeric silica comprises colloidal silica.

35. The process of claim 31 wherein the weight ratio of the silica contained in the polymeric silica stream to the silica contained in the product compound stream is at least 2:1.

36. The process of claim 31 wherein the product compound stream further comprises monosilicic acid, and the product compound stream is further processed in a selective nanofiltration membrane apparatus to separate the product compound stream into a permeate stream comprising the soluble silica species having a molecular weight below the molecular weight cut-off of the membrane and a retentate stream comprising the product compound and the soluble silica species having a molecular weight above the molecular weight cutoff of the membrane.

37. The process of claim 36 wherein the permeate stream and retentate stream are processed in continuous or discontinuous diafiltration.

38. The process of claim 37 wherein the number of diafiltrations is from 3 to 15.

39. The process of claim 36 further comprising isolating the product compound from the retentate stream, wherein the final silica content of the product compound is less than about 0.1 percent by weight.

40. The process of claim 39 wherein the final silica content of the product compound is less than about 0.01 percent by weight.

41. The process of claim 40 wherein the final silica content of the product compound is less than about 0.005 percent by weight.

42. The process of claim 31 wherein the product compound is an x-ray contrast agent.

43. The process of claim 42 wherein the x-ray contrast agent is selected from iopamidol, iomeprol, iohexyl, iopentol, iopromide, iosimide, ioversol, iotrolan, iotasul, iodixanol, iodecimol, ioglucamide, ioglunide, iogulamide, iosarcol, ioxilan, iopamiron, metrizamide, iobitridol and iosimenol.

44. The process of claim 31 wherein the product compound is a magnetic resonance imaging contrast agent.

45. The process of claim 44 wherein the magnetic resonance imaging contrast agent is selected from gadofosveset trisodium, gadoxdetate, gadomelitol, gadobenate dimeglumine, and the corresponding ligands thereof.

Assignments (6)
RELEASE OF PATENT SECURITY INTERESTS RECORDED AT REEL 032480, FRAME 0001 Recorded Nov 16, 2023
From: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
To: THERAKOS, INC.; MALLINCKRODT INTERNATIONAL FINANCE S.A.; MALLINCKRODT CB LLC; MALLINCKRODT FINANCE GMBH; MALLINCKRODT US HOLDINGS LLC (F/K/A MALLINCKRODT US HOLDINGS INC.); MALLINCKRODT CARRIBEAN, INC.; MALLINCKRODT US POOL LLC; MNK 2011 LLC (F/K/A MALLINCKRODT INC.); LUDLOW LLC (F/K/A LUDLOW CORPORATION); CNS THERAPEUTICS, INC.; MALLINCKRODT ENTERPRISES HOLDINGS LLC (F/K/A MALLINCKRODT ENTERPRISES HOLDINGS, INC.); MALLINCKRODT ENTERPRISES LLC; MALLINCKRODT LLC; LAFAYETTE PHARMACEUTICALS LLC; LIEBEL-FLARSHEIM COMPANY LLC; MALLINCKRODT BRAND PHARMACEUTICALS LLC (F/K/A MALLINCKRODT BRAND PHARMACEUTICALS, INC.); MALLINCKRODT VETERINARY, INC.; MALLINCKRODT US HOLDINGS LLC; IMC EXPLORATION COMPANY; MEH, INC.; MALLINCKRODT HOSPITAL PRODUCTS IP UNLIMITED COMPANY (F/K/A MALLINCKRODT HOSPITAL PRODUCTS IP LIMITED); MALLINCKRODT ARD IP UNLIMITED COMPANY (F/K/A MALLINCKRODT ARD IP LIMITED); OCERA THERAPEUTICS LLC (F/K/A OCERA THERAPEUTICS, INC.); SPECGX LLC; STRATATECH CORPORATION; SUCAMPO PHARMA AMERICAS LLC; VTESSE LLC (F/K/A VTESSE INC.); MALLINCKRODT PHARMACEUTICALS IRELAND LIMITED; MALLINCKRODT PHARMA IP TRADING UNLIMITED COMPANY (F/K/A MALLINCKRODT PHARMA IP TRADING D.A.C.); INFACARE PHARMACEUTICAL CORPORATION; ST SHARED SERVICES LLC; IKARIA THERAPEUTICS LLC; INO THERAPEUTICS LLC
Reel/Frame 065609/0322 →
RELEASE OF SECURITY INTEREST Recorded Nov 30, 2015
From: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
To: LIEBEL-FLARSHEIM COMPANY LLC
Reel/Frame 037172/0094 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 31, 2014
From: MALLINCKRODT LLC
To: LIEBEL-FLARSHEIM COMPANY LLC
Reel/Frame 034715/0531 →
SECURITY INTEREST Recorded Mar 19, 2014
From: MALLINCKRODT INTERNATIONAL FINANCE S.A.; MALLINCKRODT CB LLC; MALLINCKRODT FINANCE GMBH; MALLINCKRODT US HOLDINGS INC.; MALLINCKRODT CARIBBEAN, INC.; MALLINCKRODT US POOL LLC; MALLINCKRODT INC.; LUDLOW CORPORATION; CNS THERAPEUTICS, INC.; ENTERPRISES HOLDINGS, INC.; MALLINCKRODT ENTERPRISES LLC; MALLINCKRODT LLC; LAFAYETTE PHARMACEUTICALS LLC; LIEBEL-FLARSHEIM COMPANY LLC; MALLINCKRODT BRAND PHARMACEUTICALS, INC; MALLINCKRODT VETERINARY, INC.; MALLINCKRODT US HOLDINGS LLC; IMC EXPLORATION COMPANY; MEH, INC; MALLINCKRODT ENTERPRISES HOLDINGS, INC.
To: DEUTSCHE BANK AG NEW YORK BRANCH
Reel/Frame 032480/0001 →
CHANGE OF LEGAL ENTITY Recorded Aug 16, 2011
From: MALLINCKRODT INC.
To: MALLINCKRODT LLC
Reel/Frame 026754/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2010
From: BAILEY, ALLAN R.; WHITE, DAVID H.; KASPAR, DERICK L.; FUKUNAGA, ANNA K.; VANDAS, ROBERT E.; GENTILCORE, MICHAEL J.; NGUYEN, HUNG V.
To: MALLINCKRODT INC.
Reel/Frame 023988/0081 →