IP Library Granted Patent US 8,128,966
Granted Patent B2
US 8,128,966 · App. 11/093,268 · Granted Mar 6, 2012

Modified pectins, compositions and methods related thereto

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,128,966
App. No.
11/093,268
Granted
Mar 6, 2012
Kind
B2
Abstract

The present invention provides compositions of modified pectin and for preparing and using them.

Claims (37)

1. A process for manufacturing a biologically active filtered pectin, comprising: (a) passing an aqueous solution comprising 1-20 mg/mL modified or unmodified pectin and 7.5%-25% w/w ethanol through a tangential flow filter with a pore size of less than 1.0 μm to provide a permeate and a retentate, wherein said permeate comprises biologically active filtered pectin having an average molecular weight from 10 kDa to 250 kDa and an IC 50 less than 200 μg/mL in a cancer cell apoptosis model; and (b) collecting said biologically active filtered pectin.

2. The process of claim 1 , wherein the pore size is about 0.2 μm.

3. The process of claim 1 , wherein the solution has a pectin concentration of 1 to 10 mg/mL.

4. The process of claim 1 , wherein the solution has a pH in the range of 2.5 to 7.5.

5. A process for manufacturing a partially de-esterified biologically active pectin, comprising:

(a) treating a first aqueous solution comprising 1-20 mg/ml modified or unmodified pectin with acid, base, or both to partially de-esterify the pectin,

(b) neutralizing the first aqueous solution to form a second aqueous solution comprising partially de-esterified pectin,

(c) passing the second aqueous solution comprising partially de-esterified pectin and 7.5%-25% w/w ethanol through a tangential flow filter with a pore size of less than 1.0 μm to provide a permeate and a retentate, wherein said permeate comprises filtered partially de-esterified biologically active pectin having an average molecular weight from 10 kDa to 250 kDa and an IC 50 less than 200 μg/mL in a cancer cell apoptosis model, and wherein the degree of esterification in the resulting partially de-esterified biologically active pectin is between 10% and 60%, and

(d) collecting said filtered partially de-esterified biologically active pectin.

6. The process of claim 5 , wherein the pore size is about 0.2 μm.

7. The process of claim 5 , wherein the first aqueous solution comprises 1 to 10 mg/ml modified or unmodified pectin.

8. The process of claim 5 , wherein the first aqueous solution has a pH in the range of 2.5 to 7.5.

9. A process for manufacturing a biologically active filtered pectin, comprising: (a) passing an aqueous solution comprising 1-20 mg/mL modified or unmodified pectin and 7.5%-25% w/w ethanol through a tangential flow filter with a pore size of 0.1 μm to 1.0 μm to provide a permeate and a retentate, wherein said permeate comprises biologically active filtered pectin having an average molecular weight from 10 kDa to 250 kDa and an IC 50 less than 200 μg/mL in a cancer cell apoptosis model; and (b) collecting said biologically active filtered pectin.

10. The process of claim 9 , wherein the pore size is 0.1 μm to 0.7 μm.

11. The process of claim 9 , wherein the pore size is about 0.2 μm.

12. The process of claim 9 , wherein the solution has a pectin concentration of 1 to 10 mg/mL.

13. The process of claim 9 , wherein the solution has a pH in the range of 2.5 to 7.5.

14. A process for manufacturing a partially de-esterified biologically active filtered pectin, comprising:

(a) treating a first aqueous solution comprising 1-20 mg/ml modified or unmodified pectin with acid, base, or both to partially de-esterify the pectin,

(b) neutralizing the first aqueous solution to form a second aqueous solution comprising partially de-esterified pectin,

(c) passing the second aqueous solution comprising partially de-esterified pectin and 7.5%-25% w/w ethanol through a tangential flow filter with a pore size of 0.1 μm to 1.0 μm to provide a permeate and a retentate, wherein said permeate comprises filtered partially de-esterified biologically active filtered pectin having an average molecular weight from 10 kDa to 250 kDa and an IC 50 less than 200 μg/mL in a cancer cell apoptosis model, and wherein the degree of esterification in the resulting partially de-esterified pectin is between 10% and 60%, and

(d) collecting said partially de-esterified biologically active filtered pectin.

15. The process of claim 14 , wherein the pore size is about 0.2 μm.

16. The process of claim 14 , wherein the first aqueous solution comprises 1 to 10 mg/ml modified or unmodified pectin.

17. The process of claim 14 , wherein the first aqueous solution has a pH in the range of 2.5 to 7.5.

18. The process of claim 1 , wherein the average molecular weight of the biologically active filtered pectin is selected from the group consisting of 50 kDa-200 kDa, 80 kDa-150 kDa, 70 kDa-150 kDa and 80 kDa-100 kDa.

19. The process of claim 5 , wherein the average molecular weight of the biologically active filtered pectin is selected from the group consisting of 50 kDa-200 kDa, 80 kDa-150 kDa, 70 kDa-150 kDa and 80 kDa-100 kDa.

20. The process of claim 9 , wherein the average molecular weight of the biologically active filtered pectin is selected from the group consisting of 50 kDa-200 kDa, 80 kDa-150 kDa, 70 kDa-150 kDa and 80 kDa-100 kDa.

21. The process of claim 14 , wherein the average molecular weight of the biologically active filtered pectin is selected from the group consisting of 50 kDa-200 kDa, 80 kDa-150 kDa, 70 kDa-150 kDa and 80 kDa-100 kDa.

22. The process of claim 1 , wherein the biologically active filtered pectin inhibits cancer cell proliferation in a cancer cell apoptosis model with an IC 50 less than 100 μg/mL.

23. The process of claim 5 , wherein the biologically active filtered pectin inhibits cancer cell proliferation in a cancer cell apoptosis model with an IC 50 less than 100 μg/mL.

24. The process of claim 9 , wherein the biologically active filtered pectin inhibits cancer cell proliferation in a cancer cell apoptosis model with an IC 50 less than 100 μg/mL.

25. The process of claim 14 , wherein the biologically active filtered pectin inhibits cancer cell proliferation in a cancer cell apoptosis model with an IC 50 less than 100 μg/mL.

26. The process of claim 1 , wherein the solution comprises 10%-20% w/w ethanol or 15%-25% w/w ethanol.

27. The process of claim 5 , wherein the second aqueous solution comprises 10%-20% w/w ethanol or 15%-25% w/w ethanol.

28. The process of claim 9 , wherein the solution comprises 10%-20% w/w ethanol or 15%-25% w/w ethanol.

29. The process of claim 14 , wherein the second aqueous solution comprises 10%-20% w/w ethanol or 15%-25% w/w ethanol.

Assignments (13)
CHANGE OF NAME Recorded Jul 3, 2012
From: LJPC MERGER SUB, INC.
To: LA JOLLA PHARMACEUTICAL COMPANY
Reel/Frame 028484/0884 →
MERGER Recorded Jun 29, 2012
From: LA JOLLA PHARMACEUTICAL COMPANY
To: LJPC MERGER SUB, INC.
Reel/Frame 028467/0776 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2012
From: SOLANA THERAPEUTICS, INC.
To: LA JOLLA PHARMACEUTICAL COMPANY
Reel/Frame 027583/0268 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2010
From: PROSPECT THERAPEUTICS, INC.
To: TANG CAPITAL PARTNERS L.P.
Reel/Frame 024114/0769 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2010
From: PROSPECT PHARMACEUTICALS, INC.
To: TANG CAPITAL PARTNERS LP
Reel/Frame 024103/0753 →
ASSET PURCHASE AGREEMENT Recorded Mar 19, 2010
From: TANG CAPITAL PARTNERS LP
To: SOLANA THERAPEUTICS, INC.
Reel/Frame 024103/0764 →
RELEASE OF ATTORNEY'S LIEN Recorded Sep 23, 2009
From: ROPES & GRAY LLP
To: PROSPECT THERAPEUTICS, INC.
Reel/Frame 023273/0037 →
NOTICE OF ATTORNEY'S LIEN Recorded Jun 18, 2009
From: PROSPECT THERAPEUTICS, INC.
To: ROPES & GRAY LLP
Reel/Frame 022846/0200 →
CHANGE OF NAME Recorded Feb 20, 2007
From: MARLBOROUGH RESEARCH AND DEVELOPMENT, INC.
To: PROSPECT PHARMACEUTICALS, INC.
Reel/Frame 018917/0374 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2007
From: DEGIACOMO, MARK G., CHAPTER 7 TRUSTEE GLYCOGENESYS, INC.
To: MARLBOROUGH RESEARCH AND DEVELOPMENT INC.
Reel/Frame 018917/0380 →
CHANGE OF NAME Recorded Feb 20, 2007
From: PROSPECT PHARMACEUTICALS, INC.
To: PROSPECT THERAPEUTICS, INC.
Reel/Frame 018917/0395 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2007
From: DEGIACOMO, MARK G., CHAPTER 7 TRUSTEE, GLYCOGENESYS, INC.
To: MARLBOROUGH RESEARCH AND DEVELOPMENT INC.
Reel/Frame 018777/0643 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 25, 2005
From: STAPLES, MARK; ROLKE, JAMES
To: GLYCOGENESYS, INC.
Reel/Frame 016568/0411 →