IP Library Granted Patent US 10,844,345
Granted Patent B2
US 10,844,345 · App. 15/303,735 · Granted Nov 24, 2020

High density fill and draw fermentation process

Inventor: Mads Laustsen (Gentofte, DK)
Assignee: CMC BIOLOGICS A/S
C12M47/10C12M33/14C12P21/02
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 10,844,345
App. No.
15/303,735
Granted
Nov 24, 2020
Kind
B2
Abstract

The present invention relates to a high cell density fermentation fill and draw process for producing a product in a bioreactor system wherein during the fermentation, medium comprising impurities is removed via the impurity filter unit while new fresh medium is added to the cell culture vessel to replenish consumed nutrients and expelled medium.

Claims (39)

1. A method for producing a product selected from:

A) a biopolymer expressed by a cell,

B) a cell, and

C) a microorganism

in a bioreactor system in a fill and draw process, wherein the bioreactor system comprises:

a cell culture vessel ( 1 ) comprising cells or microorganisms in a suitable medium;

a cell culture vessel inlet ( 2 ) for providing medium to the cell culture vessel ( 1 );

an impurity filter unit ( 3 ), which allows impurities with a molecular weight (MW) below the MW of the product, to be removed from the cell culture vessel ( 1 ), while retaining the product inside the cell culture vessel ( 1 ) and wherein the impurity filter unit ( 3 ) is in fluid connection with the medium inside the cell culture vessel ( 1 ); and

a harvest outlet ( 4 ), which allows the medium comprising the product and impurities to be removed from the cell culture vessel ( 1 );

wherein the method comprises the following steps:

(a) fermenting the cells expressing the biopolymer, the cells, or the microorganisms in the cell culture vessel ( 1 ) in a suitable medium under suitable conditions and for a sufficient time until;

(i) the biopolymer reaches a specified concentration of at least 0.1 g/L,

(ii) the cells reach a cell density of at least 40 million cells/ml, or

(iii) the microorganisms reaches a specified cell density or density of the microorganisms is higher than that obtainable with the bioreactor system without the impurity filter unit ( 3 ) under identical conditions, wherein during the fermentation, medium comprising impurities is removed via the impurity filter unit ( 3 ), and a first fresh medium is added through the cell culture vessel inlet ( 2 ) to replace or partly replace the medium removed through the impurity filter unit ( 3 );

(b) removing a specified volume of the medium comprising the product and impurities from the cell culture vessel (i) through the harvest outlet ( 4 ) before nutrients in said medium become exhausted, and

(c) after said removal of medium in step (b), adding a second fresh medium to the cell culture vessel ( 1 ) via the cell culture vessel inlet ( 2 ) to replace or partly replace the medium removed through the harvest outlet ( 4 ) in step (b); and

(d) optionally, adding a third fresh medium through the cell culture vessel inlet ( 2 ) during step (b), during step (c), or during both step (b) and (c), after removing the medium comprising impurities via the impurity filter unit ( 3 );

(e) optionally, repeating step (b) and (c),

(f) optionally repeating step (d), and

(g) optionally, purifying the product, from the specified volume of medium comprising the product selected from the biopolymer expressed by the cell, the cell, or the microorganism, and impurities.

2. The method according to claim 1 , wherein during step (a) fermenting the cells expressing the biopolymer, the cells, or the microorganisms in the cell culture vessel ( 1 ) in a suitable medium under suitable conditions and for a sufficient time until the biopolymer reaches a concentration of 0.1 g/L, the cells reach a cell density of 40 million cells/mL, or the microorganism reach a specified density before removing impurities via the impurity filter unit ( 3 ).

3. The method according to claim 1 , wherein preceding step (a) fermenting the cells expressing the biopolymer, the cells, or the microorganism in the cell culture vessel ( 1 ) in a suitable medium under suitable conditions and for a sufficient time until the biopolymer reaches a concentration of 0.1 g/L, the cells reach a cell density of 40 million cells/mL, or the microorganisms reaches a specified density without removing impurities via the impurity filter unit ( 3 ).

4. The method according to claim 1 , wherein the first, second and optionally third fresh medium are selected from the same composition of medium.

5. The method according to claim 1 , further comprising step (d).

6. The method according to claim 1 , further comprising step (e) wherein steps (b) and (c) are repeated from at least 2 to 30 times.

7. The method according to claim 1 , further comprising step (f) wherein step (d) is repeated from at least 2 to 30 times.

8. The method according to claim 1 , further comprising step (g), purifying the product, from the specified volume of medium comprising the product selected from the biopolymer expressed by the cell, the cell, or the microorganism, and impurities.

9. The method according to claim 1 , wherein in step (a) fermenting in the cell culture vessel ( 1 ) is performed with at least 50 L of suitable medium.

10. The method according to claim 1 , wherein in step (a) fermenting in the cell culture vessel ( 1 ) is performed until the cells reach a cell density of at least 50 million cells/ml.

11. The method according to claim 1 , wherein in step (b) a specified volume of at least 30% of the medium comprising the product and impurities is removed from the cell culture vessel (i) through the product harvest module ( 4 ).

12. The method according claim 1 , wherein the cell expressing the biopolymer is a mammalian cell.

13. The method according to claim 1 , wherein the biopolymer is a recombinant protein.

14. The method according to claim 1 , wherein the biopolymer is an antibody or a fragment thereof or a blood-coagulation factor.

15. The method according to claim 1 , wherein the impurity filter has a pore size with a nominal molecular weight cut-off (NMWC) with a maximum of at least 10% of the molecular weight of the biopolymer.

16. The method according to claim 1 , wherein in step (b) a specified volume of at least 50% of the medium comprising the product and impurities is removed from the cell culture vessel ( 1 ) through the product harvest module ( 4 ).

17. The method according to claim 1 , wherein in step (b) a specified volume of at least 80% of the medium comprising the product and impurities is removed from the cell culture vessel ( 1 ) through the product harvest module ( 4 ).

18. The method according claim 1 , wherein the cell expressing the biopolymer is a mammalian cell selected from a CHO, NSO, PER.C6®, BHK, or HEK cell.

19. The method according to claim 1 , wherein the biopolymer is a recombinant protein selected from Human growth hormone, Follicle-stimulating hormone, Factor VIII, Factor VII, Factor IX Erythropoietin (EPO), Granulocyte colony-stimulating factor (G-CSF), Interferon (IF), Insulin, Insulin derivative or Insulin-like growth factor 1.

20. The method according to claim 1 , wherein the impurity filter has a pore size with a nominal molecular weight cut-off (NMWC) with a maximum of at least 40% of the molecular weight of the biopolymer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 27, 2016
From: LAUSTEN, MADS
To: CMS BIOLOGICS A/S
Reel/Frame 040772/0377 →
Priority Claims (1)
EP 14164862 · Apr 16, 2014 · regional
Continuity (1)
Related Publication 20170067010A1 · Mar 9, 2017