IP Library Granted Patent US 11,553,712
Granted Patent B2
US 11,553,712 · App. 13/994,207 · Granted Jan 17, 2023

Glycols as pathogen inactivating agents

Inventor: Sami Chtourou (Elancourt, FR)
Assignee: Laboratoire Français du Fractionnement et des Biotechnologies
A01N31/02A61L2/0088A61L2/18A61L2202/22
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Quick Facts
Patent No.
US 11,553,712
App. No.
13/994,207
Granted
Jan 17, 2023
Kind
B2
Abstract

The disclosure relates to uses, methods and compositions for the inactivation of pathogens in biological compositions, using a glycol as a pathogen inactivating agent.

Claims (20)

1. A method for inactivating and/or eliminating an enveloped virus for the production of a recombinant protein, said method comprising conducting affinity chromatography on a biological composition containing a recombinant protein, wherein the recombinant protein is eluted during the affinity chromatography with an elution buffer comprising propylene glycol, wherein the biological composition is a blood composition, a milk composition, urine, sweat, sputum, feces, spinal fluid, or cellular or tissue extracts, wherein the concentration of propylene glycol in the elution buffer is between 40 and 50% (v/v), and wherein the propylene glycol is not combined with arginine.

2. The method of claim 1 , wherein said method is performed at a temperature between 15 and 25° C.

3. The method of claim 1 , wherein said method is performed at a pH between 7.0 and 8.0.

4. The method of claim 1 , wherein the affinity chromatography column is washed with a wash buffer prior to elution of the recombinant protein, wherein the concentration of propylene glycol in the wash buffer is between 30 and 40% (v/v).

5. The method of claim 1 , wherein recombinant protein is maintained in the elution buffer with a concentration of propylene glycol between 40 and 50% (v/v) for less than 6 hours.

6. A method for inactivating and/or eliminating a virus during a purification of a protein from a biological composition, said method comprising contacting said biological composition during the purification of the protein with a glycol to inactivate the virus, wherein the concentration of glycol after the contacting step is between 40 and 50% (v/v) of the biological composition, and wherein the glycol is not combined with arginine.

7. The method of claim 6 , wherein said glycol is propylene glycol.

8. The method of claim 6 , wherein said biological composition is a blood composition or a milk composition.

9. The method of claim 6 , wherein the virus is an enveloped virus.

10. The method of claim 6 , wherein said method results in a viral elimination equal or greater than 4 Log 10 TCID, wherein the TCID is according to the methods of Kärber and/or Spearman-Kärber.

11. The method of claim 6 , wherein said method is performed at a temperature between 15 and 25° C.

12. The method of claim 6 , wherein said method is performed at a pH between 7.0 and 8.0.

13. A method for inactivating a virus during the purification of a protein from a biological composition, said method comprising contacting an eluate with a glycol during the process of purification of the protein from the biological composition to inactivate and/or eliminate the virus, wherein the concentration of glycol after the contacting step is between 40 and 50% (v/v) of the elute, and wherein the glycol is not combined with arginine.

14. The method of claim 13 , wherein said glycol is propylene glycol.

15. The method of claim 13 , wherein said biological composition is a blood composition or a milk composition.

16. The method of claim 13 , wherein the virus is an enveloped virus.

17. The method of claim 16 , wherein said enveloped virus is selected from the group consisting of X-MuLV, PRV, BVDV and TGEV virus.

18. The method of claim 13 , wherein said method results in a viral elimination equal or greater than 4 Log 10 TCID, wherein the TCID is according to the methods of Kärber and/or Spearman-Kärber.

19. The method of claim 13 , wherein said method is performed at a temperature between 15 and 25° C.

20. The method of claim 13 , wherein said method is performed at a pH between 7.0 and 8.0.

Assignments (4)
CHANGE OF OWNER/APPLICANT'S ADDRESS Recorded Apr 3, 2023
From: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
To: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 063237/0439 →
CHANGE OF OWNER/APPLICANT'S ADDRESS Recorded Sep 21, 2022
From: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
To: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 061493/0885 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2013
From: CHTOUROU, SAMI
To: LABORATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 030835/0488 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2013
From: LFB-BIOTECHNOLOGIES
To: LABORATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 030802/0820 →
Continuity (2)
Provisional Application 61428416 · Dec 30, 2010
Related Publication 20130324619A1 · Dec 5, 2013