IP Library Granted Patent US 12,397,283
Granted Patent B1
US 12,397,283 · App. 18/439,667 · Granted Aug 26, 2025

Chromatography media and methods for producing them

Inventors: Marc Hummersone (Hertfordshire, GB); Benjamin Wallis (Hertfordshire, GB); Frederic Leroux (Hertfordshire, GB); William Howard Albert Law (Hertfordshire, GB)
Assignee: CYTIVA BIOPROCESS R&D AB
B01J20/285B01D15/327B01D15/362B01D15/363B01J20/265B01J20/3212B01J20/3274B01J20/3278B01J39/05B01J39/07B01J41/05B01J41/07B01J2219/00844B01J2219/00846
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Quick Facts
Patent No.
US 12,397,283
App. No.
18/439,667
Granted
Aug 26, 2025
Kind
B1
Abstract

The invention discloses a functionalised chromatography medium, comprising: i) at least one non-woven layer of polymeric nanofibres comprising a plurality of nanofibre-nanofibre fusion points; ii) a grafted polymer coating covering the polymeric nanofibres and the nanofibre-nanofibre fusion points; iii) a plurality of ligand groups covalently bound to the grafted polymer coating, wherein the ligand groups are capable of interacting with a target biomolecule.

Claims (28)

1. A functionalised chromatography medium, comprising:

i) at least one non-woven layer of polymeric nanofibres comprising a plurality of nanofibre-nanofibre fusion points;

ii) a plurality of grafted polymer molecules single-point covalently tethered to said polymeric nanofibers, wherein the plurality of grafted polymer molecules are formed from a plurality of compounds of formula

and

iii) a plurality of ligand groups covalently bound to said grafted polymer molecules, wherein the plurality of ligand groups comprise weak or strong anion exchange ligand groups, weak or strong cation exchange ligand groups, hydrophobic interaction chromatography ligand groups, mixed mode chromatography ligand groups, or affinity ligand groups.

2. A functionalised chromatography medium, comprising:

i) at least one non-woven layer of polymeric nanofibres comprising a plurality of nanofibre-nanofibre fusion points;

ii) a grafted polymer coating covering said polymeric nanofibres and said nanofibre-nanofibre fusion points, wherein the grafted polymer coating comprises polymer molecules which are single-point covalently tethered to said polymeric nanofibres, and wherein the polymer molecules comprise glycidol monomer residues formed from a plurality of compounds of formula

and

iii) a plurality of ligand groups covalently bound to said grafted polymer coating, wherein the plurality of ligand groups comprise weak or strong anion exchange ligand groups, weak or strong cation exchange ligand groups, hydrophobic interaction chromatography ligand groups, mixed mode chromatography ligand groups, or affinity ligand groups.

3. The functionalised chromatography medium of claim 2 , wherein said grafted polymer coating is a conformal coating.

4. The functionalised chromatography medium of claim 1 , comprising 500-60,000 μmol/g of the grafted polymer on the functionalised chromatography medium.

5. The functionalised chromatography medium of claim 1 , comprising 100-2,000 μmol/g of the ligand groups on the functionalised chromatography medium.

6. The functionalised chromatography medium of claim 1 , wherein said polymer nanofibres with said grafted polymer coating have diameters of 100-1000 nm.

7. The functionalised chromatography medium of claim 1 , having an average pore size of 200-800 nm.

8. The functionalised chromatography medium of claim 1 , having a bubblepoint pore size of 0.9-1.2 μm.

9. The functionalised chromatography medium of claim 1 , having a pore volume fraction of 50-90%.

10. The functionalised chromatography medium of claim 1 , wherein the polymeric nanofibres comprise regenerated cellulose.

11. The functionalised chromatography medium of claim 10 , wherein the polymeric nanofibres comprise saponified cellulose acetate.

12. The functionalised chromatography medium of claim 1 , wherein the grafted polymer molecules comprise branched polymer molecules.

13. The functionalised chromatography medium of claim 1 , wherein the grafted polymer coating comprises divinylsulfone monomer residues.

14. The functionalised chromatography medium of claim 1 , wherein said ligand groups are weak or strong anion exchange ligand groups selected from —N + (CH 3 ) 3 , —N + (C 2 H 5 ) 2 H, CH 2 CH 2 N + (C 2 H 5 ) 2 H, —CH 2 CH 2 N + (C 2 H 5 ) 2 (CH 2 CH(OH)CH 3 ), —O—CH 2 CH 2 —N + (CH 3 ) 3 , —CH 2 CH 2 N + (CH 3 ) 3 , and —CH 2 CH 2 N + (CH 3 ) 2 H moieties.

15. The functionalised chromatography medium of claim 1 , wherein said ligand groups are weak or strong cation exchange ligand groups selected from —O—CH 2 COO, —CH 2 COO, —SO 3 , —CH 2 CH 2 CH 2 SO 3 , —CH 2 CH 2 SO 3 , and —P(OH) 2 O— moieties.

16. The functionalised chromatography medium of claim 1 , wherein said ligand groups are hydrophobic interaction chromatography ligand groups selected from propyl, butyl, phenyl, and octyl groups.

17. The functionalised chromatography medium of claim 1 , wherein said ligand groups are affinity ligand groups comprising metal cations selected from Cu 2+ , Ni 2+ , Zn 2+ , and Co 2+ .

18. The functionalised chromatography medium of claim 1 , wherein said ligand groups are affinity ligand groups, and wherein said affinity ligand groups comprise mutated immunoglobulin-binding domains of Protein A.

19. The functionalised chromatography medium of claim 1 , wherein said ligand groups comprise native domains of Protein A.

20. A chromatography cartridge comprising the functionalised chromatography medium of claim 1 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2024
From: LEROUX, FREDERIC; LAW, WILLIAM; WALLIS, BENJAMIN; HUMMERSONE, MARC
To: PURIDIFY LTD.
Reel/Frame 066826/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2024
From: PURIDIFY LTD.
To: CYTIVA BIOPROCESS R&D AB
Reel/Frame 066826/0919 →
Priority Claims (1)
GB 1800448 · Jan 11, 2018 · national
Continuity (1)
Continuation 16959373
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