IP Library Granted Patent US 12,161,993
Granted Patent B2
US 12,161,993 · App. 16/638,512 · Granted Dec 10, 2024

Chromatography carrier, ligand-immobilizing carrier, chromatography column, target substance purification method, and chromatography carrier production method

Inventor: Tomoya Norinobu (Minato-ku, JP)
Assignees: JSR CORPORATION; JSR LIFE SCIENCES CORPORATION; JSR Life Sciences, LLC; JSR MICRO N.V.
B01J20/267B01D15/10B01D15/3809B01D15/3828B01J20/285B01J20/3085B01J20/3208B01J20/3219C07K1/22C07K16/32
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Quick Facts
Patent No.
US 12,161,993
App. No.
16/638,512
Granted
Dec 10, 2024
Kind
B2
Abstract

To provide a chromatography carrier that has excellent antifouling properties and exhibits excellent pressure-resistant performance and shatter-resistant performance. A chromatography carrier comprising: a polymer having a partial structure containing at least two groups represented by —C(═O)—NH—.

Claims (30)

1. A ligand-immobilizing carrier, comprising:

a chromatography carrier; and

an antibody affinity ligand immobilized to the chromatography carrier,

wherein the chromatography carrier comprises a polymer having a structural unit (A) of formula (9) and a structural unit (B) of formula (10), and wherein a residue of a functional group capable of immobilizing a ligand in the structural unit (B) is crosslinked by a crosslinked structure of formula (2-1) or (2-4), the formula (9) is

where R 8 is a hydrogen atom or a methyl group, R 9 is a single bond or a divalent linking group, and Z 1 is a functional group capable of immobilizing a ligand, and the formula (10) is

where R 10 is a hydrogen atom or a methyl group, R 11 is a single bond or a divalent linking group, Z 2 is a residue of a functional group capable of immobilizing a ligand, and ** is a bond that is bonded to the crosslinked structure of the formula (2-1) or (2-4)

where R 2 is a single bond or a divalent linking group, * is a chemical bond, and each of R 4a and R 4b is independently a divalent linking group.

2. The ligand-immobilizing carrier of claim 1 , wherein the crosslinked structure has the formula (2-1).

3. The ligand-immobilizing carrier of claim 1 , wherein the polymer further comprises a structural unit derived from an aromatic vinyl-based crosslinkable monomer.

4. The ligand-immobilizing carrier of claim 1 , wherein the antibody affinity ligand is an immunoglobulin-binding protein.

5. The ligand-immobilizing carrier of claim 1 , wherein R 2 is (i) a divalent hydrocarbon group having 1 to 40 carbon atoms or (ii) a group comprising an ether bond, an amide bond, an ester bond, or two or more of any of these, between carbon-carbon atoms of a divalent hydrocarbon group having 2 to 40 carbon atoms.

6. The ligand-immobilizing carrier of claim 1 , wherein R 2 is (i) an alkanediyl group having 1 to 40 carbon atoms or (ii) a group comprising an ether bond, an amide bond, an ester bond, or two or more of any of these, between carbon-carbon atoms of an alkanediyl group having 2 to 40 carbon atoms.

7. The ligand-immobilizing carrier of claim 1 , wherein the antibody affinity ligand is protein A, protein G, or protein L.

8. The ligand-immobilizing carrier of claim 1 , wherein the chromatography carrier is a particulate chromatography carrier.

9. The ligand-immobilizing carrier of claim 1 , wherein the chromatography carrier is a porous chromatography carrier.

10. The ligand-immobilizing carrier of claim 2 , wherein the polymer further comprises a structural unit derived from an aromatic vinyl-based crosslinkable monomer.

11. The ligand-immobilizing carrier of claim 2 , wherein the antibody affinity ligand is an immunoglobulin-binding protein.

12. The ligand-immobilizing carrier of claim 2 , wherein R 2 is (i) a divalent hydrocarbon group having 1 to 40 carbon atoms or (ii) a group comprising an ether bond, an amide bond, an ester bond, or two or more of any of these, between carbon-carbon atoms of a divalent hydrocarbon group having 2 to 40 carbon atoms.

13. The ligand-immobilizing carrier of claim 2 , wherein R 2 is (i) an alkanediyl group having 1 to 40 carbon atoms or (ii) a group comprising an ether bond, an amide bond, an ester bond, or two or more of any of these, between carbon-carbon atoms of an alkanediyl group having 2 to 40 carbon atoms.

14. The ligand-immobilizing carrier of claim 2 , wherein the antibody affinity ligand is protein A, protein G, or protein L.

15. The ligand-immobilizing carrier of claim 2 , wherein the chromatography carrier is a particulate chromatography carrier.

16. The ligand-immobilizing carrier of claim 2 , wherein the chromatography carrier is a porous chromatography carrier.

17. A chromatography column, comprising:

the ligand-immobilizing carrier recited in claim 1 ; and

a column container,

wherein the carrier is comprised in the column container.

18. A method for purifying a target substance by chromatography, comprising:

bringing the ligand-immobilizing carrier recited in claim 1 into contact with the target substance.

19. A method for purifying a target substance by chromatography, comprising:

bringing the ligand-immobilizing carrier recited in claim 1 into contact with a sample containing the target substance.

Assignments (8)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2026
From: MBL MATERIALS CO., LTD.
To: JSR CORPORATION
Reel/Frame 074227/0181 →
CHANGE OF NAME Recorded Mar 25, 2026
From: JSR LIFE SCIENCES CORPORATION
To: MBL MATERIALS CO., LTD.
Reel/Frame 075228/0228 →
CHANGE OF ADDRESS Recorded Mar 25, 2026
From: MBL MATERIALS CO., LTD.
To: MBL MATERIALS CO., LTD.
Reel/Frame 075228/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2026
From: JSR MICRO NV
To: JSR CORPORATION
Reel/Frame 074082/0011 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2026
From: JSR LIFE SCIENCES, LLC
To: JSR CORPORATION
Reel/Frame 074082/0107 →
MERGER AND CHANGE OF NAME Recorded Feb 18, 2025
From: JSR CORPORATION; JICC-02 CO., LTD.
To: JSR CORPORATION
Reel/Frame 070242/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2021
From: JSR MICRO, INC.
To: JSR LIFE SCIENCES, LLC
Reel/Frame 057092/0068 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2020
From: NORINOBU, TOMOYA
To: JSR CORPORATION; JSR LIFE SCIENCES CORPORATION; JSR MICRO INC.; JSR MICRO N.V.
Reel/Frame 051792/0844 →
Priority Claims (1)
JP 2017-160120 · Aug 23, 2017 · national
Continuity (1)
Related Publication 20200360894A1 · Nov 19, 2020