Anionic exchange-hydrophobic mixed mode chromatography resins
AssigneeBio-Rad Laboratories, Inc.
InventorsCHRISTOPHER BELISLE, XUEMEI HE, HONG CHEN, YUEPING XU, JIALI LIAO
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Abstract
Chromatography resins having anionic exchange-hydrophobic mixed mode ligands and methods of using such resins are provided.
Claims23
A chromatography matrix covalently linked to a ligand having the following formula:
- Chromatography matrix-(X)—N(R1)—(R2-L)n-Ar
- or an anionic salt thereof,
- wherein:
- X is a spacer;
- R1 is hydrogen or C1 to C6 alkyl optionally substituted with an —OH;
- R2 is C2 to C6 alkyl or C4 to C6 cycloalkyl;
- L is NR4, O, or S;
- n=1 or 2;
- and
- Ar is a 6-10 membered ring and:
- if Ar is aryl, the aryl is optionally substituted with up to five C1 to C3 unsubstituted alkyl, C3 to C6 branched alkyl, unsubstituted aryl, or fluorine groups;
- or
- if Ar is heteroaryl, the heteroaryl is optionally substituted with up to four unsubstituted alkyl groups,
- with the proviso that when R1 is hydrogen, R2 is C2 alkyl, L is NR4 or O, and n is 1, Ar is not phenyl.
A chromatography resin having the following formula:
- Chromatography matrix-(X)—N—[(R2-L)n-Ar]2
- or an anionic salt thereof,
- wherein:
- X is a spacer;
- R2 is C2 to C6 alkyl or C4 to C6 cycloalkyl;
- L is NR4, O, or S;
- n=1 or 2;
- and
- Ar is a 6-10 membered ring and:
- if Ar is aryl, the aryl is optionally substituted with up to five C1 to C3 unsubstituted alkyl, C3 to C6 branched alkyl, unsubstituted aryl, or fluorine groups;
- or
- if Ar is heteroaryl, the heteroaryl is optionally substituted with up to four unsubstituted alkyl groups.
A chromatography resin prepared by reacting any one of the ligands of Table 1 with a chromatography matrix by any one of reductive amination, epoxide chemistry, or azalactone chemistry.
A chromatography resin prepared by reacting any one of the ligands of Table 2 with a chromatography matrix by epoxide chemistry.
Dependencies are inferred from the claim text.