Adsorptive membranes for trapping viruses

US10316296B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10316296-B2
Application numberUS-201715820766-A
CountryUS
Kind codeB2
Filing dateNov 22, 2017
Priority dateJul 14, 2006
Publication dateJun 11, 2019
Grant dateJun 11, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A disposable, virus-trapping membrane, and a corresponding method to remove viruses from solution are described. The membrane includes a disposable, micro-porous filter membrane and a ligand immobilized on the membrane. The ligand irreversibly and selectively binds viruses. The ligand also has a pKa sufficiently high to repel antibodies via electrostatic charge repulsion.

First claim

Opening claim text (preview).

What is claimed is: 1. A disposable, virus-trapping membrane comprising: a disposable, micro-porous filter membrane; and a multi-modal anion-exchange ligand that has a pKa sufficiently high to repel basic proteins via electrostatic charge repulsion immobilized on the filter membrane, wherein the ligand comprises one or more of tyrosinol, tryptophanol, octopamine, 1,3-diamino-2-hydroxypropane, tris(2-aminoethyl)amine, and agmatine, wherein the virus-trapping membrane: (a) binds neutral viruses; and (b) yields a log-reduction value (LRV) of at least 1.0 for the neutral viruses disposed in a solution comprising 50 mM salt. 2. The virus-trapping membrane of claim 1 , wherein the ligand comprises one or more of tryptophanol, tris(2-aminoethyl)amine, and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 1.0 for neutral viruses disposed in a solution comprising 150 mM salt. 3. The virus-trapping membrane of claim 1 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 50 mM salt. 4. The virus-trapping membrane of claim 1 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 150 mM salt. 5. The virus-trapping membrane of claim 1 , wherein the filter membrane comprises a polymer substrate selected from the group consisting of polyvinylidene difluoride, polytetrafluorethylene, polyamides, polyamide-imides, polysulfones, polyethersulfones, and polyphenylsulfones. 6. The virus-trapping membrane of claim 1 , wherein the ligand comprises agmatine. 7. The virus-trapping membrane of claim 6 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 1.0 for neutral viruses disposed in a solution comprising 150 mM salt. 8. The virus-trapping membrane of claim 6 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 50 mM salt. 9. The virus-trapping membrane of claim 6 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 150 mM salt. 10. The virus-trapping membrane of claim 6 , wherein the filter membrane comprises a polymer substrate selected from the group consisting of polyvinylidene difluoride, polytetrafluorethylene, polyamides, polyamide-imides, polysulfones, polyethersulfones, and polyphenylsulfones. 11. The virus-trapping membrane of claim 1 , wherein the ligand comprises tris(2-aminoethyl)amine. 12. The virus-trapping membrane of claim 11 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 1.0 for neutral viruses disposed in a solution comprising 150 mM salt. 13. The virus-trapping membrane of claim 11 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 50 mM salt. 14. The virus-trapping membrane of claim 11 , wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 150 mM salt. 15. The virus-trapping membrane of claim 11 , wherein the filter membrane comprises a polymer substrate selected from the group consisting of polyvinylidene difluoride, polytetrafluorethylene, polyamides, polyamide-imides, polysulfones, polyethersulfones, and polyphenylsulfones. 16. The method of claim 1 , wherein the filter membrane has a membrane pore size of from 0.1 μm to 10 μm. 17. The virus-trapping membrane of claim 16 , wherein the ligand comprises one or more of tryptophanol, tris(2-aminoethyl)amine, and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 1.0 for neutral viruses disposed in a solution comprising 150 mM salt. 18. The virus-trapping membrane of claim 16 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 50 mM salt. 19. The virus-trapping membrane of claim 16 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine, and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 150 mM salt. 20. The virus-trapping membrane of claim 16 , wherein the filter membrane comprises a polymer substrate selected from the group consisting of polyvinylidene difluoride, polytetrafluorethylene, polyamides, polyamide-imides, polysulfones, polyethersulfones, and polyphenylsulfones. 21. The virus-trapping membrane of claim 16 , wherein the ligand comprises agmatine. 22. The virus-trapping membrane of claim 16 , wherein the ligand comprises tris(2-aminoethyl)amine. 23. A method of removing viruses from a solution suspected of containing viruses, the method comprising contacting a solution suspected of containing viruses with the virus-trapping membrane of claim 1 .

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Classifications

  • consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds · CPC title

  • being less than 2 nm, i.e. micropores or nanopores · CPC title

  • involving a particular spacer or linking group, e.g. for attaching an active group · CPC title

  • Adsorbents being present on the surface of the membranes or in the pores · CPC title

  • Coating or impregnation layers comprising different type of functional groups or interactions, e.g. different ligands in various parts of the sorbent, mixed mode, dual zone, bimodal, multimodal, ionic or hydrophobic, cationic or anionic, hydrophilic or hydrophobic · CPC title

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What does patent US10316296B2 cover?
A disposable, virus-trapping membrane, and a corresponding method to remove viruses from solution are described. The membrane includes a disposable, micro-porous filter membrane and a ligand immobilized on the membrane. The ligand irreversibly and selectively binds viruses. The ligand also has a pKa sufficiently high to repel antibodies via electrostatic charge repulsion.
Who is the assignee on this patent?
Wisconsin Alumni Res Found
What technology area does this patent fall under?
Primary CPC classification C12N7/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).