IP Library Granted Patent US 8,008,476
Granted Patent B2
US 8,008,476 · App. 12/661,979 · Granted Aug 30, 2011

Room temperature stable agarose solutions

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Quick Facts
Patent No.
US 8,008,476
App. No.
12/661,979
Granted
Aug 30, 2011
Kind
B2
Abstract

The present invention provides methods for making porous crosslinked polysaccharide hydrogel coated structures. The methods include impregnating a porous substrate with a room temperature stable aqueous polysaccharide solution containing, water, a polysaccharide having a concentration in the aqueous solution from about 0.1% to about 20%, a gel-inhibiting agent having a concentration in the aqueous solution from about 18 to about 54%, and an anionic fluorosurfactant having a concentration in the aqueous solution from about 0.001% to about 10% by total weight of the aqueous solution. Followed by evaporating the water from the polysaccharide coating; and exposing the dehydrated polysaccharide coating to a gelling agent form a porous polysaccharide hydrogel coated substrate. The hydrogel coated substrate is exposed to a crosslinking agent to form a porous crosslinked polysaccharide hydrogel coated substrate.

Claims (34)

1. A method for making porous crosslinked polysaccharide hydrogel coated structures comprising:

a) impregnating a porous substrate selected from the group consisting of fibers, woven fabrics, non-woven fabrics, membranes, mats, monolithic honeycomb structures, felt sheets, poly(HIPES) monolithic structures, three dimensional structures, sponges, and porous beads, with a room temperature stable aqueous polysaccharide solution forming a room temperature stable aqueous polysaccharide coating on the substrate, the aqueous solution containing,

i) water,

ii) a polysaccharide having a concentration in the aqueous solution from about 0.1% to about 20%, and selected from the group consisting of agarose, dextrans, cyclodextrins and blends thereof,

iii) a gel-inhibiting agent having a concentration in the aqueous solution from about 18 to about 54%, and selected from the group consisting of ZnCl 2 , LiCl, NaOH, LiNO 3 , LiOH, LiSCN and mixtures thereof, and

iv) an anionic fluorosurfactant having a concentration in the aqueous solution from about 0.001% to about 10% by total weight of the aqueous solution;

b) evaporating the water from the polysaccharide coating;

c) exposing the dehydrated polysaccharide coating to a gelling agent selected from the group consisting of acetone and acetone in water to form a porous polysaccharide hydrogel coated substrate; and

d) exposing the hydrogel coated substrate to a crosslinking agent selected from the group consisting of epichlorohydrin, multifunctional epoxy compounds, multifunctional halide compounds, formaldehyde, gluteraldehyde, multifunctional aldehyde compounds, bis(2-hydroxy ethyl)sulfone, dimethyldichlorosilane, dimethylolurea, dimethylol ethylene urea, diisocyanate compounds, and polyisocyanate compounds to form a porous crosslinked polysaccharide hydrogel coated substrate.

2. The method according to claim 1 , further comprising step f) rinsing the crosslinked polysaccharide hydrogel coated substrate with water.

3. The method according to claim 1 , wherein the polysaccharide is agarose.

4. The method according to claim 1 , wherein the polysaccharide is dextran.

5. The method according to claim 1 , wherein the porous beads are selected from the group consisting of porous glass beads, porous styrene beads, porous silica beads, and porous zirconia beads.

6. A method for making porous crosslinked agarose hydrogel coated structures comprising:

a) impregnating a porous substrate selected from the group consisting of fibers, woven fabrics, non-woven fabrics, membranes, mats, monolithic honeycomb structures, felt sheets, poly(HIPES) monolithic structures, three dimensional structures, sponges, and porous beads, with a room temperature stable aqueous agarose solution containing,

i) water,

ii) agarose having a concentration in the aqueous solution from about 0.1% to about 20%, and

iii) a gel-inhibiting agent having a concentration in the aqueous solution from about 18 to about 54%, and selected from the group consisting of ZnCl 2 , LiCl, NaOH, LiNO 3 , LiOH, LiSCN and mixtures thereof;

b) forming a room temperature stable aqueous agarose coating on the substrate;

c) evaporating the water from the agarose coating;

d) exposing the agarose coating to a gelling agent selected from the group consisting of acetone and acetone in water to form a porous agarose hydrogel coated substrate; and

e) exposing the agarose hydrogel coated substrate to a crosslinking agent selected form the group consisting of epichlorohydrin, multifunctional epoxy compounds, multifunctional halide compounds, formaldehyde, gluteraldehyde, multifunctional aldehyde compounds, bis(2-hydroxy ethyl)sulfone, dimethyldichlorosilane, dimethylolurea, dimethylol ethylene urea, diisocyanate compounds, and polyisocyanate compounds to form a porous crosslinked agarose hydrogel coated substrate.

7. The method according to claim 6 , further comprising step f) rinsing the crosslinked agarose hydrogel coated substrate with water.

8. The method according to claim 6 , further comprising an anionic fluorosurfactant having a concentration in the aqueous solution from about 0.001% to about 10% by total weight of the aqueous solution.

9. A method for making a liquid chromatography media comprising: a

a) impregnating a porous substrate selected from the group consisting of fibers, woven fabrics, non-woven fabrics, membranes, mats, monolithic honeycomb structures, felt sheets, poly(HIPES) monolithic structures, three dimensional structures, sponges, and porous beads, with a room temperature stable aqueous agarose solution, the aqueous agarose solution containing,

i) water,

ii) agarose having a concentration in the aqueous solution from about 0.1% to about 20%,

iii) a gel-inhibiting agent having a concentration in the aqueous solution from about 18 to about 54%, and selected from the group consisting of ZnCl 2 , LiCl, NaOH, LiNO 3 , LiOH, LiSCN and mixtures thereof, and

iv) an anionic fluorosurfactant having a concentration in the aqueous solution from about 0.001% to about 10% by total weight of the aqueous solution;

b) forming a room temperature stable aqueous agarose coating on the substrate;

c) evaporating the water from the agarose coating;

d) exposing the agarose coating to a gelling agent selected from the group consisting of acetone and acetone in water to form a porous polysaccharide hydrogel coated substrate; and

e) exposing the hydrogel coated substrate to a crosslinking agent selected form the group consisting of epichlorohydrin, multifunctional epoxy compounds, multifunctional halide compounds, formaldehyde, gluteraldehyde, multifunctional aldehyde compounds, bis(2-hydroxy ethyl)sulfone, dimethyldichlorosilane, dimethylolurea, dimethylol ethylene urea, diisocyanate compounds, and polyisocyanate compounds to form a porous crosslinked agarose hydrogel coated substrate.

Assignments (3)
CHANGE OF ADDRESS Recorded Feb 15, 2018
From: EMD MILLIPORE CORPORATION
To: EMD MILLIPORE CORPORATION
Reel/Frame 045341/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2012
From: SADER, JON DENNIS
To: GREEN KNIGHT, LLC
Reel/Frame 027807/0939 →
CHANGE OF NAME Recorded Jan 31, 2012
From: MILLIPORE CORPORATION
To: EMD MILLIPORE CORPORATION
Reel/Frame 027620/0891 →