Ligand functional substrates
View Patent ↗A substrate comprising a crosslinked polymer primer layer, and grafted thereto a ligand-functionalized polymer is provided. The grafted polymer has the requisite affinity for binding neutral or negatively charged biomaterials, such as cells, cell debris, bacteria, spores, viruses, nucleic acids, and proteins, at pH's near or below the pI's of the biomaterials.
1. A ligand functional substrate comprising:
a) a substrate
b) a primer layer disposed on the substrate comprising:
a crosslinked polyamine polymer having ethylenically unsaturated polymerizable groups;
c) a ligand-functional alkenyl (co)polymer layer grafted to the ethylenically unsaturated polymerizable group of the primer layer.
2. The ligand-functional substrate of claim 1 , wherein the crosslinked polyamine polymer having ethylenically unsaturated polymerizable groups is the reaction product of:
1) a polyamine polymer
2) a polyfunctional crosslinking agent for the polyamine polymer; and
3) a monomer having an amine-reactive functional group and an ethylenically unsaturated polymerizable group.
3. The ligand-functional substrate of claim 1 , wherein said ligand is selected from the group consisting of tyrosinol, tryptophanol, octopamine, 2-aminobenzimidazole, 1,3-diamino-2-hydroxypropane, tris(2-aminoethyl)amine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, agmatine, guanidine and biguanide ligands.
4. The ligand-functional substrate of claim 1 , wherein the ligand-functional alkenyl (co)polymer comprises polymerized monomer units of the formula:
wherein
R 1 is H or C 1 -C 4 alkyl;
R 2 is a (hetero)hydrocarbyl group;
X 1 is —O—or —NR 3 —, where R 3 is independently H or C 1 -C 4 alkyl;
R lig is a ligand-containing group,
p is 0 or 1; and
m is 0 or 1.
5. The ligand-functional substrate of claim 1 , wherein the ligand-functional alkenyl (co)polymer comprises polymerized monomer units of the formula:
wherein
R 1 is H or C 1 -C 4 alkyl;
R 2 is a (hetero)hydrocarbyl group;
each R 3 is independently H or hydrocarbyl;
R 4 is H, C 1 -C4 alkyl or —N(R 3 )2;
R 5 is H or hydrocarbyl;
X 1 is —O—or —NR 3 —,
o is 0 or 1, and
n is 1 or 2.
6. The ligand-functional substrate of claim 1 , wherein the ligand-functional alkenyl (co)polymer further comprises polymerized polar monomer units.
7. The ligand-functional substrate of claim 6 , wherein the ligand-functional alkenyl (co)polymer further comprises polymerized cationic or anionic monomer units.
8. The ligand-functional substrate of claim 6 , wherein the polar monomer units comprise the poly(oxyalkylene) (meth)acrylate monomer units.
9. The ligand-functional substrate of claim 8 , wherein the poly(oxyalkylene) (meth)acrylate monomer units are of the formula: CH 2 ═CR 1 —C(O)—X 1 —(CH(R 1 )—CH2—O) n —R 1 , wherein each R 1 is independently H or C 1 -C 4 alkyl, X 1 is —O—or —NR 3 —, where R 3 is H or C 1 -C 4 alkyl and n is 2 to 100.
10. The ligand-functional substrate of claim 2 wherein the polyamine polymer is selected from the group consisting of polyethylenimine, polylysine, polyaminoamides, polydimethylamine-epichlorohydrin-ethylenediamine, polyaminosiloxanes and dendrimers formed from polyamidoamine and polypropylenimine.
11. The ligand-functional substrate of claim 1 wherein said primer layer comprises 0.1 to 5 wt. % of the substrate.
12. The ligand-functional substrate of claim 1 wherein said ligand-functional alkenyl (co)polymer comprises 5 to 30 wt.% of the ligand functional substrate.
13. The ligand-functional substrate of claim 1 wherein said ligand groups are of the formula:
wherein
each R 3 is independently H or C 1 -C 4 alkyl;
R 4 is H, C 1 -C 4 alkyl or —N(R 3 ) 2 ; and
n is 1 or 2.
14. The ligand-functionalized substrate of claim 1 comprising a ligand-functional alkenyl (co)polymer layer of the formula:
-(M Lig ) y -(M Hydrophil ) x -(M crosslink ) z -,
wherein
(M Hydrophil ) x are hydrophilic monomer units having “x” polymerized monomer units,
(M Lig ) y are ligand functional monomer units having “y” polymerized monomer units,
(M crosslink )are multifunctional (meth)acryloyl monomer units having “z” polymerized monomer units,
y is 10 to 100 wt. % of the monomer units;
x is 0 to 90 wt. % of the monomer units and;
z is 0 to 5 wt. % of the monomer units, based on 100 wt. % total monomers.
15. The ligand-functionalized substrate of claim 2 wherein the polyfunctional crosslinking agent is of the formula:
R 8 —(Z) y ,
where R 8 is a (hetero)hydrocarbyl group, Z is an amine-reactive group, and y is ≧2.
16. The ligand-functionalized substrate of claim 2 wherein said polyfunctional crosslinking agent of the formula:
where
R 6 is an alkylene or arylene having a valence of n;
X 1 is —O—or —NR 1 13 , where R 1 is H or C 1 -C 4 alkyl,
and n is 2 to 6.
17. The ligand-functionalized substrate of claim 2 wherein said monomer having an amine-reactive functional group is of the formula:
wherein
X 1 is —O—or —NR 1 —, where R 1 is H or C 1 -C 4 alkyl,
R 1 is H or C 1 -C 4 alkyl;
R 7 is a single bond or a hydrocarbyl linking group,
A is a functional group that is reactive with the amino groups of the polyamine polymer, and
x is 0 or 1.
18. The ligand-functionalized substrate of claim 15 wherein the crosslinking agent for the polyamine polymer is used in amounts wherein the number of equivalents of amine reactive groups Z is at least 2% to 20%, relative to the equivalent of amine groups in the polyamine polymer.