Phosphonate-containing polymer and use thereof and phosphonate-containing polymer viscosity reducer for drilling fluid
US-9206342-B2 · Dec 8, 2015 · US
US11873358B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11873358-B2 |
| Application number | US-201816618252-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 29, 2018 |
| Priority date | May 30, 2017 |
| Publication date | Jan 16, 2024 |
| Grant date | Jan 16, 2024 |
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A novel synthetic functionalized backbone polymer is provided which is a polyanionic side-chain functionalized back-bone polymer comprising a hydrophilic backbone polymer functionalized with an activated alkene or epoxy group. The functionalized backbone polymer may be combined with a free or protected thiol-containing compound to form a crosslinked hydrogel having bio-medical application, and may additionally be combined with a hydrogel matrix to yield a hydrogel system useful for in vivo delivery of cells and other therapeutic agents.
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The invention claimed is: 1. A crosslinked hydrogel comprising a first side-chain functionalized backbone polymer functionalized with an activated alkene, which is a vinylsulfone, acrylate, methacrylate or an alkynyl group, crosslinked with a free or protected thiol-containing compound that is a polar, water-soluble compound comprising two or more thiol groups or a second side-chain functionalized backbone polymer functionalized with an amine-containing crosslinkable compound comprising a thiopyridine, a dithiocarbamate or a thioester. 2. The crosslinked hydrogel of claim 1 , wherein the thiol-containing compound is a polyethylene glycol (PEG)-dithiol having a molecular weight in the range of from about 200 to 1,000,000 Daltons. 3. The crosslinked hydrogel of claim 1 , wherein the second side-chain functionalized backbone polymer is functionalized with S-(2-aminoethylthio)-2-thiopyridine. 4. The crosslinked hydrogel of claim 1 , comprising a hydrogel matrix core or a hydrogel matrix shell. 5. A hydrogel system comprising a crosslinked hydrogel as defined in claim 1 dispersed within a water soluble polymer matrix capable of being gelled using divalent cation binding or thermal gellation. 6. The hydrogel system of claim 5 , wherein the polymer matrix is selected from alginate, agarose, cellulose sulphate and combinations thereof. 7. A method of making a hydrogel system as defined in claim 5 , comprising: i) combining an aqueous solution of a first side-chain functionalized backbone polymer functionalized with an activated alkene or epoxy group with a polymer matrix selected from alginate, agarose, cellulose sulphate and combinations thereof; and ii) adding an aqueous solution of a polyethylene glycol (PEG)-dithiol having a molecular weight in the range of from about 200 to 1,000,000 Daltons under conditions that permit crosslinking, or combining the first side-chain functionalized backbone polymer with a second side-chain functionalized backbone polymer functionalized with a protected thiol group in a polymer matrix selected from alginate, agarose, cellulose sulphate and combinations thereof, and adding a deprotecting agent to the solution which exposes the thiol group of the second side-chain functionalized backbone polymer. 8. The method of claim 7 , wherein the deprotecting agent is selected from a phosphine, a dithiothreitol, cysteamine, cysteine, and an amino sugar. 9. The method of claim 8 , wherein the deprotecting agent is tris(2-carboxyethyl) phosphine or tris(3-hydroxypropyl)phosphine (THPP). 10. The crosslinked hydrogel as defined in claim 1 , formed by reacting an amount of about 0.5 to 15 wt % of a synthetic side-chain functionalized polymer comprising poly(methyl-vinylether-alt-maleic anhydride) (PMMA) functionalized with cysteamine vinyl sulfone or S-(2-aminoethylthio)-2-thiopyridine, wherein cysteamine vinyl sulfone or S-(2-aminoethylthio)-2-thiopyridine comprises between 5 and 40 mol % of the anhydride groups present in the PMMA in aqueous solution with i) an aqueous solution containing di- or poly-thiol poly(ethylene glycol), wherein the poly(ethylene glycol) is present in a concentration that results in a molar ratio ranging from 1:4 to 4:1 of cysteamine vinyl sulfone groups on the synthetic polymer to thiols on the poly(ethylene glycol), or with ii) an aqueous solution of the protected polythiol polymer comprising poly(methylvinylether-alt-maleic anhydride)(PMMA) functionalized with S-(2-aminoethylthio)-2-thiopyridine, wherein crosslinking is initiated by addition of triscarboxyethylphosphine or its sodium salt, or THPP. 11. The crosslinked hydrogel of claim 1 , wherein the backbone polymer is selected from homopolymers of polyacrylic acid or polymethacrylic acid; copolymers of acrylic acid or methacrylic acid with anionic, uncharged or cationic monomer;, copolymers of an alkyl vinyl ether with an acid anhydride monomer; copolymers of vinyl ethers of ethylene oxide oligomers with an acid anhydride monomer, polyanhydride and carboxylic acid anhydride polymers; copolymers of aromatic monomers with an acid anhydride monomer; polymers containing epoxy groups, and optionally including neutral or anionic monomers. 12. The crosslinked hydrogel of claim 1 , wherein the backbone polymer is a copolymer of an alkyl vinyl ether with an acid anhydride monomer. 13. The crosslinked hydrogel of claim 12 , wherein the acid anhydride is maleic, itaconic or citraconic anhydride. 14. The crosslinked hydrogel of claim 1 , which is cysteamine vinyl sulfone-functionalized poly(methyl vinyl ether-alt-maleic acid). 15. The crosslinked hydrogel of claim 10 , wherein the polymer is a polyanionic, polyfunctional Michael acceptor suitable for crosslinking with Michael donors selected from free and protected dithiols and polythiols.
leading to a crosslinking, either explicitly or inherently · CPC title
Maleic anhydride · CPC title
Chemical modification by after-treatment (graft polymers, block polymers, crosslinking with unsaturated monomers or with polymers C08F251/00 - C08F299/00; of conjugated diene rubbers C08C) · CPC title
Introducing sulfur atoms or sulfur-containing groups · CPC title
Macromolecular gels · CPC title
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