Biocompatible, biomimetic ampholyte materials
New ampholyte biomaterial compounds containing ampholyte moieties are synthesized and integrated into polymeric assemblies to provide hydrophilic polymers exhibiting improved biocompatibility, haemocompatibility, hydrophilicity non-thrombogenicity, anti-bacterial ability, and mechanical strength, as well as suitability as a drug delivery platform.
1. A hydrophilic ampholyte compound represented by a general formula of
wherein R 1 is hydrophilic and selected from the group consisting of (a) a substituted alkyl group, (b) a substituted cycloalkyl group, (c) a substituted cycloalkenyl group, (d) a substituted or unsubstituted heterocycle group, and (e) a substituted alkenyl group, wherein the R 1 group terminates with a methoxy group;
wherein R 2 and R 3 , are independently selected from the group consisting of
(a) a substituted or unsubstituted alkyl group, (b) a substituted or unsubstituted aryl group,(c) a substituted or unsubstituted cycloalkyl group, (d) a substituted or unsubstituted cycloalkenyl group, (e) a substituted or unsubstituted heterocycle group, and (f) a substituted or unsubstituted alkenyl group;
wherein m and p independently range from 0 to 6, with an m of 1 to 6 denoting a hydrocarbon chain referred to as the m-hydrocarbon chain and a p in a range from 1 to 6 denoting a hydrocarbon chain referred to as the p-hydrocarbon chain;
wherein the m-hydrocarbon chain and/or the p-hydrocarbon chain are substituted or unsubstituted hydrocarbon chains, wherein if the hydrocarbon chain is substituted substitution is an attachment to the hydrocarbon chain or is a heteroatom within the hydrocarbon chain; and
wherein Z represents a polymerizable group comprising a vinylic or allylic group that is capable of undergoing free radical polymerization.
2. The ampholyte compound of claim 1 wherein Z represents a group represented by a general formula of
wherein X represents a hydrogen or a methyl, and Y represents an oxygen in an ester moiety or a secondary amine in an amide moiety.
3. The ampholyte compound of claim 1 wherein the m-hydrocarbon chain and/or the p-hydrocarbon chain comprises one or more substituents.
4. The ampholyte compound of claim 1 represented by the general formula:
wherein R 1 comprises an ether functional group; and
wherein X represents a hydrogen or a methyl, and Y represents an oxygen in an ester moiety or a secondary amine in an amide moiety.
5. The ampholyte compound of claim 4 wherein m=1, p=1, Y is oxygen, X is a methyl, and R 1 is a methoxyethyl whereby the compound is 2-((2-(methacryloyloxy)ethyl)dimethylammonio)ethyl 2-methoxyethyl phosphate.
6. The ampholyte compound of claim 4 wherein m=1, p=2, Y is an oxygen, X is a methyl, and R 1 is a methoxyethyl whereby the compound is 2-((2-(methacryloyloxy)propyl)dimethylammonio)ethyl 2-methoxyethyl phosphate.
7. The ampholyte compound of claim 4 , the compound being represented by a formula:
8. The ampholyte compound of claim 1 wherein R 1 comprises an ether functional group.
9. A method of making a polymer comprising polymerizing an ampholyte compound represented by a general formula of
wherein R 1 is hydrophilic and selected from the group consisting of (a) a substituted alkyl group, (b) a substituted group, (c) a substituted cycloalkenyl group, (d) a substituted or unsubstituted heterocycle group, and (e) a substituted alkenyl group, wherein the R 1 group terminates with a methoxy group;
wherein R 2 and R 3 , are independently selected from the group consisting of
(a) a substituted or unsubstituted alkyl group, (b) a substituted or unsubstituted aryl group,(c) a substituted or unsubstituted cycloalkyl group, (d) a substituted or unsubstituted cycloalkenyl group, (e) a substituted or unsubstituted heterocycle group, and (f) a substituted or unsubstituted alkenyl group;
wherein m and p independently range from 0 to 6, with an m of 1 to 6 denoting a hydrocarbon chain referred to as the m-hydrocarbon chain and a p in a range from 1 to 6 denoting a hydrocarbon chain referred to as the p-hydrocarbon chain;
wherein the m-hydrocarbon chain and/or the p-hydrocarbon chain are substituted or unsubstituted hydrocarbon chains, wherein if the hydrocarbon chain is substituted substitution is an attachment to the hydrocarbon chain or is a heteroatom within the hydrocarbon chain; and
wherein Z represents a polymerizable group comprising a vinylic or allylic group that is capable of undergoing free radical polymerization.
10. The method of claim 9 further comprising other monomers with the ampholyte compound.
11. The method of claim 10 wherein the other monomers comprise glycerol mono methacrylate, acrylates, methacrylates, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylate, n-butyl methacrylate, tert-butyl methacrylate, n-hexyl methacrylate, 2-methoxyethyl methacrylate, poly(hexanide) methacrylate, poly(hexanide) polyethylene oxide methacrylate, alkyl derivatized poly(hexanide) methacrylate, heparin derivatized polyethylene oxide macromer, vinyl sulfonic acid monomer, monomers comprising poly(ethylene glycol), N-vinyl pyrrolidone monomers, 4-benzoylphenyl methacrylate, allyl methyl carbonate, allyl alcohol, allyl isocyanate, methacryloyloxyethyl phosphorylcholine, derivatized glycoaminoglycan, derivatized polysaccharides, hyaluronic acid and derivatives, methacrylic acid, glycidyl methacrylate, or combinations thereof.