Crosslinked, degradable polymers and uses thereof
Acrylate-terminated poly(beta-amino esters) are cross-linked to form materials useful in the medical as well as non-medical field. The polymeric starting material is combined with a free radical initiator, either a thermal initiator or a photoinitiator, and the mixture for cross-linking is heated or exposed to light depending on the initiator used. The resulting materials due to the hydrolysable ester bond in the polymer backbone are biodegradable under physiological conditions. These cross-linked materials are particular useful as drug delivery vehicles, tissue engineering scaffolds, and in fabricating microdevices. The materials may also be used as plastics, coating, adhesives, inks, etc. The cross-linked materials prepared exhibit a wide range of degradation times, mass loss profiles, and mechanical properties. Therefore, the properties of the material may be tuned for the desired use. The high-throughput approach to preparing a library of cross-linked poly(beta-amino esters) allows for the rapid screening and design of degradable polymers for a variety of applications.
1. A cross-linked poly(beta-amino ester) prepared by a method comprising steps of:
combining a poly(beta-amino ester) with a photoinitiator or thermal initiator to form a mixture; and
exposing the mixture to light or heating the mixture to a temperature ranging from 30° C. to 200° C.:
wherein the poly(beta-amino ester) before cross-linking is of the formula:
or a salt thereof, wherein:
linker A and linker B are each independently selected from the group consisting of carbon chains of 1 to 30 carbon atoms, heteroatom-containing carbon chains of 1 to 30 atoms, and carbon chains and heteroatom-containing carbon chains optionally substituted with a group selected from the group consisting of branched and unbranched, substituted or unsubstituted, cyclic or acyclic aliphatic; branched and unbranched, substituted or substituted, cyclic or acyclic heteroaliphatic; substituted or unsubstituted acyl; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; amino, alkylamino, dialkylamino, trialkylamino, aryl, ureido, heterocyclic, aromatic heterocyclic, cyclic, aromatic cyclic, halogen, hydroxyl, alkoxy, cyano, amide, carbamoyl, carboxylic acid, ester, carbonyl, carbonyldioxyl, alkylthioether, and thiol groups;
R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each independently selected from the group consisting of hydrogen; branched and unbranched, substituted or unsubstituted, cyclic or acyclic aliphatic; branched and unbranched, substituted or unsubstituted, cyclic or acyclic heteroaliphatic; substituted or unsubstituted acyl; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; halogen, hydroxyl, alkoxy, carbamoyl, carboxyl ester, carbonyldioxyl, amide, thiohydroxyl, alkylthioether, amino, alkylamino, dialkylamino, trialkylamino, cyano, ureido, a substituted alkanoyl group, cyclic, cyclic aromatic, heterocyclic, and aromatic heterocyclic groups, each of which may be substituted with at least one substituent selected from the group consisting of branched and unbranched alkyl, branched and unbranched alkenyl, branched and unbranched alkynyl, amino, alkylamino, dialkylamino, trialkylamino, aryl, ureido, heterocyclic, aromatic heterocyclic, cyclic, aromatic cyclic, halogen, hydroxyl, alkoxy, cyano, amide, carbamoyl, carboxylic acid, ester, carbonyl, carbonyldioxyl, alkylthioether, and thiol groups; and
n is an integer between 5 and 10,000;
wherein at least one cross-link between polymer chains is formed between terminal acrylate moieties and is a carbon-carbon cross-link selected from the group consisting of:
wherein the cross-linked poly(beta-amino ester) exhibits an elastic modulus ranging from approximately 4 to approximately 350 MPa.
2. The cross-linked poly(beta-amino ester) of claim 1 , wherein the poly(beta-amino ester) before cross-linking is of the formula:
or a salt thereof.
3. The cross-linked poly(beta-amino ester) of claim 1 , wherein the poly(beta-amino ester) before cross-linking is of the formula:
or a salt thereof.
4. The cross-linked poly(beta-amino ester) of claim 1 , wherein A is
and n is an integer between 1 and 20, inclusive.
5. The cross-linked poly(beta-amino ester) of claim 1 , wherein A is
and n is an integer between 1 and 10, inclusive.
6. The cross-linked poly(beta-amino ester) of claim 1 , wherein A is
m is an integer between 1 and 6, inclusive; and n is an integer between 1 and 10, inclusive.
7. A cross-linked poly(beta-amino ester) prepared by a method comprising steps of:
combining a poly(beta-amino ester) with a photoinitiator or thermal initiator to form a mixture; and
exposing the mixture to light or heating the mixture to a temperature ranging from 30° C. to 200° C.:
wherein the poly(beta-amino ester) before cross-linking is of the formula:
or a salt thereof, wherein:
linker B is selected from the group consisting of carbon chains of 1 to 30 carbon atoms, heteroatom-containing carbon chains of 1 to 30 atoms, and carbon chains and heteroatom-containing carbon chains optionally substituted with a group selected from the group consisting of branched and unbranched, substituted or unsubstituted, cyclic or acyclic aliphatic; branched and unbranched, substituted or substituted, cyclic or acyclic heteroaliphatic; substituted or unsubstituted acyl; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; amino, alkylamino, dialkylamino, trialkylamino, aryl, ureido, heterocyclic, aromatic heterocyclic, cyclic, aromatic cyclic, halogen, hydroxyl, alkoxy, cyano, amide, carbamoyl, carboxylic acid, ester, carbonyl, carbonyldioxyl, alkylthioether, and thiol groups;
R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are each independently selected from the group consisting of hydrogen; branched and unbranched, substituted or unsubstituted, cyclic or acyclic aliphatic; branched and unbranched, substituted or unsubstituted, cyclic or acyclic heteroaliphatic; substituted or unsubstituted acyl; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; halogen, hydroxyl, alkoxy, carbamoyl, carboxyl ester, carbonyldioxyl, amide, thiohydroxyl, alkylthioether, amino, alkylamino, dialkylamino, trialkylamino, cyano, ureido, a substituted alkanoyl group, cyclic, cyclic aromatic, heterocyclic, and aromatic heterocyclic groups, each of which may be substituted with at least one substituent selected from the group consisting of branched and unbranched alkyl, branched and unbranched alkenyl, branched and unbranched alkynyl, amino, alkylamino, dialkylamino, trialkylamino, aryl, ureido, heterocyclic, aromatic heterocyclic, cyclic, aromatic cyclic, halogen, hydroxyl, alkoxy, cyano, amide, carbamoyl, carboxylic acid, ester, carbonyl, carbonyldioxyl, alkylthioether, and thiol groups; and
n is an integer between 5 and 10,000;
wherein at least one cross-link between polymer chains is formed between terminal acrylate moieties and is a carbon-carbon cross-link selected from the group consisting of:
wherein the cross-linked poly(beta-amino ester) exhibits an elastic modulus ranging from approximately 4 to approximately 350 MPa.
8. The cross-linked poly(beta-amino ester) of claim 7 , wherein the poly(beta-amino ester) before cross-linking is of formula:
or a salt thereof.
9. The cross-linked poly(beta-amino ester) of claim 7 , wherein the poly(beta-amino ester) before cross-linking of formula:
or a salt thereof.
10. The cross-linked poly(beta-amino ester) of claim 7 , wherein R 1 is selected from the group consisting of:
11. The cross-linked poly(beta-amino ester) of claim 7 , wherein B is
and n is an integer between 1 and 20, inclusive.
12. The cross-linked poly(beta-amino ester) of claim 7 , wherein B is
and n is an integer between 1 and 10, inclusive.
13. The cross-linked poly(beta-amino ester) of claim 7 , wherein B is
m is an integer between 1 and 6, inclusive; and n is an integer between 1 and 10, inclusive.
14. The cross-linked poly(beta-amino ester) of claim 7 , wherein B is selected from the group consisting of:
15. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) is prepared by a method comprising steps of:
combining a poly(beta-amino ester) with a photoinitiator to form a mixture; and
exposing the resulting mixture to light.
16. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) is prepared by a method comprising steps of:
combining a poly(beta-amino ester) with a thermal initiator to form a mixture; and
heating the resulting mixture to a temperature ranging from 30° C. to 200° C.
17. A pharmaceutical composition comprising a cross-linked poly(beta-amino ester) of claim 1 or 7 , and a therapeutic agent or cell.
18. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) is biodegradable.
19. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) is biocompatible.
20. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) exhibits greater than 90% mass loss within 24 hours in phosphate-buffered saline (PBS) at 37° C.
21. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) exhibits greater than 90% mass loss within 1 week in phosphate-buffered saline (PBS) at 37° C.
22. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) exhibits greater than 90% mass loss within 1 month in phosphate-buffered saline (PBS) at 37° C.
23. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) exhibits greater than 90% mass loss within 6 months in phosphate-buffered saline (PBS) at 37° C.
24. The cross-linked poly(beta-amino ester) of claim 1 or 7 , wherein the cross-linked poly(beta-amino ester) exhibits an elastic modulus ranging from approximately 10 to approximately 100 MPa.
25. The cross-linked poly(beta-amino ester) of claim 1 , wherein R 1 and R 2 are both C 1 -C 6 alkyl.
26. The cross-linked poly(beta-amino ester) of claim 1 , wherein R 1 and R 2 are both methyl.
27. The cross-linked poly(beta-amino ester) of claim 4 , wherein n is 2.
28. The cross-linked poly(beta-amino ester) of claim 7 , wherein R 1 is:
29. The cross-linked poly(beta-amino ester) of claim 15 , wherein the photoinitiator is selected from the group consisting of acetophenone; anisoin; anthraquinone; anthraquinone-2-sulfonic acid, sodium salt monohydrate; (benzene) tricarbonylchromium; benzin; benzoin; benzoin ethyl ether; benzoin isobutyl ether; benzoin methyl ether; benzophenone; benzophenone/1-hydroxycyclohexyl phenyl ketone; 3,3′,4,4′-benzophenonetetracarboxylic dianhydride; 4-benzoylbiphenyl; 2-benzyl-2-(dimethylamino)-4′-morpholinobutyrophenone; 4,4′-bis(diethylamino)benzophenone; 4,4′-bis(dimethylamino)benzophenone; camphorquinone; 2-chlorothioxanthen-9-one; (cumene)cyclopentadienyliron(II) hexafluorophosphate; dibenzosuberenone; 2,2-diethoxyacetophenone; 4,4′-dihydroxybenzophenone; 2,2-dimethoxy-2-phenylacetophenone; 4-(dimethylamino)benzophenone; 4,4′-dimethylbenzil; 2,5-dimethylbenzophenone; 3,4-dimethylbenzophenone; diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide/2-hydroxy-2-methylpropiophenone; 4′-ethoxyacetophenone; 2-ethylanthraquinone; ferrocene; 3′-hydroxyacetophenone; 4′-hydroxyacetophenone; 3-hydroxybenzophenone; 4-hydroxybenzophenone; 1-hydroxycyclohexyl phenyl ketone; 2-hydroxy-2-methylpropiophenone; 2-methylbenzophenone; 3-methylbenzophenone; methybenzoylformate; 2-methyl-4′-(methylthio)-2-morpholinopropiophenone; phenanthrenequinone; 4′-phenoxyacetophenone; thioxanthen-9-one; triarylsulfonium hexafluoroantimonate salts; triarylsulfonium hexafluorophosphate salts; hydrogen peroxide; benzoyl peroxide; benzoin; 2,2-dimethoxy-2-phenylacetophenone; dibenzoyl disulphides; diphenyldithiocarbonate; 2,2′-azobisisobutyronitrile (AIBN); camphorquinone (CQ); eosin; dimethylaminobenzoate (DMAB); dimethoxy-2-phenyl-acetophenone (DMPA); ethyl-4-N,N-dimethylaminobenzoate (4EDMAB); 1-[-(4-benzoylphenylsulfanyl)phenyl]-2-methyl-2-(4-methylphenylsulfonyl) propan-1-one; 1-hydroxy-cyclohexyl-phenyl-ketone; 2,4,6-trimethylbenzoyldiphenylphosphine oxide; 2-ethylhexyl-4-dimethylaminobenzoate; 2-hydroxy-2-methyl-1-phenyl-1-propane; benzyl dimethyl ketal; benzophenone; alpha-hydroxy-cyclohexyl-phenyl-ketone; phosphine oxide; difunctional alpha-hydroxy ketone; ethyl 4-(dimethylamino)benzoate; isopropyl thioxanthone; 4-methylbenzophenone; oligo(2-hydroxy-2 methyl-1-4 (1-methylvinyl)phenyl propanone; oligo(2-hydroxy-2-methyl-1-4 (1-methylvinyl)phenyl propanone; 2-hydroxy-2-methyl-1-phenyl-1-propanone (monomeric); oligo (2-hydroxy-2-methyl-1-4 (1-methylvinyl) phenyl propanone; 2-hydroxy-2-methyl-1-phenyl-1-propanone (polymeric); trimethylbenzophenone; methylbenzophenone; 2,4,6-trimethylbenzoylphosphine oxide; bis-acylphosphine oxide; alpha hydroxyketone; trimethylbenzophenone; and 4-methyl benzophenone.
30. The cross-linked poly(beta-amino ester) of claim 15 , wherein the photoinitiator is dimethoxy-2-phenyl-acetophenone (DMPA).
31. The cross-linked poly(beta-amino ester) of claim 15 , wherein the photoinitiator is acetophenone.
32. The cross-linked poly(beta-amino ester) of claim 15 , wherein the photoinitiator is benzophenone.
33. The cross-linked poly(beta-amino ester) of claim 15 , wherein the photoinitiator is benzoin.
34. The cross-linked poly(beta-amino ester) of claim 15 , wherein the light is UV light.
35. The cross-linked poly(beta-amino ester) of claim 16 , wherein the temperature ranges from 50° C. to 180° C.
36. The cross-linked poly(beta-amino ester) of claim 16 , wherein the thermal initiator is selected from the group consisting of tert-amyl peroxybenzoate; 4,4-azobis(4-cyanovaleric acid); 1,1′-azobis(cyclohexanecarbonitrile); 2,2′-azobisisobutyronitrile (AIBN); benzoyl peroxide; 2,2-bis(tert-butylperoxy)butane; 1,1-bis(tert-butylperoxy)cyclohexane; 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane; 2,5-bis(tert-butylperoxy)-2,5-dimethyl-3-hexyne; bis(1-(tert-butylperoxy)-1-methylethyl)benzene; 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane; tert-butyl hydroperoxide; tert-butyl peracetate; tert-butyl peroxide; tert-butyl peroxybenzoate; tert-butylperoxy isopropyl carbonate; cumene hydroperoxide; cyclohexanone peroxide; dicumyl peroxide; lauroyl peroxide; 2,4-pentanedione peroxide; peracetic acid; and potassium persulfate.