Biocompatible hydrogels made with small molecule precursors
Biocompatible crosslinked polymers, and methods for their preparation and use, are disclosed in which the biocompatible crosslinked polymers are formed from water soluble precursors having electrophilic and nucleophilic functional groups capable of reacting and crosslinking in situ. Methods for making the resulting biocompatible crosslinked polymers biodegradable, or not, are provided, as are methods for controlling the rate of degradation. The crosslinking reactions may be carried out in situ on organs or tissues or outside the body. Applications for such biocompatible crosslinked polymers and their precursors include controlled delivery of drugs, prevention of post-operative adhesions, coating of medical devices such as vascular grafts, wound dressings and surgical sealants. Visualization agents may be included with the crosslinked polymers. Embodiments that include hydrogels having isolated hydrolytically degradable esters are set forth. Embodiments including the use of low molecular weight amines to make degradable hydrogels are also set forth.
1. A method for making a medical device, the method comprising:
providing at least a first biocompatible precursor having least two electrophilic functional groups, and providing at least a second biocompatible precursor comprising at least two primary amine functional groups; wherein the first biocompatible precursor and the second biocompatible precursor are resistant to enzymatic degradation and at least one of the first biocompatible precursor or second biocompatible precursor comprises at least one isolated hydrolytically degradable ester group; and
mixing at least the first biocompatible precursor and the second biocompatible precursor in situ to form a device comprising a crosslinked hydrogel that comprises covalent bonds formed by reaction of the functional groups of the first biocompatible precursor and second biocompatible precursor with each other and further comprising the at least one isolated hydrolytically degradable ester group; wherein the crosslinked hydrogel is resistant to enzymatic degradation, is degradable by hydrolysis of the at least one isolated hydrolytically degradable ester group so that the device is degradable in less than about 180 days, and wherein the second biocompatible precursor has a molecular weight of less than about 2000, wherein the second precursor is a member of the group consisting of ornithine, spermine, spermidine, urea, guanidine, dianmiopimelic acid, diaminobutyric acid, methylornithine, diaminopropionic acid, cystine, lanthionine, cystamine, trioxatridecanediamine, cyclohexanebis(methylamine), tetraethylenepentamine, pentaethylenehexamine, methylenebis(methylcyclohexamine), diaminocyclohexane, n-(2-aminoethyl)-1,3-propanediamine, diaminomethyldipropylamine, iminobispropylamine, bis(hexamethlyene)triamine, triethylenetetramine, bis(aminopropyl)ethylenediamine, bis(2-aminoethyl)-1,3-propanediamine, bis(aminopropyl)propanediamine, diamniomethylpropane, 1,2-diamino-2-methylpropane, 1,3-diaminopentane, dimethylpropanediamine, 2,2-dimethyl 1,3-propanediamine, methylpentanediamine, 2-methyl-1,5 pentanediamine, diaminoheptane, diaminooctane, diaminononane, and diaminododecane.
2. A method for making a medical device, the method comprising:
providing at least a first biocompatible precursor having least two electrophilic functional groups, and providing at least a second biocompatible precursor comprising at least two primary amine functional groups; wherein the first biocompatible precursor and the second biocompatible precursor are resistant to enzymatic degradation and at least one of the first biocompatible precursor or second biocompatible precursor comprises at least one isolated hydrolytically degradable ester group; and
mixing at least the first biocompatible precursor and the second biocompatible precursor in situ to form a device comprising a crosslinked hydrogel that comprises covalent bonds formed by reaction of the functional groups of the first biocompatible recursor and second biocompatible precursor with each other and further comprising the at least one isolated hydrolytically degradable ester group; wherein the crosslinked hydrogel is resistant to enzymatic degradation, is degradable by hydrolysis of the at least one isolated hydrolytically degradable ester group so that the device is degradable in less than about 180 days, and wherein the second biocompatible precursor has a molecular weight of less than about 2000, and
further comprising a third biocompatible precursor reacted with the first biocompatible precursor, wherein the third biocompatible precursor is a member of the group consisting of dilysine, trilysine, tetralysine, and Tris.
3. A method for making a medical device, the method comprising:
providing at least a first biocompatible precursor having least two electrophilic functional groups, and providing at least a second biocompatible precursor comprising at least two primary amine functional groups; wherein the first biocompatible precursor and the second biocompatible precursor are resistant to enzymatic degradation and at least one of the first biocompatible precursor or second biocompatible precursor comprises at least one isolated hydrolytically degradable ester group; and
mixing at least the first biocompatible recursor and the second biocompatible precursor in situ to form a device comprising a crosslinked hydrogel that comprises covalent bonds formed by reaction of the functional groups of the first biocompatible precursor and second biocompatible precursor with each other and further comprising the at least one isolated hydrolytically degradable ester group; wherein the crosslinked hydrogel is resistant to enzymatic degradation, is degradable by hydrolysis of the at least one isolated hydrolytically degradable ester group so that the device is degradable in less than about 180 days, and wherein the second biocompatible precursor has a molecular weight of less than about 2000, further comprising a third biocompatible precursor reacted with the first biocompatible precursor, wherein the second biocompatible precursor and the third biocompatible precursor are selected from the group consisting of dilysine, trilysine, tetralysine, and Tris.
4. A kit comprising:
a first biocompatible precursor having at least two electrophilic functional groups, and a second biocompatible precursor comprising at least two primary amine functional groups, a third biocompatible precursor comprising at least two primary amine functional groups and, an applicator;
wherein the first biocompatible precursor, the second biocompatible precursor, and the third biocompatible precursor are reactable with each other to form a crosslinked hydrogel, are resistant to enzymatic degradation, and at least one of the first, second, or third biocompatible precursors comprises at least one isolated hydrolytically degradable ester group;
wherein the applicator is configured to mix at least the first precursor, the second precursor, and the third precursor to form a crosslinked hydrogel in situ comprising covalent bonds formed by reaction of the functional groups of the precursors and further comprising the at least one isolated hydrolytically degradable ester group;
wherein the hydrogel comprises a sufficient number of the at least one isolated hydrolytically degradable ester groups in the crosslinked hydrogel so that the crosslinked hydrogel is degradable in less than about 180 days, is resistant to enzymatic degradation, and is degradable by hydrolysis of the at least one isolated hydrolytically degradable ester group; and
wherein the kit further comprises instructions that comprise directions for making a hydrogel that is degradable in an amount of time, with the amount of time being less than about 180 days.
5. The kit of claim 4 wherein the second biocompatible precursor and the third biocompatible precursor each have a molecular weight of less than about 1000.
6. The kit of claim 4 wherein the amount of time is less than about 90 days.
7. The kit of claim 4 wherein the amount of time is less than about 45 days.
8. The kit of claim 4 wherein the second biocompatible precursor and the third biocompatible precursor are selected from the group consisting of dilysine, trilysine, tetralysine, and Tris.
9. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of ornithine, spermine, and spermidine.
10. A readily degradable material comprising:
a crosslinked biocompatible hydrogel that comprises a products of a reaction between a first biocompatible precursor, a second biocompatible precursor, and a third biocompatible precursor, with at least one of the biocompatible precursors comprising an isolated hydrolytically degradable ester group, wherein the crosslinked hydrogel is resistant to enzymatic degradation and is degradable by hydrolysis of the isolated hydrolytically degradable ester groups, and
with the second biocompatible precursor, before reaction, being chosen from a group consisting of dilysine, trilysine, and tetralysine; and
with the third biocompatible precursor, before reaction, being chosen from the group consisting of Tris, ornithine, spermine, spermidine, urea, guanidine, diamniopimelic acid, diaminobutyric acid, methylornithine, diaminopropionic acid, cystine, lanthionine, cystamine, trioxatridecanediamine, cyclohexanebis(methylamine), tetraethylenepentamine, pentaethylenehexamine, methylenebis(methylcyclohexamine), diaminocyclohexane, n-(2-aminoethyl)-1,3-propanediamine, diaminomethyldipropylamine, iminobispropylamine, bis(hexamethlyene)triamine, triethylenetetramine, bis(aminopropyl)ethylenediamine, bis(2-aminoethyl)-1,3-propanediamine, bis(aminopropyl)propanediamine, diamniomethylpropane, 1,2-diamino-2-methylpropane, 1,3-diaminopentane, dimethylpropanediamine, 2,2-dimethyl 1,3-propanediamine, methylpentanediamine, 2-methyl-1,5 pentanediamine, diaminoheptane, diaminooctane, diaminononane, and diaminododecane.
11. A method of making a hydrogel, the method comprising:
providing a first biocompatible precursor having at least two electrophilic functional groups, a second biocompatible precursor comprising at least two primary amine functional groups, a third biocompatible precursor comprising at least two primary amine functional groups; wherein at least one of the first, the second, or the third biocompatible precursors comprises at least one isolated hydrolytically degradable ester group; wherein the first, the second, and the third biocompatible precursors are resistant to enzymatic degradation; and
mixing, in situ, the first biocompatible precursor, the second biocompatible precursor, and the third biocompatible precursor to form a crosslinked hydrogel that comprises covalent bonds formed by reaction of the functional groups of the first, the second, and the third biocompatible precursors, with the hydrogel being resistant to enzymatic degradation and comprising the at least one isolated hydrolytically degradable ester group;
wherein the hydrogel comprises a sufficient number of the at least one isolated hydrolytically degradable ester groups in the crosslinked hydrogel so that the crosslinked hydrogel is degradable in less than about 180 days and is degradable by hydrolysis of the at least one isolated hydrolytically degradable ester group.
12. The method of claim 11 wherein the second biocompatible precursor and the third biocompatible precursor each have a molecular weight of less than about 1000.
13. The method of claim 11 wherein the hydrogel is degradable in less than about 90 days.
14. The method of claim 11 wherein the hydrogel is degradable in less than about 45 days.
15. The method of claim 11 wherein the second biocompatible precursor and the third biocompatible precursor are selected from the group consisting of dilysine, trilysine, tetralysine, and Tris.
16. The method of claim 11 wherein the second biocompatible precursor is a member of the group consisting of ornithine, spermine, spermidine, urea, guanidine, diamniopimelic acid, diaminobutyric acid, methylornithine, diaminopropionic acid, cystine, lanthionine, cystamine, trioxatridecanediamine, cyclohexanebis(methylamine), tetraethylenepentamine, pentaethylenehexamine, methylenebis(methylcyclohexamine), diaminocyclohexane,n-(2-aminoethyl)-1,3-propanediamine, diaminomethyldipropylamine, iminobispropylamine, bis(hexamethlyene)triamine, triethylenetetramine, bis(aminopropyl)ethylenediamine, bis(2-aminoethyl)-1,3-propanediamine, bis(aminopropyl)propanediamine, diamniomethylpropane, 1,2-diamino-2-methylpropane, 1,3-diaminopentane, dimethylpropanediamine, 2,2-dimethyl 1,3-propanediamine, methylpentanediamine, 2-methyl-1,5 pentanediamine, diaminoheptane, diaminooctane, diaminononane, and diaminododecane.
17. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of urea, guanidine, diamniopimelic acid, diaminobutyric acid, methylornithine, and diaminopropionic acid.
18. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of cystine, lanthionine, cystamine, trioxatridecanediamine, and cyclohexanebis(methylamine).
19. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of tetraethylenepentamine, pentaethylenehexamine, methylenebis(methylcyclohexamine), diaminocyclohexane, n-(2-aminoethyl)-1,3-propanediamine, diaminomethyldipropylamine, and iminobispropylamine.
20. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of bis(hexamethlyene)triamine, triethylenetetramine, bis(aminopropyl)ethylenediamine, bis(2-aminoethyl)-1,3-propanediamine, bis(aminopropyl)propanediamine, diamniomethylpropane, and 1,2-diamino-2-methylpropane.
21. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of 1,3-diaminopentane, dimethylpropanediamine, 2,2-dimethyl 1,3-propanediamine, and methylpentanediamine.
22. The kit of claim 4 wherein the second biocompatible precursor is a member of the group consisting of 2-methyl-1,5 pentanediamine, diaminoheptane, diaminooctane, diaminononane, and diaminododecane.