Hydrophobic tissue adhesives
Pre-polymers for use as tissue sealants and adhesives, and methods of making and using thereof are provided. The pre-polymers have flow characteristics such that they can be applied through a syringe or catheter but are sufficiently viscous to remain in place at the site of application and not run off the tissue. The pre-polymers are also sufficiently hydrophobic to resist washout by bodily fluids. The pre-polymers are stable in bodily fluids; that is the pre-polymer does not spontaneously crosslink in bodily fluids absent the presence of an intentionally applied stimulus to initiate crosslinking. Upon crosslinking, the adhesive exhibits significant adhesive strength in the presence of blood and other bodily fluids. The adhesive is sufficiently elastic that it is able to resist movement of the underlying tissue. The adhesive can provide a hemostatic seal. The adhesive is biodegradable and biocompatible, causing minimal inflammatory response.
1. A surgical glue comprising a hydrophobic viscous pre-polymer,
wherein the pre-polymer is a polyester having the formula (-A-B-) n ,
wherein A is derived from a substituted or unsubstituted polyol moiety and B is derived from a substituted or unsubstituted diacid, and n represents an integer greater than 1;
wherein the pre-polymer comprises a plurality of polymeric backbones which are activated with functional groups comprising substituted or unsubstituted vinyl groups,
wherein degree of activation of the plurality of polymeric backbones is from about 0.2 to about 0.9,
wherein the functional groups on the plurality of polymeric backbones are crosslinkable by exposure to a stimulus selected from the group consisting of light, heat, and a chemical initiator,
wherein the pre-polymer has a weight average molecular weight of between about 1,000 and less than 20,000 Daltons,
wherein crosslinking of the pre-polymer is not initiated by bodily fluids, and
wherein the pre-polymer when crosslinked exhibits a 90° pull off adhesive strength which is greater than 1.5 N/cm 2 .
2. The surgical glue of claim 1 , wherein the substituted or unsubstituted vinyl groups are substituted or unsubstituted acrylate groups.
3. The surgical glue of claim 1 , wherein the degree of activation is from about 0.3 to about 0.8.
4. The surgical glue of claim 1 , wherein the weight average molecular weight of the pre-polymer is from about 3,000 Daltons to about 10,000 Daltons.
5. The surgical glue of claim 1 , wherein the viscosity of the pre-polymer is from 0.5 to about 100 Pa's.
6. The surgical glue of claim 1 , wherein A is selected from the group consisting of triols, tetraols, and higher polyols.
7. The surgical glue of claim 6 , wherein A is a triol and the triol is glycerol.
8. The surgical glue of claim 1 , wherein the substituted or unsubstituted diacid is an aliphatic diacid selected from the group consisting of glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, and diacids having more than 10 carbons.
9. The surgical glue of claim 2 , wherein the substituted or unsubstituted acrylate groups comprise
wherein, R 1 represents methyl or hydrogen.
10. A crosslinked polyester prepared from the surgical glue of claim 1 , wherein the crosslinked polyester comprises a crosslink density of at least about 10%.
11. The crosslinked polyester of claim 10 , wherein the crosslinked polyester has wet adhesion force to a wet substrate of at least 1.5 times greater than wet adhesion force of the pre-polymer.
12. The crosslinked polyester of claim 11 , wherein the wet substrate is a tissue.
13. The crosslinked polyester of claim 10 , wherein wet adhesion force of the crosslinked polyester is greater than 1.5 N/cm 2 .
14. The crosslinked polyester of claim 10 , wherein the crosslinked polyester is elastic with a maximum compression strain above 30%.
15. The crosslinked polyester of claim 10 , wherein the crosslinked polyester is elastic with a maximum compressive modulus above 0.5 MPa.
16. The crosslinked polyester of claim 10 , wherein adhesive strength of the crosslinked polyester is not substantially altered when the crosslinked polyester is adhered to a wet substrate in the presence of blood and having contact with blood for 5 minutes.
17. The crosslinked polyester of claim 10 , wherein the crosslinked polyester has a burst pressure of above 150 mmHg.
18. The crosslinked polyester of claim 10 , wherein the crosslinked polyester is capable of adhering to a dynamic substrate for a period of at least 7 days.
19. The crosslinked polyester of claim 10 , wherein the crosslinked polyester is capable of transmitting at least 5% of incident UV light.
20. The crosslinked polyester of claim 10 , wherein the crosslinked polyester is biocompatible and biodegradable.
21. The crosslinked polyester of claim 10 , wherein the crosslinked polyester comprises a crosslink density of at least about 15%.
22. A kit comprising a first container comprising the surgical glue of claim 1 and a second container comprising a photoinitiator.
23. A patch comprising the surgical glue of claim 1 .
24. The patch of claim 23 , wherein the surgical glue is on a surface of the patch.
25. The patch of claim 23 , wherein the patch further comprises a photoinitiator.
26. The patch of claim 25 , wherein the patch is transparent to the wavelength of radiation for activating the photoinitiator.
27. A method for gluing or sealing tissue, the method comprising applying the surgical glue of claim 1 to the surface of the tissue and crosslinking the pre-polymer to form a crosslinked pre-polymer, wherein the crosslinked pre-polymer has a 90° pull off adhesive strength of at least about 2 N/cm 2 .
28. A method for adhering tissue to the surface of a medical device, the method comprising applying the surgical glue of claim 1 to the surface of the tissue and/or medical device, contacting the tissue to the medical device, and crosslinking the pre-polymer to form a crosslinked pre-polymer, wherein the medical device adheres to the tissue with a 90° pull off adhesive strength of at least about 2 N/cm 2 .
29. The surgical glue of claim 1 , wherein the substituted or unsubstituted vinyl groups are selected from the group consisting of substituted or unsubstituted acrylate groups, vinyl ester, vinyl carbamates, vinyl ketones, vinyl amide, vinyl carbonate, vinyl ether groups, and allyl groups.
30. The surgical glue of claim 1 , wherein the degree of activation is from about 0.4 to about 0.6.