NITRIC OXIDE INFUSED SURGICAL TISSUE REPAIR TECHNOLOGIES

Abstract

Surgical tissue repair technologies incorporating nitric oxide releasing materials which release nitric oxide into the surrounding tissue. The surgical tissue repair technologies include tissue repair devices, such as surgical meshes, vascular stents, surgical grafts, irrigation solutions, and other internal surgical tissue repair materials. The nitric oxide releasing compound may be a S-nitrosothiol compound, such as s-nitroso-n-acetyl penicillamine (SNAP), s-nitrosoglutathione (GSNO), and mixtures thereof. The tissue repair devices may further include a catalyst to facilitate release of nitric oxide. The devices may include a substrate coated with a coating incorporating the same or different nitric oxide releasing compound. The devices may include a substrate impregnated with the nitric oxide releasing compound and coated with a polymer-based coating incorporating the same or different nitric oxide releasing compound. The polymer-based coating may include diazeniumdiolate groups (NONOate groups). The polymer-based coating may include a polyethyleneimine cellulose NONOate polymer.

Claims

1. A surgical tissue repair device configured to be implanted during tissue repair surgery and which releases nitric oxide into the surrounding tissue, wherein the device comprises a substrate incorporating a nitric oxide releasing compound.

2. The surgical tissue repair device of claim 1, wherein the nitric oxide releasing compound is a S-nitrosothiol compound.

3. The surgical tissue repair device of claim 1, wherein the nitric oxide releasing compound is selected from s-nitroso-n-acetyl penicillamine (SNAP), s-nitrosoglutathione (GSNO), and mixtures thereof.

4. The surgical tissue repair device of claim 1, wherein the nitric oxide releasing compound reacts in the presence of a physiological fluid to release nitric oxide into the surrounding tissue.

5. The surgical tissue repair device of claim 4, wherein the physiological fluid is selected from interstitial fluid and blood.

6. The surgical tissue repair device of claim 1, wherein the substrate further incorporates a catalyst to facilitate release of nitric oxide.

7. The surgical tissue repair device of claim 6, wherein the catalyst is selected from copper, iron, zinc, selenium, and silver.

8. The surgical tissue repair device of claim 1, wherein the substrate comprises a surgical mesh.

9. The surgical tissue repair device of claim 1, wherein the substrate comprises a surgical graft.

10. The surgical tissue repair device of claim 1, wherein the substrate comprises a vascular stent.

11. The surgical tissue repair device of claim 1, wherein the substrate is a polymeric material impregnated with the nitric oxide releasing compound.

12. The surgical tissue repair device of claim 1, wherein the substrate is coated with a polymer-based coating incorporating the same or different nitric oxide releasing compound.

13. The surgical tissue repair device of claim 1, wherein the substrate is impregnated with the nitric oxide releasing compound and coated with a polymer-based coating incorporating the same or different nitric oxide releasing compound.

14. The surgical tissue repair device of claim 12, wherein the polymer-based coating comprises diazeniumdiolate groups (NONOate groups).

15. The surgical tissue repair device of claim 12, wherein the polymer-based coating comprises a polyethyleneimine cellulose NONOate polymer.

16. The surgical tissue repair device of claim 13, wherein the polymer-based coating comprises diazeniumdiolate groups (NONOate groups).

17. The surgical tissue repair device of claim 13, wherein the polymer-based coating comprises a polyethyleneimine cellulose NONOate polymer.

18. A surgical tissue repair device configured to be implanted during tissue repair surgery which releases nitric oxide into the surrounding tissue, wherein the device comprises a polymeric substrate incorporating a S-nitrosothiol compound selected from s-nitroso-n-acetyl penicillamine (SNAP), s-nitrosoglutathione (GSNO), and mixtures thereof, which releases the nitric oxide, wherein the tissue repair device is selected from a surgical mesh, a surgical graft, and a vascular stent.

19. The surgical tissue repair device of claim 18, wherein the substrate further incorporates a catalyst to facilitate release of nitric oxide.

20. The surgical tissue repair device of claim 19, wherein the catalyst is selected from copper, iron, zinc, selenium, and silver.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

[0034] Example embodiments will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:

[0035] FIG. 1 is cross-sectional representation of portion of a surgical tissue repair device fabricated to contain a nitric oxide releasing compound according to an embodiment.

[0036] FIG. 2 is cross-sectional representation of portion of a surgical tissue repair device fabricated to contain a nitric oxide releasing compound according to an embodiment.

[0037] FIG. 3 is cross-sectional representation of portion of a surgical tissue repair device fabricated to contain a nitric oxide releasing compound according to an embodiment.

DESCRIPTION OF EMBODIMENTS

[0038] The disclosure relates to a biomedical technologies involved in internal surgical tissue repair which release nitric oxide to accelerate or enhance the healing process.

[0039] In an embodiment, a surgical tissue repair device is configured to be implanted during tissue repair surgery and which releases nitric oxide into the surrounding tissue, wherein the device comprises a substrate incorporating a nitric oxide releasing compound.

[0040] Any physiologically compatible nitric oxide releasing compound may be used herein. Non-limiting examples of nitric oxide releasing compounds include s-nitrosoglutathione (GSNO), s-nitroso-n-acetylpenicillamine (SNAP), and mixtures thereof. S-nitrosoglutathione (GSNO) and s-nitroso-n-acetylpenicillamine (SNAP) are naturally occurring and/or biocompatible materials that release in-vivo and degrade to form nitric oxide at physiologically relevant concentrations.

[0041] Nitric oxide is a messenger molecule expressed naturally in the inflammatory and proliferative phases of the wound healing process. It is responsible for promoting collagen synthesis and deposition, chemotaxis and reepithelialization, and angiogenesis. Additionally, it has anti-platelet activation properties—leading to a decrease in contact activated thrombogenesis.

[0042] Incorporating nitric oxide into wound repair technologies such as surgical meshes, surgical grafts, and vascular stents may reduce adverse inflammatory reactions and enhance adoption of foreign material into the surrounding tissues through increased angiogenesis and reepithelialization. Because of its anti-platelet activation characteristics, nitric oxide has the potential to reduce or eliminate the need for dual antiplatelet therapy following vascular stent implantation, which is associated with bleeding events following coronary stent implantation.

[0043] Lastly, nitric oxide has natural antimicrobial properties. At low concentrations it acts as a signaling molecule that promotes growth and activity of immune cells. At higher concentrations (respiratory burst of a neutrophil) NO covalently binds DNA, proteins and lipids of pathogens and kills them. There are also reactive species created by the auto-oxidation of nitric oxide, which directly react with DNA structure, inhibit DNA repair, and increase generation of alkylating agents and H.sub.2O.sub.2, which are genotoxic. These natural antimicrobial properties are an important aspect of the present disclosure since infections are a serious complication associated with all wound repair technologies.

[0044] The nitric oxide releasing compound may be impregnated in the surgical tissue repair device substrate, and particularly to surfaces of the device substrate that may be exposed to blood and interstitial fluid.

[0045] The impregnating step may be accomplished by exposing the surgical tissue repair device substrate to a solvent having the nitric oxide releasing compound dissolved therein. The substrate is exposed to the solvent solution for sufficient time to permit the nitric oxide releasing compound to penetrate the substrate. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the nitric oxide releasing compound and device substrate may be used. The nitric oxide releasing compound may be dissolved in tetrahydrofuran (THF), dioxolane, methyl ethyl ketone (MEK), methanol, ethanol, isopropyl alcohol, water, or combinations thereof. The device substrate may be soaked in these solutions containing the nitric oxide releasing compound for sufficient time to impregnate the device substrate with the nitric oxide releasing compound. The exposure time may range between 5 minutes and 24 hours.

[0046] The device substrate may be further impregnated with a catalyst to facilitate release of nitric oxide. Non-limiting examples of such catalysts include copper, iron, zinc, selenium, and silver. The catalyst may be impregnated into the device substrate by exposing the device substrate to a solvent having the catalyst dissolved therein. The catalyst may be impregnated into the device substrate using the same solvent system as the nitric oxide releasing compound, discussed above, either during the same impregnation step, a subsequent impregnation step, or a prior impregnation step. The device substrate is exposed to the solvent solution for sufficient time to permit the catalyst to penetrate the device substrate. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the catalyst and device substrate may be used, including those described above in relation to the nitric oxide releasing compound.

[0047] Reference is made to the figures which illustrate portions of a surgical tissue repair device. The surgical tissue repair device may be configured in any form useful for tissue repair surgery. Non-limiting examples of surgical tissue repair devices include a surgical mesh, a surgical graft, and a vascular stent.

[0048] FIG. 1 is cross-sectional representation of a portion of a surgical tissue repair device 100 fabricated to contain a nitric oxide (NO) releasing compound. The tissue repair device 100 includes a device substrate 110 impregnated with a nitric oxide releasing compound.

[0049] The nitric oxide releasing compound may be impregnated in the device substrate 110 by exposing the device substrate 110 to a solvent having the nitric oxide releasing compound dissolved therein. The device substrate 110 is exposed to the solvent solution for sufficient time to permit the nitric oxide releasing compound to penetrate the device substrate 110. The impregnating step may occur at any suitable temperature. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the device substrate and the nitric oxide releasing compound may be used.

[0050] The nitric oxide releasing compound may be dissolved in tetrahydrofuran (THF), dioxolane, methyl ethyl ketone (MEK), methanol, ethanol, isopropyl alcohol, water, or combinations thereof. The device substrate may be soaked in these solutions containing the nitric oxide releasing compound for sufficient time to impregnate the device substrate with the nitric oxide releasing compound. The exposure time may range between 5 minutes and 24 hours.

[0051] The device substrate 110 may be further impregnated with a catalyst to facilitate release of nitric oxide. Non-limiting examples of such catalysts include copper, iron, zinc, selenium, and silver. The catalyst may be impregnated into the device substrate 110 by exposing the device substrate to a solvent having the catalyst dissolved therein. The catalyst may be impregnated into the device substrate using the same solvent system as the nitric oxide releasing compound, discussed above, either during the same impregnation step, a subsequent impregnation step, or a prior impregnation step. The device substrate is exposed to the solvent solution for sufficient time to permit the catalyst to penetrate the device substrate. The impregnating step may occur at any suitable temperature. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the device substrate and the catalyst may be used.

[0052] FIG. 2 is a cross-sectional representation of a portion of a surgical tissue repair device 200 fabricated to contain a nitric oxide (NO) releasing compound. The tissue repair device 200 includes a substrate 210 coated with a polymer-based coating 220 incorporating a nitric oxide releasing compound.

[0053] In one non-limiting embodiment, the coating 220 may be coated onto the substrate 210 and then infused or impregnated with one or more nitric oxide releasing compounds. The coating 220 may be infused or impregnated with a nitric oxide releasing compound by exposing the coating 220 to a solvent having the nitric oxide releasing compound dissolved therein, in a manner similar to the discussion of FIG. 1, above.

[0054] The coating 220 is exposed to the solvent solution for sufficient time to permit the nitric oxide releasing compound to penetrate the coating 220. The impregnating step may occur at any suitable temperature. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the coating and the nitric oxide releasing compound may be used.

[0055] The nitric oxide releasing compound may be dissolved in tetrahydrofuran (THF), dioxolane, methyl ethyl ketone (MEK), methanol, ethanol, isopropyl alcohol, water, or combinations thereof. The coating 220 may be soaked in these solutions containing the nitric oxide releasing compound for sufficient time to impregnate the coating with the nitric oxide releasing compound. The exposure time may range between 5 minutes and 24 hours.

[0056] The coating 220 may be further impregnated with a catalyst to facilitate release of nitric oxide. Non-limiting examples of such catalysts include copper, iron, zinc, selenium, and silver. The catalyst may be impregnated into the coating 220 by exposing the coating to a solvent having the catalyst dissolved therein. The catalyst may be impregnated into the coating using the same solvent system as the nitric oxide releasing compound, discussed above, either during the same impregnation step, a subsequent impregnation step, or a prior impregnation step. The coating is exposed to the solvent solution for sufficient time to permit the catalyst to penetrate the coating. The impregnating step may occur at any suitable temperature. The impregnating step may occur at room temperature. The impregnating step may occur at a temperature in the range from about 20 to 60° C. Any solvent that is compatible with the coating and the catalyst may be used.

[0057] In one non-limiting embodiment, a polymer coating material incorporating one or more nitric oxide releasing compounds may be coated onto the substrate 210 to form coating 220.

[0058] Non-limiting examples of a polymer material incorporating one or more nitric oxide releasing compounds, which can release nitric oxide directly, include, but are not limited to, polymers containing diazeniumdiolate groups (NONOate groups) and polyethyleneimine (PEI) cellulose NONOate. NONOates carry an [N(O—)N═O] group on a nucleophile adduct, usually an amine. NONOates decompose spontaneously in solution at physiological pH and temperature to generate NO. The NONOate groups may be noncovalently dispersed within the polymer matrix, covalently bound to pendent polymer side chains, or covalently bound directly to the polymer backbone.

[0059] FIG. 3 is a cross-sectional representation of a portion of a surgical tissue repair device 300 fabricated to contain a nitric oxide (NO) releasing compound. The tissue repair device 300 includes a device substrate 310 impregnated with a nitric oxide releasing compound, similar to device substrate 110 described above. The device substrate 310 is further coated with a polymer-based coating 320 incorporating the same or a different nitric oxide releasing compound, similar to the coating 220 described above.

[0060] All examples and conditional language recited herein are intended for pedagogical objects to aid the reader in understanding the invention and the concepts contributed by the inventor to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions. Although embodiments of the present inventions have been described in detail, it should be understood that the various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention. Additionally, the words “including,” “having,” and variants thereof (e.g., “include,” “includes,” “have,” and “has”) as used in the present disclosure, including the claims, shall be open ended and have the same meaning as the word “comprising” and variants thereof (e.g., “comprise” and “comprises”).