IP Library › Granted Patent US 11,975,123
Granted Patent B2
US 11,975,123 · App. 16/590,189 · Granted May 7, 2024

Adhesion prevention with shear-thinning polymeric hydrogels

Inventors: Eric Andrew Appel (Palo Alto, CA); Y. Joseph Woo (Atherton, CA); Lyndsay Stapleton (Stanford, CA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
A61L31/041A61L31/042A61L31/145A61L31/148C08L1/08C08L67/025A61L2300/424A61L2400/06C08L2203/02C08L2205/22
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Quick Facts
Patent No.
US 11,975,123
App. No.
16/590,189
Granted
May 7, 2024
Kind
B2
Abstract

A method of preventing tissue adhesion includes forming an incision in tissue, applying a hydrogel to tissue through the incision, and closing the incision with the hydrogel therein. The hydrogel includes a polymer non-covalently cross-linked with a plurality of nanoparticles and prevents a formation of adhesions between tissues and/or organs.

Claims (31)

1. A method of preventing tissue adhesion, comprising:

forming an incision in a tissue;

applying a dynamically cross-linked supramolecular hydrogel to the tissue through the incision, the dynamically cross-linked supramolecular hydrogel comprising a hydrophobically modified cellulose derivative non-covalently cross-linked with a plurality of nanoparticles; and

closing the incision with the dynamically cross-linked supramolecular hydrogel therein, wherein the dynamically cross-linked supramolecular hydrogel prevents a formation of adhesions between the tissue and other tissues and/or organs.

2. The method of claim 1 , wherein forming the incision in the tissue is part of a surgical procedure.

3. The method of claim 1 , wherein the hydrophobically modified cellulose derivative comprises hydrophobically modified hydroxypropylmethylcellulose (HPMC).

4. The method of claim 1 , wherein the nanoparticles comprise poly(ethylene glycol)-b-poly(lactic acid) (PEG-PLA).

5. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel remains on the tissue for at least 7 days after closing the incision.

6. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel remains on the tissue for at least 14 days after closing the incision.

7. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel dissipates from the tissue in less than 120 days after closing.

8. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel dissipates from the tissue in less than 30 days after closing.

9. The method of claim 1 , wherein the applying comprises spraying the dynamically cross-linked supramolecular hydrogel onto the tissue.

10. The method of claim 1 , wherein the applying comprises spreading the dynamically cross-linked supramolecular hydrogel onto the tissue.

11. The method of claim 1 , wherein the applying comprises injecting the dynamically cross-linked supramolecular hydrogel onto the tissue.

12. The method of claim 1 , wherein the applying comprises applying a shear to the dynamically cross-linked supramolecular hydrogel to allow the dynamically cross-linked supramolecular hydrogel to achieve a viscous flow so as to conform to and cover the tissue.

13. The method of claim 12 , wherein the dynamically cross-linked supramolecular hydrogel adheres to the tissue without delaminating after conforming to and covering the tissue.

14. The method of claim 12 , wherein the viscous flow stops and the dynamically cross-linked supramolecular hydrogel recovers its mechanical properties within 5 seconds after the applying of the shear.

15. The method of claim 1 , wherein the tissue comprises abdominal tissue.

16. The method of claim 1 , wherein the tissue comprises orthopedic tissue.

17. The method of claim 1 , wherein the tissue comprises thoracic tissue.

18. The method of claim 1 , wherein the tissue comprises cardiac tissue.

19. The method of claim 1 , wherein the tissue comprises gynecologic tissue.

20. The method of claim 1 , wherein a storage modulus of the dynamically cross-linked supramolecular hydrogel is 50-500 Pa.

21. The method of claim 1 , wherein a yield stress of the dynamically cross-linked supramolecular hydrogel is 50-500 Pa.

22. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel maintains a linear viscoelasticity at strains up to at least 0.5%.

23. The method of claim 1 , wherein a tan delta of the dynamically cross-linked supramolecular hydrogel is less than 1.

24. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel is shear-thinning.

25. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel is self-healing.

26. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel comprises 1 wt % of the hydrophobically modified cellulose derivative or more.

27. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel comprise 5 wt % of the nanoparticles or more.

28. The method of claim 1 , wherein the dynamically cross-linked supramolecular hydrogel comprises approximately 1 wt % of the hydrophobically modified cellulose derivative and 10 wt % of the nanoparticles.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2022
From: APPEL, ERIC ANDREW; WOO, Y. JOSEPH; STAPLETON, LYNDSAY
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 059934/0723 →
Continuity (3)
Continuation In Part 15943358 · Apr 2, 2018
Provisional Application 62739550 · Oct 1, 2018
Related Publication 20200164113A1 · May 28, 2020
Cited By (8)
US 12,241,570 US 12,433,785 US 12,496,215 US 12,599,706 US 12,642,693 US 12,702,586 US 12,734,066 US 12,746,150