IP Library Granted Patent US 9,687,582
Granted Patent B2
US 9,687,582 · App. 14/056,281 · Granted Jun 27, 2017

Negative-swelling and exceptionally robust adhesive hydrogels

Inventors: Phillip B. Messersmith (Clarendon Hills, IL); Devin G. Barrett (Evanston, IL)
Assignee: Northwestern University
A61L24/046A61L24/0031C08G65/324C08G65/332C08G65/3317C08G65/3332C08G65/33303C08G65/33306C08K3/20C08G2210/00C08G2650/30
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Quick Facts
Patent No.
US 9,687,582
App. No.
14/056,281
Granted
Jun 27, 2017
Kind
B2
Abstract

The present invention provides adhesive hydrogels that negatively swell at physiological temperature. By combining mussel-mimetic chemistry and the thermosensitive nature of poly(ethylene oxide)-poly(propylene oxide) copolymers, novel materials were designed that are suitable as medical sealants and adhesives.

Claims (29)

1. A method for making a non-swelling medical adhesive comprising a hydrogel in a PBS solution at physiological temperature, the method comprising:

(a) contacting a composition comprising a catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer having four linear PPO-PEO arms emanating from a tetrafunctional ethylenediamine core with a biocompatible oxidant in a PBS solution at room temperature or below, whereby the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer is chemically cross-linked to form a hydrogel;

(b) increasing the temperature of the resulting hydrogel in the PBS solution to physiological temperature; and

(c) thermally equilibrating the hydrogel at physiological temperature, whereby the hydrogen exhibits no or negative swelling after at least one day in PBS solution at 37° C.

2. The method of claim 1 , wherein room temperature is about 20° C. or about 22° C.

3. The method of claim 1 , wherein physiological temperature is about 37° C.

4. The method of claim 1 , wherein one or more terminal ends of the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer includes a catechol moiety.

5. The method of claim 4 , wherein the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer has the structure A(B—C) 4 ,

wherein A is,

B is

wherein x is about 19 and y is about 59; and,

C is a catechol-terminating moiety.

6. The method of claim 5 , wherein C is

7. The method of claim 1 , wherein the oxidant is a periodate.

8. The method of claim 7 , wherein the periodate is sodium periodate.

9. The method of claim 7 , wherein the mole ratio of catechol present in the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer to the periodate oxidant is 2:1.

10. A non-swelling medical adhesive in a PBS solution at 37° C. made by the method of claim 1 , wherein the poly(propylene oxide) block within the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer that is chemically cross-linked to form the hydrogel comprises a hydrophobic domain.

11. A non-swelling medical adhesive comprising a hydrogel in a PBS solution at physiological temperature made by mixing a solution of two or more catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer molecules having four linear PPO-PEO arms emanating from a tetrafunctional ethylenediamine core with a biocompatible oxidant in a PBS solution at room temperature or below for at least fifteen minutes, whereby the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymers are chemically cross-linked to each other between the catechol moieties of adjacent block copolymer molecules, and increasing the temperature of the resulting hydrogel in the PBS solution to equilibrate the hydrogen to physiological temperature for at least one day wherein the hydrogel exhibits no or negative swelling while being exposed to a PBS solution at 37° C. after temperature equilibration.

12. The medical adhesive of claim 11 , wherein one or more terminal ends of the block copolymer molecules include a catechol moiety.

13. The medical adhesive of claim 12 , wherein the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer molecules have the structure A(B—C) 4 ,

wherein A is

B is

wherein x is about 19 and y is about 59; and

C is a catechol-terminating moiety.

14. The medical adhesive of claim 13 , wherein C is

15. The method of claim 1 , wherein the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer comprises about 70% by weight of poly(polypropylene oxide) and about 30% weight of poly(ethylene oxide).

16. The non-swelling medical adhesive of claim 10 , wherein the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer comprises about 70% by weight of poly(polypropylene oxide) and about 30% weight of poly(ethylene oxide).

17. The non-swelling medical adhesive of claim 11 , wherein the catechol-modified poly(ethylene oxide)-poly(propylene oxide) block copolymer comprises about 70% by weight of poly(polypropylene oxide) and about 30% weight of poly(ethylene oxide).

18. The non-swelling medical adhesive of claim 10 , wherein the adhesive exhibits an adhesion strength of about 31-49 kPa.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2014
From: MESSERSMITH, PHILLIP B.; BARRETT, DEVIN G.
To: NORTHWESTERN UNIVERSITY
Reel/Frame 031983/0563 →
CONFIRMATORY LICENSE Recorded Dec 16, 2013
From: NORTHWESTERN UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031817/0629 →
Continuity (2)
Provisional Application 61715403 · Oct 18, 2012
Related Publication 20140113989A1 · Apr 24, 2014