IP Library Granted Patent US 11,179,470
Granted Patent B2
US 11,179,470 · App. 16/248,537 · Granted Nov 23, 2021

Hydrogels with biodegradable crosslinking

Inventors: Gary W. Ashley (Alameda, CA); Daniel V. Santi (San Francisco, CA); Jeffrey C. Henise (San Francisco, CA)
Assignee: ProLynx LLC
A61K47/34
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Quick Facts
Patent No.
US 11,179,470
App. No.
16/248,537
Granted
Nov 23, 2021
Kind
B2
Abstract

Hydrogels that degrade under appropriate conditions of pH and temperature by virtue of crosslinking compounds that cleave through an elimination reaction are described. The hydrogels may be used for delivery of various agents, such as pharmaceuticals.

Claims (49)

1. A hydrogel that is biodegradable under physiological conditions which hydrogel comprises one or more multi-armed PEG polymers crosslinked by a linker that decomposes by a beta elimination reaction,

wherein said linker is

of Formula (1):

wherein for each linker of formula (1):

m of formula (1) is 0 or 1;

X of formula (1) is

wherein

T* is O, S, or NR 6 ;

z is 1-6;

Y is (OCH 2 CH 2 ) p , wherein p is 1-100; and

Z 2 is a first functional group that is coupled to a first cognate group of a first multi-armed polyethylene glycol (PEG) polymer; and

one of R 1 , R 2 , or R 5 comprises a second functional group that is coupled to a second cognate group of a second multi-armed PEG polymer,

wherein each said first functional group and said second functional group independently comprises N 3 , NH 2 , NH—CO 2 t Bu, SH, S t Bu, maleimide, CO 2 H, CO 2 t Bu, 1,3-diene, cyclopentadiene, furan, alkyne, cyclooctyne, acrylate, or acrylamide;

with the proviso that:

(1) when one of R 5 of formula (1) comprises a second functional group that is coupled to a second cognate group of a second multi-armed PEG polymer, the remaining R 5 of formula (1) is H, optionally substituted alkyl, optionally substituted alkenylalkyl, optionally substituted alkynylalkyl, (OCH 2 CH 2 ) p O-alkyl wherein p=1-1000, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl: and

(a) R 1 and R 2 of formula (1) are independently CN, NO 2 , optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkenyl, optionally substituted alkynyl, COR 3 , SOR 3 , SO 2 R 3 , or SR 4 ;

(b) R 1 and R 2 of formula (1) may be joined to form a 3-8 membered ring;

(c) R 1 of formula (1) is CN, NO 2 , optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkenyl, optionally substituted alkynyl, COR 3 , SOR 3 , SO 2 R 3 , or SR 4 ; and R 2 of formula (1) is H, optionally substituted alkyl, optionally substituted arylalkyl, or optionally substituted heteroarylalkyl; or

(d) R 2 of formula (1) is CN, NO 2 , optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkenyl, optionally substituted alkynyl, COR 3 , SOR 3 , SO 2 R 3 , or SR 4 ; and R 1 of formula (1) is H, optionally substituted alkyl, optionally substituted arylalkyl, or optionally substituted heteroarylalkyl; or

(2) when R 1 of formula (1) comprises a second functional group that is coupled to a second cognate group of a second multi-armed PEG polymer: R 2 of formula (1) is CN, NO 2 , optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkenyl, optionally substituted alkynyl, COR 3 , SOR 3 , SO 2 R 3 , or SR 4 ; and each R 5 of formula (1) is independently H, optionally substituted alkyl, optionally substituted alkenylalkyl, optionally substituted alkynylalkyl, (OCH 2 CH 2 ) p O-alkyl wherein p=1-1000, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; or

(3) when R 2 of formula (1) comprises a second functional group that is coupled to a second cognate group of a second multi-armed PEG polymer: R 1 of formula (1) is CN, NO 2 , optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkenyl, optionally substituted alkynyl, COR 3 , SOR 3 , SO 2 R 3 , or SR 4 ; and each R 5 of formula (1) is independently H, optionally substituted alkyl, optionally substituted alkenylalkyl, optionally substituted alkynylalkyl, (OCH 2 CH 2 ) p O-alkyl wherein p=1-1000, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl;

wherein

R 3 is selected from the group consisting of: (i) H; (ii) optionally substituted alkyl; (iii) optionally substituted aryl; (iv) optionally substituted arylalkyl; (v) optionally substituted heteroaryl; (vi) optionally substituted heteroarylalkyl; (vii) OR 9 ; and (viii) NR 9 2 ;

R 4 is selected from the group consisting of: (i) optionally substituted alkyl; (ii) optionally substituted aryl; (iii) optionally substituted arylalkyl; (iv) optionally substituted heteroaryl; and (v) optionally substituted heteroarylalkyl; and

each R 9 is independently H or optionally substituted alkyl, or both R 9 groups taken together with the nitrogen to which they are attached form a heterocyclic ring.

2. The biodegradable hydrogel of claim 1 , wherein each said first functional group comprises N 3 .

3. The biodegradable hydrogel of claim 1 , wherein in Formula (1)

R 2 is H; and/or

one of R 5 is H and the other is (CH 2 ) n Z, wherein n is 1-6 and Z includes said second functional group.

4. The biodegradable hydrogel of claim 1 , wherein in Formula (1) R 1 is CN or SO 2 R 3 .

5. The biodegradable hydrogel of claim 1 , wherein the first multi-armed PEG polymer and/or second multi-armed PEG polymer comprises the formula [—(CH 2 ) s (CH 2 CH 2 O) n ] t Q, wherein

n is 10-1000;

s is 0-2;

t is 2,4, 8, 16 or 32 and independently represents the number of arms of said multi-armed PEG polymer; and

Q is a core group having a valency t.

6. The biodegradable hydrogel of claim 5 , wherein Q is pentaerythritol, tripentaerythritol, or hexaglycerin.

7. The biodegradable hydrogel of claim 1 , wherein the coupling of the first functional group and the first cognate group comprises a product of:

a reaction of N 3 with acetylene, cyclooctyne, or maleimide;

a reaction of SH with maleimide, acrylate, acrylamide, vinylsulfone, vinylsulfonamide, or halocarbonyl;

a reaction of NH 2 with carboxylic acid or activated carboxylic acid; or

a reaction of maleimide with 1,3-diene, cyclopentadiene, or furan.

8. The biodegradable hydrogel of claim 1 , wherein the coupling of the first functional group and the first cognate group comprises a product of a reaction of N 3 with cyclooctyne.

9. The biodegradable hydrogel of claim 1 , wherein each said second functional group comprises N 3 .

10. The biodegradable hydrogel of claim 1 , wherein the coupling of the second functional group and the second cognate group comprises a product of:

a reaction of N 3 with acetylene, cyclooctyne, or maleimide;

a reaction of SH with maleimide, acrylate, acrylamide, vinylsulfone, vinylsulfonamide, or halocarbonyl;

a reaction of NH 2 with carboxylic acid or activated carboxylic acid; or

a reaction of maleimide with 1,3-diene, cyclopentadiene, or furan.

11. The biodegradable hydrogel of claim 1 , wherein the coupling of the second functional group and the second cognate group comprises a product of a reaction of N 3 with cyclooctyne.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 20, 2019
From: ASHLEY, GARY W.; SANTI, DANIEL V.; HENISE, JEFFREY C.
To: PROLYNX LLC
Reel/Frame 049236/0102 →
Continuity (4)
Continuation 15486215 · Apr 12, 2017
Continuation 14343819
Provisional Application 61531990 · Sep 7, 2011
Related Publication 20190209691A1 · Jul 11, 2019
Cited By (8)
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