IP Library Granted Patent US 10,646,578
Granted Patent B2
US 10,646,578 · App. 15/885,477 · Granted May 12, 2020

Polymer derivatives having particular atom arrangements

Inventors: J. Milton Harris (Huntsville, AL); Antoni Kozlowski (Huntsville, AL); Samuel P. McManus (Guntersville, AL); Michael D. Bentley (Huntsville, AL); Stephen A. Charles (San Jose, CA)
Assignee: Nektar Therapeutics
A61K47/60A61K31/357A61K31/4025A61K31/52A61K38/095A61K38/1816A61K38/193A61K38/212A61K38/215A61K38/24A61K38/27A61K38/37C08G65/329C08G65/33337C08G65/33344
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Quick Facts
Patent No.
US 10,646,578
App. No.
15/885,477
Granted
May 12, 2020
Kind
B2
Abstract

Polymeric reagents are provided comprising a moiety of atoms arranged in a specific order, wherein the moiety is positioned between a water-soluble polymer and a reactive group. The polymeric reagents are useful for, among other things, forming polymer-active agent conjugates. Related methods, compositions, preparations, and so forth are also provided.

Claims (33)

1. A linear polymeric reagent comprising a structure:

wherein:

POLY 1 is a water-soluble polymer;

(a) is 0, 1, 2 or 3;

(b) is 0, 1, 2 or 3;

R 1 is H or an organic radical;

X 1 , when present, is a first spacer moiety;

X 2 , when present, is a second spacer moiety; and

Z is a reactive group.

2. The polymeric reagent of claim 1 , wherein R 1 is H.

3. The polymeric reagent of claim 1 , wherein R 1 is an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl and substituted aryl.

4. The polymeric reagent of claim 1 , wherein R 1 is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, and piperidonyl.

5. The polymeric reagent of claim 1 , wherein the water-soluble polymer portion is a polymer selected from the group consisting of a poly(alkylene oxide), poly(vinyl pyrrolidone), poly(vinyl alcohol), polyoxazoline, poly(acryloylmorpholine), and poly(oxyethylated polyols).

6. The polymeric reagent of claim 1 , wherein the water-soluble polymer portion is a poly(alkylene oxide).

7. The polymeric reagent of claim 6 , wherein the poly(alkylene oxide) is a poly(ethylene glycol).

8. The polymeric reagent of claim 7 , wherein the poly(ethylene glycol) is terminally capped with an end-capping moiety selected from the group consisting hydroxyl and alkoxy.

9. The polymeric reagent of claim 7 , wherein the poly(ethylene glycol) is terminally capped with methoxy.

10. The polymeric reagent of claim 8 , wherein the poly(ethylene glycol) has a molecular weight of from about 100 Daltons to about 100,000 Daltons.

11. The polymeric reagent of claim 10 , wherein the poly(ethylene glycol) has a molecular weight of from about 1,000 Daltons to about 60,000 Daltons.

12. The polymeric reagent of claim 11 , wherein the poly(ethylene glycol) has a nominal average molecular mass of from about 2,000 Daltons to about 50,000 Daltons.

13. The polymeric reagent of claim 1 , wherein the water-soluble polymer is a homopolymer.

14. The polymeric reagent of claim 1 , wherein the nitrogen atom of the

moiety is linked to the water-soluble polymer through a direct covalent bond.

15. The polymeric reagent of claim 1 , wherein the nitrogen atom of the

moiety is linked to the water-soluble polymer through a first spacer moiety.

16. The polymeric reagent of claim 1 , wherein the reactive group is selected from the group consisting of hydroxyl, ester, ester, orthoester, carbonate, carbonate, acetal, aldehyde, aldehyde hydrate, ketone, vinyl ketone, ketone hydrate, thione, monothiohydrate, dithiohydrate, hemiketal, monothioketal hemiketal, dithiohemiketal, ketal, dithioketal, alkenyl, acrylate, methacrylate, acrylamide, sulfone, sulfone, amine, hydrazide, thiol, disulfide, thiol hydrate, carboxylic acid, isocyanate, isothiocyanate, maleimide, succinimide, benzotriazole, vinylsulfone, chloroethylsulfone, dithiopyridine, vinylpyridine, iodoacetamide, epoxide, glyoxals, diones, mesylates, tosylates, thiosulfonate, tresylate, silane, —(CH 2 ) r CO 2 H, —(CH 2 ) r′ CO 2 NS,

(CH 2 ) r′ CO 2 Bt, —(CH 2 ) r CH(OR) 2 , —(CH 2 ) r CHO, —(CH 2 ) 2 —NH 2 , —(CH 2 ) r M, —(CH 2 ) r —S—SO 2 —R, where r is 1-5, r′ is 0-5, R is aryl or alkyl, NS is N-succinimidyl, Bt is 1-benzotriazolyl, and M is N-maleimidyl, and protected and activated forms of any of the foregoing.

17. The polymeric reagent of claim 1 , wherein (a) is 0 or 1; and (b) is 0 or 1.

18. The polymeric reagent of claim 1 , wherein POLY 1 -(X 1 ) a -N(R 1 )˜ is selected from:

where (m) is 2 to 4,000.

19. The polymeric reagent of claim 1 , having a structure selected from:

20. The polymeric reagent of claim 1 , having a structure:

where Z is selected from N-hydroxysuccinimide ester, aldehyde, maleimide, and thiol.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2020
From: TC LENDING, LLC, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 053180/0009 →
SECURITY INTEREST Recorded Apr 19, 2018
From: NEKTAR THERAPEUTICS
To: TC LENDING, LLC, AS COLLATERAL AGENT
Reel/Frame 045591/0051 →
Continuity (8)
Continuation 15184182 · Jun 16, 2016
Continuation 14720213 · May 22, 2015
Continuation 14136497 · Dec 20, 2013
Continuation 13043438 · Mar 8, 2011
Continuation 11389431 · Mar 23, 2006
Continuation In Part 10851691 · May 21, 2004
Provisional Application 60473213 · May 23, 2003
Related Publication 20190022236A1 · Jan 24, 2019