IP Library Granted Patent US 8,722,032
Granted Patent B2
US 8,722,032 · App. 13/681,357 · Granted May 13, 2014

Thiol-selective water-soluble polymer derivatives

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Quick Facts
Patent No.
US 8,722,032
App. No.
13/681,357
Granted
May 13, 2014
Kind
B2
Abstract

The present invention provides water-soluble, polymer derivatives having a thiol-selective terminus suitable for selective coupling to thiol groups, such as those contained in the cysteine residues of proteins, as well as methods for preparing the water-soluble, polymer derivatives having a thiol-selective terminus.

Claims (17)

1. A method for a preparing a conjugate, said method comprising:

reacting a water-soluble polymer, POLY-L 0,1 -E, comprising a water-soluble polymer segment (“POLY”), an optional linker, “L,” and having one terminus activated with an electrophile (“-E”) with a symmetrical disulfide reagent, (NU—Y—S-) 2 ,wherein NU is a nucleophile (“-NU”) Y is a linear group (“-Y-”) and S and is a sulfur atom, under conditions effective to promote reaction between said electrophile and said nucleophile to form a polymer product of the structure POLY-L 0,1 -X—Y—S—S—Y—X-L 0,1 -POLY,

wherein the molecular mass of the water-soluble polymer segment is from 1,000 Daltons to 50,000 Daltons;

reducing the disulfide bond in POLY-L 0,1 -X—Y—S—S—Y—X-L 0,1 -POLY to form POLY-L 0,1 -X—Y-SH and

reacting the POLY-L 0,1 -X—Y—SH with a biologically active agent comprising a thiol group, to thereby result in a conjugate.

2. The method of claim 1 , wherein said water-soluble polymer segment is selected from the group consisting of poly(alkylene oxide), poly(vinyl pyrrolidone), poly(vinyl alcohol), polyoxazoline, poly(acryloylmorpholine), and poly(oxyethylated polyol).

3. The method of claim 2 , wherein the water-soluble polymer segment is a polyalkylene oxide.

4. The method of claim 3 , wherein said-water soluble polymer segment is a polyethylene glycol (PEG).

5. The method of claim 4 , wherein said polyethylene glycol is end-capped.

6. The method of claim 1 , wherein said electrophile is a carboxylic acid or a carboxylic acid derivative.

7. The method of claim 1 , wherein said electrophile is selected from the group consisting of carboxylic acid ester, carbonate ester, carbonic acid, acid halide, and anhydride.

8. The method of claim 1 , further comprising the step of purifying said water-soluble polymer prior to said reacting.

9. The method of claim 1 , wherein said nucleophile is selected from the group consisting of primary amino, secondary amino, hydroxy, imino, thiol, and thioester.

10. The method of claim 9 , wherein said nucleophile is primary or secondary amino.

11. The method of claim 5 , wherein said polyethylene glycol is end-capped with a group selected from the group consisting of alkoxy, substituted alkoxy, alkenyloxy, substituted alkenyloxy, alkynyloxy, substituted alkynyloxy, aryloxy, and substituted aryloxy.

12. The method of claim 4 , wherein said polyethylene glycol has a structure selected from the group consisting of linear, branched, forked, and multi-armed.

13. The method of claim 1 , wherein said symmetrical disulfide reagent is cystamine.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Apr 17, 2020
From: TC LENDING, LLC, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 053180/0009 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL 30040, FRAME 0952 Recorded Oct 14, 2015
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 036855/0793 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Oct 6, 2015
From: NEKTAR THERAPEUTICS
To: TC LENDING, LLC, AS COLLATERAL AGENT
Reel/Frame 036796/0562 →
SECURITY AGREEMENT Recorded Mar 19, 2013
From: NEKTAR THERAPEUTICS
To: WELLS FARGO, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 030040/0952 →