IP Library Granted Patent US 8,309,680
Granted Patent B2
US 8,309,680 · App. 12/224,201 · Granted Nov 13, 2012

Segmented degradable polymers and conjugates made therefrom

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Quick Facts
Patent No.
US 8,309,680
App. No.
12/224,201
Granted
Nov 13, 2012
Kind
B2
Abstract

The present invention provides, among other things, segmented, degradable polymeric reagents suitable for reaction with biologically active agents to form conjugates, the polymeric reagents comprising one or more polymer chains divided or separated by one or more degradable linkages into polymer segments having a molecular weight suitable for renal clearance. The polymeric reagents can have a substantially linear structure, a branched structure, or a multiarm structure. Each structure includes one or more linkages capable of degradation in vivo.

Claims (26)

1. A polymeric reagent having a structure of the following formula:

Z—[(X 1 ) a -POLY 1 -(X 2 ) b -L 1 -(X 3 ) c ] m —(X 4 ) d —POLY 2 -Z  Formula (Ia),

wherein:

each POLY 1 and POLY 2 , which may be the same or different, is a water-soluble and non-peptidic polymer;

each X 1 , X 2 , X 3 , and X 4 , which may be the same or different, is a spacer moiety;

each L 1 is a disulfide linkage;

each Z, which may be the same or different, is a capping group or a functional group, and may optionally include a spacer moiety, with the proviso that at least one Z is a functional group;

each a, b, c, and d, which may be the same or different, is either zero or one;

m is an integer in the range of 1-10 and represents the number of polymer segments, POLY 1 , covalently attached in series;

wherein the polymeric reagent is not in the form of a hydrogel.

2. The polymer reagent of claim 1 , wherein each of POLY 1 and POLY 2 have a number average molecular weight of less than or equal to about 20,000 Da.

3. The polymer reagent of claim 1 , wherein each of POLY 1 and POLY 2 have a number average molecular weight of less than or equal to about 10,000 Da.

4. The polymer reagent of claim 1 , wherein each of POLY 1 and POLY 2 have a number average molecular weight of less than or equal to about 8,000 Da.

5. The polymer reagent of claim 1 , wherein each of m and o, which may be the same or different, are in the range of 1-5.

6. The polymer reagent of claim 1 , wherein each of POLY 1 and POLY 2 are selected from the group consisting of poly(alkylene glycols), poly(olefinic alcohol), poly(vinylpyrrolidone), poly(hydroxyalkylmethacrylamide), poly(hydroxyalkylmethacrylate), poly(saccharides), poly(α-hydroxy acid), poly(acrylic acid), poly(vinyl alcohol), polyphosphazene, polyoxazoline, poly(N-acryloylmorpholine), and copolymers, terpolymers, or mixtures thereof.

7. The polymer reagent of claim 1 , wherein POLY 1 and POLY 2 are poly(ethylene glycol).

8. The polymer reagent of claim 1 , wherein each of X 1 , X 2 , X 3 , and X 4 , when present, is selected from the group consisting of —C(O)—, —C(O)—NH—, —NH—C(O)—NH—, —O—C(O)—NH—, —C(S)—, —CH 2 —, —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —, —O—CH 2 —, —O—CH 2 —CH 2 —, —CH 2 —O—CH 2 —, —O—CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —O—, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—O—CH 2 —, —CH 2 —C(O)—O—CH 2 —, —CH 2 —CH 2 —C(O)—O—CH 2 —, —C(O)—O—CH 2 —CH 2 —, —NH—C(O)—CH 2 —, —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —, —NH—C(O)—CH 2 —CH 2 —, —CH 2 —NH—C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —O—C(O)—NH—CH 2 —, —O—C(O)—NH—CH 2 —CH 2 —, —NH—CH 2 —, —NH—CH 2 —CH 2 —, —CH 2 —NH—CH 2 —, —CH 2 —CH 2 —NH—CH 2 —, —C(O)—CH 2 —, —C(O)—CH 2 —CH 2 —, —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, —NH—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, and —O—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, —O—C(O)—NH—[CH 2 ] h —(OCH 2 CH 2 ) j —, —NH—C(O)—O—[CH 2 ] h —(OCH 2 CH 2 ) j —, bivalent cycloalkyl group, —O—, —S—, —N(R 6 )—, and combinations thereof, wherein R 6 is H or an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl and substituted aryl, (h) is zero to six, and (j) is zero to 20.

9. The polymeric reagent of claim 1 , wherein the reagent has the structure:

Z—[(X 1 ) a -POLY 1 -(X 2 ) b -L 1 -(X 3 ) c ] m —(X 4 ) d —POLY 2 -Z  Formula (Ia)

wherein:

POLY 1 and POLY 2 are each branched poly(ethylene glycol) molecules comprising a polyol core and at least two polymer arms extending from the polyol core;

L 1 is a disulfide bond;

m is 1; and

each of X 1 , X 2 , X 3 , and X 4 , when present, is selected from the group consisting of —C(O)—, —C(O)—NH—, —NH—C(O)—NH—, —O—C(O)—NH—, —C(S)—, —CH 2 —, —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —, —O—CH 2 —, —CH 2 —O—, —O—CH 2 —CH 2 —, —CH 2 —O—CH 2 —, —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —O—, —O—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —O—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —O—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —O—CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —O—, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—NH—CH 2 —CH 2 —CH 2 —CH 2 —, —CH 2 —C(O)—NH—CH 2 —CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —CH 2 —C(O)—NH—, —C(O)—O—CH 2 —, —CH 2 —C(O)—O—CH 2 —, —CH 2 —CH 2 —C(O)—O—CH 2 —, —C(O)—O—CH 2 —CH 2 —, —NH—C(O)—CH 2 —, —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —, —NH—C(O)—CH 2 —CH 2 —, —CH 2 —NH—C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —C(O)—NH—CH 2 —, —C(O)—NH—CH 2 —CH 2 —, —O—C(O)—NH—CH 2 —, —O—C(O)—NH—CH 2 —CH 2 —, —NH—CH 2 —, —NH—CH 2 —CH 2 —, —CH 2 —NH—CH 2 —, —CH 2 —CH 2 —NH—CH 2 —, —C(O)—CH 2 —, —C(O)—CH 2 —CH 2 —, —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —, —CH 2 —CH 2 —C(O)—CH 2 —CH 2 —, —CH 2 —CH 2 —C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —, —CH 2 —CH 2 —CH 2 —C(O)—NH—CH 2 —CH 2 —NH—C(O)—CH 2 —CH 2 —, —C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, —NH—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, and —O—C(O)—NH—(CH 2 ) 1-6 —NH—C(O)—, —O—C(O)—NH—[CH 2 ] h —(OCH 2 CH 2 ) j —, —NH—C(O)—O—[CH 2 ] h -(OCH 2 CH 2 ) j —, bivalent cycloalkyl group, —O—, —S—, —N(R 6 )—, and combinations thereof, wherein R 6 is H or an organic radical selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl and substituted aryl, (h) is zero to six, and (j) is zero to 20.

10. The polymeric reagent of claim 9 , wherein each polymer arm comprising two polymer segments linked by a linkage that is cleavable in vivo.

11. A conjugate comprising the reaction product of a biologically active agent and a polymeric reagent according to claim 1 .

Assignments (6)
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 28571, FRAME 0141 Recorded Oct 14, 2015
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: NEKTAR THERAPEUTICS
Reel/Frame 036866/0700 →
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 →
GRANT OF SECURITY INTEREST Recorded Jul 17, 2012
From: NEKTAR THERAPEUTICS
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 028571/0141 →
MERGER Recorded Aug 31, 2009
From: NEKTAR THERAPEUTICS AL, CORPORATION
To: NEKTAR THERAPEUTICS
Reel/Frame 023196/0394 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2008
From: MCMANUS, SAMUEL P.; KOZLOWSKI, ANTONI
To: NEKTAR THERAPEUTICS AL, CORPORATION
Reel/Frame 021919/0929 →