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US4766106A Expired / Lapsed US ⏱️ 0.0 years remaining

Solubilization of proteins for pharmaceutical compositions using polymer conjugation

Assignee: Cetus Oncology Corp
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Filing: 1988-01-25
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Granted: 1988-08-23
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Expires: 2008-01-25
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Abstract

Abstract A pharmaceutical composition is prepared wherein a biologically active conjugated protein which is β-interferon, interleukin-2, or an immunotoxin is dissolved in an aqueous carrier medium without the presence of a solubilizing agent. The unconjugated protein, which is not water-soluble or not readily soluble in water at pH 6-8 without such solubilizing agent, is selectively conjugated to a water-soluble polymer selected from polyethylene glycol homopolymers or polyoxyethylated polyols.

Inventors

  • 👤 Nandini Katre
  • 👤 Michael J. Knauf

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 17:53
CPC Classifications
C; C07; C07K; C07K1/00; C07K1/107; C07K1/1072; C07K1/1077; A; A61; A61K; A61K38/00; A61K38/16; A61K38/17; A61K38/19; A61K38/20; A61K38/2013; A61K38/21; A61K38/215; A61K47/00; A61K47/50; A61K47/51; A61K47/56; A61K47/59; A61K47/60; A61K47/68; A61K47/6801; A61K47/6803; A61K47/6811; A61K47/6817; A61K47/6819; A61K47/6825; A61K47/6827

Claims Analysis

Total Claims: 17
Claim 1
Independent Claim 90 words
A pharmaceutical preparation comprising a non-toxic, inert, pharmaceutically acceptable aqueous carrier medium in which is dissolved an immunotherapeutic effective amount of biologically active, selectively conjugated, recombinant interleukin-2 protein, wherein the protein is covalently conjugated via up to ten amino acid residues on the protein to a water-soluble polymer selected from the group consisting of polyethylene glycol homopolymers and polyoxyethylated polyols, wherein said homopolymer is unsubstituted or substituted at one end with an alkyl group and said polyol is unsubstituted and wherein said protein in its unconjugated form is normally hydrophobic.
Claim 2
Dependent Claim 90 words
A pharmaceutical preparation comprising a non-toxic, inert, pharmaceutically acceptable aqueous carrier medium in which is dissolved an immunotherapeutic effective amount of biologically active, selectively conjugated, recombinant interleukin-2 protein, wherein the protein is covalently conjugated via up to ten amino acid residues on the protein to a water-soluble polymer selected from the group consisting of polyethylene glycol homopolymers and polyoxyethylated polyols, wherein said homopolymer is unsubstituted or substituted at one end with an alkyl group and said polyol is unsubstituted and wherein said protein in its unconjugated form is normally hydrophobic.
Claim 3
Dependent Claim 17 words
The preparation of claim 1 wherein said polymer has a molecular weight of about 300 to 100,000.
Claim 4
Dependent Claim 16 words
The preparation of claim 1 wherein said polymer has a molecular weight of 350 to 40,000.
Claim 5
Dependent Claim 29 words
The preparation of claim 1 wherein said polymer is conjugated to the protein via the 4-hydroxy-3-nitrobenzene sulfonate ester or the N-hydroxysuccinimide ester of a carboxylic acid of said polymer.
Claim 6
Dependent Claim 23 words
The preparation of claim 4 wherein said polymer is an unsubstituted polyethylene glycol homopolymer, a monomethyl polyethylene glycol homopolymer or a polyoxyethylated glycerol.
Claim 7
Dependent Claim 19 words
The preparation of claim 1 wherein the medium is at a pH of about 5-8 and contains a buffer.
Claim 8
Dependent Claim 19 words
The preparation of claim 1 wherein the medium is at a pH of about 6.5-7.8 and contains a buffer.
Claim 9
Dependent Claim 13 words
The preparation of claim 1 wherein the protein is from a human source.
Claim 10
Dependent Claim 20 words
The preparation of claim 1 wherein said protein is selectively conjugated via one or two lysine residues on the protein.
Claim 11
Dependent Claim 20 words
The preparation of claim 1 wherein said protein is selectively conjugated via three to ten lysine residues on the protein.
Claim 12
Dependent Claim 12 words
The preparation of claim 8 wherein the protein is an interleukin-2 mutein.
Claim 13
Dependent Claim 29 words
The preparation of claim 11 wherein said mutein has the amino acid(s) which are at position(s) 104 and/or 125 in the native protein substituted with a neutral amino acid.
Claim 14
Dependent Claim 33 words
The preparation of claim 12 wherein said mutein is ser 125 IL-2, des-ala 1 IL-2, des-ala 1 ser 125 IL-2, des-ala 1 ala 104 IL-2, or des-ala 1 ala 104 ser 125 IL-2.
Claim 15
Dependent Claim 20 words
The preparation of claim 1 wherein said protein is selectively conjugated via up to ten lysine residues on the protein.
Claim 16
Dependent Claim 59 words
A composition comprising biologically active, normally hydrophobic recombinant interleukin-2 protein that is covalently conjugated via up to ten amino acid residues on the protein to a water-soluble polymer selected from the group consisting of polyethylene glycol homopolymers and polyoxyethylated polyols, wherein said homopolymer is unsubstituted or substituted at one end with an alkyl group and said polyol is unsubstituted.
Claim 17
Dependent Claim 59 words
A composition comprising biologically active, normally hydrophobic recombinant interleukin-2 protein that is covalently conjugated via up to ten amino acid residues on the protein to a water-soluble polymer selected from the group consisting of polyethylene glycol homopolymers and polyoxyethylated polyols, wherein said homopolymer is unsubstituted or substituted at one end with an alkyl group and said polyol is unsubstituted.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-08-23 1992-02-22 1992-08-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-08-23 1996-02-22 1996-08-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-08-23 2000-02-22 2000-08-23 $7700.00 Window Closed / Lapsed

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