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EP0875253A2 Expired / Lapsed EP ⏱️ 0.0 years remaining

Chondroitinase compositions

Assignee: Seikagaku Corp
•
Filing: 1998-04-30
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Granted: —
•
Expires: 2018-04-30
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Abstract

Abstract This invention provides pharmaceutical compositions containing chondroitinase wherein a decrease in enzyme activity is very little even after long-term storage, and the pharmaceutical compositions are characterized in that they contain chondroitinase and a pharmaceutical carrier, and that an amount of reducing impurities per 1 g of said pharmaceutical carrier is 0.4 mL or less as a titer by a titration method with 0.01 N of ammonium ceric nitrate.

Inventors

  • 👤 Shin-Ichi Ishikawa
  • 👤 Mine Higuchi

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-10-29 22:12
CPC Classifications
A; A61; A61K; A61K47/00; A61K47/06; A61K47/26; A61K38/00; A61K38/16; A61K38/43; A61K38/51; A61K47/08; A61K47/10; A61K9/00; A61K9/0012; A61K9/0019; A61P; A61P3/00

Claims Analysis

Total Claims: 17
Claim 1
Independent Claim 46 words
A pharmaceutical composition, characterized in that it contain chondroitinase and a pharmaceutical carrier, and that an amount of reducing impurities contained in 1 g of said pharmaceutical carrier is 0.4 mL or less as a titer by a titration method with 0.01 N ammonium ceric nitrate.
Claim 2
Dependent Claim 20 words
The pharmaceutical composition according to claim 1, wherein a peroxide content in the pharmaceutical carrier is 20 ppm or less.
Claim 3
Dependent Claim 39 words
The pharmaceutical composition according to claim 1, wherein an amount of reducing impurities contained in 1 g of the pharmaceutical carrier is 0.36 mL or less as a titer by a titration method with 0.01 N ammonium ceric nitrate.
Claim 4
Dependent Claim 16 words
The pharmaceutical composition according to claim 1, wherein the pharmaceutical carrier is treated with activated carbon.
Claim 5
Dependent Claim 16 words
The pharmaceutical composition according to claim 1, wherein the pharmaceutical carrier is sucrose and/or polyethylene glycol.
Claim 6
Dependent Claim 14 words
The pharmaceutical composition according to claim 1, wherein the pharmaceutical carrier is polyethylene glycol.
Claim 7
Dependent Claim 19 words
The pharmaceutical composition according to claim 1, wherein the pharmaceutical carrier is a mixture of sucrose and polyethylene glycol.
Claim 8
Dependent Claim 24 words
The pharmaceutical composition according to claim 5, wherein the mixed ratio of polyethylene glycol and sucrose is 0/1-10/1 by weight ratio of polyethylene glycol/sucrose.
Claim 9
Dependent Claim 25 words
The pharmaceutical composition according to claim 7, wherein the mixed ratio of polyethylene glycol and sucrose is 2/1 by the weight ratio of polyethylene glycol/sucrose.
Claim 10
Dependent Claim 19 words
The pharmaceutical composition according to claim 5 or 6, wherein polyethylene glycol has an average molecular weight of 3000-4000.
Claim 11
Dependent Claim 17 words
The pharmaceutical composition according to claim 1, wherein the pharmaceutical carrier is polyoxyethylene sorbitan fatty acid ester.
Claim 12
Dependent Claim 12 words
The pharmaceutical composition according to claim 1, wherein chondroitinase is chondroitinase ABC.
Claim 13
Dependent Claim 19 words
The pharmaceutical composition according to claim 1, wherein specific activity of chondroitinase ABC is 300 U/mg protein or more.
Claim 14
Dependent Claim 14 words
The pharmaceutical composition according to claim 1 in the form of a freeze-dried preparation,
Claim 15
Dependent Claim 18 words
An agent consisting of the pharmaceutical composition according to claim 1 for the treatment of intervertebral disc herniation.
Claim 16
Dependent Claim 32 words
A method for the treatment of mammals with herniation, characterized in that an effective amount of the pharmaceutical composition according to claim 1 is injected into the intervertebral disc of the mammals.
Claim 17
Dependent Claim 15 words
Use of the pharmaceutical composition according to claim 1 in the intervertebral disc dissolution method.

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