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US4738843A Expired / Lapsed US ⏱️ 0.0 years remaining

Anti-tumor substance of immunoglobulin and melphalan and process for producing the same

Assignee: Kureha Corp
•
Filing: 1987-01-20
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Granted: 1988-04-19
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Expires: 2007-01-20
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Abstract

Abstract Disclosed herein are an anti-tumor substance obtained by bonding an anti-tumor agent to human immunoglobulin, and a process for producing the same.

Inventors

  • 👤 Yoshiharu Oguchi
  • 👤 Koichi Niimura
  • 👤 Takayoshi Fujii
  • 👤 Masahiko Fujii
  • 👤 Kenichi Matsunaga
  • 👤 Chikao Yoshikumi

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 12:32
CPC Classifications
A; A61; A61K; A61K39/00; A61K39/395; A61K47/00; A61K47/50; A61K47/51; A61K47/68; A61K47/6801; A61K47/6803; A61K47/6807; A61K47/6809; A61P; A61P35/00; Y; Y10; Y10S; Y10S424/00; Y10S424/809; Y10S530/00; Y10S530/866

Claims Analysis

Total Claims: 24
Claim 1
Independent Claim 108 words
An anti-tumor substance manufactured by a process comprising: (a) dissolving melphalan or ester thereof in aqueous solvent; (b) adding a bonding agent, selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid, to the aqueous solution, and then adding human immunoglobulin obtained from a normal healthy person to said aqueous solution, and thereby reacting said human immunoglobulin and said melphalan or ester thereof at a temperature of -30° to 50° C. for 1 minute to 48 hours; and (c) subjecting the thus produced reaction product to purification by means of a method selected from the group consisting of salting out, precipitation, recrystallization, elution and column-fractionation.
Claim 2
Dependent Claim 108 words
An anti-tumor substance manufactured by a process comprising: (a) dissolving melphalan or ester thereof in aqueous solvent; (b) adding a bonding agent, selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid, to the aqueous solution, and then adding human immunoglobulin obtained from a normal healthy person to said aqueous solution, and thereby reacting said human immunoglobulin and said melphalan or ester thereof at a temperature of -30° to 50° C. for 1 minute to 48 hours; and (c) subjecting the thus produced reaction product to purification by means of a method selected from the group consisting of salting out, precipitation, recrystallization, elution and column-fractionation.
Claim 3
Dependent Claim 14 words
The anti-tumor substance according to claim 1, wherein said bonding agent is a carbodiimide.
Claim 4
Dependent Claim 25 words
The anti-tumor substance according to claim 2, wherein said carbodiimide is one selected from the group consisting of 1-ethyl-3,3-dimethylaminopropyl carbodiimide, dicyclohexyl carbodiimide and morpholinoethyl carbodiimide.
Claim 5
Dependent Claim 15 words
The anti-tumor substance according to claim 1, wherein said ester is a lower alkyl ester.
Claim 6
Dependent Claim 16 words
The anti-tumor substance according to claim 4, wherein said lower alkyl ester is a methyl ester.
Claim 7
Dependent Claim 13 words
The anti-tumor substance according to claim 1, wherein said human immunoglobulin is IgG.
Claim 8
Dependent Claim 15 words
The anti-tumor substance according to claim 1, wherein said human immunoglobulin is F(ab') 2 .
Claim 9
Dependent Claim 53 words
A pharmaceutical composition in dosage unit form comprising an effective amount of an anti-tumor substance obtained by bonding melphalan or ester thereof to human immunoglobulin derived from a normal healthy person using a bonding agent, selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid, as the active ingredient thereof.
Claim 10
Dependent Claim 53 words
A pharmaceutical composition in dosage unit form comprising an effective amount of an anti-tumor substance obtained by bonding melphalan or ester thereof to human immunoglobulin derived from a normal healthy person using a bonding agent, selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid, as the active ingredient thereof.
Claim 11
Dependent Claim 13 words
The pharmaceutical composition according to claim 8, wherein said bonding agent is carbodiimide.
Claim 12
Dependent Claim 25 words
The pharmaceutical composition according to claim 9, wherein said carbodiimide is one selected from the group consisting of 1-ethyl-3,3-dimethylaminopropyl carbodiimide, dicyclohexyl carbodiimide and morpholinoethyl carbodiimide.
Claim 13
Dependent Claim 15 words
The pharmaceutical composition according to claim 8, wherein said ester is a lower alkyl ester.
Claim 14
Dependent Claim 16 words
The pharmaceutical composition according to claim 11, wherein said lower alkyl ester is a methyl ester.
Claim 15
Dependent Claim 13 words
The pharmaceutical composition according to claim 8, wherein said human immunoglobulin is IgG.
Claim 16
Dependent Claim 15 words
The pharmaceutical composition according to claim 8, wherein said human immunoglobulin is F(ab') 2 .
Claim 17
Independent Claim 68 words
A method for treating a tumor selected from the group consisting of human cancers of breast, lung, esophagus, stomach, colon, kidney, prostate, gallbladder and bone marrow, which comprises administering an effective amount of a compound obtained by bonding melphalan or ester thereof to human immunoglobulin derived from a normal healthy person using a bonding agent selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid.
Claim 18
Independent Claim 68 words
A method for treating a tumor selected from the group consisting of human cancers of breast, lung, esophagus, stomach, colon, kidney, prostate, gallbladder and bone marrow, which comprises administering an effective amount of a compound obtained by bonding melphalan or ester thereof to human immunoglobulin derived from a normal healthy person using a bonding agent selected from the group consisting of carbodiimides, glutaraldehyde, diethylmalonimidate, isocyanate and polyglutamic acid.
Claim 19
Dependent Claim 13 words
The method according to claim 15, wherein said bonding agent is a carbodiimide.
Claim 20
Dependent Claim 24 words
The method according to claim 16, wherein said carbodiimide is one selected from the group consisting of 1-ethyl-3,3-dimethylaminopropyl carbodiimide, dicyclohexyl carbodiimide and morpholinoethyl carbodiimide.
Claim 21
Dependent Claim 14 words
The method according to claim 15, wherein said ester is a lower alkyl ester.
Claim 22
Dependent Claim 15 words
The method according to claim 18, wherein said lower alkyl ester is a methyl ester.
Claim 23
Dependent Claim 13 words
The method according to claim 15, wherein said human immunoglobulin is Ig G.
Claim 24
Dependent Claim 14 words
The method according to claim 15, wherein said human immunoglobulin is F(ab') 2 .

References Cited (Backward Citations)

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US4093607A Cited
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US4340535A Cited
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US4414148A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-04-19 1991-10-19 1992-04-19 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-04-19 1995-10-19 1996-04-19 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-04-19 1999-10-19 2000-04-19 $7700.00 Window Closed / Lapsed

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