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US3717502A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for providing anticoagulant surfaces onto articles

Assignee: Tokyo Medical and Dental University
•
Filing: 1970-06-15
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Granted: 1973-02-20
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Expires: 1990-06-15
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Abstract

Abstract This invention relates to a method for providing anticoagulant surfaces onto articles by treating said articles with an organic solvent solution of a co-precipitated material produced by mixing an aqueous solution of heparin and an aqueous solution of a certain cation surface active agent. Said solution may include an organic solvent-soluble plastic material.

Inventors

  • 👤 E Masuhara
  • 👤 I Yohji

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-22 21:51
CPC Classifications
A; A61; A61L; A61L33/00; A61L33/0005; A61L33/0011; A61L33/0017; C; C03; C03C; C03C17/00; C03C17/28; Y; Y10; Y10S; Y10S623/00; Y10S623/92; Y10S623/921

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 50 words
A method for providing anticoagulant surfaces onto articles made of plastic materials or glass or metals, characterized by coating said articles with an organic solvent solution containing an organic solvent-soluble plastic material and a co-precipitated material produced by mixing heparin with a cationic surface active agent in an aqueous medium.
Claim 2
Independent Claim 50 words
A method for providing anticoagulant surfaces onto articles made of plastic materials or glass or metals, characterized by coating said articles with an organic solvent solution containing an organic solvent-soluble plastic material and a co-precipitated material produced by mixing heparin with a cationic surface active agent in an aqueous medium.
Claim 3
Dependent Claim 37 words
A method according to claim 1 wherein the cationic surface active agent is selected from the group consisting of dimethyl alkyl benzyl ammonium chloride, benzyldimethyl-2-(2-(p-1,1,3,3-tetramethylbutyl phenoxy) ethoxy) ethyl ammonium chloride, alkyl-trimethyl ammonium chloride and dilauryl-dimethyl ammonium chloride.
Claim 4
Dependent Claim 62 words
A method according to claim 1 wherein the organic solvent-soluble plastic material is selected from the group consisting of polyvinyl chloride, polymethacrylic esters, polyacrylic esters, polyacrylonitrile, polyvinylbutyral, polyepichlorohydrin, polyurethane and polyamides, and the cationic surface active agent is selected from the group consisting of dimethyl alkyl benzyl ammonium chloride, benzyldimethyl-2-(2-(p-1,1,3,3-tetramethylbutyl phenoxy) ethoxy) ethyl ammonium chloriDe, alkyl-trimethyl ammonium chloride and dilauryl-dimethyl ammonium chloride.
Claim 5
Independent Claim 59 words
A method for providing anticoagulant surfaces onto articles made of plastic materials or glass or metals, characterized by coating said articles with an organic solvent solution containing an organic solvent-soluble plastic material, a member selected from 4,4''-diphenylmethane diisocyanate and tolylene diisocyanate and a co-precipitated material produced by mixing heparin with a cationic surface active agent in an aqueous medium.
Claim 6
Independent Claim 59 words
A method for providing anticoagulant surfaces onto articles made of plastic materials or glass or metals, characterized by coating said articles with an organic solvent solution containing an organic solvent-soluble plastic material, a member selected from 4,4''-diphenylmethane diisocyanate and tolylene diisocyanate and a co-precipitated material produced by mixing heparin with a cationic surface active agent in an aqueous medium.
Claim 7
Dependent Claim 62 words
A method according to claim 4 wherein the organic solvent-soluble plastic material is selected from the group consisting of polyvinyl chloride, polymethacrylic esters, polyacrylic esters, polyacrylonitrile, polyvinylbutyral, polyepichlorohydrin, polyurethane and polyamides, and the cationic surface active agent is selected from the group consisting of dimethyl alkyl benzyl ammonium chloride, benzyldimethyl-2-(2-(p-1,1,3,3-tetramethylbutyl phenoxy) ethoxy) ethyl ammonium chloride, alkyl-trimethyl ammonium chloride and dilauryl-dimethyl ammonium chloride.

References Cited (Backward Citations)

US2970066A Cited
FR1459646A Cited
US3634123A Cited
US3453194A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1976-02-20 1976-08-21 1977-02-20 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1980-02-20 1980-08-21 1981-02-20 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1984-02-20 1984-08-21 1985-02-20 $7700.00 Window Closed / Lapsed

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