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US4251510A Expired / Lapsed US ⏱️ 0.0 years remaining

Intravenously injectable solution of plasma protein fraction free from bradykinin, kininogen and prekallikrein activators and processes for its production

Assignee: Bayer Corp
•
Filing: 1979-08-15
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Granted: 1981-02-17
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Expires: 1999-08-15
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Abstract

Abstract Plasma Protein Fraction substantially free of bradykinin, kininogen and prekallikrein activators is obtained by treating Cohn Supernatant II plus III at about neutrality with a siliceous substance for a period of time sufficient to bring about essentially complete conversion of intrinsic kininogen into bradykinin. Subsequently, after being separated from Cohn Fraction IV-1, the Plasma Protein Fraction is reconstituted and held for a period of time sufficient to allow substantially complete destruction of bradykinin by kininase. Methods are disclosed for the destruction of prekallikrein activators which may be present in Plasma Protein Fraction.

Inventors

  • 👤 Donald L. Tankersley

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 06:56
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; C07K14/76; C07K14/765; C07K14/46; C07K14/47; A; A61; A61K; A61K38/00; Y; Y10; Y10S; Y10S530/00; Y10S530/827; Y10S530/829; Y10S530/83; Y10S530/831

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 121 words
A sterile aqueous solution of heat-stable Plasma Protein Fraction (Human) suitable for injection, wherein about 5 grams of Plasma Protein Fraction (Human) per 100 milliliters of sterile aqueous solution contains no greater than about 16 milli-units per milliliter Factor XIIa and fragments thereof capable of activating prekallikrein, no greater than about 10 nanograms bradykinin equivalents per milliliter of kininogen, and less than about 10 nanograms per milliliter of bradykinin, said Plasma Protein Fraction (Human) being a mixture of constituent plasma protein isolated from human plasma by a modified Cohn fractionation process and containing at least 83% albumin and no more than 17% alpha and beta globulins having molecular weights similar to that of albumin and no more than 1% gamma globulin.
Claim 2
Dependent Claim 121 words
A sterile aqueous solution of heat-stable Plasma Protein Fraction (Human) suitable for injection, wherein about 5 grams of Plasma Protein Fraction (Human) per 100 milliliters of sterile aqueous solution contains no greater than about 16 milli-units per milliliter Factor XIIa and fragments thereof capable of activating prekallikrein, no greater than about 10 nanograms bradykinin equivalents per milliliter of kininogen, and less than about 10 nanograms per milliliter of bradykinin, said Plasma Protein Fraction (Human) being a mixture of constituent plasma protein isolated from human plasma by a modified Cohn fractionation process and containing at least 83% albumin and no more than 17% alpha and beta globulins having molecular weights similar to that of albumin and no more than 1% gamma globulin.
Claim 3
Dependent Claim 13 words
The solution of claim 1 wherein the protein concentration is about 5 percent.
Claim 4
Dependent Claim 20 words
The solution of claim 1 which includes a stabilizer selected from the group consisting of sodium acetyltryptophan and sodium caprylate.

References Cited (Backward Citations)

US2958628A Cited
US3100737A Cited
US3686395A Cited
US3876775A Cited
US4000121A Cited
US4017470A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-02-17 1984-08-18 1985-02-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-02-17 1988-08-18 1989-02-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-02-17 1992-08-18 1993-02-17 $7700.00 Window Closed / Lapsed

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