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US4027013A Expired / Lapsed US ⏱️ 0.0 years remaining

Clottable fibrinogen free factor VIII and albumin product and process

Assignee: Individual
•
Filing: 1976-01-22
•
Granted: 1977-05-31
•
Expires: 1996-01-22
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Abstract

Abstract Lyophilizable, clottable fibrinogen free, Factor VIII is produced on a commercial scale from a fibrinogen containing Factor VIII concentrate by sequentially, precipitating a major portion of the clottable fibrinogen by the addition of an ethylene oxide-polyoxypropylene block copolymer, clotting the remainder of the clottable fibrinogen by the addition of a small amount of a thrombin mimetic enzyme which does not decrease the potency of the Factor VIII, and adding human albumin to the resultant clottable fibrinogen free Factor VIII to stabilize its potency during lyophilization.

Inventors

  • 👤 Rodger L. Bick
  • 👤 Lajos F. Fekete

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 16:47
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; C07K14/745; C07K14/755; A; A61; A61K; A61K38/00; Y; Y10; Y10S; Y10S530/00; Y10S530/827; Y10S530/829; Y10S530/83

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 119 words
Process comprising: selecting an admixture containing clottable fibrinogen and Factor VIII; removing most of the clottable fibrinogen from said admixture to produce a clottable fibrinogen lean Factor VIII product; concentrating said product to produce a concentrate; admixing said concentrate with an amount of thrombin mimetic reagent sufficient to clot all of the clottable fibrinogen in said concentrate within approximately 24 hours without significantly impairing the potency of said Factor VIII, and allowing said clottable fibrinogen to form a clot; separating said clot and retaining a clottable fibrinogen free Factor VIII concentrate; admixing said retained clottable fibrinogen free Factor VIII concentrate with an amount of human albumin sufficient to stabilize said Factor VIII; and lyophilizing the resultant stabilized Factor VIII.
Claim 2
Dependent Claim 119 words
Process comprising: selecting an admixture containing clottable fibrinogen and Factor VIII; removing most of the clottable fibrinogen from said admixture to produce a clottable fibrinogen lean Factor VIII product; concentrating said product to produce a concentrate; admixing said concentrate with an amount of thrombin mimetic reagent sufficient to clot all of the clottable fibrinogen in said concentrate within approximately 24 hours without significantly impairing the potency of said Factor VIII, and allowing said clottable fibrinogen to form a clot; separating said clot and retaining a clottable fibrinogen free Factor VIII concentrate; admixing said retained clottable fibrinogen free Factor VIII concentrate with an amount of human albumin sufficient to stabilize said Factor VIII; and lyophilizing the resultant stabilized Factor VIII.
Claim 3
Dependent Claim 17 words
Process of claim 1 wherein approximately 90 percent of the clottable fibrinogen is removed from said admixture.
Claim 4
Dependent Claim 25 words
Process of claim 1 wherein said clottable fibrinogen lean Factor VIII product is concentrated to a Factor VIII potency of at least approximately 15 units.
Claim 5
Dependent Claim 20 words
Process of claim 1 wherein said process is carried out at a temperature of from about 10° to 35° centigrade.
Claim 6
Dependent Claim 23 words
Process of claim 1 wherein said process is carried out at a salt concentration of from about 0.05 to 0.25 molar sodium chloride.
Claim 7
Dependent Claim 19 words
Process of claim 1 wherein said process is carried out at a pH of from about 6.0 to 8.0.
Claim 8
Dependent Claim 31 words
Process of claim 1 wherein said resultant stabilized Factor VIII is lyophilized to produce a lyophilized product containing at least about 20 units of Factor VIII per milligram of human albumin.
Claim 9
Dependent Claim 42 words
A process of lyophilizing clottable fibrinogen free Factor VIII concentrate comprising: preparing an aqueous liquid admixture of said Factor VIII concentrate and at least about 0.5 percent on a weight per volume basis of human albumin; and lyophilizing said aqueous liquid admixture.
Claim 10
Dependent Claim 42 words
A process of lyophilizing clottable fibrinogen free Factor VIII concentrate comprising: preparing an aqueous liquid admixture of said Factor VIII concentrate and at least about 0.5 percent on a weight per volume basis of human albumin; and lyophilizing said aqueous liquid admixture.
Claim 11
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least about 10 units of Factor VIII per milligram of albumin.
Claim 12
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least about 10 units of Factor VIII per milligram of albumin.
Claim 13
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least approximately 100 units of Factor VIII per milligram of albumin.
Claim 14
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least approximately 100 units of Factor VIII per milligram of albumin.
Claim 15
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least approximately 250 units of Factor VIII per milligram of albumin.
Claim 16
Dependent Claim 31 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and human albumin and containing at least approximately 250 units of Factor VIII per milligram of albumin.
Claim 17
Dependent Claim 29 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and at least about 0.5 percent on a weight per volume basis of human albumin.
Claim 18
Dependent Claim 29 words
A lyophilized clottable fibrinogen free Factor VIII product comprising clottable fibrinogen free Factor VIII and at least about 0.5 percent on a weight per volume basis of human albumin.
Claim 19
Dependent Claim 118 words
Process comprising: admixing a clottable fibrinogen lean Factor VIII concentrate containing less than approximately 0.2 milligrams of clottable fibrinogen per unit of Factor VIII with from about 0.5 to 3 units per 1000 milligrams of clottable fibrinogen of a thrombin mimetic reagent that does not significantly impair the potency of said Factor VIII, and allowing the clottable fibrinogen to form a clot in the resultant admixture separating said clot from said resultant admixture and recovering a clottable fibrinogen free Factor VIII concentrate; admixing said clottable fibrinogen free Factor VIII concentrate with at least about 0.5 percent on a weight per volume basis of human albumin to stabilize said Factor VIII; and lyophilizing the resultant stabilized Factor VIII concentrate.
Claim 20
Dependent Claim 118 words
Process comprising: admixing a clottable fibrinogen lean Factor VIII concentrate containing less than approximately 0.2 milligrams of clottable fibrinogen per unit of Factor VIII with from about 0.5 to 3 units per 1000 milligrams of clottable fibrinogen of a thrombin mimetic reagent that does not significantly impair the potency of said Factor VIII, and allowing the clottable fibrinogen to form a clot in the resultant admixture separating said clot from said resultant admixture and recovering a clottable fibrinogen free Factor VIII concentrate; admixing said clottable fibrinogen free Factor VIII concentrate with at least about 0.5 percent on a weight per volume basis of human albumin to stabilize said Factor VIII; and lyophilizing the resultant stabilized Factor VIII concentrate.

References Cited (Backward Citations)

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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) 1980-05-30 1980-11-29 1981-05-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-05-30 1984-11-29 1985-05-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-05-30 1988-11-29 1989-05-31 $7700.00 Window Closed / Lapsed

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