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US4278592A Expired / Lapsed US ⏱️ 0.0 years remaining

Process and apparatus for the production of sterile filtered blood clotting factors

Assignee: Individual
•
Filing: 1979-03-30
•
Granted: 1981-07-14
•
Expires: 1999-03-30
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Abstract

Abstract A process and apparatus for the manufacture of sterile filtered blood clotting factore from fibrinogen with an enrichment of Factor I is provided. The process includes the step of extracting blood from at least one donor, manufacturing fibrinogen from the blood extracted in a known manner, dissolving the fibrinogen in a buffer, and effecting a sterile filtration of the buffer-dissolved fibrinogen by means of a static filtration device at a pressure of less than 0.5 atmospheres.

Inventors

  • 👤 Arnold Seufert

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 03:42
CPC Classifications
C; C07; C07K; C07K14/00; C07K14/435; C07K14/745; C07K14/755; A; A61; A61K; A61K35/00; A61K35/12; A61K35/14; A61L; A61L2/00; A61L2/02; A61L2/022; C07K14/75; A61K38/00; A61L2103/00; A61L2103/05; A61L2103/09; Y; Y10; Y10S; Y10S530/00; Y10S530/827; Y10S530/829; Y10S530/83

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 135 words
A process for the manufacture of sterile filtered blood clotting products from fibrinogen with an enrichment of Factor 1, comprising the steps of: extracting blood from at least one donor; physically separating the blood to obtain substantially purified plasma, free of cellular componets, said separating step being carried out in a sequence of at least two centrifuging steps, to obtain plasma with an increasing degree of purity; deep freezing the purified plasma at a temperature below about minus 22° C.; thawing the plasma to produce a cyro-precipitate; drawing off the plasma present above the cyro-precipitate and manufacturing fibrinogen from said plasma in a known manner; dissolving the fibrinogen in a buffer; and effecting a sterile filtration of the buffer-dissolved fibrinogen by means of a static filtration device at a pressure of less tha 0.5 atm.
Claim 2
Dependent Claim 135 words
A process for the manufacture of sterile filtered blood clotting products from fibrinogen with an enrichment of Factor 1, comprising the steps of: extracting blood from at least one donor; physically separating the blood to obtain substantially purified plasma, free of cellular componets, said separating step being carried out in a sequence of at least two centrifuging steps, to obtain plasma with an increasing degree of purity; deep freezing the purified plasma at a temperature below about minus 22° C.; thawing the plasma to produce a cyro-precipitate; drawing off the plasma present above the cyro-precipitate and manufacturing fibrinogen from said plasma in a known manner; dissolving the fibrinogen in a buffer; and effecting a sterile filtration of the buffer-dissolved fibrinogen by means of a static filtration device at a pressure of less tha 0.5 atm.
Claim 3
Dependent Claim 15 words
The process according to claim 1, wherein said blood is extracted from a single donor.
Claim 4
Dependent Claim 22 words
The process according to claim 1, wherein said sterile filtration step is carried out in a sterile chamber to prevent secondary contamination.
Claim 5
Dependent Claim 30 words
The process according to claim 1, additionally including the step of carrying out a bubble-point test after said sterile filtration step, to ensure that the process has proceeded without error.
Claim 6
Dependent Claim 21 words
The process according to claim 1, wherein said process steps are repeated following purification and autoclaving of the filtration apparatus employed.
Claim 7
Dependent Claim 58 words
The process according to claim 1, wherein said manufacturing step comprises the following substeps: cooling the plasma drawn off down to 0° C. and mixing said cooled plasma with alcohol so as to achieve a solution containing about 8% alcohol and to thereby obtain a fibrinogen precipitate; and physicially separating said fibrinogen precipitate from said solution by centrifuging.

References Cited (Backward Citations)

US4141887A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-07-13 1985-01-12 1985-07-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-07-13 1989-01-12 1989-07-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-07-13 1993-01-12 1993-07-14 $7700.00 Window Closed / Lapsed

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