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US3933996A Expired / Lapsed US ⏱️ 0.0 years remaining

Composition comprising radioactive labeled-fibrinogen and albumin

Assignee: GE Healthcare Ltd
•
Filing: 1973-06-19
•
Granted: 1976-01-20
•
Expires: 1993-06-19
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Abstract

Abstract The stability of fibrinogen is improved by mixing it with albumin, preferably at least 5 parts by weight of albumin per part by weight of fibrinogen. By this invention, iodinated (125I) human fibrinogen can be stabilised with human serum albumin for use in the diagnosis of thrombi.

Inventors

  • 👤 John Cecil Charlton
  • 👤 David Lawrence Gravett

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 00:30
CPC Classifications
A; A61; A61K; A61K51/00; A61K51/02; A61K51/04; A61K51/08; A61K38/00; A61K38/16; A61K38/17; A61K38/36; A61K38/363; A61K2121/00

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 35 words
A solid product comprising one part by weight of fibrinogen labelled with a radioactive iodine isotope, and from 1 to 1,000 parts by weight of albumin to reduce or prevent unwanted decomposition of the fibrinogen.
Claim 2
Dependent Claim 35 words
A solid product comprising one part by weight of fibrinogen labelled with a radioactive iodine isotope, and from 1 to 1,000 parts by weight of albumin to reduce or prevent unwanted decomposition of the fibrinogen.
Claim 3
Dependent Claim 15 words
A solid product as claimed in claim 1, wherein the fibrinogen is labelled with iodine-125.
Claim 4
Dependent Claim 21 words
A solid product as claimed in claim 1, wherein the fibrinogen is human fibrinogen and the albumin is human serum albumin.
Claim 5
Dependent Claim 25 words
A solid product as claimed in claim 1, containing at least 5 parts by weight of the albumin per part by weight of the fibrinogen.
Claim 6
Dependent Claim 25 words
A solid product as claimed in claim 1, containing 20 - 1,000 parts by weight of the albumin per part by weight of the fibrinogen.
Claim 7
Dependent Claim 49 words
A method of making the solid product claimed in claim 1, which comprises removing water from an aqueous solution or suspension of one part by weight of the fibrinogen containing from 1 to 1,000 parts by weight of the albumin to reduce or prevent unwanted decomposition of the fibrinogen.
Claim 8
Dependent Claim 16 words
A method as claimed in claim 6, wherein the removal of water is effected by freeze-drying.
Claim 9
Dependent Claim 30 words
A method as claimed in claim 6, wherein the aqueous solution or suspension contains 20 - 1,000 parts by weight of the albumin per part by weight of the fibrinogen.
Claim 10
Dependent Claim 38 words
A solid product comprising fibrinogen iodinated with iodine-125 and from 5 to 1000 parts by weight of albumin per part by weight of fibrinogen, wherein the proportion ##EQU2## remains above 0.5 during storage for one month at 2°C.
Claim 11
Dependent Claim 38 words
A solid product comprising fibrinogen iodinated with iodine-125 and from 5 to 1000 parts by weight of albumin per part by weight of fibrinogen, wherein the proportion ##EQU2## remains above 0.5 during storage for one month at 2°C.
Claim 12
Dependent Claim 25 words
A solid product as claimed in claim 9, containing 20 - 1,000 parts by weight of the albumin per part by weight of the fibrinogen.

References Cited (Backward Citations)

US2085391A Cited
US3674900A Cited
US3803299A Cited
US3784453A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-01-19 1979-07-21 1980-01-20 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-01-19 1983-07-21 1984-01-20 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-01-19 1987-07-21 1988-01-20 $7700.00 Window Closed / Lapsed

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