Abstract A therapeutic composition effective on contact with thrombin at a site of treatment in a patient as a tissue adhesive, hemostat or sealant, said composition comprising non-autologous, non-single donor mammalian fibrinogen that is capable of polymerizing when provided in solution at said site at a concentration of about 30 mg/ml thereof or less, to a fibrin network having therapeutically effective strength, wherein said composition contains less than about 30% (w/w), based on total protein mass present therein, of proteins other than fibrinogen, and further comprises a sufficient amount of one or more low molecular weight physiologically-compatible solutes such that said composition, if formulated as a lyophilized material, can be reconstituted therefrom at room temperature in sterile water for injection in about 30 minutes or less, at about 25 mg/ml of said fibrinogen. Additionally, methods for producing and maintaining said composition, and methods for the use thereof.
A method for producing a therapeutic fibrinogen composition comprising three or more steps including at least the steps of: (A) precipitating fibrinogen from a sample of mammalian blood plasma with polyethylene glycol 1000; (B) resuspending said fibrinogen in solution; and (C) reprecipitating said fibrinogen with glycine; wherein precipitation of said fibrinogen with polyethylene glycol is performed only once; and wherein about 90 to 95% of the fibrinogen present in said sample is recovered.
Claim 2
Independent Claim
73 words
A method for producing a therapeutic fibrinogen composition comprising three or more steps including at least the steps of: (A) precipitating fibrinogen from a sample of mammalian blood plasma with polyethylene glycol 1000; (B) resuspending said fibrinogen in solution; and (C) reprecipitating said fibrinogen with glycine; wherein precipitation of said fibrinogen with polyethylene glycol is performed only once; and wherein about 90 to 95% of the fibrinogen present in said sample is recovered.