Fibrinogen purification
View Patent ↗The present invention relates to a process for purifying fibrinogen, which comprises one or more process steps in which one or more contaminating proteins are depleted by negative chromatography and/or negative adsorption using cation exchanger, hydrophobic gel and/or dye gel. In addition, the invention relates to the fibrinogen which is obtained by the process of the invention and which is notable for improved stability, and to the production and use of pharmaceutical preparations comprising this fibrinogen.
1. A process for purifying fibrinogen from a fibrinogen solution containing at least one contaminating protein, comprising:
subjecting the fibrinogen solution to negative chromatography using at least one of a cation exchanger, hydrophobic gel and dye gel, wherein the negative chromatography is performed using either column chromatography or batch chromatography, wherein interaction of the at least one contaminating protein with a stationary phase over which the fibrinogen solution passes is stronger than interaction of fibrinogen with the stationary phase, such that a majority of the fibrinogen is eluted from a column of the column chromatography, or remains in a supernatant of the batch chromatography, at the same time that the at least one contaminating protein is mainly bound to the stationary phase.
2. The process as claimed in claim 1 , wherein the functional group of the cation exchanger is a sulfomethyl group, sulfopropyl group, or carboxymethyl group or other suitable negatively charged functional group.
3. The process as claimed in claim 1 , wherein the hydrophobic gel comprises alkyl groups as functional groups.
4. The process as claimed in claim 1 , wherein the hydrophobic gel comprises phenyl groups or derivatized phenyl groups as functional groups.
5. The process as claimed in claim 3 , wherein the hydrophobic gel comprises propyl, butyl, pentyl, hexyl or octyl groups as functional groups.
6. The process as claimed in claim 1 , wherein the dye gel is a blue dye gel.
7. The process as claimed in claim 1 , wherein the dye gel is a red or green dye gel.
8. The process as claimed in claim 1 , wherein the dye gel is at least one of Blue Hyper D, Mimetic Blue Agarose, Mimetic Blue SA P6XL, Mimetic Blue 1 P6XL, Blue Trisacryl Plus LS, Blue Uniflow, Blue Sepharose 6FF, Blue Sepharose CL 6B, Red Sepharose CL 6B, Fractogel TSK AF Green and Matrex gel Green A.
9. The process as claimed in claim 1 , wherein the negative chromatography is carried out at a pH between 5.5 and 9.
10. The process as claimed in claim 1 , wherein the yield of fibrinogen in a flow-through of the column chromatography or in a supernatant of the batch chromatography is ≧50%.
11. The process as claimed in claim 1 , wherein the negative chromatography is carried out in the presence of substances which weaken the binding of plasminogen to fibrinogen.
12. The process as claimed in claim 1 , wherein the fibrinogen solution comprises at least one of blood, milk from transgenic animals or a fermentation supernatant or a fraction produced therefrom.
13. The process as claimed in claim 12 , wherein the fibrinogen solution comprises human plasma, a plasma fraction or cryoprecipitate.
14. The process as claimed in claim 1 , further comprising at least one precipitation of fibrinogen.
15. The process as claimed in claim 14 , wherein the fibrinogen is precipitated with at least one amino acid.
16. The process as claimed in claim 1 , further comprising removing plasminogen on gel material comprising lysine or lysine analogs as the functional group.
17. The process as claimed in claim 1 , further comprising inactivation or depletion of infectious particles.
18. The process as claimed in claim 10 , wherein the yield of fibrinogen in the flow-through of the negative chromatography is ≧70%.
19. The process as claimed in claim 15 , wherein the at least one amino acid is glycine.
20. A process for purifying fibrinogen from a fibrinogen solution containing at least one contaminating protein, consisting essentially of:
subjecting the fibrinogen solution to negative chromatography using at least one of a cation exchanger, hydrophobic gel and dye gel, wherein the negative chromatography is performed using either column chromatography or batch chromatography;
wherein interaction of at least one contaminating protein with a stationary phase is stronger than interaction of fibrinogen with the stationary phase, such that a majority of the fibrinogen is eluted from a column of the column chromatography, or remains in a supernatant of the batch chromatography, at the same time that the at least one contaminating protein is mainly bound to the stationary phase.
21. A process for purifying fibrinogen from a fibrinogen solution containing at least one contaminating protein, comprising:
subjecting the fibrinogen solution to negative chromatography using at least one of a cation exchanger, hydrophobic gel and dye gel, wherein the negative chromatography is performed using either column chromatography or batch chromatography;
wherein interaction of at least one contaminating protein with a stationary phase over which the fibrinogen solution passes is stronger than interaction of fibrinogen with the stationary phase, such that fibrinogen is mainly eluted from a column of the column chromatography, or remains in a supernatant of the batch chromatography, at the same time that the at least one contaminating protein is mainly bound to the stationary phase; and
wherein throughout the process no more than 50% of the fibrinogen is bound within the negative chromatography.