Isolation of human fibrinogen by axial and radial flow chromatography from Nitschmann fraction I

An axial column (3 x 2.6 cm) and a radial flow column (3.5 x 5 cm) packed with DEAE Sepharose Fast Flow media had been evaluated for the separation of human fibrinogen. Nitschmann fraction I dissolved in buffered saline (0.015 M NaCl buffered with 0.06 M Tris/HCl to pH 7.5) was the starting material. Under radial flow conditions, sample flow up to 15 ml min super(-1) (i.e., 18 bed volumes h super(-1)) was achieved. The operating pressures were below 0.2 MPa, even though the elution velocity was 30 ml min super(-1) (i.e., 36 bed volumes h super(-1)).