We used chromatography to remove endotoxin during the purification of rHSA-IFNα2b (recombinant human serum albumin-Interferon alpha 2b, rHSA- IFNα2b). Affinity chromatography of Blue-sepharose, hydrophobic interaction chromatography of SOURCE 15 ISO, ion exchange chromatography of Q Sepharose Fast Flow and gel filtration of sephadex G25 Coarse were applied consequently. The endotoxin levels were measured by Limulus Amebocyte Lysate gel-clot assay. Protein purity and concentration were determined by RP-HPLC. Up to 99.9% endotoxin of rHSA-IFNα2b was removed and to a concentration of 1 EU/mg. This process was effective to purify rHSA-IFNα2b and remove exdotoxin simultaneously.