This article presents the multicolumn countercurrent solvent gradient purification (MCSGP) process, which uses three chromatographic columns, and incorporates the principle of countercurrent operation and the possibility of using solvent gradients. A MCSGP prototype has been built using commercial chromatographic equipment. The application of this prototype for purifying a MAb from a clarified cell culture supernatant using only a commercial, preparative cation exchange resin shows that the MCSGP process can result in purities and yields comparable to those of purification using Protein A. The second application example for the MCSGP prototype is the separation of three MAb variants using a preparative weak cation-exchange resin. Although the intermediately eluting MAb variant can only be obtained with 80% purity at recoveries close to zero in a batch chromatographic process, the MCSGP process can provide 90% purity at 93% yield. A numerical comparison of the MCSGP process with the batch chromatographic process, and a batch chromatographic process including ideal recycling, has been performed using an industrial polypeptide purification as the model system. It shows that the MCSGP process can increase the productivity by a factor of 10 and reduce the solvent requirement by 90%.
Besides batch solvent gradient chromatography and its derivative including a recycle, the multicolumn countercurrent solvent gradient purification (MCSGP) process is a third suitable process developed recently to perform three-fraction separations of biomolecules.3–5 This process involves three columns and continuously purifies a complex feed mixture into three fractions, thereby incorporating solvent gradients.
Conventional multicolumn processes such as simulated-moving-bed (SMB) chromatography cannot be used for the purification of biomolecules, because an SMB can only perform a binary separation and solvent gradients can not be implemented properly. SMB chromatography is therefore more suitable for a binary separation of small molecules.
This work explains the principle of the MCSGP process and shows experimental results from the MCSGP prototype for purifying a MAb from clarified cell culture supernatant (cCCS) without using protein A resin, and a separation of three MAb variants.
A numerical comparison between the conventional batch chromatography process and the MCSGP process with respect to yield and process productivity is also performed for a polypeptide purification. The Pareto curves obtained from the optimization procedure are compared and the performance superiority of the MCSGP process is explained.
Principle of the MCSGP Process