Login / Signup

Membrane Adsorber for the Fast Purification of a Monoclonal Antibody Using Protein A Chromatography.

Chantal BrämerLisa TünnermannAlina Gonzalez SalcedoOscar-Werner ReifDörte SolleThomas ScheperSascha Beutel
Published in: Membranes (2019)
Monoclonal antibodies are conquering the biopharmaceutical market because they can be used to treat a variety of diseases. Therefore, it is very important to establish robust and optimized processes for their production. In this article, the first step of chromatography (Protein A chromatography) in monoclonal antibody purification was optimized with a focus on the critical elution step. Therefore, different buffers (citrate, glycine, acetate) were tested for chromatographic performance and product quality. Membrane chromatography was evaluated because it promises high throughputs and short cycle times. The membrane adsorber Sartobind® Protein A 2 mL was used to accelerate the purification procedure and was further used to perform a continuous chromatographic run with a four-membrane adsorber-periodic counter-current chromatography (4MA-PCCC) system. It was found that citrate buffer at pH 3.5 and 0.15 M NaCl enabled the highest recovery of >95% and lowest total aggregate content of 0.26%. In the continuous process, the capacity utilization of the membrane adsorber was increased by 20%.
Keyphrases
  • monoclonal antibody
  • mass spectrometry
  • high speed
  • tandem mass spectrometry
  • liquid chromatography
  • high performance liquid chromatography
  • simultaneous determination
  • protein protein
  • amino acid
  • high resolution