Experimental designs for optimizing the purification of immunoglobulin G by mixed-mode chromatography

J Chromatogr B Analyt Technol Biomed Life Sci. 2019 Sep 1:1125:121719. doi: 10.1016/j.jchromb.2019.121719. Epub 2019 Jul 16.

Abstract

The main aim of this study was to define the optimal adsorption and elution conditions for the purification of human immunoglobulin G (IgG) by mixed-mode chromatography using the multimodal resin Capto MMC. To this end, Central Composite Experimental Design (ED) was performed for both the adsorption and desorption stages. In the first case, the conditions were systematically studied in batch mode while in the latter case, these were performed in column. For both studies, the experimental design was conducted using high-purity human IgG samples. Buffer pH and concentration as well as the salt concentration were the parameters under study in the ED. Adsorption kinetics and equilibrium experiments were performed under the best conditions defined in the ED (phosphate buffer 60 mmol/L, pH 6.75, no salt). The equilibrium experimental data were fit to the Langmuir equation, with maximum uptake qmax equal to 549.2 mg/g. The qmax value found for IgG in Capto MMC was quite high as compared to other chromatographic techniques that employ single modes of interaction. Regarding elution, the best conditions were obtained with acetate buffer (56.40 mmol/L), pH 5.2 and 0.2 mol/L NaCl. An ultimate recovery of 46.96% for high-purity IgG was achieved. Thus, the effectiveness of Capto MMC for IgG adsorption and recovery could be confirmed. Moreover, electrophoretic runs in the human serum indicated that although co-elution of HSA and IgG proteins occurs, substantial HSA removal and a high IgG recovery were achieved in the elution step.

Keywords: Capto MMC; Human serum; Protein.

Publication types

  • Evaluation Study

MeSH terms

  • Adsorption
  • Chromatography / instrumentation
  • Chromatography / methods*
  • Humans
  • Immunoglobulin G / chemistry
  • Immunoglobulin G / isolation & purification*
  • Kinetics
  • Research Design

Substances

  • Immunoglobulin G