Radar chart array analysis to visualize effects of formulation variables on IgG1 particle formation as measured by multiple analytical techniques

J Pharm Sci. 2013 Dec;102(12):4256-67. doi: 10.1002/jps.23738. Epub 2013 Oct 9.

Abstract

This study presents a novel method to visualize protein aggregate and particle formation data to rapidly evaluate the effect of solution and stress conditions on the physical stability of an immunoglobulin G (IgG) 1 monoclonal antibody (mAb). Radar chart arrays were designed so that hundreds of microflow digital imaging (MFI) solution measurements, evaluating different mAb formulations under varying stresses, could be presented in a single figure with minimal loss of data resolution. These MFI radar charts show measured changes in subvisible particle number, size, and morphology distribution as a change in the shape of polygons. Radar charts were also created to visualize mAb aggregate and particle formation across a wide size range by combining data sets from size-exclusion chromatography, Archimedes resonant mass measurements, and MFI. We found that the environmental/mechanical stress condition (e.g., heat vs. agitation) was the most important factor in influencing the particle size and morphology distribution with this IgG1 mAb. Additionally, the presence of NaCl exhibited a pH and stress-dependent behavior resulting in promotion or inhibition mAb particle formation. This data visualization technique provides a comprehensive analysis of the aggregation tendencies of this IgG1 mAb in different formulations with varying stresses as measured by different analytical techniques.

Keywords: Archimedes; data visualization; formulation; microflow imaging; monoclonal antibody; morphology; particle size; protein aggregation; stability.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calorimetry, Differential Scanning
  • Chromatography, Gel
  • Image Processing, Computer-Assisted / methods
  • Immunoglobulin G / chemistry*
  • Microscopy / methods
  • Particle Size
  • Protein Conformation
  • Protein Stability*
  • Sodium Chloride / chemistry
  • Spectrometry, Fluorescence

Substances

  • Immunoglobulin G
  • Sodium Chloride