The Role of Phase Separation and Local Mobility in the Stabilization of a Lyophilized IgG2 Formulation

AAPS PharmSciTech. 2024 Nov 19;25(8):268. doi: 10.1208/s12249-024-02984-7.

Abstract

The utility of employing solid-state NMR (SSNMR) to assess parameters governing the stability of a lyophilized IgG2 protein was the focus of the present work. Specifically, the interaction between the sugar stabilizer (sucrose) and protein component was measured using SSNMR and compared to physical and chemical stability data obtained from thermally stressed samples. 1H T1 and 1H T1⍴ relaxation times were measured by SSMNR for 5 different formulation conditions, and the resultant values were used to examine local mobility and phase separation, respectively. From the SSNMR measurements, it was found local mobility decreased as the sucrose to protein weight ratio increased. The decrease in local mobility corresponded to an increase in storage stability (both chemical and physical) of the lyophilized solids up to a critical weight ratio of sucrose to protein. Additionally, 1H T1⍴ measurements obtained on formulations having higher protein to sucrose weight ratios indicated phase separation of the protein and sucrose phases was occurring, at least on a small scale. Along with an increase in local mobility, phase separation in these specific formulations is thought to have played a role in their decreased storage stability in the solid state.

Keywords: local mobility; lyophilization; protein formulation; solid-state NMR spectroscopy.

MeSH terms

  • Chemistry, Pharmaceutical* / methods
  • Drug Stability*
  • Excipients / chemistry
  • Freeze Drying* / methods
  • Immunoglobulin G* / chemistry
  • Magnetic Resonance Spectroscopy / methods
  • Phase Separation
  • Protein Stability
  • Sucrose* / chemistry

Substances

  • Immunoglobulin G
  • Sucrose
  • Excipients