Raman spectroscopic analysis of highly-concentrated antibodies under the acid-treated conditions

TL;DR

This study uses Raman spectroscopy to analyze conformational changes in highly-concentrated antibodies at low pH, revealing insights into aggregation behavior and stability relevant for antibody formulation.

Contribution

It demonstrates the application of Raman spectroscopy to monitor pH-induced conformational changes in high-concentration antibodies, highlighting its potential for quality evaluation.

Findings

Significant conformational changes at pH 3 detected via Raman markers.

Highest aggregation temperature observed at pH 3, indicating increased stability.

Acid-induced conformational changes are not fully reversible.

Abstract

Antibody drugs are usually formulated as highly-concentrated solutions, which would easily generate oligomer and aggregation, resulting in loss of efficacy. Although low pH increases the colloidal dispersion of antibodies, acid denaturation can be an issue. Therefore, knowing the physical properties of antibodies at low pH under high concentration conditions is an important insight into the quality evaluation of high concentration antibodies. Raman spectroscopy is a powerful tool to obtain conformational information derived from amino acid residues and secondary structures without dilution. In this study, Raman spectroscopy was used to investigate pH-induced conformational changes of antibodies at high concentrations. Raman experiments in pH 3 to 7 were performed for human serum IgG and recombinant rituximab. We detected the evident changes at pH 3 in Tyr and Trp Raman bands, which are the sensitive markers of intermolecular interactions. Thermal transition analysis over the pH range demonstrated that the transition temperature (aggregation temperature, Tagg) was highest at pH 3. Acid-treated and neutralized one showed higher Tagg than that of pH 7, indicating that acid-induced conformational changes were not completely reversible. Colloidal analyses confirmed the findings of the Raman analysis, validating Raman spectroscopy as a method for evaluating antibody conformation associated with colloidal information.